CPXM1 - carboxypeptidase X, M14 family member 1 Gene

Also Known as CPX1; CPXM

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 56265

About CPXM1

Cytogenetic location: 20p13 Genomic coordinates (GRCh38): 20:2,794,074-2,800,627 (from NCBI)

This gene has 1 transcript (splice variant), 263 orthologues and 7 paralogues. Biased expression in endometrium (RPKM 64.0), gall bladder (RPKM 53.3) and 10 other tissues.

Summary

This gene likely encodes a member of the Carboxypeptidase family of proteins. Cloning of a comparable locus in mouse indicates that the encoded protein contains a discoidin domain and a Carboxypeptidase domain, but the protein appears to lack residues necessary for Carboxypeptidase activity.[provided by RefSeq, May 2010]

CPXM1 Products (2)

mRNA Protein Name
NM_001184699.2 NP_001171628.1 probable carboxypeptidase X1 isoform 2 precursor
NM_019609.5 NP_062555.1 probable carboxypeptidase X1 isoform 1 precursor

CPXM1 Protein Structure

F5_F8_type_C

F5_F8_type_C: F5/8 type C domain (150 - 271)

Peptidase_M14

Peptidase_M14: Zinc carboxypeptidase (305 - 612)

CarboxypepD_reg

CarboxypepD_reg: Carboxypeptidase regulatory-like domain (625 - 688)

  • 0
  • 200
  • 400
  • 600
  • 734 a.a.
Protein Preferred Names Protein Names

probable carboxypeptidase X1

  • carboxypeptidase X (M14 family), member 1

Related Diseases

Diseases Alias
Mirror Movements 1

  • Congenital Mirror Movement Disorder

  • Bimanual Synergia

  • Congenital Mirror Movements

  • Familial Congenital Controlateral Synkinesia

  • Familial Congenital Mirror Movements

  • Hereditary Congenital Controlateral Synkinesia

  • Hereditary Congenital Mirror Movements

  • Isolated Congenital Controlateral Synkinesia

  • Isolated Congenital Mirror Movements

  • Mirror Movements

  • MRMV1

  • Mirror Movements 1 And/Or Agenesis Of The Corpus Callosum

  • Mirror Movements, Congenital

  • Bimanual Synkinesis

  • Cmm

  • Mirror Movements, Type 1
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-RS03128 CPXM1 Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Bos taurus CPXM1 VGNC VGNC:27681
Felis catus CPXM1 VGNC VGNC:61151
Macaca mulatta CPXM1 VGNC VGNC:71413
Canis familiaris CPXM1 VGNC VGNC:39585
Rattus norvegicus CPXM1 RGD RGD:1306937
Mus musculus CPXM1 MGD MGI:1934569
Others CPXM1 NCBI