WormBase Tree Display for Gene: HGNC:26113
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HGNC:26113 | Identity | Name | CGC_name | Tctn1 | Inferred_automatically | AGR_import |
---|---|---|---|---|---|---|
Other_name | RGD:1606246 | |||||
FLJ21127 | ||||||
JBTS13 | ||||||
TECT1 | ||||||
tectonic 1 | ||||||
tectonic-1 | ||||||
Public_name | Tctn1 | |||||
DB_info | Database | HGNC | id | 26113 | ||
AGR | cURI | HGNC:26113 | ||||
EnsEMBL | ENSEMBL_geneID | ENSG00000204852 | ||||
UniProt | UniProt_AC | Q2MV58 | ||||
OMIM | gene | 609863 | ||||
DO | id | DOID:0110982 | ||||
Species | Homo sapiens | |||||
Status | Live | |||||
Gene_info | Biotype | SO:0001217 | ||||
Ortholog | WBGene00017120 | Caenorhabditis elegans | From_analysis | EnsEMBL-Compara | ||
OrthoFinder | ||||||
Panther | ||||||
Structured_description | Automated_description | This gene encodes a member of a family of secreted and transmembrane proteins. The orthologous gene in mouse functions downstream of smoothened and rab23 to modulate hedgehog signal transduction. This protein is a component of the tectonic-like complex, which forms a barrier between the ciliary axoneme and the basal body. A mutation in this gene was found in a family with Joubert syndrome-13. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016] | Inferred_automatically | AGR_import |