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Symbol Name ID |
Tmem67
transmembrane protein 67 MGI:1923928 |
| Darker colors indicate more annotations |
| Human Phenotypes | Biparietal narrowing |
Retrognathia |
Dandy-Walker malformation |
Macrocephaly |
Encephalocele |
Occipital encephalocele |
Short neck |
Fifth finger distal phalanx clinodactyly |
Postaxial hand polydactyly |
Postaxial foot polydactyly |
Polydactyly |
Postaxial polydactyly |
Brachydactyly |
Syndactyly |
Finger syndactyly |
Joint hypermobility |
Scoliosis |
| Disease(s) Associated with TMEM67 | |||||||||||||||||
| Bardet-Biedl syndrome | |||||||||||||||||
| Bardet-Biedl syndrome 14 | |||||||||||||||||
| COACH syndrome | |||||||||||||||||
| Meckel syndrome 3 |
| Mouse Phenotypes | abnormal posterior cranial fossa morphology |
mandible hypoplasia |
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| Availability | Mouse Genotype | ||
| Tmem67tm1Dgen/Tmem67tm1Dgen | |||
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 04/23/2024 MGI 6.23 |
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