PAMR1 - peptidase domain containing associated with muscle regeneration 1 Gene

Also Known as RAMP; FP938; DKFZP586H2123

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 25891

About 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.

Summary

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 Products (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 Protein Structure

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.
Protein Preferred Names Protein Names

inactive serine protease PAMR1

  • peptidase domain-containing protein associated with muscle regeneration 1

Related Diseases

Diseases Alias
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
Diseases Alias
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

Related Agents

  • Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (1)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-RS10013 PAMR1 Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source 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
Others PAMR1 NCBI