RTBDN - retbindin Gene

Homo sapiens

Gene ID: 83546 | Gene type: protein coding

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%

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

Related Agents

Pre-clinical Phase

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS12314	RTBDN Human Pre-designed siRNA Set A		/	Unkown

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

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