Symbol Name ID |
Mdfic
MyoD family inhibitor domain containing MGI:104611 |
Reference
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J:326462 Byrne AB, Brouillard P, Sutton DL, Kazenwadel J, Montazaribarforoushi S, Secker GA, Oszmiana A, Babic M, Betterman KL, Brautigan PJ, White M, Piltz SG, Thomas PQ, Hahn CN, Rath M, Felbor U, Korenke GC, Smith CL, Wood KH, Sheppard SE, Adams DM, Kariminejad A, Helaers R, Boon LM, Revencu N, Moore L, Barnett C, Haan E, Arts P, Vikkula M, Scott HS, Harvey NL, Pathogenic variants in MDFIC cause recessive central conducting lymphatic anomaly with lymphedema. Sci Transl Med. 2022 Mar 2;14(634):eabm4869 |
Age | E16.5 | E17.5 | E18.5 |
Immunohistochemistry (section) | ![]() |
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In situ RNA (section) | ![]() |
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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) |
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last database update 08/02/2024 MGI 6.24 |
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