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"
711 to 720 of 1165 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

711
Adaptor related protein complex 4 subunit mu 1
CPSQ3, MU-4, MU-ARP2, SPG50
Alzheimer disease, Ap-4 deficiency syndrome, Ap4-related intellectual disability and spastic paraplegia, Brain atrophy, Congenital neurologic anomalies, Global developmental delay, Intellectual developmental disorder, Intellectual disability, Spastic paraplegia, Hereditary spastic paraplegia

712
Adaptor related protein complex 4 subunit sigma 1
AP47B, CLA20, CLAPS4, CPSQ6, SPG52
Ap-4 deficiency syndrome, Ap4-related intellectual disability and spastic paraplegia, Intellectual developmental disorder, Neurodevelopmental disorder, Schizophrenia, Intellectual disability, Spastic paraplegia, Hereditary spastic paraplegia

713
Adaptor related protein complex 5 subunit beta 1
AP-5, PP1030
Asthma, Eczema, Kidney disease, Gout, Hypertensive nephropathy, Hyperuricemia, Kidney failure, Psoriasis, Respiratory system disease, Hereditary spastic paraplegia, Systemic lupus erythematosus

714
Adaptor related protein complex 5 subunit mu 1
C14orf108, MUDENG, Mu5, MuD
Astrocytoma, Renal cell carcinoma, Central nervous system cancer, Glioma, Scoliosis

715
Adaptor related protein complex 5 subunit zeta 1
KIAA0415, SPG48, zeta
Spastic paraplegia, Central nervous system cancer, Glioblastoma, Glioma, Optic atrophy, Peripheral arterial disease, Willis-ekbom disease, Myopia, Hereditary spastic paraplegia

716
Apoptotic peptidase activating factor 1
APAF-1, CED4
Renal cell carcinoma, Transitional cell carcinoma, Color vision deficiency, Congenital skin anomaly, Craniofacial abnormalities, Major depressive disorder, Eye abnormalities, Neural tube defect, Retinal detachment, Skin abnormalities, Depression

717
Amyloid beta precursor protein binding family A member 1
D9S411E, LIN10, MINT1, X11, X11A, X11ALPHA
Alzheimer disease, Schizophrenia, Scoliosis

718
Amyloid beta precursor protein binding family A member 2
D15S1518E, HsT16821, LIN-10, MGC:14091, MINT2, X11-BETA, X11L
Dermatologic disorder, Epilepsy, Glioma, Synovitis, acne, pustulosis, hyperostosis, and osteitis, Schizophrenia, Skin disease

719
Amyloid beta precursor protein binding family B member 1
FE65, MGC:9072, RIR
Alzheimer disease, Niemann-pick disease

720
Amyloid beta precursor protein binding family B member 1 interacting protein
INAG1, PREL1, RARP1, RIAM
Scoliosis, Diabetes mellitus type 2, Upper aerodigestive tract neoplasm