Incidental Mutation 'R4771:Adamts20'
ID 367547
Institutional Source Beutler Lab
Gene Symbol Adamts20
Ensembl Gene ENSMUSG00000022449
Gene Name ADAM metallopeptidase with thrombospondin type 1 motif 20
Synonyms ADAMTS-20, bt
Accession Numbers
Essential gene? Probably non essential (E-score: 0.233) question?
Stock # R4771 (G1)
Quality Score 225
Status Not validated
Chromosome 15
Chromosomal Location 94166177-94329966 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) C to T at 94249516 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000121696 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000035342] [ENSMUST00000155907]
AlphaFold P59511
Predicted Effect probably null
Transcript: ENSMUST00000035342
SMART Domains Protein: ENSMUSP00000036330
Gene: ENSMUSG00000022449

DomainStartEndE-ValueType
signal peptide 1 19 N/A INTRINSIC
Pfam:Pep_M12B_propep 41 186 1.4e-30 PFAM
Pfam:Reprolysin_5 253 445 3.6e-13 PFAM
Pfam:Reprolysin_4 253 460 1.1e-7 PFAM
Pfam:Reprolysin 255 464 1.5e-26 PFAM
Pfam:Reprolysin_2 272 454 1.8e-10 PFAM
Pfam:Reprolysin_3 276 410 5.8e-10 PFAM
TSP1 556 608 7.73e-11 SMART
Pfam:ADAM_spacer1 718 836 2.6e-34 PFAM
TSP1 846 901 1.47e-1 SMART
TSP1 904 958 2.83e0 SMART
TSP1 965 1019 4.28e-4 SMART
TSP1 1020 1074 1.89e-5 SMART
TSP1 1075 1131 4.87e-8 SMART
TSP1 1152 1201 6.05e-4 SMART
TSP1 1204 1260 1.22e-8 SMART
TSP1 1304 1356 1.37e-2 SMART
TSP1 1357 1411 6e-8 SMART
TSP1 1416 1470 1.69e-2 SMART
TSP1 1471 1526 2.3e0 SMART
TSP1 1530 1579 1.23e0 SMART
TSP1 1653 1706 5.27e-4 SMART
Pfam:GON 1708 1905 5.8e-80 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000129195
Predicted Effect probably null
Transcript: ENSMUST00000155907
SMART Domains Protein: ENSMUSP00000121696
Gene: ENSMUSG00000022449

DomainStartEndE-ValueType
signal peptide 1 19 N/A INTRINSIC
Pfam:Pep_M12B_propep 40 186 1e-31 PFAM
Pfam:Reprolysin_5 253 445 2.7e-13 PFAM
Pfam:Reprolysin_4 253 460 7.2e-8 PFAM
Pfam:Reprolysin 255 464 2.4e-28 PFAM
Pfam:Reprolysin_2 272 454 4e-10 PFAM
Pfam:Reprolysin_3 276 410 1.1e-10 PFAM
TSP1 556 608 7.73e-11 SMART
Pfam:ADAM_spacer1 718 836 2e-34 PFAM
TSP1 846 901 1.47e-1 SMART
TSP1 904 958 2.83e0 SMART
TSP1 965 1019 4.28e-4 SMART
TSP1 1020 1074 1.89e-5 SMART
TSP1 1075 1131 4.87e-8 SMART
TSP1 1152 1201 6.05e-4 SMART
TSP1 1204 1260 1.22e-8 SMART
TSP1 1304 1356 1.37e-2 SMART
TSP1 1357 1411 6e-8 SMART
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.1%
  • 20x: 95.0%
Validation Efficiency
MGI Phenotype FUNCTION: This gene encodes a member of "a disintegrin and metalloproteinase with thrombospondin motifs" (ADAMTS) family of multi-domain matrix-associated metalloendopeptidases that have diverse roles in tissue morphogenesis and pathophysiological remodeling, in inflammation and in vascular biology. The encoded preproprotein undergoes proteolytic processing to generate an active protease. Certain mutations in this gene cause defective development of neural crest-derived melanoblasts resulting in a "belted" phenotype that is characterized by white spots in the lumbar region. [provided by RefSeq, Jul 2016]
PHENOTYPE: Mice homozygous for spontaneous or ENU-induced mutations exhibit abnormal coat/hair pigmentation, including a typical white belt phenotype. [provided by MGI curators]
Allele List at MGI

All alleles(17) : Targeted, other(1) Spontaneous(11) Chemically induced(5)

Other mutations in this stock
Total: 111 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2310022B05Rik T C 8: 125,366,300 (GRCm39) T148A probably benign Het
Abcc4 G T 14: 118,721,796 (GRCm39) N1234K probably benign Het
Aqp9 C T 9: 71,030,152 (GRCm39) G212S probably damaging Het
Asb15 A T 6: 24,570,621 (GRCm39) N533I probably damaging Het
Brwd1 A G 16: 95,804,518 (GRCm39) V1884A probably benign Het
Ccdc106 G A 7: 5,060,521 (GRCm39) probably null Het
Cfap46 A T 7: 139,210,524 (GRCm39) L1774Q probably null Het
Cfap95 A G 19: 23,536,337 (GRCm39) L190P probably damaging Het
Cibar1 T A 4: 12,155,689 (GRCm39) Q311L probably benign Het
Clec2h G A 6: 128,651,118 (GRCm39) E133K probably damaging Het
Cntn1 T A 15: 92,202,972 (GRCm39) F751L possibly damaging Het
Col20a1 A T 2: 180,630,917 (GRCm39) M62L probably benign Het
Col7a1 T C 9: 108,800,993 (GRCm39) V1899A probably damaging Het
Cpa5 T A 6: 30,612,684 (GRCm39) L28* probably null Het
Crb1 T A 1: 139,255,942 (GRCm39) E264D probably damaging Het
Creb3l2 A T 6: 37,311,512 (GRCm39) S426T probably benign Het
Cspg5 T A 9: 110,080,195 (GRCm39) N373K probably damaging Het
Ctso T C 3: 81,840,047 (GRCm39) S26P probably benign Het
Depdc1b A C 13: 108,519,434 (GRCm39) D348A probably benign Het
Diaph1 A T 18: 37,986,604 (GRCm39) M1127K probably damaging Het
Dlgap1 A T 17: 70,900,375 (GRCm39) K397* probably null Het
Dock3 T A 9: 106,829,557 (GRCm39) H1119L possibly damaging Het
Dok4 G T 8: 95,591,795 (GRCm39) probably null Het
Dram2 A G 3: 106,480,361 (GRCm39) T225A probably damaging Het
Dst G A 1: 34,288,565 (GRCm39) R5603H probably damaging Het
Ehbp1l1 A G 19: 5,775,996 (GRCm39) F18S probably damaging Het
Epha5 A G 5: 84,298,278 (GRCm39) V427A probably damaging Het
Exoc4 A T 6: 33,418,884 (GRCm39) probably null Het
Exph5 C T 9: 53,284,965 (GRCm39) T682I possibly damaging Het
Fnbp1l A T 3: 122,351,752 (GRCm39) S264T possibly damaging Het
Ggnbp2 A T 11: 84,725,314 (GRCm39) D580E probably benign Het
Gm10277 G A 11: 77,676,534 (GRCm39) probably benign Het
Golm2 T A 2: 121,756,126 (GRCm39) V352E probably damaging Het
Gtf2a1l C A 17: 88,997,448 (GRCm39) P93Q probably benign Het
Hydin A T 8: 111,259,515 (GRCm39) I2496F probably benign Het
Ighv7-2 A C 12: 113,876,087 (GRCm39) I6S probably benign Het
Irs1 A G 1: 82,265,696 (GRCm39) V840A probably benign Het
Itgal A G 7: 126,927,405 (GRCm39) E965G probably damaging Het
Izumo1 T G 7: 45,272,233 (GRCm39) F5V probably benign Het
Izumo1 T A 7: 45,272,234 (GRCm39) F5Y probably damaging Het
Kif13a A G 13: 46,978,687 (GRCm39) S175P probably damaging Het
Klf14 A G 6: 30,934,960 (GRCm39) F225L probably damaging Het
Kpna1 T C 16: 35,853,773 (GRCm39) Y468H probably damaging Het
Krt5 T A 15: 101,617,494 (GRCm39) Q413L probably damaging Het
Lbr T C 1: 181,665,986 (GRCm39) Y41C probably damaging Het
Lmcd1 A T 6: 112,292,834 (GRCm39) N229Y probably damaging Het
Marchf3 T A 18: 56,916,170 (GRCm39) H175L probably benign Het
Mcmbp A G 7: 128,300,124 (GRCm39) probably null Het
Med27 T A 2: 29,303,515 (GRCm39) L16Q probably damaging Het
Mex3b A T 7: 82,518,273 (GRCm39) Q196L possibly damaging Het
Mga T C 2: 119,794,775 (GRCm39) S2820P probably damaging Het
Mroh2a C T 1: 88,179,087 (GRCm39) L1104F probably damaging Het
Mta3 A G 17: 84,063,103 (GRCm39) E166G probably damaging Het
Mthfd2l A G 5: 91,096,727 (GRCm39) E116G possibly damaging Het
Musk A G 4: 58,301,706 (GRCm39) I155V probably benign Het
Myh7b G A 2: 155,468,314 (GRCm39) W834* probably null Het
Myo18b T A 5: 112,840,093 (GRCm39) R2567* probably null Het
Nars2 A T 7: 96,684,452 (GRCm39) E325V probably damaging Het
Nploc4 A G 11: 120,312,260 (GRCm39) V106A possibly damaging Het
Nudcd1 A T 15: 44,268,878 (GRCm39) S167R probably damaging Het
Nup133 T A 8: 124,656,137 (GRCm39) D448V probably damaging Het
Or5al1 G T 2: 85,990,417 (GRCm39) T99N probably benign Het
Or5p70 A T 7: 107,995,229 (GRCm39) K301* probably null Het
Pax6 C A 2: 105,526,847 (GRCm39) P251Q probably benign Het
Pcdh8 C T 14: 80,005,710 (GRCm39) A893T possibly damaging Het
Per3 A T 4: 151,093,716 (GRCm39) V1033E probably damaging Het
Polr1e T C 4: 45,019,282 (GRCm39) S44P probably damaging Het
Pou4f2 T A 8: 79,161,865 (GRCm39) H246L possibly damaging Het
Psmd2 G A 16: 20,481,429 (GRCm39) R828Q probably damaging Het
Ptprq A G 10: 107,524,288 (GRCm39) S482P probably benign Het
Rbm14 G T 19: 4,852,671 (GRCm39) probably benign Het
Reln T C 5: 22,254,698 (GRCm39) D557G probably damaging Het
Rhobtb2 A G 14: 70,034,499 (GRCm39) I242T probably benign Het
Runx1 C A 16: 92,492,629 (GRCm39) V5L possibly damaging Het
Shld2 G A 14: 33,990,663 (GRCm39) T81M probably damaging Het
Slc13a1 A T 6: 24,100,339 (GRCm39) Y381* probably null Het
Smyd3 A T 1: 178,921,961 (GRCm39) C180S probably damaging Het
Sntg2 T A 12: 30,326,658 (GRCm39) probably null Het
Snx19 G A 9: 30,344,934 (GRCm39) V678I probably damaging Het
Spag5 G A 11: 78,195,592 (GRCm39) A300T probably damaging Het
Spdl1 T A 11: 34,704,154 (GRCm39) R560W probably damaging Het
Spen T C 4: 141,199,907 (GRCm39) T2884A probably benign Het
Spg11 G A 2: 121,895,963 (GRCm39) Q1752* probably null Het
Srrm4 C A 5: 116,613,234 (GRCm39) probably null Het
Ssc4d A G 5: 135,999,074 (GRCm39) L43P probably damaging Het
Sspo A G 6: 48,437,813 (GRCm39) D1324G probably damaging Het
Tkt T G 14: 30,288,982 (GRCm39) I238S probably damaging Het
Tmem184b A T 15: 79,261,377 (GRCm39) N76K probably benign Het
Trpm6 A G 19: 18,790,857 (GRCm39) M631V probably damaging Het
Ttll6 A C 11: 96,024,655 (GRCm39) E15A possibly damaging Het
Ttn T C 2: 76,569,296 (GRCm39) D27199G probably damaging Het
Ubn2 A T 6: 38,464,088 (GRCm39) probably null Het
Ubr5 A C 15: 38,018,541 (GRCm39) I866M possibly damaging Het
Urb1 T C 16: 90,550,406 (GRCm39) T2149A probably benign Het
Ush2a G T 1: 188,529,966 (GRCm39) V3252L possibly damaging Het
Usp24 A G 4: 106,219,377 (GRCm39) probably null Het
Vill T A 9: 118,897,502 (GRCm39) M259K probably damaging Het
Vldlr T C 19: 27,217,290 (GRCm39) I411T probably damaging Het
Vmn2r120 A T 17: 57,831,887 (GRCm39) W301R probably damaging Het
Vps13b G A 15: 35,910,946 (GRCm39) S3570N probably damaging Het
Vps13c T C 9: 67,836,821 (GRCm39) V1773A probably benign Het
Vtn A G 11: 78,392,400 (GRCm39) D326G probably benign Het
Wdr93 A T 7: 79,426,511 (GRCm39) H592L probably damaging Het
Zdhhc19 A G 16: 32,317,953 (GRCm39) D94G probably damaging Het
Zfand4 A T 6: 116,291,311 (GRCm39) E188V probably damaging Het
Zfp523 C A 17: 28,420,312 (GRCm39) probably null Het
Zfp536 T C 7: 37,268,309 (GRCm39) D369G probably damaging Het
Zfp608 T A 18: 55,121,372 (GRCm39) T72S probably benign Het
Zfp804a T A 2: 82,088,286 (GRCm39) V705E probably benign Het
Zfp974 T C 7: 27,625,733 (GRCm39) T46A probably damaging Het
Zkscan4 C T 13: 21,663,416 (GRCm39) Q52* probably null Het
Other mutations in Adamts20
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00433:Adamts20 APN 15 94,292,522 (GRCm39) missense probably benign
IGL00491:Adamts20 APN 15 94,171,113 (GRCm39) missense possibly damaging 0.89
IGL00502:Adamts20 APN 15 94,301,278 (GRCm39) missense probably damaging 0.99
IGL00672:Adamts20 APN 15 94,238,986 (GRCm39) missense probably damaging 0.99
IGL00840:Adamts20 APN 15 94,180,363 (GRCm39) missense probably damaging 1.00
IGL00909:Adamts20 APN 15 94,277,694 (GRCm39) missense probably damaging 1.00
IGL01101:Adamts20 APN 15 94,241,923 (GRCm39) missense probably damaging 1.00
IGL01137:Adamts20 APN 15 94,292,492 (GRCm39) critical splice donor site probably null
IGL01457:Adamts20 APN 15 94,229,329 (GRCm39) missense probably damaging 0.97
IGL01685:Adamts20 APN 15 94,301,327 (GRCm39) missense possibly damaging 0.81
IGL01949:Adamts20 APN 15 94,223,987 (GRCm39) missense probably benign 0.08
IGL02525:Adamts20 APN 15 94,180,959 (GRCm39) splice site probably null
IGL03088:Adamts20 APN 15 94,227,795 (GRCm39) critical splice donor site probably null
IGL03175:Adamts20 APN 15 94,171,136 (GRCm39) nonsense probably null
belt UTSW 15 94,243,871 (GRCm39) missense probably damaging 1.00
buckeye UTSW 15 94,238,968 (GRCm39) missense probably damaging 1.00
jack_white UTSW 15 0 () unclassified
meowth UTSW 15 94,229,339 (GRCm39) missense probably damaging 1.00
nidoking UTSW 15 94,301,326 (GRCm39) missense probably damaging 1.00
panda UTSW 15 94,224,580 (GRCm39) intron probably benign
pikachu UTSW 15 94,243,871 (GRCm39) missense probably damaging 1.00
poliwag UTSW 15 94,292,503 (GRCm39) nonsense probably null
splotch2 UTSW 15 94,233,442 (GRCm39) intron probably benign
wash UTSW 15 94,245,551 (GRCm39) nonsense probably null
whitebelly UTSW 15 0 () unclassified
whopper UTSW 15 94,245,691 (GRCm39) missense probably damaging 1.00
R0483:Adamts20 UTSW 15 94,251,452 (GRCm39) missense probably benign 0.00
R0514:Adamts20 UTSW 15 94,168,257 (GRCm39) missense probably damaging 1.00
R0568:Adamts20 UTSW 15 94,189,594 (GRCm39) splice site probably benign
R0730:Adamts20 UTSW 15 94,245,571 (GRCm39) missense probably benign 0.00
R0973:Adamts20 UTSW 15 94,184,252 (GRCm39) missense probably benign 0.00
R1339:Adamts20 UTSW 15 94,220,777 (GRCm39) missense probably benign 0.19
R1721:Adamts20 UTSW 15 94,236,340 (GRCm39) missense probably benign 0.44
R1809:Adamts20 UTSW 15 94,238,968 (GRCm39) missense probably damaging 1.00
R1832:Adamts20 UTSW 15 94,184,225 (GRCm39) missense probably benign 0.00
R1846:Adamts20 UTSW 15 94,243,871 (GRCm39) missense probably damaging 1.00
R1867:Adamts20 UTSW 15 94,236,340 (GRCm39) missense probably benign 0.44
R1875:Adamts20 UTSW 15 94,229,277 (GRCm39) missense probably benign 0.01
R1930:Adamts20 UTSW 15 94,301,891 (GRCm39) missense probably benign 0.03
R1931:Adamts20 UTSW 15 94,301,891 (GRCm39) missense probably benign 0.03
R1932:Adamts20 UTSW 15 94,301,891 (GRCm39) missense probably benign 0.03
R2001:Adamts20 UTSW 15 94,245,599 (GRCm39) missense possibly damaging 0.96
R2116:Adamts20 UTSW 15 94,253,243 (GRCm39) missense probably damaging 1.00
R2162:Adamts20 UTSW 15 94,229,339 (GRCm39) missense probably damaging 1.00
R2350:Adamts20 UTSW 15 94,181,797 (GRCm39) missense probably damaging 1.00
R2887:Adamts20 UTSW 15 94,228,459 (GRCm39) missense probably benign 0.00
R2889:Adamts20 UTSW 15 94,228,459 (GRCm39) missense probably benign 0.00
R2890:Adamts20 UTSW 15 94,228,459 (GRCm39) missense probably benign 0.00
R3109:Adamts20 UTSW 15 94,243,785 (GRCm39) splice site probably benign
R3719:Adamts20 UTSW 15 94,259,719 (GRCm39) missense probably damaging 0.99
R3832:Adamts20 UTSW 15 94,229,339 (GRCm39) missense probably damaging 1.00
R3901:Adamts20 UTSW 15 94,226,726 (GRCm39) missense possibly damaging 0.81
R4398:Adamts20 UTSW 15 94,231,576 (GRCm39) missense possibly damaging 0.93
R4402:Adamts20 UTSW 15 94,277,827 (GRCm39) missense probably benign
R4431:Adamts20 UTSW 15 94,241,924 (GRCm39) missense probably damaging 1.00
R4479:Adamts20 UTSW 15 94,301,326 (GRCm39) missense probably damaging 1.00
R4482:Adamts20 UTSW 15 94,243,801 (GRCm39) missense probably damaging 1.00
R4503:Adamts20 UTSW 15 94,277,631 (GRCm39) missense probably damaging 0.99
R4671:Adamts20 UTSW 15 94,301,206 (GRCm39) missense possibly damaging 0.48
R4700:Adamts20 UTSW 15 94,292,503 (GRCm39) nonsense probably null
R4707:Adamts20 UTSW 15 94,231,528 (GRCm39) missense possibly damaging 0.53
R4725:Adamts20 UTSW 15 94,249,643 (GRCm39) missense probably damaging 0.99
R4829:Adamts20 UTSW 15 94,224,277 (GRCm39) missense probably benign 0.01
R4937:Adamts20 UTSW 15 94,277,656 (GRCm39) missense probably benign
R4960:Adamts20 UTSW 15 94,277,655 (GRCm39) missense probably benign
R5270:Adamts20 UTSW 15 94,180,400 (GRCm39) missense probably benign 0.00
R5388:Adamts20 UTSW 15 94,243,659 (GRCm39) missense possibly damaging 0.81
R5410:Adamts20 UTSW 15 94,179,838 (GRCm39) missense possibly damaging 0.94
R5453:Adamts20 UTSW 15 94,223,969 (GRCm39) missense possibly damaging 0.69
R5611:Adamts20 UTSW 15 94,171,161 (GRCm39) missense possibly damaging 0.65
R5687:Adamts20 UTSW 15 94,223,852 (GRCm39) missense probably benign 0.36
R5758:Adamts20 UTSW 15 94,292,531 (GRCm39) missense probably benign 0.00
R5801:Adamts20 UTSW 15 94,245,551 (GRCm39) nonsense probably null
R5834:Adamts20 UTSW 15 94,251,465 (GRCm39) missense probably damaging 0.99
R5993:Adamts20 UTSW 15 94,236,604 (GRCm39) missense probably damaging 0.99
R5997:Adamts20 UTSW 15 94,277,628 (GRCm39) missense probably damaging 1.00
R6044:Adamts20 UTSW 15 94,180,364 (GRCm39) missense probably damaging 1.00
R6058:Adamts20 UTSW 15 94,227,928 (GRCm39) nonsense probably null
R6217:Adamts20 UTSW 15 94,236,596 (GRCm39) missense probably benign 0.00
R6283:Adamts20 UTSW 15 94,249,602 (GRCm39) missense probably benign
R6354:Adamts20 UTSW 15 94,245,691 (GRCm39) missense probably damaging 1.00
R6415:Adamts20 UTSW 15 94,222,540 (GRCm39) critical splice donor site probably null
R6419:Adamts20 UTSW 15 94,231,556 (GRCm39) missense possibly damaging 0.84
R6476:Adamts20 UTSW 15 94,259,691 (GRCm39) missense probably benign 0.22
R6485:Adamts20 UTSW 15 94,241,852 (GRCm39) missense probably benign 0.17
R6517:Adamts20 UTSW 15 94,180,985 (GRCm39) splice site probably null
R6675:Adamts20 UTSW 15 94,229,197 (GRCm39) critical splice donor site probably null
R6863:Adamts20 UTSW 15 94,277,627 (GRCm39) nonsense probably null
R7186:Adamts20 UTSW 15 94,220,689 (GRCm39) missense possibly damaging 0.76
R7263:Adamts20 UTSW 15 94,220,772 (GRCm39) missense possibly damaging 0.52
R7441:Adamts20 UTSW 15 94,251,554 (GRCm39) missense probably damaging 1.00
R7519:Adamts20 UTSW 15 94,223,869 (GRCm39) missense possibly damaging 0.64
R7747:Adamts20 UTSW 15 94,189,468 (GRCm39) nonsense probably null
R7770:Adamts20 UTSW 15 94,231,579 (GRCm39) missense probably benign 0.02
R7816:Adamts20 UTSW 15 94,220,725 (GRCm39) missense probably benign 0.00
R7827:Adamts20 UTSW 15 94,223,814 (GRCm39) missense probably damaging 1.00
R7853:Adamts20 UTSW 15 94,243,871 (GRCm39) missense probably damaging 1.00
R7894:Adamts20 UTSW 15 94,249,641 (GRCm39) missense probably damaging 1.00
R7951:Adamts20 UTSW 15 94,238,947 (GRCm39) missense probably damaging 1.00
R8233:Adamts20 UTSW 15 94,189,533 (GRCm39) missense probably benign 0.19
R8458:Adamts20 UTSW 15 94,251,521 (GRCm39) missense probably benign 0.02
R8709:Adamts20 UTSW 15 94,238,947 (GRCm39) missense probably damaging 1.00
R8719:Adamts20 UTSW 15 94,241,903 (GRCm39) missense probably damaging 0.99
R8728:Adamts20 UTSW 15 94,229,281 (GRCm39) missense probably benign 0.00
R8787:Adamts20 UTSW 15 94,184,294 (GRCm39) missense possibly damaging 0.83
R8801:Adamts20 UTSW 15 94,258,490 (GRCm39) missense probably damaging 1.00
R9055:Adamts20 UTSW 15 94,181,867 (GRCm39) missense probably damaging 0.98
R9069:Adamts20 UTSW 15 94,236,349 (GRCm39) missense probably benign 0.00
R9297:Adamts20 UTSW 15 94,301,321 (GRCm39) missense possibly damaging 0.88
R9318:Adamts20 UTSW 15 94,301,321 (GRCm39) missense possibly damaging 0.88
R9362:Adamts20 UTSW 15 94,236,626 (GRCm39) missense possibly damaging 0.86
R9658:Adamts20 UTSW 15 94,249,626 (GRCm39) missense probably damaging 1.00
R9747:Adamts20 UTSW 15 94,180,943 (GRCm39) missense probably damaging 1.00
R9769:Adamts20 UTSW 15 94,251,459 (GRCm39) missense probably damaging 1.00
R9795:Adamts20 UTSW 15 94,301,180 (GRCm39) missense possibly damaging 0.78
Predicted Primers PCR Primer
(F):5'- TGCTGTGGCTATACCTTCCG -3'
(R):5'- GCCATGTGTACACGTGTATTC -3'

Sequencing Primer
(F):5'- CTGTGGCTATACCTTCCGAATAGG -3'
(R):5'- GTATTCACACTGTCCTGTTTTCTG -3'
Posted On 2015-12-29