Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "H"
211 to 220 of 426 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

211
H2A clustered histone 21
H2AB, HIST2H2AB

212
Heterogeneous nuclear ribonucleoprotein A1
ALS19, ALS20, HNRPA1, HNRPA1L3, IBMPFD3, MPD3, UP 1, hnRNP A1, hnRNP-A1
Amyotrophic lateral sclerosis, Carcinoma, Distal muscular dystrophy, Multiple sclerosis

213
Heterogeneous nuclear ribonucleoprotein A2/B1
HNRNPA2, HNRNPB1, HNRPA2, HNRPA2B1, HNRPB1, IBMPFD2, OPMD2, RNPA2, SNRPB1
Amyotrophic lateral sclerosis, Frontotemporal dementia, T-cell leukemia-lymphoma, Oculopharyngeal muscular dystrophy, Vacuolar myopathy

214
Heterogeneous nuclear ribonucleoprotein H1
HNRPH, HNRPH1, NEDCDS, hnRNPH
Intellectual developmental disorder, x-linked, Neurodevelopmental disorder, Neurodevelopmental disorders, Prostatic neoplasm, Sjogren syndrome

215
Heterogeneous nuclear ribonucleoprotein H2
FTP3, HNRPH', HNRPH2, MRXSB, NRPH2, hnRNPH'
Fabry disease, Intellectual developmental disorder, x-linked, Neurodevelopmental disorder, Neurodevelopmental disorders, X-linked complex neurodevelopmental disorder

216
Heterogeneous nuclear ribonucleoprotein K
AUKS, CSBP, HNRPK, TUNP
Attention deficit hyperactivity disorder, Au-kline syndrome, Breast neoplasm, Intellectual developmental disorder, Neurodevelopmental disorder, Raynaud disease

217
Heterogeneous nuclear ribonucleoprotein L
HNRPL, P/OKcl.14, hnRNP-L
Breast neoplasm, Neurodevelopmental disorder, Non-specific syndromic intellectual disability, Stomach neoplasms, Systemic sclerosis

218
Heterogeneous nuclear ribonucleoprotein U
DEE54, EIEE54, GRIP120, HNRNPU-AS1, HNRPU, SAF-A, SAFA, U21.1, hnRNP U, pp120
1q44 microdeletion syndrome, Neurodevelopmental disorder, Developmental and epileptic encephalopathy, Epilepsy, Intellectual developmental disorder, Neurodevelopmental disorders, Non-specific syndromic intellectual disability, Oligodendroglioma

219
Homeobox A1
BSAS, HOX1, HOX1F
Athabaskan brainstem dysgenesis, Autism, Bosley-salih-alorainy syndrome, Congenital heart defects, Congenital neurologic anomalies , Craniofacial abnormalities, Congenital heart defect, Intellectual developmental disorder, Multiple sclerosis

220
Homeobox A2
HOX1K, MCOHI
Hearing impairment, Microtia, Stomach neoplasms