|
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, Amyotrophy, Anaplastic carcinoma, Anxiety disorder, Aphasia, Brain atrophy, Carcinoma, Cardiomyopathy, Cataract, Cerebral atrophy, Congestive heart failure, Cranial nerve compression, Dwarfism, Dyscalculia, Fatty liver, Frontotemporal dementia, Inclusion body myopathy with paget disease and frontotemporal dementia, Inclusion body myopathy with paget disease with or without frontotemporal dementia, Language disorders, Laryngospasm, Limb-girdle muscular dystrophy, Lung adenocarcinoma, Mental depression, Mental retardation, Mood swings, Muscular dystrophy, Myopathy, Respiratory failureView all (13 more) |
|
213
|
|
|
Heterogeneous nuclear ribonucleoprotein A2/B1 |
HNRNPA2, HNRNPB1, HNRPA2, HNRPA2B1, HNRPB1, IBMPFD2, OPMD2, RNPA2, SNRPB1 |
Amyotrophic lateral sclerosis, Amyotrophy, Aphasia, Brain atrophy, Cardiomyopathy, Cataract, Cerebral atrophy, Congestive heart failure, Cranial nerve compression, Dwarfism, Dyscalculia, Fatty liver, Frontotemporal dementia, Inclusion body myopathy with paget disease and frontotemporal dementia, Inclusion body myopathy with paget disease with or without frontotemporal dementia, Language disorders, Mental retardation, Muscular dystrophy, Myopathy, Myositis, T-cell lymphoma/leukemiaView all (6 more) |
|
214
|
|
|
Heterogeneous nuclear ribonucleoprotein H1 |
HNRPH, HNRPH1, NEDCDS, hnRNPH |
|
|
215
|
|
|
Heterogeneous nuclear ribonucleoprotein H2 |
FTP3, HNRPH', HNRPH2, MRXSB, NRPH2, hnRNPH' |
Anxiety disorder, Autism, Congenital epicanthus, Congenital pectus carinatum, Developmental delay, Developmental regression, Dwarfism, Dysmorphic features, Gastroesophageal reflux disease, High palate, Macrostomia, Mental retardation, Micrognathism, Obsessive-compulsive disorder, Scoliosis, Syndromic mental retardation, x-linkedView all (1 more) |
|
216
|
|
|
Heterogeneous nuclear ribonucleoprotein K |
AUKS, CSBP, HNRPK, TUNP |
Atrial septal defect, Au-kline syndrome, Bilateral fetal pyelectasis, Brachycephaly, Breast cancer, Mammary neoplasms, Breast carcinoma, Clinodactyly, Congenital dermal melanocytosis, Congenital pectus excavatum, Craniosynostosis, Cryptorchidism, Developmental delay, Dolichocephaly, Dysmorphic features, High palate, Hypertrichosis, Hypodontia, Macrotia, Malocclusion, Marfan syndrome, Mental retardation, Microtia, Multiple congenital anomalies, Muscular ventricular septal defect, Neck webbing, Hypotonia, Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome, Oligodontia, Patent ductus arteriosus, Patent foramen ovale, Polydactyly, Ptosis, Sagittal craniosynostosis, Scoliosis, Supernumerary mesiodens tooth, Ventricular septal defectView all (22 more) |
|
217
|
|
|
Heterogeneous nuclear ribonucleoprotein L |
HNRPL, P/OKcl.14, hnRNP-L |
|
|
218
|
|
|
Heterogeneous nuclear ribonucleoprotein U |
DEE54, EIEE54, GRIP120, HNRNPU-AS1, HNRPU, SAF-A, SAFA, U21.1, hnRNP U, pp120 |
1q44 microdeletion syndrome, Agenesis of corpus callosum, Congenital epicanthus, Congenital malrotation of intestine, Cytochrome-c oxidase deficiency, Developmental delay, Dwarfism, Dysmorphic features, Epilepsy, Epileptic encephalopathy, Frontal bossing, Heart septal defects, High palate, Horseshoe kidney, Hydrocephalus, Hypoplasia of optic disc, Mental retardation, Microcephaly, Micrognathism, Neurodevelopmental disorders, Scoliosis, Seizure, Strabismus, Synophrys, Vesicoureteral refluxView all (10 more) |
|
219
|
|
|
Homeobox A1 |
BSAS, HOX1, HOX1F |
|
|
220
|
|
|
Homeobox A2 |
HOX1K, MCOHI |
Attention deficit hyperactivity disorder, Bilateral microtia-deafness-cleft palate syndrome, Anotia, Gastric cancer, Hearing loss, Holoprosencephaly, Microtia, Microtia with or without hearing impairment, Microtia without hearing impairment, Microtia, hearing impairment, and cleft palate, Stomach neoplasms |
