We use cookies to enhance the usability of our website. If you continue, we'll assume that you are happy to receive all cookies. More information. Don't show this again.
FAM111A
HPA
RESOURCES
  • TISSUE
  • BRAIN
  • SINGLE CELL
  • SUBCELLULAR
  • CANCER
  • BLOOD
  • CELL LINE
  • STRUCTURE & INTERACTION
ABOUT
  • INTRODUCTION
  • HISTORY
  • ORGANIZATION
  • PUBLICATIONS
  • ANTIBODY SUBMISSION
  • ANTIBODY AVAILABILITY
  • ACKNOWLEDGMENTS
  • CONTACT
NEWS
  • NEWS ARTICLES
  • PRESS ROOM
LEARN
  • DICTIONARY
  • PROTEIN CLASSES
  • PROTEIN EVIDENCE
  • METHODS
  • EDUCATIONAL VIDEOS
DATA
  • DOWNLOADABLE DATA
  • PUBLICATION DATA
  • RELEASE HISTORY
HELP
  • ANTIBODY VALIDATION
  • ASSAYS & ANNOTATION
  • DISCLAIMER
  • HELP & FAQ
  • PRIVACY STATEMENT
  • LICENCE & CITATION
Fields »
Search result

Field
Term
Gene name
Class
Subclass
Class
Keyword
Chromosome
External id
Tissue
Cell type
Expression
Antibody panel
Tissue
Main location
Patient ID
Annotation
Tissue
Category
Tau score
Cluster
Reliability
Brain region
Category
Tau score
Brain region
Category
Tau score
Brain region
Category
Tau score
Cluster
Reliability
Tissue
Cell type
Enrichment
Cell type
Category
Tau score
Cell type
Category
Tau score
Cell type
Category
Tau score
Cell lineage
Category
Tau score
Cluster
Cluster
Location
Searches
Location
Cell line
Class
Type
Phase
Reliability
Cancer
Prognosis
Cancer
Category
Cancer
Category
Tau score
Cluster
Variants
Interacting gene (ensg_id)
Type
Number of interactions
Pathway
Category
Score
Score
Score
Validation
Validation
Validation
Validation
Antibodies
Data type
Column


  • SUMMARY

  • TISSUE

  • BRAIN

  • SINGLE CELL

  • SUBCELL

  • CANCER

  • BLOOD

  • CELL LINE

  • STRUCT & INT

  • FAM111A
PROTEIN SUMMARY GENE INFORMATION RNA DATA ANTIBODY DATA
GENERAL INFORMATIONi

General description of the gene and the encoded protein(s) using information from HGNC and Ensembl, as well as predictions made by the Human Protein Atlas project.

Gene namei

Official gene symbol, which is typically a short form of the gene name, according to HGNC.

FAM111A
Synonyms FLJ22794, KIAA1895
Gene descriptioni

Full gene name according to HGNC.

FAM111 trypsin like peptidase A
Protein classi

Assigned HPA protein class(es) for the encoded protein(s).

Disease related genes
Human disease related genes
Predicted locationi

All transcripts of all genes have been analyzed regarding the location(s) of corresponding protein based on prediction methods for signal peptides and transmembrane regions.

  • Genes with at least one transcript predicted to encode a secreted protein, according to prediction methods or to UniProt location data, have been further annotated and classified with the aim to determine if the corresponding protein(s) are secreted or actually retained in intracellular locations or membrane-attached.

  • Remaining genes, with no transcript predicted to encode a secreted protein, will be assigned the prediction-based location(s).

The annotated location overrules the predicted location, so that a gene encoding a predicted secreted protein that has been annotated as intracellular will have intracellular as the final location.

Intracellular
Protein evidence Evidence at protein level (all genes)
GENE INFORMATIONi

Gene information from Ensembl and Entrez, as well as links to available gene identifiers are displayed here. Information was retrieved from Ensembl if not indicated otherwise.

Chromosome 11
Cytoband q12.1
Chromosome location (bp) 59142748 - 59155039
Number of transcriptsi

Number of protein-coding transcripts from the gene as defined by Ensembl.

15
Ensembl ENSG00000166801 (version 109)
Entrez gene 63901
HGNC HGNC:24725
UniProt Q96PZ2 (UniProt - Evidence at protein level)
neXtProt NX_Q96PZ2
GeneCards FAM111A
Antibodypedia FAM111A antibodies


PROTEIN FUNCTION
Protein function (UniProt)i

Useful information about the protein provided by UniProt.

Single-stranded DNA-binding serine protease that mediates the proteolytic cleavage of covalent DNA-protein cross-links (DPCs) during DNA synthesis, thereby playing a key role in maintaining genomic integrity 1. DPCs are highly toxic DNA lesions that interfere with essential chromatin transactions, such as replication and transcription, and which are induced by reactive agents, such as UV light or formaldehyde 2. Protects replication fork from stalling by removing DPCs, such as covalently trapped topoisomerase 1 (TOP1) adducts on DNA lesion, or poly(ADP-ribose) polymerase 1 (PARP1)- DNA complexes trapped by PARP inhibitors 3. Required for PCNA loading on replication sites 4. Promotes S-phase entry and DNA synthesis 5. Acts also as a restriction factor for some viruses including SV40 polyomavirus and vaccinia virus 6, 7. Mechanistically, affects nuclear barrier function during viral replication by mediating the disruption of the nuclear pore complex (NPC) via its protease activity 8, 9. In turn, interacts with vaccinia virus DNA-binding protein OPG079 in the cytoplasm and promotes its degradation without the need of its protease activity but through autophagy 10.... show less
Molecular function (UniProt)i

Keywords assigned by UniProt to proteins due to their particular molecular function.

DNA-binding, Hydrolase, Protease
Biological process (UniProt)i

Keywords assigned by UniProt to proteins because they are involved in a particular biological process.

DNA damage, DNA repair, DNA replication, Host-virus interaction
Gene summary (Entrez)i

Useful information about the gene from Entrez

The protein encoded by this gene is cell-cycle regulated, and has nuclear localization. The C-terminal half of the protein shares homology with trypsin-like peptidases and it contains a PCNA-interacting peptide (PIP) box, that is necessary for its co-localization with proliferating cell nuclear antigen (PCNA). Reduced expression of this gene resulted in DNA replication defects, consistent with the demonstrated role for this gene in Simian Virus 40 (SV40) viral replication. Mutations in this gene have been associated with Kenny-Caffey syndrome (KCS) type 2 and the more severe osteocraniostenosis (OCS, also known as Gracile Bone Dysplasia), both characterized by short stature, hypoparathyroidism, bone development abnormalities, and hypocalcemia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2015]... show less
PROTEIN INFORMATIONi

The protein information section displays alternative protein-coding transcripts (splice variants) encoded by this gene according to the Ensembl database.

The Splice variant identifier links to the Ensembl website protein summary for the selected splice variant. The data in the Swissprot and TrEMBL columns links to corresponding pages in the UniProt database.

The protein classes assigned to this protein are shown if expanding the data in the protein class column. Parent protein classes are in bold font and subclasses are listed under the parent class.

The length of the protein (amino acid residues according to Ensembl), molecular mass (kDalton), predicted signal peptide and number of predicted transmembrane region(s) according to in-house majority decision methods based on sets of predictors are also reported.
Splice variant SwissProt TrEMBL Protein class Gene ontology Length & mass Signal peptide
(predicted)
Transmembrane regions
(predicted)
FAM111A-201
ENSP00000355264
ENST00000361723
Q96PZ2
[Direct mapping] Serine protease FAM111A
Show all
A0A024R4Z3
[Target identity:100%; Query identity:100%] Family with sequence similarity 111, member A, isoform CRA_a
Show all
   THUMBUP predicted membrane proteins
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Disease related genes
Human disease related genes
   Congenital malformations
   Congenital malformations of the musculoskeletal system
   Other congenital malformations
Mapped to neXtProt
   neXtProt - Evidence at protein level
Protein evidence (Kim et al 2014)
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0000785 [chromatin]
GO:0001650 [fibrillar center]
GO:0003677 [DNA binding]
GO:0003697 [single-stranded DNA binding]
GO:0005515 [protein binding]
GO:0005634 [nucleus]
GO:0005654 [nucleoplasm]
GO:0005694 [chromosome]
GO:0005737 [cytoplasm]
GO:0006260 [DNA replication]
GO:0006281 [DNA repair]
GO:0006508 [proteolysis]
GO:0006974 [cellular response to DNA damage stimulus]
GO:0008233 [peptidase activity]
GO:0016540 [protein autoprocessing]
GO:0016787 [hydrolase activity]
GO:0031297 [replication fork processing]
GO:0045071 [negative regulation of viral genome replication]
GO:0106300 [protein-DNA covalent cross-linking repair]
Show all
611 aa
70.2 kDa
No 0
FAM111A-202
ENSP00000406683
ENST00000420244
Q96PZ2
[Direct mapping] Serine protease FAM111A
Show all
A0A024R4Z3
[Target identity:100%; Query identity:100%] Family with sequence similarity 111, member A, isoform CRA_a
Show all
   THUMBUP predicted membrane proteins
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Disease related genes
Human disease related genes
   Congenital malformations
   Congenital malformations of the musculoskeletal system
   Other congenital malformations
Mapped to neXtProt
   neXtProt - Evidence at protein level
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0000785 [chromatin]
GO:0001650 [fibrillar center]
GO:0003677 [DNA binding]
GO:0003697 [single-stranded DNA binding]
GO:0005515 [protein binding]
GO:0005634 [nucleus]
GO:0005654 [nucleoplasm]
GO:0005694 [chromosome]
GO:0005737 [cytoplasm]
GO:0006260 [DNA replication]
GO:0006281 [DNA repair]
GO:0006508 [proteolysis]
GO:0006974 [cellular response to DNA damage stimulus]
GO:0008233 [peptidase activity]
GO:0016540 [protein autoprocessing]
GO:0016787 [hydrolase activity]
GO:0031297 [replication fork processing]
GO:0045071 [negative regulation of viral genome replication]
GO:0106300 [protein-DNA covalent cross-linking repair]
Show all
611 aa
70.2 kDa
No 0
FAM111A-203
ENSP00000436128
ENST00000527629
Q96PZ2
[Direct mapping] Serine protease FAM111A
Show all
E9PR18
[Direct mapping] Serine protease FAM111A
A0A024R4Z3
[Target identity:100%; Query identity:100%] Family with sequence similarity 111, member A, isoform CRA_a
Show all
   THUMBUP predicted membrane proteins
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Disease related genes
Human disease related genes
   Congenital malformations
   Congenital malformations of the musculoskeletal system
   Other congenital malformations
Mapped to neXtProt
   neXtProt - Evidence at protein level
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0000785 [chromatin]
GO:0001650 [fibrillar center]
GO:0003677 [DNA binding]
GO:0003697 [single-stranded DNA binding]
GO:0005515 [protein binding]
GO:0005634 [nucleus]
GO:0005654 [nucleoplasm]
GO:0005694 [chromosome]
GO:0005737 [cytoplasm]
GO:0006260 [DNA replication]
GO:0006281 [DNA repair]
GO:0006508 [proteolysis]
GO:0006974 [cellular response to DNA damage stimulus]
GO:0008233 [peptidase activity]
GO:0016540 [protein autoprocessing]
GO:0016787 [hydrolase activity]
GO:0031297 [replication fork processing]
GO:0045071 [negative regulation of viral genome replication]
GO:0106300 [protein-DNA covalent cross-linking repair]
Show all
611 aa
70.2 kDa
No 0
FAM111A-204
ENSP00000434435
ENST00000528737
Q96PZ2
[Direct mapping] Serine protease FAM111A
Show all
A0A024R4Z3
[Target identity:100%; Query identity:100%] Family with sequence similarity 111, member A, isoform CRA_a
Show all
   THUMBUP predicted membrane proteins
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Disease related genes
Human disease related genes
   Congenital malformations
   Congenital malformations of the musculoskeletal system
   Other congenital malformations
Mapped to neXtProt
   neXtProt - Evidence at protein level
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0000785 [chromatin]
GO:0001650 [fibrillar center]
GO:0003677 [DNA binding]
GO:0003697 [single-stranded DNA binding]
GO:0005515 [protein binding]
GO:0005634 [nucleus]
GO:0005654 [nucleoplasm]
GO:0005694 [chromosome]
GO:0005737 [cytoplasm]
GO:0006260 [DNA replication]
GO:0006281 [DNA repair]
GO:0006508 [proteolysis]
GO:0006974 [cellular response to DNA damage stimulus]
GO:0008233 [peptidase activity]
GO:0016540 [protein autoprocessing]
GO:0016787 [hydrolase activity]
GO:0031297 [replication fork processing]
GO:0045071 [negative regulation of viral genome replication]
GO:0106300 [protein-DNA covalent cross-linking repair]
Show all
611 aa
70.2 kDa
No 0
FAM111A-206
ENSP00000502754
ENST00000529985
Q96PZ2
[Direct mapping] Serine protease FAM111A
Show all
A0A6Q8PHI8
[Direct mapping] Serine protease FAM111A
A0A024R4Z3
[Target identity:100%; Query identity:100%] Family with sequence similarity 111, member A, isoform CRA_a
Show all
   THUMBUP predicted membrane proteins
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Disease related genes
Human disease related genes
   Congenital malformations
   Congenital malformations of the musculoskeletal system
   Other congenital malformations
Mapped to neXtProt
   neXtProt - Evidence at protein level
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0000785 [chromatin]
GO:0001650 [fibrillar center]
GO:0003677 [DNA binding]
GO:0003697 [single-stranded DNA binding]
GO:0005515 [protein binding]
GO:0005634 [nucleus]
GO:0005654 [nucleoplasm]
GO:0005694 [chromosome]
GO:0005737 [cytoplasm]
GO:0006260 [DNA replication]
GO:0006281 [DNA repair]
GO:0006508 [proteolysis]
GO:0006974 [cellular response to DNA damage stimulus]
GO:0008233 [peptidase activity]
GO:0016540 [protein autoprocessing]
GO:0016787 [hydrolase activity]
GO:0031297 [replication fork processing]
GO:0045071 [negative regulation of viral genome replication]
GO:0106300 [protein-DNA covalent cross-linking repair]
Show all
611 aa
70.2 kDa
No 0
FAM111A-207
ENSP00000431631
ENST00000531147
Q96PZ2
[Direct mapping] Serine protease FAM111A
Show all
A0A024R4Z3
[Target identity:100%; Query identity:100%] Family with sequence similarity 111, member A, isoform CRA_a
Show all
   THUMBUP predicted membrane proteins
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Disease related genes
Human disease related genes
   Congenital malformations
   Congenital malformations of the musculoskeletal system
   Other congenital malformations
Mapped to neXtProt
   neXtProt - Evidence at protein level
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0000785 [chromatin]
GO:0001650 [fibrillar center]
GO:0003677 [DNA binding]
GO:0003697 [single-stranded DNA binding]
GO:0005515 [protein binding]
GO:0005634 [nucleus]
GO:0005654 [nucleoplasm]
GO:0005694 [chromosome]
GO:0005737 [cytoplasm]
GO:0006260 [DNA replication]
GO:0006281 [DNA repair]
GO:0006508 [proteolysis]
GO:0006974 [cellular response to DNA damage stimulus]
GO:0008233 [peptidase activity]
GO:0016540 [protein autoprocessing]
GO:0016787 [hydrolase activity]
GO:0031297 [replication fork processing]
GO:0045071 [negative regulation of viral genome replication]
GO:0106300 [protein-DNA covalent cross-linking repair]
Show all
611 aa
70.2 kDa
No 0
FAM111A-208
ENSP00000432821
ENST00000531408
Q96PZ2
[Direct mapping] Serine protease FAM111A
Show all
E9PNQ0
[Direct mapping] Serine protease FAM111A
A0A024R4Z3
[Target identity:100%; Query identity:100%] Family with sequence similarity 111, member A, isoform CRA_a
Show all
   THUMBUP predicted membrane proteins
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Disease related genes
Human disease related genes
   Congenital malformations
   Congenital malformations of the musculoskeletal system
   Other congenital malformations
Mapped to neXtProt
   neXtProt - Evidence at protein level
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0000785 [chromatin]
GO:0001650 [fibrillar center]
GO:0003677 [DNA binding]
GO:0003697 [single-stranded DNA binding]
GO:0005515 [protein binding]
GO:0005634 [nucleus]
GO:0005654 [nucleoplasm]
GO:0005694 [chromosome]
GO:0005737 [cytoplasm]
GO:0006260 [DNA replication]
GO:0006281 [DNA repair]
GO:0006508 [proteolysis]
GO:0006974 [cellular response to DNA damage stimulus]
GO:0008233 [peptidase activity]
GO:0016540 [protein autoprocessing]
GO:0016787 [hydrolase activity]
GO:0031297 [replication fork processing]
GO:0045071 [negative regulation of viral genome replication]
GO:0106300 [protein-DNA covalent cross-linking repair]
Show all
611 aa
70.2 kDa
No 0
FAM111A-211
ENSP00000433154
ENST00000533703
Q96PZ2
[Direct mapping] Serine protease FAM111A
Show all
A0A024R4Z3
[Target identity:100%; Query identity:100%] Family with sequence similarity 111, member A, isoform CRA_a
Show all
   THUMBUP predicted membrane proteins
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Disease related genes
Human disease related genes
   Congenital malformations
   Congenital malformations of the musculoskeletal system
   Other congenital malformations
Mapped to neXtProt
   neXtProt - Evidence at protein level
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0000785 [chromatin]
GO:0001650 [fibrillar center]
GO:0003677 [DNA binding]
GO:0003697 [single-stranded DNA binding]
GO:0005515 [protein binding]
GO:0005634 [nucleus]
GO:0005654 [nucleoplasm]
GO:0005694 [chromosome]
GO:0005737 [cytoplasm]
GO:0006260 [DNA replication]
GO:0006281 [DNA repair]
GO:0006508 [proteolysis]
GO:0006974 [cellular response to DNA damage stimulus]
GO:0008233 [peptidase activity]
GO:0016540 [protein autoprocessing]
GO:0016787 [hydrolase activity]
GO:0031297 [replication fork processing]
GO:0045071 [negative regulation of viral genome replication]
GO:0106300 [protein-DNA covalent cross-linking repair]
Show all
611 aa
70.2 kDa
No 0
FAM111A-212
ENSP00000501786
ENST00000674617
Q96PZ2
[Direct mapping] Serine protease FAM111A
Show all
A0A024R4Z3
[Target identity:100%; Query identity:100%] Family with sequence similarity 111, member A, isoform CRA_a
Show all
   THUMBUP predicted membrane proteins
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Disease related genes
Human disease related genes
   Congenital malformations
   Congenital malformations of the musculoskeletal system
   Other congenital malformations
Mapped to neXtProt
   neXtProt - Evidence at protein level
Protein evidence (Kim et al 2014)
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0000785 [chromatin]
GO:0001650 [fibrillar center]
GO:0003677 [DNA binding]
GO:0003697 [single-stranded DNA binding]
GO:0005515 [protein binding]
GO:0005634 [nucleus]
GO:0005654 [nucleoplasm]
GO:0005694 [chromosome]
GO:0005737 [cytoplasm]
GO:0006260 [DNA replication]
GO:0006281 [DNA repair]
GO:0006508 [proteolysis]
GO:0006974 [cellular response to DNA damage stimulus]
GO:0008233 [peptidase activity]
GO:0016540 [protein autoprocessing]
GO:0016787 [hydrolase activity]
GO:0031297 [replication fork processing]
GO:0045071 [negative regulation of viral genome replication]
GO:0106300 [protein-DNA covalent cross-linking repair]
Show all
611 aa
70.2 kDa
No 0
FAM111A-213
ENSP00000501952
ENST00000675163
Q96PZ2
[Direct mapping] Serine protease FAM111A
Show all
A0A024R4Z3
[Target identity:100%; Query identity:100%] Family with sequence similarity 111, member A, isoform CRA_a
Show all
   THUMBUP predicted membrane proteins
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Disease related genes
Human disease related genes
   Congenital malformations
   Congenital malformations of the musculoskeletal system
   Other congenital malformations
Mapped to neXtProt
   neXtProt - Evidence at protein level
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0000785 [chromatin]
GO:0001650 [fibrillar center]
GO:0003677 [DNA binding]
GO:0003697 [single-stranded DNA binding]
GO:0005515 [protein binding]
GO:0005634 [nucleus]
GO:0005654 [nucleoplasm]
GO:0005694 [chromosome]
GO:0005737 [cytoplasm]
GO:0006260 [DNA replication]
GO:0006281 [DNA repair]
GO:0006508 [proteolysis]
GO:0006974 [cellular response to DNA damage stimulus]
GO:0008233 [peptidase activity]
GO:0016540 [protein autoprocessing]
GO:0016787 [hydrolase activity]
GO:0031297 [replication fork processing]
GO:0045071 [negative regulation of viral genome replication]
GO:0106300 [protein-DNA covalent cross-linking repair]
Show all
611 aa
70.2 kDa
No 0
FAM111A-214
ENSP00000501617
ENST00000675806
Q96PZ2
[Direct mapping] Serine protease FAM111A
Show all
A0A6Q8PF34
[Direct mapping] Serine protease FAM111A
A0A024R4Z3
[Target identity:100%; Query identity:100%] Family with sequence similarity 111, member A, isoform CRA_a
Show all
   THUMBUP predicted membrane proteins
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Disease related genes
Human disease related genes
   Congenital malformations
   Congenital malformations of the musculoskeletal system
   Other congenital malformations
Mapped to neXtProt
   neXtProt - Evidence at protein level
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0000785 [chromatin]
GO:0001650 [fibrillar center]
GO:0003677 [DNA binding]
GO:0003697 [single-stranded DNA binding]
GO:0005515 [protein binding]
GO:0005634 [nucleus]
GO:0005654 [nucleoplasm]
GO:0005694 [chromosome]
GO:0005737 [cytoplasm]
GO:0006260 [DNA replication]
GO:0006281 [DNA repair]
GO:0006508 [proteolysis]
GO:0006974 [cellular response to DNA damage stimulus]
GO:0008233 [peptidase activity]
GO:0016540 [protein autoprocessing]
GO:0016787 [hydrolase activity]
GO:0031297 [replication fork processing]
GO:0045071 [negative regulation of viral genome replication]
GO:0106300 [protein-DNA covalent cross-linking repair]
Show all
611 aa
70.2 kDa
No 0
FAM111A-215
ENSP00000501909
ENST00000676340
Q96PZ2
[Direct mapping] Serine protease FAM111A
Show all
A0A024R4Z3
[Target identity:100%; Query identity:100%] Family with sequence similarity 111, member A, isoform CRA_a
Show all
   THUMBUP predicted membrane proteins
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Disease related genes
Human disease related genes
   Congenital malformations
   Congenital malformations of the musculoskeletal system
   Other congenital malformations
Mapped to neXtProt
   neXtProt - Evidence at protein level
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0000785 [chromatin]
GO:0001650 [fibrillar center]
GO:0003677 [DNA binding]
GO:0003697 [single-stranded DNA binding]
GO:0005515 [protein binding]
GO:0005634 [nucleus]
GO:0005654 [nucleoplasm]
GO:0005694 [chromosome]
GO:0005737 [cytoplasm]
GO:0006260 [DNA replication]
GO:0006281 [DNA repair]
GO:0006508 [proteolysis]
GO:0006974 [cellular response to DNA damage stimulus]
GO:0008233 [peptidase activity]
GO:0016540 [protein autoprocessing]
GO:0016787 [hydrolase activity]
GO:0031297 [replication fork processing]
GO:0045071 [negative regulation of viral genome replication]
GO:0106300 [protein-DNA covalent cross-linking repair]
Show all
611 aa
70.2 kDa
No 0
FAM111A-216
ENSP00000501771
ENST00000676459
Q96PZ2
[Direct mapping] Serine protease FAM111A
Show all
A0A024R4Z3
[Target identity:100%; Query identity:100%] Family with sequence similarity 111, member A, isoform CRA_a
Show all
   THUMBUP predicted membrane proteins
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Disease related genes
Human disease related genes
   Congenital malformations
   Congenital malformations of the musculoskeletal system
   Other congenital malformations
Mapped to neXtProt
   neXtProt - Evidence at protein level
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0000785 [chromatin]
GO:0001650 [fibrillar center]
GO:0003677 [DNA binding]
GO:0003697 [single-stranded DNA binding]
GO:0005515 [protein binding]
GO:0005634 [nucleus]
GO:0005654 [nucleoplasm]
GO:0005694 [chromosome]
GO:0005737 [cytoplasm]
GO:0006260 [DNA replication]
GO:0006281 [DNA repair]
GO:0006508 [proteolysis]
GO:0006974 [cellular response to DNA damage stimulus]
GO:0008233 [peptidase activity]
GO:0016540 [protein autoprocessing]
GO:0016787 [hydrolase activity]
GO:0031297 [replication fork processing]
GO:0045071 [negative regulation of viral genome replication]
GO:0106300 [protein-DNA covalent cross-linking repair]
Show all
611 aa
70.2 kDa
No 0
FAM111A-217
ENSP00000507215
ENST00000682018
Q96PZ2
[Direct mapping] Serine protease FAM111A
Show all
A0A024R4Z3
[Target identity:100%; Query identity:100%] Family with sequence similarity 111, member A, isoform CRA_a
Show all
   THUMBUP predicted membrane proteins
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Disease related genes
Human disease related genes
   Congenital malformations
   Congenital malformations of the musculoskeletal system
   Other congenital malformations
Mapped to neXtProt
   neXtProt - Evidence at protein level
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0000785 [chromatin]
GO:0001650 [fibrillar center]
GO:0003677 [DNA binding]
GO:0003697 [single-stranded DNA binding]
GO:0005515 [protein binding]
GO:0005634 [nucleus]
GO:0005654 [nucleoplasm]
GO:0005694 [chromosome]
GO:0005737 [cytoplasm]
GO:0006260 [DNA replication]
GO:0006281 [DNA repair]
GO:0006508 [proteolysis]
GO:0006974 [cellular response to DNA damage stimulus]
GO:0008233 [peptidase activity]
GO:0016540 [protein autoprocessing]
GO:0016787 [hydrolase activity]
GO:0031297 [replication fork processing]
GO:0045071 [negative regulation of viral genome replication]
GO:0106300 [protein-DNA covalent cross-linking repair]
Show all
611 aa
70.2 kDa
No 0
FAM111A-218
ENSP00000508374
ENST00000684135
A0A804HLI8
[Direct mapping] Serine protease FAM111A
Show all
   THUMBUP predicted membrane proteins
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Human disease related genes
   Congenital malformations
   Congenital malformations of the musculoskeletal system
   Other congenital malformations
Protein evidence (Ezkurdia et al 2014)
Show all
571 aa
65.5 kDa
No 0

Contact

  • NEWS ARTICLES
  • PRESS ROOM

The Project

  • INTRODUCTION
  • ORGANIZATION
  • PUBLICATIONS

The Human Protein Atlas

  • DOWNLOADABLE DATA
  • LICENCE & CITATION
  • HELP & FAQ
The Human Protein Atlas project is funded
by the Knut & Alice Wallenberg Foundation.


contact@proteinatlas.org