Incidental Mutation 'IGL01347:Gbp11'
ID 75127
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gbp11
Ensembl Gene ENSMUSG00000092021
Gene Name guanylate binding protein 11
Synonyms Gm7141
Accession Numbers
Essential gene? Probably non essential (E-score: 0.050) question?
Stock # IGL01347
Quality Score
Status
Chromosome 5
Chromosomal Location 105470908-105494338 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) G to A at 105479194 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000132552 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000100960] [ENSMUST00000171587]
AlphaFold A9YVJ5
Predicted Effect probably benign
Transcript: ENSMUST00000100960
SMART Domains Protein: ENSMUSP00000098520
Gene: ENSMUSG00000092021

DomainStartEndE-ValueType
Pfam:GBP 16 279 1.5e-122 PFAM
Pfam:GBP_C 281 574 3.4e-114 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000171587
SMART Domains Protein: ENSMUSP00000132552
Gene: ENSMUSG00000092021

DomainStartEndE-ValueType
Pfam:GBP 16 279 4.9e-117 PFAM
Pfam:GBP_C 281 442 2.7e-75 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 55 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aoc1l2 A T 6: 48,909,477 (GRCm39) Y574F probably benign Het
Apc C T 18: 34,450,723 (GRCm39) P2506S probably damaging Het
Bdp1 T A 13: 100,206,711 (GRCm39) K610N possibly damaging Het
Bri3bp T G 5: 125,531,581 (GRCm39) C176G probably damaging Het
Carnmt1 A G 19: 18,668,818 (GRCm39) I248V probably benign Het
Ccdc88b A G 19: 6,822,454 (GRCm39) L1475P probably damaging Het
Cfap100 C T 6: 90,383,103 (GRCm39) V511M possibly damaging Het
Chchd3 T C 6: 32,780,838 (GRCm39) N78S probably benign Het
Cnnm4 G A 1: 36,537,115 (GRCm39) E480K possibly damaging Het
Cyp2d34 T A 15: 82,500,978 (GRCm39) I385F possibly damaging Het
D930048N14Rik T A 11: 51,545,615 (GRCm39) probably benign Het
Dgkg A T 16: 22,419,340 (GRCm39) D53E probably benign Het
Dlx3 T A 11: 95,011,359 (GRCm39) L71H probably damaging Het
Egln2 A C 7: 26,859,717 (GRCm39) V332G probably null Het
Entpd2 A G 2: 25,288,746 (GRCm39) Q250R probably benign Het
Epyc A G 10: 97,510,593 (GRCm39) D132G probably damaging Het
Fxr2 A G 11: 69,543,114 (GRCm39) D637G probably benign Het
Gapvd1 A G 2: 34,596,708 (GRCm39) probably null Het
Gm17175 A T 14: 51,808,307 (GRCm39) C162S probably damaging Het
Gm5499 C T 17: 87,386,339 (GRCm39) noncoding transcript Het
Gps1 T C 11: 120,679,086 (GRCm39) V378A probably benign Het
Grik1 C T 16: 87,754,481 (GRCm39) R368Q probably benign Het
Gsap A G 5: 21,431,318 (GRCm39) E214G probably benign Het
H2bc13 A G 13: 21,900,064 (GRCm39) Y84H probably damaging Het
Jdp2 T C 12: 85,655,020 (GRCm39) S28P probably benign Het
Kif26b T C 1: 178,698,240 (GRCm39) F577S probably damaging Het
Kl G A 5: 150,904,130 (GRCm39) G294D probably damaging Het
Lgsn T A 1: 31,243,041 (GRCm39) D374E probably damaging Het
Lman1 T C 18: 66,124,681 (GRCm39) I353V probably damaging Het
Lmna T C 3: 88,392,270 (GRCm39) H374R probably benign Het
Lrrc57 A G 2: 120,439,286 (GRCm39) S31P probably benign Het
Lum T A 10: 97,404,547 (GRCm39) N147K probably damaging Het
Or6n2 T C 1: 173,897,632 (GRCm39) I256T probably benign Het
Or7a41 A G 10: 78,871,445 (GRCm39) T272A probably benign Het
P4ha3 C A 7: 99,955,140 (GRCm39) L332I probably damaging Het
Pelp1 A G 11: 70,286,505 (GRCm39) I541T probably damaging Het
Pja2 A C 17: 64,620,023 (GRCm39) S2A probably benign Het
Rhbdl3 T C 11: 80,244,268 (GRCm39) L325P probably damaging Het
Robo2 T C 16: 74,149,744 (GRCm39) D28G probably damaging Het
Rpa1 A G 11: 75,198,111 (GRCm39) Y470H probably damaging Het
Rtn3 T C 19: 7,434,645 (GRCm39) N430S probably benign Het
Scg2 T A 1: 79,414,538 (GRCm39) I62L probably benign Het
Scn5a T A 9: 119,391,507 (GRCm39) K62* probably null Het
Sec23ip T C 7: 128,364,129 (GRCm39) V469A probably benign Het
Shank1 A G 7: 43,991,544 (GRCm39) T663A unknown Het
Slco1a7 A T 6: 141,700,192 (GRCm39) Y113* probably null Het
Stab2 G T 10: 86,737,567 (GRCm39) probably null Het
Tmcc3 T C 10: 94,418,147 (GRCm39) L305P probably damaging Het
Tmem145 A G 7: 25,014,260 (GRCm39) N458S probably damaging Het
Tpr G A 1: 150,302,738 (GRCm39) R1412Q probably damaging Het
Wdr1 A T 5: 38,703,058 (GRCm39) F173I possibly damaging Het
Wdr17 C T 8: 55,104,380 (GRCm39) V898I probably benign Het
Wdr64 A T 1: 175,547,899 (GRCm39) L145F probably benign Het
Wnt10b A G 15: 98,674,826 (GRCm39) probably benign Het
Zfyve26 A T 12: 79,298,957 (GRCm39) probably null Het
Other mutations in Gbp11
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01329:Gbp11 APN 5 105,475,482 (GRCm39) critical splice acceptor site probably null
IGL01762:Gbp11 APN 5 105,475,473 (GRCm39) missense probably benign
IGL02157:Gbp11 APN 5 105,475,374 (GRCm39) missense possibly damaging 0.95
Quilt UTSW 5 105,473,374 (GRCm39) missense probably damaging 1.00
Tilted UTSW 5 105,478,919 (GRCm39) missense probably damaging 1.00
R0550:Gbp11 UTSW 5 105,491,616 (GRCm39) missense probably benign 0.28
R0647:Gbp11 UTSW 5 105,478,830 (GRCm39) missense possibly damaging 0.93
R1530:Gbp11 UTSW 5 105,475,355 (GRCm39) missense probably damaging 0.99
R1612:Gbp11 UTSW 5 105,474,462 (GRCm39) missense possibly damaging 0.72
R1677:Gbp11 UTSW 5 105,475,277 (GRCm39) missense probably damaging 1.00
R1738:Gbp11 UTSW 5 105,474,510 (GRCm39) missense probably benign 0.02
R2063:Gbp11 UTSW 5 105,476,450 (GRCm39) nonsense probably null
R2869:Gbp11 UTSW 5 105,478,866 (GRCm39) missense probably benign 0.00
R2869:Gbp11 UTSW 5 105,478,866 (GRCm39) missense probably benign 0.00
R2870:Gbp11 UTSW 5 105,478,866 (GRCm39) missense probably benign 0.00
R2870:Gbp11 UTSW 5 105,478,866 (GRCm39) missense probably benign 0.00
R2873:Gbp11 UTSW 5 105,478,866 (GRCm39) missense probably benign 0.00
R3915:Gbp11 UTSW 5 105,478,978 (GRCm39) missense probably damaging 1.00
R4854:Gbp11 UTSW 5 105,473,374 (GRCm39) missense probably damaging 1.00
R5140:Gbp11 UTSW 5 105,478,919 (GRCm39) missense probably damaging 1.00
R5534:Gbp11 UTSW 5 105,478,904 (GRCm39) missense probably damaging 1.00
R6091:Gbp11 UTSW 5 105,479,254 (GRCm39) missense possibly damaging 0.95
R6336:Gbp11 UTSW 5 105,473,355 (GRCm39)
R6351:Gbp11 UTSW 5 105,475,464 (GRCm39) missense probably benign 0.07
R6956:Gbp11 UTSW 5 105,476,241 (GRCm39) critical splice donor site probably null
R7371:Gbp11 UTSW 5 105,489,971 (GRCm39) missense probably benign 0.06
R7393:Gbp11 UTSW 5 105,475,443 (GRCm39) missense possibly damaging 0.60
R7410:Gbp11 UTSW 5 105,491,774 (GRCm39) missense probably damaging 1.00
R7443:Gbp11 UTSW 5 105,478,816 (GRCm39) critical splice donor site probably null
R7898:Gbp11 UTSW 5 105,472,798 (GRCm39) missense probably benign 0.00
R8465:Gbp11 UTSW 5 105,472,928 (GRCm39) missense probably benign 0.00
R8467:Gbp11 UTSW 5 105,475,457 (GRCm39) missense probably damaging 1.00
R8672:Gbp11 UTSW 5 105,491,675 (GRCm39) missense probably damaging 1.00
R8858:Gbp11 UTSW 5 105,473,392 (GRCm39) nonsense probably null
R8960:Gbp11 UTSW 5 105,479,251 (GRCm39) missense probably damaging 0.98
R9097:Gbp11 UTSW 5 105,474,347 (GRCm39) makesense probably null
R9232:Gbp11 UTSW 5 105,476,290 (GRCm39) missense possibly damaging 0.76
R9380:Gbp11 UTSW 5 105,475,202 (GRCm39) missense probably benign 0.00
R9400:Gbp11 UTSW 5 105,478,841 (GRCm39) missense probably damaging 1.00
R9438:Gbp11 UTSW 5 105,474,471 (GRCm39) nonsense probably null
Posted On 2013-10-07