Incidental Mutation 'IGL02260:Gm5581'
ID 286699
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm5581
Ensembl Gene ENSMUSG00000061969
Gene Name predicted gene 5581
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.072) question?
Stock # IGL02260
Quality Score
Status
Chromosome 6
Chromosomal Location 131143329-131144284 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) T to C at 131144909 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
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: 57,754,891 (GRCm39) A663V probably benign Het
Atg2b A T 12: 105,602,699 (GRCm39) probably benign Het
B4galt6 T C 18: 20,833,804 (GRCm39) I194V probably benign Het
Caprin1 T C 2: 103,609,714 (GRCm39) Y188C probably damaging Het
Ccdc85a A G 11: 28,526,672 (GRCm39) F284S possibly damaging Het
Ccdc88b A T 19: 6,832,717 (GRCm39) probably benign Het
Cox18 C T 5: 90,365,384 (GRCm39) V272I possibly damaging Het
Dars1 A T 1: 128,299,898 (GRCm39) M362K probably benign Het
Ddi1 A T 9: 6,265,760 (GRCm39) M203K probably benign Het
Dlg4 G A 11: 69,933,093 (GRCm39) G500R probably damaging Het
Ebf3 G A 7: 136,807,919 (GRCm39) P375S probably damaging Het
Eif5b T A 1: 38,084,537 (GRCm39) L842M possibly damaging Het
Fhdc1 G A 3: 84,352,042 (GRCm39) A1061V possibly damaging Het
Mapk10 A T 5: 103,186,534 (GRCm39) D29E probably benign Het
Mib2 C T 4: 155,745,628 (GRCm39) R61H probably damaging Het
Mki67 A G 7: 135,303,697 (GRCm39) S724P probably benign Het
Mtor T C 4: 148,622,758 (GRCm39) I1946T probably damaging Het
Myh14 A G 7: 44,260,995 (GRCm39) L1873P probably damaging Het
Myom1 C T 17: 71,415,310 (GRCm39) Q1226* probably null Het
Neb A G 2: 52,095,668 (GRCm39) L4858P probably damaging Het
Or51f5 A T 7: 102,424,114 (GRCm39) I128F probably damaging Het
Or5m9b C A 2: 85,905,816 (GRCm39) T244K possibly damaging Het
Or5p76 T C 7: 108,122,492 (GRCm39) I222V probably benign Het
Pcdhb14 C T 18: 37,583,086 (GRCm39) H731Y probably benign Het
Prdm16 T C 4: 154,412,744 (GRCm39) N1087S probably benign Het
Prdm2 C T 4: 142,861,157 (GRCm39) G711D probably damaging Het
Proser1 G A 3: 53,386,365 (GRCm39) G749D probably damaging Het
Ptch1 A T 13: 63,713,166 (GRCm39) probably benign Het
Pus10 A T 11: 23,657,548 (GRCm39) K233* probably null Het
Rasa2 A G 9: 96,426,372 (GRCm39) Y825H probably benign Het
Tbcd T C 11: 121,494,104 (GRCm39) F969S probably damaging Het
Tbp T A 17: 15,724,878 (GRCm39) S133T probably damaging Het
Tnks C T 8: 35,310,137 (GRCm39) G1062D probably damaging Het
Tnrc6b T A 15: 80,764,372 (GRCm39) S625T probably damaging Het
Triobp T C 15: 78,850,562 (GRCm39) S239P probably benign Het
Ubiad1 T C 4: 148,528,564 (GRCm39) D115G probably benign Het
Uckl1 A G 2: 181,211,381 (GRCm39) S483P probably damaging Het
Vill A G 9: 118,887,509 (GRCm39) D91G probably benign Het
Wdr62 C A 7: 29,970,207 (GRCm39) C200F probably damaging Het
Zfp341 G A 2: 154,483,969 (GRCm39) C586Y possibly damaging Het
Zfp687 G A 3: 94,918,575 (GRCm39) T399I possibly damaging Het
Zp1 G T 19: 10,894,078 (GRCm39) probably benign Het
Zzz3 T A 3: 152,157,720 (GRCm39) D263E probably benign Het
Other mutations in Gm5581
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00533:Gm5581 APN 6 131,144,604 (GRCm39) unclassified noncoding transcript
IGL01372:Gm5581 APN 6 131,145,366 (GRCm39) exon noncoding transcript
IGL01630:Gm5581 APN 6 131,145,259 (GRCm39) exon noncoding transcript
IGL01667:Gm5581 APN 6 131,144,735 (GRCm39) unclassified noncoding transcript
IGL03212:Gm5581 APN 6 131,158,413 (GRCm39) exon noncoding transcript
IGL03306:Gm5581 APN 6 131,145,044 (GRCm39) unclassified noncoding transcript
R0366:Gm5581 UTSW 6 131,143,410 (GRCm39) unclassified noncoding transcript
R1764:Gm5581 UTSW 6 131,158,362 (GRCm39) exon noncoding transcript
R1961:Gm5581 UTSW 6 131,145,125 (GRCm39) unclassified noncoding transcript
R2129:Gm5581 UTSW 6 131,145,247 (GRCm39) exon noncoding transcript
R3177:Gm5581 UTSW 6 131,143,928 (GRCm39) unclassified noncoding transcript
R4026:Gm5581 UTSW 6 131,144,031 (GRCm39) unclassified noncoding transcript
R4289:Gm5581 UTSW 6 131,144,519 (GRCm39) unclassified noncoding transcript
R4943:Gm5581 UTSW 6 131,144,088 (GRCm39) unclassified noncoding transcript
R4961:Gm5581 UTSW 6 131,144,190 (GRCm39) unclassified noncoding transcript
R5817:Gm5581 UTSW 6 131,144,132 (GRCm39) unclassified noncoding transcript
R5944:Gm5581 UTSW 6 131,145,363 (GRCm39) exon noncoding transcript
Posted On 2015-04-16