Homo sapiens mRNA for DYNC2H1/KIAA1997 variant protein, complete cds

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Ellis-van Creveld Syndrome. [GeneReviews(®). 1993]
Ellis-van Creveld Syndrome.
Da Silva JD, Tkachenko N, Soares AR. GeneReviews(®). 1993-2024. 2023 Oct 26
Antagonistic roles of canonical and Alternative-RPA in disease-associated tandem CAG repeat instability. [Cell. 2023]
Antagonistic roles of canonical and Alternative-RPA in disease-associated tandem CAG repeat instability.
Gall-Duncan T, Luo J, Jurkovic CM, Fischer LA, Fujita K, Deshmukh AL, Harding RJ, Tran S, Mehkary M, Li V, et al. Cell. 2023 Oct 26; 186(22):4898-4919.e25. Epub 2023 Oct 11.
Clinical variability in DYNC2H1-related skeletal ciliopathies includes Ellis-van Creveld syndrome. [Eur J Hum Genet. 2023]
Clinical variability in DYNC2H1-related skeletal ciliopathies includes Ellis-van Creveld syndrome.
Piceci-Sparascio F, Micale L, Torres B, Guida V, Consoli F, Torrente I, Onori A, Frustaci E, D'Asdia MC, Petrizzelli F, et al. Eur J Hum Genet. 2023 Apr; 31(4):479-484. Epub 2023 Jan 4.

RefSeq alternative splicing
See 10 reference mRNA sequence splice variants for the DYNC2H1 gene.

Homo sapiens NK2 homeobox 5 (NKX2-5), transcript variant 2, mRNA
Homo sapiens NK2 homeobox 5 (NKX2-5), transcript variant 2, mRNA
gi|1674985859|ref|NM_001166175.2|

Nucleotide
Homo sapiens chromosome 5 open reading frame 25, mRNA (cDNA clone MGC:87612 IMAG...
Homo sapiens chromosome 5 open reading frame 25, mRNA (cDNA clone MGC:87612 IMAGE:4821958), complete cds
gi|44890779|gb|BC066980.1|

Nucleotide

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Nucleotide