DCLRE1C
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 10[12]
- Cytogenetic location
- 10p13[15]
- Encodes
- DNA cross-link repair 1C, Protein artemis[9][10]
- Expressed in
- buccal mucosa cell, tendon of biceps brachii, epithelium of nasopharynx, sperm, nipple, pylorus, cardia, superior surface of tongue, endothelial cell, amniotic fluid[16][17][18][19][20][21][22][23][24][25]
- Found in taxon
- Homo sapiens[11]
- Genetic association
- Omenn syndrome[13]
- HomoloGene ID
- 32547[3]
- Strand orientation
- reverse strand[14]
🏷️ Also known as
en A-SCID
en DCLRE1C
en DCLREC1C
en DNA cross-link repair 1C
en RS-SCID
en SCIDA
en SNM1C
ja アルテミス
🔖 Identifiers · 12
- Image (Wikimedia Commons)
- DCLRE1C.png ↗
- Ensembl gene ID
- ENSG00000152457
- Ensembl transcript ID
- ENST00000492201, ENST00000357717, ENST00000378241, ENST00000378242, ENST00000378246, ENST00000378249, ENST00000378254, ENST00000378255, ENST00000378258, ENST00000378278, ENST00000378289, ENST00000396817, ENST00000418843, ENST00000456122, ENST00000489161, ENST00000489845
- Entrez Gene ID
- 64421
- Exact match
- identifiers.org
- Freebase ID
- /m/03cx0v9
- HGNC ID
- 17642
- HGNC gene symbol
- DCLRE1C
- Microsoft Academic ID (discontinued)
- 106681099
- OMIM ID
- 605988
- RefSeq RNA ID
- XR_930515, NM_001033855, NM_001033857, NM_001033858, NM_001289076, NM_001289077, NM_001289078, NM_001289079, NM_022487, NR_110297, XM_011519620, XM_011519621, NM_001350965, NM_001350966, NM_001350967, NR_146960, NR_146961, NR_146962, XM_047425648, XM_047425649, XM_047425650, XM_047425651, XM_047425652
- UMLS CUI
- C1425020
🔗 Connections
Expressed in 5
Chromosome 1
Found in taxon 1
Genetic association 1
Instance of 1
← Genetic association 1
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