Full name: transmembrane protein 107

Gene type: protein coding

RefSeq status: VALIDATED

Also known as: 1110004B13Rik; 2810049P21Rik

Summary: Involved in several processes, including embryonic digit morphogenesis; non-motile cilium assembly; and protein localization to ciliary transition zone. Acts upstream of or within several processes, including craniofacial suture morphogenesis; detection of nodal flow; and roof of mouth development. Located in ciliary transition zone. Is expressed in brain ventricle and choroid plexus; nasal cavity epithelium; node; and pharynx. Human ortholog(s) of this gene implicated in Meckel syndrome 13 and orofaciodigital syndrome XVI. Orthologous to human TMEM107 (transmembrane protein 107). [provided by Alliance of Genome Resources, Apr 2022]

Expression: Ubiquitous expression in testis adult (RPKM 30.6), ovary adult (RPKM 12.8) and 27 other tissues

Gene size: 2485bp

Exon count: 4