Homo sapiens homeobox D13 (HOXD13), mRNA

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Sequence variants in DLX5, HOXD13 and 445 kb-microduplication surrounding BTRC cause split-hand/foot malformation in three different families. [Clin Genet. 2024]
Sequence variants in DLX5, HOXD13 and 445 kb-microduplication surrounding BTRC cause split-hand/foot malformation in three different families.
Abdullah, Hussain S, Ji W, Khan H, Mis EK, Mushtaq R, Chodhary M, Raza MH, Jan A, Ullah I, et al. Clin Genet. 2024 Jan; 105(1):109-111. Epub 2023 Sep 30.
Identification of motif-based interactions between SARS-CoV-2 protein domains and human peptide ligands pinpoint antiviral targets. [Nat Commun. 2023]
Identification of motif-based interactions between SARS-CoV-2 protein domains and human peptide ligands pinpoint antiviral targets.
Mihalič F, Benz C, Kassa E, Lindqvist R, Simonetti L, Inturi R, Aronsson H, Andersson E, Chi CN, Davey NE, et al. Nat Commun. 2023 Sep 13; 14(1):5636. Epub 2023 Sep 13.
HOXD13-associated synpolydactyly: Extending and validating the genotypic and phenotypic spectrum with 38 new and 49 published families. [Genet Med. 2023]
HOXD13-associated synpolydactyly: Extending and validating the genotypic and phenotypic spectrum with 38 new and 49 published families.
Gottschalk A, Sczakiel HL, Hülsemann W, Schwartzmann S, Abad-Perez AT, Grünhagen J, Ott CE, Spielmann M, Horn D, Mundlos S, et al. Genet Med. 2023 Nov; 25(11):100928. Epub 2023 Jul 7.

RefSeq alternative splicing
See 3 reference mRNA sequence splice variants for the HOXD13 gene.
RefSeq protein product
See the reference protein sequence for homeobox protein Hox-D13 (NP_000514.2).

Protein
Protein sequence from Nucleotide coding region
PubMed
PubMed articles cited by Nucleotide sequence record
Taxonomy
Taxonomy sequences associated with Nucleotide record
Annotated Genomic
Genomic sequence records that have the current RNA records as annotated features marking the exons of genes.
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BioSystems
CCDS
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Components (Core)
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Functional Class
Functional class of the sequence domain architecture
Gene
Link to related Genes
OMIM
OMIM records associated with Nucleotide sequence
Probe
Related Probe entry
PubMed (RefSeq)
Link to RefSeq PubMed articles
PubMed (Weighted)
Links to pubmed

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SH3GL3 SH3 domain containing GRB2 like 3, endophilin A3 [Homo sapiens]
SH3GL3 SH3 domain containing GRB2 like 3, endophilin A3 [Homo sapiens]
Gene ID:6457

Gene
Vcam1 vascular cell adhesion molecule 1 [Mus musculus]
Vcam1 vascular cell adhesion molecule 1 [Mus musculus]
Gene ID:22329

Gene

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Nucleotide