Incidental Mutation 'R4807:Vsig10l'
ID 370752
Institutional Source Beutler Lab
Gene Symbol Vsig10l
Ensembl Gene ENSMUSG00000070604
Gene Name V-set and immunoglobulin domain containing 10 like
Synonyms 2210412E05Rik
MMRRC Submission 042426-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.204) question?
Stock # R4807 (G1)
Quality Score 225
Status Validated
Chromosome 7
Chromosomal Location 43112575-43121443 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 43113173 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Alanine at position 144 (T144A)
Ref Sequence ENSEMBL: ENSMUSP00000103611 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000107977] [ENSMUST00000203042] [ENSMUST00000203633] [ENSMUST00000203769] [ENSMUST00000204680]
AlphaFold D3YZF7
Predicted Effect possibly damaging
Transcript: ENSMUST00000107977
AA Change: T144A

PolyPhen 2 Score 0.528 (Sensitivity: 0.88; Specificity: 0.90)
SMART Domains Protein: ENSMUSP00000103611
Gene: ENSMUSG00000070604
AA Change: T144A

DomainStartEndE-ValueType
signal peptide 1 21 N/A INTRINSIC
low complexity region 28 52 N/A INTRINSIC
IG 183 285 1.92e0 SMART
IG 298 383 2.15e-3 SMART
IGc2 406 465 4.19e-6 SMART
Blast:IG_like 582 649 1e-13 BLAST
transmembrane domain 764 786 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000203042
Predicted Effect noncoding transcript
Transcript: ENSMUST00000203152
Predicted Effect probably benign
Transcript: ENSMUST00000203633
SMART Domains Protein: ENSMUSP00000145061
Gene: ENSMUSG00000107482

DomainStartEndE-ValueType
ETF 26 216 2.7e-65 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000203769
AA Change: T42A

PolyPhen 2 Score 0.166 (Sensitivity: 0.92; Specificity: 0.87)
SMART Domains Protein: ENSMUSP00000144692
Gene: ENSMUSG00000070604
AA Change: T42A

DomainStartEndE-ValueType
IG 81 183 8.1e-3 SMART
IG 196 281 9.2e-6 SMART
IGc2 304 363 1.8e-8 SMART
Blast:IG_like 480 547 9e-14 BLAST
transmembrane domain 662 684 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000204680
SMART Domains Protein: ENSMUSP00000145493
Gene: ENSMUSG00000107482

DomainStartEndE-ValueType
ETF 26 168 2.4e-17 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000205247
Meta Mutation Damage Score 0.0848 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.5%
  • 10x: 96.9%
  • 20x: 94.2%
Validation Efficiency 98% (86/88)
Allele List at MGI
Other mutations in this stock
Total: 84 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca16 C T 7: 120,139,832 (GRCm39) A1499V probably damaging Het
Agap3 T A 5: 24,682,114 (GRCm39) D386E probably damaging Het
Ahdc1 C A 4: 132,791,624 (GRCm39) T955K possibly damaging Het
Ankrd9 A G 12: 110,943,669 (GRCm39) Y122H probably benign Het
Apc2 G T 10: 80,150,196 (GRCm39) R1721L probably benign Het
Arfgef3 A G 10: 18,522,385 (GRCm39) V547A probably benign Het
Arhgap42 T C 9: 9,046,629 (GRCm39) N203D possibly damaging Het
Arl6ip1 AAAATAAATAAATAAATAAATAAATA AAAATAAATAAATAAATAAATAAATAAATA 7: 117,721,122 (GRCm39) probably benign Het
Arsi G A 18: 61,049,723 (GRCm39) G202E probably benign Het
Aspm T A 1: 139,405,657 (GRCm39) F1515I probably damaging Het
Baz1a T C 12: 54,945,267 (GRCm39) T1363A probably benign Het
Cacng3 C T 7: 122,353,732 (GRCm39) A72V probably benign Het
Casp8ap2 T C 4: 32,644,505 (GRCm39) C1193R possibly damaging Het
Ccr3 A G 9: 123,829,334 (GRCm39) Y223C probably damaging Het
Clcn3 C A 8: 61,387,564 (GRCm39) L201F probably damaging Het
Cltc A C 11: 86,591,902 (GRCm39) probably benign Het
Cyp19a1 G T 9: 54,083,930 (GRCm39) T86K possibly damaging Het
Ddx24 A T 12: 103,385,720 (GRCm39) F248L probably damaging Het
Ddx60 G A 8: 62,432,372 (GRCm39) V885I probably damaging Het
Dync2h1 T C 9: 7,139,422 (GRCm39) I1404M probably benign Het
Emilin2 A T 17: 71,580,443 (GRCm39) V761E probably damaging Het
Endou C T 15: 97,629,113 (GRCm39) C13Y probably benign Het
Ep400 C A 5: 110,843,444 (GRCm39) probably null Het
Fbxo33 C A 12: 59,265,998 (GRCm39) D90Y probably damaging Het
Fryl A G 5: 73,198,705 (GRCm39) F2641L probably benign Het
Gbp2b A G 3: 142,304,006 (GRCm39) I34V probably benign Het
Ghdc T C 11: 100,661,051 (GRCm39) H38R probably damaging Het
Gm10722 T C 9: 3,000,937 (GRCm39) C6R probably benign Het
Gpr63 A C 4: 25,007,446 (GRCm39) M57L probably benign Het
Gprc5c A G 11: 114,755,324 (GRCm39) S3G probably damaging Het
Grk4 A T 5: 34,909,552 (GRCm39) M539L probably benign Het
Gulo C T 14: 66,227,833 (GRCm39) M366I probably benign Het
Heatr5a T C 12: 51,924,303 (GRCm39) H1970R probably damaging Het
Hmbox1 T C 14: 65,062,998 (GRCm39) probably benign Het
Ighg2b T C 12: 113,267,965 (GRCm39) probably benign Het
Il1b A T 2: 129,212,226 (GRCm39) C9S probably benign Het
Itpkb A T 1: 180,162,440 (GRCm39) probably benign Het
Kcnn1 T A 8: 71,300,822 (GRCm39) H473L probably damaging Het
Kidins220 C T 12: 25,107,284 (GRCm39) S1579L probably damaging Het
Kif1b A T 4: 149,332,378 (GRCm39) probably benign Het
Lyg2 A T 1: 37,950,148 (GRCm39) M60K possibly damaging Het
Mak16 G T 8: 31,656,161 (GRCm39) H107Q probably benign Het
Mapkap1 G A 2: 34,487,434 (GRCm39) probably null Het
Mastl A G 2: 23,022,855 (GRCm39) S623P probably benign Het
Mccc1 T C 3: 36,039,195 (GRCm39) Y46C probably damaging Het
Mdn1 T G 4: 32,685,651 (GRCm39) probably null Het
Med25 T A 7: 44,534,043 (GRCm39) T31S probably benign Het
Mprip G A 11: 59,648,846 (GRCm39) G850D probably benign Het
Mrpl10 T C 11: 96,932,449 (GRCm39) I8T probably benign Het
Msr1 T C 8: 40,095,668 (GRCm39) probably benign Het
Myo3b T A 2: 69,936,056 (GRCm39) I99N probably damaging Het
Neurod6 A T 6: 55,655,640 (GRCm39) N332K probably damaging Het
Npc1l1 T C 11: 6,168,723 (GRCm39) Y886C probably damaging Het
Nsmaf T C 4: 6,398,542 (GRCm39) probably null Het
Ntn4 C T 10: 93,480,362 (GRCm39) R29C probably damaging Het
Or5d47 T A 2: 87,804,095 (GRCm39) I305L probably benign Het
Plppr2 A G 9: 21,855,810 (GRCm39) N261S probably damaging Het
Prkar2a T A 9: 108,617,584 (GRCm39) probably benign Het
Pxk G A 14: 8,144,133 (GRCm38) V294M probably damaging Het
Rars1 A G 11: 35,699,973 (GRCm39) F608L possibly damaging Het
Rasa3 A G 8: 13,664,633 (GRCm39) F60L probably damaging Het
Rbm47 C T 5: 66,176,647 (GRCm39) A490T possibly damaging Het
Sardh T C 2: 27,079,539 (GRCm39) I918V probably benign Het
Saxo5 A G 8: 3,529,004 (GRCm39) K193R possibly damaging Het
Sdhc T C 1: 170,963,626 (GRCm39) Y80C probably damaging Het
Selp T A 1: 163,971,505 (GRCm39) M653K probably damaging Het
Slc6a17 T C 3: 107,407,803 (GRCm39) D56G possibly damaging Het
Slco1b2 T C 6: 141,615,195 (GRCm39) S367P probably damaging Het
Spry4 TTGAGGTCC T 18: 38,723,328 (GRCm39) probably null Het
Strip2 T A 6: 29,925,092 (GRCm39) Y143* probably null Het
Sycp2 T C 2: 178,035,754 (GRCm39) probably benign Het
Tex30 C A 1: 44,126,118 (GRCm39) V204L possibly damaging Het
Tln2 G T 9: 67,239,015 (GRCm39) T1087K probably benign Het
Tmeff2 A C 1: 51,018,546 (GRCm39) N176T probably benign Het
Togaram2 C G 17: 72,004,918 (GRCm39) T324R probably damaging Het
Trpc3 C T 3: 36,688,531 (GRCm39) R836Q probably benign Het
Trpm7 A C 2: 126,673,149 (GRCm39) L535V probably benign Het
Vmn1r213 G A 13: 23,195,775 (GRCm39) W119* probably null Het
Vps29 T G 5: 122,500,951 (GRCm39) V176G probably damaging Het
Wdr11 T C 7: 129,229,746 (GRCm39) Y844H probably benign Het
Zbp1 A T 2: 173,053,999 (GRCm39) M174K probably damaging Het
Zfp341 G A 2: 154,487,786 (GRCm39) probably benign Het
Zfp638 G A 6: 83,920,040 (GRCm39) R546H probably damaging Het
Zfp820 A T 17: 22,042,853 (GRCm39) M1K probably null Het
Other mutations in Vsig10l
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01319:Vsig10l APN 7 43,114,678 (GRCm39) missense probably damaging 1.00
IGL01390:Vsig10l APN 7 43,115,889 (GRCm39) missense probably damaging 0.97
IGL02401:Vsig10l APN 7 43,113,468 (GRCm39) missense probably damaging 1.00
IGL02404:Vsig10l APN 7 43,113,171 (GRCm39) missense possibly damaging 0.85
IGL02514:Vsig10l APN 7 43,113,338 (GRCm39) missense probably benign 0.02
IGL02636:Vsig10l APN 7 43,113,002 (GRCm39) missense possibly damaging 0.53
IGL02805:Vsig10l APN 7 43,114,666 (GRCm39) missense probably damaging 1.00
IGL02823:Vsig10l APN 7 43,115,888 (GRCm39) missense probably damaging 1.00
IGL02827:Vsig10l APN 7 43,114,293 (GRCm39) missense probably damaging 1.00
R0111:Vsig10l UTSW 7 43,117,525 (GRCm39) missense probably damaging 0.97
R0394:Vsig10l UTSW 7 43,114,879 (GRCm39) missense probably damaging 0.97
R0465:Vsig10l UTSW 7 43,116,866 (GRCm39) missense probably damaging 1.00
R0632:Vsig10l UTSW 7 43,113,561 (GRCm39) missense probably damaging 0.97
R1689:Vsig10l UTSW 7 43,114,792 (GRCm39) missense possibly damaging 0.93
R1991:Vsig10l UTSW 7 43,116,892 (GRCm39) missense possibly damaging 0.89
R2103:Vsig10l UTSW 7 43,116,892 (GRCm39) missense possibly damaging 0.89
R2358:Vsig10l UTSW 7 43,118,185 (GRCm39) missense probably benign 0.00
R3015:Vsig10l UTSW 7 43,116,881 (GRCm39) missense possibly damaging 0.73
R4024:Vsig10l UTSW 7 43,117,510 (GRCm39) missense probably benign 0.33
R4031:Vsig10l UTSW 7 43,114,798 (GRCm39) missense probably damaging 1.00
R5020:Vsig10l UTSW 7 43,114,741 (GRCm39) nonsense probably null
R5261:Vsig10l UTSW 7 43,120,274 (GRCm39) missense probably damaging 1.00
R5317:Vsig10l UTSW 7 43,114,247 (GRCm39) missense probably damaging 1.00
R5426:Vsig10l UTSW 7 43,114,247 (GRCm39) missense probably damaging 0.97
R5656:Vsig10l UTSW 7 43,113,575 (GRCm39) nonsense probably null
R5842:Vsig10l UTSW 7 43,118,396 (GRCm39) missense probably benign 0.15
R6012:Vsig10l UTSW 7 43,117,439 (GRCm39) missense probably damaging 1.00
R6235:Vsig10l UTSW 7 43,118,396 (GRCm39) missense probably benign 0.15
R6309:Vsig10l UTSW 7 43,120,397 (GRCm39) splice site probably null
R6994:Vsig10l UTSW 7 43,114,491 (GRCm39) missense possibly damaging 0.71
R7250:Vsig10l UTSW 7 43,113,099 (GRCm39) missense probably benign
R7397:Vsig10l UTSW 7 43,117,431 (GRCm39) missense probably damaging 1.00
R7767:Vsig10l UTSW 7 43,113,141 (GRCm39) missense probably damaging 0.96
R7956:Vsig10l UTSW 7 43,117,494 (GRCm39) missense probably benign
R8086:Vsig10l UTSW 7 43,114,876 (GRCm39) missense possibly damaging 0.92
R8139:Vsig10l UTSW 7 43,113,153 (GRCm39) missense probably benign 0.00
R8297:Vsig10l UTSW 7 43,113,531 (GRCm39) missense possibly damaging 0.50
R8341:Vsig10l UTSW 7 43,113,378 (GRCm39) missense probably damaging 1.00
R8519:Vsig10l UTSW 7 43,114,326 (GRCm39) missense probably benign 0.33
R8925:Vsig10l UTSW 7 43,116,020 (GRCm39) missense probably benign 0.41
R8927:Vsig10l UTSW 7 43,116,020 (GRCm39) missense probably benign 0.41
R8948:Vsig10l UTSW 7 43,117,623 (GRCm39) missense possibly damaging 0.53
R9157:Vsig10l UTSW 7 43,112,948 (GRCm39) missense
R9203:Vsig10l UTSW 7 43,112,657 (GRCm39) start codon destroyed probably null
R9481:Vsig10l UTSW 7 43,112,795 (GRCm39) nonsense probably null
X0028:Vsig10l UTSW 7 43,112,788 (GRCm39) utr 3 prime probably benign
X0067:Vsig10l UTSW 7 43,116,914 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- ACCAATGTTTCCGCTGAGG -3'
(R):5'- AATTAGTGGAGCCTGTGACCC -3'

Sequencing Primer
(F):5'- GGAACAGTATCTCAGCCCTGATGTC -3'
(R):5'- AATACCTTGGAACCCCGGCG -3'
Posted On 2016-02-04