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Rattus norvegicus P-glycoprotein-like ATP-binding cassette transporter mRNA, complete cds

GenBank: AF106563.1

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Articles about the Abcb6 gene

Mutations in ABCB6 cause dyschromatosis universalis hereditaria. [J Invest Dermatol. 2013]
Mutations in ABCB6 cause dyschromatosis universalis hereditaria.
Zhang C, Li D, Zhang J, Chen X, Huang M, Archacki S, Tian Y, Ren W, Mei A, Zhang Q, et al. J Invest Dermatol. 2013 Sep; 133(9):2221-8. Epub 2013 Mar 21.
ABCB6 mutations cause ocular coloboma. [Am J Hum Genet. 2012]
ABCB6 mutations cause ocular coloboma.
Wang L, He F, Bu J, Zhen Y, Liu X, Du W, Dong J, Cooney JD, Dubey SK, Shi Y, et al. Am J Hum Genet. 2012 Jan 13; 90(1):40-8. Epub 2012 Jan 5.
Recessive mutations in ELOVL4 cause ichthyosis, intellectual disability, and spastic quadriplegia. [Am J Hum Genet. 2011]
Recessive mutations in ELOVL4 cause ichthyosis, intellectual disability, and spastic quadriplegia.
Aldahmesh MA, Mohamed JY, Alkuraya HS, Verma IC, Puri RD, Alaiya AA, Rizzo WB, Alkuraya FS. Am J Hum Genet. 2011 Dec 9; 89(6):745-50. Epub 2011 Nov 17.

Reference sequence information

RefSeq alternative splicing
See 3 reference mRNA sequence splice variants for the Abcb6 gene.

More about the Abcb6 gene

Predicted to enable several functions, including ABC-type heme transporter activity; ATP binding activity; and ATP hydrolysis activity. Invo...
Also Known As: MTABC3

Related information

Protein
Protein sequence from Nucleotide coding region
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reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

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