1. Gene
  2. PARVA - parvin alpha Gene

PARVA - parvin alpha Gene

Homo sapiens

Also known as MXRA2; CH-ILKBP

Gene ID: 55742 | Gene type: protein coding

About PARVA

Cytogenetic location: 11p15.3 Genomic coordinates (GRCh38): 11:12,376,436-12,535,356 (from NCBI)

This gene has 6 transcripts (splice variants), 229 orthologues and 2 paralogues. Ubiquitous expression in endometrium (RPKM 30.7), fat (RPKM 26.7) and 24 other tissues.

Summary

This gene encodes a member of the parvin family of actin-binding proteins. Parvins are associated with focal contacts and contain calponin homology domains that bind to actin filaments. The encoded protein is part of the integrin-linked kinase signaling complex and plays a role in cell adhesion, motility and survival. [provided by RefSeq, Dec 2010]

PARVA Products(1)

mRNA Protein Name
NM_018222.5 NP_060692.3 alpha-parvin

PARVA Protein Structure

CH

CH: Calponin homology (CH) domain (140 - 241)

CH

CH: Calponin homology (CH) domain (305 - 408)

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

alpha-parvin

actopaxin

Recombinant PARVA Proteins

Cat. No. Product Name Accession Purity
HY-P7493 PARVA/alpha-Parvin Protein, Human (His) Q9NVD7 (M1-E372) ≥95%
HY-P76535 PARVA/alpha-Parvin Protein, Human (GST) Q9NVD7 (M1-E372) ≥95%

Related Diseases

Diseases Alias
Breast Giant Fibroadenoma

Giant Fibroadenoma

Giant Fibroadenoma Of Breast

Focal Segmental Glomerulosclerosis

Familial Idiopathic Steroid-Resistant Nephrotic Syndrome

Focal Glomerulosclerosis

Fsgs

Segmental Glomerulosclerosis

Glomerulosclerosis, Focal Segmental

Fgs

Focal Glomerular Sclerosis

Familial Idiopathic Nephrotic Syndrome

Focal Sclerosis With Hyalinosis

Glomerulosclerosis, Focal

Glomerulosclerosis Focal

Glomerulosclerosis, Segmental, Focal

Focal Segmental Glomerulosclerosis, Not Otherwise Specified

Adams-Oliver Syndrome

Adams Oliver Syndrome

Aos

Congenital Scalp Defects With Distal Limb Reduction Anomalies

Aplasia Cutis Congenita With Terminal Transverse Limb Defects

Congenital Scalp Defects With Distal Limb Anomalies

Limb, Scalp And Skull Defects

Limb Scalp And Skull Defects

Absence Defect Of Limbs, Scalp, And Skull

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
Macaca mulatta PARVA VGNC VGNC:75605
Mus musculus PARVA MGD MGI:1931144
Felis catus PARVA VGNC VGNC:64045
Canis familiaris PARVA VGNC VGNC:49689
Bos taurus PARVA VGNC VGNC:32589
Rattus norvegicus PARVA RGD RGD:71021
Others PARVA NCBI