1. Gene
  2. Mmp13 - matrix metallopeptidase 13 Gene

Mmp13 - matrix metallopeptidase 13 Gene

中文名称:基质金属肽酶 13

种属: Rattus norvegicus

基因 ID: 171052 | 基因类型: protein coding

关于 Mmp13

Primary_assembly 8: 4,497,960-4,508,239 forward strand.mRatBN7.2:CM026981.1

This gene has 1 transcript (splice variant), 203 orthologues, 23 paralogues and is associated with 44 phenotypes. Biased expression in Thymus (RPKM 2.9), Muscle (RPKM 1.6) and 5 other tissues.

功能概要

该基因编码的蛋白可启动多种功能,包括纤连蛋白结合活性;低密度脂蛋白颗粒受体结合活性;和金属离子结合活性。参与多个过程,包括动物器官发育;胚胎后肢形态发生;和动情周期。位于多种细胞成分中,包括高尔基体;细胞间小管;和溶酶体。用于研究脑缺血;退行性椎间盘疾病;和心肌梗塞。多种疾病的生物标志物,包括退行性椎间盘疾病;胃溃疡;肝硬化(多发性);脑膜炎球菌性脑膜炎;和矽肺。该基因的人类直系同源物与无牙症有关;动脉疾病(多发性);骨关节炎;卵巢癌;和脊柱骨骺发育不良,密苏里型。与人 MMP13(基质金属肽酶 13)同源。 [由基因组资源联盟提供,2022 年 4 月]

Enables several functions, including fibronectin binding activity; low-density lipoprotein particle receptor binding activity; and metal ion binding activity. Involved in several processes, including animal organ development; embryonic hindlimb morphogenesis; and estrous cycle. Located in several cellular components, including Golgi apparatus; intercellular canaliculus; and lysosome. Used to study brain ischemia; degenerative disc disease; and myocardial infarction. Biomarker of several diseases, including degenerative disc disease; gastric ulcer; liver cirrhosis (multiple); meningococcal meningitis; and silicosis. Human ortholog(s) of this gene implicated in anodontia; artery disease (multiple); osteoarthritis; ovarian carcinoma; and spondyloepimetaphyseal dysplasia, Missouri type. Orthologous to human MMP13 (matrix metallopeptidase 13). [provided by Alliance of Genome Resources, Apr 2022]

Mmp13 基因产物(1)

mRNA Protein Name
NM_133530.1 NP_598214.1 collagenase 3 precursor

Mmp13 蛋白结构

PG_binding_1

PG_binding_1: pfam01471 (39 - 91)

Peptidase_M10

Peptidase_M10: pfam00413 (112 - 267)

HX

HX: cd00094 (281 - 471)

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  • 472 a.a.
蛋白主名 其他名称

collagenase 3

MMP-13

UMRCASE

interstitial collagenase

matrix metalloproteinase-13

直系同源

种属 基因名 来源 基因 ID
Homo sapiens Mmp13 NCBI NCBI:4322