Incidental Mutation 'R0197:1700016H13Rik'
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Institutional Source Beutler Lab
Gene Symbol 1700016H13Rik
Ensembl Gene ENSMUSG00000029320
Gene NameRIKEN cDNA 1700016H13 gene
MMRRC Submission 038456-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.035) question?
Stock #R0197 (G1)
Quality Score204
Status Validated
Chromosomal Location103648039-103656010 bp(-) (GRCm38)
Type of Mutationmakesense
DNA Base Change (assembly) T to C at 103648821 bp
Amino Acid Change Stop codon to Tryptophan at position 118 (*118W)
Ref Sequence ENSEMBL: ENSMUSP00000114503 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000031261] [ENSMUST00000119824] [ENSMUST00000120108] [ENSMUST00000120688] [ENSMUST00000134926] [ENSMUST00000154096] [ENSMUST00000154408]
Predicted Effect probably benign
Transcript: ENSMUST00000031261
Predicted Effect probably null
Transcript: ENSMUST00000119824
AA Change: *118W
SMART Domains Protein: ENSMUSP00000113935
Gene: ENSMUSG00000029320
AA Change: *118W

Pfam:DUF4522 1 117 3.5e-75 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000120108
AA Change: *118W
SMART Domains Protein: ENSMUSP00000113969
Gene: ENSMUSG00000029320
AA Change: *118W

Pfam:DUF4522 1 117 3.5e-75 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000120688
AA Change: *118W
SMART Domains Protein: ENSMUSP00000113469
Gene: ENSMUSG00000029320
AA Change: *118W

Pfam:DUF4522 1 117 3.5e-75 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000134926
AA Change: *118W
SMART Domains Protein: ENSMUSP00000114503
Gene: ENSMUSG00000029320
AA Change: *118W

Pfam:DUF4522 1 117 9.7e-66 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000154096
Predicted Effect probably benign
Transcript: ENSMUST00000154408
Meta Mutation Damage Score 0.524 question?
Coding Region Coverage
  • 1x: 98.6%
  • 3x: 97.3%
  • 10x: 92.5%
  • 20x: 75.9%
Validation Efficiency 97% (121/125)
Allele List at MGI
Other mutations in this stock
Total: 68 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1110002E22Rik T C 3: 138,069,871 L1607P probably damaging Het
1700061G19Rik A T 17: 56,883,835 N468Y probably benign Het
2610507B11Rik A C 11: 78,269,704 probably benign Het
4930452B06Rik C T 14: 8,518,695 G254R probably damaging Het
Abcc2 A T 19: 43,826,614 R1147* probably null Het
Agap2 A G 10: 127,091,702 T1131A possibly damaging Het
Aldh9a1 A G 1: 167,361,847 D388G probably damaging Het
Ap3d1 G T 10: 80,730,042 A97E probably damaging Het
Arhgef10 T A 8: 14,962,636 V320E probably damaging Het
Baiap2l1 C A 5: 144,266,010 V498L probably damaging Het
Ccdc189 T C 7: 127,584,862 E261G probably damaging Het
Cdh2 T C 18: 16,629,576 N437S probably benign Het
Chd1 C A 17: 15,725,431 N72K probably benign Het
Col4a3bp T A 13: 96,549,287 Y63N probably benign Het
Cstf2t A T 19: 31,084,626 M521L probably benign Het
Dlx5 T C 6: 6,881,619 K90E possibly damaging Het
Dmp1 A G 5: 104,207,630 E32G possibly damaging Het
Espnl T G 1: 91,344,489 Y524D probably damaging Het
Fam20c T C 5: 138,755,724 L30P probably damaging Het
Fat1 G T 8: 45,026,553 A2879S probably benign Het
Gabrg1 A T 5: 70,774,389 V337D probably damaging Het
Gart C A 16: 91,623,403 D851Y possibly damaging Het
Gcc1 T C 6: 28,420,616 H234R probably damaging Het
Gemin6 T A 17: 80,228,095 H161Q probably damaging Het
Glt6d1 A G 2: 25,794,070 I308T probably benign Het
Gm10320 T C 13: 98,491,983 T7A probably benign Het
Gm10912 T C 2: 104,066,530 S5P probably benign Het
Gm13088 C T 4: 143,656,440 E70K possibly damaging Het
Gmpr2 T A 14: 55,672,735 D7E possibly damaging Het
Hc A G 2: 34,984,750 Y1620H probably damaging Het
Hoxa3 T C 6: 52,170,143 probably benign Het
Ift140 A G 17: 25,090,933 T1105A probably benign Het
Kdr G T 5: 75,968,422 T188N possibly damaging Het
Lepr A T 4: 101,752,152 D312V possibly damaging Het
Mcm3 A G 1: 20,810,105 V501A probably damaging Het
Mcur1 T C 13: 43,545,740 Y267C probably damaging Het
Med13 T A 11: 86,307,038 T736S probably benign Het
Med13l T C 5: 118,671,002 probably benign Het
Mroh2a G C 1: 88,246,042 A871P probably damaging Het
Ndrg2 T A 14: 51,907,003 probably benign Het
Oas3 G A 5: 120,756,145 R39C probably damaging Het
Olfr1258 A G 2: 89,930,201 T131A probably benign Het
Olfr1298 C T 2: 111,645,791 V69I probably benign Het
Olfr272 G A 4: 52,910,849 T315M probably benign Het
Olfr558 T A 7: 102,709,995 H245Q probably damaging Het
Onecut2 T A 18: 64,341,472 S365T possibly damaging Het
Pds5b C A 5: 150,754,431 Q505K probably benign Het
Rfx2 T C 17: 56,803,722 Y88C probably damaging Het
Rpl6 T C 5: 121,208,478 V214A probably benign Het
Samd3 T A 10: 26,271,854 C476S possibly damaging Het
Sfi1 TCGC TC 11: 3,146,254 probably null Het
Shank1 C T 7: 44,352,294 R1146W unknown Het
Smcr8 T C 11: 60,778,115 Y30H probably damaging Het
Smpd4 T A 16: 17,641,597 probably null Het
Strip1 C A 3: 107,614,613 D750Y probably damaging Het
Svep1 T C 4: 58,070,851 K2312E possibly damaging Het
Taf1c A T 8: 119,599,983 I438N probably damaging Het
Tnfaip1 A T 11: 78,530,014 probably benign Het
Unc45b T A 11: 82,940,205 L797Q possibly damaging Het
Usp24 T A 4: 106,407,133 W1754R probably damaging Het
Utp20 G A 10: 88,777,516 P1301L probably benign Het
Vmn2r115 T A 17: 23,359,781 S743T probably damaging Het
Vps41 T G 13: 18,854,663 probably null Het
Vps72 G T 3: 95,122,583 L304F probably damaging Het
Wiz A T 17: 32,356,441 I907N probably damaging Het
Zfp521 T C 18: 13,845,062 T765A probably benign Het
Zfp616 A T 11: 74,085,674 H923L probably damaging Het
Zp2 A T 7: 120,143,576 probably benign Het
Other mutations in 1700016H13Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01086:1700016H13Rik APN 5 103648863 missense probably damaging 0.97
R0414:1700016H13Rik UTSW 5 103649490 missense probably benign 0.00
R0883:1700016H13Rik UTSW 5 103648821 makesense probably null
R5655:1700016H13Rik UTSW 5 103648880 missense probably benign 0.09
Z1088:1700016H13Rik UTSW 5 103649568 missense probably damaging 1.00
Predicted Primers PCR Primer

Sequencing Primer
(R):5'- gaaatctacctgcctctgcc -3'
Posted On2013-04-16