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loading...| Preferred Name |
SEC23 HOMOLOG B, COAT COMPLEX II COMPONENT |
| Synonyms |
SEC23B |
| ID |
http://purl.bioontology.org/ontology/OMIM/610512 |
| altLabel |
SEC23B SEC23, S. CEREVISIAE, HOMOLOG OF, B COWDEN SYNDROME 7 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE II |
| cui |
C4225179 C1419926 C1306589 |
| Gene Locus |
20p11.2 |
| Gene Symbol |
SEC23B HEMPAS CDAN2 CWS7 |
| Has allelic variant |
http://purl.bioontology.org/ontology/OMIM/610512.0003 http://purl.bioontology.org/ontology/OMIM/610512.0005 http://purl.bioontology.org/ontology/OMIM/610512.0004 http://purl.bioontology.org/ontology/OMIM/610512.0001 http://purl.bioontology.org/ontology/OMIM/610512.0006 http://purl.bioontology.org/ontology/OMIM/610512.0002 |
| MIMTYPEMEANING |
Gene with known sequence |
| notation |
610512 |
| OMIM Entry Type |
1 |
| OMIM MimType Value |
star |
| prefLabel |
SEC23 HOMOLOG B, COAT COMPLEX II COMPONENT |
| tui |
T028 T047 |
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| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://purl.bioontology.org/ontology/MESH/D000742 | Medical Subject Headings / 医学主题词表 | CUI |