|
Symbol Name ID |
Man1b1
mannosidase, alpha, class 1B, member 1 MGI:2684954 |
|
Reference
|
J:371576 Zang L, Han Y, Zhang Q, Luo S, Hu Z, Xia K, Ahmed A, Tian Q, Bi-Allelic Loss-of-Function Variant in MAN1B1 Cause Rafiq Syndrome and Developmental Delay. Int J Mol Sci. 2025 Aug 14;26(16) |
Indicates gene expression was analyzed but not necessarily detected.
| Age | E12.5 | E14.5 | E16.5 | E18.5 | P |
| Immunohistochemistry (section) | |||||
| In situ RNA (section) | |||||
| Immunohistochemistry (whole mount) | |||||
| In situ RNA (whole mount) | |||||
| In situ reporter (knock in) | |||||
| Northern blot | |||||
| Western blot | |||||
| RT-PCR | ![]() |
![]() |
![]() |
![]() |
![]() |
| cDNA clones | |||||
| RNase protection | |||||
| Nuclease S1 | |||||
| Primer Extension |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
||
|
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 12/30/2025 MGI 6.24 |
|
|
|
||