dmX-like protein 2 isoform 1 [Homo sapiens]

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A novel variant in DMXL2 gene is associated with autosomal dominant non-syndromic hearing impairment (DFNA71) in a Cameroonian family. [Exp Biol Med (Maywood). 2021]
A novel variant in DMXL2 gene is associated with autosomal dominant non-syndromic hearing impairment (DFNA71) in a Cameroonian family.
Wonkam-Tingang E, Schrauwen I, Esoh KK, Bharadwaj T, Nouel-Saied LM, Acharya A, Nasir A, Leal SM, Wonkam A. Exp Biol Med (Maywood). 2021 Jul; 246(13):1524-1532. Epub 2021 Mar 9.
Biallelic DMXL2 mutations impair autophagy and cause Ohtahara syndrome with progressive course. [Brain. 2019]
Biallelic DMXL2 mutations impair autophagy and cause Ohtahara syndrome with progressive course.
Esposito A, Falace A, Wagner M, Gal M, Mei D, Conti V, Pisano T, Aprile D, Cerullo MS, De Fusco A, et al. Brain. 2019 Dec 1; 142(12):3876-3891.
Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disorders. [J Neurodev Disord. 2019]
Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disorders.
Costain G, Walker S, Argiropoulos B, Baribeau DA, Bassett AS, Boot E, Devriendt K, Kellam B, Marshall CR, Prasad A, et al. J Neurodev Disord. 2019 Feb 7; 11(1):3. Epub 2019 Feb 7.

RefSeq genomic sequence
See the genomic reference sequence for the DMXL2 gene (NG_017155.1).
RefSeq mRNA
See reference mRNA sequence for the DMXL2 gene (NM_001174116.3).
RefSeq protein isoforms
See 25 reference sequence protein isoforms for the DMXL2 gene.

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Ensembl [Ensembl]
Ensembl
GlyGen glycoinformatics resource [GlyGen glycoinformatics resou...]
GlyGen glycoinformatics resource
OncoMX cancer biomarker resource [OncoMX cancer biomarker resou...]
OncoMX cancer biomarker resource
Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System
reagent reviews [ExactAntigen/Labome]
reagent reviews
ExactAntigen/Labome
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

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