MFAP5

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

MFAP5

Microfibrillar-associated protein 5 is a protein that in humans is encoded by the MFAP5 gene.[5][6][7]

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MFAP5
Identifiers
AliasesMFAP5, MAGP-2, MAGP2, MFAP-5, MP25, AAT9, microfibrillar associated protein 5, microfibril associated protein 5
External IDsOMIM: 601103; MGI: 1354387; HomoloGene: 2599; GeneCards: MFAP5; OMA:MFAP5 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001297709
NM_001297710
NM_001297711
NM_001297712
NM_003480

NM_015776
NM_001347434

RefSeq (protein)

NP_001284638
NP_001284639
NP_001284640
NP_001284641
NP_003471

NP_001334363
NP_056591

Location (UCSC)Chr 12: 8.64 – 8.66 MbChr 6: 122.48 – 122.51 Mb
PubMed search[3][4]
Wikidata
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This gene encodes a 25-kD microfibril-associated glycoprotein which is rich in serine and threonine residues. It lacks a hydrophobic carboxyl terminus and proline-, glutamine-, and tyrosine-rich regions, which are characteristics of a related 31-kDa microfibril-associated glycoprotein (MFAP2). The close similarity between these two proteins is confined to a central region of 60 aa where precise alignment of 7 cysteine residues occurs. The structural differences suggest that this encoded protein has some functions that are distinct from those of MFAP2.[7]

References

Further reading

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