DDB2

GENERAL INFORMATION

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Gene name

DDB2

Gene description

Damage-specific DNA binding protein 2, 48kDa

Protein class

Cancer-related genes
Disease related genes
Predicted intracellular proteins

Predicted localization

Intracellular

Number of transcripts

6
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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

General nuclear expression, most abundant in squamous epithelium.

ANTIBODY RELIABILITY

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Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Supportive based on 2 antibodies.
HPA058406 , CAB025912
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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

Skin



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

DDB2 (HGNC Symbol)

Synonyms

DDBB, FLJ34321, UV-DDB2

Description

Damage-specific DNA binding protein 2, 48kDa (HGNC Symbol)

Entrez gene summary

This gene encodes a protein that is necessary for the repair of ultraviolet light-damaged DNA. This protein is the smaller subunit of a heterodimeric protein complex that participates in nucleotide excision repair, and this complex mediates the ubiquitylation of histones H3 and H4, which facilitates the cellular response to DNA damage. This subunit appears to be required for DNA binding. Mutations in this gene cause xeroderma pigmentosum complementation group E, a recessive disease that is characterized by an increased sensitivity to UV light and a high predisposition for skin cancer development, in some cases accompanied by neurological abnormalities. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2014]

Chromosome

11

Cytoband

p11.2

Chromosome location (bp)

47214465 - 47239240

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000134574 (version 78.38)

Entrez gene

1643

UniProt

Q92466 (UniProt - Evidence at protein level)

neXtProt

NX_Q92466

Antibodypedia

DDB2 antibodies


PROTEIN BROWSER

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ENST00000256996
 
ENST00000378600
 
ENST00000378603
 
ENST00000614825
 
ENST00000622090
 
ENST00000622878
 
 
 
 


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)

DDB2-001 ENSP00000256996
ENST00000256996
Q92466
Show all »
Show » Show » 427 47.9 No 0
DDB2-006 ENSP00000367863
ENST00000378600
Q92466
Show all »
Show » Show » 238 26.7 No 0
DDB2-007 ENSP00000367866
ENST00000378603
Q92466
Show all »
Show » Show » 363 40.8 No 0
DDB2-011 ENSP00000479196
ENST00000622878
Show » 93 10.4 No 0
DDB2-012 ENSP00000483718
ENST00000614825
Show » Show » 228 25.1 No 0
DDB2-013 ENSP00000479994
ENST00000622090
Show » Show » 163 17.9 No 0