Other mutations in this stock |
Total: 34 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930590J08Rik |
C |
T |
6: 91,927,003 (GRCm39) |
L888F |
probably damaging |
Het |
Aftph |
G |
T |
11: 20,642,507 (GRCm39) |
A842E |
probably damaging |
Het |
Ankrd13d |
A |
T |
19: 4,323,592 (GRCm39) |
M257K |
probably benign |
Het |
Anks1 |
T |
C |
17: 28,270,558 (GRCm39) |
F786L |
probably damaging |
Het |
Cd2ap |
A |
T |
17: 43,163,365 (GRCm39) |
I20N |
probably damaging |
Het |
Dnah5 |
C |
T |
15: 28,331,872 (GRCm39) |
R2153C |
probably damaging |
Het |
Fap |
G |
A |
2: 62,374,655 (GRCm39) |
P248L |
possibly damaging |
Het |
Hps4 |
T |
A |
5: 112,512,377 (GRCm39) |
|
probably benign |
Het |
Igdcc4 |
C |
A |
9: 65,029,889 (GRCm39) |
T313K |
probably benign |
Het |
Klhl30 |
G |
A |
1: 91,281,761 (GRCm39) |
V121I |
probably damaging |
Het |
Ldb3 |
C |
A |
14: 34,264,519 (GRCm39) |
E526D |
probably damaging |
Het |
Ldc1 |
T |
A |
4: 130,109,218 (GRCm39) |
Y274F |
probably benign |
Het |
Lhfpl4 |
T |
A |
6: 113,171,082 (GRCm39) |
I35F |
probably benign |
Het |
Lpin1 |
A |
G |
12: 16,612,358 (GRCm39) |
|
probably benign |
Het |
Nek1 |
T |
A |
8: 61,502,860 (GRCm39) |
C436S |
probably benign |
Het |
Nek5 |
C |
A |
8: 22,573,385 (GRCm39) |
A524S |
probably benign |
Het |
Nkx2-3 |
C |
T |
19: 43,601,094 (GRCm39) |
T52M |
possibly damaging |
Het |
Or1e33 |
A |
G |
11: 73,738,036 (GRCm39) |
I305T |
probably benign |
Het |
Or2w2 |
A |
T |
13: 21,758,627 (GRCm39) |
|
probably null |
Het |
Or8b56 |
G |
A |
9: 38,739,895 (GRCm39) |
V303I |
possibly damaging |
Het |
Pappa |
T |
C |
4: 65,107,536 (GRCm39) |
V649A |
probably damaging |
Het |
Parp4 |
T |
A |
14: 56,859,661 (GRCm39) |
Y920N |
possibly damaging |
Het |
Pdgfra |
G |
A |
5: 75,324,313 (GRCm39) |
S56N |
probably benign |
Het |
Pigg |
T |
C |
5: 108,484,067 (GRCm39) |
V438A |
possibly damaging |
Het |
Ptn |
A |
T |
6: 36,720,298 (GRCm39) |
C85S |
probably damaging |
Het |
Sh3rf1 |
A |
C |
8: 61,782,365 (GRCm39) |
E169A |
possibly damaging |
Het |
Slc30a10 |
T |
A |
1: 185,187,616 (GRCm39) |
V119E |
probably damaging |
Het |
Speg |
A |
G |
1: 75,364,471 (GRCm39) |
E178G |
probably damaging |
Het |
Sspo |
A |
G |
6: 48,455,665 (GRCm39) |
Y3105C |
probably damaging |
Het |
Supt3 |
A |
G |
17: 45,430,045 (GRCm39) |
E366G |
possibly damaging |
Het |
Top2a |
A |
T |
11: 98,901,856 (GRCm39) |
L458Q |
probably damaging |
Het |
Ttc21b |
G |
A |
2: 66,082,234 (GRCm39) |
|
probably benign |
Het |
Usp24 |
T |
C |
4: 106,219,429 (GRCm39) |
F542L |
probably benign |
Het |
Vmn1r234 |
T |
A |
17: 21,449,171 (GRCm39) |
D28E |
possibly 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 |
IGL00743:Cdh20
|
APN |
1 |
104,875,153 (GRCm39) |
missense |
probably benign |
0.06 |
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 |
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 |
|