B6;129P2-Tmem67tm1Dgen/H
Status | Available to order |
EMMA ID | EM:02370 |
International strain name | B6;129P2-Tmem67tm1Dgen/H |
Alternative name | DELTAGEN_T4738 |
Strain type | Targeted Mutant Strains : Knock-out |
Allele/Transgene symbol | Tmem67tm1Dgen |
Gene/Transgene symbol | Tmem67 |
Information from provider
Provider | Deltagen Inc. |
Provider affiliation | Deltagen Inc. |
Phenotypic information | No phenotype data was provided |
References | None available |
Information from EMMA
Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
MGI allele-associated human disease models
Orphanet associated rare diseases, based on orthologous gene matching
- Joubert syndrome with hepatic defect / Orphanet_1454
- Senior-Boichis syndrome / Orphanet_84081
- Joubert syndrome / Orphanet_475
- Meckel syndrome / Orphanet_564
- RHYNS syndrome / Orphanet_140976
IMPC phenotypes (gene matching)
MGI phenotypes (allele matching)
- abnormal cell morphology / MGI
- microcephaly / MGI
- mandible hypoplasia / MGI
- abnormal corpus callosum morphology / MGI
- dilated fourth ventricle / MGI
- small cerebellum / MGI
- cerebellum vermis hypoplasia / MGI
- exencephaly / MGI
- abnormal roof plate morphology / MGI
- incomplete rostral neuropore closure / MGI
- abnormal dorsal-ventral axis patterning / MGI
- postnatal growth retardation / MGI
- perinatal lethality / MGI
- postnatal lethality / MGI
- abnormal neural tube morphology / MGI
- abnormal forebrain development / MGI
- abnormal nervous system morphology / MGI
- kidney cysts / MGI
- abnormal midbrain development / MGI
- abnormal hepatobiliary system development / MGI
- absent embryonic cilia / MGI
- abnormal embryonic neuroepithelium morphology / MGI
- holoprosencephaly / MGI
- limbs/digits/tail phenotype / MGI
- cellular phenotype / MGI
- abnormal basal ganglion morphology / MGI
- abnormal tegmentum morphology / MGI
- absent anterior commissure / MGI
- enlarged hippocampus / MGI
- abnormal neural tube ventricular layer morphology / MGI
- meningomyelocele / MGI
- abnormal brain ependyma motile cilium morphology / MGI
- abnormal renal tubule epithelial cell primary cilium morphology / MGI
- postnatal lethality, incomplete penetrance / MGI
- neonatal lethality, incomplete penetrance / MGI
- abnormal neural fold morphology / MGI
- decreased forebrain size / MGI
- increased forebrain size / MGI
- encephalomeningocele / MGI
- decreased hindbrain size / MGI
- abnormal posterior cranial fossa morphology / MGI
MGI phenotypes (gene matching)
- double outlet right ventricle / MGI
- abnormal cell morphology / MGI
- microcephaly / MGI
- mandible hypoplasia / MGI
- abnormal corpus callosum morphology / MGI
- dilated fourth ventricle / MGI
- small cerebellum / MGI
- cerebellum vermis hypoplasia / MGI
- exencephaly / MGI
- abnormal roof plate morphology / MGI
- incomplete rostral neuropore closure / MGI
- abnormal dorsal-ventral axis patterning / MGI
- postnatal growth retardation / MGI
- perinatal lethality / MGI
- postnatal lethality / MGI
- abnormal neural tube morphology / MGI
- abnormal forebrain development / MGI
- abnormal nervous system morphology / MGI
- kidney cysts / MGI
- abnormal midbrain development / MGI
- abnormal hepatobiliary system development / MGI
- absent embryonic cilia / MGI
- heterotaxia / MGI
- interrupted aortic arch / MGI
- abnormal embryonic neuroepithelium morphology / MGI
- holoprosencephaly / MGI
- limbs/digits/tail phenotype / MGI
- cellular phenotype / MGI
- abnormal basal ganglion morphology / MGI
- abnormal tegmentum morphology / MGI
- absent anterior commissure / MGI
- enlarged hippocampus / MGI
- polycystic kidney / MGI
- abnormal neural tube ventricular layer morphology / MGI
- meningomyelocele / MGI
- atrioventricular septal defect / MGI
- heart right ventricle hypoplasia / MGI
- right-sided stomach / MGI
- abnormal brain ependyma motile cilium morphology / MGI
- abnormal renal tubule epithelial cell primary cilium morphology / MGI
- postnatal lethality, incomplete penetrance / MGI
- neonatal lethality, incomplete penetrance / MGI
- situs inversus with levocardia / MGI
- abnormal neural fold morphology / MGI
- decreased forebrain size / MGI
- increased forebrain size / MGI
- encephalomeningocele / MGI
- decreased hindbrain size / MGI
- abnormal posterior cranial fossa morphology / MGI
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