C57BL/6N-Shhtm1a(EUCOMM)Wtsi/H
Status | Available to order |
EMMA ID | EM:07782 |
International strain name | C57BL/6N-Shhtm1a(EUCOMM)Wtsi/H |
Alternative name | EPD0339_3_A12 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Shhtm1a(EUCOMM)Wtsi, |
Gene/Transgene symbol | Shh |
Disclaimer | Please note that for EUCOMM and KOMP-CSD mice supplied to the scientific community by INFRAFRONTIER/EMMA:
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Information from provider
Provider | MRC, Medical Research Council |
Provider affiliation | Mammalian Genetics Unit, Mary Lyon Centre at MRC Harwell |
Genetic information | This mouse line originates from EUCOMM ES clone EPD0339_3_A12. For further details on the construction of this clone see the page at the IMPC portal. |
Phenotypic information | Potential phenotyping data in the IMPC portal |
References | None available |
Information from EMMA
Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Alobar holoprosencephaly / Orphanet_93925
- Triphalangeal thumb-polysyndactyly syndrome / Orphanet_2950
- Midline interhemispheric variant of holoprosencephaly / Orphanet_93926
- Colobomatous microphthalmia / Orphanet_98938
- Polydactyly of a triphalangeal thumb / Orphanet_93336
- Syndactyly type 4 / Orphanet_93405
- Hypoplastic tibiae-postaxial polydactyly syndrome / Orphanet_3332
- Lobar holoprosencephaly / Orphanet_93924
- Autosomal dominant preaxial polydactyly-upperback hypertrichosis syndrome / Orphanet_476119
- Microform holoprosencephaly / Orphanet_280200
- Septopreoptic holoprosencephaly / Orphanet_280195
- Radial hemimelia / Orphanet_93321
- Semilobar holoprosencephaly / Orphanet_220386
- Holoprosencephaly / Orphanet_2162
- Tibial hemimelia-polysyndactyly-triphalangeal thumb syndrome / Orphanet_988
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