Incidental Mutation 'R4960:Adamtsl1'
ID |
382251 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Adamtsl1
|
Ensembl Gene |
ENSMUSG00000066113 |
Gene Name |
ADAMTS-like 1 |
Synonyms |
punctin-1, 5930437A14Rik, 6720426B09Rik |
MMRRC Submission |
042557-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.238)
|
Stock # |
R4960 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
4 |
Chromosomal Location |
85432409-86346622 bp(+) (GRCm39) |
Type of Mutation |
nonsense |
DNA Base Change (assembly) |
C to T
at 86342410 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Glutamine to Stop codon
at position 1642
(Q1642*)
|
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 null
Transcript: ENSMUST00000107178
AA Change: Q1650*
|
SMART Domains |
Protein: ENSMUSP00000102796 Gene: ENSMUSG00000066113 AA Change: Q1650*
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 null
Transcript: ENSMUST00000141889
AA Change: Q1642*
|
SMART Domains |
Protein: ENSMUSP00000119278 Gene: ENSMUSG00000066113 AA Change: Q1642*
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: 99.3%
- 3x: 98.5%
- 10x: 96.8%
- 20x: 93.8%
|
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: 102 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc9 |
A |
T |
6: 142,566,509 (GRCm39) |
|
probably null |
Het |
Abtb3 |
A |
C |
10: 85,487,526 (GRCm39) |
N998T |
probably benign |
Het |
Adamts20 |
T |
C |
15: 94,277,655 (GRCm39) |
H269R |
probably benign |
Het |
Adamtsl3 |
A |
C |
7: 82,216,185 (GRCm39) |
T863P |
probably damaging |
Het |
Adcy3 |
G |
T |
12: 4,184,896 (GRCm39) |
V191L |
probably benign |
Het |
Akap9 |
G |
T |
5: 4,007,664 (GRCm39) |
R244L |
probably benign |
Het |
Anapc1 |
C |
T |
2: 128,526,514 (GRCm39) |
V95M |
probably benign |
Het |
Arhgap17 |
G |
T |
7: 122,886,149 (GRCm39) |
|
probably benign |
Het |
Art2b |
T |
A |
7: 101,229,437 (GRCm39) |
Y154F |
probably damaging |
Het |
Atrn |
C |
T |
2: 130,836,967 (GRCm39) |
R1144* |
probably null |
Het |
Atxn3 |
T |
C |
12: 101,914,638 (GRCm39) |
S29G |
possibly damaging |
Het |
Batf3 |
C |
T |
1: 190,830,707 (GRCm39) |
P18S |
probably benign |
Het |
Bmal1 |
T |
A |
7: 112,898,642 (GRCm39) |
|
probably null |
Het |
Bmpr1b |
A |
T |
3: 141,576,546 (GRCm39) |
C96S |
probably damaging |
Het |
Bola1 |
A |
G |
3: 96,104,370 (GRCm39) |
S75P |
probably benign |
Het |
Cela3a |
G |
A |
4: 137,129,959 (GRCm39) |
R221* |
probably null |
Het |
Chat |
A |
G |
14: 32,142,771 (GRCm39) |
V406A |
possibly damaging |
Het |
Chd1 |
T |
A |
17: 15,962,493 (GRCm39) |
M750K |
probably damaging |
Het |
Clip1 |
T |
A |
5: 123,792,066 (GRCm39) |
K35* |
probably null |
Het |
Cnr2 |
G |
A |
4: 135,644,918 (GRCm39) |
G332D |
probably benign |
Het |
Cnrip1 |
A |
G |
11: 17,002,228 (GRCm39) |
D20G |
probably damaging |
Het |
Col2a1 |
T |
C |
15: 97,874,030 (GRCm39) |
Y1384C |
unknown |
Het |
Col6a3 |
T |
A |
1: 90,731,940 (GRCm39) |
I831F |
probably damaging |
Het |
Cp |
G |
A |
3: 20,027,961 (GRCm39) |
V456I |
probably damaging |
Het |
Cspp1 |
T |
A |
1: 10,196,688 (GRCm39) |
N900K |
probably damaging |
Het |
Ctbp2 |
T |
C |
7: 132,615,967 (GRCm39) |
I323V |
probably benign |
Het |
Ctnna2 |
C |
T |
6: 77,630,094 (GRCm39) |
R120H |
probably damaging |
Het |
Cyp2a12 |
A |
G |
7: 26,733,575 (GRCm39) |
H318R |
probably benign |
Het |
Cyp2c66 |
A |
T |
19: 39,151,766 (GRCm39) |
|
probably null |
Het |
Cyp2j8 |
T |
C |
4: 96,395,614 (GRCm39) |
T4A |
probably benign |
Het |
Cyp4v3 |
A |
G |
8: 45,773,674 (GRCm39) |
V165A |
possibly damaging |
Het |
D5Ertd579e |
G |
A |
5: 36,773,571 (GRCm39) |
R275* |
probably null |
Het |
Deup1 |
G |
T |
9: 15,512,264 (GRCm39) |
Q160K |
possibly damaging |
Het |
Dhx36 |
A |
T |
3: 62,404,280 (GRCm39) |
I221K |
probably damaging |
Het |
Dnah7b |
T |
A |
1: 46,272,886 (GRCm39) |
M2338K |
probably benign |
Het |
Dync2li1 |
T |
G |
17: 84,940,969 (GRCm39) |
L62V |
probably benign |
Het |
Ephb3 |
A |
G |
16: 21,039,245 (GRCm39) |
K367R |
probably benign |
Het |
Etv3 |
A |
G |
3: 87,435,368 (GRCm39) |
K80E |
probably damaging |
Het |
Flacc1 |
T |
A |
1: 58,706,965 (GRCm39) |
E234V |
probably damaging |
Het |
Gdap1l1 |
T |
C |
2: 163,295,779 (GRCm39) |
F346L |
probably benign |
Het |
Gm4787 |
C |
T |
12: 81,426,090 (GRCm39) |
V23M |
probably damaging |
Het |
Greb1l |
T |
A |
18: 10,547,306 (GRCm39) |
I1508N |
probably damaging |
Het |
Heatr5b |
G |
A |
17: 79,139,013 (GRCm39) |
T43I |
probably benign |
Het |
Hephl1 |
T |
C |
9: 14,997,586 (GRCm39) |
Y360C |
probably damaging |
Het |
Itgam |
A |
C |
7: 127,715,012 (GRCm39) |
T865P |
possibly damaging |
Het |
Kcnma1 |
T |
C |
14: 24,054,186 (GRCm39) |
|
probably benign |
Het |
Kidins220 |
T |
A |
12: 25,042,259 (GRCm39) |
C185* |
probably null |
Het |
Klhl35 |
G |
T |
7: 99,118,275 (GRCm39) |
G273V |
probably damaging |
Het |
Lama5 |
A |
G |
2: 179,850,045 (GRCm39) |
|
probably null |
Het |
Lamc3 |
A |
G |
2: 31,805,966 (GRCm39) |
Q689R |
probably benign |
Het |
Lnx2 |
C |
T |
5: 146,955,850 (GRCm39) |
V649I |
probably benign |
Het |
Lrrc43 |
A |
G |
5: 123,637,675 (GRCm39) |
I281V |
probably benign |
Het |
Ly6g6d |
C |
A |
17: 35,290,730 (GRCm39) |
A67S |
probably benign |
Het |
Map1b |
A |
G |
13: 99,568,720 (GRCm39) |
S1334P |
probably benign |
Het |
Mast1 |
T |
A |
8: 85,644,500 (GRCm39) |
T810S |
probably benign |
Het |
Matcap1 |
G |
T |
8: 106,009,843 (GRCm39) |
R369S |
probably damaging |
Het |
Mbnl1 |
A |
G |
3: 60,503,117 (GRCm39) |
M1V |
probably null |
Het |
Mc5r |
T |
G |
18: 68,471,890 (GRCm39) |
M83R |
possibly damaging |
Het |
Mkln1 |
T |
C |
6: 31,435,941 (GRCm39) |
F300S |
probably damaging |
Het |
Mrgpre |
A |
T |
7: 143,335,088 (GRCm39) |
C138* |
probably null |
Het |
Mtarc2 |
T |
A |
1: 184,566,116 (GRCm39) |
M186L |
probably benign |
Het |
Ncbp1 |
C |
T |
4: 46,165,273 (GRCm39) |
Q529* |
probably null |
Het |
Nherf1 |
A |
G |
11: 115,067,289 (GRCm39) |
D180G |
probably benign |
Het |
Nrcam |
A |
G |
12: 44,613,082 (GRCm39) |
D591G |
probably benign |
Het |
Nrxn3 |
A |
T |
12: 88,761,971 (GRCm39) |
H6L |
possibly damaging |
Het |
Nsmaf |
T |
A |
4: 6,423,342 (GRCm39) |
D342V |
probably damaging |
Het |
Oip5 |
TGAGAAA |
T |
2: 119,448,342 (GRCm39) |
|
probably benign |
Het |
Omt2a |
T |
A |
9: 78,220,305 (GRCm39) |
E31D |
possibly damaging |
Het |
Or4f62 |
A |
G |
2: 111,986,697 (GRCm39) |
T134A |
probably benign |
Het |
Or52n2b |
A |
G |
7: 104,565,915 (GRCm39) |
I196T |
probably benign |
Het |
Or5ac20 |
A |
G |
16: 59,104,348 (GRCm39) |
S171P |
probably benign |
Het |
Or6c88 |
A |
C |
10: 129,406,895 (GRCm39) |
I124L |
probably damaging |
Het |
Or9a2 |
C |
A |
6: 41,749,003 (GRCm39) |
V77F |
probably damaging |
Het |
Phyhipl |
A |
G |
10: 70,404,815 (GRCm39) |
V131A |
probably benign |
Het |
Pik3r5 |
A |
G |
11: 68,384,464 (GRCm39) |
M619V |
probably benign |
Het |
Pramel19 |
T |
C |
4: 101,798,661 (GRCm39) |
Y211H |
probably benign |
Het |
Ptprg |
A |
T |
14: 12,237,837 (GRCm38) |
E1431D |
probably benign |
Het |
Rnf20 |
A |
G |
4: 49,638,029 (GRCm39) |
T85A |
probably damaging |
Het |
Rtn3 |
A |
T |
19: 7,433,886 (GRCm39) |
I683K |
probably damaging |
Het |
Rwdd3 |
A |
G |
3: 120,952,470 (GRCm39) |
F174L |
probably damaging |
Het |
Ryr1 |
T |
C |
7: 28,778,208 (GRCm39) |
Q2096R |
possibly damaging |
Het |
Scrn1 |
T |
C |
6: 54,511,407 (GRCm39) |
D111G |
probably damaging |
Het |
Sema3e |
A |
G |
5: 14,302,646 (GRCm39) |
R724G |
possibly damaging |
Het |
She |
A |
G |
3: 89,741,544 (GRCm39) |
M232V |
possibly damaging |
Het |
Skic3 |
T |
A |
13: 76,333,275 (GRCm39) |
V1508E |
possibly damaging |
Het |
Slc25a54 |
A |
T |
3: 109,020,132 (GRCm39) |
N382I |
possibly damaging |
Het |
Slc26a2 |
T |
C |
18: 61,331,875 (GRCm39) |
M519V |
probably damaging |
Het |
Slc9a1 |
T |
A |
4: 133,097,967 (GRCm39) |
L38H |
probably damaging |
Het |
Snap47 |
A |
T |
11: 59,319,369 (GRCm39) |
D256E |
probably damaging |
Het |
Tacc3 |
A |
G |
5: 33,829,326 (GRCm39) |
T610A |
probably benign |
Het |
Tbc1d30 |
G |
A |
10: 121,103,121 (GRCm39) |
T637M |
probably benign |
Het |
Tbcd |
T |
A |
11: 121,464,681 (GRCm39) |
M572K |
probably benign |
Het |
Thoc7 |
A |
T |
14: 13,953,460 (GRCm38) |
D68E |
probably benign |
Het |
Tmpo |
G |
A |
10: 90,989,171 (GRCm39) |
T250M |
probably damaging |
Het |
Tmtc1 |
TGTCCGCCAGGCCCTTGCCCCAGAAGTC |
TGTC |
6: 148,345,445 (GRCm39) |
|
probably benign |
Het |
Tnfaip1 |
A |
T |
11: 78,418,396 (GRCm39) |
C224S |
possibly damaging |
Het |
Tshz1 |
T |
C |
18: 84,032,987 (GRCm39) |
T474A |
probably benign |
Het |
Tspoap1 |
C |
T |
11: 87,657,222 (GRCm39) |
Q345* |
probably null |
Het |
Ttc21a |
A |
G |
9: 119,774,067 (GRCm39) |
E258G |
possibly damaging |
Het |
Ttyh1 |
T |
C |
7: 4,131,225 (GRCm39) |
L232P |
probably damaging |
Het |
Usp2 |
T |
A |
9: 43,987,110 (GRCm39) |
L136Q |
probably damaging |
Het |
Usp31 |
T |
C |
7: 121,247,868 (GRCm39) |
S1192G |
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 |
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 |
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'- TTCTTGGGTCATGAAGAAGAGC -3'
(R):5'- ACATGGAGTGACGTTGCAG -3'
Sequencing Primer
(F):5'- ATGGATGCTCAGGACAATGGC -3'
(R):5'- GCAGCGTTGCCAGTTGG -3'
|
Posted On |
2016-04-27 |