Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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6071 to 6080 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

6071
HtrA serine peptidase 1
ARMD7, CADASIL2, CARASIL, HtrA, L56, ORF480, PRSS11
Breast cancer, Butterfly-shaped pigmentary macular dystrophy, Cadasil, Carasil syndrome, Cerebral arteriopathy with subcortical infarcts and leukoencephalopathy, Cerebral microangiopathy, Obstructive pulmonary disease, Coronary artery disease, Macular and posterior pole degeneration, Vascular dementia, Age-related macular degeneration, Glaucoma, Hypertension, Lung neoplasms, Macular degeneration
View all (8 more)

6072
HtrA serine peptidase 2
MGCA8, OMI, PARK13, PRSS25
3-methylglutaconic aciduria, Motor neuron disease, Parkinson disease, Transient ischemic attack

6073
HtrA serine peptidase 4
-
Autism

6074
Huntingtin
HD, IT15, LOMARS
Attention deficit hyperactivity disorder, Cerebral palsy, Major depressive disorder, Diffuse gastric adenocarcinoma, Dyslexia, Gastric cancer, Huntington disease, Metabolic syndrome, Mood disorder, Movement disorder, Myocardial infarction, Non-specific syndromic intellectual disability, Parkinson disease, Diabetes mellitus type 2

6075
Hormonally up-regulated Neu-associated kinase
-
Astrocytoma, Crohn disease, Hearing loss, Inflammatory bowel disease, Periodontitis, Rosacea, Diabetes mellitus type 2, Vitiligo

6076
HUS1 checkpoint clamp component B
-
Neurodevelopmental disorder

6077
HECT, UBA and WWE domain containing E3 ubiquitin protein ligase 1
ARF-BP1, HECTH9, HSPC272, Ib772, LASU1, MRXST, MULE, URE-B1, UREB1
Atrial septal defect, Autism, Bipolar disorder, Global developmental delay, Hypothyroidism, Intellectual developmental disorder, x-linked, Intellectual developmental disorder, Intellectual developmental disorder hypotonic x-linked, Male infertility single gene azoospermia, Non-specific syndromic intellectual disability, X-linked intellectual disability, Say meyer syndrome, Diabetes mellitus type 2, Ventricular septal defect

6078
Hydrogen voltage gated channel 1
HV1, VSOP
Atrial fibrillation, Gout

6079
Hyaluronidase 1
HYAL-1, LUCA1, MPS9, NAT6
Hyaluronoglucosaminidase deficiency, Mucopolysaccharidosis, Schizophrenia

6080
Hyaluronidase 2
LUCA2, MCCS
Alzheimer disease, Cleft lip and palate, craniofacial dysmorphism, congenital heart defect, hearing loss syndrome, Gastroesophageal reflux disease, Muggenthaler-chowdhury-chioza syndrome, Orofacial cleft, Peptic ulcer disease, Schizophrenia