Incidental Mutation 'R3801:Mb21d2'
ID273014
Institutional Source Beutler Lab
Gene Symbol Mb21d2
Ensembl Gene ENSMUSG00000051065
Gene NameMab-21 domain containing 2
Synonyms
MMRRC Submission 040760-MU
Accession Numbers
Is this an essential gene? Non essential (E-score: 0.000) question?
Stock #R3801 (G1)
Quality Score225
Status Not validated
Chromosome16
Chromosomal Location28826176-28929673 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to T at 28828003 bp
ZygosityHeterozygous
Amino Acid Change Aspartic acid to Glutamic Acid at position 406 (D406E)
Ref Sequence ENSEMBL: ENSMUSP00000097600 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000100023]
Predicted Effect possibly damaging
Transcript: ENSMUST00000100023
AA Change: D406E

PolyPhen 2 Score 0.946 (Sensitivity: 0.80; Specificity: 0.95)
SMART Domains Protein: ENSMUSP00000097600
Gene: ENSMUSG00000051065
AA Change: D406E

DomainStartEndE-ValueType
Mab-21 120 405 8.7e-75 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000232571
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.2%
  • 20x: 95.0%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 66 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700011L22Rik C T 8: 79,248,293 E54K probably benign Het
Als2 A C 1: 59,167,199 M1634R probably damaging Het
Ankfy1 T C 11: 72,749,420 S531P probably benign Het
Atp6v1e1 A G 6: 120,801,059 Y172H probably benign Het
Brd1 C T 15: 88,717,040 V464M probably damaging Het
Btaf1 A T 19: 36,986,548 T840S probably benign Het
Btaf1 A T 19: 36,988,973 H1047L probably benign Het
Cacnb2 A G 2: 14,824,263 D3G possibly damaging Het
Capn13 G A 17: 73,339,401 P339L probably benign Het
Cgrrf1 G T 14: 46,832,363 G30C probably damaging Het
Crnkl1 T C 2: 145,919,795 D614G probably benign Het
Cyp2c23 C T 19: 44,007,039 V430I probably benign Het
Dazl G A 17: 50,281,281 R289W probably benign Het
Dsg1b C T 18: 20,390,203 P96S probably damaging Het
Dusp14 A G 11: 84,048,709 S169P possibly damaging Het
Egfem1 A G 3: 29,151,926 D91G probably benign Het
Eif1 A G 11: 100,320,824 K95E probably damaging Het
Fap C T 2: 62,546,650 V191I probably benign Het
Flnc T C 6: 29,447,404 Y1069H probably damaging Het
Fndc7 T C 3: 108,869,148 T526A possibly damaging Het
Fras1 A T 5: 96,733,932 T2508S probably benign Het
Gast T C 11: 100,336,810 S73P probably damaging Het
Grap2 A G 15: 80,623,746 T4A possibly damaging Het
Grm8 T G 6: 28,125,636 N164H possibly damaging Het
Hyal5 A T 6: 24,876,524 H132L probably benign Het
Iqcm C A 8: 75,669,393 T188K possibly damaging Het
Kank4 A G 4: 98,780,133 S26P probably damaging Het
Lipo1 C T 19: 33,784,857 C80Y probably damaging Het
Lrrk2 A G 15: 91,737,111 R963G probably benign Het
Lrtm2 G A 6: 119,317,483 T229I probably damaging Het
Meikin T A 11: 54,399,871 probably null Het
Mybl1 A T 1: 9,673,214 F538I probably damaging Het
Nectin2 T C 7: 19,717,636 D491G probably benign Het
Nf1 A G 11: 79,559,521 D511G probably null Het
Nid2 T C 14: 19,809,997 C1328R probably damaging Het
Nlrp1a T A 11: 71,122,703 M574L probably benign Het
Nrap C T 19: 56,321,779 D1595N probably damaging Het
Nrg3 G A 14: 38,376,434 P496S probably damaging Het
Olfr1287 A T 2: 111,449,565 I142F probably benign Het
Pak3 G A X: 143,709,731 V87I probably damaging Het
Phf8 T C X: 151,572,576 S512P possibly damaging Het
Phkb G T 8: 85,922,229 E225* probably null Het
Plaa T C 4: 94,569,888 D615G probably damaging Het
Prdm12 A G 2: 31,651,947 K223E probably damaging Het
Prkd1 C A 12: 50,383,422 R634L possibly damaging Het
Rassf3 T A 10: 121,414,366 I181F possibly damaging Het
Samd8 G A 14: 21,775,065 V30M probably damaging Het
Sema4f A T 6: 82,918,627 H308Q possibly damaging Het
Skint4 G T 4: 112,118,181 V113L probably damaging Het
Slc16a10 G C 10: 40,056,624 H314D possibly damaging Het
Slpi A G 2: 164,356,238 L12P probably damaging Het
Smco1 A G 16: 32,273,898 Y129C probably benign Het
Spag17 A G 3: 100,053,853 K985R possibly damaging Het
Stc1 T C 14: 69,038,475 I239T probably benign Het
Suclg2 A T 6: 95,497,668 I372N probably damaging Het
Tmed4 C A 11: 6,274,233 V80F probably damaging Het
Tnpo2 T A 8: 85,055,171 probably null Het
Top1 A G 2: 160,702,768 H268R probably damaging Het
Triobp A T 15: 78,973,700 Q1167L probably benign Het
Txndc16 G A 14: 45,151,352 P536L possibly damaging Het
Usp13 C T 3: 32,881,508 A360V possibly damaging Het
Vhl G A 6: 113,629,462 V147I probably benign Het
Vldlr A T 19: 27,217,621 T3S probably damaging Het
Vps54 T A 11: 21,268,832 D130E probably benign Het
Zfp808 T A 13: 62,172,083 H375Q probably damaging Het
Zfp87 A T 13: 67,521,215 N37K probably damaging Het
Other mutations in Mb21d2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01958:Mb21d2 APN 16 28827743 utr 3 prime probably benign
IGL02153:Mb21d2 APN 16 28929488 missense probably benign 0.31
IGL02678:Mb21d2 APN 16 28828049 missense probably benign 0.00
R0570:Mb21d2 UTSW 16 28929572 missense probably benign 0.01
R0571:Mb21d2 UTSW 16 28929572 missense probably benign 0.01
R0630:Mb21d2 UTSW 16 28929572 missense probably benign 0.01
R1728:Mb21d2 UTSW 16 28828421 missense probably benign 0.00
R1729:Mb21d2 UTSW 16 28828421 missense probably benign 0.00
R1866:Mb21d2 UTSW 16 28828515 missense possibly damaging 0.67
R6403:Mb21d2 UTSW 16 28828517 missense possibly damaging 0.53
R7384:Mb21d2 UTSW 16 28828912 missense probably benign
R7464:Mb21d2 UTSW 16 28929546 missense possibly damaging 0.85
R8030:Mb21d2 UTSW 16 28827803 missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TCATCGGGGTTAATAAAGACCG -3'
(R):5'- TGCCAGCTACTTGGCTCAAG -3'

Sequencing Primer
(F):5'- AGATGGACTTCCCTGGATTCTCAG -3'
(R):5'- GAAGACTATGCAGCCCACTTTTTG -3'
Posted On2015-03-25