PPP1R3F - protein phosphatase 1 regulatory subunit 3F Gene

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

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 89801

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
Molecular Function GO Annotation Evidence References Source
enables glycogen binding IDA
IDA: Inferred from direct assay
21668450 GOA
enables protein phosphatase binding IPI
IPI: Inferred from physical interaction
21668450 GOA
Biological Process GO Annotation Evidence References Source
acts upstream of or within regulation of glycogen (starch) synthase activity IDA
IDA: Inferred from direct assay
21668450 GOA
acts upstream of or within regulation of glycogen biosynthetic process IDA
IDA: Inferred from direct assay
21668450 GOA
Cellular Component GO Annotation Evidence References Source
located in membrane IDA
IDA: Inferred from direct assay
21668450 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern
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

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
Others PPP1R3F NCBI