Approved symbol | NIPBL |
---|---|
Approved name | NIPBL cohesin loading factor |
HGCN ID | HGNC:28862 |
Previous symbols | |
Inheritance | |
OMIM | 608667 |
Chromosome | 5p13.2 |
Panel(s) |
NGS Cornelia de Lange syndrome NGS Intellectual disability NGS Mendeliome NGS Microcephaly NGS Skeletal Dysplasia NIPBL Analysis |