Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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3631 to 3640 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

3631
Dynein axonemal assembly factor 9
C20orf194
Asthma, Color vision deficiency, Nonalcoholic fatty liver disease, Diabetes mellitus type 2

3632
Dynein axonemal heavy chain 1
CILD37, DNAHC1, HDHC7, HL-11, HL11, HSRF-1, SPGF18, XLHSRF-1
Ciliary dyskinesia, Congenital impairment of spermatozoa motility, Gout, Hypertrophic cardiomyopathy, Schizophrenia, Spermatogenic failure, Teratozoospermia, Tumor predisposition syndrome, Diabetes mellitus type 2

3633
Dynein axonemal heavy chain 10
SPGF56
Atrial fibrillation, Ciliary dyskinesia, Coronary artery disease, Diabetes mellitus, Insomnia, Male infertility, Male infertility large polyploid spermatozoa, Male infertility single gene azoospermia, Metabolic syndrome, Myocardial infarction, Osteoarthritis, Schizophrenia, Spermatogenic failure, Teratozoospermia, Tourette syndrome
View all (1 more)

3634
Dynein axonemal heavy chain 11
CILD7, DNAHBL, DNAHC11, DNHBL, DPL11
Autism, Bone remodeling disease, Breast cancer, Ciliary dyskinesia, with or without situs inversus, Ciliary dyskinesia, Color vision deficiency, Congenital nasopharyngeal atresia, Coronary artery disease, Dyslexia, Gastric cancer, Hyperlipidemia, Iga nephropathy, Insomnia, Lung cancer, Major depressive disorder
View all (8 more)

3635
Dynein axonemal heavy chain 12
DHC3, DLP12, DLP3, DNAH12L, DNAH7L, DNAHC12, DNAHC3, DNHD2, HDHC3, HL-19, HL19, SPGF100
Alzheimer disease, Gastroesophageal reflux disease, Spermatogenic failure

3636
Dynein axonemal heavy chain 14
C1orf67, Dnahc14, HL-18, HL18
Alzheimer disease, Astrocytoma, Neurodevelopmental disorder, Pancreatic neoplasms, Ciliary dyskinesia, Prostate cancer, Scoliosis, Intellectual disability

3637
Dynein axonemal heavy chain 17
DNAHL1, DNEL2, SPGF39
Color vision deficiency, Congenital impairment of spermatozoa motility, Dilated cardiomyopathy, Male infertility spermatogenesis disorder, Parkinson disease, Spermatogenic failure

3638
Dynein axonemal heavy chain 2
DNAHC2, DNHD3, SPGF45
Atrial fibrillation, Cancer, Central nervous system cancer, Congenital microcephaly, Coronary artery disease, Diabetes mellitus, Glioblastoma, Glioma, Heart failure, Non-melanoma skin carcinoma, Spermatogenic failure, Stroke, Diabetes mellitus type 1, Diabetes mellitus type 2, Uterine fibroid

3639
Dynein axonemal heavy chain 3
DNAHC3-B, DNAHC3B, HDHC8, HEL-36, HSADHC3
Gout, Intellectual developmental disorder, Male infertility, Spermatogenic failure

3640
Dynein axonemal heavy chain 5
CILD3, DNAHC5, HL1, KTGNR, PCD
Asthma, Autism, Obstructive pulmonary disease, Ciliary dyskinesia, with or without situs inversus, Ciliary dyskinesia, Color vision deficiency, Congenital nasopharyngeal atresia, Corneal astigmatism, Gout, Male infertility, Neuroblastoma, Polynesian bronchiectasis, Seasonal allergic rhinitis, Situs ambiguus, Situs inversus
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