Genesⓘ

Dataset:
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "A"
351 to 360 of 912 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

351
Ataxin 10
ATX10, E46L, HUMEEP, SCA10
Cerebellar ataxia, Cerebellar atrophy, Ciliopathies, Dementia, Dysarthria, Dyscognitive seizures, Dyskinetic syndrome, Dysphagia, Dyssomnia, Epilepsy, Mental depression, Nephronophthisis, Nystagmus, Seizure, Sleep disorders
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352
Ankyrin repeat and BTB domain containing 2
ABTB2A, BTBD22, CCA3
Leukemia

353
Anti-silencing function 1A histone chaperone
CGI-98, CIA, HSPC146
Melanoma

354
Armadillo repeat containing 8
GID5, HSPC056, S863-2, VID28
Polydactyly

355
ABI family member 3 binding protein
NESHBP, TARSH
Asthma, Diabetes mellitus, Endometrioma, Endometriosis, Leukemia, Mental depression, Urticaria

356
Alpha-1-microglobulin/bikunin precursor
A1M, EDC1, HCP, HI30, IATIL, ITI, ITIL, ITILC, UTI
Kidney failure, Mood disorder, Acute kidney insufficiency

357
Anaphase promoting complex subunit 15
APC15, C11orf51, HSPC020
Deafness

358
ALS2 C-terminal like
RN49018
Breast cancer, Schizophrenia

359
Atlastin GTPase 3
AT3, ATL-3, HSN1F
Acrosteolysis, Arthropathy, Hereditary sensory and autonomic neuropathy, Hyperkeratosis, Neuropathy, Osteomyelitis, Sensory and autonomic neuropathy

360
Assembly factor for spindle microtubules
ASP, Calmbp1, MCPH5
Adenocarcinoma, Agenesis of corpus callosum, Arthrogryposis multiplex congenita, Attention deficit hyperactivity disorder, Congenital microcephaly, Developmental delay, Dwarfism, Dysmorphic features, Hypoplasia of corpus callosum, Mental retardation, Liver carcinoma, Malformation of cortical development, Microcephaly, Motor delay, Multiple congenital anomalies
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