|Institutional Source||Beutler Lab|
|Gene Name||mitogen-activated protein kinase kinase kinase 20|
|Synonyms||MLTKalpha, Zak, MLTKbeta, B230120H23Rik|
|Is this an essential gene?||Non essential (E-score: 0.000)|
|Stock #||R2655 (G1)|
|Chromosomal Location||72285637-72442610 bp(+) (GRCm38)|
|Type of Mutation||missense|
|DNA Base Change (assembly)||C to A at 72433420 bp|
|Amino Acid Change||Threonine to Lysine at position 471 (T471K)|
|Ref Sequence||ENSEMBL: ENSMUSP00000088334 (fasta)|
|Gene Model||predicted gene model for transcript(s): [ENSMUST00000090824]|
|Predicted Effect||probably damaging
AA Change: T471K
PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
AA Change: T471K
|Meta Mutation Damage Score||0.0632|
|Coding Region Coverage||
|Validation Efficiency||100% (39/39)|
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene is a member of the MAPKKK family of signal transduction molecules and encodes a protein with an N-terminal kinase catalytic domain, followed by a leucine zipper motif and a sterile-alpha motif (SAM). This magnesium-binding protein forms homodimers and is located in the cytoplasm. The protein mediates gamma radiation signaling leading to cell cycle arrest and activity of this protein plays a role in cell cycle checkpoint regulation in cells. The protein also has pro-apoptotic activity. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit complete lethality at E9.5 with growth retardation. Mice homozygous for an allele lacking the SAM domain exhibit low penetrant unilateral complex hindlimb duplication phenotype. [provided by MGI curators]
|Allele List at MGI|
|Other mutations in this stock||
|Other mutations in Map3k20||
(F):5'- ATAAGGCGCTCCCACATGAC -3'
(R):5'- AATCCTTCTAACACTGAAGAGCTC -3'
(F):5'- CTCCCACATGACTTCATTTAGAATAC -3'
(R):5'- GCTTGAGACCGAGCTGATG -3'