QuickView for TTC7A (gene)

Gene Symbol:

TTC7A Homo sapiens

Full name:

tetratricopeptide repeat domain 7A

Synonyms:

GIDID, MINAT, TTC7, tetratricopeptide repeat protein 7A, TPR repeat protein 7A

Genomic Location:

Chr 2: 47021817-47156779

Description:

This gene encodes a protein containing tetratricopeptide repeats. Mutations in this gene disrupt intestinal development and can cause early onset inflammatory bowel disease and intestinal atresia. Alternative splicing results in multiple transcript variants.

This gene encodes a protein containing tetratricopeptide repeats. Mutations in this gene disrupt intestinal development and can cause early onset inflammatory bowel disease and intestinal atresia. Alternative splicing results in multiple transcript variants.

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Orthologs:

Mus musculus ,  Rattus norvegicus ,  Macaca mulatta ,  Gallus gallus ,  Pan troglodytes ,  Canis lupus familiaris ,  Danio rerio ,  Bos taurus

External Links:

Entrez Gene

miRNA binding sites
(Source: miRecords):

hsa-miR-124 Targeted Genes

Cytogenetic Map:

2p21

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