2. Gene
  3. PRRC2B - proline rich coiled-coil 2B Gene

PRRC2B - proline rich coiled-coil 2B Gene

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

Also known as BAT2L; BAT2L1; LQFBS-1; KIAA0515

Gene ID: 84726 | Gene type: protein coding

About PRRC2B

Cytogenetic location: 9q34.13 Genomic coordinates (GRCh38): 9:131,373,651-131,500,193 (from NCBI)

This gene has 10 transcripts (splice variants), 210 orthologues and 2 paralogues. Ubiquitous expression in brain (RPKM 18.3), ovary (RPKM 17.4) and 25 other tissues.

Summary

Enables RNA binding activity. Predicted to be involved in cell differentiation. Predicted to act upstream of or within in utero embryonic development. [provided by Alliance of Genome Resources, Apr 2022]

PRRC2B Products(5)

mRNA Protein Name
NM_001384818.1 NP_001371747.1 protein PRRC2B isoform 1
NM_001384821.1 NP_001371750.1 protein PRRC2B isoform 2
NM_001384822.1 NP_001371751.1 protein PRRC2B isoform 3
NM_001384823.1 NP_001371752.1 protein PRRC2B isoform 4
NM_013318.4 NP_037450.2 protein PRRC2B isoform 1
Gene Ontology
  • Molecular Function
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
16189514 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

PRRC2B Protein Structure

BAT2_N

BAT2_N: BAT2 N-terminus (1 - 192)

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  • 2229 a.a.
Protein Preferred Names Protein Names

protein PRRC2B

HLA-B associated transcript 2-like

Related Diseases

Diseases Alias
Spinocerebellar Ataxia, Autosomal Recessive, With Axonal Neuropathy 2

Aoa2

Ataxia With Oculomotor Apraxia Type 2

Scar1

SCAN2

Ataxia-Oculomotor Apraxia 2

Ataxia-Ocular Apraxia 2

Ataxia-Oculomotor Apraxia Type 2

Scan 2

Spinocerebellar Ataxia With Axonal Neuropathy Type 2

Spinocerebellar Ataxia, Autosomal Recessive 1, Formerly

Scar1, Formerly

Autosomal Recessive Spinocerebellar Ataxia-1

Spinocerebellar Ataxia, Autosomal Recessive, 1

Ataxia-Ocular Apraxia-2

Spinocerebellar Ataxia, Autosomal Recessive 1
Spinocerebellar Ataxia 36

Spinocerebellar Ataxia Type 36

SCA36

Asidan Ataxia

Costa De Morte Ataxia

Asidan

Ataxia, Spinocerebellar, Type 36
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-RS11237 PRRC2B Human Pre-designed siRNA Set A Pre-designed Sets / Unkown

Orthologs Information

Species Symbol Source ID
Mus musculus PRRC2B MGD MGI:1923304
Canis familiaris PRRC2B VGNC VGNC:45053
Rattus norvegicus PRRC2B RGD RGD:1595906
Bos taurus PRRC2B VGNC VGNC:33405
Macaca mulatta PRRC2B VGNC VGNC:76327