| Description: | transmembrane protein 237 [Source:MGI Symbol;Acc:MGI:2138365] |
| Synonyms: | AI853305, Gm972, Als2cr4 |
| Other ID(s): | ENSMUSG00000038079, MGI:2138365 |
| Protein Accession Numbers: | NP_001032901, XP_006496159, NP_001028621, NP_001348342, XP_006496160 |
| Statistics: |
∙ Please click the name of species for the protein accession number used in the alignment.
∙ A p letter used as a pointer to positions of post translational modifications in human.
∙ Protein domains illustrated above belong to Homo sapiens (Human).
∙ ClinVar stacked bar chart represents whole protein isoforms of the gene. Please, check the other protein isoforms of the gene below.
∙ If more than one transcripts below are active (with blue background color), it means all the active transcripts have the same sequence.
ENST00000286196
ENST00000409444
ENST00000409883
ENST00000432684
ENST00000444047
NP_001037850
NP_689601
| Pfam Domain filter_list | Domain Name filter_list | Description filter_list | Positions filter_list | Clan filter_list | Clan Name filter_list | Organism filter_list |
|---|---|---|---|---|---|---|
| NO RESULT FOUND | ||||||
| PF15383 | TMEM237 | Transmembrane protein 237 | 108-367 | Caenorhabditis elegans | ||
| Disease Name filter_list | Disease Category filter_list | DSI* filter_list | DPI** filter_list | ||
|---|---|---|---|---|---|
| Congenital ocular coloboma (disorder) | Eye Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; | 0.652 | 0.345 | ||
| Polydactyly | Musculoskeletal Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; | 0.652 | 0.345 | ||
| Familial aplasia of the vermis | Eye Diseases ; Male Urogenital Diseases ; Female Urogenital Diseases and Pregnancy Complications ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; | 0.652 | 0.345 | ||
| Cystic Kidney Diseases | Male Urogenital Diseases ; Female Urogenital Diseases and Pregnancy Complications ; | 0.652 | 0.345 | ||
| JOUBERT SYNDROME 4 (disorder) | Nervous System Diseases ; Eye Diseases ; Male Urogenital Diseases ; Female Urogenital Diseases and Pregnancy Complications ; | 0.652 | 0.345 | ||
| Arima syndrome | Nervous System Diseases ; Eye Diseases ; Male Urogenital Diseases ; Female Urogenital Diseases and Pregnancy Complications ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; | 0.652 | 0.345 | ||
| Intellectual Disability | Nervous System Diseases ; Pathological Conditions, Signs and Symptoms ; Behavior and Behavior Mechanisms ; Mental Disorders ; | 0.652 | 0.345 | ||
| Ciliopathies | Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; | 0.652 | 0.345 | ||
| NO RESULT FOUND | |||||