Genesⓘ

Dataset:
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "H"
111 to 120 of 426 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

111
H1.2 linker histone, cluster member
H1.2, H1C, H1F2, H1s-1, HIST1H1C
Breast cancer, Mammary neoplasms, Breast carcinoma, Gout, Gouty arthritis, Leukemia, Marfan syndrome, Myeloid leukemia

112
H1.4 linker histone, cluster member
H1.4, H1E, H1F4, H1s-4, HIST1H1E, RMNS, dJ221C16.5
Acquired kyphoscoliosis, Adenocarcinoma, Astigmatism, Colorectal cancer, Congenital camptodactyly, Congenital clubfoot, Congenital kyphoscoliosis, Developmental delay, Dysmorphic features, Macrocephaly, Mental retardation, Hypotonia, Nevus, Rahman syndrome, Schizophrenia
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113
H1.5 linker histone, cluster member
H1, H1.5, H1B, H1F5, H1s-3, HIST1H1B
Colorectal cancer, Schizophrenia

114
H1.6 linker histone, cluster member
H1.6, H1FT, H1t, HIST1H1T, dJ221C16.2
Gout, Gouty arthritis

115
H2A clustered histone 8
H2A.1, H2A.2, H2A/a, H2AC4, H2AFA, HIST1H2AE
Arthritis, Juvenile arthritis, Seronegative polyarthritis, Polyarthritis, rheumatoid factor positive, Still disease

116
H2A.X variant histone
H2A.X, H2A/X, H2AFX
Breast cancer, Mammary neoplasms, Breast carcinoma, Giant cell glioblastoma, Glioblastoma, Marfan syndrome, Schizophrenia

117
H3.3 histone A
BRYLIB1, H3-3B, H3.3A, H3F3, H3F3A
Adrenocortical carcinoma, Astigmatism, Astrocytoma, Brain neoplasms, Brain stem glioma, Camptodactyly, Craniosynostosis, Cryptorchidism, Deafness, Developmental delay, Dolichocephaly, Dysmorphic features, Dysphagia, Exotropia, Frontal bossing
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118
H3.3 histone B
BRYLIB2, H3-3A, H3.3B, H3F3B
Chondroblastoma

119
Hyaluronan binding protein 2
FSAP, HABP, HGFAL, NMTC5, PHBP, PHBSP
Nonmedullary thyroid carcinoma, Colonic neoplasms, Follicular thyroid carcinoma, Head and neck neoplasms, Lung diseases, Miscarriage, Nodular goiter, Papillary renal carcinoma, Papillary thyroid carcinoma, Spinal cord compression, Thrombophilia, Thrombosis, Thyroid cancer, Thyroid carcinoma

120
Hydroxysteroid 17-beta dehydrogenase 10
17b-HSD10, ABAD, CAMR, DUPXp11.22, ERAB, HADH2, HCD2, HSD10MD, MHBD, MRPP2, MRX17, MRX31, MRXS10, SCHAD, SDR5C1
Cerebral cortical atrophy, Choreoathetosis, Developmental delay, Developmental regression, Dysarthria, Hearing loss, Hsd10 disease, Hypertrophic cardiomyopathy, Hypoglycemia, Lung adenocarcinoma, Mental retardation, Mental retardation, x-linked, Movement disorders, Nystagmus, Optic atrophy
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