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
5771 to 5780 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

5771
Hes family bHLH transcription factor 5
bHLHb38
Brain neoplasms, Nervous system disease

5772
Hes family bHLH transcription factor 6
C-HAIRY1, HES-6, bHLHb41, bHLHc23
Irritable bowel syndrome, Mood disorder

5773
Hes family bHLH transcription factor 7
SCDO4, bHLHb37, hHes7
Spondylocostal dysostosis, Desbuquois syndrome, Iga nephropathy, Jarcho-levin syndrome, Hypertension

5774
HESX homeobox 1
ANF, CPHD5, RPX
Alzheimer disease, Anophthalmia/microphthalmia-esophageal atresia syndrome, Combined pituitary hormone deficiency, Desbuquois syndrome, Growth hormone deficiency with pituitary anomalies, Hypothyroidism, Kallmann syndrome, Male infertility spermatogenesis disorder, Panhypopituitarism, Pituitary hormone deficiency, Pituitary stalk interruption syndrome, Septo-optic dysplasia

5775
Hexosaminidase subunit alpha
TSD
Beta-hexosaminidase a deficiency, Global developmental delay, Gm2 gangliosidosis, Hearing impairment, Intellectual developmental disorder, Leukodystrophy, Tay-sachs disease

5776
Hexosaminidase subunit beta
ENC-1AS, HEL-248, HEL-S-111
Kidney failure, Sandhoff disease, Spinal muscular atrophy

5777
Hexosaminidase D
HEXDC
Colorectal adenoma, Colorectal cancer

5778
HEXIM P-TEFb complex subunit 1
CLP1, EDG1, HIS1, MAQ1
Asthma, Insomnia, Osteoarthritis

5779
HEXIM P-TEFb complex subunit 2
L3
Androgenetic alopecia, Insomnia

5780
Hes related family bHLH transcription factor with YRPW motif 1
BHLHb31, CHF2, HERP2, HESR1, HRT-1, NERP2, OAF1, hHRT1
Astrocytoma, Autism, Breast neoplasms, Pancreatic ductal carcinoma, Congenital heart disease, Glioblastoma, Lung neoplasms, Oligodendroglioma, Urethral obstruction