|
561
|
|
|
Rho guanine nucleotide exchange factor 4 |
ASEF, ASEF1, GEF4, SMIM39, STM6 |
|
|
562
|
|
|
ArfGAP with SH3 domain, ankyrin repeat and PH domain 1 |
AMAP1, CENTB4, DDEF1, PAG2, PAP, ZG14P |
|
|
563
|
|
|
Acyl-CoA oxidase 1 |
ACOX, AOX, MITCH, PALMCOX, SCOX |
Brachycephaly, Central nervous system demyelination, Congenital epicanthus, Developmental delay, Developmental regression, Dysphagia, Frontal bossing, Hearing loss, Hypodontia, Mental retardation, Leukodystrophy, Liver carcinoma, Myopia, Hypotonia, Nystagmus, Optic atrophy, Peroxisomal acyl-coa oxidase deficiency, Retinitis pigmentosa, Rod-cone dystrophy, Sensorineural hearing loss, Speech disorders, StrabismusView all (7 more) |
|
564
|
|
|
Amidohydrolase domain containing 2 |
CGI-14 |
|
|
565
|
|
|
Activating signal cointegrator 1 complex subunit 1 |
ASC1p50, CGI-18, SMABF2, p50 |
Arthrogryposis multiplex congenita, Barrett epithelium, Barrett esophagus, Congenital alveolar dysplasia, Pulmonary hypoplasia, Developmental delay, Dysphagia, Esophageal carcinoma, Gastroesophageal reflux disease, Patent ductus arteriosus, Patent foramen ovale, Pena shokeir syndrome, Peripheral axonal neuropathy, Respiratory failure, Spinal muscular atrophy, Spinal muscular atrophy with congenital bone fractures, Ulcer of esophagusView all (2 more) |
|
566
|
|
|
Atlastin GTPase 1 |
AD-FSP, ATL-1, FSP1, GBP3, HSN1D, SPG3, SPG3A, atlastin1 |
Cardiovascular diseases, Distal amyotrophy, Distal lower limb amyotrophy, Dupuytren contracture, Dysarthria, Hereditary sensory and autonomic neuropathy, Mental retardation, Motor delay, Movement disorders, Myocardial infarction, Nail diseases, Nail dysplasia, Nail dystrophy, Neuropathy, Osteomyelitis, Paraplegia, Penetrating foot ulcers, Peripheral axonal neuropathy, Scoliosis, Sensory and autonomic neuropathy, Sensory neuropathy, hereditary, Spastic paraplegiaView all (7 more) |
|
567
|
|
|
Adiponectin receptor 1 |
ACDCR1, CGI-45, CGI45, PAQR1, TESBP1A |
|
|
568
|
|
|
Abhydrolase domain containing 5, lysophosphatidic acid acyltransferase |
CGI58, IECN2, NCIE2 |
Alopecia, Cardiomyopathy, Congenital nonbullous ichthyosiform erythroderma, Developmental delay, Dwarfism, Ectropion, Fatty liver, Hearing loss, Mental retardation, Micronodular cirrhosis, Microtia, Myopathy, Neutral lipid storage disease with ichthyosis, Nystagmus, Ptosis, Strabismus, Subcapsular cataract, Triglyceride storage disease with ichthyosisView all (3 more) |
|
569
|
|
|
Angiopoietin like 4 |
ARP4, FIAF, HARP, HFARP, NL2, PGAR, TGQTL, UNQ171, pp1158 |
Anaplastic carcinoma, Breast cancer, Mammary neoplasms, Breast carcinoma, Carcinoma, Coronary arteriosclerosis, Coronary artery disease, Dyslipidemias, Fatty liver, Lymphatic metastasis, Marfan syndrome, Obesity |
|
570
|
|
|
Ankyrin repeat and SOCS box containing 3 |
ASB-3 |
|
