Incidental Mutation 'R1458:Adamtsl3'
ID |
161879 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Adamtsl3
|
Ensembl Gene |
ENSMUSG00000070469 |
Gene Name |
ADAMTS-like 3 |
Synonyms |
9230119C12Rik, punctin-2 |
MMRRC Submission |
039513-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R1458 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
7 |
Chromosomal Location |
81984902-82263658 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to A
at 82172528 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Methionine to Lysine
at position 497
(M497K)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000133637
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000173287]
[ENSMUST00000173828]
|
AlphaFold |
G3UXC7 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000173287
AA Change: M497K
PolyPhen 2
Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
|
SMART Domains |
Protein: ENSMUSP00000133637 Gene: ENSMUSG00000070469 AA Change: M497K
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
38 |
N/A |
INTRINSIC |
TSP1
|
90 |
136 |
6.43e-8 |
SMART |
TSP1
|
355 |
414 |
1.59e-1 |
SMART |
TSP1
|
433 |
492 |
3.72e-4 |
SMART |
TSP1
|
494 |
547 |
4.28e-4 |
SMART |
TSP1
|
579 |
638 |
1.85e-2 |
SMART |
TSP1
|
660 |
717 |
1.75e-2 |
SMART |
TSP1
|
719 |
773 |
3.45e-8 |
SMART |
TSP1
|
775 |
833 |
3.67e-3 |
SMART |
TSP1
|
836 |
894 |
8.99e-2 |
SMART |
IGc2
|
938 |
1002 |
7.59e-4 |
SMART |
IG
|
1213 |
1296 |
4.87e0 |
SMART |
IGc2
|
1326 |
1388 |
1.01e-13 |
SMART |
TSP1
|
1441 |
1498 |
1.95e-2 |
SMART |
TSP1
|
1500 |
1559 |
6.76e-2 |
SMART |
TSP1
|
1616 |
1666 |
3.84e-1 |
SMART |
Pfam:PLAC
|
1674 |
1704 |
2.4e-11 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000173828
|
SMART Domains |
Protein: ENSMUSP00000133337 Gene: ENSMUSG00000070469
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
20 |
N/A |
INTRINSIC |
Blast:IG
|
22 |
79 |
1e-26 |
BLAST |
SCOP:d1biha4
|
27 |
77 |
2e-5 |
SMART |
IG
|
283 |
366 |
4.87e0 |
SMART |
IGc2
|
396 |
458 |
1.01e-13 |
SMART |
TSP1
|
511 |
568 |
1.95e-2 |
SMART |
TSP1
|
570 |
629 |
6.76e-2 |
SMART |
TSP1
|
686 |
736 |
3.84e-1 |
SMART |
|
Meta Mutation Damage Score |
0.1382 |
Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.3%
- 10x: 96.3%
- 20x: 92.8%
|
Validation Efficiency |
98% (95/97) |
Allele List at MGI |
All alleles(10) : Targeted(7) Gene trapped(2) Spontaneous(1)
|
Other mutations in this stock |
Total: 94 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700036A12Rik |
A |
G |
9: 60,677,043 (GRCm39) |
|
noncoding transcript |
Het |
A430110L20Rik |
T |
A |
1: 181,055,423 (GRCm39) |
|
noncoding transcript |
Het |
Abce1 |
T |
C |
8: 80,433,864 (GRCm39) |
K63R |
possibly damaging |
Het |
Acp6 |
A |
G |
3: 97,081,104 (GRCm39) |
|
probably benign |
Het |
Adamts13 |
T |
A |
2: 26,878,366 (GRCm39) |
L579Q |
probably damaging |
Het |
Adgrb2 |
T |
A |
4: 129,908,384 (GRCm39) |
M1042K |
possibly damaging |
Het |
Akap12 |
A |
T |
10: 4,303,693 (GRCm39) |
S168C |
probably damaging |
Het |
Akap3 |
A |
T |
6: 126,842,517 (GRCm39) |
M379L |
probably damaging |
Het |
Aldh6a1 |
C |
T |
12: 84,486,437 (GRCm39) |
M135I |
probably null |
Het |
Arhgef12 |
A |
G |
9: 42,900,294 (GRCm39) |
S860P |
probably damaging |
Het |
Atp11b |
A |
C |
3: 35,843,707 (GRCm39) |
T185P |
probably damaging |
Het |
Bcas1 |
T |
C |
2: 170,229,871 (GRCm39) |
D243G |
probably damaging |
Het |
Cdhr2 |
T |
A |
13: 54,865,685 (GRCm39) |
S228T |
probably damaging |
Het |
Cic |
T |
C |
7: 24,979,162 (GRCm39) |
|
probably benign |
Het |
Cimap1d |
A |
T |
10: 79,481,392 (GRCm39) |
|
probably benign |
Het |
Cmya5 |
T |
A |
13: 93,201,835 (GRCm39) |
I3376L |
probably benign |
Het |
Ctrc |
C |
A |
4: 141,573,535 (GRCm39) |
|
probably null |
Het |
Dchs1 |
G |
T |
7: 105,404,451 (GRCm39) |
P2697Q |
probably damaging |
Het |
Dmbt1 |
A |
G |
7: 130,646,217 (GRCm39) |
|
probably benign |
Het |
Drd2 |
G |
A |
9: 49,313,512 (GRCm39) |
R227H |
probably damaging |
Het |
Dscc1 |
C |
A |
15: 54,950,160 (GRCm39) |
C195F |
probably damaging |
Het |
Dzip1 |
T |
A |
14: 119,160,125 (GRCm39) |
M28L |
probably benign |
Het |
Edar |
A |
T |
10: 58,443,188 (GRCm39) |
S313T |
probably benign |
Het |
Eef1e1 |
C |
A |
13: 38,840,099 (GRCm39) |
A69S |
probably damaging |
Het |
Fbn1 |
A |
G |
2: 125,143,849 (GRCm39) |
V2760A |
probably benign |
Het |
Fez1 |
GACAAACA |
GACA |
9: 36,781,845 (GRCm39) |
|
probably null |
Het |
Fgl1 |
C |
G |
8: 41,663,496 (GRCm39) |
A11P |
possibly damaging |
Het |
Fras1 |
T |
C |
5: 96,748,592 (GRCm39) |
V689A |
probably benign |
Het |
Fry |
T |
A |
5: 150,304,324 (GRCm39) |
D571E |
probably damaging |
Het |
Gm11232 |
T |
A |
4: 71,675,450 (GRCm39) |
R104* |
probably null |
Het |
Gm1527 |
A |
G |
3: 28,972,199 (GRCm39) |
I439V |
possibly damaging |
Het |
Gm4922 |
C |
A |
10: 18,659,640 (GRCm39) |
G361* |
probably null |
Het |
Gm7052 |
T |
A |
17: 22,259,447 (GRCm39) |
|
probably benign |
Het |
Gpatch8 |
A |
T |
11: 102,372,055 (GRCm39) |
S494R |
unknown |
Het |
Gria2 |
A |
T |
3: 80,639,352 (GRCm39) |
V220E |
possibly damaging |
Het |
Grik4 |
G |
A |
9: 42,432,418 (GRCm39) |
H860Y |
probably benign |
Het |
Gtpbp1 |
A |
C |
15: 79,591,930 (GRCm39) |
S93R |
probably damaging |
Het |
Gucy2g |
C |
A |
19: 55,203,468 (GRCm39) |
|
probably benign |
Het |
H2ac8 |
C |
A |
13: 23,755,221 (GRCm39) |
|
probably benign |
Het |
Hmcn1 |
G |
A |
1: 150,485,451 (GRCm39) |
R4384C |
probably damaging |
Het |
Hspa12b |
G |
C |
2: 130,987,112 (GRCm39) |
A678P |
probably damaging |
Het |
Igsf21 |
T |
A |
4: 139,755,435 (GRCm39) |
N407Y |
probably damaging |
Het |
Insig2 |
A |
G |
1: 121,234,885 (GRCm39) |
Y174H |
probably benign |
Het |
Itpr3 |
T |
A |
17: 27,337,346 (GRCm39) |
M2413K |
probably benign |
Het |
Kalrn |
A |
T |
16: 33,994,857 (GRCm39) |
I1322N |
probably damaging |
Het |
Klk1b24 |
T |
A |
7: 43,840,890 (GRCm39) |
M106K |
possibly damaging |
Het |
Krt81 |
G |
T |
15: 101,358,198 (GRCm39) |
Q352K |
probably benign |
Het |
Lca5l |
A |
T |
16: 95,961,059 (GRCm39) |
S468T |
possibly damaging |
Het |
Lvrn |
T |
C |
18: 47,015,452 (GRCm39) |
|
probably benign |
Het |
Mcpt1 |
T |
A |
14: 56,256,621 (GRCm39) |
|
probably benign |
Het |
Med13l |
T |
C |
5: 118,876,524 (GRCm39) |
M900T |
probably benign |
Het |
Med16 |
A |
G |
10: 79,743,312 (GRCm39) |
|
probably benign |
Het |
Megf6 |
G |
T |
4: 154,261,578 (GRCm39) |
V68L |
probably benign |
Het |
Mep1a |
T |
C |
17: 43,802,563 (GRCm39) |
H154R |
probably damaging |
Het |
Mrc2 |
A |
T |
11: 105,228,598 (GRCm39) |
D659V |
probably benign |
Het |
Mroh8 |
T |
A |
2: 157,063,224 (GRCm39) |
E799V |
probably damaging |
Het |
Mrpl21 |
A |
G |
19: 3,334,808 (GRCm39) |
Y50C |
possibly damaging |
Het |
Msl1 |
A |
G |
11: 98,694,808 (GRCm39) |
|
probably benign |
Het |
Myo1a |
C |
A |
10: 127,555,806 (GRCm39) |
Q932K |
probably benign |
Het |
Nav3 |
A |
C |
10: 109,555,905 (GRCm39) |
S1675R |
probably damaging |
Het |
Neurl2 |
A |
G |
2: 164,674,666 (GRCm39) |
V232A |
possibly damaging |
Het |
Nfatc1 |
T |
A |
18: 80,708,482 (GRCm39) |
|
probably benign |
Het |
Or2w4 |
C |
T |
13: 21,795,992 (GRCm39) |
C49Y |
probably benign |
Het |
Or5k8 |
T |
A |
16: 58,645,039 (GRCm39) |
E11V |
probably null |
Het |
P4hb |
A |
G |
11: 120,453,381 (GRCm39) |
|
probably benign |
Het |
Papss1 |
T |
G |
3: 131,311,615 (GRCm39) |
I281S |
probably damaging |
Het |
Pde10a |
A |
T |
17: 9,183,540 (GRCm39) |
D832V |
probably damaging |
Het |
Pfkfb2 |
A |
T |
1: 130,635,927 (GRCm39) |
Y35N |
possibly damaging |
Het |
Phaf1 |
T |
C |
8: 105,973,188 (GRCm39) |
|
probably null |
Het |
Phf20l1 |
T |
A |
15: 66,476,662 (GRCm39) |
F253Y |
probably damaging |
Het |
Pkhd1l1 |
G |
A |
15: 44,379,511 (GRCm39) |
V1046I |
probably benign |
Het |
Plin3 |
C |
T |
17: 56,591,337 (GRCm39) |
A148T |
probably benign |
Het |
Ppp1r8 |
T |
C |
4: 132,567,942 (GRCm39) |
|
probably benign |
Het |
Ppp2r3d |
A |
G |
9: 101,088,511 (GRCm39) |
L604P |
probably damaging |
Het |
Prdm5 |
T |
C |
6: 65,860,585 (GRCm39) |
V239A |
probably damaging |
Het |
Prickle1 |
A |
G |
15: 93,398,519 (GRCm39) |
S770P |
probably damaging |
Het |
Prl2c5 |
T |
A |
13: 13,365,310 (GRCm39) |
I155N |
probably benign |
Het |
Prom1 |
T |
C |
5: 44,190,274 (GRCm39) |
|
probably benign |
Het |
Psg25 |
C |
T |
7: 18,263,512 (GRCm39) |
G104R |
probably damaging |
Het |
Rbm19 |
T |
C |
5: 120,282,094 (GRCm39) |
V817A |
probably benign |
Het |
Ryr2 |
T |
A |
13: 11,741,908 (GRCm39) |
Y2091F |
probably damaging |
Het |
Slc16a4 |
A |
G |
3: 107,208,248 (GRCm39) |
T253A |
probably benign |
Het |
Smg7 |
A |
T |
1: 152,731,594 (GRCm39) |
|
probably null |
Het |
Spink5 |
C |
A |
18: 44,140,786 (GRCm39) |
H662N |
probably benign |
Het |
Taf2 |
A |
T |
15: 54,923,311 (GRCm39) |
M322K |
probably damaging |
Het |
Tmc2 |
T |
C |
2: 130,090,682 (GRCm39) |
F676S |
probably damaging |
Het |
Tmem177 |
A |
G |
1: 119,837,915 (GRCm39) |
S255P |
possibly damaging |
Het |
Trim46 |
A |
T |
3: 89,142,375 (GRCm39) |
|
probably null |
Het |
Tubb1 |
T |
A |
2: 174,292,596 (GRCm39) |
|
probably null |
Het |
Upf1 |
T |
C |
8: 70,796,904 (GRCm39) |
T110A |
probably benign |
Het |
Vmn2r9 |
T |
A |
5: 108,996,850 (GRCm39) |
I140L |
probably benign |
Het |
Zfp638 |
T |
A |
6: 83,921,638 (GRCm39) |
H588Q |
probably damaging |
Het |
Zfp780b |
T |
A |
7: 27,664,252 (GRCm39) |
N101I |
probably damaging |
Het |
Zpld2 |
T |
C |
4: 133,924,144 (GRCm39) |
D467G |
probably benign |
Het |
|
Other mutations in Adamtsl3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01549:Adamtsl3
|
APN |
7 |
82,261,656 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01936:Adamtsl3
|
APN |
7 |
82,244,579 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02819:Adamtsl3
|
APN |
7 |
82,223,329 (GRCm39) |
missense |
probably damaging |
0.99 |
P0012:Adamtsl3
|
UTSW |
7 |
82,223,465 (GRCm39) |
missense |
probably benign |
0.27 |
R0096:Adamtsl3
|
UTSW |
7 |
82,114,907 (GRCm39) |
intron |
probably benign |
|
R0096:Adamtsl3
|
UTSW |
7 |
82,114,907 (GRCm39) |
intron |
probably benign |
|
R0180:Adamtsl3
|
UTSW |
7 |
82,225,198 (GRCm39) |
missense |
probably benign |
0.00 |
R0270:Adamtsl3
|
UTSW |
7 |
82,206,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R0295:Adamtsl3
|
UTSW |
7 |
82,197,213 (GRCm39) |
critical splice donor site |
probably null |
|
R0329:Adamtsl3
|
UTSW |
7 |
82,171,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R0330:Adamtsl3
|
UTSW |
7 |
82,171,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R0548:Adamtsl3
|
UTSW |
7 |
82,178,191 (GRCm39) |
critical splice donor site |
probably null |
|
R0611:Adamtsl3
|
UTSW |
7 |
82,178,120 (GRCm39) |
missense |
probably damaging |
1.00 |
R0671:Adamtsl3
|
UTSW |
7 |
82,172,390 (GRCm39) |
missense |
probably damaging |
1.00 |
R0711:Adamtsl3
|
UTSW |
7 |
82,114,907 (GRCm39) |
intron |
probably benign |
|
R0845:Adamtsl3
|
UTSW |
7 |
82,225,204 (GRCm39) |
missense |
probably damaging |
1.00 |
R1119:Adamtsl3
|
UTSW |
7 |
82,189,525 (GRCm39) |
missense |
probably damaging |
0.96 |
R1644:Adamtsl3
|
UTSW |
7 |
82,099,298 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1691:Adamtsl3
|
UTSW |
7 |
82,148,814 (GRCm39) |
missense |
probably damaging |
1.00 |
R1838:Adamtsl3
|
UTSW |
7 |
82,142,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R2131:Adamtsl3
|
UTSW |
7 |
82,227,802 (GRCm39) |
missense |
probably damaging |
1.00 |
R2245:Adamtsl3
|
UTSW |
7 |
82,099,308 (GRCm39) |
missense |
probably damaging |
1.00 |
R2274:Adamtsl3
|
UTSW |
7 |
82,255,766 (GRCm39) |
missense |
probably benign |
0.37 |
R2275:Adamtsl3
|
UTSW |
7 |
82,255,766 (GRCm39) |
missense |
probably benign |
0.37 |
R2448:Adamtsl3
|
UTSW |
7 |
82,148,956 (GRCm39) |
missense |
probably damaging |
1.00 |
R3725:Adamtsl3
|
UTSW |
7 |
82,261,612 (GRCm39) |
missense |
possibly damaging |
0.80 |
R3757:Adamtsl3
|
UTSW |
7 |
81,986,415 (GRCm39) |
missense |
probably benign |
0.01 |
R3821:Adamtsl3
|
UTSW |
7 |
82,255,687 (GRCm39) |
splice site |
probably benign |
|
R4618:Adamtsl3
|
UTSW |
7 |
82,255,728 (GRCm39) |
missense |
probably benign |
0.41 |
R4842:Adamtsl3
|
UTSW |
7 |
82,178,069 (GRCm39) |
missense |
probably damaging |
1.00 |
R4887:Adamtsl3
|
UTSW |
7 |
82,223,822 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4888:Adamtsl3
|
UTSW |
7 |
82,223,822 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4925:Adamtsl3
|
UTSW |
7 |
82,251,507 (GRCm39) |
critical splice donor site |
probably null |
|
R4960:Adamtsl3
|
UTSW |
7 |
82,216,185 (GRCm39) |
missense |
probably damaging |
0.99 |
R5026:Adamtsl3
|
UTSW |
7 |
82,225,262 (GRCm39) |
missense |
probably benign |
0.07 |
R5152:Adamtsl3
|
UTSW |
7 |
82,223,752 (GRCm39) |
missense |
probably benign |
0.11 |
R5198:Adamtsl3
|
UTSW |
7 |
82,261,006 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5244:Adamtsl3
|
UTSW |
7 |
82,247,277 (GRCm39) |
missense |
probably benign |
0.02 |
R5281:Adamtsl3
|
UTSW |
7 |
82,178,142 (GRCm39) |
missense |
probably damaging |
1.00 |
R5323:Adamtsl3
|
UTSW |
7 |
82,206,269 (GRCm39) |
missense |
probably damaging |
1.00 |
R5523:Adamtsl3
|
UTSW |
7 |
82,223,650 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5602:Adamtsl3
|
UTSW |
7 |
82,206,447 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5638:Adamtsl3
|
UTSW |
7 |
82,260,958 (GRCm39) |
missense |
probably damaging |
0.99 |
R5682:Adamtsl3
|
UTSW |
7 |
82,255,758 (GRCm39) |
missense |
probably damaging |
0.99 |
R5782:Adamtsl3
|
UTSW |
7 |
82,189,494 (GRCm39) |
splice site |
probably null |
|
R5946:Adamtsl3
|
UTSW |
7 |
82,225,265 (GRCm39) |
missense |
probably damaging |
0.98 |
R6091:Adamtsl3
|
UTSW |
7 |
82,114,829 (GRCm39) |
missense |
probably damaging |
1.00 |
R6258:Adamtsl3
|
UTSW |
7 |
82,178,191 (GRCm39) |
critical splice donor site |
probably null |
|
R6500:Adamtsl3
|
UTSW |
7 |
82,227,818 (GRCm39) |
missense |
probably benign |
0.00 |
R6765:Adamtsl3
|
UTSW |
7 |
82,216,232 (GRCm39) |
missense |
possibly damaging |
0.60 |
R6785:Adamtsl3
|
UTSW |
7 |
82,171,212 (GRCm39) |
missense |
probably damaging |
0.99 |
R6982:Adamtsl3
|
UTSW |
7 |
82,164,271 (GRCm39) |
missense |
probably damaging |
1.00 |
R7109:Adamtsl3
|
UTSW |
7 |
82,261,069 (GRCm39) |
missense |
|
|
R7341:Adamtsl3
|
UTSW |
7 |
82,206,082 (GRCm39) |
missense |
probably damaging |
1.00 |
R7402:Adamtsl3
|
UTSW |
7 |
82,227,825 (GRCm39) |
missense |
probably damaging |
0.96 |
R7506:Adamtsl3
|
UTSW |
7 |
82,164,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R7549:Adamtsl3
|
UTSW |
7 |
82,223,117 (GRCm39) |
missense |
probably damaging |
1.00 |
R7575:Adamtsl3
|
UTSW |
7 |
82,223,756 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7592:Adamtsl3
|
UTSW |
7 |
81,986,459 (GRCm39) |
missense |
probably benign |
0.00 |
R7617:Adamtsl3
|
UTSW |
7 |
82,206,054 (GRCm39) |
splice site |
probably null |
|
R7654:Adamtsl3
|
UTSW |
7 |
82,223,702 (GRCm39) |
missense |
probably benign |
|
R7721:Adamtsl3
|
UTSW |
7 |
82,255,728 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7784:Adamtsl3
|
UTSW |
7 |
82,223,197 (GRCm39) |
missense |
probably damaging |
1.00 |
R7858:Adamtsl3
|
UTSW |
7 |
82,099,371 (GRCm39) |
missense |
probably damaging |
1.00 |
R8109:Adamtsl3
|
UTSW |
7 |
82,251,487 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8125:Adamtsl3
|
UTSW |
7 |
82,099,541 (GRCm39) |
splice site |
probably null |
|
R8211:Adamtsl3
|
UTSW |
7 |
82,172,371 (GRCm39) |
missense |
probably damaging |
1.00 |
R8348:Adamtsl3
|
UTSW |
7 |
82,253,007 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8360:Adamtsl3
|
UTSW |
7 |
82,197,187 (GRCm39) |
missense |
probably damaging |
1.00 |
R8448:Adamtsl3
|
UTSW |
7 |
82,253,007 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8465:Adamtsl3
|
UTSW |
7 |
82,247,330 (GRCm39) |
missense |
probably benign |
0.43 |
R8547:Adamtsl3
|
UTSW |
7 |
82,077,621 (GRCm39) |
missense |
probably damaging |
1.00 |
R8551:Adamtsl3
|
UTSW |
7 |
82,189,678 (GRCm39) |
missense |
probably benign |
0.34 |
R8558:Adamtsl3
|
UTSW |
7 |
82,077,600 (GRCm39) |
missense |
possibly damaging |
0.59 |
R8709:Adamtsl3
|
UTSW |
7 |
82,077,642 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8722:Adamtsl3
|
UTSW |
7 |
82,244,745 (GRCm39) |
critical splice donor site |
probably null |
|
R8930:Adamtsl3
|
UTSW |
7 |
82,261,069 (GRCm39) |
missense |
|
|
R8932:Adamtsl3
|
UTSW |
7 |
82,261,069 (GRCm39) |
missense |
|
|
R9131:Adamtsl3
|
UTSW |
7 |
82,244,722 (GRCm39) |
missense |
probably benign |
0.00 |
R9169:Adamtsl3
|
UTSW |
7 |
82,223,188 (GRCm39) |
missense |
probably damaging |
0.99 |
R9272:Adamtsl3
|
UTSW |
7 |
82,189,753 (GRCm39) |
missense |
probably damaging |
1.00 |
R9276:Adamtsl3
|
UTSW |
7 |
82,206,710 (GRCm39) |
intron |
probably benign |
|
R9351:Adamtsl3
|
UTSW |
7 |
82,169,929 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9352:Adamtsl3
|
UTSW |
7 |
82,091,656 (GRCm39) |
missense |
probably damaging |
1.00 |
R9749:Adamtsl3
|
UTSW |
7 |
82,099,394 (GRCm39) |
missense |
probably benign |
0.04 |
R9750:Adamtsl3
|
UTSW |
7 |
82,244,589 (GRCm39) |
missense |
probably benign |
0.11 |
RF005:Adamtsl3
|
UTSW |
7 |
82,261,603 (GRCm39) |
missense |
|
|
X0003:Adamtsl3
|
UTSW |
7 |
82,260,967 (GRCm39) |
nonsense |
probably null |
|
X0063:Adamtsl3
|
UTSW |
7 |
82,223,365 (GRCm39) |
missense |
probably benign |
0.25 |
Z1088:Adamtsl3
|
UTSW |
7 |
82,189,533 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Adamtsl3
|
UTSW |
7 |
82,148,922 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- TGAGCTGGGAACATAATCCCTGGAC -3'
(R):5'- TGAGGTGACTTCTCATCCTGTGCC -3'
Sequencing Primer
(F):5'- ACTGCATGTTCGGTGTCC -3'
(R):5'- agcatggctcagggattac -3'
|
Posted On |
2014-03-14 |