Incidental Mutation 'R1387:Adamtsl1'
ID |
162411 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Adamtsl1
|
Ensembl Gene |
ENSMUSG00000066113 |
Gene Name |
ADAMTS-like 1 |
Synonyms |
punctin-1, 5930437A14Rik, 6720426B09Rik |
MMRRC Submission |
039449-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.238)
|
Stock # |
R1387 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
4 |
Chromosomal Location |
85432409-86346622 bp(+) (GRCm39) |
Type of Mutation |
splice site |
DNA Base Change (assembly) |
T to C
at 86293230 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000119278
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000107178]
[ENSMUST00000141889]
|
AlphaFold |
Q8BLI0 |
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000107177
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000107178
|
SMART Domains |
Protein: ENSMUSP00000102796 Gene: ENSMUSG00000066113
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
28 |
N/A |
INTRINSIC |
TSP1
|
36 |
82 |
8.95e-7 |
SMART |
TSP1
|
301 |
360 |
4.35e-2 |
SMART |
TSP1
|
362 |
421 |
2.05e-2 |
SMART |
TSP1
|
422 |
476 |
3.99e-4 |
SMART |
TSP1
|
508 |
567 |
6.39e-3 |
SMART |
TSP1
|
593 |
650 |
7.86e-3 |
SMART |
TSP1
|
652 |
712 |
3.78e-5 |
SMART |
TSP1
|
715 |
772 |
2.66e-2 |
SMART |
TSP1
|
774 |
833 |
1.62e-4 |
SMART |
IGc2
|
873 |
937 |
4.19e-6 |
SMART |
low complexity region
|
1123 |
1142 |
N/A |
INTRINSIC |
IGc2
|
1175 |
1240 |
1.31e-7 |
SMART |
IGc2
|
1282 |
1351 |
7.81e-15 |
SMART |
IGc2
|
1400 |
1467 |
2.39e-10 |
SMART |
TSP1
|
1481 |
1537 |
2.12e-1 |
SMART |
TSP1
|
1540 |
1599 |
1.74e-4 |
SMART |
TSP1
|
1600 |
1658 |
8.2e0 |
SMART |
TSP1
|
1660 |
1717 |
1.96e-1 |
SMART |
Pfam:PLAC
|
1721 |
1751 |
1.4e-9 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000141889
|
SMART Domains |
Protein: ENSMUSP00000119278 Gene: ENSMUSG00000066113
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
28 |
N/A |
INTRINSIC |
TSP1
|
36 |
82 |
8.95e-7 |
SMART |
TSP1
|
301 |
360 |
4.35e-2 |
SMART |
TSP1
|
379 |
438 |
2.05e-2 |
SMART |
TSP1
|
439 |
493 |
3.99e-4 |
SMART |
TSP1
|
525 |
584 |
6.39e-3 |
SMART |
TSP1
|
610 |
667 |
7.86e-3 |
SMART |
TSP1
|
707 |
764 |
2.66e-2 |
SMART |
TSP1
|
766 |
825 |
1.62e-4 |
SMART |
IGc2
|
865 |
929 |
4.19e-6 |
SMART |
low complexity region
|
1115 |
1134 |
N/A |
INTRINSIC |
IGc2
|
1167 |
1232 |
1.31e-7 |
SMART |
IGc2
|
1274 |
1343 |
7.81e-15 |
SMART |
IGc2
|
1392 |
1459 |
2.39e-10 |
SMART |
TSP1
|
1473 |
1529 |
2.12e-1 |
SMART |
TSP1
|
1532 |
1591 |
1.74e-4 |
SMART |
TSP1
|
1592 |
1650 |
8.2e0 |
SMART |
TSP1
|
1652 |
1709 |
1.96e-1 |
SMART |
Pfam:PLAC
|
1712 |
1744 |
5.6e-12 |
PFAM |
|
Coding Region Coverage |
- 1x: 98.9%
- 3x: 97.9%
- 10x: 95.1%
- 20x: 88.4%
|
Validation Efficiency |
99% (82/83) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a secreted protein and member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motif) family. This protein lacks the metalloproteinase and disintegrin-like domains, which are typical of the ADAMTS family, but contains other ADAMTS domains, including the thrombospondin type 1 motif. This protein may have important functions in the extracellular matrix. Alternative splicing results in multiple transcript variants encoding distinct proteins. [provided by RefSeq, Jul 2008]
|
Allele List at MGI |
All alleles(3) : Gene trapped(3) |
Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610303G11Rik |
T |
A |
9: 98,068,812 (GRCm39) |
|
noncoding transcript |
Het |
4930447C04Rik |
C |
A |
12: 72,962,208 (GRCm39) |
R52L |
probably benign |
Het |
Abca13 |
C |
T |
11: 9,632,085 (GRCm39) |
Q5002* |
probably null |
Het |
Acacb |
T |
C |
5: 114,338,573 (GRCm39) |
I761T |
probably benign |
Het |
Acap3 |
G |
T |
4: 155,983,937 (GRCm39) |
L134F |
probably benign |
Het |
Adgrv1 |
A |
G |
13: 81,641,295 (GRCm39) |
V3278A |
possibly damaging |
Het |
Agxt2 |
T |
C |
15: 10,380,696 (GRCm39) |
Y196H |
probably damaging |
Het |
Akap13 |
T |
C |
7: 75,235,941 (GRCm39) |
V172A |
probably damaging |
Het |
Aqp8 |
A |
G |
7: 123,065,891 (GRCm39) |
I229V |
probably benign |
Het |
Atp8a2 |
T |
C |
14: 60,097,719 (GRCm39) |
K770E |
probably benign |
Het |
Brd10 |
A |
G |
19: 29,700,853 (GRCm39) |
I812T |
probably benign |
Het |
Cacng8 |
T |
C |
7: 3,463,672 (GRCm39) |
S275P |
possibly damaging |
Het |
Catsperg1 |
T |
C |
7: 28,906,289 (GRCm39) |
Y138C |
probably damaging |
Het |
Ccdc93 |
T |
G |
1: 121,418,918 (GRCm39) |
L491R |
probably damaging |
Het |
Cntnap2 |
T |
C |
6: 47,084,848 (GRCm39) |
V1103A |
probably benign |
Het |
Col12a1 |
C |
T |
9: 79,588,657 (GRCm39) |
|
probably benign |
Het |
Col6a3 |
A |
G |
1: 90,750,138 (GRCm39) |
|
probably benign |
Het |
Csf2rb2 |
C |
T |
15: 78,182,414 (GRCm39) |
A6T |
probably damaging |
Het |
Cyp2j5 |
T |
A |
4: 96,522,522 (GRCm39) |
S351C |
probably damaging |
Het |
Cyth1 |
A |
G |
11: 118,073,172 (GRCm39) |
|
probably benign |
Het |
Dock2 |
A |
G |
11: 34,223,309 (GRCm39) |
|
probably benign |
Het |
Duoxa1 |
T |
A |
2: 122,134,468 (GRCm39) |
I262F |
possibly damaging |
Het |
Dync2h1 |
T |
C |
9: 7,125,816 (GRCm39) |
D1930G |
probably benign |
Het |
Eeig1 |
T |
C |
2: 32,455,635 (GRCm39) |
S254P |
possibly damaging |
Het |
Eno1 |
C |
T |
4: 150,332,590 (GRCm39) |
|
probably benign |
Het |
Fam98a |
T |
A |
17: 75,845,264 (GRCm39) |
H494L |
unknown |
Het |
Fcamr |
C |
A |
1: 130,732,379 (GRCm39) |
T122K |
possibly damaging |
Het |
Foxq1 |
A |
G |
13: 31,743,288 (GRCm39) |
D130G |
probably damaging |
Het |
Glb1 |
T |
A |
9: 114,249,431 (GRCm39) |
W5R |
probably damaging |
Het |
Gm17661 |
GA |
GAA |
2: 90,917,709 (GRCm38) |
|
noncoding transcript |
Het |
Gm5431 |
T |
A |
11: 48,785,842 (GRCm39) |
R178W |
possibly damaging |
Het |
Gys2 |
C |
T |
6: 142,407,009 (GRCm39) |
V116M |
probably benign |
Het |
Hif1a |
C |
T |
12: 73,989,066 (GRCm39) |
T651I |
possibly damaging |
Het |
Itgb5 |
T |
A |
16: 33,720,885 (GRCm39) |
Y3* |
probably null |
Het |
Kank3 |
A |
G |
17: 34,035,205 (GRCm39) |
N7S |
possibly damaging |
Het |
Kdm2b |
G |
T |
5: 123,018,331 (GRCm39) |
H981Q |
probably damaging |
Het |
Kdm6a |
C |
T |
X: 18,120,235 (GRCm39) |
|
probably benign |
Het |
Kif1a |
A |
T |
1: 92,983,672 (GRCm39) |
|
probably benign |
Het |
Knl1 |
T |
A |
2: 118,901,211 (GRCm39) |
S971T |
possibly damaging |
Het |
Lcn6 |
T |
C |
2: 25,567,149 (GRCm39) |
V50A |
possibly damaging |
Het |
Llgl2 |
G |
T |
11: 115,743,958 (GRCm39) |
V762F |
probably damaging |
Het |
Lpcat4 |
T |
C |
2: 112,075,021 (GRCm39) |
F342L |
probably benign |
Het |
Lrp2 |
C |
A |
2: 69,287,262 (GRCm39) |
G3725V |
probably damaging |
Het |
Map1b |
T |
C |
13: 99,569,158 (GRCm39) |
T1188A |
unknown |
Het |
Mecp2 |
G |
A |
X: 73,079,394 (GRCm39) |
P362S |
possibly damaging |
Het |
Mideas |
C |
A |
12: 84,199,705 (GRCm39) |
R1005L |
probably damaging |
Het |
Mmp13 |
T |
A |
9: 7,282,033 (GRCm39) |
F445Y |
possibly damaging |
Het |
Myo5b |
G |
T |
18: 74,777,272 (GRCm39) |
|
probably benign |
Het |
Myo7b |
A |
G |
18: 32,116,805 (GRCm39) |
|
probably benign |
Het |
Nadk2 |
C |
A |
15: 9,106,870 (GRCm39) |
L384I |
possibly damaging |
Het |
Napg |
A |
G |
18: 63,119,283 (GRCm39) |
I98V |
possibly damaging |
Het |
Ncoa1 |
G |
T |
12: 4,324,790 (GRCm39) |
N1041K |
probably benign |
Het |
Nmu |
A |
T |
5: 76,497,992 (GRCm39) |
C64* |
probably null |
Het |
Nobox |
T |
A |
6: 43,284,132 (GRCm39) |
K13M |
probably damaging |
Het |
Nos1 |
T |
C |
5: 118,091,848 (GRCm39) |
|
probably benign |
Het |
Nrg2 |
A |
G |
18: 36,329,792 (GRCm39) |
V141A |
probably damaging |
Het |
Or1b1 |
T |
G |
2: 36,994,880 (GRCm39) |
I261L |
probably benign |
Het |
Or2aj5 |
T |
C |
16: 19,424,777 (GRCm39) |
I214V |
probably damaging |
Het |
Or55b4 |
T |
A |
7: 102,133,911 (GRCm39) |
I139L |
probably benign |
Het |
Phldb2 |
C |
T |
16: 45,646,357 (GRCm39) |
E71K |
possibly damaging |
Het |
Pik3r4 |
T |
A |
9: 105,521,490 (GRCm39) |
Y19N |
probably damaging |
Het |
Pkhd1 |
A |
C |
1: 20,625,447 (GRCm39) |
|
probably benign |
Het |
Pogk |
G |
T |
1: 166,227,707 (GRCm39) |
P148Q |
possibly damaging |
Het |
Pten |
G |
T |
19: 32,775,496 (GRCm39) |
A79S |
probably benign |
Het |
Ptpdc1 |
A |
T |
13: 48,739,796 (GRCm39) |
V545E |
possibly damaging |
Het |
Qdpr |
G |
C |
5: 45,607,480 (GRCm39) |
|
probably benign |
Het |
Rhbdd3 |
T |
A |
11: 5,054,121 (GRCm39) |
H83Q |
probably damaging |
Het |
Rnf6 |
A |
G |
5: 146,148,055 (GRCm39) |
V321A |
probably benign |
Het |
Rtf1 |
T |
A |
2: 119,536,126 (GRCm39) |
|
probably null |
Het |
Serpina10 |
C |
T |
12: 103,594,500 (GRCm39) |
V240I |
probably benign |
Het |
Siah2 |
A |
G |
3: 58,598,935 (GRCm39) |
V101A |
possibly damaging |
Het |
Taok3 |
A |
G |
5: 117,344,720 (GRCm39) |
K46R |
probably damaging |
Het |
Tcaf2 |
A |
C |
6: 42,601,512 (GRCm39) |
L849R |
probably damaging |
Het |
Upf3a |
T |
C |
8: 13,842,118 (GRCm39) |
F178S |
probably damaging |
Het |
Vmn1r218 |
G |
A |
13: 23,321,478 (GRCm39) |
G195D |
probably damaging |
Het |
Vmn2r59 |
A |
G |
7: 41,695,521 (GRCm39) |
V297A |
probably damaging |
Het |
Vmn2r70 |
T |
A |
7: 85,207,969 (GRCm39) |
Q836L |
probably benign |
Het |
Zfp473 |
A |
G |
7: 44,382,365 (GRCm39) |
V655A |
probably benign |
Het |
Zic5 |
A |
G |
14: 122,696,897 (GRCm39) |
S573P |
unknown |
Het |
|
Other mutations in Adamtsl1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00231:Adamtsl1
|
APN |
4 |
86,303,877 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00741:Adamtsl1
|
APN |
4 |
86,195,185 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00770:Adamtsl1
|
APN |
4 |
86,306,776 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL00774:Adamtsl1
|
APN |
4 |
86,306,776 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL00826:Adamtsl1
|
APN |
4 |
86,075,041 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00938:Adamtsl1
|
APN |
4 |
86,260,515 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01012:Adamtsl1
|
APN |
4 |
86,260,426 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01728:Adamtsl1
|
APN |
4 |
86,029,074 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01801:Adamtsl1
|
APN |
4 |
86,117,559 (GRCm39) |
missense |
probably benign |
0.23 |
IGL01922:Adamtsl1
|
APN |
4 |
86,168,139 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02006:Adamtsl1
|
APN |
4 |
86,117,582 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02192:Adamtsl1
|
APN |
4 |
86,146,253 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02351:Adamtsl1
|
APN |
4 |
86,075,110 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02358:Adamtsl1
|
APN |
4 |
86,075,110 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02373:Adamtsl1
|
APN |
4 |
86,168,042 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02660:Adamtsl1
|
APN |
4 |
86,150,847 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02964:Adamtsl1
|
APN |
4 |
86,342,594 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03233:Adamtsl1
|
APN |
4 |
86,260,357 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03297:Adamtsl1
|
APN |
4 |
86,341,663 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03326:Adamtsl1
|
APN |
4 |
86,170,985 (GRCm39) |
splice site |
probably benign |
|
PIT4378001:Adamtsl1
|
UTSW |
4 |
86,117,601 (GRCm39) |
missense |
possibly damaging |
0.93 |
PIT4418001:Adamtsl1
|
UTSW |
4 |
86,161,961 (GRCm39) |
missense |
probably damaging |
1.00 |
R0131:Adamtsl1
|
UTSW |
4 |
86,260,960 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0131:Adamtsl1
|
UTSW |
4 |
86,260,960 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0132:Adamtsl1
|
UTSW |
4 |
86,260,960 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0453:Adamtsl1
|
UTSW |
4 |
86,150,852 (GRCm39) |
missense |
probably damaging |
1.00 |
R0480:Adamtsl1
|
UTSW |
4 |
86,171,055 (GRCm39) |
missense |
probably benign |
0.08 |
R0496:Adamtsl1
|
UTSW |
4 |
86,259,435 (GRCm39) |
missense |
probably damaging |
1.00 |
R0538:Adamtsl1
|
UTSW |
4 |
86,261,358 (GRCm39) |
missense |
probably benign |
0.27 |
R0547:Adamtsl1
|
UTSW |
4 |
86,274,592 (GRCm39) |
missense |
probably benign |
0.37 |
R0567:Adamtsl1
|
UTSW |
4 |
86,146,253 (GRCm39) |
missense |
probably damaging |
1.00 |
R0568:Adamtsl1
|
UTSW |
4 |
86,336,789 (GRCm39) |
missense |
probably damaging |
1.00 |
R0639:Adamtsl1
|
UTSW |
4 |
86,195,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R0931:Adamtsl1
|
UTSW |
4 |
86,168,084 (GRCm39) |
missense |
probably benign |
0.05 |
R1186:Adamtsl1
|
UTSW |
4 |
86,306,746 (GRCm39) |
missense |
probably benign |
0.00 |
R1459:Adamtsl1
|
UTSW |
4 |
86,344,102 (GRCm39) |
missense |
probably damaging |
1.00 |
R1518:Adamtsl1
|
UTSW |
4 |
86,260,840 (GRCm39) |
missense |
probably damaging |
0.99 |
R1532:Adamtsl1
|
UTSW |
4 |
86,166,302 (GRCm39) |
missense |
probably benign |
0.02 |
R1603:Adamtsl1
|
UTSW |
4 |
86,333,767 (GRCm39) |
missense |
probably benign |
|
R1931:Adamtsl1
|
UTSW |
4 |
86,260,648 (GRCm39) |
missense |
possibly damaging |
0.62 |
R2086:Adamtsl1
|
UTSW |
4 |
86,146,249 (GRCm39) |
missense |
probably damaging |
1.00 |
R2221:Adamtsl1
|
UTSW |
4 |
86,306,762 (GRCm39) |
missense |
probably benign |
0.19 |
R2223:Adamtsl1
|
UTSW |
4 |
86,306,762 (GRCm39) |
missense |
probably benign |
0.19 |
R2396:Adamtsl1
|
UTSW |
4 |
86,261,356 (GRCm39) |
nonsense |
probably null |
|
R2397:Adamtsl1
|
UTSW |
4 |
86,117,594 (GRCm39) |
missense |
probably damaging |
1.00 |
R2426:Adamtsl1
|
UTSW |
4 |
86,075,025 (GRCm39) |
missense |
probably benign |
0.01 |
R3121:Adamtsl1
|
UTSW |
4 |
86,255,246 (GRCm39) |
missense |
probably damaging |
1.00 |
R3715:Adamtsl1
|
UTSW |
4 |
86,135,213 (GRCm39) |
missense |
probably benign |
0.01 |
R3848:Adamtsl1
|
UTSW |
4 |
86,336,783 (GRCm39) |
missense |
probably damaging |
1.00 |
R3849:Adamtsl1
|
UTSW |
4 |
86,336,783 (GRCm39) |
missense |
probably damaging |
1.00 |
R3850:Adamtsl1
|
UTSW |
4 |
86,336,783 (GRCm39) |
missense |
probably damaging |
1.00 |
R4194:Adamtsl1
|
UTSW |
4 |
85,972,245 (GRCm39) |
intron |
probably benign |
|
R4354:Adamtsl1
|
UTSW |
4 |
86,074,921 (GRCm39) |
missense |
probably damaging |
1.00 |
R4795:Adamtsl1
|
UTSW |
4 |
86,162,006 (GRCm39) |
critical splice donor site |
probably null |
|
R4830:Adamtsl1
|
UTSW |
4 |
86,274,619 (GRCm39) |
missense |
probably damaging |
0.97 |
R4874:Adamtsl1
|
UTSW |
4 |
86,260,729 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4939:Adamtsl1
|
UTSW |
4 |
86,161,962 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4942:Adamtsl1
|
UTSW |
4 |
86,259,451 (GRCm39) |
nonsense |
probably null |
|
R4947:Adamtsl1
|
UTSW |
4 |
85,683,037 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4960:Adamtsl1
|
UTSW |
4 |
86,342,410 (GRCm39) |
nonsense |
probably null |
|
R4971:Adamtsl1
|
UTSW |
4 |
86,255,168 (GRCm39) |
missense |
probably damaging |
1.00 |
R5141:Adamtsl1
|
UTSW |
4 |
86,075,087 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5213:Adamtsl1
|
UTSW |
4 |
86,303,865 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5237:Adamtsl1
|
UTSW |
4 |
86,303,906 (GRCm39) |
critical splice donor site |
probably null |
|
R5250:Adamtsl1
|
UTSW |
4 |
86,135,182 (GRCm39) |
nonsense |
probably null |
|
R5411:Adamtsl1
|
UTSW |
4 |
86,306,650 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5554:Adamtsl1
|
UTSW |
4 |
86,195,182 (GRCm39) |
missense |
possibly damaging |
0.69 |
R5631:Adamtsl1
|
UTSW |
4 |
86,195,160 (GRCm39) |
nonsense |
probably null |
|
R5739:Adamtsl1
|
UTSW |
4 |
86,150,901 (GRCm39) |
missense |
probably damaging |
1.00 |
R5905:Adamtsl1
|
UTSW |
4 |
86,260,561 (GRCm39) |
missense |
probably damaging |
1.00 |
R6028:Adamtsl1
|
UTSW |
4 |
86,260,561 (GRCm39) |
missense |
probably damaging |
1.00 |
R6044:Adamtsl1
|
UTSW |
4 |
86,130,928 (GRCm39) |
missense |
probably damaging |
1.00 |
R6261:Adamtsl1
|
UTSW |
4 |
86,255,115 (GRCm39) |
missense |
probably benign |
0.09 |
R6300:Adamtsl1
|
UTSW |
4 |
86,166,254 (GRCm39) |
missense |
probably damaging |
1.00 |
R6332:Adamtsl1
|
UTSW |
4 |
86,135,248 (GRCm39) |
missense |
probably damaging |
0.96 |
R6560:Adamtsl1
|
UTSW |
4 |
86,255,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R6693:Adamtsl1
|
UTSW |
4 |
86,261,123 (GRCm39) |
missense |
probably benign |
0.27 |
R6736:Adamtsl1
|
UTSW |
4 |
86,260,484 (GRCm39) |
missense |
probably damaging |
1.00 |
R6964:Adamtsl1
|
UTSW |
4 |
86,075,091 (GRCm39) |
missense |
probably damaging |
1.00 |
R7064:Adamtsl1
|
UTSW |
4 |
86,260,278 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7434:Adamtsl1
|
UTSW |
4 |
86,344,115 (GRCm39) |
missense |
probably damaging |
0.99 |
R7477:Adamtsl1
|
UTSW |
4 |
86,333,888 (GRCm39) |
missense |
probably damaging |
1.00 |
R7545:Adamtsl1
|
UTSW |
4 |
85,683,092 (GRCm39) |
missense |
probably damaging |
1.00 |
R7556:Adamtsl1
|
UTSW |
4 |
86,195,358 (GRCm39) |
missense |
probably benign |
0.19 |
R7580:Adamtsl1
|
UTSW |
4 |
85,972,301 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7593:Adamtsl1
|
UTSW |
4 |
86,259,450 (GRCm39) |
missense |
probably damaging |
1.00 |
R7710:Adamtsl1
|
UTSW |
4 |
86,150,810 (GRCm39) |
missense |
|
|
R7908:Adamtsl1
|
UTSW |
4 |
86,274,676 (GRCm39) |
missense |
probably benign |
0.02 |
R7934:Adamtsl1
|
UTSW |
4 |
86,161,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R8056:Adamtsl1
|
UTSW |
4 |
86,260,269 (GRCm39) |
missense |
possibly damaging |
0.76 |
R8109:Adamtsl1
|
UTSW |
4 |
86,166,306 (GRCm39) |
missense |
|
|
R8143:Adamtsl1
|
UTSW |
4 |
86,260,492 (GRCm39) |
missense |
possibly damaging |
0.71 |
R8205:Adamtsl1
|
UTSW |
4 |
86,117,650 (GRCm39) |
makesense |
probably null |
|
R8215:Adamtsl1
|
UTSW |
4 |
86,261,382 (GRCm39) |
missense |
probably benign |
0.45 |
R8250:Adamtsl1
|
UTSW |
4 |
86,260,846 (GRCm39) |
missense |
probably damaging |
1.00 |
R8261:Adamtsl1
|
UTSW |
4 |
86,195,120 (GRCm39) |
missense |
probably damaging |
0.99 |
R8417:Adamtsl1
|
UTSW |
4 |
86,074,926 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8494:Adamtsl1
|
UTSW |
4 |
86,240,221 (GRCm39) |
missense |
probably damaging |
0.99 |
R8516:Adamtsl1
|
UTSW |
4 |
86,260,780 (GRCm39) |
missense |
probably damaging |
1.00 |
R8525:Adamtsl1
|
UTSW |
4 |
86,195,247 (GRCm39) |
missense |
probably damaging |
1.00 |
R8688:Adamtsl1
|
UTSW |
4 |
86,166,263 (GRCm39) |
missense |
|
|
R8698:Adamtsl1
|
UTSW |
4 |
86,306,714 (GRCm39) |
missense |
probably benign |
0.01 |
R8778:Adamtsl1
|
UTSW |
4 |
85,432,687 (GRCm39) |
missense |
probably benign |
0.01 |
R9015:Adamtsl1
|
UTSW |
4 |
86,150,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R9127:Adamtsl1
|
UTSW |
4 |
86,208,027 (GRCm39) |
missense |
probably benign |
|
R9326:Adamtsl1
|
UTSW |
4 |
86,150,804 (GRCm39) |
missense |
possibly damaging |
0.70 |
R9336:Adamtsl1
|
UTSW |
4 |
86,240,264 (GRCm39) |
missense |
probably benign |
0.00 |
R9394:Adamtsl1
|
UTSW |
4 |
86,135,225 (GRCm39) |
missense |
|
|
R9416:Adamtsl1
|
UTSW |
4 |
86,342,477 (GRCm39) |
missense |
probably damaging |
1.00 |
R9571:Adamtsl1
|
UTSW |
4 |
86,117,543 (GRCm39) |
missense |
probably benign |
0.00 |
R9627:Adamtsl1
|
UTSW |
4 |
86,306,762 (GRCm39) |
missense |
possibly damaging |
0.48 |
R9675:Adamtsl1
|
UTSW |
4 |
86,161,989 (GRCm39) |
missense |
probably damaging |
1.00 |
R9798:Adamtsl1
|
UTSW |
4 |
86,074,927 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1176:Adamtsl1
|
UTSW |
4 |
86,260,930 (GRCm39) |
missense |
probably benign |
0.30 |
Z1176:Adamtsl1
|
UTSW |
4 |
86,260,414 (GRCm39) |
missense |
probably damaging |
0.99 |
|
Predicted Primers |
PCR Primer
(F):5'- AGTTTCTCCTCCAGGCAAAACATGG -3'
(R):5'- TAGCGCCTCCTTTAGTCTACCAGG -3'
Sequencing Primer
(F):5'- CGATGTTGTTGATGAGAGATCAC -3'
(R):5'- CTCCTTTAGTCTACCAGGCTTAG -3'
|
Posted On |
2014-03-17 |