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) |
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 | ![]() |
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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) |
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last database update 10/07/2025 MGI 6.24 |
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