Other mutations in this stock |
Total: 24 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700037C18Rik |
T |
A |
16: 3,724,146 (GRCm39) |
D130V |
probably damaging |
Het |
4930596D02Rik |
T |
C |
14: 35,533,880 (GRCm39) |
T9A |
probably benign |
Het |
Anapc1 |
C |
A |
2: 128,501,772 (GRCm39) |
A757S |
probably benign |
Het |
Bpifa6 |
A |
T |
2: 153,834,192 (GRCm39) |
D328V |
probably benign |
Het |
Cdh19 |
T |
A |
1: 110,853,616 (GRCm39) |
K275I |
probably benign |
Het |
Col18a1 |
A |
G |
10: 76,895,217 (GRCm39) |
I1148T |
possibly damaging |
Het |
Commd1 |
A |
T |
11: 22,850,017 (GRCm39) |
V222D |
probably damaging |
Het |
Crim1 |
T |
A |
17: 78,677,427 (GRCm39) |
M876K |
possibly damaging |
Het |
Dhx57 |
T |
C |
17: 80,582,268 (GRCm39) |
T393A |
probably benign |
Het |
Dnai7 |
T |
C |
6: 145,123,090 (GRCm39) |
Y592C |
probably damaging |
Het |
Gabrb2 |
G |
T |
11: 42,482,721 (GRCm39) |
R193L |
probably benign |
Het |
Gm5828 |
T |
A |
1: 16,839,342 (GRCm39) |
|
noncoding transcript |
Het |
Gm6483 |
C |
T |
8: 19,741,629 (GRCm39) |
P55S |
probably damaging |
Het |
Hsp90ab1 |
T |
C |
17: 45,879,364 (GRCm39) |
Y619C |
possibly damaging |
Het |
Kctd19 |
A |
G |
8: 106,123,006 (GRCm39) |
I136T |
probably damaging |
Het |
Or2n1 |
G |
T |
17: 38,486,577 (GRCm39) |
V201L |
probably benign |
Het |
Or2w6 |
A |
C |
13: 21,843,170 (GRCm39) |
F108V |
probably benign |
Het |
Sel1l |
T |
C |
12: 91,781,789 (GRCm39) |
Y532C |
probably damaging |
Het |
Sirpb1a |
A |
G |
3: 15,475,469 (GRCm39) |
|
probably null |
Het |
Ush2a |
C |
T |
1: 187,995,466 (GRCm39) |
T79M |
possibly damaging |
Het |
Usp24 |
T |
C |
4: 106,244,690 (GRCm39) |
V1215A |
probably damaging |
Het |
Vdac3-ps1 |
T |
C |
13: 18,205,379 (GRCm39) |
|
noncoding transcript |
Het |
Vmn2r75 |
T |
C |
7: 85,814,348 (GRCm39) |
T382A |
probably benign |
Het |
Vps53 |
T |
C |
11: 75,937,949 (GRCm39) |
Y728C |
probably benign |
Het |
|
Other mutations in Dennd1b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00417:Dennd1b
|
APN |
1 |
138,990,678 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00510:Dennd1b
|
APN |
1 |
139,029,809 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00671:Dennd1b
|
APN |
1 |
139,061,475 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL00937:Dennd1b
|
APN |
1 |
139,097,977 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00959:Dennd1b
|
APN |
1 |
139,071,626 (GRCm39) |
splice site |
probably benign |
|
IGL01446:Dennd1b
|
APN |
1 |
138,950,848 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL01610:Dennd1b
|
APN |
1 |
139,097,504 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02851:Dennd1b
|
APN |
1 |
139,096,705 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02995:Dennd1b
|
APN |
1 |
139,008,980 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03089:Dennd1b
|
APN |
1 |
139,029,767 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03240:Dennd1b
|
APN |
1 |
139,067,130 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL03267:Dennd1b
|
APN |
1 |
138,990,599 (GRCm39) |
nonsense |
probably null |
|
Dendrite
|
UTSW |
1 |
138,981,155 (GRCm39) |
critical splice donor site |
probably null |
|
LCD18:Dennd1b
|
UTSW |
1 |
139,042,502 (GRCm39) |
intron |
probably benign |
|
PIT4418001:Dennd1b
|
UTSW |
1 |
139,008,999 (GRCm39) |
missense |
|
|
PIT4504001:Dennd1b
|
UTSW |
1 |
138,967,742 (GRCm39) |
missense |
probably benign |
0.28 |
R0426:Dennd1b
|
UTSW |
1 |
139,097,934 (GRCm39) |
missense |
probably benign |
|
R0445:Dennd1b
|
UTSW |
1 |
139,095,503 (GRCm39) |
splice site |
probably benign |
|
R0497:Dennd1b
|
UTSW |
1 |
138,967,724 (GRCm39) |
splice site |
probably benign |
|
R0627:Dennd1b
|
UTSW |
1 |
139,008,957 (GRCm39) |
missense |
probably damaging |
1.00 |
R1027:Dennd1b
|
UTSW |
1 |
138,969,700 (GRCm39) |
missense |
probably damaging |
1.00 |
R1599:Dennd1b
|
UTSW |
1 |
139,095,468 (GRCm39) |
missense |
probably benign |
0.01 |
R1703:Dennd1b
|
UTSW |
1 |
139,097,492 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1844:Dennd1b
|
UTSW |
1 |
139,018,143 (GRCm39) |
splice site |
probably null |
|
R1943:Dennd1b
|
UTSW |
1 |
139,096,690 (GRCm39) |
utr 3 prime |
probably benign |
|
R2504:Dennd1b
|
UTSW |
1 |
139,097,908 (GRCm39) |
utr 3 prime |
probably benign |
|
R2866:Dennd1b
|
UTSW |
1 |
139,098,019 (GRCm39) |
missense |
possibly damaging |
0.58 |
R3109:Dennd1b
|
UTSW |
1 |
138,969,654 (GRCm39) |
splice site |
probably benign |
|
R3843:Dennd1b
|
UTSW |
1 |
138,981,092 (GRCm39) |
missense |
probably damaging |
1.00 |
R3926:Dennd1b
|
UTSW |
1 |
139,071,697 (GRCm39) |
missense |
probably benign |
0.00 |
R4258:Dennd1b
|
UTSW |
1 |
138,990,678 (GRCm39) |
missense |
probably damaging |
1.00 |
R4504:Dennd1b
|
UTSW |
1 |
139,013,665 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4805:Dennd1b
|
UTSW |
1 |
138,981,122 (GRCm39) |
missense |
probably damaging |
1.00 |
R4922:Dennd1b
|
UTSW |
1 |
139,013,652 (GRCm39) |
missense |
probably damaging |
0.99 |
R4954:Dennd1b
|
UTSW |
1 |
138,981,124 (GRCm39) |
missense |
probably damaging |
1.00 |
R5098:Dennd1b
|
UTSW |
1 |
139,061,459 (GRCm39) |
missense |
probably damaging |
0.97 |
R5205:Dennd1b
|
UTSW |
1 |
138,982,306 (GRCm39) |
missense |
probably benign |
0.00 |
R5240:Dennd1b
|
UTSW |
1 |
138,990,615 (GRCm39) |
missense |
probably damaging |
1.00 |
R5383:Dennd1b
|
UTSW |
1 |
139,095,409 (GRCm39) |
missense |
probably benign |
|
R5504:Dennd1b
|
UTSW |
1 |
139,018,246 (GRCm39) |
missense |
probably benign |
0.07 |
R5702:Dennd1b
|
UTSW |
1 |
139,061,413 (GRCm39) |
missense |
probably damaging |
1.00 |
R5801:Dennd1b
|
UTSW |
1 |
138,967,727 (GRCm39) |
splice site |
probably null |
|
R6144:Dennd1b
|
UTSW |
1 |
139,008,993 (GRCm39) |
missense |
probably damaging |
1.00 |
R6190:Dennd1b
|
UTSW |
1 |
139,061,413 (GRCm39) |
missense |
probably damaging |
1.00 |
R6192:Dennd1b
|
UTSW |
1 |
139,095,456 (GRCm39) |
missense |
probably benign |
0.00 |
R6289:Dennd1b
|
UTSW |
1 |
139,096,683 (GRCm39) |
utr 3 prime |
probably benign |
|
R6453:Dennd1b
|
UTSW |
1 |
139,071,686 (GRCm39) |
missense |
probably benign |
0.07 |
R6479:Dennd1b
|
UTSW |
1 |
138,969,698 (GRCm39) |
intron |
probably benign |
|
R6940:Dennd1b
|
UTSW |
1 |
138,981,155 (GRCm39) |
critical splice donor site |
probably null |
|
R6954:Dennd1b
|
UTSW |
1 |
139,096,683 (GRCm39) |
utr 3 prime |
probably benign |
|
R7183:Dennd1b
|
UTSW |
1 |
139,097,990 (GRCm39) |
missense |
unknown |
|
R7710:Dennd1b
|
UTSW |
1 |
138,990,670 (GRCm39) |
missense |
probably damaging |
1.00 |
R7742:Dennd1b
|
UTSW |
1 |
138,990,611 (GRCm39) |
missense |
probably damaging |
1.00 |
R7796:Dennd1b
|
UTSW |
1 |
138,990,611 (GRCm39) |
missense |
probably damaging |
1.00 |
R7871:Dennd1b
|
UTSW |
1 |
138,990,611 (GRCm39) |
missense |
probably damaging |
1.00 |
R7920:Dennd1b
|
UTSW |
1 |
138,990,611 (GRCm39) |
missense |
probably damaging |
1.00 |
R7921:Dennd1b
|
UTSW |
1 |
138,990,611 (GRCm39) |
missense |
probably damaging |
1.00 |
R7991:Dennd1b
|
UTSW |
1 |
139,013,634 (GRCm39) |
missense |
|
|
R8025:Dennd1b
|
UTSW |
1 |
139,038,158 (GRCm39) |
missense |
|
|
R8239:Dennd1b
|
UTSW |
1 |
138,969,673 (GRCm39) |
missense |
probably benign |
0.02 |
R8526:Dennd1b
|
UTSW |
1 |
138,950,858 (GRCm39) |
nonsense |
probably null |
|
R8532:Dennd1b
|
UTSW |
1 |
139,097,912 (GRCm39) |
utr 3 prime |
probably benign |
|
R8691:Dennd1b
|
UTSW |
1 |
138,969,774 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9229:Dennd1b
|
UTSW |
1 |
138,981,100 (GRCm39) |
nonsense |
probably null |
|
R9577:Dennd1b
|
UTSW |
1 |
139,018,196 (GRCm39) |
missense |
|
|
RF008:Dennd1b
|
UTSW |
1 |
138,981,135 (GRCm39) |
missense |
probably damaging |
1.00 |
|