Incidental Mutation 'R8070:9830107B12Rik'
ID620265
Institutional Source Beutler Lab
Gene Symbol 9830107B12Rik
Ensembl Gene ENSMUSG00000073386
Gene NameRIKEN cDNA 9830107B12 gene
Synonyms
Accession Numbers
Is this an essential gene? Not available question?
Stock #R8070 (G1)
Quality Score225.009
Status Not validated
Chromosome17
Chromosomal Location48125605-48146307 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to G at 48145510 bp
ZygosityHeterozygous
Amino Acid Change Phenylalanine to Serine at position 86 (F86S)
Ref Sequence ENSEMBL: ENSMUSP00000070138 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000063481]
Predicted Effect probably damaging
Transcript: ENSMUST00000063481
AA Change: F86S

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000070138
Gene: ENSMUSG00000073386
AA Change: F86S

DomainStartEndE-ValueType
low complexity region 8 17 N/A INTRINSIC
IG 26 122 3.65e-6 SMART
low complexity region 144 158 N/A INTRINSIC
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.8%
  • 20x: 99.3%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 65 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
0610040J01Rik A G 5: 63,898,167 E82G probably benign Het
Aamdc A T 7: 97,575,648 Y2* probably null Het
Acta1 T A 8: 123,893,621 D26V possibly damaging Het
Adra1d A C 2: 131,561,582 L196R probably damaging Het
Agbl2 G A 2: 90,791,565 C132Y probably benign Het
Amd1 A G 10: 40,294,230 V92A probably benign Het
Arid4b T A 13: 14,136,259 I149K probably benign Het
Atg7 A G 6: 114,697,080 M312V probably benign Het
Bap1 T A 14: 31,256,686 V381E probably damaging Het
Cbfa2t3 C T 8: 122,642,981 V207I possibly damaging Het
Cdh24 T C 14: 54,632,573 Q629R probably benign Het
Cdhr2 G T 13: 54,719,793 V479L probably benign Het
Chd2 A G 7: 73,451,758 S1407P probably benign Het
Clstn2 A G 9: 97,799,470 V39A possibly damaging Het
Cwh43 T A 5: 73,421,463 M357K possibly damaging Het
Dcdc2a T A 13: 25,202,197 D351E probably benign Het
Dennd6b T C 15: 89,185,373 I517V probably benign Het
Dnah17 T C 11: 118,024,671 E4374G probably damaging Het
Emsy A G 7: 98,626,715 S336P possibly damaging Het
Enoph1 A T 5: 100,060,982 E65D probably benign Het
Fam83f T A 15: 80,672,080 L55Q probably damaging Het
Fry T C 5: 150,478,007 F379L Het
Fscb A T 12: 64,474,608 M28K probably benign Het
Gas7 G A 11: 67,683,434 V412M probably damaging Het
Gatad1 T C 5: 3,643,540 R210G probably benign Het
Gcn1l1 T A 5: 115,588,998 V638E probably benign Het
Ggt1 A T 10: 75,578,899 I184F probably damaging Het
Gigyf2 A G 1: 87,440,907 N1103S probably benign Het
Gm13757 G T 2: 88,446,659 T93K probably benign Het
Gm5592 G A 7: 41,286,463 A130T possibly damaging Het
Gys2 T C 6: 142,448,504 probably null Het
Hmcn1 C A 1: 150,649,992 E3327* probably null Het
Ighv1-36 C T 12: 114,880,036 G68E probably damaging Het
Igkv6-32 G A 6: 70,074,105 T89M probably damaging Het
Ipo7 A G 7: 110,052,807 D931G probably benign Het
Jakmip1 A G 5: 37,173,287 E437G probably benign Het
Lingo3 C T 10: 80,836,121 probably benign Het
Lnpep A G 17: 17,538,638 S815P probably damaging Het
Ly6a T C 15: 74,997,600 D2G probably damaging Het
Madd C A 2: 91,158,014 E1223* probably null Het
Mapk8ip3 A T 17: 24,901,104 probably null Het
Mecom T C 3: 29,979,838 E239G probably damaging Het
Mug1 T C 6: 121,875,879 V889A probably benign Het
Myo18b T A 5: 112,791,120 N1675I probably benign Het
Ndrg4 T C 8: 95,700,128 F50L possibly damaging Het
Ndst4 A G 3: 125,714,644 Y286C probably damaging Het
Nrp2 C T 1: 62,745,408 R239C probably damaging Het
Olfm3 A G 3: 115,101,955 D195G probably damaging Het
Olfr1384 A T 11: 49,514,114 T159S probably damaging Het
Pds5a A G 5: 65,652,398 L407P possibly damaging Het
Pgm1 A G 5: 64,112,082 N504S probably benign Het
Plce1 A G 19: 38,701,839 M656V probably damaging Het
Pou6f2 T C 13: 18,239,624 T189A unknown Het
Ppp1r12b T C 1: 134,876,069 S451G probably benign Het
Prox1 T G 1: 190,160,910 N446T probably damaging Het
Ralgapa2 T A 2: 146,353,279 R1195S probably damaging Het
Rere A G 4: 150,617,375 D37G probably damaging Het
Tfip11 T A 5: 112,334,930 M560K possibly damaging Het
Thop1 T C 10: 81,079,486 V260A probably damaging Het
Tle6 A G 10: 81,598,642 M41T possibly damaging Het
Trav13-4-dv7 T C 14: 53,757,792 S68P possibly damaging Het
Trim24 A G 6: 37,957,726 N826S probably damaging Het
Tuba3a T C 6: 125,278,470 E414G probably damaging Het
Vmn2r78 A G 7: 86,922,487 I502V probably benign Het
Vmn2r79 A T 7: 87,002,128 Y245F probably benign Het
Other mutations in 9830107B12Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00771:9830107B12Rik APN 17 48145684 missense possibly damaging 0.74
IGL01457:9830107B12Rik APN 17 48128583 splice site probably benign
IGL01586:9830107B12Rik APN 17 48128515 missense unknown
IGL01792:9830107B12Rik APN 17 48145509 missense probably damaging 1.00
IGL01978:9830107B12Rik APN 17 48145993 missense probably damaging 0.99
IGL02347:9830107B12Rik APN 17 48145664 nonsense probably null
R0044:9830107B12Rik UTSW 17 48146186 utr 5 prime probably benign
R4613:9830107B12Rik UTSW 17 48128557 missense probably benign 0.15
R5984:9830107B12Rik UTSW 17 48128555 missense probably benign 0.00
R7565:9830107B12Rik UTSW 17 48145579 missense possibly damaging 0.76
Predicted Primers PCR Primer
(F):5'- TGAGTCCTCTTCAACTCTGGAG -3'
(R):5'- AGGAAGCATTTATTCCCAGGC -3'

Sequencing Primer
(F):5'- TCAACTCTGGAGCCTTGCGAC -3'
(R):5'- ACCCAGAGTTACTTCGAGTACTGG -3'
Posted On2020-01-23