Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930474N05Rik |
C |
T |
14: 35,817,121 (GRCm39) |
T57I |
probably benign |
Het |
Adgrv1 |
T |
A |
13: 81,684,483 (GRCm39) |
I1073F |
possibly damaging |
Het |
Akap3 |
A |
G |
6: 126,843,439 (GRCm39) |
D686G |
probably damaging |
Het |
Alg2 |
A |
T |
4: 47,471,881 (GRCm39) |
I309N |
probably benign |
Het |
Ankrd36 |
A |
G |
11: 5,639,168 (GRCm39) |
E1360G |
probably benign |
Het |
Aox1 |
C |
A |
1: 58,370,051 (GRCm39) |
Q788K |
probably damaging |
Het |
Apoc2 |
A |
T |
7: 19,407,282 (GRCm39) |
D26E |
possibly damaging |
Het |
Bbx |
G |
A |
16: 50,022,851 (GRCm39) |
T703I |
possibly damaging |
Het |
C2cd4d |
T |
C |
3: 94,271,378 (GRCm39) |
Y215H |
probably benign |
Het |
C3 |
C |
T |
17: 57,525,809 (GRCm39) |
E858K |
probably benign |
Het |
Ciita |
T |
C |
16: 10,329,171 (GRCm39) |
L482P |
probably damaging |
Het |
Cldn9 |
T |
C |
17: 23,902,052 (GRCm39) |
E191G |
probably benign |
Het |
Cnst |
T |
A |
1: 179,438,133 (GRCm39) |
S566T |
probably damaging |
Het |
Col5a2 |
A |
G |
1: 45,417,609 (GRCm39) |
I1322T |
possibly damaging |
Het |
Cp |
G |
A |
3: 20,024,137 (GRCm39) |
V326M |
probably damaging |
Het |
Cyp7b1 |
G |
A |
3: 18,151,782 (GRCm39) |
Q144* |
probably null |
Het |
Dnah10 |
T |
C |
5: 124,864,490 (GRCm39) |
S2232P |
probably damaging |
Het |
Dnah17 |
T |
C |
11: 118,009,697 (GRCm39) |
E625G |
possibly damaging |
Het |
Dnah7c |
T |
A |
1: 46,571,910 (GRCm39) |
D794E |
probably benign |
Het |
Dusp10 |
G |
A |
1: 183,769,414 (GRCm39) |
V127M |
probably benign |
Het |
Dysf |
G |
C |
6: 84,090,962 (GRCm39) |
W1015C |
probably damaging |
Het |
Fbxw17 |
T |
C |
13: 50,577,808 (GRCm39) |
Y104H |
probably damaging |
Het |
Gm6408 |
G |
A |
5: 146,420,647 (GRCm39) |
E176K |
probably damaging |
Het |
Gp1bb |
T |
A |
16: 18,439,689 (GRCm39) |
D135V |
possibly damaging |
Het |
Gprin1 |
C |
T |
13: 54,886,069 (GRCm39) |
C735Y |
probably damaging |
Het |
Heatr9 |
T |
A |
11: 83,411,446 (GRCm39) |
M30L |
possibly damaging |
Het |
Hhat |
G |
A |
1: 192,376,134 (GRCm39) |
T333I |
possibly damaging |
Het |
Htr5b |
A |
G |
1: 121,438,223 (GRCm39) |
F336S |
probably damaging |
Het |
Ippk |
T |
G |
13: 49,590,181 (GRCm39) |
|
probably null |
Het |
Jph1 |
T |
A |
1: 17,074,410 (GRCm39) |
H11L |
possibly damaging |
Het |
Kif12 |
T |
A |
4: 63,084,717 (GRCm39) |
I534L |
probably benign |
Het |
Lemd3 |
A |
T |
10: 120,788,137 (GRCm39) |
F523I |
probably benign |
Het |
Lgsn |
C |
A |
1: 31,229,508 (GRCm39) |
H76Q |
probably benign |
Het |
Lipm |
T |
A |
19: 34,089,497 (GRCm39) |
W152R |
probably damaging |
Het |
Mei1 |
A |
T |
15: 81,978,200 (GRCm39) |
R216W |
probably damaging |
Het |
Mybpc1 |
C |
T |
10: 88,389,274 (GRCm39) |
G379S |
probably damaging |
Het |
Myh8 |
A |
G |
11: 67,179,142 (GRCm39) |
T512A |
probably benign |
Het |
Nf1 |
A |
G |
11: 79,337,849 (GRCm39) |
|
probably null |
Het |
Npc1 |
T |
C |
18: 12,343,605 (GRCm39) |
T463A |
probably benign |
Het |
Or12e10 |
A |
G |
2: 87,640,230 (GRCm39) |
N22S |
probably damaging |
Het |
Or2y13 |
G |
A |
11: 49,415,011 (GRCm39) |
V154M |
probably benign |
Het |
Or6c7 |
A |
T |
10: 129,323,277 (GRCm39) |
I133F |
probably damaging |
Het |
Osbpl11 |
T |
G |
16: 33,047,309 (GRCm39) |
I424R |
possibly damaging |
Het |
Pnma8b |
A |
T |
7: 16,680,181 (GRCm39) |
K388N |
possibly damaging |
Het |
Ppp1r26 |
A |
T |
2: 28,341,171 (GRCm39) |
K267I |
probably damaging |
Het |
Psmb5 |
A |
T |
14: 54,854,166 (GRCm39) |
M104K |
probably damaging |
Het |
Ptges2 |
T |
C |
2: 32,292,318 (GRCm39) |
V378A |
probably benign |
Het |
Rcan2 |
C |
T |
17: 44,147,216 (GRCm39) |
S18F |
probably benign |
Het |
Saxo5 |
A |
T |
8: 3,526,309 (GRCm39) |
D154V |
probably damaging |
Het |
Sf3b2 |
C |
T |
19: 5,324,545 (GRCm39) |
R859Q |
probably benign |
Het |
Slc7a1 |
G |
A |
5: 148,289,256 (GRCm39) |
|
|
Het |
Spata31d1a |
T |
A |
13: 59,851,448 (GRCm39) |
T227S |
probably benign |
Het |
Sptbn2 |
T |
A |
19: 4,794,173 (GRCm39) |
V1459E |
possibly damaging |
Het |
Srgap2 |
T |
C |
1: 131,247,275 (GRCm39) |
I586V |
probably benign |
Het |
St6galnac1 |
G |
A |
11: 116,657,833 (GRCm39) |
R356* |
probably null |
Het |
Taf5 |
T |
A |
19: 47,059,650 (GRCm39) |
F265I |
probably damaging |
Het |
Tkfc |
T |
A |
19: 10,573,727 (GRCm39) |
I229L |
probably benign |
Het |
Tmem132c |
T |
A |
5: 127,436,679 (GRCm39) |
L56Q |
probably damaging |
Het |
Togaram2 |
C |
T |
17: 72,016,638 (GRCm39) |
A665V |
probably damaging |
Het |
Ttn |
G |
A |
2: 76,537,390 (GRCm39) |
T34846I |
probably benign |
Het |
Tyr |
G |
A |
7: 87,142,548 (GRCm39) |
A4V |
probably benign |
Het |
Ubap2 |
A |
C |
4: 41,206,221 (GRCm39) |
F549L |
probably damaging |
Het |
Usp2 |
T |
C |
9: 44,001,339 (GRCm39) |
S294P |
probably damaging |
Het |
Vrk3 |
A |
G |
7: 44,407,187 (GRCm39) |
N53D |
probably damaging |
Het |
Zfp324 |
T |
C |
7: 12,705,142 (GRCm39) |
S444P |
probably damaging |
Het |
Zfp597 |
T |
C |
16: 3,683,791 (GRCm39) |
I322V |
probably benign |
Het |
|
Other mutations in Adcy8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00589:Adcy8
|
APN |
15 |
64,659,216 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00690:Adcy8
|
APN |
15 |
64,571,151 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00990:Adcy8
|
APN |
15 |
64,694,162 (GRCm39) |
missense |
probably benign |
0.07 |
IGL01083:Adcy8
|
APN |
15 |
64,659,191 (GRCm39) |
missense |
probably benign |
0.21 |
IGL01296:Adcy8
|
APN |
15 |
64,655,628 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01433:Adcy8
|
APN |
15 |
64,609,263 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL01584:Adcy8
|
APN |
15 |
64,687,170 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01729:Adcy8
|
APN |
15 |
64,678,511 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02023:Adcy8
|
APN |
15 |
64,694,069 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02420:Adcy8
|
APN |
15 |
64,659,303 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02613:Adcy8
|
APN |
15 |
64,655,833 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL02662:Adcy8
|
APN |
15 |
64,618,744 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03180:Adcy8
|
APN |
15 |
64,655,799 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL03327:Adcy8
|
APN |
15 |
64,792,116 (GRCm39) |
missense |
probably damaging |
1.00 |
revolutionary
|
UTSW |
15 |
64,571,236 (GRCm39) |
missense |
probably damaging |
1.00 |
whirligig
|
UTSW |
15 |
64,571,134 (GRCm39) |
missense |
probably damaging |
1.00 |
F0336:Adcy8
|
UTSW |
15 |
64,694,083 (GRCm39) |
missense |
probably benign |
0.38 |
K7894:Adcy8
|
UTSW |
15 |
64,694,083 (GRCm39) |
missense |
probably benign |
0.38 |
PIT4581001:Adcy8
|
UTSW |
15 |
64,626,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R0035:Adcy8
|
UTSW |
15 |
64,571,217 (GRCm39) |
missense |
probably benign |
0.29 |
R0119:Adcy8
|
UTSW |
15 |
64,588,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R0129:Adcy8
|
UTSW |
15 |
64,618,862 (GRCm39) |
missense |
probably benign |
0.18 |
R0299:Adcy8
|
UTSW |
15 |
64,588,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R0573:Adcy8
|
UTSW |
15 |
64,694,044 (GRCm39) |
missense |
probably damaging |
1.00 |
R0961:Adcy8
|
UTSW |
15 |
64,626,711 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1203:Adcy8
|
UTSW |
15 |
64,618,780 (GRCm39) |
missense |
probably damaging |
1.00 |
R1239:Adcy8
|
UTSW |
15 |
64,587,911 (GRCm39) |
missense |
probably damaging |
0.98 |
R1615:Adcy8
|
UTSW |
15 |
64,743,625 (GRCm39) |
missense |
probably benign |
0.25 |
R1881:Adcy8
|
UTSW |
15 |
64,678,503 (GRCm39) |
missense |
probably damaging |
0.96 |
R2013:Adcy8
|
UTSW |
15 |
64,639,727 (GRCm39) |
missense |
probably benign |
0.00 |
R2014:Adcy8
|
UTSW |
15 |
64,639,727 (GRCm39) |
missense |
probably benign |
0.00 |
R2015:Adcy8
|
UTSW |
15 |
64,639,727 (GRCm39) |
missense |
probably benign |
0.00 |
R2164:Adcy8
|
UTSW |
15 |
64,792,783 (GRCm39) |
missense |
probably benign |
|
R2228:Adcy8
|
UTSW |
15 |
64,694,056 (GRCm39) |
missense |
possibly damaging |
0.58 |
R2229:Adcy8
|
UTSW |
15 |
64,694,056 (GRCm39) |
missense |
possibly damaging |
0.58 |
R2241:Adcy8
|
UTSW |
15 |
64,571,230 (GRCm39) |
missense |
possibly damaging |
0.78 |
R3177:Adcy8
|
UTSW |
15 |
64,571,008 (GRCm39) |
missense |
probably benign |
0.10 |
R3277:Adcy8
|
UTSW |
15 |
64,571,008 (GRCm39) |
missense |
probably benign |
0.10 |
R3404:Adcy8
|
UTSW |
15 |
64,571,449 (GRCm39) |
missense |
probably damaging |
1.00 |
R3688:Adcy8
|
UTSW |
15 |
64,743,556 (GRCm39) |
missense |
probably damaging |
0.99 |
R3709:Adcy8
|
UTSW |
15 |
64,597,384 (GRCm39) |
splice site |
probably benign |
|
R3710:Adcy8
|
UTSW |
15 |
64,597,384 (GRCm39) |
splice site |
probably benign |
|
R3778:Adcy8
|
UTSW |
15 |
64,618,846 (GRCm39) |
missense |
probably damaging |
1.00 |
R4037:Adcy8
|
UTSW |
15 |
64,597,319 (GRCm39) |
missense |
probably benign |
0.06 |
R4685:Adcy8
|
UTSW |
15 |
64,609,287 (GRCm39) |
missense |
probably benign |
0.09 |
R4731:Adcy8
|
UTSW |
15 |
64,626,711 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4732:Adcy8
|
UTSW |
15 |
64,626,711 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4733:Adcy8
|
UTSW |
15 |
64,626,711 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5071:Adcy8
|
UTSW |
15 |
64,659,207 (GRCm39) |
missense |
probably damaging |
1.00 |
R5073:Adcy8
|
UTSW |
15 |
64,659,207 (GRCm39) |
missense |
probably damaging |
1.00 |
R5074:Adcy8
|
UTSW |
15 |
64,659,207 (GRCm39) |
missense |
probably damaging |
1.00 |
R5091:Adcy8
|
UTSW |
15 |
64,678,553 (GRCm39) |
missense |
probably damaging |
1.00 |
R5285:Adcy8
|
UTSW |
15 |
64,639,706 (GRCm39) |
missense |
possibly damaging |
0.68 |
R5287:Adcy8
|
UTSW |
15 |
64,588,001 (GRCm39) |
missense |
probably benign |
0.04 |
R5403:Adcy8
|
UTSW |
15 |
64,588,001 (GRCm39) |
missense |
probably benign |
0.04 |
R5521:Adcy8
|
UTSW |
15 |
64,687,199 (GRCm39) |
missense |
probably damaging |
1.00 |
R5633:Adcy8
|
UTSW |
15 |
64,571,134 (GRCm39) |
missense |
probably damaging |
1.00 |
R5712:Adcy8
|
UTSW |
15 |
64,626,715 (GRCm39) |
missense |
probably damaging |
1.00 |
R5745:Adcy8
|
UTSW |
15 |
64,792,320 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5787:Adcy8
|
UTSW |
15 |
64,576,067 (GRCm39) |
missense |
probably damaging |
0.98 |
R5839:Adcy8
|
UTSW |
15 |
64,588,031 (GRCm39) |
missense |
probably damaging |
1.00 |
R5890:Adcy8
|
UTSW |
15 |
64,687,266 (GRCm39) |
missense |
probably damaging |
1.00 |
R6156:Adcy8
|
UTSW |
15 |
64,689,488 (GRCm39) |
splice site |
probably null |
|
R6338:Adcy8
|
UTSW |
15 |
64,792,466 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6516:Adcy8
|
UTSW |
15 |
64,571,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R6525:Adcy8
|
UTSW |
15 |
64,609,243 (GRCm39) |
nonsense |
probably null |
|
R6636:Adcy8
|
UTSW |
15 |
64,659,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R6823:Adcy8
|
UTSW |
15 |
64,626,735 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7070:Adcy8
|
UTSW |
15 |
64,792,404 (GRCm39) |
missense |
probably damaging |
1.00 |
R7092:Adcy8
|
UTSW |
15 |
64,743,619 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7371:Adcy8
|
UTSW |
15 |
64,571,067 (GRCm39) |
missense |
probably benign |
0.19 |
R7457:Adcy8
|
UTSW |
15 |
64,792,529 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7611:Adcy8
|
UTSW |
15 |
64,792,882 (GRCm39) |
missense |
probably benign |
|
R7644:Adcy8
|
UTSW |
15 |
64,571,218 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7697:Adcy8
|
UTSW |
15 |
64,618,850 (GRCm39) |
missense |
probably benign |
|
R7735:Adcy8
|
UTSW |
15 |
64,655,629 (GRCm39) |
missense |
probably benign |
0.10 |
R7789:Adcy8
|
UTSW |
15 |
64,743,623 (GRCm39) |
nonsense |
probably null |
|
R7860:Adcy8
|
UTSW |
15 |
64,571,322 (GRCm39) |
missense |
probably damaging |
0.97 |
R7894:Adcy8
|
UTSW |
15 |
64,792,054 (GRCm39) |
missense |
possibly damaging |
0.60 |
R7948:Adcy8
|
UTSW |
15 |
64,687,199 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7966:Adcy8
|
UTSW |
15 |
64,573,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R8024:Adcy8
|
UTSW |
15 |
64,792,095 (GRCm39) |
missense |
probably damaging |
1.00 |
R8097:Adcy8
|
UTSW |
15 |
64,743,711 (GRCm39) |
splice site |
probably null |
|
R8158:Adcy8
|
UTSW |
15 |
64,655,655 (GRCm39) |
missense |
probably benign |
0.32 |
R8463:Adcy8
|
UTSW |
15 |
64,792,874 (GRCm39) |
missense |
probably benign |
|
R8474:Adcy8
|
UTSW |
15 |
64,576,638 (GRCm39) |
missense |
probably damaging |
0.98 |
R8696:Adcy8
|
UTSW |
15 |
64,687,235 (GRCm39) |
missense |
probably benign |
0.30 |
R8955:Adcy8
|
UTSW |
15 |
64,576,554 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8973:Adcy8
|
UTSW |
15 |
64,570,984 (GRCm39) |
makesense |
probably null |
|
R9015:Adcy8
|
UTSW |
15 |
64,597,206 (GRCm39) |
intron |
probably benign |
|
R9041:Adcy8
|
UTSW |
15 |
64,609,287 (GRCm39) |
missense |
probably benign |
0.31 |
R9052:Adcy8
|
UTSW |
15 |
64,792,764 (GRCm39) |
missense |
probably benign |
0.00 |
R9074:Adcy8
|
UTSW |
15 |
64,573,940 (GRCm39) |
missense |
probably damaging |
0.96 |
R9183:Adcy8
|
UTSW |
15 |
64,694,116 (GRCm39) |
missense |
probably damaging |
0.98 |
R9259:Adcy8
|
UTSW |
15 |
64,576,604 (GRCm39) |
missense |
probably damaging |
1.00 |
R9498:Adcy8
|
UTSW |
15 |
64,792,045 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9522:Adcy8
|
UTSW |
15 |
64,792,560 (GRCm39) |
missense |
probably damaging |
0.99 |
R9800:Adcy8
|
UTSW |
15 |
64,571,095 (GRCm39) |
missense |
probably benign |
0.19 |
Z1176:Adcy8
|
UTSW |
15 |
64,597,367 (GRCm39) |
missense |
probably benign |
0.16 |
Z1177:Adcy8
|
UTSW |
15 |
64,571,026 (GRCm39) |
missense |
probably benign |
|
|