|
1321
|
|
|
Intraflagellar transport 27 |
BBS19, CFAP156, FAP156, RABL4, RAYL |
Bardet-biedl syndrome, Bipolar disorder, Hypoplasia of the ovary, Congenital hypoplasia of penis, Cryptorchidism, Dwarfism, Hypertension, Hypogonadism, Liver fibrosis, Mental retardation, Multicystic renal dysplasia, Nephrotic syndrome, Nystagmus, Obesity, Polydactyly, Renal insufficiency, Retinitis pigmentosa, Rod-cone dystrophy, Speech disorders, Syndactyly of fingers, Postaxial hand polydactylyView all (6 more) |
|
1322
|
|
|
Tudor and KH domain containing |
TDRD2 |
|
|
1323
|
|
|
Ventral anterior homeobox 1 |
MCOPS11 |
|
|
1324
|
|
|
PITX2 adjacent non-coding RNA |
- |
|
|
1325
|
|
|
Leukocyte immunoglobulin like receptor A1 |
CD85I, LIR-6, LIR6 |
|
|
1326
|
|
|
Choline O-acetyltransferase |
CHOACTASE, CMS1A, CMS1A2, CMS6 |
Acquired kyphoscoliosis, Angle closure glaucoma, Arthrogryposis multiplex congenita, Bulbar palsy, Clonic seizures, Developmental dysplasia of the hip, Congenital kyphoscoliosis, Myasthenic syndrome, Congenital pectus carinatum, Distal amyotrophy, Dysphagia, Esotropia, External ophthalmoplegia, Febrile seizures, Gastroesophageal reflux disease, Hearing loss, High palate, Hypotonic seizures, Jacksonian seizure, Mental depression, Mental retardation, Motor delay, Myasthenia gravis, Nystagmus, Polyneuropathy, Ptosis, Retinal diseases, Schizophrenia, Seizure, Sleep apnea, Strabismus, Sudden episodic apneaView all (17 more) |
|
1327
|
|
|
RAB31, member RAS oncogene family |
Rab22B |
|
|
1328
|
|
|
Destrin, actin depolymerizing factor |
ACTDP, ADF, HEL32, bA462D18.2 |
|
|
1329
|
|
|
Receptor interacting serine/threonine kinase 3 |
RIP3 |
|
|
1330
|
|
|
General transcription factor IIA subunit 1 like |
ALF |
|
