MXRA7
Description
The MXRA7 (matrix remodeling associated 7) is a protein-coding gene located on chromosome 17.
MXRA7 is a human gene found on chromosome 17 that encodes the protein Matrix Remodeling Associated 7. Studies in mice without the MXRA7 gene indicate its involvement in various biological processes, both normal and disease-related.
MXRA7, also known as Matrix Remodeling Associated 7, is a human gene located on chromosome 17. Studies in mice lacking the MXRA7 gene suggest that this gene plays a role in various biological processes, both healthy and disease-related.
MXRA7 is also known as -.
Associated Diseases
- Gollop-Wolfgang complex
- tibia, hypoplasia or aplasia of, with polydactyly
- Blount disease
- acheiropody
- syndactyly type 4
- acromesomelic dysplasia 2C, Hunter-Thompson type
- laurin-Sandrow syndrome
- spondyloepimetaphyseal dysplasia, Missouri type
- fibular aplasia-ectrodactyly syndrome
- acromesomelic dysplasia 2A
- tibial hemimelia