Incidental Mutation 'R0076:Gm11437'
ID16503
Institutional Source Beutler Lab
Gene Symbol Gm11437
Ensembl Gene ENSMUSG00000051452
Gene Namepredicted gene 11437
Synonyms
MMRRC Submission 038363-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.128) question?
Stock #R0076 (G1)
Quality Score
Status Validated
Chromosome11
Chromosomal Location84148351-84167476 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to C at 84148636 bp
ZygosityHeterozygous
Amino Acid Change Threonine to Alanine at position 288 (T288A)
Ref Sequence ENSEMBL: ENSMUSP00000056084 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000050771] [ENSMUST00000133811]
Predicted Effect possibly damaging
Transcript: ENSMUST00000050771
AA Change: T288A

PolyPhen 2 Score 0.907 (Sensitivity: 0.81; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000056084
Gene: ENSMUSG00000051452
AA Change: T288A

DomainStartEndE-ValueType
Pfam:DUF4711 1 226 7.4e-102 PFAM
low complexity region 227 238 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000133811
SMART Domains Protein: ENSMUSP00000116174
Gene: ENSMUSG00000020532

DomainStartEndE-ValueType
signal peptide 1 22 N/A INTRINSIC
PDB:2YL2|B 115 157 2e-21 PDB
Meta Mutation Damage Score 0.1099 question?
Coding Region Coverage
  • 1x: 89.9%
  • 3x: 87.5%
  • 10x: 81.6%
  • 20x: 72.8%
Validation Efficiency 92% (83/90)
Allele List at MGI
Other mutations in this stock
Total: 58 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca15 T G 7: 120,373,685 probably benign Het
Acpp A G 9: 104,324,218 probably benign Het
Ada T A 2: 163,727,603 probably benign Het
Ankrd17 T A 5: 90,244,406 K1693* probably null Het
Arhgef38 T A 3: 133,160,746 H210L possibly damaging Het
Car10 G A 11: 93,490,597 E129K possibly damaging Het
Cask A G X: 13,678,274 probably benign Het
Cd19 T C 7: 126,410,862 D406G probably damaging Het
Cd93 T C 2: 148,442,136 D430G probably benign Het
Cds1 T C 5: 101,817,840 probably benign Het
Cerkl A T 2: 79,343,289 S259T possibly damaging Het
Cog8 T C 8: 107,054,133 I164M possibly damaging Het
Col4a1 G A 8: 11,218,713 P1009L probably damaging Het
Col9a1 G A 1: 24,237,497 probably null Het
Dcc G A 18: 71,321,046 Q1241* probably null Het
Dock3 A C 9: 106,911,486 probably benign Het
Dus1l A T 11: 120,792,808 probably benign Het
Dvl2 G A 11: 70,008,100 E438K probably damaging Het
Eif3g A G 9: 20,897,753 F85S probably damaging Het
Fam234b A G 6: 135,227,226 M456V probably benign Het
Fbxo47 G A 11: 97,857,655 probably benign Het
Fyb2 A G 4: 104,945,464 T188A possibly damaging Het
Gm5546 T A 3: 104,353,132 noncoding transcript Het
Gmfb C A 14: 46,817,455 A11S probably benign Het
Gpat4 G A 8: 23,190,705 probably benign Het
Ifitm6 T A 7: 141,016,007 R124S possibly damaging Het
Il17rd T A 14: 27,094,854 L172Q probably damaging Het
Il4 A T 11: 53,613,914 L13Q probably damaging Het
Kif2b A G 11: 91,575,909 M516T probably damaging Het
Kmt2a A G 9: 44,830,059 probably benign Het
Maats1 G A 16: 38,302,684 Q661* probably null Het
Mark1-ps1 T A 17: 53,947,877 noncoding transcript Het
Mndal G T 1: 173,874,447 C96* probably null Het
Mroh1 T C 15: 76,451,140 S1365P probably benign Het
Mrpl12 A G 11: 120,485,442 probably benign Het
Mthfsd C A 8: 121,098,739 V270F probably benign Het
Nbas T A 12: 13,324,336 V555D probably damaging Het
Pcdhb16 T C 18: 37,478,359 V124A probably damaging Het
Pla2g10 T A 16: 13,715,518 Y131F possibly damaging Het
Plec T C 15: 76,191,414 probably benign Het
Polr2b T A 5: 77,326,561 V415E possibly damaging Het
Pou6f1 G A 15: 100,587,836 Q106* probably null Het
Ptprd T C 4: 75,947,039 probably benign Het
Rad54b G A 4: 11,609,480 probably benign Het
Rspo1 G A 4: 124,991,397 R22Q probably benign Het
Scn7a A G 2: 66,714,037 V370A probably benign Het
Sec1 A G 7: 45,678,891 V244A probably damaging Het
Serac1 A G 17: 6,064,937 probably benign Het
Slco2b1 A T 7: 99,685,501 Y254* probably null Het
Steap3 G A 1: 120,227,730 R500C probably damaging Het
Stk10 A G 11: 32,603,722 T580A probably benign Het
Tpo C T 12: 30,104,023 G228R probably damaging Het
Tpx2 T C 2: 152,893,683 F744L probably damaging Het
Ube3b G T 5: 114,408,217 probably null Het
Vmn2r84 A G 10: 130,394,193 S17P probably damaging Het
Vps13d A T 4: 145,164,694 probably benign Het
Zfp532 T A 18: 65,685,627 S851R probably benign Het
Zfp623 G A 15: 75,947,209 E5K probably benign Het
Other mutations in Gm11437
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00959:Gm11437 APN 11 84148622 intron probably benign
IGL01354:Gm11437 APN 11 84167318 intron probably benign
IGL02051:Gm11437 APN 11 84152766 missense probably benign 0.00
IGL03184:Gm11437 APN 11 84156264 intron probably benign
R0076:Gm11437 UTSW 11 84148636 missense possibly damaging 0.91
R1241:Gm11437 UTSW 11 84164628 missense possibly damaging 0.93
R2135:Gm11437 UTSW 11 84153812 missense probably damaging 0.97
R4065:Gm11437 UTSW 11 84164511 missense probably benign 0.13
R4067:Gm11437 UTSW 11 84164511 missense probably benign 0.13
R5356:Gm11437 UTSW 11 84152687 missense possibly damaging 0.90
R6571:Gm11437 UTSW 11 84156212 missense probably benign 0.13
R6594:Gm11437 UTSW 11 84164560 missense probably null 0.03
R7173:Gm11437 UTSW 11 84164548 missense probably benign 0.39
R7368:Gm11437 UTSW 11 84167472 intron probably benign
X0026:Gm11437 UTSW 11 84165327 missense possibly damaging 0.92
X0028:Gm11437 UTSW 11 84156100 critical splice donor site probably null
Posted On2013-01-20