Symbol
Name
ID
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Synonyms
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Hox-1.10
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Genetic Map
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Sequence Map
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Mammalian homology
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Sequences
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All sequences(17)
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Alleles and phenotypes
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All alleles(6) :
Targeted, knock-out(2)
Targeted, other(3)
Spontaneous(1)
| Homozygotes for a targeted null mutation exhibit agenesis of both the urinary bladder and the caudal portion of the Mullerian ducts, premature stenosis of the umbilical arteries, loss of the most anterior digit of all feet, and death around mid-gestation. |
Associated Human Diseases (1)
Alleles Annotated to Human Diseases (2)
Phenotype Images (1)
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Polymorphisms
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RFLP(1)
SNPs within 2kb(1 from dbSNP Build 128)
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Gene Ontology (GO) classifications
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Expression
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Literature Summary: (47 records)
Data Summary:
Assays (22)
Results (170)
Tissues (107)
Images (47)
Theiler Stages: 17,18,19,20,21,23,24,25,28
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Assay Type |
Assays |
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Results |
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Western blot |
3 |
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10 |
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RT-PCR |
8 |
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80 |
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In situ reporter (knock in) |
1 |
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24 |
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RNA in situ |
9 |
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55 |
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RNase protection |
1 |
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1 |
cDNA source data(3)
External Resources:
GEO
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Molecular reagents
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All nucleic(21)
Genomic(10)
cDNA(3)
Primer pair(4)
Other(4)
Antibodies(2)
Microarray probesets(2)
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Other database links
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Protein domains
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Graphical View
of Protein Domain Structure
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References
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(Earliest)
J:64253
Hummel KP et al.,
"Hd - hypodactyly"
Mouse News Lett 1966;34():31
(Latest)
J:153164
Cocquempot O et al.,
"Fork stalling and template switching as a mechanism for polyalanine tract expansion affecting the DYC mutant of HOXD13, a new murine model of synpolydactyly."
Genetics 2009 Sep;183(1):23-30
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All references(81)
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Other accession IDs
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MGD-MRK-10679, MGD-MRK-10816, MGD-MRK-10874, MGI:96061
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