1. Gene
  2. PRRX2 - paired related homeobox 2 Gene

PRRX2 - paired related homeobox 2 Gene

中文名称:配对相关同源框 2

种属: Homo sapiens

同用名: PMX2; PRX2

基因 ID: 51450 | 基因类型: protein coding

关于 PRRX2

Cytogenetic location: 9q34.11 Genomic coordinates (GRCh38): 9:129,665,647-129,722,674 (from NCBI)

This gene has 1 transcript (splice variant), 124 orthologues and 50 paralogues. Broad expression in skin (RPKM 3.1), prostate (RPKM 3.0) and 17 other tissues.

功能概要

由该基因编码的 DNA 相关蛋白是同源框蛋白配对家族的成员。表达局限于增殖的胎儿成纤维细胞和发育中的真皮层,在成人皮肤中表达下调。该基因在胎儿而非成人伤口愈合过程中表达增加表明可能在控制哺乳动物真皮再生和防止疤痕反应形成的机制中发挥作用。表达模式提供的证据与胎儿皮肤发育中的作用和细胞增殖中的可能作用一致。[RefSeq 提供,2008 年 7 月]

The DNA-associated protein encoded by this gene is a member of the paired family of homeobox proteins. Expression is localized to proliferating fetal fibroblasts and the developing dermal layer, with downregulated expression in adult skin. Increases in expression of this gene during fetal but not adult wound healing suggest a possible role in mechanisms that control mammalian dermal regeneration and prevent formation of scar response to wounding. The expression patterns provide evidence consistent with a role in fetal skin development and a possible role in cellular proliferation. [provided by RefSeq, Jul 2008]

PRRX2 基因产物(1)

mRNA Protein Name
NM_016307.4 NP_057391.1 paired mesoderm homeobox protein 2
基因本体论
  • 分子功能
分子功能 GO 注释 逻辑证据 参考文献 来源
enables sequence-specific double-stranded DNA binding IDA
IDA: 通过直接分析推断
28473536 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

PRRX2 蛋白结构

Homeobox

Homeobox: Homeobox domain (105 - 161)

OAR

OAR: OAR domain (227 - 245)

  • 0
  • 100
  • 200
  • 253 a.a.
蛋白主名 其他名称

paired mesoderm homeobox protein 2

PRX-2

关联疾病

疾病名称 别名
Agnathia-Otocephaly Complex

Otocephaly

Holoprosencephaly-Agnathia

Dysgnathia Complex Agnathia-Holoprosencephaly

AGOTC

Agnathia-Holoprosencephaly-Situs Inversus Syndrome

Dysgnathia Complex

Agnathia-Holoprosencephaly

Cervical Auricle

Hypoplastic Right Heart Syndrome

Right Hypoplastic Heart Syndrome

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
Mus musculus PRRX2 MGD MGI:98218
Canis familiaris PRRX2 VGNC VGNC:49775
Rattus norvegicus PRRX2 RGD RGD:1311471
Bos taurus PRRX2 VGNC VGNC:58400
Felis catus PRRX2 VGNC VGNC:64396