|
1641
|
|
|
Phosphatase and actin regulator 3 |
C20orf101, H17739, PPP1R123, SCAPIN1, SCAPININ |
|
|
1642
|
|
|
Cytochrome c oxidase assembly factor COX20 |
FAM36A, MC4DN11 |
Anemia, Cytochrome-c oxidase deficiency, Developmental delay, Fanconi syndrome, Hearing loss, High palate, Hypertrophic cardiomyopathy, Isolated cytochrome c oxidase deficiency, Leukoencephalopathy, Mental retardation, Motor delay, Optic atrophy, Phosphate diabetes, Ptosis, Renal tubular disorder, Retinitis pigmentosaView all (1 more) |
|
1643
|
|
|
Acyl-CoA synthetase medium chain family member 1 |
BUCS1, MACS1 |
|
|
1644
|
|
|
Chromosome 8 open reading frame 34 |
VEST-1, VEST1 |
|
|
1645
|
|
|
Solute carrier family 26 member 8 |
AZON, SPGF3, TAT1 |
|
|
1646
|
|
|
CDC28 protein kinase regulatory subunit 2 |
CKSHS2 |
|
|
1647
|
|
|
RAB39B, member RAS oncogene family |
BGMR, MRX72, WSMN, WSN, XLID72 |
Attention deficit hyperactivity disorder, Autism, Developmental delay, Dolichocephaly, Dysarthria, Dyskinetic syndrome, Epilepsy, Facial paralysis, Frontal bossing, Macrocephaly, Meckel diverticulum, Mental retardation, Mental retardation, x-linked, Movement disorders, Neurosensory hearing impairment, Non-syndromic intellectual disability, x-linked, Obesity, Parkinson disease, Seizure, Speech disorders, Stereotyped behavior, Strabismus, Syndactyly of the toes, Waisman syndromeView all (9 more) |
|
1648
|
|
|
Glutamate ionotropic receptor NMDA type subunit 3A |
GluN3A, NMDAR-L, NMDAR3A, NR3A |
|
|
1649
|
|
|
Cytokine dependent hematopoietic cell linker |
MIST |
|
|
1650
|
|
|
TRNA splicing endonuclease subunit 15 |
C1orf19, PCH2F, sen15 |
|