PPP1R3F - protein phosphatase 1 regulatory subunit 3F Gene

Homo sapiens

Also known as R3F; HB2E; LL0XNC01-7P3.1

Gene ID: 89801 | Gene type: protein coding

About PPP1R3F

This gene has 6 transcripts (splice variants), 112 orthologues and 6 paralogues. Broad expression in brain (RPKM 2.6), heart (RPKM 1.4) and 23 other tissues.

Summary

This gene encodes a protein that has been identified as one of several type-1 protein Phosphatase (PP1) regulatory subunits. One or two of these subunits, together with the well-conserved catalytic subunit, can form the PP1 holoenzyme, where the regulatory subunit functions to regulate substrate specificity and/or targeting to a particular cellular compartment. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2010]

PPP1R3F Products(2)

mRNA	Protein	Name
NM_001184745.2	NP_001171674.1	protein phosphatase 1 regulatory subunit 3F isoform 2
NM_033215.5	NP_149992.3	protein phosphatase 1 regulatory subunit 3F isoform 1

Protein Preferred Names

Protein Names

protein phosphatase 1 regulatory subunit 3F

protein phosphatase 1, regulatory (inhibitor) subunit 3F

Related Diseases

Diseases

Alias

Joubert Syndrome 23

JBTS23

Joubert Syndrome, Type 23

Spinocerebellar Ataxia 29

Spinocerebellar Ataxia Type 29	SCA29
Cnpca	Cerebellar Vermis Aplasia
Aplasia Of Cerebellar Vermis	Acv
Cerebellar Ataxia, Congenital Nonprogressive, Autosomal Dominant	Spinocerebellar Ataxia 29, Congenital Nonprogressive
Congenital Nonprogressive Spinocerebellar Ataxia	Autosomal Dominant Congenital Nonprogressive Cerebellar Ataxia
Ataxia, Spinocerebellar, Type 29, Congenital Nonprogressive	Familial Aplasia Of The Vermis

Parkinsonism With Spasticity, X-Linked

X-Linked Parkinsonism-Spasticity Syndrome	XPDS
X-Linked Parkinsonism With Spasticity

Stocco Dos Santos Type X-Linked Intellectual Disability

X-Linked Intellectual Disability, Stocco Dos Santos Type	Stocco Dos Santos Syndrome
Sdsx	Stocco Dos Santos X-Linked Mental Retardation Syndrome

Spinocerebellar Ataxia 13

Spinocerebellar Ataxia Type 13	SCA13
Autosomal Dominant Cerebellar Ataxia With Intellectual Disability	Cerebellar Ataxia, Autosomal Dominant With Intellectual Disability
Spinocerebellar Ataxia-13	Ataxia, Spinocerebellar, Type 13

Spinocerebellar Ataxia 5

Spinocerebellar Ataxia Type 5	SCA5
Spinocerebellar Ataxia-5	Ataxia, Spinocerebellar, Type 5

Adenoiditis

Chronic Adenoiditis

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-RS11001	PPP1R3F Human Pre-designed siRNA Set A		/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Bos taurus	PPP1R3F	VGNC	VGNC:33247
Mus musculus	PPP1R3F	MGD	MGI:1859617
Canis familiaris	PPP1R3F	VGNC	VGNC:44901
Rattus norvegicus	PPP1R3F	RGD	RGD:1566398

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