1. Gene
  2. RBP2 - retinol binding protein 2 Gene

RBP2 - retinol binding protein 2 Gene

Homo sapiens

Also known as CRBP2; RBPC2; CRBPII; CRABP-II

Gene ID: 5948 | Gene type: protein coding

About RBP2

Cytogenetic location: 3q23 Genomic coordinates (GRCh38): 3:139,452,884-139,476,516 (from NCBI)

This gene has 3 transcripts (splice variants), 249 orthologues and 15 paralogues. Biased expression in duodenum (RPKM 1065.7) and small intestine (RPKM 769.4).

Summary

This gene encodes an abundant protein present in the small intestinal epithelium. It is thought to participate in the uptake and/or intracellular metabolism of vitamin A. Vitamin A is a fat-soluble vitamin necessary for growth, reproduction, differentiation of epithelial tissues, and vision. This protein may also modulate the supply of retinoic acid to the nuclei of endometrial cells during the menstrual cycle. [provided by RefSeq, Aug 2015]

RBP2 Products(1)

mRNA Protein Name
NM_004164.3 NP_004155.2 retinol-binding protein 2

RBP2 Protein Structure

Lipocalin

Lipocalin: Lipocalin / cytosolic fatty-acid binding protein family (6 - 133)

  • 0
  • 100
  • 134 a.a.
Protein Preferred Names Protein Names

retinol-binding protein 2

CRBP-II

Recombinant RBP2 Proteins

Cat. No. Product Name Accession Purity
HY-P71249 RBP2 Protein, Human P50120 (M1-K134) ≥95%

Related Diseases

Diseases Alias
Hypervitaminosis A

Hypervitaminosis A, Susceptibility To

Hyperalimentation Of Vitamin A

Diaphragmatic Hernia, Congenital

Congenital Diaphragmatic Hernia

Diaphragmatic Hernia

Cdh

Congenital Diaphragmatic Defect

Hernia, Diaphragmatic

Dih

Hernia, Congenital Diaphragmatic

Hcd

Diaphragmatic Defect, Congenital

Diaphragm, Unilateral Agenesis Of

Hemidiaphragm, Agenesis Of

Diaphragmatic Hernia 1

Agenesis Of Hemidiaphragm

Unilateral Agenesis Of Diaphragm

Hernia Diaphragmatic

Hernia Diaphragmatic Congenital

Hernia, Diaphragmatic, Type 1

Hiatus Hernia

Oesophageal Hiatus Hernia

Paraoesophageal Hernia

Sliding Hiatus Hernia

Congenital Diaphragm Hernia

Congenital Diaphragm Defect With Hernia

Gross Congenital Diaphragm Defect

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
Canis familiaris RBP2 VGNC VGNC:45430
Felis catus RBP2 VGNC VGNC:69272
Bos taurus RBP2 VGNC VGNC:33813
Macaca mulatta RBP2 VGNC VGNC:110345
Rattus norvegicus RBP2 RGD RGD:3544
Mus musculus RBP2 MGD MGI:97877
Others RBP2 NCBI