Variant position: 736 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 1435 The length of the canonical sequence.
Location on the sequence:
The residue change on the sequence. Unless the variant is located at the beginning or at the end of the protein sequence, both residues upstream (20) and downstream (20) of the variant will be shown.
Residue conservation: The multiple alignment of the region surrounding the variant against various orthologous sequences.
Human VEWIRSTLLYIRALKNPSHY- GFASGLNKDGIE-AKLQELCLK
Mouse LDWIRSTMLYIRALKNPSHY- GFSSGLNKDGIE-AKLQELC
Xenopus tropicalis LEWIRSTFLYIRALKNPAYY- GFSEGLDKIGIE-AKLQELC
Baker's yeast VNWLRNTFFYVRFGKNPAAYQ EVNRYVSFHSVEDSQINQFC
Sequence annotation in neighborhood: The regions or sites of interest surrounding the variant. In general the features listed are posttranslational modifications, binding sites, enzyme active sites, local secondary structure or other characteristics reported in the cited references. The "Sequence annotation in neighborhood" lines have a fixed format:
Type: the type of sequence feature. Positions: endpoints of the sequence feature. Description: contains additional information about the feature.
Type Positions Description
1 – 1435 Probable ATP-dependent DNA helicase HFM1
1 – 768 Missing. In isoform 2.
Mutations in HFM1 in recessive primary ovarian insufficiency.
Wang J.; Zhang W.; Jiang H.; Wu B.L.; Wu B.L.; An Y.; Wu B.; Yu L.; Zhou W.; Jiang H.; Zhang W.; Song X.; Zhang W.; Jiang H.; Wu J.; Pu D.; Zhang M.; Wu B.L.; Shen Y.; Wu B.L.; Wang J.; Zhang W.; Shen Y.; Lin C.; Grimmett L.; Liao E.; Shao H.; Shen X.; Platt O.;
N. Engl. J. Med. 370:972-974(2014)
Cited for: POSSIBLE INVOLVEMENT IN POF9; VARIANTS POF9 SER-736 AND SER-884;
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