Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "H"

11 to 20 of 426 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
11	100288742	H2BC2P	H2B clustered histone 2, pseudogene	H2BFVP, HIST1H2BPS1, bA317E16.4	Gout, Gouty arthritis
12	100316868	HOTTIP	HOXA distal transcript antisense RNA	HOXA-AS6, HOXA13-AS1, NCRNA00213	Cardiovascular diseases, Hand-foot-genital syndrome, Hypertension
13	10042	HMGXB4	HMG-box containing 4	HMG2L1, HMGBCG, P53N, THC211630	Bipolar disorder, Major affective disorder
14	100421397	HNRNPA1P68	Heterogeneous nuclear ribonucleoprotein A1 pseudogene 68	-	Multiple sclerosis
15	100506311	HOTAIRM1	HOXA transcript antisense RNA, myeloid-specific 1	HOXA-AS1, HOXA1-AS1, NCRNA00179	Bosley-salih-alorainy syndrome, Human hoxa1 syndromes
16	100506783	HOXD-AS2	HOXD cluster antisense RNA 2	-	Alopecia, Alopecia, male pattern, Androgenetic alopecia, Kidney failure, Narcolepsy
17	100529241	HSPE1-MOB4	HSPE1-MOB4 readthrough	HSPE1-PHOCN	Development disorder, Schizophrenia
18	100534595	HNRNPUL2-BSCL2	HNRNPUL2-BSCL2 readthrough (NMD candidate)	-	Congenital lipodystrophy, Dysautonomia, Encephalopathy, with or without lipodystrophy, Lipodystrophy, Monogenic diabetes, Neuronopathy, Partial lipodystrophy, Sensorimotor neuropathy, Spastic paraplegia
19	10075	HUWE1	HECT, UBA and WWE domain containing E3 ubiquitin protein ligase 1	ARF-BP1, HECTH9, HSPC272, Ib772, LASU1, MRXST, MULE, URE-B1, UREB1	Cubitus valgus, Autism, Blepharophimosis, Brachycephaly, Brachydactyly, Camptodactyly of fingers, Cerebral atrophy, Clinodactyly, Congenital camptodactyly, Congenital epicanthus, Congenital pectus excavatum, Craniosynostosis, Cryptorchidism, Developmental delay, Dwarfism View all (33 more)
20	100750326	HTT-AS	HTT antisense RNA	HTT-AS1, HTTAS	Huntington disease

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