1. Gene
  2. MIA - MIA SH3 domain containing Gene

MIA - MIA SH3 domain containing Gene

Homo sapiens

Also known as CD-RAP

Gene ID: 8190 | Gene type: protein coding

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%
HY-P70846A MIA Protein, Human (N-His) Q16674 (G25-Q131) ≥95%

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
Macaca fascicularis MIA NCBI NCBI:102118191
Macaca mulatta MIA NCBI NCBI:114669743
Others MIA NCBI