Genes?

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?All genes including those with curated and unreviewed disease associations.
Log in to save this view

Save This View

Selected (0) TSV CSV PDF
This Page (10) TSV CSV PDF
All Matching (3040) TSV CSV PDF
Chromosome:
Gene type:
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
Showing genes starting with "P"
2581 to 2590 of 3040 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

2581
PTPN13 like Y-linked
PRY1, PTPN13LY

Curated: N/A

Unreviewed: Azoospermia, Nonobstructive Spermatogenic Failure, Y-Linked, Prostate cancer

2582
PTPN13 like Y-linked 2
PTPN13LY2

Curated: N/A

Unreviewed: Azoospermia, Nonobstructive Spermatogenic Failure, Y-Linked

2583
PTPN13 like Y-linked pseudogene 1
PRY4P, PRYP7

Curated: N/A

Unreviewed: N/A

2584
PTPN13 like Y-linked pseudogene 2
-

Curated: N/A

Unreviewed: N/A

2585
PTPN13 like Y-linked pseudogene 3
-

Curated: N/A

Unreviewed: N/A

2586
PTPN13 like Y-linked pseudogene 4
-

Curated: N/A

Unreviewed: N/A

2587
PTPN13 like Y-linked pseudogene 5
-

Curated: N/A

Unreviewed: N/A

2588
PTPN13 like Y-linked pseudogene 6
-

Curated: N/A

Unreviewed: N/A

2589
Prosaposin
GLBA, PARK24, PSAPD, SAP1, SAP2

Curated: Asthma, Atypical femoral fracture, Gaucher disease, Parkinson disease, Bipolar disorder, Combined psap deficiency, Combined saposin deficiency, Coronary artery disease, Deafness, Eosinophilia, Metachromatic leukodystrophy, Major depressive disorder, Neuromuscular disease, Hereditary parkinson disease, Retinitis pigmentosa-deafness syndrome, Usher syndrome, Gaucher disease due to saposin C deficiency, Krabbe disease due to saposin A deficiency

Unreviewed: N/A

2590
Prosaposin like 1
-

Curated: N/A

Unreviewed: Stomach neoplasms