full name
tectonic family member 3

synonyms
C10orf61, JBTS18, OFD4, TECT3, TCTN3, ENSG00000119977

HGNC
HGNC:24519

Entrez Gene
Gene:26123

ENSEMBL
ENSG00000119977

location
chr: 10
start: 97423153
stop: 97453900
strand: -

OMIM
OMIM:613847: TCTN3 (Autosomal recessive inheritance)
OMIM:614815: Joubert syndrome 18
OMIM:258860: Orofaciodigital syndrome IV

transcripts
NM_001143973.1
NM_015631.5

pathways
Anchoring of the basal body to the plasma membrane [NCBI:1268847] [REACTOME:R-HSA-5620912] [PUBMED:21816947] [PUBMED:23747070] [PUBMED:19575670] [PUBMED:13978319] [PUBMED:23348840] [PUBMED:25047614] [PUBMED:20819941] [PUBMED:5661997] [PUBMED:21422230] [PUBMED:24469809] [PUBMED:23530209] [PUBMED:21725307] [PUBMED:21680046] [PUBMED:23351793] [PUBMED:21427764] [PUBMED:11676918] [PUBMED:22653444]
Cilium Assembly [NCBI:1268846] [REACTOME:R-HSA-5617833] [PUBMED:21427764] [PUBMED:23351793] [PUBMED:25040720] [PUBMED:17955020] [PUBMED:22118932] [PUBMED:22653444] [PUBMED:22389062] [PUBMED:20399632] [PUBMED:25047619] [PUBMED:20395968] [PUBMED:23945166] [PUBMED:19575670] [PUBMED:24296415] [PUBMED:20145001] [PUBMED:19602418]
Organelle biogenesis and maintenance [NCBI:1268838] [REACTOME:R-HSA-1852241] [PUBMED:8608592] [PUBMED:16103713]