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.
CUL1
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

  • CUL1
STRUCTURE & INTERACTION STRUCTURE INTERACTION
Protein structures
Protein interactions
Human metabolism
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.

CUL1
Synonyms
Gene descriptioni

Full gene name according to HGNC.

Cullin 1
Protein classi

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

Cancer-related genes
Plasma proteins
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)

HUMAN PROTEIN ATLAS INFORMATIONi

Summary of RNA expression analysis and annotation data generated within the Human Protein Atlas project.

Single cell type
expression clusteri

The RNA data was used to cluster genes according to their expression across single cell types. Clusters contain genes that have similar expression patterns, and each cluster has been manually annotated to describe common features in terms of function and specificity.

Late spermatids - Unknown function (mainly)
Single cell type specificityi

The RNA specificity category is based on mRNA expression levels in the analyzed cell types based on scRNA-seq data from normal tissues. The categories include: cell type enriched, group enriched, cell type enhanced, low cell type specificity and not detected.

Group enriched (Early spermatids, Late spermatids)
Tissue expression
cluster (RNA)i

The RNA data was used to cluster genes according to their expression across tissues. Clusters contain genes that have similar expression patterns, and each cluster has been manually annotated to describe common features in terms of function and specificity.

Non-specific - Transcription (mainly)
Tissue specificity (RNA)i

The RNA specificity category is based on mRNA expression levels in the consensus dataset which is calculated from the RNA expression levels in samples from HPA and GTEX. The categories include: tissue enriched, group enriched, tissue enhanced, low tissue specificity and not detected.

Low tissue specificity
Subcellular locationi

Main subcellular location based on data generated in the subcellular section of the Human Protein Atlas.

Localized to the Nucleoplasm, Cytosol In addition localized to the Nucleoli
Secretome annotationi

All genes with at least one predicted secreted isoform have been annotated and classified with the aim to determine if the corresponding protein(s) are:

  • secreted into blood
  • locally secreted
  • or actually being attached to membrane or retained in intracellular locations like mitochondria, endoplasmatic reticulum (ER), Golgi apparatus or lysosomes.

Not available
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 q36.1
Chromosome location (bp) 148697914 - 148801110
Number of transcriptsi

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

12
Ensembl ENSG00000055130 (version 109)
Entrez gene 8454
HGNC HGNC:2551
UniProt Q13616 (UniProt - Evidence at protein level)
neXtProt NX_Q13616
GeneCards CUL1
ASSAYSi

Links to data of the different assays available in the Structure & Interaction resource of the Human Protein Atlas. Click on the miniature images to directly get to the respective section.

Proteinstructure Interaction
PROTEIN BROWSERi

The Structure section provides in-house generated structures, predicted using the Alphafold source code, for the majority of the proteins and their related isoforms.

Displaying protein features on the AlphaFold structures

Individual splice variants can be selected in the top part of the Protein Browser (see below) and different transcript-related features such as transmembrane regions, InterPro domains and antigen sequences for antibodies can be displayed in the structure by clicking on the respective features in the Protein Browser.

Clinical and population-based amino acid variants based on data from the Ensembl variation database and AlphaMissense (AM) predictions can be highlighted using the sliders to the right of the structure. These can also be used to colour the entire structure by residue index or make the structure autorotate.The structures are displayed using the NGL Viewer and can also be zoomed-in and rotated manually.

The Protein Browser

The ProteinBrowser displays the antigen location on the target protein(s) and the features of the target protein. Transcript names and schematic transcript structures including exons, introns and UTRs for the different isoforms are shown on top, and can be used to switch between the structures for the different splice variants.

At the top of the view, the position of the antigen (identified by the corresponding HPA identifier) is shown as a green bar. A yellow triangle on the bar indicates a <100% sequence identity to the protein target.

Below the antigens, the maximum percent sequence identity of the protein to all other proteins from other human genes is displayed, using a sliding window of 10 aa residues (HsID 10) or 50 aa residues (HsID 50). The region with the lowest possible identity is always selected for antigen design, with a maximum identity of 60% allowed for designing a single-target antigen (read more).

The curve in blue displays the predicted antigenicity i.e. the tendency for different regions of the protein to generate an immune response, with peak regions being predicted to be more antigenic.The curve shows average values based on a sliding window approach using an in-house propensity scale. (read more).

Signal peptides (turquoise) and membrane regions (orange) based on predictions using the majority decision methods MDM and MDSEC are also displayed.

Low complexity regions are shown in yellow and InterPro regions in green. Common (purple) and unique (grey) regions between different splice variants of the gene are also displayed (read more), and at the bottom of the protein view is the protein scale.
«
CUL1-201
CUL1-202
CUL1-203
CUL1-204
CUL1-206
CUL1-207
CUL1-208
CUL1-210
CUL1-212
CUL1-213
CUL1-214
CUL1-215
»

Description:

Color scheme:
Confidence
Residue index
Your selection
Variants:
Off
Population
Clinical
Alphamissense variants:
Off
Benign
Pathogenic
Autorotate:
Off
On
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 Length & mass Signal peptide
(predicted)
Transmembrane regions
(predicted)
CUL1-201
Q13616
Show all
A0A090N7U0
Show all
Predicted intracellular proteins
Plasma proteins
Cancer-related genes
Mapped to neXtProt
Protein evidence (Kim et al 2014)
Protein evidence (Ezkurdia et al 2014)
Show all
776 aa
89.7 kDa
No 0
CUL1-202
Q13616
Show all
A0A090N7U0
Show all
Predicted intracellular proteins
Plasma proteins
Cancer-related genes
Mapped to neXtProt
Protein evidence (Ezkurdia et al 2014)
Show all
776 aa
89.7 kDa
No 0
CUL1-203
Q13616
Show all
A0A090N7U0
Show all
Predicted intracellular proteins
Plasma proteins
Cancer-related genes
Mapped to neXtProt
Protein evidence (Ezkurdia et al 2014)
Show all
776 aa
89.7 kDa
No 0
CUL1-204
A0A590UK34
Show all
Predicted intracellular proteins
Cancer-related genes
Protein evidence (Ezkurdia et al 2014)
Show all
720 aa
83.2 kDa
No 0
CUL1-206
A0A590UJA0
Show all
Predicted intracellular proteins
Cancer-related genes
Protein evidence (Ezkurdia et al 2014)
Show all
281 aa
32.4 kDa
No 0
CUL1-207
A0A590UJC4
Show all
Predicted intracellular proteins
Cancer-related genes
Protein evidence (Ezkurdia et al 2014)
Show all
678 aa
78.4 kDa
No 0
CUL1-208
A0A590UJ50
Show all
Predicted intracellular proteins
Cancer-related genes
Protein evidence (Ezkurdia et al 2014)
Show all
759 aa
87.6 kDa
No 0
CUL1-210
Q13616
Show all
A0A090N7U0
Show all
Predicted intracellular proteins
Plasma proteins
Cancer-related genes
Mapped to neXtProt
Protein evidence (Ezkurdia et al 2014)
Show all
776 aa
89.7 kDa
No 0
CUL1-212
Q13616
Show all
A0A090N7U0
Show all
Predicted intracellular proteins
Plasma proteins
Cancer-related genes
Mapped to neXtProt
Protein evidence (Ezkurdia et al 2014)
Show all
776 aa
89.7 kDa
No 0
CUL1-213
A0A590UJR3
Show all
Predicted intracellular proteins
Cancer-related genes
Protein evidence (Ezkurdia et al 2014)
Show all
732 aa
84.6 kDa
No 0
CUL1-214
Q13616
Show all
A0A090N7U0
Show all
Predicted intracellular proteins
Plasma proteins
Cancer-related genes
Mapped to neXtProt
Protein evidence (Ezkurdia et al 2014)
Show all
776 aa
89.7 kDa
No 0
CUL1-215
A0A590UJ21
Show all
Predicted intracellular proteins
Cancer-related genes
Protein evidence (Ezkurdia et al 2014)
Show all
732 aa
84.3 kDa
No 0
Show allShow less
INTERACTIONi

In the Interaction part of this page network plots showing the gene's interaction partners according to four different datasets are displayed, including a consensus network plot showing only interactions present in at least two of the datasets. In the network plots the nodes represent genes and edge color represent the number of datasets the interaction belongs to.

The highlight bar in the top of the plot can be used to color the nodes according to subcellular location (based on data in the Subcellular section), predicted location (based on signalpeptide and transmembrane region predictions), tissue specificity (based on RNA tissue expression profiles) or proteinclass. For genes categorised as single cell type or group specific the option to highlight interaction partners expressed in the same cell type will also be available in the highlight bar.

Custom highlighting of nodes is possible using the top left Filter option in which a query of choice can be built to for example label all nodes that are tissue enriched in both human and mouse brain or those that belongs to a certain tissue expression cluster. The expression cluster for the gene is stated in the box Human Protein Atlas Information above the network plot. Click on Filter in the top left in the plot to find the query builder and some example queries.

Interactions included are direct interaction and physical associations with high and medium confidence from IntAct, physical multivalidated interactions from BioGRID, interactions with>75% probability from BioPlex and significant physical interactions from OpenCell.

Filter menu »
Fields »
e.g. Brain enriched, Localized to mitochondria, Non-specific - Transcription

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


Consensus
IntAct
BioGrid
OpenCell
BioPlex
Highlight:
Off
Subcell location
Predicted location
Cell type specificity
Protein class
In same cell type



Number of interactions: 32
Interaction# Consensus# IntAct# BioGrid# OpenCell# BioPlex
ARIH1244703
BTRC324518500
CAND1774506
CCDC222020251924
CCNF4462401
CDC34252404
CDKN1B283158214
COPS55251161117
COPS6515678427
DCUN1D12151701
FBXL1421705
FBXL1532507
FBXO176157015
FBXO22222000
FBXO3221300
FBXO3333301
FBXO436804
FBXO42551504
FBXO641385052
FBXO714852024
FBXW11252714200
FBXW2391000
FBXW562313049
FBXW79715003
MDM2476125900
NEDD811246602
RBX1121412821
SKP16354147853
SKP215139516
UBE2M676360
UBXN79223021
YBX121311151236
Show allShow less
Highlight:
Off
Subcell location
Predicted location
Cell type specificity
Protein class
In same cell type



Number of interactions: 31 View all protein interaction data in IntAct
Interaction# Consensus# IntAct# BioGrid# OpenCell# BioPlex
ARIH1244703
BTRC324518500
CAND1774506
CCDC222020251924
CCNF4462401
CDC34252404
CDKN1B283158214
CFTR3410423400
COPS55251161117
COPS6515678427
DCUN1D12151701
FBXO176157015
FBXO22222000
FBXO3221300
FBXO3333301
FBXO436804
FBXO641385052
FBXW11252714200
FBXW2391000
FBXW562313049
FBXW79715003
HSP90AB1631431642219
MDM2476125900
NEDD811246602
RBX1121412821
SKP16354147853
SKP215139516
UBE2D2334113004
UBE2M676360
UBXN79223021
YBX121311151236
Show allShow less
Highlight:
Off
Subcell location
Predicted location
Cell type specificity
Protein class
In same cell type



Number of interactions: 160
Interaction# Consensus# IntAct# BioGrid# OpenCell# BioPlex
ARIH1244703
ATXN33746310
BRD43548702
BTRC324518500
CAND1774506
CAND204800
CAPRIN1163451350
CARM16104430
CCDC222020251924
CCNA1232400
CCNA214556122
CCND1141454011
CCNF4462401
CDC25A672920
CDC34252404
CDC5L40481281829
CDCA3341606
CDK229261391024
CDK91714124190
CDKN1B283158214
CDT1553201
CENPW11400
CFLAR332700
CHEK1695171
CHUK131967714
CKS1B12431707
COMMD12523432726
COMMD813717816
COPS210145240
COPS3184347228
COPS4141543114
COPS55251161117
COPS6515678427
COPS7A12539214
COPS7B151124124
COPS8151628122
COPS9411113
CRY1631716
CUL3364168420
CUL4A91213700
DCUN1D12151701
DCUN1D200900
DCUN1D3111300
DCUN1D400800
DCUN1D5061111
DDB13922169649
DDX1653565
DVL216447407
E2F110197500
FAF1576005
FBH1031000
FBXL12351010
FBXL1421705
FBXL1532507
FBXL176418010
FBXL1811800
FBXL2131501
FBXL2012500
FBXL322504
FBXL411902
FBXL5231501
FBXL6114600
FBXL813201
FBXO1000201
FBXO11561400
FBXO176157015
FBXO213130154
FBXO2122700
FBXO22222000
FBXO2511600
FBXO2711302
FBXO28111617415
FBXO3221300
FBXO3042854
FBXO3123801
FBXO32111210
FBXO3333301
FBXO34018501
FBXO38111500
FBXO436804
FBXO42551504
FBXO4424800
FBXO452121310
FBXO4611201
FBXO5932060
FBXO641385052
FBXO714852024
FBXO913200
FBXW11252714200
FBXW2391000
FBXW48111010
FBXW562313049
FBXW79715003
FBXW8221700
FBXW922300
FZR111710450
GLMN5321113
GPS111133820
H4C1325635205
HNRNPL334112701
HSP90AA15156349230
HSPA4155126545
IKBKB15218066
KDM2B222200
KPNA2303680437
LRWD1001303
MAGEC2111700
MATR341411200
MATR380112140
MCL19133505
MDM2476125900
MMD016300
MYC6588126320
NEDD811246602
NFKBIA15236242
NLRP3002500
NUDT111500
PDE6D7913217
PML121415950
POLD191031218
PRKN1111140500
PSMA2429634029
PSMA43715614110
PSMA5405624422
PSMA6282565279
PSMA7331967318
PSMB43331542123
PSMD43835972416
PTTG1231600
RBPJ9125400
RBX1121412821
RICTOR1057690
RIPK4873020
RNF710733020
RPA171041711
RPA2111537520
RPA35631311
RUVBL2671113910333
SENP39830159
SENP801501
SF3B33411805845
SKP16354147853
SKP215139516
SMAD3285212702
SNRNP701611164110
SQSTM1314030520
SREK1572710
STAU13213369390
STIP1132187166
SUN291410341
TPD52221040
TRIM213249300
UBC345845240
UBE2M676360
UBXN1342700
UBXN79223021
VCP5453347435
YBX121311151236
ZC3HC11210046
ZXDA02500
Show allShow less
Highlight:
Off
Subcell location
Predicted location
Cell type specificity
Protein class
In same cell type



Number of interactions: 1
Interaction# Consensus# IntAct# BioGrid# OpenCell# BioPlex
POLR3H16217210
Highlight:
Off
Subcell location
Predicted location
Cell type specificity
Protein class
In same cell type



Number of interactions: 11
Interaction# Consensus# IntAct# BioGrid# OpenCell# BioPlex
FBXL1421705
FBXL1532507
FBXO176157015
FBXO436804
FBXO4000009
FBXO42551504
FBXO641385052
FBXO714852024
IDS010060
KHDRBS26381102
SKP16354147853
Show allShow less
METABOLIC SUMMARYi

In this summary the pathway/subsystems to which the gene belongs is shown together with the associated cellular compartment for the reactions based on metabolite information. The number of proteins and metabolites in the pathway is shown as well as the number of reactions for the selected gene. By clicking on a pathway in the summary table the associated metabolic network map is shown, together with a gene-tissue heatmap that shows the expression of genes in that pathway in different tissues.

CUL1 is not a metabolic protein

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