SEC23B (S. cerevisiae) (predicted), isoform CRA_b [Rattus norvegicus]

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Germline Heterozygous Variants in SEC23B Are Associated with Cowden Syndrome and Enriched in Apparently Sporadic Thyroid Cancer. [Am J Hum Genet. 2015]
Germline Heterozygous Variants in SEC23B Are Associated with Cowden Syndrome and Enriched in Apparently Sporadic Thyroid Cancer.
Yehia L, Niazi F, Ni Y, Ngeow J, Sankunny M, Liu Z, Wei W, Mester JL, Keri RA, Zhang B, et al. Am J Hum Genet. 2015 Nov 5; 97(5):661-76. Epub 2015 Oct 29.
Codanin-1 mutations in congenital dyserythropoietic anemia type 1 affect HP1{alpha} localization in erythroblasts. [Blood. 2011]
Codanin-1 mutations in congenital dyserythropoietic anemia type 1 affect HP1{alpha} localization in erythroblasts.
Renella R, Roberts NA, Brown JM, De Gobbi M, Bird LE, Hassanali T, Sharpe JA, Sloane-Stanley J, Ferguson DJ, Cordell J, et al. Blood. 2011 Jun 23; 117(25):6928-38. Epub 2011 Mar 1.
Yeast two-hybrid screens imply that GGNBP1, GGNBP2 and OAZ3 are potential interaction partners of testicular germ cell-specific protein GGN1. [FEBS Lett. 2005]
Yeast two-hybrid screens imply that GGNBP1, GGNBP2 and OAZ3 are potential interaction partners of testicular germ cell-specific protein GGN1.
Zhang J, Wang Y, Zhou Y, Cao Z, Huang P, Lu B. FEBS Lett. 2005 Jan 17; 579(2):559-66.

RefSeq protein isoforms
See 4 reference sequence protein isoforms for the Sec23b gene.

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