Citations for
1AMN, CUBN
Amnionless-mediated glycosylation is crucial for cell surface targeting of cubilin in renal and intestinal cells.
Udagawa T, Harita Y, Miura K, Mitsui J, Ode KL, Morishita S, Urae S, Kanda S, Kajiho Y, Tsurumi H, Ueda HR, Tsuji S, Saito A, Oka A.
Sci Rep 8(1):2351. doi: 10.1038/s41598-018-20731-4. 2018
2MGA1, MGA2, AMN, CUBN
Genetic heterogeneity of megaloblastic anaemia type 1 in Tunisian patients.
Bouchlaka C, Maktouf C, Mahjoub B, Ayadi A, Sfar MT, Sioud M, Gueddich N, Belhadjali Z, Rebai A, Abdelhak S, Dellagi K.
J Hum Genet 52(3):262-70. Epub 2007 Feb 7. 2007
3MGA1, AMN, CUBN, GIF, MGA2, MGA3
Hereditary juvenile cobalamin deficiency caused by mutations in the intrinsic factor gene.
Tanner SM, Li Z, Perko JD, Oner C, Cetin M, Altay C, Yurtsever Z, David KL, Faivre L, Ismail EA, Grasbeck R, de la Chapelle A.
Proc Natl Acad Sci U S A 102(11):4130-3. Epub 2005 Feb 28. 2005
4AMN, CUBN
Amnionless function is required for cubilin brush-border expression and intrinsic factor-cobalamin (vitamin B12) absorption in vivo.
He Q, Madsen M, Kilkenney A, Gregory B, Christensen EI, Vorum H, Hojrup P, Schaffer AA, Kirkness EF, Tanner SM, de la Chapelle A, Giger U, Moestrup SK, Fyfe JC.
Blood 106(4):1447-53. Epub 2005 Apr 21. 2005
5AMN, CUBN
The functional cobalamin (vitamin B12)-intrinsic factor receptor is a novel complex of cubilin and amnionless.
Fyfe JC, Madsen M, Hojrup P, Christensen EI, Tanner SM, de la Chapelle A, He Q, Moestrup SK.
Blood 103(5):1573-9. Epub 2003 Oct 23. 2004
6AMN
The amnionless gene, essential for mouse gastrulation, encodes a visceral-endoderm-specific protein with an extracellular cysteine-rich domain.
Kalantry S, Manning S, Haub O, Tomihara-Newberger C, Lee HG, Fangman J,Disteche CM, Manova K, Lacy E.
Nat Genet 27(4):412-6. 2001