Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca6 |
CTGTAGGAAATCTTCAATGT |
CTGT |
11: 110,101,019 (GRCm39) |
|
probably null |
Het |
Adgra2 |
T |
A |
8: 27,604,232 (GRCm39) |
L24* |
probably null |
Het |
Ampd2 |
C |
A |
3: 107,992,685 (GRCm39) |
|
probably benign |
Het |
Ankrd26 |
T |
G |
6: 118,502,752 (GRCm39) |
E806A |
probably damaging |
Het |
Apol9b |
A |
G |
15: 77,619,639 (GRCm39) |
D145G |
probably benign |
Het |
Ash1l |
T |
A |
3: 88,892,726 (GRCm39) |
M1535K |
probably benign |
Het |
Atf6 |
A |
G |
1: 170,622,304 (GRCm39) |
M439T |
probably damaging |
Het |
B3glct |
A |
T |
5: 149,677,621 (GRCm39) |
M417L |
probably damaging |
Het |
Cep192 |
A |
T |
18: 67,953,431 (GRCm39) |
T483S |
probably damaging |
Het |
Cep290 |
G |
A |
10: 100,354,657 (GRCm39) |
E914K |
probably damaging |
Het |
Chst15 |
C |
T |
7: 131,872,114 (GRCm39) |
A56T |
probably damaging |
Het |
Col27a1 |
A |
T |
4: 63,143,661 (GRCm39) |
T450S |
probably benign |
Het |
Cpsf2 |
A |
G |
12: 101,951,594 (GRCm39) |
N177S |
probably damaging |
Het |
Csmd3 |
CCTTTGCGCTT |
CCTT |
15: 47,604,632 (GRCm39) |
|
probably null |
Het |
Ctc1 |
C |
T |
11: 68,926,441 (GRCm39) |
A859V |
possibly damaging |
Het |
Dcakd |
A |
G |
11: 102,888,183 (GRCm39) |
Y134H |
possibly damaging |
Het |
Dctn3 |
G |
T |
4: 41,723,065 (GRCm39) |
Y22* |
probably null |
Het |
Dync2h1 |
T |
A |
9: 7,124,797 (GRCm39) |
D2025V |
probably damaging |
Het |
Dync2li1 |
T |
C |
17: 84,943,702 (GRCm39) |
S92P |
probably damaging |
Het |
Eml5 |
A |
G |
12: 98,853,356 (GRCm39) |
V81A |
probably damaging |
Het |
Espl1 |
C |
T |
15: 102,228,023 (GRCm39) |
R1625C |
probably damaging |
Het |
Fam181a |
T |
C |
12: 103,282,785 (GRCm39) |
V230A |
probably benign |
Het |
Fanci |
T |
A |
7: 79,045,743 (GRCm39) |
D28E |
probably benign |
Het |
Fmn1 |
A |
G |
2: 113,195,962 (GRCm39) |
N554S |
unknown |
Het |
Frem2 |
T |
C |
3: 53,444,751 (GRCm39) |
Y2460C |
probably damaging |
Het |
Fscb |
G |
A |
12: 64,520,567 (GRCm39) |
P300S |
probably damaging |
Het |
Gm28042 |
A |
G |
2: 119,867,229 (GRCm39) |
D438G |
probably benign |
Het |
Ldaf1 |
A |
G |
7: 119,719,462 (GRCm39) |
E157G |
possibly damaging |
Het |
Map1b |
C |
T |
13: 99,565,846 (GRCm39) |
V2292M |
unknown |
Het |
Nbas |
A |
G |
12: 13,380,647 (GRCm39) |
D635G |
possibly damaging |
Het |
Ncapg2 |
A |
G |
12: 116,414,095 (GRCm39) |
|
probably null |
Het |
Nrp2 |
A |
T |
1: 62,783,514 (GRCm39) |
E205V |
probably damaging |
Het |
Pcdhb3 |
A |
T |
18: 37,435,239 (GRCm39) |
T402S |
possibly damaging |
Het |
Phc1 |
T |
C |
6: 122,299,296 (GRCm39) |
N638D |
possibly damaging |
Het |
Plcb1 |
A |
G |
2: 135,188,250 (GRCm39) |
N781S |
possibly damaging |
Het |
Prkdc |
T |
A |
16: 15,523,071 (GRCm39) |
D1164E |
probably damaging |
Het |
Proser2 |
T |
A |
2: 6,105,506 (GRCm39) |
R353W |
possibly damaging |
Het |
Prxl2b |
T |
G |
4: 154,982,606 (GRCm39) |
Y56S |
probably damaging |
Het |
Ptges |
T |
A |
2: 30,782,708 (GRCm39) |
T115S |
probably benign |
Het |
Ptprk |
A |
T |
10: 28,436,138 (GRCm39) |
D833V |
probably damaging |
Het |
Pum1 |
T |
A |
4: 130,455,394 (GRCm39) |
L173* |
probably null |
Het |
Pum1 |
G |
T |
4: 130,455,395 (GRCm39) |
L269F |
probably damaging |
Het |
Rasgrp4 |
A |
G |
7: 28,838,470 (GRCm39) |
Y106C |
probably damaging |
Het |
Rbbp6 |
T |
A |
7: 122,598,697 (GRCm39) |
|
probably benign |
Het |
Rdh1 |
A |
G |
10: 127,596,041 (GRCm39) |
T79A |
possibly damaging |
Het |
Relb |
A |
C |
7: 19,347,686 (GRCm39) |
|
probably null |
Het |
Rnf122 |
G |
A |
8: 31,602,192 (GRCm39) |
W6* |
probably null |
Het |
Rnf31 |
A |
G |
14: 55,829,994 (GRCm39) |
E138G |
possibly damaging |
Het |
Scaf8 |
G |
A |
17: 3,247,485 (GRCm39) |
R936Q |
probably damaging |
Het |
Scube3 |
T |
A |
17: 28,385,108 (GRCm39) |
V686D |
possibly damaging |
Het |
Snrnp27 |
A |
T |
6: 86,653,196 (GRCm39) |
C141S |
probably benign |
Het |
Spns2 |
C |
T |
11: 72,349,497 (GRCm39) |
V252M |
possibly damaging |
Het |
Tomm40l |
C |
T |
1: 171,047,703 (GRCm39) |
S220N |
probably damaging |
Het |
Trim17 |
A |
G |
11: 58,862,237 (GRCm39) |
D423G |
probably damaging |
Het |
Trpc6 |
A |
AT |
9: 8,610,466 (GRCm39) |
|
probably null |
Het |
Tut4 |
G |
A |
4: 108,360,226 (GRCm39) |
R481Q |
possibly damaging |
Het |
Uba5 |
A |
T |
9: 103,937,442 (GRCm39) |
M89K |
probably damaging |
Het |
Vav2 |
T |
C |
2: 27,163,718 (GRCm39) |
D628G |
probably damaging |
Het |
Vmn2r107 |
T |
C |
17: 20,595,904 (GRCm39) |
L819P |
probably damaging |
Het |
Vmn2r25 |
A |
T |
6: 123,816,518 (GRCm39) |
D354E |
possibly damaging |
Het |
Xrn1 |
A |
G |
9: 95,888,873 (GRCm39) |
E984G |
possibly damaging |
Het |
Zbtb17 |
T |
C |
4: 141,191,557 (GRCm39) |
V223A |
probably benign |
Het |
Zfp592 |
T |
C |
7: 80,691,186 (GRCm39) |
S1122P |
possibly damaging |
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 |
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 |
|
R7007:Adcy8
|
UTSW |
15 |
64,576,565 (GRCm39) |
missense |
possibly damaging |
0.88 |
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 |
|
|