1. Gene
  2. ADAM19 - ADAM metallopeptidase domain 19 Gene

ADAM19 - ADAM metallopeptidase domain 19 Gene

Homo sapiens

Also known as MLTNB; FKSG34; MADDAM

Gene ID: 8728 | Gene type: protein coding

About ADAM19

Cytogenetic location: 5q33.3 Genomic coordinates (GRCh38): 5:157,477,304-157,575,775 (from NCBI)

This gene has 5 transcripts (splice variants), 196 orthologues and 20 paralogues. Broad expression in lymph node (RPKM 12.3), appendix (RPKM 11.1) and 18 other tissues.

Summary

This gene encodes a member of the ADAM (a disintegrin and metalloprotease domain) family. Members of this family are membrane-anchored proteins structurally related to snake venom disintegrins and have been implicated in a variety of biological processes involving cell-cell and cell-matrix interactions, including fertilization, muscle development, and neurogenesis. This member is a type I transmembrane protein and serves as a marker for dendritic cell differentiation. It has been demonstrated to be an active metalloproteinase, which may be involved in normal physiological processes such as cell migration, cell adhesion, cell-cell and cell-matrix interactions, and signal transduction. It is proposed to play a role in pathological processes, such as Cancer, inflammatory diseases, renal diseases, and Alzheimer's disease. [provided by RefSeq, May 2013]

ADAM19 Products(1)

mRNA Protein Name
NM_033274.5 NP_150377.1 disintegrin and metalloproteinase domain-containing protein 19 preproprotein
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables metalloendopeptidase activity IMP
IMP: Inferred from mutant phenotype
11162584 GOA
enables metalloendopeptidase activity involved in amyloid precursor protein catabolic process IMP
IMP: Inferred from mutant phenotype
17112471 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
11162584 GOA
Biological Process GO Annotation Evidence Reference Source
involved in amyloid precursor protein catabolic process IMP
IMP: Inferred from mutant phenotype
17112471 GOA
involved in placenta development IEP
IEP: Inferred from expression pattern
19727588 GOA
involved in positive regulation of cell-cell adhesion mediated by cadherin IDA
IDA: Inferred from direct assay
19727588 GOA
involved in positive regulation of gene expression IDA
IDA: Inferred from direct assay
19727588 GOA
involved in protein processing IMP
IMP: Inferred from mutant phenotype
17112471 GOA
Cellular Component GO Annotation Evidence Reference Source
located in nucleus IDA
IDA: Inferred from direct assay
19727588 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

ADAM19 Protein Structure

Pep_M12B_propep

Pep_M12B_propep: Reprolysin family propeptide (44 - 162)

Reprolysin

Reprolysin: Reprolysin (M12B) family zinc metalloprotease (210 - 408)

Disintegrin

Disintegrin: Disintegrin (425 - 499)

ADAM_CR

ADAM_CR: ADAM cysteine-rich (502 - 617)

  • 0
  • 200
  • 400
  • 600
  • 800
  • 955 a.a.
Protein Preferred Names Protein Names

disintegrin and metalloproteinase domain-containing protein 19

a disintegrin and metalloproteinase domain 19 (meltrin beta)

ADAM19 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
ADAM19 Q9H013 SH3PXD2A Homo sapiens Q5TCZ1 25825872
Intra
ADAM19 Q9H013 SH3PXD2A Homo sapiens Q5TCZ1 33961781
Intra
ADAM19 Q9H013 TSPOAP1 Homo sapiens O95153 25825872
Intra
ADAM19 Q9H013 TSPOAP1 Homo sapiens O95153 25825872
Intra
ADAM19 Q9H013 EPS8L1 Homo sapiens Q8TE68 25825872
Intra
ADAM19 Q9H013 EPS8L1 Homo sapiens Q8TE68 25825872
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Fanconi Renotubular Syndrome 1

Renal Fanconi Syndrome

Adult Fanconi Syndrome

FRTS1

Fanconi Renotubular Syndrome

Frts

Rfs

Fanconi Syndrome Without Cystinosis

Luder-Sheldon Syndrome

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
Canis familiaris ADAM19 VGNC VGNC:37577
Rattus norvegicus ADAM19 RGD RGD:1585017
Mus musculus ADAM19 MGD MGI:105377
Felis catus ADAM19 VGNC VGNC:59578
Bos taurus ADAM19 VGNC VGNC:25608
Macaca mulatta ADAM19 VGNC VGNC:69479
Others ADAM19 NCBI