Incidental Mutation 'IGL02514:Vsig10l'
ID 296683
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vsig10l
Ensembl Gene ENSMUSG00000070604
Gene Name V-set and immunoglobulin domain containing 10 like
Synonyms 2210412E05Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.204) question?
Stock # IGL02514
Quality Score
Status
Chromosome 7
Chromosomal Location 43112575-43121443 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 43113338 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Alanine at position 199 (T199A)
Ref Sequence ENSEMBL: ENSMUSP00000103611 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000107977] [ENSMUST00000203042] [ENSMUST00000203633] [ENSMUST00000203769] [ENSMUST00000204680]
AlphaFold D3YZF7
Predicted Effect probably benign
Transcript: ENSMUST00000107977
AA Change: T199A

PolyPhen 2 Score 0.017 (Sensitivity: 0.95; Specificity: 0.80)
SMART Domains Protein: ENSMUSP00000103611
Gene: ENSMUSG00000070604
AA Change: T199A

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: T97A

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000144692
Gene: ENSMUSG00000070604
AA Change: T97A

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
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 53 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2310009B15Rik A T 1: 138,779,909 (GRCm39) C114* probably null Het
4933421I07Rik A G 7: 42,096,981 (GRCm39) M110T probably damaging Het
Amer1 A G X: 94,470,117 (GRCm39) V667A possibly damaging Het
Casr C T 16: 36,320,687 (GRCm39) G487E probably damaging Het
Catsperd G A 17: 56,968,271 (GRCm39) G552D probably damaging Het
Ceacam3 A G 7: 16,896,906 (GRCm39) D624G possibly damaging Het
Celsr2 A G 3: 108,304,826 (GRCm39) V2208A probably benign Het
Cibar1 T G 4: 12,164,080 (GRCm39) probably benign Het
Clca4a G A 3: 144,660,832 (GRCm39) S664F probably damaging Het
Ddx23 A T 15: 98,556,199 (GRCm39) S40T unknown Het
Dhodh G A 8: 110,332,896 (GRCm39) R58* probably null Het
Dhx36 A G 3: 62,408,319 (GRCm39) L173S possibly damaging Het
Dnaaf5 C T 5: 139,159,872 (GRCm39) probably benign Het
Dnah3 T C 7: 119,565,470 (GRCm39) D2546G probably damaging Het
Eef2 T G 10: 81,015,427 (GRCm39) I316S probably benign Het
Efcab6 T C 15: 83,917,143 (GRCm39) D139G possibly damaging Het
Efcab6 A T 15: 83,755,512 (GRCm39) probably benign Het
Eif4g3 T A 4: 137,853,505 (GRCm39) I357N possibly damaging Het
Elovl2 G A 13: 41,348,247 (GRCm39) T44M probably benign Het
Fbln1 T A 15: 85,128,463 (GRCm39) C553* probably null Het
Fip1l1 T C 5: 74,731,813 (GRCm39) V310A probably damaging Het
Gast A G 11: 100,227,718 (GRCm39) D100G probably benign Het
Gk G A X: 84,756,970 (GRCm39) probably benign Het
Gm1330 G A 2: 148,841,305 (GRCm39) probably benign Het
Hspg2 C A 4: 137,296,887 (GRCm39) T4355K probably benign Het
Ipo7 T C 7: 109,648,035 (GRCm39) V639A possibly damaging Het
Lrrc7 T C 3: 157,865,929 (GRCm39) M1271V probably damaging Het
Msantd1 T A 5: 35,078,887 (GRCm39) S141T probably damaging Het
Myo9b T C 8: 71,743,650 (GRCm39) I237T probably damaging Het
Or10ag59 G A 2: 87,405,537 (GRCm39) M36I probably benign Het
Or13a21 A T 7: 139,999,507 (GRCm39) Y60N probably damaging Het
Or2w3 T C 11: 58,556,469 (GRCm39) F28S probably damaging Het
Or4k40 A C 2: 111,251,117 (GRCm39) Y60D probably damaging Het
Pan2 A T 10: 128,146,610 (GRCm39) M416L possibly damaging Het
Pank4 T C 4: 155,054,922 (GRCm39) F209L probably damaging Het
Pcdhb13 A T 18: 37,576,044 (GRCm39) I141L possibly damaging Het
Pik3r2 A G 8: 71,223,236 (GRCm39) Y422H probably benign Het
Pramel14 T C 4: 143,719,772 (GRCm39) K198E probably benign Het
Prdm4 A T 10: 85,743,781 (GRCm39) I158N probably damaging Het
Prl T G 13: 27,243,377 (GRCm39) L14R probably damaging Het
Rabl6 C A 2: 25,498,188 (GRCm39) A23S probably damaging Het
Rbm15b T A 9: 106,762,176 (GRCm39) H664L probably damaging Het
Rhobtb1 T A 10: 69,125,471 (GRCm39) H618Q probably benign Het
Slc15a1 T C 14: 121,724,452 (GRCm39) K140R probably damaging Het
Slc6a17 A G 3: 107,402,993 (GRCm39) S145P possibly damaging Het
Snx31 T C 15: 36,525,728 (GRCm39) T324A probably damaging Het
Spatc1l T C 10: 76,405,490 (GRCm39) probably benign Het
Taar7b A G 10: 23,876,882 (GRCm39) N349S probably benign Het
Tbx19 T C 1: 164,981,273 (GRCm39) I74V probably benign Het
Tmtc2 G A 10: 105,025,960 (GRCm39) T836I possibly damaging Het
Vmn2r72 C A 7: 85,387,907 (GRCm39) M552I possibly damaging Het
Washc4 A T 10: 83,405,947 (GRCm39) E481V probably damaging Het
Zc3h15 T A 2: 83,483,725 (GRCm39) N33K probably damaging 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
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
R4807:Vsig10l UTSW 7 43,113,173 (GRCm39) missense possibly damaging 0.53
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
Posted On 2015-04-16