RecName: Full=Cobalamin binding intrinsic factor; AltName: Full=Gastri - Protein

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Pancytopenia and megaloblastic erythropoiesis reveal a novel GIF mutation. [Br J Haematol. 2018]
Pancytopenia and megaloblastic erythropoiesis reveal a novel GIF mutation.
Saultier P, Loosveld M, Benoist JF, Michel G. Br J Haematol. 2018 May; 181(3):304. Epub 2018 Jan 25.
Acute lymphoblastic leukemia and vitamin B12 deficiency secondary to a gastric intrinsic factor gene mutation. [Pediatr Blood Cancer. 2012]
Acute lymphoblastic leukemia and vitamin B12 deficiency secondary to a gastric intrinsic factor gene mutation.
Zia A, Fışgin T, Sokolowski C, Tanner SM, Savaşan S. Pediatr Blood Cancer. 2012 Oct; 59(4):766-7. Epub 2012 May 3.
Juvenile cobalamin deficiency in individuals of African ancestry is caused by a founder mutation in the intrinsic factor gene GIF. [Br J Haematol. 2009]
Juvenile cobalamin deficiency in individuals of African ancestry is caused by a founder mutation in the intrinsic factor gene GIF.
Ament AE, Li Z, Sturm AC, Perko JD, Lawson S, Masterson M, Quadros EV, Tanner SM. Br J Haematol. 2009 Feb; 144(4):622-4. Epub 2008 Nov 19.

RefSeq genomic sequence
See the genomic reference sequence for the CBLIF gene (NG_008120.1).
RefSeq protein isoforms
See 3 reference sequence protein isoforms for the CBLIF gene.

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P27352 [Domain Mapping of Disease Mut...]
P27352
Domain Mapping of Disease Mutations
Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System
Reactome [Reactome]
Reactome
reagent reviews [ExactAntigen/Labome]
reagent reviews
ExactAntigen/Labome
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome
Evolutionary Trace of Functional Site [Evolutionary Trace of Functio...]
Evolutionary Trace of Functional Site

RecName: Full=Cobalamin binding intrinsic factor; AltName: Full=Gastric intrinsi...
RecName: Full=Cobalamin binding intrinsic factor; AltName: Full=Gastric intrinsic factor; AltName: Full=Intrinsic factor; Short=IF; Short=INF; Flags: Precursor
gi|62906845|sp|P27352.2|IF_HUMAN

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