Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
6081 to 6090 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

6081
Hyaluronidase 3
HYAL-3, LUCA-3, LUCA3
Auroneurodental syndrome, Metabolic syndrome, Diabetes mellitus type 2

6082
Hyccin PI4KA lipid kinase complex subunit 1
DRCTNNB1A, FAM126A, HCC, HLD5
Astrocytoma, Bipolar disorder, Hypomyelinating leukodystrophy, Intellectual developmental disorder, Parkinson disease, Periodontitis, Scoliosis

6083
Hyccin PI4KA lipid kinase complex subunit 2
FAM126B
Breast cancer, Lymphocytic leukemia, Non-melanoma skin carcinoma

6084
HYDIN axonemal central pair apparatus protein
CILD5, HYDIN1, HYDIN2, PPP1R31
Alzheimer disease, Astrocytoma, Celiac disease, Obstructive pulmonary disease, Ciliary dyskinesia, Color vision deficiency, Congenital nasopharyngeal atresia, Glioma, Hydrocephalus, Hypertension, Paroxysmal tachycardia, Scoliosis, Teratozoospermia

6085
Hydroxypyruvate isomerase (putative)
HT036
Alzheimer disease, Developmental and epileptic encephalopathy

6086
Hydroxylysine kinase
AGPHD1
Brain aneurysm, Obstructive airway disease, Obstructive pulmonary disease, Color vision deficiency, Lysine metabolism disorder, Heart failure, Lung cancer, Osteoarthritis, Peripheral arterial disease, Schizophrenia, Squamous cell carcinoma

6087
HYLS1 centriolar and ciliogenesis associated
HLS
Anencephaly, Cerebellar atrophy, Congenital heart defects, Dandy-walker syndrome, Desbuquois syndrome, Aplasia of the vermis, Hydrolethalus syndrome, Joubert syndrome, Neurodevelopmental disorder

6088
Hypoxia up-regulated 1
GRP-170, Grp170, HSP12A, IMD59, ORP-150, ORP150
B-cell acute lymphoblastic leukemia, Immunodeficiency, Spinocerebellar ataxia

6089
Islet amyloid polypeptide
DAP, IAP
Diabetes mellitus type 1, Diabetes mellitus type 2, Gastric ulcer

6090
Isoleucyl-tRNA synthetase 1
GRIDHH, IARS, ILERS, ILRS, IRS, PRO0785
Global developmental delay, Growth retardation, impaired intellectual development, hypotonia, and hepatopathy