2. Gene
  3. PNISR - PNN interacting serine and arginine rich protein Gene

PNISR - PNN interacting serine and arginine rich protein Gene

  • Gene
  • Protein
  • Disease
  • Agent
  • Ortholog
Homo sapiens

Also known as SFRS18; HSPC306; SRrp130; C6orf111; bA98I9.2

Gene ID: 25957 | Gene type: protein coding

About PNISR

Cytogenetic location: 6q16.2 Genomic coordinates (GRCh38): 6:99,398,050-99,425,308 (from NCBI)

This gene has 14 transcripts (splice variants) and 170 orthologues. Ubiquitous expression in lymph node (RPKM 25.8), spleen (RPKM 24.5) and 25 other tissues.

Summary

Enables RNA binding activity. Located in cytosol; nuclear speck; and plasma membrane. [provided by Alliance of Genome Resources, Apr 2022]

PNISR Products(14)

mRNA Protein Name
NM_001322405.2 NP_001309334.1 arginine/serine-rich protein PNISR isoform a
NM_001322406.2 NP_001309335.1 arginine/serine-rich protein PNISR isoform a
NM_001322408.2 NP_001309337.1 arginine/serine-rich protein PNISR isoform a
NM_001322410.2 NP_001309339.1 arginine/serine-rich protein PNISR isoform b
NM_001322412.2 NP_001309341.1 arginine/serine-rich protein PNISR isoform b
NM_001322413.2 NP_001309342.1 arginine/serine-rich protein PNISR isoform b
NM_001322414.2 NP_001309343.1 arginine/serine-rich protein PNISR isoform c
NM_001322415.2 NP_001309344.1 arginine/serine-rich protein PNISR isoform c
NM_001322416.2 NP_001309345.1 arginine/serine-rich protein PNISR isoform d
NM_001322417.2 NP_001309346.1 arginine/serine-rich protein PNISR isoform e
NM_001322418.2 NP_001309347.1 arginine/serine-rich protein PNISR isoform f
NM_001322419.2 NP_001309348.1 arginine/serine-rich protein PNISR isoform f
NM_015491.3 NP_056306.1 arginine/serine-rich protein PNISR isoform a
NM_032870.4 NP_116259.2 arginine/serine-rich protein PNISR isoform a
Protein Preferred Names Protein Names

arginine/serine-rich protein PNISR

PNN-interacting serine/arginine-rich protein

Related Diseases

Diseases Alias
Unilateral Focal Polymicrogyria
Night Blindness, Congenital Stationary, Autosomal Dominant 1

Congenital Stationary Night Blindness Autosomal Dominant 1

CSNBAD1

Rhodopsin-Related Congenital Stationary Night Blindness

Night Blindness, Congenital Stationary, Rhodopsin-Related

Blindness, Night, Stationary, Congenital, Autosomal Dominant, Type 1
Cleft Soft Palate

Cleft Velum

Cleft Velum Palatinum

Soft Cleft Palate

Soft Palate Perforation
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-RS10776 PNISR Human Pre-designed siRNA Set A / Unkown

Orthologs Information

Species Symbol Source ID
Felis catus PNISR VGNC VGNC:64259
Macaca mulatta PNISR VGNC VGNC:76090
Mus musculus PNISR MGD MGI:1913875
Rattus norvegicus PNISR RGD RGD:1307395
Canis familiaris PNISR VGNC VGNC:44741