2. Gene
  3. PAMR1 - peptidase domain containing associated with muscle regeneration 1 Gene

PAMR1 - peptidase domain containing associated with muscle regeneration 1 Gene

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

中文名称：含肽酶结构域与肌肉再生相关 1

种属: Homo sapiens

同用名: RAMP; FP938; DKFZP586H2123

基因 ID: 25891 | 基因类型: protein coding

关于 PAMR1

This gene has 8 transcripts (splice variants), 252 orthologues and 1 paralogue. Biased expression in endometrium (RPKM 38.4), placenta (RPKM 23.8) and 13 other tissues.

功能概要

预测可启用钙离子结合活性和丝氨酸型内肽酶活性。预计参与蛋白水解。预测位于细胞外区域。 [由基因组资源联盟提供，2022 年 4 月]

Predicted to enable calcium ion binding activity and serine-type endopeptidase activity. Predicted to be involved in proteolysis. Predicted to be located in extracellular region. [provided by Alliance of Genome Resources, Apr 2022]

PAMR1 基因产物(4)

mRNA Protein Name
NM_001001991.3 NP_001001991.1 inactive serine protease PAMR1 isoform b precursor
NM_001282675.2 NP_001269604.1 inactive serine protease PAMR1 isoform c
NM_001282676.2 NP_001269605.1 inactive serine protease PAMR1 isoform d precursor
NM_015430.4 NP_056245.2 inactive serine protease PAMR1 isoform a precursor

PAMR1 蛋白结构

CUB

CUB: CUB domain (128 - 233)

EGF

EGF: EGF-like domain (239 - 270)

Sushi

Sushi: Sushi repeat (SCR repeat) (297 - 359)

Sushi

Sushi: Sushi repeat (SCR repeat) (411 - 459)

Trypsin

Trypsin: Trypsin (474 - 732)

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

inactive serine protease PAMR1

peptidase domain-containing protein associated with muscle regeneration 1

关联疾病

疾病名称 别名
Pericytoma With T(7;12)
Muscular Dystrophy

Muscular Dystrophies

Congenital Md

Congenital Muscular Dystrophy

Cmd

Mdc

Dystrophy, Muscular

Gower'S Muscular Dystrophy

Progressive Musclular Dystrophy

Pseudohypertrophic Atrophy

Pseudohypertrophic Muscle Paralysis

Pseudohypertrophic Muscular Atrophy

Pseudohypertrophic Muscular Dystrophy

Pseudohypertrophic Paralysis

Pseudomuscular Hypertrophy
Adams-Oliver Syndrome

Adams Oliver Syndrome

Aos

Congenital Scalp Defects With Distal Limb Reduction Anomalies

Aplasia Cutis Congenita With Terminal Transverse Limb Defects

Congenital Scalp Defects With Distal Limb Anomalies

Limb, Scalp And Skull Defects

Limb Scalp And Skull Defects

Absence Defect Of Limbs, Scalp, And Skull
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-RS10013 PAMR1 Human Pre-designed siRNA Set A Pre-designed Set / 否

直系同源

种属 基因名 来源 基因 ID
Mus musculus PAMR1 MGD MGI:2445082
Bos taurus PAMR1 VGNC VGNC:32562
Macaca mulatta PAMR1 VGNC VGNC:75673
Rattus norvegicus PAMR1 RGD RGD:1308745
Felis catus PAMR1 VGNC VGNC:64030
Canis familiaris PAMR1 VGNC VGNC:44251
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