MIA - MIA SH3 domain containing Gene

Also Known as CD-RAP

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 8190

About MIA

Cytogenetic location: 19q13.2 Genomic coordinates (GRCh38): 19:40,775,160-40,777,490 (from NCBI)

This gene has 7 transcripts (splice variants), 163 orthologues and 10 paralogues. Biased expression in stomach (RPKM 20.5), salivary gland (RPKM 4.7) and 2 other tissues.

Summary

Predicted to enable growth factor activity. Predicted to be involved in extracellular matrix organization. Predicted to act upstream of or within cell-matrix adhesion. Predicted to be located in extracellular space. [provided by Alliance of Genome Resources, Apr 2022]

MIA Products (2)

mRNA Protein Name
NM_001202553.2 NP_001189482.1 melanoma-derived growth regulatory protein precursor
NM_006533.4 NP_006524.1 melanoma-derived growth regulatory protein precursor

MIA Protein Structure

SH3_2

SH3_2: Variant SH3 domain (48 - 110)

  • 0
  • 100
  • 131 a.a.
Protein Preferred Names Protein Names

melanoma-derived growth regulatory protein

  • melanoma inhibitory activity

Recombinant MIA Proteins

Cat. No. Product Name Accession Purity
HY-P70846 MIA Protein, Human (His) Q16674 (G25-Q131) ≥ 95%, as determined by reducing SDS-PAGE.
HY-P70846A MIA Protein, Human (N-His) Q16674 (G25-Q131) ≥ 95%, as determined by reducing SDS-PAGE.

Related Diseases

Diseases Alias
Melanoma
  • Malignant Melanoma

  • Cutaneous Melanoma

  • Naevocarcinoma

  • Malignant Melanomas

Familial Isolated Hypoparathyroidism
  • Fih

Melanoma, Uveal
  • Uveal Melanoma

  • Choroidal Melanoma

  • Melanoma Of Uvea

  • Iris Melanoma

  • Malignant Melanoma Of Choroid

  • Malignant Melanoma Of Iris

Melanoma, Cutaneous Malignant 1
  • Familial Melanoma

  • Melanoma, Cutaneous Malignant, Susceptibility To, 1

  • Melanoma, Malignant

  • CMM1

  • Melanoma, Cutaneous Malignant

  • Cmm

  • Familial Atypical Mole-Malignant Melanoma Syndrome

  • Fammm

  • Melanoma, Familial

  • Mlm

  • Dysplastic Nevus Syndrome, Hereditary

  • Dns

  • B-K Mole Syndrome

  • Melanoma, Cutaneous Malignant, 1

  • Malignant Melanoma, Cutaneous

  • Melanoma, Cutaneous, Malignant, Susceptibility To, Type 1

  • Dysplastic Nevus Syndrome

  • Cutaneous Melanoma

  • Familial Atypical Mole Melanoma Syndrome

  • Hereditary Melanoma

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
Rattus norvegicus MIA RGD RGD:620883
Mus musculus MIA MGD MGI:109615
Others MIA NCBI