ERCC5

GENERAL INFORMATION

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Gene name

ERCC5

Gene description

Excision repair cross-complementation group 5

Protein class

Cancer-related genes
Disease related genes
Plasma proteins
Predicted intracellular proteins

Predicted localization

Intracellular

Number of transcripts

4
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Expressed in all
GTEx:Expressed in all

Protein evidence

Evidence at protein level

Protein localization

Ubiquitous nuclear and cytoplasmic expression.

ANTIBODY RELIABILITY

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Data reliability
description

Pending RNA-based expert annotation. Caution, targets protein from more than one gene.

Data reliability

Supportive based on 2 antibodies.
HPA045845 , HPA050374
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
Endocrine tissues
Bone marrow & immune system
Muscle tissues
Lung
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Lymph node

Liver

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Expressed in all

Organ

Expression

GTEx dataset
RNA tissue category:  Expressed in all

Organ

Expression



GENE INFORMATION

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Gene name

ERCC5 (HGNC Symbol)

Synonyms

ERCM2, XPGC

Description

Excision repair cross-complementation group 5 (HGNC Symbol)

Entrez gene summary

This gene encodes a single-strand specific DNA endonuclease that makes the 3' incision in DNA excision repair following UV-induced damage. The protein may also function in other cellular processes, including RNA polymerase II transcription, and transcription-coupled DNA repair. Mutations in this gene cause xeroderma pigmentosum complementation group G (XP-G), which is also referred to as xeroderma pigmentosum VII (XP7), a skin disorder characterized by hypersensitivity to UV light and increased susceptibility for skin cancer development following UV exposure. Some patients also develop Cockayne syndrome, which is characterized by severe growth defects, mental retardation, and cachexia. Read-through transcription exists between this gene and the neighboring upstream BIVM (basic, immunoglobulin-like variable motif containing) gene. [provided by RefSeq, Feb 2011]

Chromosome

13

Cytoband

q33.1

Chromosome location (bp)

102844844 - 102876001

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000134899 (version 78.38)

Entrez gene

2073

UniProt

P28715 (UniProt - Evidence at protein level)

neXtProt

NX_P28715

Antibodypedia

ERCC5 antibodies


PROTEIN BROWSER

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ENST00000355739
 
ENST00000375954
 
ENST00000535557
 
ENST00000610537
 
 
 
 


PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

ERCC5-001 ENSP00000347978
ENST00000355739
P28715
Show all »
Show » Show » 1186 133.1 No 0
ERCC5-006 ENSP00000365121
ENST00000375954
P28715
Show all »
Show » Show » 419 47.3 No 0
ERCC5-201 ENSP00000442117
ENST00000535557
P28715
Show all »
Show » Show » 232 27.3 No 0
ERCC5-202 ENSP00000478667
ENST00000610537
Show » Show » 1185 133.1 No 0