Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acss1 |
T |
C |
2: 150,461,606 (GRCm39) |
E659G |
probably benign |
Het |
Adgrg6 |
A |
C |
10: 14,411,703 (GRCm39) |
|
probably benign |
Het |
Als2cl |
A |
G |
9: 110,718,227 (GRCm39) |
K323E |
possibly damaging |
Het |
Atm |
A |
C |
9: 53,424,416 (GRCm39) |
S628R |
probably benign |
Het |
Baz2a |
T |
C |
10: 127,950,395 (GRCm39) |
V443A |
probably benign |
Het |
Bclaf3 |
T |
A |
X: 158,341,357 (GRCm39) |
F545Y |
probably benign |
Het |
Calcr |
T |
C |
6: 3,717,196 (GRCm39) |
Y88C |
probably damaging |
Het |
Ccdc178 |
C |
T |
18: 22,278,501 (GRCm39) |
|
probably benign |
Het |
Chrnd |
G |
A |
1: 87,120,649 (GRCm39) |
W91* |
probably null |
Het |
Cntln |
T |
C |
4: 84,897,652 (GRCm39) |
F413S |
probably benign |
Het |
Ctsq |
A |
T |
13: 61,183,998 (GRCm39) |
I308N |
probably damaging |
Het |
Cyp2d34 |
A |
T |
15: 82,501,736 (GRCm39) |
V258D |
probably damaging |
Het |
Dnajc13 |
G |
A |
9: 104,039,979 (GRCm39) |
P2044S |
probably benign |
Het |
Hnrnpm |
C |
A |
17: 33,868,876 (GRCm39) |
R517L |
probably damaging |
Het |
Hps6 |
A |
T |
19: 45,992,099 (GRCm39) |
D12V |
probably damaging |
Het |
Hpse |
T |
C |
5: 100,846,865 (GRCm39) |
D188G |
probably benign |
Het |
Id2 |
C |
A |
12: 25,145,355 (GRCm39) |
E123* |
probably null |
Het |
Ints10 |
C |
T |
8: 69,271,985 (GRCm39) |
P562L |
probably damaging |
Het |
Kctd10 |
G |
A |
5: 114,505,410 (GRCm39) |
R195C |
probably damaging |
Het |
Kel |
A |
C |
6: 41,665,509 (GRCm39) |
L537R |
probably damaging |
Het |
Kif19a |
T |
C |
11: 114,675,599 (GRCm39) |
V357A |
probably damaging |
Het |
Lrrtm3 |
A |
T |
10: 63,924,988 (GRCm39) |
S60T |
probably damaging |
Het |
Myof |
C |
A |
19: 37,949,382 (GRCm39) |
R608L |
probably benign |
Het |
Naa35 |
A |
T |
13: 59,778,485 (GRCm39) |
I669F |
probably benign |
Het |
Or8g2b |
A |
T |
9: 39,751,002 (GRCm39) |
I91F |
probably benign |
Het |
Or8g53 |
A |
G |
9: 39,683,407 (GRCm39) |
S230P |
possibly damaging |
Het |
Pclo |
G |
T |
5: 14,728,035 (GRCm39) |
|
probably benign |
Het |
Pik3c3 |
C |
T |
18: 30,407,417 (GRCm39) |
S55F |
probably damaging |
Het |
Prdm6 |
T |
G |
18: 53,673,300 (GRCm39) |
D153E |
possibly damaging |
Het |
Rnf183 |
T |
C |
4: 62,346,610 (GRCm39) |
T63A |
probably benign |
Het |
Samd4b |
A |
C |
7: 28,101,302 (GRCm39) |
I108S |
probably damaging |
Het |
Slc9a7 |
T |
C |
X: 19,972,260 (GRCm39) |
D708G |
possibly damaging |
Het |
Stim2 |
A |
G |
5: 54,210,835 (GRCm39) |
D90G |
probably benign |
Het |
Tmem52b |
A |
G |
6: 129,493,678 (GRCm39) |
D97G |
probably damaging |
Het |
Tnfsf15 |
T |
C |
4: 63,652,518 (GRCm39) |
R98G |
probably benign |
Het |
Uxs1 |
C |
T |
1: 43,796,173 (GRCm39) |
V310I |
probably benign |
Het |
Vcan |
A |
C |
13: 89,873,425 (GRCm39) |
M143R |
probably damaging |
Het |
Vmn2r93 |
T |
C |
17: 18,546,504 (GRCm39) |
F792S |
probably damaging |
Het |
Zfp455 |
T |
C |
13: 67,355,962 (GRCm39) |
I345T |
probably benign |
Het |
Zfp938 |
A |
T |
10: 82,062,317 (GRCm39) |
M101K |
probably benign |
Het |
Zkscan2 |
A |
G |
7: 123,079,195 (GRCm39) |
S921P |
probably damaging |
Het |
|
Other mutations in Cdh20 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00428:Cdh20
|
APN |
1 |
104,881,612 (GRCm39) |
missense |
probably benign |
0.05 |
IGL00742:Cdh20
|
APN |
1 |
109,993,356 (GRCm39) |
missense |
probably benign |
0.22 |
IGL00848:Cdh20
|
APN |
1 |
104,861,981 (GRCm39) |
missense |
probably benign |
|
IGL00861:Cdh20
|
APN |
1 |
109,988,718 (GRCm39) |
splice site |
probably benign |
|
IGL01016:Cdh20
|
APN |
1 |
110,036,686 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01393:Cdh20
|
APN |
1 |
104,861,969 (GRCm39) |
missense |
probably benign |
|
IGL01396:Cdh20
|
APN |
1 |
104,875,154 (GRCm39) |
missense |
possibly damaging |
0.59 |
IGL01485:Cdh20
|
APN |
1 |
104,861,832 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01538:Cdh20
|
APN |
1 |
109,988,870 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01612:Cdh20
|
APN |
1 |
104,921,895 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01763:Cdh20
|
APN |
1 |
109,993,520 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01765:Cdh20
|
APN |
1 |
109,988,836 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01937:Cdh20
|
APN |
1 |
110,065,826 (GRCm39) |
missense |
probably benign |
|
IGL01947:Cdh20
|
APN |
1 |
104,921,649 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL01967:Cdh20
|
APN |
1 |
104,868,762 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02020:Cdh20
|
APN |
1 |
110,066,078 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02135:Cdh20
|
APN |
1 |
110,066,004 (GRCm39) |
nonsense |
probably null |
|
IGL02226:Cdh20
|
APN |
1 |
104,881,816 (GRCm39) |
splice site |
probably benign |
|
IGL02285:Cdh20
|
APN |
1 |
110,065,921 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02318:Cdh20
|
APN |
1 |
104,881,764 (GRCm39) |
missense |
probably null |
0.03 |
IGL02326:Cdh20
|
APN |
1 |
104,902,764 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02798:Cdh20
|
APN |
1 |
104,875,190 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02963:Cdh20
|
APN |
1 |
104,861,823 (GRCm39) |
start codon destroyed |
probably null |
0.66 |
IGL03081:Cdh20
|
APN |
1 |
104,868,982 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03237:Cdh20
|
APN |
1 |
110,066,037 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL03280:Cdh20
|
APN |
1 |
110,036,498 (GRCm39) |
nonsense |
probably null |
|
IGL03347:Cdh20
|
APN |
1 |
110,065,973 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL03385:Cdh20
|
APN |
1 |
109,993,516 (GRCm39) |
missense |
possibly damaging |
0.90 |
3-1:Cdh20
|
UTSW |
1 |
104,875,145 (GRCm39) |
missense |
possibly damaging |
0.84 |
BB002:Cdh20
|
UTSW |
1 |
104,912,473 (GRCm39) |
missense |
probably damaging |
0.99 |
BB012:Cdh20
|
UTSW |
1 |
104,912,473 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02802:Cdh20
|
UTSW |
1 |
110,065,655 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02991:Cdh20
|
UTSW |
1 |
104,861,972 (GRCm39) |
missense |
probably benign |
|
R0030:Cdh20
|
UTSW |
1 |
110,065,798 (GRCm39) |
nonsense |
probably null |
|
R0070:Cdh20
|
UTSW |
1 |
110,026,102 (GRCm39) |
missense |
probably benign |
0.37 |
R0070:Cdh20
|
UTSW |
1 |
110,026,102 (GRCm39) |
missense |
probably benign |
0.37 |
R0178:Cdh20
|
UTSW |
1 |
104,902,776 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0255:Cdh20
|
UTSW |
1 |
109,922,036 (GRCm39) |
missense |
probably benign |
0.09 |
R0365:Cdh20
|
UTSW |
1 |
110,036,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R0506:Cdh20
|
UTSW |
1 |
110,027,844 (GRCm39) |
missense |
probably damaging |
1.00 |
R0549:Cdh20
|
UTSW |
1 |
110,036,674 (GRCm39) |
missense |
probably damaging |
1.00 |
R0599:Cdh20
|
UTSW |
1 |
109,980,696 (GRCm39) |
missense |
probably damaging |
1.00 |
R0648:Cdh20
|
UTSW |
1 |
109,993,337 (GRCm39) |
splice site |
probably benign |
|
R1033:Cdh20
|
UTSW |
1 |
110,012,783 (GRCm39) |
missense |
probably damaging |
0.96 |
R1114:Cdh20
|
UTSW |
1 |
104,906,739 (GRCm39) |
missense |
probably damaging |
0.96 |
R1173:Cdh20
|
UTSW |
1 |
109,988,862 (GRCm39) |
missense |
probably benign |
0.10 |
R1174:Cdh20
|
UTSW |
1 |
109,988,862 (GRCm39) |
missense |
probably benign |
0.10 |
R1175:Cdh20
|
UTSW |
1 |
109,988,862 (GRCm39) |
missense |
probably benign |
0.10 |
R1401:Cdh20
|
UTSW |
1 |
104,875,222 (GRCm39) |
missense |
possibly damaging |
0.65 |
R1403:Cdh20
|
UTSW |
1 |
109,988,862 (GRCm39) |
missense |
probably benign |
0.10 |
R1403:Cdh20
|
UTSW |
1 |
109,988,862 (GRCm39) |
missense |
probably benign |
0.10 |
R1406:Cdh20
|
UTSW |
1 |
109,988,862 (GRCm39) |
missense |
probably benign |
0.10 |
R1406:Cdh20
|
UTSW |
1 |
109,988,862 (GRCm39) |
missense |
probably benign |
0.10 |
R1502:Cdh20
|
UTSW |
1 |
104,881,755 (GRCm39) |
missense |
probably benign |
0.06 |
R1587:Cdh20
|
UTSW |
1 |
110,027,757 (GRCm39) |
missense |
probably damaging |
0.98 |
R1728:Cdh20
|
UTSW |
1 |
109,993,465 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1729:Cdh20
|
UTSW |
1 |
109,993,465 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1730:Cdh20
|
UTSW |
1 |
109,993,465 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1739:Cdh20
|
UTSW |
1 |
109,993,465 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1762:Cdh20
|
UTSW |
1 |
109,993,465 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1764:Cdh20
|
UTSW |
1 |
104,862,070 (GRCm39) |
splice site |
probably benign |
|
R1769:Cdh20
|
UTSW |
1 |
109,980,606 (GRCm39) |
missense |
probably damaging |
1.00 |
R1783:Cdh20
|
UTSW |
1 |
109,993,465 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1785:Cdh20
|
UTSW |
1 |
109,993,465 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1940:Cdh20
|
UTSW |
1 |
109,976,754 (GRCm39) |
missense |
probably benign |
0.09 |
R1972:Cdh20
|
UTSW |
1 |
109,988,862 (GRCm39) |
missense |
probably benign |
0.10 |
R1973:Cdh20
|
UTSW |
1 |
109,988,862 (GRCm39) |
missense |
probably benign |
0.10 |
R1997:Cdh20
|
UTSW |
1 |
109,976,668 (GRCm39) |
missense |
probably damaging |
1.00 |
R2060:Cdh20
|
UTSW |
1 |
109,976,607 (GRCm39) |
missense |
probably damaging |
1.00 |
R2068:Cdh20
|
UTSW |
1 |
110,065,666 (GRCm39) |
nonsense |
probably null |
|
R2069:Cdh20
|
UTSW |
1 |
110,065,889 (GRCm39) |
missense |
probably damaging |
1.00 |
R2137:Cdh20
|
UTSW |
1 |
110,027,836 (GRCm39) |
missense |
probably damaging |
0.97 |
R2155:Cdh20
|
UTSW |
1 |
109,976,594 (GRCm39) |
missense |
probably damaging |
1.00 |
R2198:Cdh20
|
UTSW |
1 |
104,875,047 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2279:Cdh20
|
UTSW |
1 |
104,875,139 (GRCm39) |
missense |
probably damaging |
1.00 |
R2419:Cdh20
|
UTSW |
1 |
104,902,740 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2897:Cdh20
|
UTSW |
1 |
104,875,199 (GRCm39) |
missense |
probably damaging |
1.00 |
R3780:Cdh20
|
UTSW |
1 |
109,976,734 (GRCm39) |
missense |
probably benign |
0.45 |
R3781:Cdh20
|
UTSW |
1 |
109,976,734 (GRCm39) |
missense |
probably benign |
0.45 |
R3782:Cdh20
|
UTSW |
1 |
109,976,734 (GRCm39) |
missense |
probably benign |
0.45 |
R4115:Cdh20
|
UTSW |
1 |
110,066,039 (GRCm39) |
missense |
probably benign |
0.37 |
R4243:Cdh20
|
UTSW |
1 |
104,869,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R4244:Cdh20
|
UTSW |
1 |
104,869,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R4277:Cdh20
|
UTSW |
1 |
109,993,418 (GRCm39) |
missense |
probably benign |
0.00 |
R4299:Cdh20
|
UTSW |
1 |
109,988,731 (GRCm39) |
missense |
probably damaging |
0.99 |
R4349:Cdh20
|
UTSW |
1 |
104,906,814 (GRCm39) |
missense |
probably damaging |
1.00 |
R4350:Cdh20
|
UTSW |
1 |
104,906,814 (GRCm39) |
missense |
probably damaging |
1.00 |
R4352:Cdh20
|
UTSW |
1 |
104,906,814 (GRCm39) |
missense |
probably damaging |
1.00 |
R4353:Cdh20
|
UTSW |
1 |
104,906,814 (GRCm39) |
missense |
probably damaging |
1.00 |
R4719:Cdh20
|
UTSW |
1 |
104,862,035 (GRCm39) |
missense |
probably damaging |
0.97 |
R4754:Cdh20
|
UTSW |
1 |
104,912,410 (GRCm39) |
missense |
probably damaging |
0.99 |
R4777:Cdh20
|
UTSW |
1 |
109,922,055 (GRCm39) |
nonsense |
probably null |
|
R4795:Cdh20
|
UTSW |
1 |
104,868,989 (GRCm39) |
missense |
probably damaging |
1.00 |
R4796:Cdh20
|
UTSW |
1 |
104,868,989 (GRCm39) |
missense |
probably damaging |
1.00 |
R4907:Cdh20
|
UTSW |
1 |
110,066,053 (GRCm39) |
missense |
probably damaging |
1.00 |
R4955:Cdh20
|
UTSW |
1 |
104,912,528 (GRCm39) |
missense |
probably damaging |
1.00 |
R5045:Cdh20
|
UTSW |
1 |
110,026,080 (GRCm39) |
missense |
probably benign |
0.01 |
R5056:Cdh20
|
UTSW |
1 |
104,881,722 (GRCm39) |
missense |
probably benign |
0.00 |
R5059:Cdh20
|
UTSW |
1 |
109,993,430 (GRCm39) |
missense |
probably damaging |
0.98 |
R5127:Cdh20
|
UTSW |
1 |
104,875,073 (GRCm39) |
missense |
probably damaging |
1.00 |
R5146:Cdh20
|
UTSW |
1 |
109,922,042 (GRCm39) |
missense |
probably damaging |
0.97 |
R5196:Cdh20
|
UTSW |
1 |
110,065,730 (GRCm39) |
missense |
probably damaging |
0.99 |
R5269:Cdh20
|
UTSW |
1 |
104,861,882 (GRCm39) |
missense |
possibly damaging |
0.67 |
R5304:Cdh20
|
UTSW |
1 |
110,036,569 (GRCm39) |
missense |
probably damaging |
1.00 |
R5496:Cdh20
|
UTSW |
1 |
109,976,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R5563:Cdh20
|
UTSW |
1 |
104,875,082 (GRCm39) |
missense |
probably benign |
0.29 |
R5634:Cdh20
|
UTSW |
1 |
104,902,800 (GRCm39) |
missense |
probably damaging |
0.97 |
R5708:Cdh20
|
UTSW |
1 |
104,912,635 (GRCm39) |
missense |
probably damaging |
1.00 |
R5743:Cdh20
|
UTSW |
1 |
110,036,575 (GRCm39) |
missense |
probably damaging |
1.00 |
R5822:Cdh20
|
UTSW |
1 |
104,861,823 (GRCm39) |
start codon destroyed |
probably null |
0.49 |
R5867:Cdh20
|
UTSW |
1 |
109,976,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R5933:Cdh20
|
UTSW |
1 |
104,912,396 (GRCm39) |
missense |
probably damaging |
1.00 |
R6042:Cdh20
|
UTSW |
1 |
110,065,997 (GRCm39) |
missense |
probably damaging |
0.97 |
R6092:Cdh20
|
UTSW |
1 |
110,026,036 (GRCm39) |
missense |
probably benign |
0.00 |
R6109:Cdh20
|
UTSW |
1 |
104,921,739 (GRCm39) |
missense |
probably damaging |
1.00 |
R6497:Cdh20
|
UTSW |
1 |
109,993,528 (GRCm39) |
critical splice donor site |
probably null |
|
R6521:Cdh20
|
UTSW |
1 |
104,869,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R6911:Cdh20
|
UTSW |
1 |
104,912,411 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7111:Cdh20
|
UTSW |
1 |
110,065,638 (GRCm39) |
missense |
|
|
R7169:Cdh20
|
UTSW |
1 |
104,875,078 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7207:Cdh20
|
UTSW |
1 |
104,921,702 (GRCm39) |
missense |
probably damaging |
0.98 |
R7208:Cdh20
|
UTSW |
1 |
104,881,796 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7297:Cdh20
|
UTSW |
1 |
104,898,598 (GRCm39) |
missense |
probably benign |
|
R7511:Cdh20
|
UTSW |
1 |
109,925,583 (GRCm39) |
intron |
probably benign |
|
R7532:Cdh20
|
UTSW |
1 |
110,065,889 (GRCm39) |
missense |
probably damaging |
1.00 |
R7535:Cdh20
|
UTSW |
1 |
104,902,768 (GRCm39) |
missense |
probably damaging |
1.00 |
R7587:Cdh20
|
UTSW |
1 |
104,869,004 (GRCm39) |
missense |
probably damaging |
1.00 |
R7748:Cdh20
|
UTSW |
1 |
104,869,024 (GRCm39) |
missense |
probably damaging |
1.00 |
R7879:Cdh20
|
UTSW |
1 |
109,976,677 (GRCm39) |
missense |
probably benign |
0.01 |
R7879:Cdh20
|
UTSW |
1 |
104,875,047 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7915:Cdh20
|
UTSW |
1 |
104,861,898 (GRCm39) |
missense |
probably benign |
0.15 |
R7925:Cdh20
|
UTSW |
1 |
104,912,473 (GRCm39) |
missense |
probably damaging |
0.99 |
R7978:Cdh20
|
UTSW |
1 |
109,921,835 (GRCm39) |
start gained |
probably benign |
|
R8022:Cdh20
|
UTSW |
1 |
109,988,838 (GRCm39) |
missense |
probably benign |
0.02 |
R8207:Cdh20
|
UTSW |
1 |
109,922,076 (GRCm39) |
missense |
probably damaging |
1.00 |
R8224:Cdh20
|
UTSW |
1 |
109,921,933 (GRCm39) |
missense |
probably benign |
|
R8239:Cdh20
|
UTSW |
1 |
110,027,832 (GRCm39) |
missense |
probably benign |
0.11 |
R8257:Cdh20
|
UTSW |
1 |
104,921,962 (GRCm39) |
missense |
probably benign |
0.25 |
R8444:Cdh20
|
UTSW |
1 |
104,898,583 (GRCm39) |
missense |
probably benign |
0.16 |
R8546:Cdh20
|
UTSW |
1 |
104,861,769 (GRCm39) |
start gained |
probably benign |
|
R8749:Cdh20
|
UTSW |
1 |
110,027,009 (GRCm39) |
missense |
probably damaging |
1.00 |
R8870:Cdh20
|
UTSW |
1 |
104,873,048 (GRCm39) |
missense |
probably damaging |
0.99 |
R8884:Cdh20
|
UTSW |
1 |
110,027,860 (GRCm39) |
missense |
probably damaging |
1.00 |
R9030:Cdh20
|
UTSW |
1 |
110,027,843 (GRCm39) |
missense |
probably benign |
0.21 |
R9310:Cdh20
|
UTSW |
1 |
104,875,061 (GRCm39) |
missense |
probably damaging |
1.00 |
R9498:Cdh20
|
UTSW |
1 |
109,976,635 (GRCm39) |
missense |
probably benign |
0.03 |
R9542:Cdh20
|
UTSW |
1 |
104,875,067 (GRCm39) |
missense |
probably damaging |
1.00 |
R9602:Cdh20
|
UTSW |
1 |
104,868,823 (GRCm39) |
missense |
probably benign |
0.07 |
R9658:Cdh20
|
UTSW |
1 |
109,988,785 (GRCm39) |
missense |
probably damaging |
0.99 |
R9664:Cdh20
|
UTSW |
1 |
104,862,065 (GRCm39) |
missense |
probably benign |
0.10 |
Z1088:Cdh20
|
UTSW |
1 |
110,012,853 (GRCm39) |
missense |
probably benign |
0.01 |
Z1176:Cdh20
|
UTSW |
1 |
110,036,466 (GRCm39) |
missense |
probably damaging |
1.00 |
|