1. Gene
  2. PTPRR - protein tyrosine phosphatase receptor type R Gene

PTPRR - protein tyrosine phosphatase receptor type R Gene

中文名称:R 型蛋白酪氨酸磷酸酶受体

种属: Homo sapiens

同用名: PTPRQ; EC-PTP; PCPTP1; PTP-SL; PTPBR7

基因 ID: 5801 | 基因类型: protein coding

关于 PTPRR

Cytogenetic location: 12q15 Genomic coordinates (GRCh38): 12:70,638,073-70,920,738 (from NCBI)

This gene has 11 transcripts (splice variants), 198 orthologues and 35 paralogues. Biased expression in brain (RPKM 5.7), colon (RPKM 3.2) and 11 other tissues.

功能概要

该基因编码的蛋白质是蛋白酪氨酸磷酸酶 (PTP) 家族的成员。已知 PTP 是调节多种细胞过程的信号分子,包括细胞生长、分化、有丝分裂周期和致癌转化。该 PTP 具有细胞外区域、单个跨膜区域和单个细胞内催化结构域,因此代表受体型 PTP。该基因的沉默与结直肠癌有关。已发现该基因编码不同异构体的多个转录变体。该基因与另一个基因、蛋白酪氨酸磷酸酶、受体类型 Q (GeneID 374462) 共享一个符号 (PTPRQ) ,后者也位于 12 号染色体上。[RefSeq 提供,2011 年 5 月]

The protein encoded by this gene is a member of the protein tyrosine Phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This PTP possesses an extracellular region, a single transmembrane region, and a single intracellular catalytic domain, and thus represents a receptor-type PTP. Silencing of this gene has been associated with colorectal Cancer. Multiple transcript variants encoding different isoforms have been found for this gene. This gene shares a symbol (PTPRQ) with another gene, protein tyrosine Phosphatase, receptor type, Q (GeneID 374462), which is also located on chromosome 12. [provided by RefSeq, May 2011]

PTPRR 基因产物(4)

mRNA Protein Name
NM_001207015.2 NP_001193944.1 receptor-type tyrosine-protein phosphatase R isoform 3
NM_001207016.1 NP_001193945.1 receptor-type tyrosine-protein phosphatase R isoform 4
NM_002849.4 NP_002840.2 receptor-type tyrosine-protein phosphatase R isoform 1 precursor
NM_130846.3 NP_570897.2 receptor-type tyrosine-protein phosphatase R isoform 2
基因本体论
  • 分子功能
  • 生物过程
分子功能 GO 注释 逻辑证据 参考文献 来源
enables protein binding IPI
IPI: 通过物理相互作用推断
10601328 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in ERBB2 signaling pathway IMP
IMP: 通过突变表型推断
21724833 GOA
involved in in utero embryonic development IEP
IEP: 通过表达模式推断
10601328 GOA
involved in negative regulation of ERK1 and ERK2 cascade IMP
IMP: 通过突变表型推断
21724833 GOA
involved in negative regulation of epithelial cell migration IMP
IMP: 通过突变表型推断
21724833 GOA
NOT involved in regulation of homophilic cell adhesion IMP
IMP: 通过突变表型推断
21724833 GOA
EXP:通过实验结果推断 IDA:通过直接分析推断 IPI:通过物理相互作用推断 IMP:通过突变表型推断 IGI:通过遗传相互作用推断 IEP:通过表达模式推断

PTPRR 蛋白结构

Y_phosphatase

Y_phosphatase: Protein-tyrosine phosphatase (417 - 644)

  • 0
  • 200
  • 400
  • 600
  • 657 a.a.
蛋白主名 其他名称

receptor-type tyrosine-protein phosphatase R

Ch-1 PTPase

PTPRR 蛋白互作信息

分类
蛋白名称 蛋白编号 互作蛋白 互作蛋白种属 互作蛋白编号 实验方法 参考文献
种属内
PTPRR Q15256 INSR Homo sapiens P06213
Ub Reconstruction
28065597
种属内
PTPRR Q15256 ERBB2 Homo sapiens P04626
Ub Reconstruction
28065597
种属内
PTPRR Q15256 MAPK14 Homo sapiens Q16539
Anti Tag CoIP
33961781
种属内
PTPRR Q15256 MAPK14 Homo sapiens Q16539
Phosphatase Assay
10601328
种属内
PTPRR Q15256 MAPK1 Homo sapiens P28482
Phosphatase Assay
10601328
种属内
PTPRR Q15256 MAPK1 Homo sapiens P28482
IF
10601328
种属内
PTPRR Q15256 MAPK1 Homo sapiens P28482
Anti Tag CoIP
33961781
种属间: 跨种属相互作用 种属内: 同种属相互作用

PTPRR 抗体

目录号 产品名 应用 反应物种
HY-P81804 PCPTP1 Antibody (YA1549) WB Rat

关联疾病

疾病名称 别名
Deafness, Autosomal Recessive 84a

DFNB84A

Deafness, Autosomal Recessive 84

Autosomal Recessive Nonsyndromic Deafness 84a

Dfnb84

Deafness, Autosomal Recessive 84a, With Vestibular Dysfunction

Autosomal Recessive Deafness 84a

Autosomal Recessive Deafness 84a With Vestibular Dysfunction

Deafness, Autosomal Recessive, 84a

Deafness Autosomal Recessive 84

Deafness Autosomal Recessive 84a With Vestibular Dysfunction

Non-Syndromic Neurosensory Deafness Autosomal Recessive Type 84

Deafness, Autosomal Recessive, Type 84a

Autosomal Recessive Nonsyndromic Deafness 70

Deafness, Autosomal Recessive 70

Autosomal Recessive Deafness 70

Dfnb70

Deafness, Autosomal Recessive, Type 70

Deafness, Autosomal Dominant 2a

DFNA2A

Autosomal Dominant Nonsyndromic Deafness 2a

Autosomal Dominant Deafness 2a

Deafness, Autosomal Dominant, 2a

Non-Syndromic Neurosensory Deafness Autosomal Dominant Type 2a

Non-Syndromic Sensorineural Deafness Autosomal Dominant Type 2a

Deafness, Autosomal Dominant, Type 2a

Deafness, Autosomal Dominant 50

DFNA50

Autosomal Dominant Nonsyndromic Deafness 50

Autosomal Dominant Deafness 50

Deafness, Autosomal Dominant, Type 50

Myopia

Near-Sightedness

Short-Sightedness

Nearsightedness

Nearsighted

Near Vision

Close Sighted

Myopic

Short-Sighted

Near Sighted

Normal Pressure Hydrocephalus

Low Pressure Hydrocephalus

Hydrocephalus Normal Pressure

Hydrocephalus, Normal Pressure

Normal Pressure Hydrocephalus Nos

Nph - [Normal Pressure Hydrocephalus]

Normal Pressure Hydrocephaly

Deafness, Autosomal Recessive 12

DFNB12

Deafness, Autosomal Recessive 12, Modifier Of

Autosomal Recessive Nonsyndromic Deafness 12

Autosomal Recessive Deafness 12

Deafness, Autosomal Recessive, 12

Congenital Neurosensory Deafness Autosomal Recessive 12

Non-Syndromic Neurosensory Deafness Autosomal Recessive Type 12

Non-Syndromic Sensorineural Deafness Autosomal Recessive Type 12

Deafness, Autosomal Recessive, Type 12

Autosomal Recessive Nonsyndromic Deafness

Deafness, Autosomal Recessive, Nonsyndromic

Autosomal Dominant Nonsyndromic Deafness

Autosomal Dominant Deafness

Usher Syndrome

Deafness-Retinitis Pigmentosa Syndrome

Dystrophia Retinae Pigmentosa-Dysostosis Syndrome

Graefe-Usher Syndrome

Hallgren Syndrome

Usher'S Syndrome

Retinitis Pigmentosa-Deafness Syndrome

Retinitis Pigmentosa-Hearing Loss Syndrome

Ush

Usher Syndromes

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

直系同源

种属 基因名 来源 基因 ID
Macaca mulatta PTPRR VGNC VGNC:76621
Felis catus PTPRR VGNC VGNC:69180
Rattus norvegicus PTPRR RGD RGD:620780
Canis familiaris PTPRR VGNC VGNC:45197
Bos taurus PTPRR VGNC VGNC:33557
Mus musculus PTPRR MGD MGI:109559