PNRC2 - proline rich nuclear receptor coactivator 2 Gene

Homo sapiens

Gene ID: 55629 | Gene type: protein coding

About PNRC2

Cytogenetic location: 1p36.11 Genomic coordinates (GRCh38): 1:23,959,164-23,963,462 (from NCBI)

This gene has 5 transcripts (splice variants), 198 orthologues and 1 paralogue. Ubiquitous expression in thyroid (RPKM 68.8), lymph node (RPKM 67.1) and 25 other tissues.

Summary

Involved in nuclear-transcribed mRNA catabolic process, nonsense-mediated decay. Located in Golgi apparatus; P-body; and nucleoplasm. [provided by Alliance of Genome Resources, Apr 2022]

PNRC2 Products(1)

mRNA	Protein	Name
NM_017761.4	NP_060231.1	proline-rich nuclear receptor coactivator 2

PNRC2 Protein Structure

PNRC

0
100
139 a.a.

Protein Preferred Names

Protein Names

proline-rich nuclear receptor coactivator 2

Related Diseases

Diseases

Alias

Murray Valley Encephalitis

Australian Encephalitis	Australian X Disease
Encephalitis Australia	Murray River Encephalitis
Australian Arboencephalitis	Australian X Disorder
Mve - [Murray Valley Encephalitis]

Holoprosencephaly 3

HPE3	Hlp3
Holoprosencephaly-3	Holoprosencephaly, Type 3

Pancreatic Adenosquamous Carcinoma

Adenosquamous Carcinoma Of Pancreas

Adenosquamous Carcinoma Of The Pancreas

Diseases	Alias
Waldenstroem'S Macroglobulinemia	Waldenstroem'S Macroglobulinemia Waldenstroem'S Macroglobulinemia Macroglobulinemia Of Waldenstrom Lymphoplasmacytic Lymphoma With Igm Gammopathy Lymphoplasmacytic Lymphoma Waldenstroem'S Macroglobulinemia Waldenstroem'S Macroglobulinemia Macroglobulinemia Of Waldenstrom Lymphoplasmacytic Lymphoma With Igm Gammopathy Lymphoplasmacytic Lymphoma

Related Agents

Pre-clinical Phase

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS10803	PNRC2 Human Pre-designed siRNA Set A		/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Macaca mulatta	PNRC2	VGNC	VGNC:100042
Rattus norvegicus	PNRC2	RGD	RGD:1642418
Mus musculus	PNRC2	MGD	MGI:106512
Felis catus	PNRC2	VGNC	VGNC:107602
Bos taurus	PNRC2	VGNC	VGNC:33099

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