Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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10441 to 10450 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

10441
Proline rich coiled-coil 1
-
Hypertension

10442
Proline rich coiled-coil 2A
BAT2, D6S51, D6S51E, G2
Autism, Autoimmune disease, Celiac disease, Cervical cancer, Coronary artery disease, Crohn disease, Diabetes mellitus type 1, Apolipoprotein b hypobetalipoproteinemia, Gallstones, Glomerulonephritis, Hypertension, Inflammatory bowel disease, Irritable bowel syndrome, Major depressive disorder, Membranous glomerulonephritis
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10443
Proline rich coiled-coil 2B
BAT2L, BAT2L1, KIAA0515, LQFBS-1
Attention deficit hyperactivity disorder, Gout, Substance abuse

10444
Proline rich coiled-coil 2C
BAT2-iso, BAT2D1, BAT2L2, XTP2
Alzheimer disease, Glioma, Metabolic syndrome, Ocular sarcoidosis, Diabetes mellitus type 2

10445
Proline rich and Gla domain 2
PRGP2
Schizophrenia

10446
Proline rich and Gla domain 4
PRGP4, TMG4
Parkinson disease, Vascular disease

10447
Proline rich transmembrane protein 1
C6orf31, DSPD1, IFITMD7, NG5, SynDIG4
Diabetes mellitus type 2

10448
Proline rich transmembrane protein 2
BFIC2, BFIS2, DSPB3, DYT10, EKD1, FICCA, ICCA, IFITMD1, PKC
Benign infantile epilepsy, Childhood-onset glut1 deficiency syndrome 2, Familial infantile convulsions with paroxysmal choreoathetosis, Dystonia, Episodic kinesigenic dyskinesia, Paroxysmal dystonia, Generalized epilepsy with febrile seizures plus, Global developmental delay, Hemiplegic migraine, Intellectual developmental disorder, Neurodevelopmental disorder, Paroxysmal dyskinesia, Paroxysmal dystonic choreoathetosis, Paroxysmal nonkinesigenic dyskinesia, Seizures

10449
Paired related homeobox 1
AGOTC, PHOX1, PMX1, PRX-1, PRX1
Agnathia-otocephaly, Alzheimer disease, Aortic stenosis, Aortic valve disease, Atrial fibrillation, Atrial flutter, Cardiac arrhythmia, Cardiac embolism, Cardioembolic stroke, Craniosynostosis, Dementia, Demyelinating diseases, Dysgnathia complex, Otosclerosis, Prostatic neoplasms
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10450
Paired related homeobox 2
PMX2, PRX2
Color vision deficiency