RTBDN - retbindin Gene

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 83546

About RTBDN

Cytogenetic location: 19p13.13 Genomic coordinates (GRCh38): 19:12,825,482-12,835,428 (from NCBI)

This gene has 14 transcripts (splice variants), 188 orthologues and 4 paralogues. Biased expression in brain (RPKM 1.6), adrenal (RPKM 0.5) and 2 other tissues.

Summary

This gene was first identified in a study of human eye tissues. The protein encoded by this gene is preferentially expressed in the retina and may play a role in binding retinoids and Other carotenoids as it shares homology with riboflavin binding proteins. Alternative splicing results in multiple transcript variants and protein isoforms. [provided by RefSeq, Jul 2012]

RTBDN Products (8)

mRNA Protein Name
NM_001080997.3 NP_001074466.1 retbindin isoform 1 precursor
NM_001270440.2 NP_001257369.1 retbindin isoform 3
NM_001270441.2 NP_001257370.2 retbindin isoform 1 precursor
NM_001270442.2 NP_001257371.1 retbindin isoform 5 precursor
NM_001270443.2 NP_001257372.1 retbindin isoform 1 precursor
NM_001270444.2 NP_001257373.1 retbindin isoform 1 precursor
NM_001270445.2 NP_001257374.1 retbindin isoform 6 precursor
NM_031429.3 NP_113617.1 retbindin isoform 2
Protein Preferred Names Protein Names

retbindin

Recombinant RTBDN Proteins

Cat. No. Product Name Accession Purity
HY-P71268 RTBDN Protein, Human (HEK293, His) Q9BSG5 (S31-P229) ≥ 95%, as determined by reducing SDS-PAGE.

Related Diseases

Diseases Alias
Choroid Plexus Cancer
  • Choroid Plexus Carcinoma

  • Choroid Plexus Neoplasms

  • Choroid Plexus Neoplasm

  • Tumor Of Choroid Plexus

  • Tumor Of The Choroid Plexus

  • Choroid Plexus Tumor

  • Choroid Plexus Tumors

  • Anaplastic Choroid Plexus Papilloma

  • Choroid Plexus Papilloma Nos

  • Papilloma Of Choroid Plexus

  • Plexus Choroideus Papilloma

  • Choroid Plexus Papilloma In Fourth Ventricle

  • Plexus Choroideus Papilloma In Fourth Ventricle

Riboflavin Deficiency
  • Ariboflavinosis

  • Maternal Riboflavin Deficiency

  • RBFVD

  • Vitamin B2 Deficiency

  • Hyporiboflavinosis

Late-Onset Retinal Degeneration
  • LORD

  • Retinal Degeneration, Late-Onset, Autosomal Dominant

  • Autosomal Dominant Late-Onset Retinal Degeneration

  • Pigmentary Retinopathy

  • Retinal Degeneration, Late-Onset

  • Retinitis Pigmentosa

Cone-Rod Dystrophy 2
  • Cone-Rod Dystrophy

  • CORD2

  • Cone-Rod Retinal Dystrophy

  • Rcrd2

  • Cone-Rod Retinal Dystrophy 2

  • Crd2

  • Cord

  • Crd

  • Retinal Cone-Rod Dystrophy

  • Cone-Rod Retinal Dystrophy-2

  • Retinal Cone-Rod Dystrophy 2

  • Tapetoretinal Degeneration

  • Cone-Rod Degeneration

  • Cone Rod Dystrophy

  • Dystrophy, Cone-Rod

  • Dystrophy, Cone-Rod, Type 2

  • Retinitis Pigmentosa

  • Retinitis Pigmentosa 2

  • Progressive Cone-Rod Dystrophy

Fundus Dystrophy
  • Retinal Dystrophy

  • Retinal Dystrophies

  • Dystrophy, Retinal

Retinitis Pigmentosa
  • RP

  • Rod-Cone Dystrophy

  • Autosomal Recessive Retinitis Pigmentosa

  • Non-Syndromic Retinitis Pigmentosa

  • Pericentral Pigmentary Retinopathy

  • Pigmentary Retinopathy

  • Tapetoretinal Degeneration

  • Rcd

  • Retinitis Pigmentosa Autosomal Recessive

  • ARRP

  • Retinitis Pigmentosa, Autosomal Recessive

  • Retinitis Pigmentosa 1

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
Mus musculus RTBDN MGD MGI:2443686
Canis familiaris RTBDN VGNC VGNC:45786
Felis catus RTBDN VGNC VGNC:64803
Rattus norvegicus RTBDN RGD RGD:1308534
Macaca mulatta RTBDN VGNC VGNC:82228
Bos taurus RTBDN VGNC VGNC:34192
Others RTBDN NCBI