Homo sapiens DNA cross-link repair 1B (DCLRE1B), RefSeqGene (LRG_1219) - Nucleotide

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DCLRE1B promotes tumor progression and predicts immunotherapy response through METTL3-mediated m6A modification in pancreatic cancer. [BMC Cancer. 2023]
DCLRE1B promotes tumor progression and predicts immunotherapy response through METTL3-mediated m6A modification in pancreatic cancer.
Li L, Wang F, Deng Z, Zhang G, Zhu L, Zhao Z, Liu R. BMC Cancer. 2023 Nov 7; 23(1):1073. Epub 2023 Nov 7.
AP4B1-associated hereditary spastic paraplegia: Expansion of clinico-genetic phenotype and geographic range. [Eur J Med Genet. 2022]
AP4B1-associated hereditary spastic paraplegia: Expansion of clinico-genetic phenotype and geographic range.
Salayev K, Rocca C, Kaiyrzhanov R, Guliyeva U, Guliyeva S, Mursalova A, Rahman F, Anwar N, Zafar F, Jan F, et al. Eur J Med Genet. 2022 Nov; 65(11):104620. Epub 2022 Sep 16.
Inherited human Apollo deficiency causes severe bone marrow failure and developmental defects. [Blood. 2022]
Inherited human Apollo deficiency causes severe bone marrow failure and developmental defects.
Kermasson L, Churikov D, Awad A, Smoom R, Lainey E, Touzot F, Audebert-Bellanger S, Haro S, Roger L, Costa E, et al. Blood. 2022 Apr 21; 139(16):2427-2440.

RefSeq alternative splicing
See 5 reference mRNA sequence splice variants for the DCLRE1B gene.

Protein
Protein sequence from Nucleotide coding region
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RNA
RNA sequence records that are annotated on the current genomic nucleotide sequences. The RNA records represent aligned or predicted transcripts of the current records.