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MGI:Hoxd13

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Contents

Species (Taxon ID) Mus musculus (house mouse) (taxon:10090)
Gene Name(s) Hoxd13 ( synonyms: Hox-4.8, spdh )
Protein Name(s) homeobox D13,
External Links
MGI MGI:96205

Annotations

Qualifier GO ID GO term name Reference Evidence Code with/from Aspect Notes Status
GO:0001501

skeletal system development

MGI:MGI:63627
PMID:8106170[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857871

P

From MGI

GO:0001501

skeletal system development

MGI:MGI:80097
PMID:8620844[2]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2151805

P

From MGI

GO:0003677

DNA binding

MGI:MGI:3829797
PMID:19168674[3]

IDA: Inferred from Direct Assay

F

From MGI

GO:0003682

chromatin binding

MGI:MGI:3629247
PMID:16672333[4]

IDA: Inferred from Direct Assay

F

From MGI

GO:0003700

sequence-specific DNA binding transcription factor activity

MGI:MGI:3620476
PMID:16314414[5]

IDA: Inferred from Direct Assay

F

From MGI

GO:0005634

nucleus

MGI:MGI:3527920
PMID:15617687[6]

IDA: Inferred from Direct Assay

C

From MGI

GO:0006351

transcription, DNA-dependent

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0804

P

From MGI

GO:0006355

regulation of transcription, DNA-dependent

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0805

P

From MGI

GO:0006355

regulation of transcription, DNA-dependent

MGI:MGI:2152098

IEA: Inferred from Electronic Annotation

InterPro:IPR017970
InterPro:IPR001356

P

From MGI

GO:0007275

multicellular organismal development

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0217

P

From MGI

GO:0007389

pattern specification process

MGI:MGI:2177382
PMID:11850178[7]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857397

P

From MGI

GO:0007389

pattern specification process

MGI:MGI:63627
PMID:8106170[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857871

P

From MGI

GO:0007389

pattern specification process

MGI:MGI:83869
PMID:8900279[8]

IGI: Inferred from Genetic Interaction

MGI:MGI:96203
MGI:MGI:96204

P

From MGI

GO:0009952

anterior/posterior pattern specification

MGI:MGI:63627
PMID:8106170[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857871

P

From MGI

GO:0022612

gland morphogenesis

MGI:MGI:86772
PMID:9097018[9]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857871

P

From MGI

GO:0030326

embryonic limb morphogenesis

MGI:MGI:2177382
PMID:11850178[7]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857397

P

From MGI

GO:0030539

male genitalia development

MGI:MGI:63627
PMID:8106170[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857871

P

From MGI

GO:0035108

limb morphogenesis

MGI:MGI:2150573
PMID:11543619[10]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857397

P

From MGI

GO:0035108

limb morphogenesis

MGI:MGI:84613
PMID:8978698[11]

IGI: Inferred from Genetic Interaction

MGI:MGI:95462

P

From MGI

GO:0042127

regulation of cell proliferation

MGI:MGI:2177382
PMID:11850178[7]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857397

P

From MGI

GO:0042733

embryonic digit morphogenesis

MGI:MGI:1097490
PMID:9342042[12]

IGI: Inferred from Genetic Interaction

MGI:MGI:1918115

P

From MGI

GO:0042733

embryonic digit morphogenesis

MGI:MGI:3765370
PMID:17714700[13]

IGI: Inferred from Genetic Interaction

MGI:MGI:96204
MGI:MGI:96203
MGI:MGI:95729

P

From MGI

GO:0042733

embryonic digit morphogenesis

MGI:MGI:83869
PMID:8900279[8]

IGI: Inferred from Genetic Interaction

MGI:MGI:96203
MGI:MGI:96204

P

From MGI

GO:0043565

sequence-specific DNA binding

MGI:MGI:2152098

IEA: Inferred from Electronic Annotation

InterPro:IPR017970
InterPro:IPR001356

F

From MGI

GO:0045944

positive regulation of transcription from RNA polymerase II promoter

MGI:MGI:3620476
PMID:16314414[5]

IDA: Inferred from Direct Assay

P

From MGI

GO:0045944

positive regulation of transcription from RNA polymerase II promoter

MGI:MGI:3629247
PMID:16672333[4]

IDA: Inferred from Direct Assay

P

From MGI

GO:0045944

positive regulation of transcription from RNA polymerase II promoter

MGI:MGI:3829797
PMID:19168674[3]

IDA: Inferred from Direct Assay

P

From MGI

GO:0048619

embryonic hindgut morphogenesis

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

NCBI:NP_001099356

P

From MGI

GO:0060527

prostate epithelial cord arborization involved in prostate glandular acinus morphogenesis

MGI:MGI:2653645
PMID:12668621[14]

IGI: Inferred from Genetic Interaction

MGI:MGI:107730

P

From MGI

GO:0060571

morphogenesis of an epithelial fold

MGI:MGI:86772
PMID:9097018[9]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857871

P

From MGI

GO:0060602

branch elongation of an epithelium

MGI:MGI:86772
PMID:9097018[9]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857871

P

From MGI

GO:0060687

regulation of branching involved in prostate gland morphogenesis

MGI:MGI:86772
PMID:9097018[9]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857871

P

From MGI


Notes

References

See Help:References for how to manage references in GONUTS.
  1. 1.0 1.1 1.2 1.3 Dollé P et al. (1993) Disruption of the Hoxd-13 gene induces localized heterochrony leading to mice with neotenic limbs. Cell 75: 431-41 PubMed GONUTS page
  2. Davis AP & Capecchi MR (1996) A mutational analysis of the 5' HoxD genes: dissection of genetic interactions during limb development in the mouse. Development 122: 1175-85 PubMed GONUTS page
  3. 3.0 3.1 Kawakami Y et al. (2009) Sall genes regulate region-specific morphogenesis in the mouse limb by modulating Hox activities. Development 136: 585-94 PubMed GONUTS page
  4. 4.0 4.1 Capellini TD et al. (2006) Pbx1/Pbx2 requirement for distal limb patterning is mediated by the hierarchical control of Hox gene spatial distribution and Shh expression. Development 133: 2263-73 PubMed GONUTS page
  5. 5.0 5.1 Salsi V & Zappavigna V (2006) Hoxd13 and Hoxa13 directly control the expression of the EphA7 Ephrin tyrosine kinase receptor in developing limbs. J Biol Chem 281: 1992-9 PubMed GONUTS page
  6. Williams TM et al. (2005) Range of HOX/TALE superclass associations and protein domain requirements for HOXA13:MEIS interaction. Dev Biol 277: 457-71 PubMed GONUTS page
  7. 7.0 7.1 7.2 Albrecht AN et al. (2002) The synpolydactyly homolog (spdh) mutation in the mouse -- a defect in patterning and growth of limb cartilage elements. Mech Dev 112: 53-67 PubMed GONUTS page
  8. 8.0 8.1 Zákány J & Duboule D (1996) Synpolydactyly in mice with a targeted deficiency in the HoxD complex. Nature 384: 69-71 PubMed GONUTS page
  9. 9.0 9.1 9.2 9.3 Podlasek CA et al. (1997) Male accessory sex organ morphogenesis is altered by loss of function of Hoxd-13. Dev Dyn 208: 454-65 PubMed GONUTS page
  10. Bruneau S et al. (2001) The mouse Hoxd13(spdh) mutation, a polyalanine expansion similar to human type II synpolydactyly (SPD), disrupts the function but not the expression of other Hoxd genes. Dev Biol 237: 345-53 PubMed GONUTS page
  11. Hérault Y et al. (1996) Function of the Evx-2 gene in the morphogenesis of vertebrate limbs. EMBO J 15: 6727-38 PubMed GONUTS page
  12. Hérault Y et al. (1997) Ulnaless (Ul), a regulatory mutation inducing both loss-of-function and gain-of-function of posterior Hoxd genes. Development 124: 3493-500 PubMed GONUTS page
  13. Sheth R et al. (2007) Hoxd and Gli3 interactions modulate digit number in the amniote limb. Dev Biol 310: 430-41 PubMed GONUTS page
  14. Economides KD & Capecchi MR (2003) Hoxb13 is required for normal differentiation and secretory function of the ventral prostate. Development 130: 2061-9 PubMed GONUTS page
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