Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adnp |
T |
C |
2: 168,025,645 (GRCm39) |
D550G |
probably damaging |
Het |
Ano6 |
A |
G |
15: 95,839,228 (GRCm39) |
T457A |
probably damaging |
Het |
Ano8 |
A |
G |
8: 71,935,221 (GRCm39) |
V359A |
probably damaging |
Het |
Aqp2 |
G |
T |
15: 99,476,993 (GRCm39) |
|
probably benign |
Het |
Atp13a5 |
C |
T |
16: 29,075,829 (GRCm39) |
|
probably benign |
Het |
Carmil3 |
ACCCCC |
ACCCCCCCCCCCC |
14: 55,741,456 (GRCm39) |
|
probably null |
Het |
Ccr1l1 |
A |
G |
9: 123,778,030 (GRCm39) |
V139A |
probably benign |
Het |
Cecr2 |
A |
G |
6: 120,708,407 (GRCm39) |
|
probably null |
Het |
Celsr2 |
A |
G |
3: 108,310,119 (GRCm39) |
V1537A |
possibly damaging |
Het |
Chd6 |
T |
A |
2: 160,856,032 (GRCm39) |
K741N |
probably damaging |
Het |
Chrna1 |
T |
A |
2: 73,397,075 (GRCm39) |
T405S |
probably benign |
Het |
Cish |
T |
C |
9: 107,174,227 (GRCm39) |
V5A |
possibly damaging |
Het |
Cmss1 |
C |
A |
16: 57,131,649 (GRCm39) |
C159F |
probably damaging |
Het |
Col1a2 |
A |
G |
6: 4,516,916 (GRCm39) |
|
probably benign |
Het |
Cradd |
G |
T |
10: 95,011,666 (GRCm39) |
S158* |
probably null |
Het |
Dmxl1 |
G |
A |
18: 49,997,545 (GRCm39) |
A578T |
probably benign |
Het |
Drd2 |
A |
G |
9: 49,318,315 (GRCm39) |
N419S |
possibly damaging |
Het |
E4f1 |
T |
C |
17: 24,666,103 (GRCm39) |
T232A |
probably damaging |
Het |
Fat2 |
T |
A |
11: 55,171,956 (GRCm39) |
E2919V |
probably damaging |
Het |
Gc |
T |
C |
5: 89,586,309 (GRCm39) |
|
probably null |
Het |
Gprc5c |
G |
T |
11: 114,755,093 (GRCm39) |
V257L |
possibly damaging |
Het |
Hsd11b2 |
G |
A |
8: 106,249,143 (GRCm39) |
V173I |
probably benign |
Het |
Kdm6b |
C |
T |
11: 69,296,900 (GRCm39) |
A456T |
probably damaging |
Het |
Kif18b |
G |
A |
11: 102,799,015 (GRCm39) |
P729S |
possibly damaging |
Het |
Lgi1 |
A |
G |
19: 38,294,629 (GRCm39) |
D467G |
possibly damaging |
Het |
Loxl1 |
A |
G |
9: 58,219,650 (GRCm39) |
Y174H |
possibly damaging |
Het |
Mtus1 |
A |
T |
8: 41,475,592 (GRCm39) |
I824N |
probably damaging |
Het |
Myrf |
C |
T |
19: 10,192,654 (GRCm39) |
E622K |
probably benign |
Het |
Ncam1 |
A |
G |
9: 49,457,051 (GRCm39) |
Y416H |
probably damaging |
Het |
Nceh1 |
A |
G |
3: 27,280,248 (GRCm39) |
T132A |
probably benign |
Het |
Nhlrc4 |
G |
A |
17: 26,162,466 (GRCm39) |
P94S |
probably damaging |
Het |
Or2v1 |
C |
G |
11: 49,025,941 (GRCm39) |
D307E |
probably benign |
Het |
Or52s1b |
A |
T |
7: 102,822,841 (GRCm39) |
M1K |
probably null |
Het |
Or8b1 |
A |
T |
9: 38,399,821 (GRCm39) |
R165S |
possibly damaging |
Het |
Pcdhac2 |
A |
G |
18: 37,277,476 (GRCm39) |
Y152C |
probably damaging |
Het |
Pdia3 |
C |
A |
2: 121,244,611 (GRCm39) |
T8K |
possibly damaging |
Het |
Pogz |
T |
A |
3: 94,771,820 (GRCm39) |
V304E |
probably damaging |
Het |
Snrnp200 |
A |
G |
2: 127,068,007 (GRCm39) |
S835G |
possibly damaging |
Het |
Susd4 |
T |
C |
1: 182,719,635 (GRCm39) |
S417P |
probably benign |
Het |
Thsd7b |
G |
A |
1: 129,523,578 (GRCm39) |
R127H |
probably damaging |
Het |
Ttll9 |
T |
A |
2: 152,826,234 (GRCm39) |
M148K |
probably damaging |
Het |
Ubn2 |
G |
A |
6: 38,467,323 (GRCm39) |
C677Y |
probably benign |
Het |
Vmn2r98 |
T |
C |
17: 19,301,161 (GRCm39) |
I721T |
probably benign |
Het |
Wdfy4 |
C |
A |
14: 32,855,454 (GRCm39) |
C720F |
probably damaging |
Het |
Zzef1 |
G |
A |
11: 72,807,347 (GRCm39) |
D2742N |
probably damaging |
Het |
|
Other mutations in Tmco4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00741:Tmco4
|
APN |
4 |
138,723,885 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01346:Tmco4
|
APN |
4 |
138,748,260 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02552:Tmco4
|
APN |
4 |
138,785,690 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02644:Tmco4
|
APN |
4 |
138,737,920 (GRCm39) |
splice site |
probably benign |
|
IGL02676:Tmco4
|
APN |
4 |
138,750,380 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02741:Tmco4
|
APN |
4 |
138,757,188 (GRCm39) |
missense |
probably damaging |
1.00 |
R0116:Tmco4
|
UTSW |
4 |
138,781,231 (GRCm39) |
missense |
probably damaging |
1.00 |
R0611:Tmco4
|
UTSW |
4 |
138,747,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R4034:Tmco4
|
UTSW |
4 |
138,748,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R4612:Tmco4
|
UTSW |
4 |
138,717,871 (GRCm39) |
missense |
probably benign |
|
R4785:Tmco4
|
UTSW |
4 |
138,725,350 (GRCm39) |
missense |
probably damaging |
0.97 |
R4981:Tmco4
|
UTSW |
4 |
138,718,012 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5040:Tmco4
|
UTSW |
4 |
138,747,477 (GRCm39) |
missense |
probably damaging |
1.00 |
R5052:Tmco4
|
UTSW |
4 |
138,785,817 (GRCm39) |
missense |
probably benign |
|
R5074:Tmco4
|
UTSW |
4 |
138,785,433 (GRCm39) |
missense |
probably damaging |
0.98 |
R5364:Tmco4
|
UTSW |
4 |
138,779,815 (GRCm39) |
missense |
probably damaging |
0.99 |
R5445:Tmco4
|
UTSW |
4 |
138,748,178 (GRCm39) |
missense |
probably damaging |
1.00 |
R6959:Tmco4
|
UTSW |
4 |
138,737,810 (GRCm39) |
missense |
probably damaging |
0.99 |
R7539:Tmco4
|
UTSW |
4 |
138,749,010 (GRCm39) |
missense |
probably benign |
0.33 |
R7662:Tmco4
|
UTSW |
4 |
138,737,872 (GRCm39) |
missense |
probably benign |
0.00 |
R7981:Tmco4
|
UTSW |
4 |
138,785,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R7996:Tmco4
|
UTSW |
4 |
138,748,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R8543:Tmco4
|
UTSW |
4 |
138,781,251 (GRCm39) |
missense |
probably benign |
0.01 |
R9460:Tmco4
|
UTSW |
4 |
138,747,387 (GRCm39) |
missense |
probably damaging |
1.00 |
R9551:Tmco4
|
UTSW |
4 |
138,779,895 (GRCm39) |
missense |
probably damaging |
1.00 |
R9552:Tmco4
|
UTSW |
4 |
138,779,895 (GRCm39) |
missense |
probably damaging |
1.00 |
|