C20orf42

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Fermitin family member 1
Identifiers
Symbols FERMT1 ; C20orf42; DTGCU2; KIND1; UNC112A; URP1
External IDs OMIM607900 MGI2443583 HomoloGene9773 GeneCards: FERMT1 Gene
RNA expression pattern
PBB GE C20orf42 218796 at tn.png
PBB GE C20orf42 60474 at tn.png
More reference expression data
Orthologs
Species Human Mouse
Entrez 55612 241639
Ensembl ENSG00000101311 ENSMUSG00000027356
UniProt Q9BQL6 P59113
RefSeq (mRNA) NM_017671 NM_198029
RefSeq (protein) NP_060141 NP_932146
Location (UCSC) Chr 20:
6.06 – 6.1 Mb
Chr 2:
132.9 – 132.95 Mb
PubMed search [1] [2]

Fermitin family homolog 1 is a protein that in humans is encoded by the FERMT1 gene.[1][2][3]


References[edit]

  1. ^ Weinstein EJ, Bourner M, Head R, Zakeri H, Bauer C, Mazzarella R (Apr 2003). "URP1: a member of a novel family of PH and FERM domain-containing membrane-associated proteins is significantly over-expressed in lung and colon carcinomas". Biochim Biophys Acta 1637 (3): 207–16. doi:10.1016/S0925-4439(03)00035-8. PMID 12697302. 
  2. ^ Siegel DH, Ashton GH, Penagos HG, Lee JV, Feiler HS, Wilhelmsen KC, South AP, Smith FJ, Prescott AR, Wessagowit V, Oyama N, Akiyama M, Al Aboud D, Al Aboud K, Al Githami A, Al Hawsawi K, Al Ismaily A, Al-Suwaid R, Atherton DJ, Caputo R, Fine JD, Frieden IJ, Fuchs E, Haber RM, Harada T, Kitajima Y, Mallory SB, Ogawa H, Sahin S, Shimizu H, Suga Y, Tadini G, Tsuchiya K, Wiebe CB, Wojnarowska F, Zaghloul AB, Hamada T, Mallipeddi R, Eady RA, McLean WH, McGrath JA, Epstein EH (Jun 2003). "Loss of Kindlin-1, a Human Homolog of the Caenorhabditis elegans Actin–Extracellular-Matrix Linker Protein UNC-112, Causes Kindler Syndrome". Am J Hum Genet 73 (1): 174–87. doi:10.1086/376609. PMC 1180579. PMID 12789646. 
  3. ^ "Entrez Gene: C20orf42 chromosome 20 open reading frame 42". 

External links[edit]

Further reading[edit]