Incidental Mutation 'IGL00591:Gm1110'
ID 332735
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm1110
Ensembl Gene ENSMUSG00000079644
Gene Name predicted gene 1110
Synonyms LOC382064
Accession Numbers
Essential gene? Probably non essential (E-score: 0.069) question?
Stock # IGL00591
Quality Score
Status
Chromosome 9
Chromosomal Location 26790863-26834407 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) C to A at 26792170 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamic Acid to Stop codon at position 617 (E617*)
Ref Sequence ENSEMBL: ENSMUSP00000110916 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000115261]
AlphaFold F6Y113
Predicted Effect probably null
Transcript: ENSMUST00000115261
AA Change: E617*
SMART Domains Protein: ENSMUSP00000110916
Gene: ENSMUSG00000079644
AA Change: E617*

DomainStartEndE-ValueType
signal peptide 1 24 N/A INTRINSIC
Pfam:Glyco_hydro_35 55 368 2e-93 PFAM
Pfam:Glyco_hydro_42 70 229 1e-12 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000214847
Predicted Effect noncoding transcript
Transcript: ENSMUST00000217197
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 15 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Csmd3 C T 15: 47,868,279 (GRCm39) C747Y probably damaging Het
Elk3 T C 10: 93,120,689 (GRCm39) N50S probably damaging Het
Esyt2 T A 12: 116,327,064 (GRCm39) L544H probably damaging Het
Faap20 A G 4: 155,335,067 (GRCm39) N56S probably benign Het
Fnd3c2 T A X: 105,279,597 (GRCm39) Y845F probably damaging Het
Gpbp1 T C 13: 111,577,284 (GRCm39) D202G probably damaging Het
Hecw1 C T 13: 14,440,565 (GRCm39) G1242R possibly damaging Het
Iqce A T 5: 140,663,883 (GRCm39) L132* probably null Het
Mthfd1 C A 12: 76,347,213 (GRCm39) P550Q possibly damaging Het
Pabpc6 C T 17: 9,887,427 (GRCm39) V375I possibly damaging Het
Sh2d4b G T 14: 40,594,490 (GRCm39) F163L probably benign Het
Sp140 G A 1: 85,549,393 (GRCm39) R208K probably benign Het
Vps13d T C 4: 144,917,129 (GRCm39) T12A possibly damaging Het
Xkr8 A T 4: 132,455,357 (GRCm39) Y339N probably damaging Het
Zfp108 A G 7: 23,960,911 (GRCm39) K501E possibly damaging Het
Other mutations in Gm1110
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01089:Gm1110 APN 9 26,793,156 (GRCm39) missense probably benign
IGL01631:Gm1110 APN 9 26,809,212 (GRCm39) critical splice donor site probably null
IGL02008:Gm1110 APN 9 26,794,526 (GRCm39) missense probably benign 0.09
IGL02331:Gm1110 APN 9 26,824,583 (GRCm39) critical splice donor site probably null
IGL02335:Gm1110 APN 9 26,793,059 (GRCm39) missense probably benign 0.00
IGL02550:Gm1110 APN 9 26,793,130 (GRCm39) missense probably benign 0.09
IGL02614:Gm1110 APN 9 26,832,010 (GRCm39) missense probably benign 0.11
IGL03409:Gm1110 APN 9 26,807,916 (GRCm39) missense probably benign 0.21
PIT4458001:Gm1110 UTSW 9 26,792,124 (GRCm39) missense probably benign 0.00
R0189:Gm1110 UTSW 9 26,794,514 (GRCm39) missense probably null 0.99
R0271:Gm1110 UTSW 9 26,831,962 (GRCm39) missense probably damaging 1.00
R1034:Gm1110 UTSW 9 26,832,646 (GRCm39) missense probably damaging 1.00
R1229:Gm1110 UTSW 9 26,793,102 (GRCm39) missense probably benign
R1355:Gm1110 UTSW 9 26,795,057 (GRCm39) missense probably benign 0.01
R1566:Gm1110 UTSW 9 26,792,166 (GRCm39) missense probably damaging 1.00
R1574:Gm1110 UTSW 9 26,792,422 (GRCm39) splice site probably benign
R1916:Gm1110 UTSW 9 26,800,934 (GRCm39) missense probably damaging 1.00
R2011:Gm1110 UTSW 9 26,805,554 (GRCm39) missense probably benign 0.01
R2214:Gm1110 UTSW 9 26,813,786 (GRCm39) missense probably benign 0.37
R2567:Gm1110 UTSW 9 26,831,992 (GRCm39) missense probably benign
R2967:Gm1110 UTSW 9 26,792,339 (GRCm39) missense probably benign 0.05
R4271:Gm1110 UTSW 9 26,806,944 (GRCm39) critical splice donor site probably null
R4683:Gm1110 UTSW 9 26,831,890 (GRCm39) missense probably damaging 0.99
R4945:Gm1110 UTSW 9 26,831,891 (GRCm39) missense possibly damaging 0.46
R5015:Gm1110 UTSW 9 26,793,162 (GRCm39) missense probably benign 0.01
R5089:Gm1110 UTSW 9 26,793,683 (GRCm39) missense probably damaging 0.96
R5225:Gm1110 UTSW 9 26,813,774 (GRCm39) missense probably damaging 1.00
R5239:Gm1110 UTSW 9 26,804,866 (GRCm39) missense probably benign 0.00
R5395:Gm1110 UTSW 9 26,800,928 (GRCm39) missense probably benign
R5783:Gm1110 UTSW 9 26,793,632 (GRCm39) missense probably benign
R6045:Gm1110 UTSW 9 26,794,505 (GRCm39) critical splice donor site probably null
R6245:Gm1110 UTSW 9 26,832,043 (GRCm39) missense probably benign 0.04
R6357:Gm1110 UTSW 9 26,825,424 (GRCm39) splice site probably null
R6863:Gm1110 UTSW 9 26,792,360 (GRCm39) missense probably damaging 1.00
R7336:Gm1110 UTSW 9 26,825,653 (GRCm39) missense probably damaging 0.99
R7454:Gm1110 UTSW 9 26,831,945 (GRCm39) missense probably benign
R7555:Gm1110 UTSW 9 26,804,924 (GRCm39) missense probably benign 0.05
R7579:Gm1110 UTSW 9 26,795,122 (GRCm39) missense possibly damaging 0.93
R7990:Gm1110 UTSW 9 26,792,137 (GRCm39) missense possibly damaging 0.66
R8062:Gm1110 UTSW 9 26,793,117 (GRCm39) missense probably damaging 0.99
R8108:Gm1110 UTSW 9 26,831,957 (GRCm39) missense probably damaging 1.00
R8323:Gm1110 UTSW 9 26,813,719 (GRCm39) critical splice donor site probably null
R8354:Gm1110 UTSW 9 26,794,577 (GRCm39) missense probably benign 0.00
R8354:Gm1110 UTSW 9 26,794,576 (GRCm39) missense probably benign 0.01
R8454:Gm1110 UTSW 9 26,794,577 (GRCm39) missense probably benign 0.00
R8454:Gm1110 UTSW 9 26,794,576 (GRCm39) missense probably benign 0.01
R8494:Gm1110 UTSW 9 26,792,154 (GRCm39) missense probably benign 0.04
R8978:Gm1110 UTSW 9 26,807,095 (GRCm39) splice site probably benign
R9321:Gm1110 UTSW 9 26,831,891 (GRCm39) missense probably benign 0.00
R9513:Gm1110 UTSW 9 26,795,083 (GRCm39) missense possibly damaging 0.95
R9545:Gm1110 UTSW 9 26,800,977 (GRCm39) missense probably benign 0.00
R9758:Gm1110 UTSW 9 26,800,894 (GRCm39) nonsense probably null
RF002:Gm1110 UTSW 9 26,831,936 (GRCm39) missense probably damaging 1.00
X0063:Gm1110 UTSW 9 26,805,576 (GRCm39) missense probably benign 0.01
Z1088:Gm1110 UTSW 9 26,824,606 (GRCm39) missense probably benign 0.01
Posted On 2015-08-05