Transmembrane protein 138 is a protein that in humans is encoded by the TMEM138 gene. Mutations in this gene have been shown to cause a ciliopathy indistinguishable...

recessive JBTS15 614464 CEP41 7q32.2 Autosomal recessive JBTS16 614465 TMEM138 11q12.2 Autosomal recessive JBTS17 614615 C5ORF42 5p13.2 JBTS18 614815...

TMEM216, AHI1, NPHP1, CEP290, TMEM67, RPGRIP1L, ARL13B, CC2D2A, OFD1, TMEM138, TCTN3, ZNF423, AMRC9 Juvenile-onset dystonia ACTB, IMPDH2 dominant Juvenile...

16927 TMEM134 HGNC:26142 Q9H6X4 16928 TMEM135 HGNC:26167 Q86UB9 16929 TMEM138 HGNC:26944 Q9NPI0 16930 TMEM139 HGNC:22058 Q8IV31 16931 TMEM140 HGNC:21870...