SPECC1L
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 22[12]
- Cytogenetic location
- 22q11.23[16]
- Encodes
- Sperm antigen with calponin homology and coiled-coil domains 1 like[10]
- Expressed in
- Achilles tendon, testicle, endothelial cell, sural nerve, tendon of biceps brachii, parotid gland, islet of Langerhans, ventricular zone, dorsal motor nucleus of vagus nerve, ganglionic eminence[17][18][19][20][21][22][23][24][25][26]
- Found in taxon
- Homo sapiens[11]
- Genetic association
- Tessier number 4 facial cleft, Hypertelorism, Teebi type[13][14]
- HomoloGene ID
- 15610[3]
- Strand orientation
- forward strand[15]
🏷️ Also known as
en CYTSA
en GBBB2
en OBLFC1
en SPECC1L
en sperm antigen with calponin homology and coiled-coil domains 1 like
en sperm antigen with calponin homology and coiled-coil domains 1-like
en TBHS
en TBHS1
🔖 Identifiers · 10
- Ensembl gene ID
- ENSG00000100014
- Ensembl transcript ID
- ENST00000314328, ENST00000416735, ENST00000421374, ENST00000437398, ENST00000440893, ENST00000472799, ENST00000541492, ENST00000651059
- Entrez Gene ID
- 23384
- Exact match
- identifiers.org
- Google Knowledge Graph ID
- /g/11fy_qmt6f
- HGNC ID
- 29022
- HGNC gene symbol
- SPECC1L
- OMIM ID
- 614140
- RefSeq RNA ID
- NM_015330, NM_001145468, NM_001254732, NM_001254733
- UMLS CUI
- C1823097
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