Incidental Mutation 'R4939:Adamtsl1'
ID |
382893 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Adamtsl1
|
Ensembl Gene |
ENSMUSG00000066113 |
Gene Name |
ADAMTS-like 1 |
Synonyms |
punctin-1, 5930437A14Rik, 6720426B09Rik |
MMRRC Submission |
042538-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.238)
|
Stock # |
R4939 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
4 |
Chromosomal Location |
85432409-86346622 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 86161962 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Tyrosine to Phenylalanine
at position 365
(Y365F)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000119278
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000048885]
[ENSMUST00000107178]
[ENSMUST00000141889]
|
AlphaFold |
Q8BLI0 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000048885
AA Change: Y365F
PolyPhen 2
Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
|
SMART Domains |
Protein: ENSMUSP00000043073 Gene: ENSMUSG00000066113 AA Change: Y365F
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 |
|
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: ENSMUST00000136320
|
SMART Domains |
Protein: ENSMUSP00000123343 Gene: ENSMUSG00000066113
Domain | Start | End | E-Value | Type |
Pfam:ADAM_spacer1
|
15 |
125 |
2.7e-7 |
PFAM |
TSP1
|
130 |
189 |
4.35e-2 |
SMART |
TSP1
|
191 |
239 |
1.36e-1 |
SMART |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000141889
AA Change: Y365F
PolyPhen 2
Score 0.948 (Sensitivity: 0.79; Specificity: 0.95)
|
SMART Domains |
Protein: ENSMUSP00000119278 Gene: ENSMUSG00000066113 AA Change: Y365F
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: 99.1%
- 3x: 98.4%
- 10x: 96.6%
- 20x: 93.4%
|
Validation Efficiency |
|
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: 85 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Atp2a1 |
T |
C |
7: 126,049,288 (GRCm39) |
M585V |
probably benign |
Het |
Brca1 |
A |
G |
11: 101,398,876 (GRCm39) |
V1572A |
probably benign |
Het |
C1ql4 |
A |
T |
15: 98,985,521 (GRCm39) |
M30K |
probably damaging |
Het |
Ccdc73 |
A |
G |
2: 104,822,502 (GRCm39) |
|
probably null |
Het |
Cdk6 |
A |
T |
5: 3,394,377 (GRCm39) |
D4V |
probably null |
Het |
Celf3 |
ACAGCAGCAGCAGCAGCAGCAGCA |
ACAGCAGCAGCAGCAGCAGCA |
3: 94,395,537 (GRCm39) |
|
probably benign |
Het |
Clic4 |
T |
C |
4: 134,950,852 (GRCm39) |
E113G |
probably benign |
Het |
Creld1 |
C |
A |
6: 113,465,140 (GRCm39) |
H122Q |
probably benign |
Het |
Cyp4a29 |
G |
A |
4: 115,104,873 (GRCm39) |
|
probably null |
Het |
Dnaaf3 |
A |
T |
7: 4,530,144 (GRCm39) |
S246R |
probably damaging |
Het |
Dnah12 |
A |
T |
14: 26,613,481 (GRCm39) |
T3925S |
probably damaging |
Het |
Dnajc21 |
T |
A |
15: 10,449,683 (GRCm39) |
D446V |
probably damaging |
Het |
Dock8 |
A |
T |
19: 25,099,764 (GRCm39) |
Y629F |
probably damaging |
Het |
Duxf4 |
T |
C |
10: 58,071,425 (GRCm39) |
N263S |
probably benign |
Het |
E2f8 |
A |
T |
7: 48,521,886 (GRCm39) |
N405K |
probably benign |
Het |
Flg |
A |
G |
3: 93,187,154 (GRCm39) |
N202S |
probably benign |
Het |
Glyatl3 |
A |
G |
17: 41,220,914 (GRCm39) |
|
probably null |
Het |
Gm38999 |
A |
G |
7: 43,077,885 (GRCm39) |
T63A |
possibly damaging |
Het |
Grap |
A |
G |
11: 61,551,124 (GRCm39) |
Y52C |
probably damaging |
Het |
Haus2 |
T |
A |
2: 120,449,517 (GRCm39) |
I187K |
probably damaging |
Het |
Heatr5b |
T |
C |
17: 79,069,689 (GRCm39) |
E1686G |
probably benign |
Het |
Herc2 |
A |
G |
7: 55,856,484 (GRCm39) |
D3944G |
probably damaging |
Het |
Hexd |
A |
T |
11: 121,098,542 (GRCm39) |
M9L |
probably benign |
Het |
Hoxa3 |
T |
C |
6: 52,147,656 (GRCm39) |
|
probably benign |
Het |
Hspg2 |
A |
T |
4: 137,235,342 (GRCm39) |
I126F |
probably damaging |
Het |
Itpr1 |
T |
A |
6: 108,417,519 (GRCm39) |
C123* |
probably null |
Het |
Jmjd1c |
T |
A |
10: 67,081,916 (GRCm39) |
N2346K |
possibly damaging |
Het |
Kctd9 |
A |
G |
14: 67,967,135 (GRCm39) |
Y37C |
probably damaging |
Het |
Kmt5b |
A |
C |
19: 3,865,245 (GRCm39) |
S747R |
possibly damaging |
Het |
Krt26 |
T |
C |
11: 99,225,522 (GRCm39) |
M320V |
probably benign |
Het |
Lama1 |
T |
G |
17: 68,044,470 (GRCm39) |
V123G |
possibly damaging |
Het |
Lamc2 |
T |
C |
1: 153,002,582 (GRCm39) |
D1103G |
probably damaging |
Het |
Lepr |
A |
T |
4: 101,590,635 (GRCm39) |
K71I |
possibly damaging |
Het |
Llgl1 |
A |
T |
11: 60,600,805 (GRCm39) |
|
probably null |
Het |
Mcoln2 |
A |
T |
3: 145,897,996 (GRCm39) |
H39L |
probably benign |
Het |
Mtrex |
T |
C |
13: 113,046,426 (GRCm39) |
D308G |
possibly damaging |
Het |
Myh11 |
T |
A |
16: 14,057,371 (GRCm39) |
T315S |
probably benign |
Het |
Ncapd3 |
T |
C |
9: 26,975,165 (GRCm39) |
|
probably null |
Het |
Nlrp9b |
G |
T |
7: 19,758,421 (GRCm39) |
V553F |
probably damaging |
Het |
Nubpl |
A |
G |
12: 52,227,878 (GRCm39) |
N129S |
probably damaging |
Het |
Nup214 |
C |
A |
2: 31,873,171 (GRCm39) |
T255K |
probably benign |
Het |
Or10j3 |
T |
C |
1: 173,031,030 (GRCm39) |
Y36H |
possibly damaging |
Het |
Or2t46 |
G |
T |
11: 58,472,037 (GRCm39) |
M122I |
probably damaging |
Het |
Or2y17 |
A |
G |
11: 49,231,376 (GRCm39) |
T6A |
probably benign |
Het |
Or4d1 |
G |
T |
11: 87,804,950 (GRCm39) |
P261T |
probably damaging |
Het |
Or52z14 |
T |
C |
7: 103,253,458 (GRCm39) |
V199A |
probably benign |
Het |
Or5b3 |
T |
A |
19: 13,388,219 (GRCm39) |
N95K |
probably benign |
Het |
Orc3 |
G |
A |
4: 34,593,126 (GRCm39) |
Q256* |
probably null |
Het |
Pbrm1 |
A |
G |
14: 30,783,580 (GRCm39) |
M566V |
probably damaging |
Het |
Pde6b |
A |
G |
5: 108,569,363 (GRCm39) |
I357V |
probably benign |
Het |
Pkdrej |
A |
G |
15: 85,704,484 (GRCm39) |
I484T |
possibly damaging |
Het |
Plvap |
A |
G |
8: 71,964,083 (GRCm39) |
V93A |
probably benign |
Het |
Plxna4 |
T |
C |
6: 32,142,697 (GRCm39) |
Y1586C |
probably damaging |
Het |
Ppfia4 |
A |
T |
1: 134,255,817 (GRCm39) |
L196Q |
possibly damaging |
Het |
Ptpn13 |
T |
G |
5: 103,665,335 (GRCm39) |
|
probably null |
Het |
Ranbp17 |
T |
C |
11: 33,169,223 (GRCm39) |
N997S |
probably benign |
Het |
Rpap2 |
G |
T |
5: 107,751,491 (GRCm39) |
|
probably null |
Het |
Rrm1 |
T |
C |
7: 102,116,131 (GRCm39) |
V683A |
probably benign |
Het |
Ruvbl1 |
A |
G |
6: 88,460,021 (GRCm39) |
|
probably null |
Het |
Sh3pxd2a |
A |
G |
19: 47,266,843 (GRCm39) |
Y277H |
probably damaging |
Het |
Shank1 |
C |
T |
7: 43,975,586 (GRCm39) |
P477S |
unknown |
Het |
Shtn1 |
T |
C |
19: 59,010,633 (GRCm39) |
E278G |
probably benign |
Het |
Skap2 |
T |
A |
6: 51,899,303 (GRCm39) |
I109F |
possibly damaging |
Het |
Slc28a3 |
A |
C |
13: 58,706,395 (GRCm39) |
I615M |
probably benign |
Het |
Slc4a11 |
A |
G |
2: 130,526,788 (GRCm39) |
L780P |
probably damaging |
Het |
Slc5a4b |
T |
C |
10: 75,917,301 (GRCm39) |
E245G |
probably benign |
Het |
Slfn8 |
C |
T |
11: 82,894,111 (GRCm39) |
A843T |
probably benign |
Het |
Sncaip |
A |
T |
18: 53,040,335 (GRCm39) |
Q843L |
possibly damaging |
Het |
Spidr |
T |
A |
16: 15,958,610 (GRCm39) |
K51* |
probably null |
Het |
Spopfm2 |
A |
T |
3: 94,083,540 (GRCm39) |
Y90* |
probably null |
Het |
Tas2r123 |
T |
C |
6: 132,824,808 (GRCm39) |
V235A |
probably benign |
Het |
Tgfbr3 |
T |
C |
5: 107,278,335 (GRCm39) |
D757G |
probably benign |
Het |
Tmem132d |
A |
T |
5: 127,873,139 (GRCm39) |
V490D |
probably damaging |
Het |
Top2a |
T |
A |
11: 98,900,918 (GRCm39) |
H557L |
probably damaging |
Het |
Trafd1 |
A |
G |
5: 121,513,254 (GRCm39) |
I328T |
probably benign |
Het |
Trappc11 |
G |
A |
8: 47,972,700 (GRCm39) |
A291V |
probably damaging |
Het |
Tuba1c |
A |
G |
15: 98,935,835 (GRCm39) |
Y432C |
probably damaging |
Het |
Utp11 |
T |
G |
4: 124,577,043 (GRCm39) |
R109S |
possibly damaging |
Het |
Vmn1r159 |
T |
G |
7: 22,542,316 (GRCm39) |
T239P |
probably damaging |
Het |
Vwce |
A |
T |
19: 10,622,414 (GRCm39) |
N239Y |
probably damaging |
Het |
Yes1 |
T |
C |
5: 32,802,457 (GRCm39) |
|
probably null |
Het |
Zfand6 |
A |
C |
7: 84,265,030 (GRCm39) |
*224G |
probably null |
Het |
Zfp408 |
A |
T |
2: 91,475,450 (GRCm39) |
I668N |
probably damaging |
Het |
Zfp647 |
TGCACG |
TGCACGCACG |
15: 76,795,244 (GRCm39) |
|
probably null |
Het |
Zfp946 |
T |
C |
17: 22,674,418 (GRCm39) |
F391L |
probably damaging |
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 |
R1387:Adamtsl1
|
UTSW |
4 |
86,293,230 (GRCm39) |
splice site |
probably benign |
|
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 |
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'- TTTCCCCAGCCTACAACATATG -3'
(R):5'- ACGACAAGCTTAGCGTCTGAG -3'
Sequencing Primer
(F):5'- TGCTAGCATAAATATCGAACTGTTTC -3'
(R):5'- GTGGATCTGCAGAATCAACCATCTTC -3'
|
Posted On |
2016-04-27 |