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词条 ANKRD35
释义

  1. Related gene problems

  2. References

{{infobox protein
|Name=ankyrin repeat domain 35
|caption=
|image=
|width=
|HGNCid=26323
|Symbol=ANKRD35
|AltSymbols=
|EntrezGene=148741
|OMIM=
|RefSeq=NM_144698
|UniProt= Q8N283
|PDB=
|ECnumber=
|Chromosome=1
|Arm=q
|Band=21.1
|LocusSupplementaryData=
}}Ankyrin repeat domain 35 also known as ANKRD35 is a protein which in humans is encoded by the ANKRD35 gene.[1]

Related gene problems

  • TAR syndrome[2]
  • 1q21.1 deletion syndrome
  • 1q21.1 duplication syndrome

References

1. ^{{cite web | title = Entrez Gene: ANKRD35 ankyrin repeat domain 35 | url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=148741 | accessdate = }}
2. ^{{cite journal | vauthors = Klopocki E, Schulze H, Strauss G | title = Complex Inheritance Pattern Resembling Autosomal Recessive Inheritance Involving a Microdeletion in Thrombocytopenia–Absent Radius Syndrome | journal = Am. J. Hum. Genet. | volume = 80 | issue = 2 | pages = 232–40 |date=February 2007 | pmid = 17236129 | pmc = 1785342 | doi = 10.1086/510919 | url = |display-authors=etal}}
{{Gene-1-stub}}
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