Incidental Mutation 'R5771:Gm10110'
ID 445397
Institutional Source Beutler Lab
Gene Symbol Gm10110
Ensembl Gene ENSMUSG00000062093
Gene Name predicted gene 10110
Synonyms
MMRRC Submission 043371-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.184) question?
Stock # R5771 (G1)
Quality Score 178
Status Validated
Chromosome 14
Chromosomal Location 90133664-90136883 bp(-) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) C to T at 90134675 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s): [ENSMUST00000081204]
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000081204
SMART Domains Protein: ENSMUSP00000079967
Gene: ENSMUSG00000062093

DomainStartEndE-ValueType
RRM 12 85 1.47e-21 SMART
RRM 100 171 2.91e-25 SMART
RRM 192 264 1.27e-25 SMART
RRM 295 366 1.92e-25 SMART
low complexity region 478 493 N/A INTRINSIC
low complexity region 503 516 N/A INTRINSIC
PolyA 534 597 4.49e-41 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000228705
Meta Mutation Damage Score 0.0697 question?
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.7%
  • 10x: 97.4%
  • 20x: 95.8%
Validation Efficiency 95% (87/92)
Allele List at MGI
Other mutations in this stock
Total: 82 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca13 T A 11: 9,241,411 (GRCm39) N1091K probably damaging Het
Adam3 C T 8: 25,197,427 (GRCm39) V335I probably benign Het
AI504432 G A 3: 106,956,299 (GRCm39) noncoding transcript Het
Apcdd1 A G 18: 63,070,027 (GRCm39) Y98C probably damaging Het
Aqp9 C T 9: 71,030,146 (GRCm39) A214T probably damaging Het
Atp8b4 T C 2: 126,220,664 (GRCm39) D578G probably benign Het
Bcdin3d T C 15: 99,368,717 (GRCm39) M161V probably benign Het
Bicral C T 17: 47,136,284 (GRCm39) V309I possibly damaging Het
Ccdc88b C T 19: 6,831,203 (GRCm39) A580T probably benign Het
Cdhr2 T A 13: 54,874,508 (GRCm39) V860E probably damaging Het
Clhc1 A T 11: 29,513,854 (GRCm39) N302Y possibly damaging Het
Cnnm2 T A 19: 46,845,434 (GRCm39) probably null Het
Crebbp T C 16: 3,937,636 (GRCm39) N709S probably benign Het
Ctnnal1 T C 4: 56,826,328 (GRCm39) S512G probably benign Het
Dgcr8 C T 16: 18,090,632 (GRCm39) V581I probably benign Het
Dnaaf10 A G 11: 17,174,638 (GRCm39) T169A probably benign Het
Dnah7c G A 1: 46,678,825 (GRCm39) V1790I probably benign Het
Efl1 A G 7: 82,341,732 (GRCm39) K452E probably benign Het
Epb42 A C 2: 120,852,301 (GRCm39) V564G probably damaging Het
Etv4 G A 11: 101,662,282 (GRCm39) P335S probably damaging Het
Fbxw9 T A 8: 85,791,201 (GRCm39) probably null Het
Fcrl2 A T 3: 87,170,775 (GRCm39) L3Q probably damaging Het
Frmd8 C A 19: 5,919,478 (GRCm39) A190S probably benign Het
Gcm2 C T 13: 41,256,991 (GRCm39) D253N probably benign Het
Gfm1 T C 3: 67,342,895 (GRCm39) V143A probably benign Het
Gigyf2 T C 1: 87,374,050 (GRCm39) M1226T possibly damaging Het
Gm11595 G A 11: 99,663,381 (GRCm39) R100C unknown Het
Gm20939 T G 17: 95,181,767 (GRCm39) C55W possibly damaging Het
Gm5407 T A 16: 49,117,229 (GRCm39) noncoding transcript Het
Golga4 A G 9: 118,387,351 (GRCm39) E1491G probably damaging Het
Hdac11 T A 6: 91,146,364 (GRCm39) probably null Het
Hs3st3b1 C T 11: 63,780,098 (GRCm39) S343N probably benign Het
Igkv12-44 G A 6: 69,792,075 (GRCm39) P4S probably benign Het
Igkv1-35 C T 6: 69,988,231 (GRCm39) V22I probably benign Het
Kcns2 A T 15: 34,839,068 (GRCm39) T144S probably benign Het
Khdc1c T C 1: 21,439,266 (GRCm39) V84A possibly damaging Het
Kif4-ps T A 12: 101,115,544 (GRCm39) noncoding transcript Het
Lamc2 T G 1: 153,017,340 (GRCm39) Y549S probably benign Het
Lect2 T A 13: 56,696,154 (GRCm39) I8F probably benign Het
Loxl3 T A 6: 83,012,780 (GRCm39) probably null Het
Lrwd1 A T 5: 136,152,516 (GRCm39) I545N possibly damaging Het
Ltbp3 T C 19: 5,797,572 (GRCm39) C437R probably damaging Het
Lypd3 T C 7: 24,339,787 (GRCm39) S285P probably benign Het
Mast2 T A 4: 116,190,622 (GRCm39) H83L possibly damaging Het
Mfsd4b4 A G 10: 39,768,635 (GRCm39) F153L probably benign Het
Ms4a4b T A 19: 11,438,606 (GRCm39) probably null Het
Nbr1 T A 11: 101,450,364 (GRCm39) L41Q probably damaging Het
Nlrp4a G A 7: 26,152,814 (GRCm39) C628Y probably damaging Het
Nup160 C T 2: 90,553,740 (GRCm39) R1157C probably damaging Het
Obscn T A 11: 58,891,533 (GRCm39) I7000F unknown Het
Or4k41 T A 2: 111,280,406 (GRCm39) probably null Het
Or4p21 A T 2: 88,276,652 (GRCm39) V210D possibly damaging Het
Or5ac15 TGAAGAAGAA TGAAGAA 16: 58,940,335 (GRCm39) probably benign Het
Or5b122 T G 19: 13,562,872 (GRCm39) V25G probably damaging Het
Or8g2 A T 9: 39,821,546 (GRCm39) Y149F probably damaging Het
Pdilt T C 7: 119,094,217 (GRCm39) K345E probably damaging Het
Ppp1r12b A T 1: 134,701,162 (GRCm39) probably null Het
Ppp2r1b A T 9: 50,778,132 (GRCm39) Q219L probably damaging Het
Prim2 A G 1: 33,493,232 (GRCm39) S485P unknown Het
Prkdc A G 16: 15,482,097 (GRCm39) D380G probably damaging Het
Psmg1 A G 16: 95,783,369 (GRCm39) L243S probably damaging Het
Rapgef5 T A 12: 117,685,061 (GRCm39) V270D probably benign Het
Rnft1 C T 11: 86,384,032 (GRCm39) R311* probably null Het
Scaper T A 9: 55,724,075 (GRCm39) I628L probably damaging Het
Serpina3j C A 12: 104,281,185 (GRCm39) H119Q possibly damaging Het
Slamf6 G A 1: 171,745,341 (GRCm39) V23I probably damaging Het
Slc12a5 T A 2: 164,815,688 (GRCm39) M45K possibly damaging Het
Slc25a11 A C 11: 70,537,016 (GRCm39) V13G probably damaging Het
Slc7a14 T A 3: 31,292,856 (GRCm39) Y143F probably damaging Het
Spryd3 A G 15: 102,025,342 (GRCm39) probably benign Het
Stard13 C A 5: 151,113,476 (GRCm39) L28F probably damaging Het
Susd2 C T 10: 75,473,853 (GRCm39) A581T probably damaging Het
Taf2 A G 15: 54,923,335 (GRCm39) V314A probably benign Het
Tas2r106 T C 6: 131,655,086 (GRCm39) N255S possibly damaging Het
Tbxa2r T A 10: 81,168,775 (GRCm39) W155R probably damaging Het
Tcf3 A G 10: 80,257,450 (GRCm39) probably benign Het
Ticam1 TCACACA TCACA 17: 56,577,629 (GRCm39) probably null Het
Vmn2r55 T C 7: 12,404,959 (GRCm39) D148G probably damaging Het
Vmn2r77 A G 7: 86,461,235 (GRCm39) N854D probably benign Het
Vstm4 A T 14: 32,626,526 (GRCm39) H64L probably benign Het
Wnk2 T C 13: 49,256,276 (GRCm39) T282A probably damaging Het
Zscan4c A T 7: 10,743,574 (GRCm39) D391V probably benign Het
Other mutations in Gm10110
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01390:Gm10110 APN 14 90,135,677 (GRCm39) exon noncoding transcript
IGL02308:Gm10110 APN 14 90,135,031 (GRCm39) exon noncoding transcript
IGL02977:Gm10110 APN 14 90,134,768 (GRCm39) exon noncoding transcript
IGL03230:Gm10110 APN 14 90,135,733 (GRCm39) exon noncoding transcript
R0966:Gm10110 UTSW 14 90,135,555 (GRCm39) exon noncoding transcript
R1466:Gm10110 UTSW 14 90,135,511 (GRCm39) exon noncoding transcript
R1466:Gm10110 UTSW 14 90,135,511 (GRCm39) exon noncoding transcript
R1640:Gm10110 UTSW 14 90,135,679 (GRCm39) exon noncoding transcript
R1762:Gm10110 UTSW 14 90,134,825 (GRCm39) exon noncoding transcript
R1839:Gm10110 UTSW 14 90,135,272 (GRCm39) exon noncoding transcript
R2679:Gm10110 UTSW 14 90,134,852 (GRCm39) exon noncoding transcript
R3907:Gm10110 UTSW 14 90,135,583 (GRCm39) exon noncoding transcript
R4512:Gm10110 UTSW 14 90,135,151 (GRCm39) exon noncoding transcript
R4513:Gm10110 UTSW 14 90,135,151 (GRCm39) exon noncoding transcript
R4590:Gm10110 UTSW 14 90,134,982 (GRCm39) exon noncoding transcript
R4877:Gm10110 UTSW 14 90,134,785 (GRCm39) exon noncoding transcript
R6333:Gm10110 UTSW 14 90,135,733 (GRCm39) exon noncoding transcript
R6341:Gm10110 UTSW 14 90,134,144 (GRCm39) exon noncoding transcript
R8235:Gm10110 UTSW 14 90,135,677 (GRCm39) missense noncoding transcript
R8236:Gm10110 UTSW 14 90,135,677 (GRCm39) missense noncoding transcript
R8237:Gm10110 UTSW 14 90,135,677 (GRCm39) missense noncoding transcript
R8281:Gm10110 UTSW 14 90,135,677 (GRCm39) missense noncoding transcript
R8282:Gm10110 UTSW 14 90,135,677 (GRCm39) missense noncoding transcript
R8283:Gm10110 UTSW 14 90,135,677 (GRCm39) missense noncoding transcript
Predicted Primers PCR Primer
(F):5'- CAAAGTCCATAGCCAAGCGG -3'
(R):5'- CAAAGCTGTCACCGAGATGAATG -3'

Sequencing Primer
(F):5'- ACTCAGACCCAGTTGGAGC -3'
(R):5'- TGTCACCGAGATGAATGGACGC -3'
Posted On 2016-11-21