Incidental Mutation 'IGL01298:Gm11444'
ID 73213
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm11444
Ensembl Gene ENSMUSG00000069785
Gene Name predicted gene 11444
Accession Numbers
Essential gene? Probably non essential (E-score: 0.128) question?
Stock # IGL01298
Quality Score
Chromosome 11
Chromosomal Location 85846790-85850333 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) C to A at 85848094 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Tyrosine at position 58 (D58Y)
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect unknown
Transcript: ENSMUST00000146433
AA Change: D58Y
SMART Domains Protein: ENSMUSP00000116236
Gene: ENSMUSG00000069785
AA Change: D58Y

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 (GRCm38) W263C probably damaging Het
Agtpbp1 G A 13: 59,504,226 (GRCm38) H424Y possibly damaging Het
Angpt2 T G 8: 18,710,528 (GRCm38) N186T probably benign Het
Ank2 A G 3: 126,959,720 (GRCm38) V304A possibly damaging Het
Atg3 T C 16: 45,171,673 (GRCm38) M88T possibly damaging Het
Baz1a G T 12: 54,954,809 (GRCm38) P142Q probably damaging Het
Btbd1 G T 7: 81,794,307 (GRCm38) probably null Het
Cacnb3 T C 15: 98,639,853 (GRCm38) Y70H probably damaging Het
Cd4 G A 6: 124,879,378 (GRCm38) T50I probably benign Het
Cyp7a1 A T 4: 6,275,517 (GRCm38) W19R probably damaging Het
Dock10 T A 1: 80,531,245 (GRCm38) I1610F probably damaging Het
Gm7168 A T 17: 13,949,858 (GRCm38) T496S probably benign Het
Gpc5 A G 14: 115,399,188 (GRCm38) S428G probably benign Het
Haus8 T C 8: 71,253,113 (GRCm38) E309G probably damaging Het
Ice1 A G 13: 70,604,904 (GRCm38) L1021P possibly damaging Het
Krtap14 A T 16: 88,825,727 (GRCm38) H121Q probably benign Het
Nwd1 T C 8: 72,662,331 (GRCm38) V170A probably benign Het
Or1j10 T A 2: 36,377,448 (GRCm38) M224K probably benign Het
Or6c3b T C 10: 129,692,029 (GRCm38) Y4C probably damaging Het
Or8g24 G A 9: 39,078,724 (GRCm38) T7I possibly damaging Het
Pfpl T C 19: 12,428,673 (GRCm38) M96T possibly damaging Het
Pramel5 A G 4: 144,271,162 (GRCm38) probably benign Het
Proc T C 18: 32,123,552 (GRCm38) N354S probably benign Het
Prss40 T G 1: 34,560,766 (GRCm38) I47L probably benign Het
Tmprss7 T C 16: 45,664,175 (GRCm38) R541G probably benign Het
Togaram2 T C 17: 71,716,513 (GRCm38) V788A possibly damaging Het
Trbv19 T C 6: 41,178,904 (GRCm38) Y70H probably damaging Het
Ttk C T 9: 83,865,142 (GRCm38) S678L probably benign Het
Vmn2r85 T C 10: 130,418,821 (GRCm38) T665A probably benign Het
Other mutations in Gm11444
AlleleSourceChrCoordTypePredicted EffectPPH Score
R1958:Gm11444 UTSW 11 85,848,173 (GRCm38) splice site probably benign
R5199:Gm11444 UTSW 11 85,848,019 (GRCm38) missense unknown
R6283:Gm11444 UTSW 11 85,846,791 (GRCm38) splice site probably null
R7088:Gm11444 UTSW 11 85,847,036 (GRCm38) missense
R7579:Gm11444 UTSW 11 85,850,243 (GRCm38) missense unknown
R8378:Gm11444 UTSW 11 85,850,249 (GRCm38) missense
R8708:Gm11444 UTSW 11 85,846,897 (GRCm38) missense
R9803:Gm11444 UTSW 11 85,846,873 (GRCm38) nonsense probably null
Posted On 2013-10-07