Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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4071 to 4080 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

4071
ELOVL fatty acid elongase 2
SSC2
Male infertility

4072
ELOVL fatty acid elongase 3
CIG-30, CIG30
Alzheimer disease, Atrial fibrillation, Attention deficit hyperactivity disorder, Substance abuse, Systemic lupus erythematosus

4073
ELOVL fatty acid elongase 4
ADMD, CT118, ISQMR, SCA34, STGD2, STGD3
Obstructive pulmonary disease, Congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome, Corneal dystrophy, Elsahy-waters syndrome, Erythrokeratodermia with ataxia, Hereditary corneal dystrophy, Retinitis pigmentosa, Rosacea, Spastic ataxia, Spinocerebellar ataxia, Stargardt disease

4074
ELOVL fatty acid elongase 5
HELO1, SCA38, dJ483K16.1
Spinocerebellar ataxia, Colorectal cancer, Exostoses, Glaucoma, Squamous cell carcinoma, Diabetes mellitus type 2

4075
ELOVL fatty acid elongase 6
FACE, FAE, LCE, hELO2
Attention deficit hyperactivity disorder, Benign prostatic hyperplasia, Congestive heart failure, Heart failure, Obesity

4076
ELOVL fatty acid elongase 7
-
Alzheimer disease, Lewy body disease, Multiple system atrophy, Parkinson disease

4077
Elongator acetyltransferase complex subunit 1
DYS, FD, IKAP, IKBKAP, IKI3, TOT1
Asthma, Attention deficit hyperactivity disorder, Breast neoplasms, Charcot-marie-tooth disease, Dysautonomia, Gaucher disease, Medulloblastoma, Hereditary sensory and autonomic neuropathy, Riley-day syndrome, Scoliosis, Substance abuse

4078
Elongator acetyltransferase complex subunit 2
MRT58, SHINC-2, STATIP1, StIP
Intellectual developmental disorder, Major depressive disorder, Oligodendroglioma

4079
Elongator acetyltransferase complex subunit 3
KAT9
Amyotrophic lateral sclerosis, Breast neoplasms, Metabolic syndrome, Scoliosis, Systemic lupus erythematosus, Hypertension, Diabetes mellitus type 2

4080
Elongator acetyltransferase complex subunit 4
AN, AN2, C11orf19, PAX6NEB, PAXNEB, dJ68P15A.1, hELP4
Aniridia, Anophthalmia/microphthalmia-esophageal atresia syndrome, Anophthalmia, Autism, Coloboma, Congenital ocular coloboma, Gastrointestinal stromal tumor, Glaucoma, Global developmental delay, Insomnia, Anterior segment dysgenesis, Keratitis, Macular telangiectasia, Neurotic disorder, Nystagmus
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