Incidental Mutation 'IGL01298:Gm11444'
ID73213
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm11444
Ensembl Gene ENSMUSG00000069785
Gene Namepredicted gene 11444
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.131) question?
Stock #IGL01298
Quality Score
Status
Chromosome11
Chromosomal Location85846790-85850333 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) C to A at 85848094 bp
ZygosityHeterozygous
Amino Acid Change Aspartic acid to Tyrosine at position 58 (D58Y)
Gene Model predicted gene model for transcript(s):
Predicted Effect unknown
Transcript: ENSMUST00000146433
AA Change: D58Y
SMART Domains Protein: ENSMUSP00000116236
Gene: ENSMUSG00000069785
AA Change: D58Y

DomainStartEndE-ValueType
low complexity region 130 143 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 29 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adora2a G T 10: 75,333,492 W263C probably damaging Het
Agtpbp1 G A 13: 59,504,226 H424Y possibly damaging Het
Angpt2 T G 8: 18,710,528 N186T probably benign Het
Ank2 A G 3: 126,959,720 V304A possibly damaging Het
Atg3 T C 16: 45,171,673 M88T possibly damaging Het
Baz1a G T 12: 54,954,809 P142Q probably damaging Het
Btbd1 G T 7: 81,794,307 probably null Het
Cacnb3 T C 15: 98,639,853 Y70H probably damaging Het
Cd4 G A 6: 124,879,378 T50I probably benign Het
Cyp7a1 A T 4: 6,275,517 W19R probably damaging Het
Dock10 T A 1: 80,531,245 I1610F probably damaging Het
Gm7168 A T 17: 13,949,858 T496S probably benign Het
Gpc5 A G 14: 115,399,188 S428G probably benign Het
Haus8 T C 8: 71,253,113 E309G probably damaging Het
Ice1 A G 13: 70,604,904 L1021P possibly damaging Het
Krtap14 A T 16: 88,825,727 H121Q probably benign Het
Nwd1 T C 8: 72,662,331 V170A probably benign Het
Olfr338 T A 2: 36,377,448 M224K probably benign Het
Olfr803 T C 10: 129,692,029 Y4C probably damaging Het
Olfr938 G A 9: 39,078,724 T7I possibly damaging Het
Pfpl T C 19: 12,428,673 M96T possibly damaging Het
Pramel5 A G 4: 144,271,162 probably benign Het
Proc T C 18: 32,123,552 N354S probably benign Het
Prss40 T G 1: 34,560,766 I47L probably benign Het
Tmprss7 T C 16: 45,664,175 R541G probably benign Het
Togaram2 T C 17: 71,716,513 V788A possibly damaging Het
Trbv19 T C 6: 41,178,904 Y70H probably damaging Het
Ttk C T 9: 83,865,142 S678L probably benign Het
Vmn2r85 T C 10: 130,418,821 T665A probably benign Het
Other mutations in Gm11444
AlleleSourceChrCoordTypePredicted EffectPPH Score
R1958:Gm11444 UTSW 11 85848173 splice site probably benign
R5199:Gm11444 UTSW 11 85848019 missense unknown
R6283:Gm11444 UTSW 11 85846791 splice site probably null
R7088:Gm11444 UTSW 11 85847036 missense
R7579:Gm11444 UTSW 11 85850243 missense unknown
R8378:Gm11444 UTSW 11 85850249 missense
R8708:Gm11444 UTSW 11 85846897 missense
Posted On2013-10-07