Incidental Mutation 'IGL01584:Gm15446'
ID 91495
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm15446
Ensembl Gene ENSMUSG00000090015
Gene Name predicted gene 15446
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.053) question?
Stock # IGL01584
Quality Score
Status
Chromosome 5
Chromosomal Location 110081429-110089576 bp(+) (GRCm39)
Type of Mutation makesense
DNA Base Change (assembly) T to A at 110088668 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Stop codon to Lysine at position 64 (*64K)
Ref Sequence ENSEMBL: ENSMUSP00000127438 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000112544] [ENSMUST00000170826]
AlphaFold D3Z5Y8
Predicted Effect probably null
Transcript: ENSMUST00000112544
SMART Domains Protein: ENSMUSP00000108163
Gene: ENSMUSG00000090015

DomainStartEndE-ValueType
KRAB 4 60 1.74e-14 SMART
ZnF_C2H2 103 125 1.1e-2 SMART
ZnF_C2H2 131 153 1.67e-2 SMART
ZnF_C2H2 159 181 4.87e-4 SMART
ZnF_C2H2 187 209 3.39e-3 SMART
ZnF_C2H2 215 237 1.76e-1 SMART
ZnF_C2H2 243 265 1.3e-4 SMART
ZnF_C2H2 271 293 1.1e-2 SMART
ZnF_C2H2 299 321 2.27e-4 SMART
ZnF_C2H2 327 349 6.99e-5 SMART
ZnF_C2H2 355 377 5.21e-4 SMART
ZnF_C2H2 383 405 9.73e-4 SMART
ZnF_C2H2 411 433 3.39e-3 SMART
ZnF_C2H2 439 461 1.58e-3 SMART
ZnF_C2H2 467 489 5.14e-3 SMART
ZnF_C2H2 495 517 2.61e-4 SMART
ZnF_C2H2 523 545 3.21e-4 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000146564
Predicted Effect probably null
Transcript: ENSMUST00000170826
AA Change: *64K
SMART Domains Protein: ENSMUSP00000127438
Gene: ENSMUSG00000090015
AA Change: *64K

DomainStartEndE-ValueType
KRAB 3 59 1.74e-14 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 37 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca5 A G 11: 110,195,749 (GRCm39) V570A probably damaging Het
Abcb1a T C 5: 8,748,637 (GRCm39) S323P possibly damaging Het
Adcy8 C T 15: 64,687,170 (GRCm39) D445N probably damaging Het
Cdc14a A T 3: 116,186,474 (GRCm39) Y102* probably null Het
Cubn A G 2: 13,313,472 (GRCm39) probably benign Het
Dcaf7 T C 11: 105,944,653 (GRCm39) S279P probably benign Het
Dock10 T C 1: 80,511,567 (GRCm39) Q1514R probably damaging Het
Dtx2 G A 5: 136,055,420 (GRCm39) S369N possibly damaging Het
Dusp11 A G 6: 85,930,376 (GRCm39) F136S probably damaging Het
Fbxo32 T C 15: 58,047,632 (GRCm39) D227G probably damaging Het
Flg2 T A 3: 93,120,773 (GRCm39) V1215E unknown Het
Flg2 A T 3: 93,122,777 (GRCm39) D1649V unknown Het
Gabbr2 T C 4: 46,674,524 (GRCm39) K821R probably damaging Het
Gga2 T C 7: 121,590,761 (GRCm39) T516A probably benign Het
Gm5900 T C 7: 104,599,361 (GRCm39) noncoding transcript Het
Il17rb A G 14: 29,725,637 (GRCm39) F121S probably damaging Het
Ip6k3 C A 17: 27,370,034 (GRCm39) R128L probably benign Het
Kmt2d A T 15: 98,754,250 (GRCm39) probably benign Het
Lrrn4 A G 2: 132,719,996 (GRCm39) L268P probably damaging Het
Mthfd1l C A 10: 3,966,738 (GRCm39) S332R probably damaging Het
Or12d12 C T 17: 37,610,629 (GRCm39) R228H probably benign Het
Or5t17 G A 2: 86,832,495 (GRCm39) V61I probably benign Het
Pdzd2 T C 15: 12,592,569 (GRCm39) E25G probably damaging Het
Prima1 A T 12: 103,169,047 (GRCm39) probably null Het
Rbm26 A G 14: 105,368,968 (GRCm39) V737A probably damaging Het
Ryr2 C T 13: 11,616,644 (GRCm39) probably null Het
Sema5b G T 16: 35,465,793 (GRCm39) C114F probably damaging Het
Spata31f1e A C 4: 42,794,014 (GRCm39) S39R probably damaging Het
Speg T C 1: 75,407,581 (GRCm39) V3196A probably damaging Het
Svs3b T C 2: 164,097,943 (GRCm39) Y126C probably benign Het
Tmem171 T C 13: 98,828,683 (GRCm39) probably null Het
Tnrc6b T A 15: 80,763,883 (GRCm39) W462R probably benign Het
Trdmt1 T C 2: 13,524,739 (GRCm39) R239G probably benign Het
Usp5 A T 6: 124,796,350 (GRCm39) V583E probably damaging Het
Utrn A G 10: 12,602,111 (GRCm39) V639A probably benign Het
Vmn1r206 T C 13: 22,804,964 (GRCm39) K81R probably damaging Het
Vwa3a A G 7: 120,383,197 (GRCm39) I599M probably benign Het
Other mutations in Gm15446
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0278:Gm15446 UTSW 5 110,091,281 (GRCm39) missense probably benign 0.14
R0606:Gm15446 UTSW 5 110,091,347 (GRCm39) missense probably benign
R1608:Gm15446 UTSW 5 110,090,323 (GRCm39) missense probably damaging 1.00
R1874:Gm15446 UTSW 5 110,090,419 (GRCm39) missense probably damaging 0.99
R1892:Gm15446 UTSW 5 110,091,253 (GRCm39) missense probably damaging 1.00
R2000:Gm15446 UTSW 5 110,090,677 (GRCm39) missense possibly damaging 0.67
R2059:Gm15446 UTSW 5 110,090,362 (GRCm39) missense probably damaging 1.00
R3083:Gm15446 UTSW 5 110,091,158 (GRCm39) missense possibly damaging 0.48
R3883:Gm15446 UTSW 5 110,088,313 (GRCm39) missense probably damaging 0.98
R4086:Gm15446 UTSW 5 110,091,121 (GRCm39) missense probably benign 0.02
R4095:Gm15446 UTSW 5 110,088,590 (GRCm39) splice site probably null
R4459:Gm15446 UTSW 5 110,091,107 (GRCm39) missense probably benign 0.03
R4721:Gm15446 UTSW 5 110,090,866 (GRCm39) missense probably damaging 1.00
R4735:Gm15446 UTSW 5 110,090,818 (GRCm39) missense probably damaging 1.00
R5229:Gm15446 UTSW 5 110,091,036 (GRCm39) missense probably damaging 1.00
R5502:Gm15446 UTSW 5 110,088,364 (GRCm39) nonsense probably null
R6116:Gm15446 UTSW 5 110,090,902 (GRCm39) missense probably damaging 1.00
R6166:Gm15446 UTSW 5 110,090,646 (GRCm39) nonsense probably null
R6322:Gm15446 UTSW 5 110,091,383 (GRCm39) missense probably damaging 1.00
R7871:Gm15446 UTSW 5 110,091,165 (GRCm39) nonsense probably null
R7939:Gm15446 UTSW 5 110,090,360 (GRCm39) missense probably benign 0.22
R8045:Gm15446 UTSW 5 110,088,394 (GRCm39) missense probably damaging 1.00
R8069:Gm15446 UTSW 5 110,088,306 (GRCm39) nonsense probably null
R8528:Gm15446 UTSW 5 110,090,896 (GRCm39) missense possibly damaging 0.95
R9074:Gm15446 UTSW 5 110,091,299 (GRCm39) missense probably damaging 1.00
R9198:Gm15446 UTSW 5 110,090,743 (GRCm39) missense probably damaging 1.00
R9604:Gm15446 UTSW 5 110,088,314 (GRCm39) missense probably damaging 1.00
R9706:Gm15446 UTSW 5 110,091,161 (GRCm39) missense probably damaging 0.96
Posted On 2013-12-09