Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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181 to 190 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

181
Actin beta
BKRNS, BNS, BRWS1, CSMH, DDS1, PS1TP5BP1, THC8
Thrombocytopenia, Alzheimer disease, Aminoacylase deficiency, Baraitser-winter cerebrofrontofacial syndrome, Becker nevus syndrome, Bipolar disorder, Carcinoma, Hepatocellular carcinoma, Central nervous system cancer, Coloboma, Congenital neurologic anomalies, Congenital ocular coloboma, Congenital smooth muscle hamartoma, Craniofacial abnormalities, Desbuquois syndrome
View all (16 more)

182
Actin alpha cardiac muscle 1
ACTC, ASD5, CMD1R, CMH11, LVNC4
Arrhythmogenic right ventricular cardiomyopathy, Arthrogryposis, Atrial septal defect, Cardiomyopathy, Dilated cardiomyopathy, Dilatation of left cardiac ventricle, Restrictive cardiomyopathy, Hypertrophic cardiomyopathy, Left ventricular disease, Left ventricular noncompaction cardiomyopathy, Stomach neoplasms, Tetralogy of fallot, Wolff-parkinson-white syndrome

183
Actin gamma 1
ACT, ACTG, DFNA20, DFNA26, HEL-176
Isolated sensorineural deafness, Nonsyndromic hearing loss, Baraitser-winter cerebrofrontofacial syndrome, Congenital anomalies of the kidney and urinary tract, Carcinoma, Coloboma, Congenital iris coloboma, Congenital neurologic anomalies, Congenital ocular coloboma, Craniofacial abnormalities, Deafness, Alzheimer disease, Hearing impairment, Hereditary hearing loss, Insomnia
View all (2 more)

184
Actin gamma 2, smooth muscle
ACT, ACTA3, ACTE, ACTL3, ACTSG, MMIHS5, VSCM, VSCM1
Bell's palsy, Intestinal pseudo-obstruction, Colonic neoplasms, Visceral myopathy, Intestinal obstruction, Megacystis microcolon intestinal hypoperistalsis syndrome, Visceral neuropathy

185
Actin like 6A
ACTL6, ARPN-BETA, Arp4, BAF53A, INO80K, SMARCN1
Bafopathy, Atrial septal defect, Global developmental delay, Intellectual developmental disorder, Non-specific syndromic intellectual disability

186
Actin like 6B
ACTL6, BAF53B, DEE76, EIEE76, IDDSSAD, SMARCN2, arpNalpha
Alzheimer disease, Amyotrophic lateral sclerosis, Autism, Congenital generalized lipodystrophy, Developmental and epileptic encephalopathy, Global developmental delay, Intellectual developmental disorder speech ambulation, Intellectual developmental disorder, Non-specific syndromic intellectual disability

187
Actin like 7A
SPGF86
Male infertility, Spermatogenic failure

188
Actin like 8
CT57
Colorectal cancer, Erectile dysfunction, Major depressive disorder, Obesity, Prostate cancer, Psychiatric disorders, Testicular carcinoma

189
Actin like 9
HSD21, SPGF53
Eczema, Congenital impairment of spermatozoa motility, Atopic dermatitis, Scoliosis, Spermatogenic failure

190
Actin maturation protease
C19orf54
Kawasaki disease