C57BL/6N-Fgf8tm1a(KOMP)Wtsi/H
Status | Available to order |
EMMA ID | EM:07495 |
International strain name | C57BL/6N-Fgf8tm1a(KOMP)Wtsi/H |
Alternative name | EPD0383_6_A10 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Fgf8tm1a(KOMP)Wtsi |
Gene/Transgene symbol | Fgf8 |
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 | Mary Lyon Centre at MRC Harwell |
Genetic information | This mouse line originates from KOMP ES clone EPD0383_6_A10. 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
- Normosmic congenital hypogonadotropic hypogonadism / Orphanet_432
- Kallmann syndrome / Orphanet_478
- Alobar holoprosencephaly / Orphanet_93925
- Midline interhemispheric variant of holoprosencephaly / Orphanet_93926
- Microform holoprosencephaly / Orphanet_280200
- Septopreoptic holoprosencephaly / Orphanet_280195
- Semilobar holoprosencephaly / Orphanet_220386
- Lobar holoprosencephaly / Orphanet_93924
- Holoprosencephaly / Orphanet_2162
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- abnormal heart development / MGI
- abnormal heart tube morphology / MGI
- abnormal craniofacial morphology / MGI
- syndactyly / MGI
- abnormal pituitary gland morphology / MGI
- abnormal hypothalamus morphology / MGI
- absent cerebellum / MGI
- abnormal midbrain morphology / MGI
- open neural tube / MGI
- small embryonic telencephalon / MGI
- decreased body weight / MGI
- cyanosis / MGI
- abnormal ectoderm development / MGI
- abnormal mesoderm development / MGI
- absent mesoderm / MGI
- abnormal somite development / MGI
- decreased embryo size / MGI
- abnormal allantois morphology / MGI
- edema / MGI
- prenatal lethality / MGI
- postnatal lethality / MGI
- abnormal developmental patterning / MGI
- abnormal cardiovascular system morphology / MGI
- no abnormal phenotype detected / MGI
- abnormal primitive streak morphology / MGI
- abnormal chorion morphology / MGI
- abnormal pharyngeal arch morphology / MGI
- decreased neuron apoptosis / MGI
- absent olfactory bulb / MGI
- nervous system phenotype / MGI
- abnormal embryonic epiblast morphology / MGI
- abnormal craniofacial development / MGI
- fetal growth retardation / MGI
- abnormal neural fold formation / MGI
- abnormal amnion morphology / MGI
- abnormal rostral-caudal axis patterning / MGI
- absent somites / MGI
- absent inferior colliculus / MGI
- absent primitive node / MGI
- abnormal neural crest cell apoptosis / MGI
- abnormal truncus arteriosus septation / MGI
- mortality/aging / MGI
- postnatal lethality, incomplete penetrance / MGI
- neonatal lethality, complete penetrance / MGI
- embryonic lethality during organogenesis, complete penetrance / MGI
- prenatal lethality, incomplete penetrance / MGI
- absent heart / MGI
- abnormal cardiogenic mesoderm morphology / MGI
- abnormal primitive streak elongation / MGI
- third pharyngeal arch artery hypoplasia / MGI
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