Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
G |
T |
11: 9,248,304 (GRCm39) |
V2684L |
probably benign |
Het |
Adcyap1r1 |
A |
G |
6: 55,455,067 (GRCm39) |
D110G |
probably benign |
Het |
Adgrd1 |
G |
A |
5: 129,208,641 (GRCm39) |
G281D |
probably damaging |
Het |
Afg1l |
A |
T |
10: 42,330,366 (GRCm39) |
C100* |
probably null |
Het |
Atp2a2 |
G |
A |
5: 122,595,372 (GRCm39) |
Q993* |
probably null |
Het |
Baz1a |
A |
G |
12: 54,977,095 (GRCm39) |
M389T |
probably benign |
Het |
Btnl4 |
T |
A |
17: 34,693,242 (GRCm39) |
M58L |
probably benign |
Het |
Card6 |
TTGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGCGGATGAGAGGGCTTAGCATGGGAGGACTG |
TTGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGCGGATGAGAGGGCTTAGCATGGGAGGACTG |
15: 5,128,173 (GRCm39) |
|
probably benign |
Het |
Cpeb1 |
A |
T |
7: 80,998,180 (GRCm39) |
F533Y |
probably damaging |
Het |
Ctnna1 |
T |
A |
18: 35,308,179 (GRCm39) |
N166K |
possibly damaging |
Het |
Ecsit |
T |
C |
9: 21,987,580 (GRCm39) |
H153R |
probably damaging |
Het |
Gbp8 |
T |
C |
5: 105,162,955 (GRCm39) |
K480E |
probably benign |
Het |
Glyat |
A |
T |
19: 12,625,373 (GRCm39) |
T66S |
probably benign |
Het |
Gm1110 |
T |
C |
9: 26,792,124 (GRCm39) |
Q632R |
probably benign |
Het |
Gm12185 |
C |
T |
11: 48,798,738 (GRCm39) |
R585Q |
probably damaging |
Het |
Gm17669 |
TAA |
TAAA |
18: 67,695,819 (GRCm39) |
|
probably null |
Het |
Gm7489 |
A |
C |
15: 53,749,195 (GRCm39) |
E89A |
unknown |
Het |
Grb7 |
C |
T |
11: 98,344,655 (GRCm39) |
Q353* |
probably null |
Het |
Ifi207 |
G |
A |
1: 173,562,738 (GRCm39) |
T136I |
unknown |
Het |
Ighv3-1 |
T |
C |
12: 113,928,224 (GRCm39) |
Y45C |
probably benign |
Het |
Ing5 |
A |
G |
1: 93,739,668 (GRCm39) |
M92V |
possibly damaging |
Het |
Ivl |
TTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTG |
TTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTG |
3: 92,479,608 (GRCm39) |
|
probably benign |
Het |
Kdm6b |
A |
T |
11: 69,290,778 (GRCm39) |
D1630E |
unknown |
Het |
Lmo7 |
C |
T |
14: 102,124,923 (GRCm39) |
Q583* |
probably null |
Het |
Lrrc37a |
T |
C |
11: 103,395,338 (GRCm39) |
D29G |
probably benign |
Het |
Mpdz |
G |
T |
4: 81,337,263 (GRCm39) |
A10D |
probably damaging |
Het |
Myh4 |
A |
G |
11: 67,131,821 (GRCm39) |
M94V |
possibly damaging |
Het |
Nectin2 |
A |
C |
7: 19,472,252 (GRCm39) |
L46V |
probably benign |
Het |
Nynrin |
A |
T |
14: 56,101,425 (GRCm39) |
T365S |
probably benign |
Het |
Or4c120 |
A |
T |
2: 89,000,977 (GRCm39) |
I193K |
probably benign |
Het |
Pde4b |
A |
C |
4: 102,459,875 (GRCm39) |
E570A |
probably damaging |
Het |
Phf3 |
T |
C |
1: 30,855,622 (GRCm39) |
H988R |
probably damaging |
Het |
Ppfia2 |
A |
G |
10: 106,763,708 (GRCm39) |
K1234E |
probably benign |
Het |
Prl7c1 |
A |
T |
13: 27,957,741 (GRCm39) |
M233K |
probably benign |
Het |
Prp2 |
C |
T |
6: 132,577,510 (GRCm39) |
P266S |
unknown |
Het |
Ralgds |
T |
C |
2: 28,432,486 (GRCm39) |
L160P |
probably damaging |
Het |
Rasa1 |
A |
T |
13: 85,375,237 (GRCm39) |
M664K |
possibly damaging |
Het |
Ryr2 |
T |
C |
13: 11,570,334 (GRCm39) |
T4930A |
probably benign |
Het |
Senp8 |
T |
C |
9: 59,644,763 (GRCm39) |
Y131C |
probably damaging |
Het |
Sp100 |
A |
G |
1: 85,635,837 (GRCm39) |
I547M |
probably benign |
Het |
Spata20 |
A |
G |
11: 94,375,434 (GRCm39) |
M120T |
probably damaging |
Het |
Spata31 |
A |
G |
13: 65,069,664 (GRCm39) |
H604R |
probably benign |
Het |
Sycp1 |
A |
T |
3: 102,842,149 (GRCm39) |
S53T |
probably benign |
Het |
Tgm1 |
T |
C |
14: 55,950,022 (GRCm39) |
D62G |
unknown |
Het |
Trpm1 |
G |
C |
7: 63,918,309 (GRCm39) |
E1434Q |
possibly damaging |
Het |
Tshb |
A |
T |
3: 102,685,480 (GRCm39) |
Y50N |
probably damaging |
Het |
Wdr17 |
A |
T |
8: 55,126,614 (GRCm39) |
Y413* |
probably null |
Het |
Zdhhc16 |
G |
A |
19: 41,926,209 (GRCm39) |
G55R |
possibly damaging |
Het |
|
Other mutations in Adamts9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00565:Adamts9
|
APN |
6 |
92,836,883 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01352:Adamts9
|
APN |
6 |
92,837,155 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01462:Adamts9
|
APN |
6 |
92,871,247 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01551:Adamts9
|
APN |
6 |
92,784,001 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01577:Adamts9
|
APN |
6 |
92,835,128 (GRCm39) |
splice site |
probably benign |
|
IGL01638:Adamts9
|
APN |
6 |
92,849,409 (GRCm39) |
missense |
probably benign |
0.19 |
IGL01757:Adamts9
|
APN |
6 |
92,773,140 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02102:Adamts9
|
APN |
6 |
92,754,420 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02379:Adamts9
|
APN |
6 |
92,774,014 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02419:Adamts9
|
APN |
6 |
92,773,978 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02554:Adamts9
|
APN |
6 |
92,857,828 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02832:Adamts9
|
APN |
6 |
92,784,156 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03164:Adamts9
|
APN |
6 |
92,866,918 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03347:Adamts9
|
APN |
6 |
92,864,413 (GRCm39) |
nonsense |
probably null |
|
IGL03401:Adamts9
|
APN |
6 |
92,763,849 (GRCm39) |
missense |
probably damaging |
0.97 |
basilisk
|
UTSW |
6 |
92,837,170 (GRCm39) |
missense |
probably benign |
0.35 |
bluebeard
|
UTSW |
6 |
92,856,940 (GRCm39) |
nonsense |
probably null |
|
Serpent
|
UTSW |
6 |
92,885,687 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4402001:Adamts9
|
UTSW |
6 |
92,849,328 (GRCm39) |
missense |
probably benign |
|
R0047:Adamts9
|
UTSW |
6 |
92,882,287 (GRCm39) |
unclassified |
probably benign |
|
R0047:Adamts9
|
UTSW |
6 |
92,882,287 (GRCm39) |
unclassified |
probably benign |
|
R0067:Adamts9
|
UTSW |
6 |
92,867,148 (GRCm39) |
missense |
probably damaging |
0.98 |
R0141:Adamts9
|
UTSW |
6 |
92,920,066 (GRCm39) |
missense |
probably benign |
|
R0326:Adamts9
|
UTSW |
6 |
92,835,038 (GRCm39) |
nonsense |
probably null |
|
R0396:Adamts9
|
UTSW |
6 |
92,774,986 (GRCm39) |
missense |
probably benign |
0.00 |
R0490:Adamts9
|
UTSW |
6 |
92,849,847 (GRCm39) |
missense |
probably benign |
|
R0504:Adamts9
|
UTSW |
6 |
92,889,626 (GRCm39) |
missense |
probably damaging |
1.00 |
R0620:Adamts9
|
UTSW |
6 |
92,835,094 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0669:Adamts9
|
UTSW |
6 |
92,857,938 (GRCm39) |
missense |
probably damaging |
1.00 |
R0682:Adamts9
|
UTSW |
6 |
92,880,783 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1412:Adamts9
|
UTSW |
6 |
92,773,414 (GRCm39) |
missense |
probably benign |
|
R1433:Adamts9
|
UTSW |
6 |
92,826,271 (GRCm39) |
critical splice donor site |
probably null |
|
R1558:Adamts9
|
UTSW |
6 |
92,885,692 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1661:Adamts9
|
UTSW |
6 |
92,857,604 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1801:Adamts9
|
UTSW |
6 |
92,840,357 (GRCm39) |
missense |
probably benign |
0.27 |
R1855:Adamts9
|
UTSW |
6 |
92,878,350 (GRCm39) |
splice site |
probably benign |
|
R1887:Adamts9
|
UTSW |
6 |
92,849,769 (GRCm39) |
critical splice donor site |
probably null |
|
R1934:Adamts9
|
UTSW |
6 |
92,920,102 (GRCm39) |
missense |
possibly damaging |
0.59 |
R1956:Adamts9
|
UTSW |
6 |
92,836,830 (GRCm39) |
missense |
probably damaging |
1.00 |
R1986:Adamts9
|
UTSW |
6 |
92,773,375 (GRCm39) |
missense |
probably benign |
|
R2370:Adamts9
|
UTSW |
6 |
92,837,184 (GRCm39) |
missense |
probably damaging |
0.99 |
R2376:Adamts9
|
UTSW |
6 |
92,889,812 (GRCm39) |
missense |
probably benign |
|
R2432:Adamts9
|
UTSW |
6 |
92,834,881 (GRCm39) |
missense |
probably damaging |
1.00 |
R2876:Adamts9
|
UTSW |
6 |
92,772,891 (GRCm39) |
splice site |
probably benign |
|
R3015:Adamts9
|
UTSW |
6 |
92,849,913 (GRCm39) |
missense |
probably benign |
0.05 |
R3611:Adamts9
|
UTSW |
6 |
92,846,965 (GRCm39) |
missense |
probably benign |
0.05 |
R4024:Adamts9
|
UTSW |
6 |
92,849,765 (GRCm39) |
splice site |
probably benign |
|
R4292:Adamts9
|
UTSW |
6 |
92,772,977 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4403:Adamts9
|
UTSW |
6 |
92,836,845 (GRCm39) |
missense |
probably damaging |
1.00 |
R4574:Adamts9
|
UTSW |
6 |
92,856,940 (GRCm39) |
nonsense |
probably null |
|
R4677:Adamts9
|
UTSW |
6 |
92,793,587 (GRCm39) |
start codon destroyed |
probably null |
|
R5114:Adamts9
|
UTSW |
6 |
92,867,254 (GRCm39) |
missense |
probably benign |
0.03 |
R5260:Adamts9
|
UTSW |
6 |
92,784,118 (GRCm39) |
missense |
probably benign |
0.00 |
R5384:Adamts9
|
UTSW |
6 |
92,774,999 (GRCm39) |
missense |
probably damaging |
1.00 |
R5423:Adamts9
|
UTSW |
6 |
92,857,678 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5497:Adamts9
|
UTSW |
6 |
92,831,346 (GRCm39) |
missense |
probably damaging |
1.00 |
R5629:Adamts9
|
UTSW |
6 |
92,775,114 (GRCm39) |
missense |
probably damaging |
1.00 |
R5943:Adamts9
|
UTSW |
6 |
92,880,767 (GRCm39) |
missense |
probably benign |
0.02 |
R6039:Adamts9
|
UTSW |
6 |
92,885,527 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6039:Adamts9
|
UTSW |
6 |
92,885,527 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6051:Adamts9
|
UTSW |
6 |
92,867,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R6051:Adamts9
|
UTSW |
6 |
92,836,907 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6082:Adamts9
|
UTSW |
6 |
92,866,930 (GRCm39) |
missense |
probably damaging |
1.00 |
R6192:Adamts9
|
UTSW |
6 |
92,774,002 (GRCm39) |
missense |
probably damaging |
1.00 |
R6291:Adamts9
|
UTSW |
6 |
92,867,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R6502:Adamts9
|
UTSW |
6 |
92,849,316 (GRCm39) |
missense |
probably damaging |
1.00 |
R6818:Adamts9
|
UTSW |
6 |
92,882,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R6848:Adamts9
|
UTSW |
6 |
92,840,335 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7028:Adamts9
|
UTSW |
6 |
92,886,774 (GRCm39) |
nonsense |
probably null |
|
R7095:Adamts9
|
UTSW |
6 |
92,864,672 (GRCm39) |
missense |
probably benign |
0.39 |
R7287:Adamts9
|
UTSW |
6 |
92,866,984 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7294:Adamts9
|
UTSW |
6 |
92,871,270 (GRCm39) |
missense |
probably damaging |
1.00 |
R7313:Adamts9
|
UTSW |
6 |
92,835,102 (GRCm39) |
missense |
probably damaging |
1.00 |
R7581:Adamts9
|
UTSW |
6 |
92,914,319 (GRCm39) |
missense |
probably benign |
0.00 |
R7682:Adamts9
|
UTSW |
6 |
92,857,679 (GRCm39) |
missense |
possibly damaging |
0.57 |
R7691:Adamts9
|
UTSW |
6 |
92,773,219 (GRCm39) |
missense |
probably damaging |
1.00 |
R7791:Adamts9
|
UTSW |
6 |
92,849,366 (GRCm39) |
missense |
probably benign |
0.00 |
R7851:Adamts9
|
UTSW |
6 |
92,885,687 (GRCm39) |
missense |
probably damaging |
1.00 |
R7974:Adamts9
|
UTSW |
6 |
92,886,668 (GRCm39) |
critical splice donor site |
probably null |
|
R8224:Adamts9
|
UTSW |
6 |
92,773,351 (GRCm39) |
missense |
probably damaging |
0.96 |
R8328:Adamts9
|
UTSW |
6 |
92,866,993 (GRCm39) |
missense |
probably benign |
0.17 |
R8334:Adamts9
|
UTSW |
6 |
92,914,225 (GRCm39) |
splice site |
probably null |
|
R8559:Adamts9
|
UTSW |
6 |
92,784,117 (GRCm39) |
missense |
probably benign |
0.01 |
R8709:Adamts9
|
UTSW |
6 |
92,784,144 (GRCm39) |
missense |
probably damaging |
1.00 |
R8735:Adamts9
|
UTSW |
6 |
92,837,048 (GRCm39) |
intron |
probably benign |
|
R8739:Adamts9
|
UTSW |
6 |
92,831,261 (GRCm39) |
missense |
probably benign |
0.04 |
R9108:Adamts9
|
UTSW |
6 |
92,857,721 (GRCm39) |
missense |
probably damaging |
1.00 |
R9171:Adamts9
|
UTSW |
6 |
92,849,381 (GRCm39) |
missense |
probably benign |
0.03 |
R9198:Adamts9
|
UTSW |
6 |
92,837,170 (GRCm39) |
missense |
probably benign |
0.35 |
R9299:Adamts9
|
UTSW |
6 |
92,773,976 (GRCm39) |
missense |
probably benign |
0.00 |
R9300:Adamts9
|
UTSW |
6 |
92,864,371 (GRCm39) |
missense |
probably benign |
0.10 |
R9308:Adamts9
|
UTSW |
6 |
92,857,875 (GRCm39) |
missense |
probably benign |
0.03 |
R9325:Adamts9
|
UTSW |
6 |
92,849,279 (GRCm39) |
missense |
probably benign |
0.00 |
R9397:Adamts9
|
UTSW |
6 |
92,878,444 (GRCm39) |
missense |
probably damaging |
1.00 |
R9550:Adamts9
|
UTSW |
6 |
92,878,429 (GRCm39) |
missense |
probably benign |
0.00 |
R9623:Adamts9
|
UTSW |
6 |
92,857,661 (GRCm39) |
missense |
probably benign |
0.02 |
R9698:Adamts9
|
UTSW |
6 |
92,784,121 (GRCm39) |
missense |
probably damaging |
1.00 |
R9755:Adamts9
|
UTSW |
6 |
92,856,922 (GRCm39) |
missense |
probably benign |
0.15 |
RF013:Adamts9
|
UTSW |
6 |
92,920,126 (GRCm39) |
missense |
possibly damaging |
0.88 |
Z1177:Adamts9
|
UTSW |
6 |
92,831,327 (GRCm39) |
missense |
probably damaging |
0.99 |
|