Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "A"
1041 to 1050 of 1165 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1041
ATPase phospholipid transporting 11A
ATPIH, ATPIS, AUNA2, DFNA84, HLD24
Auditory neuropathy, Isolated sensorineural deafness, Nonsyndromic hearing loss, Basal cell carcinoma, Neurodevelopmental disorder, Melanoma, Deafness, Hearing loss, Hypomyelinating leukodystrophy, Idiopathic pulmonary fibrosis, Interstitial lung disease, Keratinocyte carcinoma, Machado-joseph disease, Non-specific syndromic intellectual disability, Skin cancer
View all (3 more)

1042
ATPase phospholipid transporting 11B (putative)
ATPIF, ATPIR
Alzheimer disease, Dementia, Prostate cancer

1043
ATPase phospholipid transporting 11C (ATP11C blood group)
ATPIG, ATPIQ, HACXL
Hemolytic anemia

1044
ATPase H+/K+ transporting non-gastric alpha2 subunit
ATP1AL1, H-K-ATPase, HK
Central nervous system cancer, Cystic fibrosis, Glioblastoma, Glioma, Obesity

1045
ATPase cation transporting 13A2
CLN12, HSA9947, KRPPD, PARK9, SPG78
Spastic paraplegia, Neuronal ceroid lipofuscinosis, Neurodegeneration with brain iron accumulation, Parkinson disease, Secondary parkinson disease

1046
ATPase 13A3
AFURS1, PPH5
Pulmonary hypertension, Pulmonary arterial hypertension

1047
ATPase 13A4
-
Bipolar disorder, Digestive system disease, Major depressive disorder

1048
ATPase 13A5
-
Hodgkin lymphoma

1049
ATPase Na+/K+ transporting subunit alpha 1
CMT2DD, HOMGSMR2
Charcot-marie-tooth disease, Bipolar disorder, Cushing syndrome, Hyperaldosteronism, Hypertension, Hypothyroidism, Intellectual developmental disorder, Myocardial infarction, Myocardial ischemia, Neurodevelopmental disorder, Neuromuscular disease, Vestibular disease

1050
ATPase Na+/K+ transporting subunit alpha 2
DEE98, FARIMPD, FHM2, MHP2
Alternating hemiplegia of childhood, Benign neonatal epilepsy, Bipolar disorder, Developmental and epileptic encephalopathy, Dysphasia, Epilepsy, Hemiplegic migraine, Hypertension, Migraine, Polymicrogyria, Spastic ataxia