microtubule-associated protein 1B isoform 2 [Homo sapiens]

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Epilepsy phenotypes associated with MAP1B-related brain malformations. [Epileptic Disord. 2021]
Epilepsy phenotypes associated with MAP1B-related brain malformations.
Arya R, Spaeth C, Zhang W. Epileptic Disord. 2021 Apr 1; 23(2):392-396.
Mutations of MAP1B encoding a microtubule-associated phosphoprotein cause sensorineural hearing loss. [JCI Insight. 2020]
Mutations of MAP1B encoding a microtubule-associated phosphoprotein cause sensorineural hearing loss.
Cui L, Zheng J, Zhao Q, Chen JR, Liu H, Peng G, Wu Y, Chen C, He Q, Shi H, et al. JCI Insight. 2020 Dec 3; 5(23). Epub 2020 Dec 3.
MAP1B related syndrome: Case presentation and review of literature. [Am J Med Genet A. 2019]
MAP1B related syndrome: Case presentation and review of literature.
Julca DM, Diaz J, Berger S, Leon E. Am J Med Genet A. 2019 Sep; 179(9):1703-1708. Epub 2019 Jul 17.

RefSeq mRNA
See reference mRNA sequence for the MAP1B gene (NM_001324255.2).
RefSeq protein isoforms
See the other reference sequence protein isoform for the MAP1B gene (NP_005900.2).

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Protein