XRCC4
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 5[13]
- Cytogenetic location
- 5q14.2[16]
- Encodes
- X-ray repair cross complementing 4, X-ray repair complementing defective repair in Chinese hamster cells 4, isoform CRA_b, X-ray repair complementing defective repair in Chinese hamster cells 4, isoform CRA_a[9][10][11]
- Expressed in
- testicle, monocyte, gonad, secondary oocyte, ventricular zone, Descending thoracic aorta, Achilles tendon, ganglionic eminence, islet of Langerhans, ascending aorta[17][18][19][20][21][22][23][24][25][26]
- Found in taxon
- Homo sapiens[12]
- Genetic association
- microcephalic primordial dwarfism-insulin resistance syndrome[14]
- HomoloGene ID
- 2555[3]
- Strand orientation
- forward strand[15]
🏷️ Also known as
en hXRCC4
en SSMED
en X-ray repair complementing defective repair in Chinese hamster cells 4
en X-ray repair cross complementing 4
en XRCC4
🔖 Identifiers · 13
- OpenAlex ID
- C145803527
- Image (Wikimedia Commons)
- Protein XRCC4 PDB 1fu1.png ↗
- Ensembl gene ID
- ENSG00000152422
- Ensembl transcript ID
- ENST00000542685, ENST00000282268, ENST00000338635, ENST00000396027, ENST00000509268, ENST00000511817
- Entrez Gene ID
- 7518
- Exact match
- identifiers.org
- Freebase ID
- /m/02kfpm1
- HGNC ID
- 12831
- HGNC gene symbol
- XRCC4
- Microsoft Academic ID (discontinued)
- 145803527
- OMIM ID
- 194363
- RefSeq RNA ID
- NM_003401, NM_022406, NM_022550, XM_011543626, NM_001318012, NM_001318013, XM_017009827, XM_017009828, XM_047417694, XM_047417695, XM_047417696, XM_047417697, XM_047417698
Show all 13 identifiers +1
- UMLS CUI
- C1337033
🔗 Connections
Expressed in 7
Chromosome 1
Found in taxon 1
Instance of 1
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