C2CD3
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene[2]
- Chromosome
- human chromosome 11[12]
- Cytogenetic location
- 11q13.4[15]
- Encodes
- C2 domain containing 3 centriole elongation regulator, C2 domain-containing protein 3[9][10]
- Expressed in
- sural nerve, right uterine tube, bronchial epithelial cell, epithelium of colon, right testis, left testis, ventricular zone, sperm, Brodmann area 23, ganglionic eminence[16][17][18][19][20][21][22][23][24][25]
- Found in taxon
- Homo sapiens[11]
- Genetic association
- orofaciodigital syndrome type 14[13]
- HomoloGene ID
- 19524[3]
- Strand orientation
- reverse strand[14]
🏷️ Also known as
en C2 calcium dependent domain containing 3
en C2 calcium-dependent domain containing 3
en C2CD3
en C2 domain containing 3 centriole elongation regulator
en OFD14
🔖 Identifiers · 10
- Ensembl gene ID
- ENSG00000168014
- Ensembl transcript ID
- ENST00000544293, ENST00000313663, ENST00000334126, ENST00000366334, ENST00000414160, ENST00000415191, ENST00000436679, ENST00000442398, ENST00000535954, ENST00000537285, ENST00000538361, ENST00000538625, ENST00000539061, ENST00000540057, ENST00000541922, ENST00000542452, ENST00000542484, ENST00000542930, ENST00000681385, ENST00000681000, ENST00000679906, ENST00000680173, ENST00000681233, ENST00000679940, ENST00000681143, ENST00000680665, ENST00000680231, ENST00000681291, ENST00000681811, ENST00000681310, ENST00000680645, ENST00000681609, ENST00000679415, ENST00000680306, ENST00000680839, ENST00000681829, ENST00000681924, ENST00000680718, ENST00000681345
- Entrez Gene ID
- 26005
- Exact match
- identifiers.org
- Google Knowledge Graph ID
- /g/11gbldydgv
- HGNC ID
- 24564
- HGNC gene symbol
- C2CD3
- OMIM ID
- 615944
- RefSeq RNA ID
- NM_001286577, NM_015531
- UMLS CUI
- C2240247
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Summary
C2CD3 is a gene[1].