1. Gene
  2. MMP23B - matrix metallopeptidase 23B Gene

MMP23B - matrix metallopeptidase 23B Gene

Homo sapiens

Also known as MIFR; MMP22; MIFR-1; MMP23A

Gene ID: 8510 | Gene type: protein coding

About MMP23B

Cytogenetic location: 1p36.33 Genomic coordinates (GRCh38): 1:1,632,173-1,634,654 (from NCBI)

This gene has 10 transcripts (splice variants), 186 orthologues, 23 paralogues and is associated with 1 phenotype. Broad expression in placenta (RPKM 4.1), prostate (RPKM 3.5) and 21 other tissues.

Summary

This gene (MMP23B) encodes a member of the matrix metalloproteinase (MMP) family, and it is part of a duplicated region of chromosome 1p36.3. Proteins of the matrix metalloproteinase (MMP) family are involved in the breakdown of extracellular matrix in normal physiological processes, such as embryonic development, reproduction, and tissue remodeling, as well as in disease processes, such as arthritis and metastasis. This gene belongs to the more telomeric copy of the duplicated region. [provided by RefSeq, Jul 2008]

MMP23B Products(1)

mRNA Protein Name
NM_006983.2 NP_008914.1 matrix metalloproteinase-23 precursor

MMP23B Protein Structure

Peptidase_M10

Peptidase_M10: Matrixin (87 - 254)

ShK

ShK: ShK domain-like (255 - 289)

Ig_2

Ig_2: Immunoglobulin domain (306 - 388)

  • 0
  • 100
  • 200
  • 300
  • 390 a.a.
Protein Preferred Names Protein Names

matrix metalloproteinase-23

MMP-21

Related Diseases

Diseases Alias
Chromosome 1p36 Deletion Syndrome

1p36 Deletion Syndrome

Deletion 1p36

Monosomy 1p36

Subtelomeric 1p36 Deletion

Monosomy 1p36 Syndrome

Distal Monosomy 1p36

Del(1)(P36)

Deletion 1pter

Monosomy 1pter

Primary Ciliary Dyskinesia

Immotile Cilia Syndrome

Kartagener Syndrome

Dextrocardia Bronchiectasis And Sinusitis

Pcd

Ciliary Motility Disorders

Ciliary Motility Disorder

Immotile Ciliary Syndrome

Ciliary Dyskinesia Primary

Ics

Polynesian Bronchiectasis

Dextrocardia-Bronchiectasis-Sinusitis Syndrome

Immotile Cilia Syndrome, Kartagener Type

Primary Ciliary Dyskinesia And Situs Inversus

Primary Ciliary Dyskinesia, Kartagener Type

Siewert Syndrome

Dyskinesia, Ciliary, Primary

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

Orthologs Information

Species Symbol Source ID
Bos taurus MMP23B VGNC VGNC:53594
Felis catus MMP23B VGNC VGNC:82534
Rattus norvegicus MMP23B RGD RGD:620201
Macaca mulatta MMP23B VGNC VGNC:106408
Mus musculus MMP23B MGD MGI:1347361
Canis familiaris MMP23B VGNC VGNC:53425