Genes | GeDiPNet - Gene Disease Pathway & Associations

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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

1691 to 1700 of 12229 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
1691	118461	C10orf71	Chromosome 10 open reading frame 71	CEFIP, CMD1QQ	Alzheimer disease
1692	118490	MSS51	MSS51 mitochondrial translational activator	ZMYND17	Schizophrenia
1693	118491	CFAP70	Cilia and flagella associated protein 70	SPGF41, TTC18	Non-syndromic male infertility due to sperm motility disorder
1694	1185	CLCN6	Chloride voltage-gated channel 6	CLC-6, CONRIBA	Atrial fibrillation, Atrial standstill, Cardiovascular diseases, Psoriasis
1695	1186	CLCN7	Chloride voltage-gated channel 7	CLC-7, CLC7, HOD, OPTA2, OPTB4, PPP1R63	Albers-schonberg osteopetrosis, Anemia, Arthritis, Cerebellar atrophy, Congenital osteopetrosis, Cranial nerve paralysis, Craniosynostosis, Developmental delay, Dwarfism, Facial paralysis, Frontal bossing, Hydrocephalus, Hypopigmentation disorder, Macrocephaly, Malignant osteopetrosis View all (11 more)
1696	118611	C10orf90	Chromosome 10 open reading frame 90	FATS, bA422P15.2	Leukemia, Prostate cancer, Schizophrenia
1697	118672	PSTK	Phosphoseryl-tRNA kinase	C10orf89	Hypertension
1698	1187	CLCNKA	Chloride voltage-gated channel Ka	CLCK1, ClC-K1, hClC-Ka	Bartter syndrome, Bartter syndrome with sensorineural deafness, Hearing loss, Hyperaldosteronism, Hypernatriuria, Hypertension, Hypochloremia, Hypokalemia, Mental retardation, Motor delay, Renal insufficiency
1699	118788	PIK3AP1	Phosphoinositide-3-kinase adaptor protein 1	BCAP	Colorectal neoplasms, Narcolepsy
1700	1188	CLCNKB	Chloride voltage-gated channel Kb	CLCKB, ClC-K2, ClC-Kb	Bartter syndrome, Bartter syndrome with hypocalciuria, Bartter syndrome with sensorineural deafness, Chondrocalcinosis, Conn syndrome, Diabetes mellitus, Diabetic ketoacidosis, Fanconi syndrome, Focal seizures, Gitelman syndrome, Glomerulosclerosis, Gout, Graves disease, Hashimoto disease, Hearing loss View all (23 more)

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