Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
Showing genes starting with "A"
601 to 610 of 1165 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

601
Ankyrin repeat and FYVE domain containing 1
ANKHZN, BTBD23, ZFYVE14
Idiopathic steroid-resistant nephrotic syndrome, Genetic steroid-resistant nephrotic syndrome, Hereditary steroid-resistant nephrotic syndrome, Kidney disease, Schizophrenia, Diabetes mellitus type 2, Urinary bladder neoplasms

602
ANKH inorganic pyrophosphate transport regulator
ANK, CCAL2, CMDJ, CPPDD, HANK, MANK, SLC62A1
Alzheimer disease, Calcium metabolism disorders, Chondrocalcinosis, Craniofacial abnormalities, Craniometadiaphyseal dysplasia, Craniometaphyseal dysplasia, Desbuquois syndrome, Diabetes mellitus, Diabetic neuropathy, Endometriosis, Calcium pyrophosphate deposition, Glaucoma, Intellectual developmental disorder, Open angle glaucoma, Prostate cancer
View all (4 more)

603
Ankyrin repeat and KH domain containing 1
MASK, MASK1, PP2500, VBARP
Bipolar disorder, Gallstones

604
ANKHD1-EIF4EBP3 readthrough
MASK-BP3, MASK-BP3ARF
Bipolar disorder, Gallstones, Willis-ekbom disease

605
Ankyrin repeat and IBR domain containing 1
-
Angiokeratoma, Breast cancer, Cavernous malformations of cns, Prostate cancer

606
Ankyrin repeat and kinase domain containing 1
PKK2, sgK288
Anxiety disorder, Attention deficit hyperactivity disorder, Bipolar disorder, Major depressive disorder, Language development disorders, Metabolic syndrome, Mild cognitive impairment, Neurotic disorder, Schizophrenia, Diabetes mellitus type 2

607
Ankyrin repeat and LEM domain containing 1
ANKRD41, LEM3, LEMD6
Basal cell carcinoma, Breast cancer, Essential tremor, Estrogen-receptor negative breast cancer, Ovarian cancer, Squamous cell carcinoma, Triple negative breast cancer, Upper aerodigestive tract neoplasm

608
Ankyrin repeat and LEM domain containing 2
KIAA0692, LEMD7, Lem4, MCPH16
Primary microcephaly, Childhood ataxia with cns hypomyelination, Intellectual developmental disorder, Microcephaly, Schizophrenia

609
Ankyrin repeat and MYND domain containing 2
ZMYND20
Myopia

610
Ankyrin repeat domain 1
ALRP, C-193, CARP, CVARP, MCARP, bA320F15.2
Dilated cardiomyopathy, Brugada syndrome, Cardiomyopathy, Congenital heart disease, Congenital structural myopathy, Endometriosis, Hypertrophic cardiomyopathy, Left ventricular disease, Nemaline myopathy, Spinal muscular atrophy, Tetralogy of fallot