Incidental Mutation 'IGL01081:Gm5114'
ID 51470
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm5114
Ensembl Gene ENSMUSG00000053742
Gene Name predicted gene 5114
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.076) question?
Stock # IGL01081
Quality Score
Status
Chromosome 7
Chromosomal Location 39056718-39062584 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) G to A at 39060071 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000103652 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000108017]
AlphaFold W4VSN8
Predicted Effect probably benign
Transcript: ENSMUST00000108017
SMART Domains Protein: ENSMUSP00000103652
Gene: ENSMUSG00000053742

DomainStartEndE-ValueType
Pfam:DUF4629 435 580 2.5e-65 PFAM
low complexity region 709 726 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 46 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acad8 A G 9: 26,901,890 (GRCm39) L158P probably damaging Het
Aco1 A G 4: 40,197,576 (GRCm39) Q860R probably benign Het
Actl11 A T 9: 107,806,181 (GRCm39) Q168L possibly damaging Het
Adam26b T C 8: 43,972,975 (GRCm39) I676V probably benign Het
Aldoart2 A C 12: 55,612,920 (GRCm39) I282L probably benign Het
Capns1 G T 7: 29,889,565 (GRCm39) S211R probably benign Het
Cps1 T C 1: 67,245,983 (GRCm39) V1158A probably damaging Het
Cryl1 C T 14: 57,523,821 (GRCm39) probably null Het
Cxcr5 A G 9: 44,425,607 (GRCm39) probably benign Het
Dcaf13 A G 15: 38,982,201 (GRCm39) K56E probably damaging Het
Dlx6 T G 6: 6,867,068 (GRCm39) S85A probably damaging Het
Dsg2 C T 18: 20,722,999 (GRCm39) probably benign Het
Dync1li1 T A 9: 114,549,665 (GRCm39) S412T possibly damaging Het
Ebf3 C A 7: 136,827,625 (GRCm39) probably benign Het
Fads3 T C 19: 10,030,366 (GRCm39) I168T probably benign Het
Gm10295 G A 7: 71,000,296 (GRCm39) P95S unknown Het
Gm43638 T C 5: 87,634,455 (GRCm39) T51A probably damaging Het
Gucy2c G A 6: 136,679,737 (GRCm39) T974M probably damaging Het
Ighv1-19-1 T C 12: 114,672,258 (GRCm39) probably benign Het
Kri1 A T 9: 21,191,723 (GRCm39) L173Q probably damaging Het
Lztfl1 T C 9: 123,531,338 (GRCm39) D210G probably benign Het
Morc2a T A 11: 3,638,149 (GRCm39) N958K probably damaging Het
Msl3l2 G A 10: 55,992,021 (GRCm39) A249T probably benign Het
Nlrp4a A G 7: 26,149,254 (GRCm39) E287G probably benign Het
Nlrp9a A T 7: 26,257,519 (GRCm39) N290I possibly damaging Het
Or2b28 T G 13: 21,531,185 (GRCm39) L29R probably damaging Het
Or4e2 A G 14: 52,688,484 (GRCm39) T205A probably benign Het
Or5al6 C T 2: 85,976,955 (GRCm39) G41D probably benign Het
Pcsk7 A G 9: 45,840,005 (GRCm39) D731G probably benign Het
Plppr5 T A 3: 117,480,298 (GRCm39) probably benign Het
Podxl T C 6: 31,505,639 (GRCm39) T135A possibly damaging Het
Pole T G 5: 110,485,106 (GRCm39) C407G possibly damaging Het
Prl C A 13: 27,249,024 (GRCm39) N224K possibly damaging Het
Prnp A T 2: 131,778,340 (GRCm39) probably benign Het
Proser2 A G 2: 6,105,149 (GRCm39) *472R probably null Het
Rhag T C 17: 41,122,178 (GRCm39) S38P possibly damaging Het
Rnf146 T C 10: 29,223,856 (GRCm39) D10G probably damaging Het
Rps3a1 T C 3: 86,049,085 (GRCm39) D29G probably benign Het
Sv2a A T 3: 96,097,012 (GRCm39) I446F probably benign Het
Tbc1d30 C A 10: 121,103,319 (GRCm39) R571L probably damaging Het
Tfrc T A 16: 32,443,646 (GRCm39) probably null Het
Tnfaip1 G A 11: 78,419,129 (GRCm39) P156S probably damaging Het
Vmn1r226 T C 17: 20,908,166 (GRCm39) S133P probably damaging Het
Wnt9b C T 11: 103,622,836 (GRCm39) R189K probably damaging Het
Ythdc2 A G 18: 44,983,726 (GRCm39) H564R probably benign Het
Zfp442 C A 2: 150,251,267 (GRCm39) E211* probably null Het
Other mutations in Gm5114
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01295:Gm5114 APN 7 39,057,241 (GRCm39) missense probably damaging 1.00
IGL01349:Gm5114 APN 7 39,058,531 (GRCm39) missense probably benign
IGL01633:Gm5114 APN 7 39,057,490 (GRCm39) missense probably benign
IGL01634:Gm5114 APN 7 39,058,071 (GRCm39) missense probably benign
IGL02072:Gm5114 APN 7 39,060,826 (GRCm39) missense probably benign 0.00
FR4304:Gm5114 UTSW 7 39,060,530 (GRCm39) missense probably benign 0.00
FR4304:Gm5114 UTSW 7 39,060,529 (GRCm39) missense probably benign
R0034:Gm5114 UTSW 7 39,058,282 (GRCm39) missense possibly damaging 0.83
R0127:Gm5114 UTSW 7 39,057,880 (GRCm39) missense probably benign 0.00
R0328:Gm5114 UTSW 7 39,057,885 (GRCm39) missense probably damaging 1.00
R0387:Gm5114 UTSW 7 39,058,233 (GRCm39) missense probably benign 0.15
R0693:Gm5114 UTSW 7 39,058,188 (GRCm39) missense probably benign 0.00
R1006:Gm5114 UTSW 7 39,058,510 (GRCm39) missense probably damaging 1.00
R2039:Gm5114 UTSW 7 39,058,612 (GRCm39) missense probably damaging 1.00
R3433:Gm5114 UTSW 7 39,058,621 (GRCm39) missense probably benign 0.02
R3834:Gm5114 UTSW 7 39,058,161 (GRCm39) missense possibly damaging 0.69
R4320:Gm5114 UTSW 7 39,057,051 (GRCm39) missense probably damaging 1.00
R5214:Gm5114 UTSW 7 39,057,792 (GRCm39) missense probably benign 0.19
R5443:Gm5114 UTSW 7 39,058,289 (GRCm39) missense probably benign 0.00
R5471:Gm5114 UTSW 7 39,058,534 (GRCm39) nonsense probably null
R5707:Gm5114 UTSW 7 39,060,700 (GRCm39) missense probably benign 0.01
R6129:Gm5114 UTSW 7 39,058,024 (GRCm39) missense possibly damaging 0.71
R6234:Gm5114 UTSW 7 39,058,768 (GRCm39) missense probably benign 0.19
R6326:Gm5114 UTSW 7 39,057,579 (GRCm39) missense probably benign
R6443:Gm5114 UTSW 7 39,057,141 (GRCm39) missense possibly damaging 0.91
R6530:Gm5114 UTSW 7 39,057,514 (GRCm39) missense probably damaging 1.00
R6743:Gm5114 UTSW 7 39,057,997 (GRCm39) missense probably benign 0.42
R6770:Gm5114 UTSW 7 39,057,967 (GRCm39) missense possibly damaging 0.94
R6885:Gm5114 UTSW 7 39,057,580 (GRCm39) missense probably benign 0.01
R6980:Gm5114 UTSW 7 39,058,624 (GRCm39) missense probably benign 0.01
R7100:Gm5114 UTSW 7 39,057,708 (GRCm39) missense possibly damaging 0.52
R7215:Gm5114 UTSW 7 39,060,795 (GRCm39) missense probably benign 0.02
R7254:Gm5114 UTSW 7 39,058,390 (GRCm39) missense probably benign 0.35
R7343:Gm5114 UTSW 7 39,058,180 (GRCm39) missense probably damaging 1.00
R7366:Gm5114 UTSW 7 39,058,768 (GRCm39) missense possibly damaging 0.69
R7474:Gm5114 UTSW 7 39,057,404 (GRCm39) missense probably benign 0.01
R7499:Gm5114 UTSW 7 39,058,489 (GRCm39) missense possibly damaging 0.55
R8022:Gm5114 UTSW 7 39,058,800 (GRCm39) missense probably benign
R8121:Gm5114 UTSW 7 39,057,552 (GRCm39) missense probably benign 0.15
R8201:Gm5114 UTSW 7 39,060,373 (GRCm39) missense probably damaging 0.98
R8212:Gm5114 UTSW 7 39,060,676 (GRCm39) missense probably benign 0.18
R8321:Gm5114 UTSW 7 39,060,273 (GRCm39) missense possibly damaging 0.85
R8725:Gm5114 UTSW 7 39,060,657 (GRCm39) missense probably benign 0.17
R8752:Gm5114 UTSW 7 39,057,927 (GRCm39) missense probably damaging 0.99
R8891:Gm5114 UTSW 7 39,057,718 (GRCm39) missense probably benign 0.05
R8934:Gm5114 UTSW 7 39,060,553 (GRCm39) missense probably benign 0.14
R8969:Gm5114 UTSW 7 39,058,732 (GRCm39) missense probably damaging 1.00
R9158:Gm5114 UTSW 7 39,060,486 (GRCm39) missense probably damaging 0.97
R9419:Gm5114 UTSW 7 39,057,540 (GRCm39) missense possibly damaging 0.92
R9453:Gm5114 UTSW 7 39,058,242 (GRCm39) missense probably damaging 0.99
Z1088:Gm5114 UTSW 7 39,057,871 (GRCm39) missense probably damaging 1.00
Z1177:Gm5114 UTSW 7 39,058,750 (GRCm39) missense probably benign 0.03
Posted On 2013-06-21