TCTN3
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene[2]
- Chromosome
- human chromosome 10[11]
- Cytogenetic location
- 10q24.1[15]
- Encodes
- Tectonic family member 3[9]
- Expressed in
- corpus epididymis, decidua, stromal cell of endometrium, islet of Langerhans, caput epididymis, right lobe of thyroid gland, pancreatic ductal cell, left lobe of thyroid gland, gallbladder, tail of epididymis[16][17][18][19][20][21][22][23][24][25]
- Found in taxon
- Homo sapiens[10]
- Genetic association
- orofaciodigital syndrome IV, Joubert syndrome 18[12][13]
- HomoloGene ID
- 9221[3]
- Strand orientation
- reverse strand[14]
🏷️ Also known as
en OFD4
en C10orf61
en JBTS18
en tectonic family member 3
en TCTN3
en TECT3
ar TCTN٣
🔖 Identifiers · 10
- Ensembl gene ID
- ENSG00000119977
- Ensembl transcript ID
- ENST00000614499, ENST00000265993, ENST00000371209, ENST00000371217, ENST00000430368, ENST00000478245, ENST00000497399, ENST00000679984, ENST00000681928, ENST00000681185, ENST00000681739, ENST00000680709, ENST00000680697, ENST00000679485, ENST00000680353, ENST00000680144, ENST00000681127, ENST00000680781, ENST00000679566
- Entrez Gene ID
- 26123
- Exact match
- identifiers.org
- Freebase ID
- /m/011x3rrn
- HGNC ID
- 24519
- HGNC gene symbol
- TCTN3
- OMIM ID
- 613847
- RefSeq RNA ID
- XM_011539628, NM_001143973, NM_015631, XM_005269690, XM_011539627, XM_024447935, XM_047425041, XM_047425042
- UMLS CUI
- C1538392
🔗 Connections
Expressed in 3
Chromosome 1
Found in taxon 1
Instance of 1
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Summary
TCTN3 is a gene[1].