Incidental Mutation 'IGL02260:Gm5581'
ID286699
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm5581
Ensembl Gene ENSMUSG00000061969
Gene Namepredicted gene 5581
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.070) question?
Stock #IGL02260
Quality Score
Status
Chromosome6
Chromosomal Location131166365-131182379 bp(-) (GRCm38)
Type of Mutationunclassified
DNA Base Change (assembly) T to C at 131167946 bp
ZygosityHeterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
Predicted Effect noncoding transcript
Transcript: ENSMUST00000072940
SMART Domains Protein: ENSMUSP00000072710
Gene: ENSMUSG00000061969

DomainStartEndE-ValueType
KRAB 8 68 1.79e-34 SMART
low complexity region 285 302 N/A INTRINSIC
low complexity region 355 366 N/A INTRINSIC
PDB:1MEY|G 422 507 4e-15 PDB
Blast:HNHc 445 504 4e-6 BLAST
ZnF_C2H2 509 531 9.73e-4 SMART
ZnF_C2H2 537 559 1.5e-4 SMART
ZnF_C2H2 565 587 1.98e-4 SMART
ZnF_C2H2 593 615 1.52e-5 SMART
ZnF_C2H2 621 643 9.73e-4 SMART
ZnF_C2H2 649 671 9.36e-6 SMART
ZnF_C2H2 677 699 3.49e-5 SMART
ZnF_C2H2 705 727 9.88e-5 SMART
ZnF_C2H2 733 755 9.88e-5 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000204992
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 43 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgre1 C T 17: 57,447,891 A663V probably benign Het
Atg2b A T 12: 105,636,440 probably benign Het
B4galt6 T C 18: 20,700,747 I194V probably benign Het
Caprin1 T C 2: 103,779,369 Y188C probably damaging Het
Ccdc85a A G 11: 28,576,672 F284S possibly damaging Het
Ccdc88b A T 19: 6,855,349 probably benign Het
Cox18 C T 5: 90,217,525 V272I possibly damaging Het
Dars A T 1: 128,372,161 M362K probably benign Het
Ddi1 A T 9: 6,265,760 M203K probably benign Het
Dlg4 G A 11: 70,042,267 G500R probably damaging Het
Ebf3 G A 7: 137,206,190 P375S probably damaging Het
Eif5b T A 1: 38,045,456 L842M possibly damaging Het
Fhdc1 G A 3: 84,444,735 A1061V possibly damaging Het
Mapk10 A T 5: 103,038,668 D29E probably benign Het
Mib2 C T 4: 155,661,171 R61H probably damaging Het
Mki67 A G 7: 135,701,968 S724P probably benign Het
Mtor T C 4: 148,538,301 I1946T probably damaging Het
Myh14 A G 7: 44,611,571 L1873P probably damaging Het
Myom1 C T 17: 71,108,315 Q1226* probably null Het
Neb A G 2: 52,205,656 L4858P probably damaging Het
Olfr1036 C A 2: 86,075,472 T244K possibly damaging Het
Olfr502 T C 7: 108,523,285 I222V probably benign Het
Olfr561 A T 7: 102,774,907 I128F probably damaging Het
Pcdhb14 C T 18: 37,450,033 H731Y probably benign Het
Prdm16 T C 4: 154,328,287 N1087S probably benign Het
Prdm2 C T 4: 143,134,587 G711D probably damaging Het
Proser1 G A 3: 53,478,944 G749D probably damaging Het
Ptch1 A T 13: 63,565,352 probably benign Het
Pus10 A T 11: 23,707,548 K233* probably null Het
Rasa2 A G 9: 96,544,319 Y825H probably benign Het
Tbcd T C 11: 121,603,278 F969S probably damaging Het
Tbp T A 17: 15,504,616 S133T probably damaging Het
Tnks C T 8: 34,842,983 G1062D probably damaging Het
Tnrc6b T A 15: 80,880,171 S625T probably damaging Het
Triobp T C 15: 78,966,362 S239P probably benign Het
Ubiad1 T C 4: 148,444,107 D115G probably benign Het
Uckl1 A G 2: 181,569,588 S483P probably damaging Het
Vill A G 9: 119,058,441 D91G probably benign Het
Wdr62 C A 7: 30,270,782 C200F probably damaging Het
Zfp341 G A 2: 154,642,049 C586Y possibly damaging Het
Zfp687 G A 3: 95,011,264 T399I possibly damaging Het
Zp1 G T 19: 10,916,714 probably benign Het
Zzz3 T A 3: 152,452,083 D263E probably benign Het
Other mutations in Gm5581
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00533:Gm5581 APN 6 131167641 unclassified noncoding transcript
IGL01372:Gm5581 APN 6 131168403 exon noncoding transcript
IGL01630:Gm5581 APN 6 131168296 exon noncoding transcript
IGL01667:Gm5581 APN 6 131167772 unclassified noncoding transcript
IGL03212:Gm5581 APN 6 131181450 exon noncoding transcript
IGL03306:Gm5581 APN 6 131168081 unclassified noncoding transcript
R0366:Gm5581 UTSW 6 131166447 unclassified noncoding transcript
R1764:Gm5581 UTSW 6 131181399 exon noncoding transcript
R1961:Gm5581 UTSW 6 131168162 unclassified noncoding transcript
R2129:Gm5581 UTSW 6 131168284 exon noncoding transcript
R3177:Gm5581 UTSW 6 131166965 unclassified noncoding transcript
R4026:Gm5581 UTSW 6 131167068 unclassified noncoding transcript
R4289:Gm5581 UTSW 6 131167556 unclassified noncoding transcript
R4943:Gm5581 UTSW 6 131167125 unclassified noncoding transcript
R4961:Gm5581 UTSW 6 131167227 unclassified noncoding transcript
R5817:Gm5581 UTSW 6 131167169 unclassified noncoding transcript
R5944:Gm5581 UTSW 6 131168400 exon noncoding transcript
Posted On2015-04-16