- absent neurocranium / MGI
- abnormal exoccipital bone morphology / MGI
- cleft palate / MGI
- abnormal rib morphology / MGI
- rib bifurcation / MGI
- abnormal heart looping / MGI
- abnormal interventricular septum morphology / MGI
- abnormal craniofacial morphology / MGI
- abnormal mouth morphology / MGI
- abnormal maxilla morphology / MGI
- maxilla hypoplasia / MGI
- polydactyly / MGI
- oligodactyly / MGI
- absent spleen / MGI
- exencephaly / MGI
- abnormal lung morphology / MGI
- anophthalmia / MGI
- abnormal somite development / MGI
- abnormal digit morphology / MGI
- abnormal neural tube morphology / MGI
- hydrops fetalis / MGI
- abnormal tricuspid valve morphology / MGI
- persistent truncus arteriosis / MGI
- abnormal atrioventricular valve morphology / MGI
- curly tail / MGI
- omphalocele / MGI
- spina bifida / MGI
- absent tympanic ring / MGI
- left pulmonary isomerism / MGI
- kidney cysts / MGI
- abnormal neural tube closure / MGI
- abnormal aortic arch morphology / MGI
- right aortic arch / MGI
- absent alisphenoid bone / MGI
- absent palatine bone / MGI
- cervical vertebral fusion / MGI
- premaxilla hypoplasia / MGI
- abnormal heart ventricle morphology / MGI
- abnormal limb bud morphology / MGI
- abnormal costovertebral joint morphology / MGI
- heart hemorrhage / MGI
- exostosis / MGI
- palatal shelf hypoplasia / MGI
- atrioventricular septal defect / MGI
- fusion of atlas and occipital bones / MGI
- prenatal growth retardation / MGI
- embryonic lethality, complete penetrance / MGI
- embryonic lethality during organogenesis, complete penetrance / MGI
- lethality throughout fetal growth and development, complete penetrance / MGI
- lethality throughout fetal growth and development, incomplete penetrance / MGI
- abnormal hindlimb bud morphology / MGI
- abnormal primary cilium morphology / MGI
- absent facial bone / MGI
- facial bone hypoplasia / MGI
C57BL/6NTac-Ift140tm1a(KOMP)Wtsi/WtsiPh
Status | Available to order |
EMMA ID | EM:09158 |
International strain name | C57BL/6NTac-Ift140tm1a(KOMP)Wtsi/WtsiPh |
Alternative name | EPD0073_5_B02 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Ift140tm1a(KOMP)Wtsi |
Gene/Transgene symbol | Ift140 |
Disclaimer | Please note that for EUCOMM and KOMP-CSD mice supplied to the scientific community by INFRAFRONTIER/EMMA:
|
Information from provider
Provider | Wellcome Trust Sanger Institute |
Provider affiliation | Wellcome Trust Sanger Institute |
Genetic information | This mouse line originates from KOMP ES clone EPD0073_5_B02. 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 | Institute of Molecular Genetics, Prague, Czech Republic |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Leber congenital amaurosis / Orphanet_65
- Retinitis pigmentosa / Orphanet_791
- Jeune syndrome / Orphanet_474
- Saldino-Mainzer syndrome / Orphanet_140969
- Autosomal dominant polycystic kidney disease / Orphanet_730
MGI phenotypes (gene matching)
Information on how we integrate external resources can be found here
INFRAFRONTIER® and European Mouse Mutant Archive - EMMA® are registered trademarks at the European Union Intellectual Property Office (EUIPO).