Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "A"

981 to 990 of 1165 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
981	79058	ASPSCR1	ASPSCR1 tether for SLC2A4, UBX domain containing	ASPCR1, ASPL, ASPS, RCC17, TUG, UBXD9, UBXN9	Attention deficit hyperactivity disorder, Insomnia, Metabolic syndrome, Willis-ekbom disease, Sarcoma, Substance abuse, Diabetes mellitus type 2
982	80150	ASRGL1	Asparaginase and isoaspartyl peptidase 1	ALP, ALP1, CRASH	Obstructive pulmonary disease, Allergic contact dermatitis, Retinitis pigmentosa
983	445	ASS1	Argininosuccinate synthase 1	ASS, CTLN1	Citrullinemia, Cardiac arrhythmia, Diabetic angiopathies, Diabetic peripheral angiopathy, Urea cycle disorder, Glycogen storage disease, Liver disease, Liver failure, Partial epilepsy, Upper aerodigestive tract neoplasm
984	28990	ASTE1	Asteroid structure-specific endonuclease 1	HT001	Constitutional mismatch repair deficiency syndrome, Lynch syndrome, Constitutional mismatch repair deficiency
985	431705	ASTL	Astacin like metalloendopeptidase	OOMD11, OZEMA11, SAS1B	Oocyte maturation defect
986	460	ASTN1	Astrotactin 1	ASTN	Brain injuries, Major depressive disorder, Substance abuse
987	23245	ASTN2	Astrotactin 2	bA67K19.1	Amphetamine or sympathomimetic abuse, Atrial fibrillation, Attention deficit hyperactivity disorder, Autism, Bardet-biedl syndrome, Bipolar disorder, Breast cancer, Obstructive pulmonary disease, Colonic neoplasms, Common migraine, Coronary artery disease, Cystitis, Endometriosis, Estrogen-receptor negative breast cancer, Hearing loss View all (21 more)
988	171023	ASXL1	ASXL transcriptional regulator 1	BOPS, MDS	Autism, Bohring syndrome, Bohring-opitz syndrome, Myelomonocytic leukemia, Developmental delay, Global developmental delay, Gross motor development delay, Hypertrichosis, Insomnia, Intellectual developmental disorder, Promyelocytic leukemia, Myelodysplastic syndrome, Rubinstein-taybi syndrome, Intellectual disability, Systemic mastocytosis, Diabetes mellitus type 2, Wilms tumor View all (2 more)
989	55252	ASXL2	ASXL transcriptional regulator 2	ASXH2, SHAPNS	Autism, Breast cancer, Developmental disability, Gout, Myeloid leukemia, Neurodevelopmental disorder, Diabetes mellitus type 2, Urinary bladder neoplasms
990	80816	ASXL3	ASXL transcriptional regulator 3	BRPS, KIAA1713	Asthma, Autism, Bipolar disorder, Color vision deficiency, Epilepsy, Global developmental delay, Heart failure, Insomnia, Intellectual developmental disorder, Major depressive disorder, Metabolic syndrome, Neurodevelopmental disorder, Neurotic disorder, Ovarian cancer, Parkinson disease View all (4 more)

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