Incidental Mutation 'R6317:Vcan'
ID 510054
Institutional Source Beutler Lab
Gene Symbol Vcan
Ensembl Gene ENSMUSG00000021614
Gene Name versican
Synonyms PG-M, hdf, heart defect, Cspg2, DPEAAE, 5430420N07Rik
MMRRC Submission 044417-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R6317 (G1)
Quality Score 225.009
Status Validated
Chromosome 13
Chromosomal Location 89803431-89890628 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 89839716 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Leucine at position 983 (I983L)
Ref Sequence ENSEMBL: ENSMUSP00000125446 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000109543] [ENSMUST00000109544] [ENSMUST00000109546] [ENSMUST00000159910]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000109543
SMART Domains Protein: ENSMUSP00000105170
Gene: ENSMUSG00000021614

DomainStartEndE-ValueType
signal peptide 1 20 N/A INTRINSIC
IG 29 148 1.4e-7 SMART
LINK 148 245 1.4e-53 SMART
LINK 249 347 8.8e-60 SMART
EGF 351 384 2.72e-7 SMART
EGF_CA 386 422 1.16e-10 SMART
CLECT 428 549 3.08e-34 SMART
CCP 555 611 1.04e-8 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000109544
SMART Domains Protein: ENSMUSP00000105171
Gene: ENSMUSG00000021614

DomainStartEndE-ValueType
signal peptide 1 20 N/A INTRINSIC
IG 29 148 1.4e-7 SMART
LINK 148 245 1.4e-53 SMART
LINK 249 347 8.8e-60 SMART
low complexity region 728 743 N/A INTRINSIC
low complexity region 1205 1219 N/A INTRINSIC
EGF 1311 1344 2.72e-7 SMART
EGF_CA 1346 1382 1.16e-10 SMART
CLECT 1388 1509 3.08e-34 SMART
CCP 1515 1571 1.04e-8 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000109546
AA Change: I1943L

PolyPhen 2 Score 0.011 (Sensitivity: 0.96; Specificity: 0.78)
SMART Domains Protein: ENSMUSP00000105173
Gene: ENSMUSG00000021614
AA Change: I1943L

DomainStartEndE-ValueType
signal peptide 1 20 N/A INTRINSIC
IG 29 148 1.4e-7 SMART
LINK 148 245 1.4e-53 SMART
LINK 249 347 8.8e-60 SMART
low complexity region 728 743 N/A INTRINSIC
low complexity region 1205 1219 N/A INTRINSIC
low complexity region 1322 1333 N/A INTRINSIC
low complexity region 1546 1569 N/A INTRINSIC
low complexity region 1837 1852 N/A INTRINSIC
low complexity region 2013 2026 N/A INTRINSIC
low complexity region 2354 2367 N/A INTRINSIC
low complexity region 2468 2482 N/A INTRINSIC
low complexity region 2719 2728 N/A INTRINSIC
EGF 3050 3083 2.72e-7 SMART
EGF_CA 3085 3121 1.16e-10 SMART
CLECT 3127 3248 3.08e-34 SMART
CCP 3254 3310 1.04e-8 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000159910
AA Change: I983L

PolyPhen 2 Score 0.221 (Sensitivity: 0.91; Specificity: 0.88)
SMART Domains Protein: ENSMUSP00000125446
Gene: ENSMUSG00000021614
AA Change: I983L

DomainStartEndE-ValueType
signal peptide 1 20 N/A INTRINSIC
IG 29 148 1.4e-7 SMART
LINK 148 245 1.4e-53 SMART
LINK 249 347 8.8e-60 SMART
low complexity region 362 373 N/A INTRINSIC
low complexity region 586 609 N/A INTRINSIC
low complexity region 877 892 N/A INTRINSIC
low complexity region 1053 1066 N/A INTRINSIC
low complexity region 1394 1407 N/A INTRINSIC
low complexity region 1508 1522 N/A INTRINSIC
low complexity region 1759 1768 N/A INTRINSIC
EGF 2090 2123 2.72e-7 SMART
EGF_CA 2125 2161 1.16e-10 SMART
CLECT 2167 2288 3.08e-34 SMART
CCP 2294 2350 1.04e-8 SMART
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.4%
  • 20x: 98.2%
Validation Efficiency 100% (62/62)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene is a member of the aggrecan/versican proteoglycan family. The protein encoded is a large chondroitin sulfate proteoglycan and is a major component of the extracellular matrix. This protein is involved in cell adhesion, proliferation, proliferation, migration and angiogenesis and plays a central role in tissue morphogenesis and maintenance. Mutations in this gene are the cause of Wagner syndrome type 1. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2009]
PHENOTYPE: Homozygotes for an insertional mutation exhibit anterior-posterior segmental defects of the heart, lack endocardial cushions of the conus and atrioventricular region, and die and around embryonic day 10.5. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 61 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930503L19Rik T C 18: 70,601,264 (GRCm39) N206S probably damaging Het
Abcf2 A T 5: 24,774,156 (GRCm39) Y315* probably null Het
Adck1 T G 12: 88,368,921 (GRCm39) V133G probably damaging Het
Aoc2 T C 11: 101,216,292 (GRCm39) F125S probably damaging Het
As3mt A G 19: 46,713,410 (GRCm39) D319G probably benign Het
Atp1a2 C G 1: 172,116,903 (GRCm39) R238P probably damaging Het
Baz1a T C 12: 55,001,585 (GRCm39) Q145R possibly damaging Het
Bhlhe22 A G 3: 18,109,778 (GRCm39) E276G probably damaging Het
Cdo1 C A 18: 46,861,104 (GRCm39) V36L probably benign Het
Ces1h A G 8: 94,084,046 (GRCm39) F388S unknown Het
Col6a5 T A 9: 105,766,266 (GRCm39) N1885Y probably damaging Het
Corin A T 5: 72,496,388 (GRCm39) C522S probably damaging Het
Csmd1 G T 8: 16,760,658 (GRCm39) T159K possibly damaging Het
Cspg4b T A 13: 113,504,802 (GRCm39) L1977H probably benign Het
Cwc27 T A 13: 104,940,769 (GRCm39) K197* probably null Het
Cyp20a1 T C 1: 60,391,283 (GRCm39) S26P probably damaging Het
Daxx T A 17: 34,130,949 (GRCm39) D321E probably damaging Het
Gria2 A C 3: 80,648,311 (GRCm39) Y142D possibly damaging Het
Gspt1 T C 16: 11,041,072 (GRCm39) probably null Het
Ighv1-80 A T 12: 115,876,265 (GRCm39) V17D probably damaging Het
Ints4 T A 7: 97,178,425 (GRCm39) L675* probably null Het
Kif13a C T 13: 46,980,233 (GRCm39) R173Q probably damaging Het
Map3k2 T C 18: 32,336,086 (GRCm39) I91T probably damaging Het
Map3k8 A G 18: 4,348,979 (GRCm39) probably null Het
Mcemp1 G A 8: 3,717,284 (GRCm39) W101* probably null Het
Naca T C 10: 127,879,993 (GRCm39) I1675T probably benign Het
Nol9 T C 4: 152,125,514 (GRCm39) F155S probably damaging Het
Obscn C A 11: 58,960,721 (GRCm39) D3406Y probably damaging Het
Obsl1 A G 1: 75,466,273 (GRCm39) V1485A possibly damaging Het
Oga A T 19: 45,760,119 (GRCm39) probably null Het
Or8a1 T C 9: 37,641,725 (GRCm39) K185E possibly damaging Het
Otog C A 7: 45,950,639 (GRCm39) P337H probably damaging Het
Patl1 T C 19: 11,898,242 (GRCm39) L140P probably damaging Het
Pcca G A 14: 122,820,035 (GRCm39) V60M probably damaging Het
Pex11g G T 8: 3,514,092 (GRCm39) D23E probably damaging Het
Phactr2 A T 10: 13,137,626 (GRCm39) M172K probably damaging Het
Plce1 G A 19: 38,512,974 (GRCm39) W91* probably null Het
Plch1 C T 3: 63,688,811 (GRCm39) W131* probably null Het
Podn A G 4: 107,884,357 (GRCm39) F44S probably damaging Het
Polr3e A G 7: 120,527,205 (GRCm39) D87G possibly damaging Het
Prmt2 T A 10: 76,058,351 (GRCm39) I153F probably benign Het
Prpf6 T C 2: 181,273,229 (GRCm39) V258A probably benign Het
Ptpn21 G T 12: 98,655,521 (GRCm39) A482E probably damaging Het
Qrich1 A T 9: 108,411,491 (GRCm39) N339Y probably damaging Het
Rabgap1 T A 2: 37,432,659 (GRCm39) V750D possibly damaging Het
Reg3d G A 6: 78,354,428 (GRCm39) P58S probably damaging Het
Rp1 A G 1: 4,112,212 (GRCm39) L1213P unknown Het
Sema6b A G 17: 56,431,047 (GRCm39) L872S probably benign Het
Serpinb7 T C 1: 107,379,436 (GRCm39) I281T probably damaging Het
Shank2 T C 7: 143,838,821 (GRCm39) V685A possibly damaging Het
Slc28a2 A G 2: 122,284,980 (GRCm39) I323V possibly damaging Het
Slc7a6 A T 8: 106,919,099 (GRCm39) I228F probably damaging Het
Slc9a9 A G 9: 94,821,512 (GRCm39) T300A possibly damaging Het
Spta1 A G 1: 174,068,653 (GRCm39) N2151S probably damaging Het
Sult2a1 T A 7: 13,569,945 (GRCm39) I96L probably benign Het
Tgm2 T C 2: 157,966,070 (GRCm39) D528G probably benign Het
Ubl7 T C 9: 57,818,456 (GRCm39) probably null Het
Vmn1r172 T C 7: 23,359,742 (GRCm39) L209P probably damaging Het
Vmn1r181 G A 7: 23,684,183 (GRCm39) R216Q probably benign Het
Vmn1r3 T C 4: 3,184,993 (GRCm39) S105G probably benign Het
Zfp644 A T 5: 106,783,711 (GRCm39) H945Q probably damaging Het
Other mutations in Vcan
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00434:Vcan APN 13 89,852,821 (GRCm39) missense probably damaging 1.00
IGL00502:Vcan APN 13 89,840,438 (GRCm39) missense probably benign
IGL00504:Vcan APN 13 89,839,394 (GRCm39) missense possibly damaging 0.70
IGL00566:Vcan APN 13 89,837,098 (GRCm39) missense probably benign 0.01
IGL00701:Vcan APN 13 89,851,845 (GRCm39) missense probably benign
IGL00743:Vcan APN 13 89,873,425 (GRCm39) missense probably damaging 0.98
IGL00962:Vcan APN 13 89,810,171 (GRCm39) missense probably damaging 1.00
IGL01085:Vcan APN 13 89,828,077 (GRCm39) missense probably damaging 1.00
IGL01317:Vcan APN 13 89,839,787 (GRCm39) missense probably benign 0.00
IGL01349:Vcan APN 13 89,852,062 (GRCm39) missense probably damaging 0.98
IGL01391:Vcan APN 13 89,852,288 (GRCm39) missense probably benign 0.19
IGL01644:Vcan APN 13 89,836,794 (GRCm39) missense probably benign 0.13
IGL01657:Vcan APN 13 89,838,705 (GRCm39) missense probably damaging 1.00
IGL01707:Vcan APN 13 89,837,864 (GRCm39) missense probably damaging 1.00
IGL01764:Vcan APN 13 89,873,507 (GRCm39) missense probably damaging 1.00
IGL01920:Vcan APN 13 89,837,324 (GRCm39) missense probably benign 0.04
IGL01989:Vcan APN 13 89,837,478 (GRCm39) missense possibly damaging 0.86
IGL01999:Vcan APN 13 89,832,557 (GRCm39) missense probably damaging 1.00
IGL02083:Vcan APN 13 89,873,684 (GRCm39) missense probably damaging 1.00
IGL02160:Vcan APN 13 89,832,612 (GRCm39) missense probably damaging 1.00
IGL02217:Vcan APN 13 89,851,196 (GRCm39) missense probably damaging 1.00
IGL02522:Vcan APN 13 89,852,968 (GRCm39) missense probably benign 0.00
IGL02527:Vcan APN 13 89,838,776 (GRCm39) missense possibly damaging 0.95
IGL02926:Vcan APN 13 89,836,742 (GRCm39) missense probably damaging 0.98
IGL03061:Vcan APN 13 89,851,394 (GRCm39) missense probably benign 0.25
IGL03331:Vcan APN 13 89,810,051 (GRCm39) missense probably damaging 1.00
IGL03352:Vcan APN 13 89,853,125 (GRCm39) missense probably benign 0.00
R0041:Vcan UTSW 13 89,810,104 (GRCm39) missense probably damaging 1.00
R0102:Vcan UTSW 13 89,851,787 (GRCm39) missense probably benign 0.01
R0102:Vcan UTSW 13 89,851,787 (GRCm39) missense probably benign 0.01
R0109:Vcan UTSW 13 89,826,192 (GRCm39) critical splice donor site probably null
R0139:Vcan UTSW 13 89,839,380 (GRCm39) missense probably damaging 1.00
R0295:Vcan UTSW 13 89,860,310 (GRCm39) missense probably benign 0.06
R0375:Vcan UTSW 13 89,839,394 (GRCm39) missense probably damaging 0.99
R0379:Vcan UTSW 13 89,851,665 (GRCm39) missense probably damaging 0.99
R0457:Vcan UTSW 13 89,851,318 (GRCm39) missense possibly damaging 0.78
R0482:Vcan UTSW 13 89,826,264 (GRCm39) missense probably damaging 1.00
R0485:Vcan UTSW 13 89,852,779 (GRCm39) missense possibly damaging 0.92
R0532:Vcan UTSW 13 89,851,891 (GRCm39) missense probably damaging 0.99
R0561:Vcan UTSW 13 89,879,583 (GRCm39) missense possibly damaging 0.86
R0561:Vcan UTSW 13 89,860,372 (GRCm39) missense probably damaging 1.00
R0636:Vcan UTSW 13 89,860,386 (GRCm39) missense probably damaging 1.00
R0636:Vcan UTSW 13 89,852,825 (GRCm39) missense probably damaging 0.99
R0680:Vcan UTSW 13 89,827,941 (GRCm39) missense probably damaging 1.00
R0849:Vcan UTSW 13 89,853,072 (GRCm39) missense possibly damaging 0.75
R1006:Vcan UTSW 13 89,833,196 (GRCm39) critical splice donor site probably null
R1104:Vcan UTSW 13 89,840,529 (GRCm39) missense probably damaging 1.00
R1118:Vcan UTSW 13 89,853,782 (GRCm39) missense probably damaging 1.00
R1137:Vcan UTSW 13 89,852,422 (GRCm39) missense probably damaging 1.00
R1199:Vcan UTSW 13 89,827,913 (GRCm39) splice site probably null
R1219:Vcan UTSW 13 89,828,023 (GRCm39) missense probably damaging 1.00
R1296:Vcan UTSW 13 89,805,675 (GRCm39) missense probably damaging 1.00
R1332:Vcan UTSW 13 89,841,174 (GRCm39) missense probably damaging 1.00
R1336:Vcan UTSW 13 89,841,174 (GRCm39) missense probably damaging 1.00
R1403:Vcan UTSW 13 89,836,603 (GRCm39) missense probably benign 0.00
R1403:Vcan UTSW 13 89,836,603 (GRCm39) missense probably benign 0.00
R1546:Vcan UTSW 13 89,841,075 (GRCm39) missense probably damaging 0.99
R1604:Vcan UTSW 13 89,837,780 (GRCm39) missense probably benign 0.42
R1616:Vcan UTSW 13 89,853,782 (GRCm39) missense probably damaging 1.00
R1636:Vcan UTSW 13 89,851,786 (GRCm39) missense possibly damaging 0.90
R1654:Vcan UTSW 13 89,810,065 (GRCm39) missense probably damaging 1.00
R1680:Vcan UTSW 13 89,851,666 (GRCm39) missense probably benign 0.19
R1694:Vcan UTSW 13 89,836,602 (GRCm39) missense probably damaging 0.98
R1712:Vcan UTSW 13 89,869,894 (GRCm39) missense probably damaging 1.00
R1754:Vcan UTSW 13 89,852,854 (GRCm39) missense probably benign 0.01
R1756:Vcan UTSW 13 89,839,800 (GRCm39) missense probably benign 0.05
R1824:Vcan UTSW 13 89,853,331 (GRCm39) missense possibly damaging 0.75
R1852:Vcan UTSW 13 89,853,511 (GRCm39) missense probably damaging 0.99
R1868:Vcan UTSW 13 89,838,990 (GRCm39) missense probably benign 0.12
R1920:Vcan UTSW 13 89,841,134 (GRCm39) missense probably damaging 1.00
R1932:Vcan UTSW 13 89,853,653 (GRCm39) missense possibly damaging 0.78
R1934:Vcan UTSW 13 89,851,045 (GRCm39) missense probably damaging 1.00
R1942:Vcan UTSW 13 89,851,543 (GRCm39) missense probably benign 0.01
R1964:Vcan UTSW 13 89,840,861 (GRCm39) missense probably benign 0.02
R1970:Vcan UTSW 13 89,837,157 (GRCm39) missense probably damaging 1.00
R2045:Vcan UTSW 13 89,839,104 (GRCm39) missense probably benign 0.00
R2110:Vcan UTSW 13 89,841,422 (GRCm39) missense probably damaging 1.00
R2111:Vcan UTSW 13 89,841,422 (GRCm39) missense probably damaging 1.00
R2112:Vcan UTSW 13 89,841,422 (GRCm39) missense probably damaging 1.00
R2136:Vcan UTSW 13 89,837,856 (GRCm39) missense probably damaging 1.00
R2158:Vcan UTSW 13 89,851,648 (GRCm39) missense possibly damaging 0.68
R2376:Vcan UTSW 13 89,851,529 (GRCm39) missense possibly damaging 0.80
R2385:Vcan UTSW 13 89,837,568 (GRCm39) missense probably damaging 1.00
R2443:Vcan UTSW 13 89,852,794 (GRCm39) missense probably damaging 1.00
R2876:Vcan UTSW 13 89,852,356 (GRCm39) missense probably damaging 1.00
R3607:Vcan UTSW 13 89,851,420 (GRCm39) missense probably damaging 0.98
R4042:Vcan UTSW 13 89,840,662 (GRCm39) missense probably benign 0.35
R4043:Vcan UTSW 13 89,840,662 (GRCm39) missense probably benign 0.35
R4044:Vcan UTSW 13 89,840,662 (GRCm39) missense probably benign 0.35
R4065:Vcan UTSW 13 89,828,006 (GRCm39) missense probably damaging 1.00
R4161:Vcan UTSW 13 89,833,277 (GRCm39) missense probably damaging 1.00
R4178:Vcan UTSW 13 89,873,666 (GRCm39) missense probably damaging 1.00
R4290:Vcan UTSW 13 89,873,605 (GRCm39) missense probably damaging 1.00
R4530:Vcan UTSW 13 89,852,147 (GRCm39) missense probably damaging 0.97
R4666:Vcan UTSW 13 89,828,053 (GRCm39) missense probably damaging 1.00
R4785:Vcan UTSW 13 89,853,908 (GRCm39) missense probably damaging 1.00
R4870:Vcan UTSW 13 89,852,858 (GRCm39) missense probably benign 0.01
R4973:Vcan UTSW 13 89,836,961 (GRCm39) missense probably benign 0.30
R5037:Vcan UTSW 13 89,852,096 (GRCm39) missense probably damaging 1.00
R5104:Vcan UTSW 13 89,805,591 (GRCm39) intron probably benign
R5124:Vcan UTSW 13 89,873,636 (GRCm39) missense probably damaging 1.00
R5129:Vcan UTSW 13 89,838,359 (GRCm39) missense probably damaging 1.00
R5198:Vcan UTSW 13 89,838,991 (GRCm39) missense probably damaging 1.00
R5240:Vcan UTSW 13 89,840,651 (GRCm39) missense probably benign 0.08
R5254:Vcan UTSW 13 89,839,719 (GRCm39) missense probably damaging 0.99
R5280:Vcan UTSW 13 89,838,405 (GRCm39) missense probably benign 0.00
R5522:Vcan UTSW 13 89,839,929 (GRCm39) missense possibly damaging 0.62
R5557:Vcan UTSW 13 89,851,231 (GRCm39) missense possibly damaging 0.77
R5568:Vcan UTSW 13 89,836,790 (GRCm39) missense probably damaging 1.00
R5578:Vcan UTSW 13 89,839,622 (GRCm39) missense probably benign 0.01
R5627:Vcan UTSW 13 89,839,254 (GRCm39) frame shift probably null
R5687:Vcan UTSW 13 89,826,253 (GRCm39) missense probably damaging 1.00
R5752:Vcan UTSW 13 89,828,069 (GRCm39) missense probably damaging 1.00
R5879:Vcan UTSW 13 89,852,071 (GRCm39) missense probably damaging 0.99
R5941:Vcan UTSW 13 89,840,810 (GRCm39) missense probably damaging 0.98
R6113:Vcan UTSW 13 89,805,655 (GRCm39) nonsense probably null
R6135:Vcan UTSW 13 89,838,045 (GRCm39) missense probably benign 0.36
R6252:Vcan UTSW 13 89,839,339 (GRCm39) nonsense probably null
R6280:Vcan UTSW 13 89,873,492 (GRCm39) missense probably damaging 1.00
R6327:Vcan UTSW 13 89,852,951 (GRCm39) missense probably damaging 0.99
R6460:Vcan UTSW 13 89,838,806 (GRCm39) missense possibly damaging 0.61
R6669:Vcan UTSW 13 89,852,850 (GRCm39) missense probably benign 0.21
R6744:Vcan UTSW 13 89,853,301 (GRCm39) missense probably damaging 1.00
R6819:Vcan UTSW 13 89,853,244 (GRCm39) missense probably benign 0.00
R6880:Vcan UTSW 13 89,860,500 (GRCm39) missense probably damaging 1.00
R6956:Vcan UTSW 13 89,837,550 (GRCm39) missense probably damaging 0.99
R6971:Vcan UTSW 13 89,826,252 (GRCm39) missense probably damaging 1.00
R6985:Vcan UTSW 13 89,828,075 (GRCm39) missense probably damaging 1.00
R6994:Vcan UTSW 13 89,841,526 (GRCm39) missense possibly damaging 0.94
R6997:Vcan UTSW 13 89,838,737 (GRCm39) missense probably damaging 0.98
R7029:Vcan UTSW 13 89,838,360 (GRCm39) missense probably damaging 1.00
R7066:Vcan UTSW 13 89,853,805 (GRCm39) missense probably damaging 1.00
R7156:Vcan UTSW 13 89,837,229 (GRCm39) missense possibly damaging 0.95
R7171:Vcan UTSW 13 89,873,710 (GRCm39) missense probably damaging 1.00
R7176:Vcan UTSW 13 89,837,055 (GRCm39) missense probably benign 0.01
R7229:Vcan UTSW 13 89,853,389 (GRCm39) missense possibly damaging 0.87
R7250:Vcan UTSW 13 89,879,576 (GRCm39) critical splice donor site probably null
R7250:Vcan UTSW 13 89,869,805 (GRCm39) missense probably damaging 1.00
R7262:Vcan UTSW 13 89,853,280 (GRCm39) missense possibly damaging 0.62
R7289:Vcan UTSW 13 89,840,852 (GRCm39) nonsense probably null
R7299:Vcan UTSW 13 89,853,385 (GRCm39) missense probably benign
R7301:Vcan UTSW 13 89,853,385 (GRCm39) missense probably benign
R7425:Vcan UTSW 13 89,837,951 (GRCm39) missense probably damaging 0.99
R7514:Vcan UTSW 13 89,852,237 (GRCm39) missense probably damaging 0.97
R7579:Vcan UTSW 13 89,840,577 (GRCm39) missense probably damaging 1.00
R7618:Vcan UTSW 13 89,840,342 (GRCm39) missense probably damaging 0.99
R7655:Vcan UTSW 13 89,833,233 (GRCm39) missense probably damaging 1.00
R7656:Vcan UTSW 13 89,833,233 (GRCm39) missense probably damaging 1.00
R7676:Vcan UTSW 13 89,839,908 (GRCm39) missense probably damaging 1.00
R7719:Vcan UTSW 13 89,852,738 (GRCm39) missense probably damaging 0.98
R7753:Vcan UTSW 13 89,837,442 (GRCm39) missense probably damaging 1.00
R7762:Vcan UTSW 13 89,841,056 (GRCm39) missense probably damaging 1.00
R7778:Vcan UTSW 13 89,836,773 (GRCm39) missense probably damaging 1.00
R7824:Vcan UTSW 13 89,836,773 (GRCm39) missense probably damaging 1.00
R7995:Vcan UTSW 13 89,839,977 (GRCm39) missense probably benign
R7998:Vcan UTSW 13 89,852,446 (GRCm39) missense probably damaging 1.00
R8033:Vcan UTSW 13 89,852,479 (GRCm39) missense probably benign 0.04
R8061:Vcan UTSW 13 89,805,409 (GRCm39) missense probably benign 0.45
R8103:Vcan UTSW 13 89,851,439 (GRCm39) nonsense probably null
R8103:Vcan UTSW 13 89,805,777 (GRCm39) missense probably damaging 1.00
R8124:Vcan UTSW 13 89,852,373 (GRCm39) missense possibly damaging 0.93
R8162:Vcan UTSW 13 89,853,106 (GRCm39) nonsense probably null
R8166:Vcan UTSW 13 89,840,855 (GRCm39) missense probably benign 0.02
R8274:Vcan UTSW 13 89,853,089 (GRCm39) missense probably benign 0.02
R8284:Vcan UTSW 13 89,852,454 (GRCm39) missense possibly damaging 0.68
R8417:Vcan UTSW 13 89,836,862 (GRCm39) missense probably benign 0.19
R8696:Vcan UTSW 13 89,839,217 (GRCm39) missense probably benign 0.00
R8738:Vcan UTSW 13 89,840,439 (GRCm39) missense probably benign 0.17
R8792:Vcan UTSW 13 89,840,230 (GRCm39) missense possibly damaging 0.91
R8887:Vcan UTSW 13 89,853,026 (GRCm39) missense probably benign
R9049:Vcan UTSW 13 89,826,224 (GRCm39) missense probably damaging 1.00
R9074:Vcan UTSW 13 89,839,146 (GRCm39) missense possibly damaging 0.95
R9095:Vcan UTSW 13 89,852,644 (GRCm39) missense probably benign 0.32
R9172:Vcan UTSW 13 89,828,050 (GRCm39) missense probably damaging 1.00
R9199:Vcan UTSW 13 89,838,615 (GRCm39) nonsense probably null
R9259:Vcan UTSW 13 89,838,989 (GRCm39) missense probably damaging 0.99
R9455:Vcan UTSW 13 89,837,452 (GRCm39) missense probably damaging 1.00
R9476:Vcan UTSW 13 89,851,531 (GRCm39) missense possibly damaging 0.95
R9477:Vcan UTSW 13 89,841,128 (GRCm39) missense probably damaging 1.00
R9555:Vcan UTSW 13 89,839,659 (GRCm39) missense
R9579:Vcan UTSW 13 89,837,713 (GRCm39) missense possibly damaging 0.67
R9606:Vcan UTSW 13 89,853,491 (GRCm39) missense probably damaging 1.00
R9645:Vcan UTSW 13 89,841,081 (GRCm39) missense probably benign 0.00
R9659:Vcan UTSW 13 89,839,860 (GRCm39) missense probably damaging 0.99
R9766:Vcan UTSW 13 89,839,247 (GRCm39) missense probably benign 0.00
R9778:Vcan UTSW 13 89,837,930 (GRCm39) missense probably damaging 1.00
X0058:Vcan UTSW 13 89,840,612 (GRCm39) missense probably benign 0.21
X0065:Vcan UTSW 13 89,853,868 (GRCm39) missense probably damaging 0.96
Z1176:Vcan UTSW 13 89,840,690 (GRCm39) missense probably benign 0.10
Z1177:Vcan UTSW 13 89,852,192 (GRCm39) missense probably damaging 1.00
Z1177:Vcan UTSW 13 89,851,907 (GRCm39) nonsense probably null
Z1177:Vcan UTSW 13 89,851,643 (GRCm39) missense probably benign 0.00
Predicted Primers PCR Primer
(F):5'- AGCTAGTGGAAGCACTGGAC -3'
(R):5'- CTGGAGTTATGAGCCAGACATC -3'

Sequencing Primer
(F):5'- CCAACAGAGCTCCTGACTGAGG -3'
(R):5'- CGCAGAAGACACTGATTTCTG -3'
Posted On 2018-04-02