Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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3851 to 3860 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

3851
Dynactin associated protein
C18orf26
Asthma, Oligodendroglioma, Uveal melanoma

3852
Dynein cytoplasmic 1 heavy chain 1
CDCBM13, CMT2O, DHC1, DHC1a, DNCH1, DNCL, DNECL, DYHC, Dnchc1, HL-3, SMALED1, p22
Amyotrophic lateral sclerosis, Arthrogryposis multiplex congenita, Autism, Cerebellar ataxia, Charcot-marie-tooth disease, Childhood-onset spinal muscular atrophy, Distal hereditary motor neuropathy, Nonsyndromic intellectual disability, Cerebellar atrophy, Congenital neurologic anomalies, Congenital pes cavus, Cortical dysplasia with other brain malformations, Dejerine-sottas disease, Distal spinal muscular atrophy, Spinal muscular atrophy
View all (23 more)

3853
Dynein cytoplasmic 1 intermediate chain 1
DNCI1, DNCIC1
Alzheimer disease, Astrocytoma, Dementia, Major depressive disorder, Non-neoplastic peripheral nervous system disease, Obesity, Osteoarthritis, Peripheral nervous system disease, Peripheral neuropathy

3854
Dynein cytoplasmic 1 intermediate chain 2
DIC74, DNCI2, IC2, NEDMIBA
Eye disease, Neurodevelopmental disorder, Prostate cancer, Schizophrenia

3855
Dynein cytoplasmic 2 heavy chain 1
ATD3, DHC1b, DHC2, DNCH2, DYH1B, SRPS2B, SRTD3, hdhc11
Jeune syndrome, Asthma, Polycystic kidney disease, Retinitis pigmentosa, Bowed long bones, Breast neoplasms, Ciliopathy, Clinodactyly, Congenital heart defects, Desbuquois syndrome, Gout, Hypertension, Intellectual developmental disorder, Jeune thoracic dystrophy, Majewski syndrome
View all (10 more)

3856
Dynein 2 intermediate chain 1
CFAP163, DIC6, FAP163, SRPS6, SRTD8, WDR60
Jeune syndrome, Cutaneous mastocytosis, Desbuquois syndrome, Jeune thoracic dystrophy, Saldino-noonan syndrome, Scoliosis, Short rib dysplasia-polydactyly syndrome, Short-rib thoracic dysplasia

3857
Dynein 2 intermediate chain 2
CFAP133, DIC5, FAP133, SRTD11, WDR34, bA216B9.3
Jeune syndrome, Desbuquois syndrome, Jeune thoracic dystrophy, Saldino-noonan syndrome, Short rib dysplasia-polydactyly syndrome, Short-rib thoracic dysplasia

3858
Dynein cytoplasmic 2 light intermediate chain 1
CGI-60, D2LIC, LIC3
Jeune syndrome, Cholecystolithiasis, Kidney disease, Desbuquois syndrome, Ellis-van creveld syndrome, Jeune thoracic dystrophy, Kidney failure, Majewski syndrome, Short rib dysplasia-polydactyly syndrome, Short-rib thoracic dysplasia, Sitosterolemia, Thrombocytopenia

3859
Dynein light chain LC8-type 1
DLC1, DLC8, DNCL1, DNCLC1, LC8, LC8a, PIN, hdlc1
Brain ischemia

3860
Dynein light chain roadblock-type 1
BITH, BLP, DNCL2A, DNLC2A, ROBLD1
Bipolar disorder