Genesⓘ

Dataset:
? Protein-coding genes with reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
711 to 720 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

711
Adaptor related protein complex 4 subunit epsilon 1
CPSQ4, SPG51, STUT1
Ap-4 deficiency syndrome, Ap4-related intellectual disability and spastic paraplegia, Cerebral amyloid angiopathy, Congenital disorder of glycosylation, Congenital neurologic anomalies, Coronary artery disease, Developmental disability, Gout, Intellectual developmental disorder, Peripheral neuropathy, Intellectual disability, Spastic paraplegia, Hereditary spastic paraplegia

712
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

713
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

714
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

715
Adaptor related protein complex 5 subunit mu 1
C14orf108, MUDENG, Mu5, MuD
Astrocytoma, Renal cell carcinoma, Central nervous system cancer, Glioma, Scoliosis

716
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

717
317
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, Liver cirrhosis, Neural tube defect, Retinal detachment, Skin abnormalities, Depression

718
320
Amyloid beta precursor protein binding family A member 1
D9S411E, LIN10, MINT1, X11, X11A, X11ALPHA
Alzheimer disease, Schizophrenia, Scoliosis

719
321
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

720
322
Amyloid beta precursor protein binding family B member 1
FE65, MGC:9072, RIR
Alzheimer disease, Niemann-pick disease