Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700049A03Rik |
C |
T |
12: 71,184,804 (GRCm39) |
T64M |
possibly damaging |
Het |
3110040N11Rik |
G |
T |
7: 81,438,208 (GRCm39) |
N49K |
probably benign |
Het |
Adrb1 |
T |
A |
19: 56,711,293 (GRCm39) |
F164I |
probably damaging |
Het |
Aplf |
C |
T |
6: 87,630,866 (GRCm39) |
V190I |
probably benign |
Het |
Aqr |
A |
G |
2: 114,000,533 (GRCm39) |
Y50H |
probably damaging |
Het |
Arfgef3 |
A |
C |
10: 18,537,135 (GRCm39) |
I182R |
probably benign |
Het |
Cacna1b |
G |
A |
2: 24,515,244 (GRCm39) |
|
probably benign |
Het |
Casp9 |
A |
G |
4: 141,532,841 (GRCm39) |
T246A |
probably damaging |
Het |
Clcn6 |
A |
G |
4: 148,099,063 (GRCm39) |
S427P |
probably damaging |
Het |
Cnga1 |
T |
C |
5: 72,761,846 (GRCm39) |
N556S |
possibly damaging |
Het |
Cntnap2 |
G |
A |
6: 45,969,018 (GRCm39) |
|
probably null |
Het |
Col11a2 |
T |
G |
17: 34,261,501 (GRCm39) |
V120G |
probably benign |
Het |
Cux2 |
A |
C |
5: 122,022,802 (GRCm39) |
|
probably benign |
Het |
Dmrt2 |
T |
C |
19: 25,656,026 (GRCm39) |
S542P |
probably damaging |
Het |
Dnah7b |
A |
G |
1: 46,316,286 (GRCm39) |
H3133R |
probably damaging |
Het |
Drosha |
G |
A |
15: 12,837,374 (GRCm39) |
R286Q |
unknown |
Het |
Eipr1 |
A |
G |
12: 28,816,784 (GRCm39) |
D47G |
probably damaging |
Het |
Fras1 |
T |
G |
5: 96,874,399 (GRCm39) |
Y2275D |
probably damaging |
Het |
Grm4 |
C |
T |
17: 27,670,865 (GRCm39) |
|
probably benign |
Het |
Hebp1 |
A |
G |
6: 135,129,918 (GRCm39) |
V100A |
possibly damaging |
Het |
Hivep2 |
G |
A |
10: 14,019,039 (GRCm39) |
V1937I |
possibly damaging |
Het |
Hs3st6 |
T |
C |
17: 24,977,168 (GRCm39) |
V216A |
probably damaging |
Het |
Hsd17b4 |
T |
C |
18: 50,324,851 (GRCm39) |
I688T |
probably benign |
Het |
Hydin |
T |
C |
8: 111,296,533 (GRCm39) |
|
probably null |
Het |
Iws1 |
A |
G |
18: 32,217,258 (GRCm39) |
E426G |
probably damaging |
Het |
Klrb1f |
T |
C |
6: 129,030,680 (GRCm39) |
S64P |
probably damaging |
Het |
Lacc1 |
C |
T |
14: 77,272,629 (GRCm39) |
G56R |
probably damaging |
Het |
Lcmt2 |
A |
G |
2: 120,969,377 (GRCm39) |
S569P |
probably benign |
Het |
Lipm |
C |
T |
19: 34,090,275 (GRCm39) |
|
probably benign |
Het |
Lum |
A |
G |
10: 97,404,471 (GRCm39) |
H122R |
probably damaging |
Het |
Magi2 |
A |
G |
5: 20,270,664 (GRCm39) |
Y15C |
probably damaging |
Het |
Mal |
A |
T |
2: 127,482,286 (GRCm39) |
I39N |
probably damaging |
Het |
Mgme1 |
A |
G |
2: 144,118,319 (GRCm39) |
H197R |
probably benign |
Het |
Mmrn1 |
A |
T |
6: 60,921,955 (GRCm39) |
K137N |
probably benign |
Het |
Myh3 |
T |
A |
11: 66,981,254 (GRCm39) |
C706S |
possibly damaging |
Het |
Myo18b |
A |
T |
5: 113,022,389 (GRCm39) |
|
probably benign |
Het |
Myom1 |
A |
G |
17: 71,352,744 (GRCm39) |
E356G |
possibly damaging |
Het |
Nfib |
A |
G |
4: 82,422,954 (GRCm39) |
|
probably benign |
Het |
Npc1l1 |
T |
C |
11: 6,173,076 (GRCm39) |
M788V |
probably benign |
Het |
Or9a2 |
C |
T |
6: 41,749,058 (GRCm39) |
M58I |
probably damaging |
Het |
Pdha2 |
A |
G |
3: 140,917,457 (GRCm39) |
V17A |
probably benign |
Het |
Pgap1 |
A |
T |
1: 54,525,617 (GRCm39) |
|
probably benign |
Het |
Polr1a |
G |
T |
6: 71,897,747 (GRCm39) |
|
probably benign |
Het |
Ppp1r16a |
C |
T |
15: 76,574,999 (GRCm39) |
|
probably benign |
Het |
Pramel20 |
A |
T |
4: 143,297,878 (GRCm39) |
|
probably benign |
Het |
Pramel21 |
A |
T |
4: 143,342,559 (GRCm39) |
D222V |
possibly damaging |
Het |
Prmt2 |
A |
T |
10: 76,044,337 (GRCm39) |
V405D |
possibly damaging |
Het |
Psg26 |
T |
A |
7: 18,209,181 (GRCm39) |
Y409F |
probably benign |
Het |
Psme3ip1 |
A |
G |
8: 95,314,639 (GRCm39) |
F73S |
probably damaging |
Het |
Ptges |
G |
T |
2: 30,793,144 (GRCm39) |
Y29* |
probably null |
Het |
Ptrhd1 |
A |
G |
12: 4,286,399 (GRCm39) |
T97A |
probably benign |
Het |
Ripk3 |
T |
A |
14: 56,024,200 (GRCm39) |
|
probably benign |
Het |
Rnf114 |
A |
T |
2: 167,353,136 (GRCm39) |
I136F |
probably benign |
Het |
Serinc5 |
A |
G |
13: 92,844,497 (GRCm39) |
|
probably null |
Het |
Slc17a3 |
C |
T |
13: 24,039,841 (GRCm39) |
S293F |
probably damaging |
Het |
Slc23a2 |
C |
A |
2: 131,902,716 (GRCm39) |
M495I |
probably benign |
Het |
Slc52a3 |
T |
A |
2: 151,849,433 (GRCm39) |
L360* |
probably null |
Het |
Snapc1 |
C |
T |
12: 74,021,806 (GRCm39) |
R81C |
probably damaging |
Het |
Syt5 |
A |
G |
7: 4,544,170 (GRCm39) |
V290A |
probably benign |
Het |
Szt2 |
G |
A |
4: 118,239,790 (GRCm39) |
A1931V |
unknown |
Het |
Tasp1 |
A |
G |
2: 139,793,378 (GRCm39) |
|
probably null |
Het |
Tcp10a |
C |
A |
17: 7,593,805 (GRCm39) |
D43E |
probably damaging |
Het |
Tnfsf11 |
A |
T |
14: 78,516,408 (GRCm39) |
Y187N |
probably benign |
Het |
Tppp2 |
T |
A |
14: 52,156,807 (GRCm39) |
N61K |
possibly damaging |
Het |
Zfp623 |
A |
G |
15: 75,820,433 (GRCm39) |
D463G |
probably benign |
Het |
Zfp990 |
A |
G |
4: 145,263,174 (GRCm39) |
I57M |
probably damaging |
Het |
Zmat5 |
G |
A |
11: 4,672,413 (GRCm39) |
C10Y |
probably damaging |
Het |
|
Other mutations in Wwtr1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00155:Wwtr1
|
APN |
3 |
57,370,942 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL00230:Wwtr1
|
APN |
3 |
57,370,912 (GRCm39) |
missense |
probably benign |
0.11 |
IGL01684:Wwtr1
|
APN |
3 |
57,483,210 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01859:Wwtr1
|
APN |
3 |
57,384,938 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01936:Wwtr1
|
APN |
3 |
57,482,241 (GRCm39) |
splice site |
probably benign |
|
IGL03235:Wwtr1
|
APN |
3 |
57,384,954 (GRCm39) |
missense |
probably benign |
0.24 |
R0586:Wwtr1
|
UTSW |
3 |
57,366,487 (GRCm39) |
missense |
probably damaging |
1.00 |
R1797:Wwtr1
|
UTSW |
3 |
57,369,996 (GRCm39) |
missense |
probably damaging |
1.00 |
R2364:Wwtr1
|
UTSW |
3 |
57,370,024 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4453:Wwtr1
|
UTSW |
3 |
57,482,680 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5325:Wwtr1
|
UTSW |
3 |
57,482,658 (GRCm39) |
missense |
probably benign |
0.09 |
R6601:Wwtr1
|
UTSW |
3 |
57,483,159 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7915:Wwtr1
|
UTSW |
3 |
57,483,020 (GRCm39) |
critical splice donor site |
probably null |
|
R8221:Wwtr1
|
UTSW |
3 |
57,366,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R8693:Wwtr1
|
UTSW |
3 |
57,369,945 (GRCm39) |
missense |
probably damaging |
0.98 |
R8827:Wwtr1
|
UTSW |
3 |
57,482,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R9535:Wwtr1
|
UTSW |
3 |
57,384,825 (GRCm39) |
missense |
possibly damaging |
0.94 |
|