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NSUN5
HPA
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  • NSUN5
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.

NSUN5
Synonyms FLJ10267, NOL1R, NSUN5A, p120(NOL1), WBSCR20, WBSCR20A, Ynl022cL
Gene descriptioni

Full gene name according to HGNC.

NOP2/Sun RNA methyltransferase 5
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 7
Cytoband q11.23
Chromosome location (bp) 73302516 - 73308826
Number of transcriptsi

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

4
Ensembl ENSG00000130305 (version 109)
Entrez gene 55695
HGNC HGNC:16385
UniProt Q96P11 (UniProt - Evidence at protein level)
neXtProt NX_Q96P11
GeneCards NSUN5
Antibodypedia NSUN5 antibodies


PROTEIN FUNCTION
Protein function (UniProt)i

Useful information about the protein provided by UniProt.

S-adenosyl-L-methionine-dependent methyltransferase that specifically methylates the C(5) position of cytosine 3782 (m5C3782) in 28S rRNA 1, 2, 3. m5C3782 promotes protein translation without affecting ribosome biogenesis and fidelity 4, 5. Required for corpus callosum and cerebral cortex development (By similarity).... show less
Molecular function (UniProt)i

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

Methyltransferase, RNA-binding, Transferase
Biological process (UniProt)i

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

rRNA processing
Ligand (UniProt)i

Keywords assigned by UniProt to proteins because they bind, are associated with, or whose activity is dependent of some molecule.

S-adenosyl-L-methionine
Gene summary (Entrez)i

Useful information about the gene from Entrez

This gene encodes a member of an evolutionarily conserved family of proteins that may function as methyltransferases. This gene is located in a larger region of chromosome 7 that is deleted in Williams-Beuren syndrome, a multisystem developmental disorder. There are two pseudogenes for this gene located in the same region of chromosome 7. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2013]... 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)
NSUN5-201
ENSP00000252594
ENST00000252594
Q96P11
[Direct mapping] 28S rRNA (cytosine-C(5))-methyltransferase
Show all
   Phobius predicted secreted proteins
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Disease related genes
Human disease related genes
   Other congenital disorders
   Chromosomal abnormalities
Mapped to neXtProt
   neXtProt - Evidence at protein level
Protein evidence (Kim et al 2014)
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0001510 [RNA methylation]
GO:0003723 [RNA binding]
GO:0005634 [nucleus]
GO:0005654 [nucleoplasm]
GO:0005730 [nucleolus]
GO:0006364 [rRNA processing]
GO:0008168 [methyltransferase activity]
GO:0009383 [rRNA (cytosine-C5-)-methyltransferase activity]
GO:0014003 [oligodendrocyte development]
GO:0016740 [transferase activity]
GO:0021987 [cerebral cortex development]
GO:0022038 [corpus callosum development]
GO:0031641 [regulation of myelination]
GO:0032259 [methylation]
GO:0045727 [positive regulation of translation]
GO:0050890 [cognition]
GO:0070475 [rRNA base methylation]
Show all
429 aa
46.7 kDa
No 0
NSUN5-202
ENSP00000309126
ENST00000310326
Q96P11
[Direct mapping] 28S rRNA (cytosine-C(5))-methyltransferase
Show all
   Phobius predicted secreted proteins
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Disease related genes
Human disease related genes
   Other congenital disorders
   Chromosomal abnormalities
Mapped to neXtProt
   neXtProt - Evidence at protein level
Protein evidence (Kim et al 2014)
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0001510 [RNA methylation]
GO:0003723 [RNA binding]
GO:0005634 [nucleus]
GO:0005654 [nucleoplasm]
GO:0005730 [nucleolus]
GO:0006364 [rRNA processing]
GO:0008168 [methyltransferase activity]
GO:0009383 [rRNA (cytosine-C5-)-methyltransferase activity]
GO:0014003 [oligodendrocyte development]
GO:0016740 [transferase activity]
GO:0021987 [cerebral cortex development]
GO:0022038 [corpus callosum development]
GO:0031641 [regulation of myelination]
GO:0032259 [methylation]
GO:0045727 [positive regulation of translation]
GO:0050890 [cognition]
GO:0070475 [rRNA base methylation]
Show all
470 aa
51.1 kDa
No 0
NSUN5-203
ENSP00000393081
ENST00000428206
Q96P11
[Direct mapping] 28S rRNA (cytosine-C(5))-methyltransferase
Show all
   Phobius predicted secreted proteins
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Disease related genes
Human disease related genes
   Other congenital disorders
   Chromosomal abnormalities
Mapped to neXtProt
   neXtProt - Evidence at protein level
Protein evidence (Kim et al 2014)
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0001510 [RNA methylation]
GO:0003723 [RNA binding]
GO:0005634 [nucleus]
GO:0005654 [nucleoplasm]
GO:0005730 [nucleolus]
GO:0006364 [rRNA processing]
GO:0008168 [methyltransferase activity]
GO:0009383 [rRNA (cytosine-C5-)-methyltransferase activity]
GO:0014003 [oligodendrocyte development]
GO:0016740 [transferase activity]
GO:0021987 [cerebral cortex development]
GO:0022038 [corpus callosum development]
GO:0031641 [regulation of myelination]
GO:0032259 [methylation]
GO:0045727 [positive regulation of translation]
GO:0050890 [cognition]
GO:0070475 [rRNA base methylation]
Show all
391 aa
42.5 kDa
No 0
NSUN5-204
ENSP00000388464
ENST00000438747
Q96P11
[Direct mapping] 28S rRNA (cytosine-C(5))-methyltransferase
Show all
   Phobius predicted secreted proteins
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Disease related genes
Human disease related genes
   Other congenital disorders
   Chromosomal abnormalities
Mapped to neXtProt
   neXtProt - Evidence at protein level
Protein evidence (Kim et al 2014)
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0001510 [RNA methylation]
GO:0003723 [RNA binding]
GO:0005634 [nucleus]
GO:0005654 [nucleoplasm]
GO:0005730 [nucleolus]
GO:0006364 [rRNA processing]
GO:0008168 [methyltransferase activity]
GO:0009383 [rRNA (cytosine-C5-)-methyltransferase activity]
GO:0014003 [oligodendrocyte development]
GO:0016740 [transferase activity]
GO:0021987 [cerebral cortex development]
GO:0022038 [corpus callosum development]
GO:0031641 [regulation of myelination]
GO:0032259 [methylation]
GO:0045727 [positive regulation of translation]
GO:0050890 [cognition]
GO:0070475 [rRNA base methylation]
Show all
466 aa
50.4 kDa
No 0

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