2. Gene
  3. RTBDN - retbindin Gene

RTBDN - retbindin Gene

  • 基因
  • 蛋白
  • 疾病
  • 相关产品
  • 直系同源

中文名称：重组蛋白

种属: Homo sapiens

基因 ID: 83546 | 基因类型: protein coding

关于 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.

功能概要

该基因最初是在对人眼组织的研究中发现的。由该基因编码的蛋白质优先在视网膜中表达，并且可能在结合类视黄醇和其他类胡萝卜素方面发挥作用，因为它与核黄素结合蛋白具有同源性。可变剪接导致多种转录本变体和蛋白质同种型。[RefSeq 提供，2012 年 7 月]

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 基因产物(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
蛋白主名 其他名称

retbindin

重组 RTBDN 蛋白

目录号 产品名 蛋白编号 纯度
HY-P71268 RTBDN Protein, Human (HEK293, His) Q9BSG5 (S31-P229) ≥95%

关联疾病

疾病名称 别名
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
疾病名称 别名
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

相关产品

Pre-clinical Phase
生物活性分子 (1)
Cat. No. 产品名 作用方式
纯度 是否罕见病
HY-RS12314 RTBDN Human Pre-designed siRNA Set A Pre-designed Sets / 否

直系同源

种属 基因名 来源 基因 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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