|
621
|
|
|
- |
SPG |
|
|
622
|
|
|
SURP and G-patch domain containing 1 |
F23858, RBP, SF4 |
|
|
623
|
|
|
SLAM family member 7 |
19A, CD319, CRACC, CS1 |
|
|
624
|
|
|
SR-related CTD associated factor 1 |
SRA1 |
|
|
625
|
|
|
SIN3-HDAC complex associated factor |
C12orf14, FAM60A, L4, TERA |
|
|
626
|
|
|
SUMO specific peptidase 2 |
AXAM2, SMT3IP2 |
|
|
627
|
|
|
Solute carrier family 25 member 19 |
DNC, MCPHA, MTPPT, MUP1, THMD3, THMD4, TPC |
Agenesis of corpus callosum, Cerebellar hypoplasia, Cleft soft palate, Congenital clubfoot, Defect of skull ossification, Lethal microcephaly, Lissencephaly, Microcephaly, Micrognathism, Optic atrophy, Osteoporosis, Partial agenesis of corpus callosum, Peripheral axonal neuropathy, Polyneuropathy, Progressive polyneuropathy with bilateral striatal necrosis, Seizure, Spina bifidaView all (2 more) |
|
628
|
|
|
Solute carrier family 5 member 7 |
CHT, CHT1, CMS20, DHMNVP, HMN7A, HMND7, hCHT1 |
Acquired kyphoscoliosis, Arthrogryposis multiplex congenita, Bulbar palsy, Developmental dysplasia of the hip, Congenital kyphoscoliosis, Myasthenic syndrome, Congenital pectus carinatum, Distal amyotrophy, Distal hereditary motor neuronopathy, Dysphagia, Esotropia, Facial paralysis, Gastroesophageal reflux disease, Hearing loss, High palate, Mental depression, Mental retardation, Mood disorder, Motor delay, Myasthenia gravis, Nervous system diseases, Neuropathy, Nystagmus, Partial paralysis vocal cords, Polyneuropathy, Ptosis, Scoliosis, Sleep apnea, Sudden episodic apnea, Vocal cord paralysisView all (15 more) |
|
629
|
|
|
Signal peptidase complex subunit 3 |
PRO3567, SPC22, SPC22/23, SPC23, SPC3, YLR066W |
|
|
630
|
|
|
- |
- |
|
