Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "O"
231 to 240 of 301 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

231
Olfactory receptor family 9 subfamily Q member 1
-
Color vision deficiency, Endometrial cancer, Endometriosis, Hypertrophic cardiomyopathy, Insomnia, Diabetes mellitus type 2

232
ORAI calcium release-activated calcium modulator 1
CRACM1, IMD9, ORAT1, TAM2, TMEM142A
Alzheimer disease, Combined immunodeficiency disease, Congenital structural myopathy, Hypertension, Immunodeficiency, Major depressive disorder, Tubular aggregate myopathy

233
ORAI calcium release-activated calcium modulator 2
C7orf19, CBCIP2, MEM142B, TMEM142B
Insomnia

234
ORAI calcium release-activated calcium modulator 3
TMEM142C
Obstructive pulmonary disease

235
Origin recognition complex subunit 1
HSORC1, ORC1L, PARC1
Hepatocellular carcinoma, Desbuquois syndrome, Dwarfism, Ear, patella, short stature syndrome, Ear patella short stature syndrome, Meier-gorlin syndrome, Microcephaly

236
Origin recognition complex subunit 3
LAT, LATHEO, ORC3L
Asthma, Gastroesophageal reflux disease, Obesity

237
Origin recognition complex subunit 4
ORC4L, ORC4P
Desbuquois syndrome, Ear, patella, short stature syndrome, Ear patella short stature syndrome, Gout, Meier-gorlin syndrome, Neurotic disorder

238
Origin recognition complex subunit 5
ORC5L, ORC5P, ORC5T, PPP1R117
Lymphocytic leukemia, Schizophrenia, Diabetes mellitus type 2

239
Origin recognition complex subunit 6
ORC6L
Desbuquois syndrome, Ear, patella, short stature syndrome, Ear patella short stature syndrome, Meier-gorlin syndrome

240
Orosomucoid 1
A1AG1, AGP-A, AGP1, HEL-S-153w, ORM
Alzheimer disease, Dementia, Kidney failure, Liver failure, Stevens-johnson syndrome