IMPC phenotypes (gene matching)
B6;129P2-Tmem67tm1Dgen/H
| Status | Available to order |
| EMMA ID | EM:02370 |
| Citation information | RRID:IMSR_EM:02370 Research Resource Identifiers (RRID) are persistent unique ID numbers assigned to help researchers cite key resources (e.g. antibodies, model organisms and software projects) in the biomedical literature to improve transparency and reproducibility in research. See https://www.rrids.org/ for more information. |
| 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
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