Genesⓘ

Dataset:
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "H"
391 to 400 of 426 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

391
Hook microtubule tethering protein 3
HK3
Breast cancer, Sclerocystic ovaries, Polycystic ovary syndrome

392
HHIP like 1
KIAA1822, UNQ9245
Coronary arteriosclerosis, Coronary artery disease, Coronary heart disease

393
Hes family bHLH transcription factor 7
SCDO4, bHLHb37, hHes7
Abnormal spinal segmentation, Congenital diaphragmatic hernia, Congenital exomphalos, Rib fusion, Congenital meningocele, Cryptorchidism, Dwarfism, Hypospadias, Jarcho-levin syndrome, Macrocephaly, Meningomyelocele, Mental retardation, Microcephaly, Pulmonary venous return anomaly, Scoliosis
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394
HDGF like 2
HDGF-2, HDGF2, HDGFRP2, HRP-2, HRP2
Leukemia

395
Hepatitis A virus cellular receptor 2
CD366, HAVcr-2, KIM-3, SPTCL, TIM3, TIMD-3, TIMD3, Tim-3
Blood coagulation disorders, Fibrinogen deficiency, Hemophagocytic lymphohistiocytosis, Hemophagocytic syndrome, Histiocytosis haematophagic, Hypofibrinogenemia, Lymphohistiocytosis, Panniculitis, Reactive hemophagocytic syndrome, Subcutaneous panniculitis-like t-cell lymphoma

396
Histone acetyltransferase 1
KAT1
Colorectal cancer, Schizophrenia

397
H2B clustered histone 12
H2B/S, H2BFAiii, H2BFT, H2BK, HIST1H2BK
Breast cancer, Mammary neoplasms, Breast carcinoma, Marfan syndrome

398
Heat shock transcription factor Y-linked 1
HSF2L, HSFY
Azoospermia, Nonobstructive spermatogenic failure, y-linked

399
Hyaluronidase 2
LUCA2, MCCS
Cleft lip and palate-craniofacial dysmorphism-congenital heart defect-hearing loss syndrome

400
HESX homeobox 1
ANF, CPHD5, RPX
Absence of septum pellucidum, Agenesis of corpus callosum, Autism, Central hypothyroidism, Congenital exomphalos, Breast hypoplasia, Congenital hypoplasia of penis, Cryptorchidism, Developmental delay, Diabetes insipidus, Dwarfism, Dysarthria, Dyssomnia, Ectopic anterior pituitary gland, Esophageal atresia
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