Incidental Mutation 'IGL02153:Foxb1'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Foxb1
Ensembl Gene ENSMUSG00000059246
Gene Nameforkhead box B1
SynonymsTWH, Mf3, C43, Foxb1b, Hfh-e5.1, Foxb1a, Fkh5
Accession Numbers
Is this an essential gene? Possibly essential (E-score: 0.621) question?
Stock #IGL02153
Quality Score
Chromosomal Location69757710-69760940 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to A at 69759703 bp
Amino Acid Change Methionine to Leucine at position 182 (M182L)
Ref Sequence ENSEMBL: ENSMUSP00000096197 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000071281]
Predicted Effect probably benign
Transcript: ENSMUST00000071281
AA Change: M182L

PolyPhen 2 Score 0.005 (Sensitivity: 0.97; Specificity: 0.74)
SMART Domains Protein: ENSMUSP00000096197
Gene: ENSMUSG00000059246
AA Change: M182L

FH 11 101 6.75e-62 SMART
low complexity region 102 113 N/A INTRINSIC
low complexity region 265 309 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000180488
Predicted Effect noncoding transcript
Transcript: ENSMUST00000180914
Coding Region Coverage
Validation Efficiency
MGI Phenotype PHENOTYPE: Targeted null mutant mice show variable embryonic lethality with neural tube defects or severe posterior reduction. Survivors have high postnatal mortality, reduced growth, motor weakness, midbrain abnormalities and females have a lactational defect. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 45 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
6820408C15Rik T C 2: 152,441,241 I275T probably benign Het
BC005561 A G 5: 104,521,083 E1157G probably benign Het
Chd9 A T 8: 90,956,494 K521* probably null Het
Csn3 A T 5: 87,930,097 N154I possibly damaging Het
Dock2 A G 11: 34,230,670 S1716P probably benign Het
Dock7 A T 4: 98,958,067 S18T probably benign Het
Esrra G A 19: 6,913,822 T190I probably benign Het
F13b T C 1: 139,516,377 I483T probably damaging Het
Fsip2 T C 2: 82,978,721 F1795L probably benign Het
Gkn2 G A 6: 87,373,408 probably null Het
Gm8439 G A 4: 120,609,590 A93T unknown Het
Ift22 T C 5: 136,911,696 S72P probably benign Het
Kcnmb2 A G 3: 32,178,844 K24E probably damaging Het
Kcnq3 C A 15: 66,025,191 V287L probably damaging Het
Lrriq1 T A 10: 103,170,479 M1262L probably benign Het
Mb21d2 A G 16: 28,929,488 I59T probably benign Het
Mogat2 A T 7: 99,223,554 M141K possibly damaging Het
Mtdh C T 15: 34,131,250 L409F possibly damaging Het
Muc5ac C T 7: 141,818,800 Q2724* probably null Het
Myo15 T G 11: 60,498,397 L2040R probably damaging Het
Nodal C T 10: 61,424,545 T325I probably damaging Het
Pappa A T 4: 65,297,437 T1194S probably damaging Het
Pcdhb13 A C 18: 37,443,685 D372A probably damaging Het
Phf14 T A 6: 11,934,016 N292K probably damaging Het
Pigr T A 1: 130,849,056 probably null Het
Plcb1 T C 2: 135,387,853 I1131T probably benign Het
Plch1 T A 3: 63,781,351 D132V probably damaging Het
Plxnb2 C A 15: 89,165,813 E502* probably null Het
Prox2 T C 12: 85,087,929 N526S probably damaging Het
Rdm1 T A 11: 101,628,454 probably null Het
Rxfp1 C T 3: 79,660,120 E308K probably benign Het
Sgca T C 11: 94,963,284 T120A probably damaging Het
Sh3tc1 G A 5: 35,703,352 R1054W probably damaging Het
Smarcal1 C T 1: 72,633,055 probably benign Het
Spata45 T A 1: 191,039,761 M60K probably benign Het
St8sia6 T C 2: 13,656,905 M372V probably damaging Het
Tas2r126 T G 6: 42,434,664 S44A probably benign Het
Tcea3 T A 4: 136,273,634 probably benign Het
Tln1 T C 4: 43,546,857 I840V possibly damaging Het
Ttn T C 2: 76,898,341 probably benign Het
Ubr4 T A 4: 139,460,160 Y3846* probably null Het
Usp47 G A 7: 112,104,049 D1171N probably benign Het
Vmn2r114 G A 17: 23,291,808 T566I probably benign Het
Wdr35 G A 12: 9,008,535 R575Q probably null Het
Xkr5 A T 8: 18,933,667 C454S probably benign Het
Other mutations in Foxb1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00234:Foxb1 APN 9 69760198 missense probably damaging 1.00
IGL01475:Foxb1 APN 9 69759268 utr 3 prime probably benign
PIT4514001:Foxb1 UTSW 9 69760221 missense probably damaging 1.00
R0570:Foxb1 UTSW 9 69759562 missense probably benign
R1618:Foxb1 UTSW 9 69760011 missense probably damaging 0.96
R1624:Foxb1 UTSW 9 69759316 missense probably benign 0.04
R1665:Foxb1 UTSW 9 69759822 missense probably damaging 0.97
R1913:Foxb1 UTSW 9 69760101 missense possibly damaging 0.51
R2243:Foxb1 UTSW 9 69759864 missense probably damaging 0.99
R4913:Foxb1 UTSW 9 69759577 missense probably benign
R4925:Foxb1 UTSW 9 69760155 missense probably damaging 1.00
R5630:Foxb1 UTSW 9 69760120 missense probably damaging 1.00
R5668:Foxb1 UTSW 9 69760246 start codon destroyed probably damaging 0.96
R7540:Foxb1 UTSW 9 69759859 nonsense probably null
Posted On2015-04-16