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Previous release (v1)
2025-10-28 01:10:20, GGRNA.v2 : RefSeq release 232 (Sep, 2025)
LOCUS NM_001105886 2483 bp mRNA linear ROD 20-MAR-2023
DEFINITION Rattus norvegicus homeo box D13 (Hoxd13), mRNA.
ACCESSION NM_001105886 XM_001063399 XM_221511
VERSION NM_001105886.1
KEYWORDS RefSeq; RefSeq Select.
SOURCE Rattus norvegicus (Norway rat)
ORGANISM Rattus norvegicus
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
Mammalia; Eutheria; Euarchontoglires; Glires; Rodentia; Myomorpha;
Muroidea; Muridae; Murinae; Rattus.
REFERENCE 1 (bases 1 to 2483)
AUTHORS Wang B, Li N, Geng J, Wang Z, Fu Q, Wang J and Xu Y.
TITLE Exome sequencing identifies a novel nonsense mutation of HOXD13 in
a Chinese family with synpolydactyly
JOURNAL Congenit Anom (Kyoto) 57 (1), 4-7 (2017)
PUBMED 27254532
REFERENCE 2 (bases 1 to 2483)
AUTHORS Kherdjemil Y, Lalonde RL, Sheth R, Dumouchel A, de Martino G,
Pineault KM, Wellik DM, Stadler HS, Akimenko MA and Kmita M.
TITLE Evolution of Hoxa11 regulation in vertebrates is linked to the
pentadactyl state
JOURNAL Nature 539 (7627), 89-92 (2016)
PUBMED 27706137
REFERENCE 3 (bases 1 to 2483)
AUTHORS Zhu YP, Li EH, Sun WL, Xu DL, Liu ZH, Zhao W, Wood K, Xia SJ and
Jiang JT.
TITLE Maternal exposure to di-n-butyl phthalate (DBP) induces combined
anorectal and urogenital malformations in male rat offspring
JOURNAL Reprod Toxicol 61, 169-176 (2016)
PUBMED 27079746
REFERENCE 4 (bases 1 to 2483)
AUTHORS Ibrahim DM, Tayebi N, Knaus A, Stiege AC, Sahebzamani A, Hecht J,
Mundlos S and Spielmann M.
TITLE A homozygous HOXD13 missense mutation causes a severe form of
synpolydactyly with metacarpal to carpal transformation
JOURNAL Am J Med Genet A 170 (3), 615-621 (2016)
PUBMED 26581570
REFERENCE 5 (bases 1 to 2483)
AUTHORS Wang F, Du M, Wang R, Zhou J, Zhang W and Li H.
TITLE Molecular mechanism of Hoxd13-mediated congenital malformations in
rat embryos
JOURNAL Int J Clin Exp Pathol 8 (12), 15591-15598 (2015)
PUBMED 26884828
REMARK GeneRIF: Hoxd13 expression was decreased in rat embryos with
congenital malformations. The administration of exogenous Hoxd13
alleviated fetal malformation probably through stimulation of Slim1
expression and Wnt/beta-catenin signaling pathway.
Publication Status: Online-Only
REFERENCE 6 (bases 1 to 2483)
AUTHORS Herault Y, Hraba-Renevey S, van der Hoeven F and Duboule D.
TITLE Function of the Evx-2 gene in the morphogenesis of vertebrate limbs
JOURNAL EMBO J 15 (23), 6727-6738 (1996)
PUBMED 8978698
REFERENCE 7 (bases 1 to 2483)
AUTHORS Zakany J and Duboule D.
TITLE Synpolydactyly in mice with a targeted deficiency in the HoxD
complex
JOURNAL Nature 384 (6604), 69-71 (1996)
PUBMED 8900279
REFERENCE 8 (bases 1 to 2483)
AUTHORS Akarsu AN, Stoilov I, Yilmaz E, Sayli BS and Sarfarazi M.
TITLE Genomic structure of HOXD13 gene: a nine polyalanine duplication
causes synpolydactyly in two unrelated families
JOURNAL Hum Mol Genet 5 (7), 945-952 (1996)
PUBMED 8817328
REFERENCE 9 (bases 1 to 2483)
AUTHORS Davis AP and Capecchi MR.
TITLE A mutational analysis of the 5' HoxD genes: dissection of genetic
interactions during limb development in the mouse
JOURNAL Development 122 (4), 1175-1185 (1996)
PUBMED 8620844
REFERENCE 10 (bases 1 to 2483)
AUTHORS Dolle P, Dierich A, LeMeur M, Schimmang T, Schuhbaur B, Chambon P
and Duboule D.
TITLE Disruption of the Hoxd-13 gene induces localized heterochrony
leading to mice with neotenic limbs
JOURNAL Cell 75 (3), 431-441 (1993)
PUBMED 8106170
COMMENT PROVISIONAL REFSEQ: This record has not yet been subject to final
NCBI review. The reference sequence was derived from CH473949.1.
On or before Oct 3, 2007 this sequence version replaced
XM_221511.3, XM_001063399.1.
Publication Note: This RefSeq record includes a subset of the
publications that are available for this gene. Please see the Gene
record to access additional publications.
##Evidence-Data-START##
RNAseq introns :: single sample supports all introns SAMN09345330,
SAMN09345331 [ECO:0000348]
##Evidence-Data-END##
##RefSeq-Attributes-START##
RefSeq Select criteria :: based on single protein-coding transcript
##RefSeq-Attributes-END##
FEATURES Location/Qualifiers
source 1..2483
/organism="Rattus norvegicus"
/mol_type="mRNA"
/db_xref="taxon:10116"
/chromosome="3"
/map="3q23"
gene 1..2483
/gene="Hoxd13"
/note="homeo box D13"
/db_xref="GeneID:288154"
/db_xref="RGD:1308417"
exon 1..768
/gene="Hoxd13"
/inference="alignment:Splign:2.1.0"
CDS 24..1019
/gene="Hoxd13"
/codon_start=1
/product="homeobox protein Hox-D13"
/protein_id="NP_001099356.1"
/db_xref="GeneID:288154"
/db_xref="RGD:1308417"
/translation="
MDGLRADGGAAGAAPASSSSSVAAPGQCRGFLSAPVFAGTHSGRAAAAAAAAAAAAAAASSFAYPGTSERTGSSSSSSSSAVIATRPEAPVAKECPAPAAAATAAAPPGAPALGYGYHFGNGYYSCRMSHGVGLQQNALKSSPHASLGGFPVEKYMDVSGLASSSVPTNEVPARAKEVSFYQGYTSPYQHVPGYIDMVSTFGSGEPRHEAYISMEGYQSWTLANGWNSQVYCAKDQPQGSHFWKSSFPGDVALNQPDMCVYRRGRKKRVPYTKLQLKELENEYAINKFINKDKRRRISAATNLSERQVTIWFQNRRVKDKKIVSKLKDTVS"
misc_feature <360..503
/gene="Hoxd13"
/note="Hox protein A13 N terminal; Region: HoxA13_N;
pfam12284"
/db_xref="CDD:463521"
misc_feature 816..986
/gene="Hoxd13"
/note="Region: Homeodomain; pfam00046"
/db_xref="CDD:459649"
exon 769..2483
/gene="Hoxd13"
/inference="alignment:Splign:2.1.0"
ORIGIN
tgagccgctcggggacttgggacatggatgggctgcgggcggacggcggggccgctggggcggcaccggcctcctcctcctcctctgtggcggcgcctggccagtgtcgcggcttcctgtcggcgccggtgttcgcggggacacattccggacgcgcggcggccgcagcggcagcggcggcggcggcggcggcggcagcctccagcttcgcgtacccagggacctctgagcgcacaggctcgtcgtcgtcgtcgtcatcctcggctgtgatcgccactcgccccgaggctccagtggccaaagagtgtcccgcgccagcggccgcggcgaccgcagcagcaccgccgggcgctcccgcgttgggctatggctaccatttcggcaacggctactacagctgccgcatgtcgcacggcgtgggcttacagcagaacgctctcaagtcgtccccgcacgcctctctcggaggtttcccagtggagaagtacatggacgtgtcgggcctggcgagcagcagcgtaccgaccaacgaggtgcccgcgcgagccaaggaagtgtccttctaccagggctacacgagtccctatcagcacgtgcctgggtatatcgacatggtgtccacttttggatccggggaacctcggcacgaggcgtacatttccatggagggctaccagtcctggacgctagccaacgggtggaacagccaggtgtattgtgccaaggaccagccgcaggggtcccatttttggaaatcatcctttccaggggatgtggctttaaaccagccggacatgtgcgtctaccgtcggggaaggaagaaaagggtaccttataccaaactgcagctcaaagaactggagaacgagtatgccattaacaagtttattaacaaggacaagcggcggcggatctcagctgccaccaacctatccgagagacaagtcaccatttggtttcagaatcgaagagtgaaggacaagaaaatcgtctccaagctcaaagatactgtctcctgatgtgggccaggttggccacagacagtttaaatgctttcagttgtctccaaaaatacctttaaaaagacttgaaaatgtatttaatttcatccccttccctgcctagaatggcaagcattgtgaattttttttctttttttctttttccccttctctctctttttcttttgacctttctctgactctaaaactttttggtgcccaatctgactttgtaattctgtttcttacttgcttattattggttttgttcttgtctaggcttgtttttataattttgaaacattgtttctccctccaggccagtataaaaaaaaaaacttgaagtatttttcaataatcccccaaaatgaatttcagaagtgtccttggatttaggggtttattttttaacaggattttatatgtgtttccagcactgattatggttataatccattaggccagaatcattttcagccattcataccctgtgattgtgtaattgaatcattagctctcagaagtttccccaaggcaagtggaaacagctcttaggcagtcaatgatttaggatctctgggagagtctgaaacttagaggttgaaggcacgtgatggctttaaaagcagctaccttattaatattaaaatgaagacaatcttccatatctctggcagtctccctgctgtttcatgtggttttaacatgccctgtagctgtaatcttttaatctgaaaacagtattcttcatgaataccttcgtttctccaactctagatgcagctagtaaaatacttaccacttggcagagtgactctggatggtataaattcatctctttccttgggtctgtgggaatggaactgagaccatttcctcaattcttggagagagactaagccaatgtggccatgggtgggaacttctgtccagaacctactgaagaaggtaattatctgaacgcacgggcctctcagagctttgaaatatctaacacgttttttaaaatggagttctaaggactaaggggggaaaatatgcttctgaaaatgatgatgaactactttcaaaaaggttgcatatttatgcgactgaaagattatttttgtagatgcaatgtgtgtgagcagtgcttcgagcatttaaaaatcacagtttactcctagggagatataaataaaaagaactctcttgtctccaccgagttttcatacatttgtgtttttcaagcttgggctgcctctagaaactgtttttatttattataaaattttgttctcctcgacatctgtagatgaaggaaacaataccagttctggtctctgaaacctccatgttctgttctccatttctgtccacctccttctaacacaaatagtgatatttaaaatgaggatatcatctgtggtgtctaaaataatcgtttttttttaaaccaggccagctcattaaaaatcaataaattttctttctttcaatatt
//
by
@meso_cacase at
DBCLS
This page is licensed under a
Creative Commons Attribution 4.0 International License (CC BY 4.0).
If you use GGRNA in your work, please cite:
Naito Y, Bono H. (2012)
GGRNA: an ultrafast, transcript-oriented search engine for genes and transcripts.
Nucleic Acids Res., 40, W592-W596.
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