Sequence 1 from Patent EP2623119

Run BLAST
Find regions of similarity between this sequence and other sequences using BLAST.
Pick Primers
Design and test primers for this sequence using Primer-BLAST.

MPZL2-a common autosomal recessive deafness gene related to moderate sensorineural hearing loss in the Chinese population. [BMC Med Genomics. 2024]
MPZL2-a common autosomal recessive deafness gene related to moderate sensorineural hearing loss in the Chinese population.
Zhang L, Yang JY, Wang QQ, Gao X, Wang GJ, Han MY, Kang DY, Han DY, Huang SS, Yuan YY. BMC Med Genomics. 2024 Jan 23; 17(1):32. Epub 2024 Jan 23.
Recurrent missense variant identified in two unrelated families with MPZL2-related hearing loss, expanding the variant spectrum associated with DFNB111. [Am J Med Genet A. 2024]
Recurrent missense variant identified in two unrelated families with MPZL2-related hearing loss, expanding the variant spectrum associated with DFNB111.
Lo E, Blair J, Yamamoto N, Diaz-Miranda MA, Bedoukian E, Gray C, Lawrence A, Dedhia K, Elden LM, Germiller JA, et al. Am J Med Genet A. 2024 May; 194(5):e63530. Epub 2024 Jan 10.
MPZL2 variant analysis with whole exome sequencing in a cohort of Chinese hearing loss patients. [Int J Pediatr Otorhinolaryngol...]
MPZL2 variant analysis with whole exome sequencing in a cohort of Chinese hearing loss patients.
Li W, Guo L, Chen B, Shu Y, Li H. Int J Pediatr Otorhinolaryngol. 2023 Aug; 171:111635. Epub 2023 Jun 12.

RefSeq alternative splicing
See 4 reference mRNA sequence splice variants for the MPZL2 gene.

Your browsing activity is empty.

Activity recording is turned off.

Nucleotide