Genes | GeDiPNet - Gene Disease Pathway & Associations

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3641 to 3650 of 12229 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
3641	23460	ABCA6	ATP binding cassette subfamily A member 6	EST155051	Colorectal cancer, Colorectal neoplasms, Dermatitis
3642	23461	ABCA5	ATP binding cassette subfamily A member 5	ABC13, DEL17q24, EST90625, HTC3, HTGH	Colorectal cancer, Colorectal neoplasms, Gingival fibromatosis-hypertrichosis syndrome, Hypertrichosis, Impaired cognition, Schizophrenia, Synophrys
3643	23462	HEY1	Hes related family bHLH transcription factor with YRPW motif 1	BHLHb31, CHF2, HERP2, HESR1, HRT-1, NERP2, OAF1, hHRT1	Anaplastic astrocytoma, Anaplastic oligodendroglioma, Astrocytoma, Autism spectrum disorder, Breast cancer, Mammary neoplasms, Breast carcinoma, Cerebral primitive neuroectodermal tumor, Ependymoblastoma, Fibrillary astrocytoma, Gemistocytic astrocytoma, Giant cell glioblastoma, Glioblastoma, Grade i astrocytoma, Intracranial astrocytoma View all (13 more)
3644	23468	CBX5	Chromobox 5	HEL25, HP1, HP1A, HP1alpha	Colorectal cancer, Colorectal neoplasms
3645	23469	PHF3	PHD finger protein 3	-	Mental depression, Retinal dystrophy, Retinitis pigmentosa, Rod-cone dystrophy
3646	23474	ETHE1	ETHE1 persulfide dioxygenase	HSCO, YF13H12	Developmental delay, Developmental regression, Epileptic encephalopathy, Ethylmalonic encephalopathy, Leigh syndrome, Mental retardation, Necrotizing encephalomyelopathy
3647	23476	BRD4	Bromodomain containing 4	CAP, CDLS6, FSHRG4, HUNK1, HUNKI, MCAP	Alopecia, Alopecia, male pattern, Androgenetic alopecia, Carcinoma, Colonic neoplasms, Congenital heart defects, Congenital muscular hypertrophy-cerebral syndrome, Cornelia de lange syndrome, Ewing sarcoma, Giant cell glioblastoma, Glioblastoma, Leukemia, Medulloblastoma, Medullomyoblastoma, Mental retardation View all (13 more)
3648	23478	SEC11A	SEC11 homolog A, signal peptidase complex subunit	1810012E07Rik, SEC11L1, SPC18, SPCS4A, sid2895	Bipolar disorder, Mental depression
3649	23479	ISCU	Iron-sulfur cluster assembly enzyme	2310020H20Rik, HML, ISU2, NIFU, NIFUN, hnifU	Hereditary myopathy with lactic acidosis, Mitochondrial myopathy, Myopathy, Sideroblastic anemia
3650	2348	FOLR1	Folate receptor alpha	FBP, FOLR, FRalpha, NCFTD	Acrania, Anencephaly, Central nervous system inborn metabolic diseases, Colonic neoplasms, Congenital heart defects, Craniorachischisis, Developmental regression, Diastematomyelia, Epilepsy, Epileptic encephalopathy, Mental retardation, Movement disorders, Narcolepsy, Neural tube defect, Neurenteric cyst View all (8 more)

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