protein unc-79 homolog isoform X12 [Homo sapiens]

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A new neurodevelopmental disorder linked to heterozygous variants in UNC79. [Genet Med. 2023]
A new neurodevelopmental disorder linked to heterozygous variants in UNC79.
Bayat A, Liu Z, Luo S, Fenger CD, Højte AF, Isidor B, Cogne B, Larson A, Zanus C, Faletra F, et al. Genet Med. 2023 Sep; 25(9):100894. Epub 2023 May 11.
Genetic variants in components of the NALCN-UNC80-UNC79 ion channel complex cause a broad clinical phenotype (NALCN channelopathies). [Hum Genet. 2018]
Genetic variants in components of the NALCN-UNC80-UNC79 ion channel complex cause a broad clinical phenotype (NALCN channelopathies).
Bramswig NC, Bertoli-Avella AM, Albrecht B, Al Aqeel AI, Alhashem A, Al-Sannaa N, Bah M, Bröhl K, Depienne C, Dorison N, et al. Hum Genet. 2018 Sep; 137(9):753-768. Epub 2018 Aug 23.
Mutations in UNC80, Encoding Part of the UNC79-UNC80-NALCN Channel Complex, Cause Autosomal-Recessive Severe Infantile Encephalopathy. [Am J Hum Genet. 2016]
Mutations in UNC80, Encoding Part of the UNC79-UNC80-NALCN Channel Complex, Cause Autosomal-Recessive Severe Infantile Encephalopathy.
Shamseldin HE, Faqeih E, Alasmari A, Zaki MS, Gleeson JG, Alkuraya FS. Am J Hum Genet. 2016 Jan 7; 98(1):210-5. Epub 2015 Dec 17.

RefSeq mRNA
See reference mRNA sequence for the UNC79 gene (XM_017021513.2).
RefSeq protein isoforms
See 93 reference sequence protein isoforms for the UNC79 gene.

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474223[BioProject] (174628)
Protein
GSM449499[Accession] (3)
GEO DataSets
tRNA-queuosine alpha-mannosyltransferase isoform X7 [Homo sapiens]
tRNA-queuosine alpha-mannosyltransferase isoform X7 [Homo sapiens]
gi|2462577215|ref|XP_054199914.1|

Protein
protein unc-79 homolog isoform X2 [Homo sapiens]
protein unc-79 homolog isoform X2 [Homo sapiens]
gi|2462541072|ref|XP_054232438.1|

Protein
Arthrobacter sp. 'SMCC G915' RecA protein (recA) gene, partial cds
Arthrobacter sp. 'SMCC G915' RecA protein (recA) gene, partial cds
gi|6694764|gb|AF214757.1|

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Protein