Homo sapiens dynein heavy chain domain 1 (DNHD1), transcript variant 1 - Nucleotide

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New Mutations in DNHD1 Cause Multiple Morphological Abnormalities of the Sperm Flagella. [Int J Mol Sci. 2023]
New Mutations in DNHD1 Cause Multiple Morphological Abnormalities of the Sperm Flagella.
Martinez G, Barbotin AL, Cazin C, Wehbe Z, Boursier A, Amiri-Yekta A, Daneshipour A, Hosseini SH, Rives N, Feraille A, et al. Int J Mol Sci. 2023 Jan 29; 24(3). Epub 2023 Jan 29.
USP7 targets XIAP for cancer progression: Establishment of a p53-independent therapeutic avenue for glioma. [Oncogene. 2022]
USP7 targets XIAP for cancer progression: Establishment of a p53-independent therapeutic avenue for glioma.
Saha G, Sarkar S, Mohanta PS, Kumar K, Chakrabarti S, Basu M, Ghosh MK. Oncogene. 2022 Nov; 41(47):5061-5075. Epub 2022 Oct 15.
Bi-allelic variants in DNHD1 cause flagellar axoneme defects and asthenoteratozoospermia in humans and mice. [Am J Hum Genet. 2022]
Bi-allelic variants in DNHD1 cause flagellar axoneme defects and asthenoteratozoospermia in humans and mice.
Tan C, Meng L, Lv M, He X, Sha Y, Tang D, Tan Y, Hu T, He W, Tu C, et al. Am J Hum Genet. 2022 Jan 6; 109(1):157-171. Epub 2021 Dec 20.

RefSeq alternative splicing
See the other reference mRNA sequence splice variant for the DNHD1 gene (NM_173589.4).
RefSeq protein product
See the reference protein sequence for dynein heavy chain domain-containing protein 1 isoform 1 (NP_653267.2).

Protein
Protein sequence from Nucleotide coding region
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Homo sapiens dynein heavy chain domain 1 (DNHD1), transcript variant 1, mRNA
Homo sapiens dynein heavy chain domain 1 (DNHD1), transcript variant 1, mRNA
gi|1805791175|ref|NM_144666.3|

Nucleotide

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Nucleotide