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SHFM3P1

From Wikipedia, the free encyclopedia
FBXW4P1
Identifiers
AliasesFBXW4P1, FBW3, FBXW3, SHFM3P1, F-box and WD repeat domain containing 4 pseudogene 1
External IDsGeneCards: FBXW4P1; OMA:FBXW4P1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_012165

n/a

RefSeq (protein)

n/a

n/a

Location (UCSC)Chr 22: 23.26 – 23.27 Mbn/a
PubMed search[2]n/a
Wikidata
View/Edit Human

Split hand/foot malformation (ectrodactyly) type 3 pseudogene 1, also known as SHFM3P1, is a human gene.[3]


References

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000230701Ensembl, May 2017
  2. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  3. ^ "Entrez Gene: SHFM3P1 split hand/foot malformation (ectrodactyly) type 3 pseudogene 1".

Further reading

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