Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933409G03Rik |
T |
A |
2: 68,446,589 (GRCm39) |
N289K |
unknown |
Het |
Adgrl2 |
T |
C |
3: 148,522,917 (GRCm39) |
I436V |
|
Het |
Agbl3 |
C |
T |
6: 34,834,549 (GRCm39) |
S911L |
probably damaging |
Het |
Ampd2 |
C |
T |
3: 107,982,613 (GRCm39) |
M714I |
probably damaging |
Het |
Asb6 |
T |
C |
2: 30,718,143 (GRCm39) |
D19G |
possibly damaging |
Het |
Atosa |
C |
A |
9: 74,933,107 (GRCm39) |
L1025I |
probably damaging |
Het |
Bbx |
T |
C |
16: 50,061,227 (GRCm39) |
Q298R |
probably damaging |
Het |
Bcl9l |
T |
A |
9: 44,420,263 (GRCm39) |
M1223K |
probably benign |
Het |
Ccr3 |
T |
A |
9: 123,829,096 (GRCm39) |
F144I |
possibly damaging |
Het |
Cfap74 |
T |
A |
4: 155,503,105 (GRCm39) |
F32L |
|
Het |
Clhc1 |
G |
A |
11: 29,511,401 (GRCm39) |
E293K |
probably damaging |
Het |
Col22a1 |
A |
T |
15: 71,878,571 (GRCm39) |
D195E |
probably benign |
Het |
Cttnbp2 |
T |
A |
6: 18,376,003 (GRCm39) |
D1512V |
probably damaging |
Het |
Cul9 |
T |
C |
17: 46,832,828 (GRCm39) |
T1372A |
possibly damaging |
Het |
Dyrk4 |
G |
T |
6: 126,857,208 (GRCm39) |
D490E |
possibly damaging |
Het |
E4f1 |
C |
T |
17: 24,663,574 (GRCm39) |
V626M |
probably damaging |
Het |
Edc3 |
C |
T |
9: 57,634,678 (GRCm39) |
R232C |
probably damaging |
Het |
Eppk1 |
A |
G |
15: 75,994,895 (GRCm39) |
I662T |
probably benign |
Het |
G3bp2 |
C |
T |
5: 92,231,356 (GRCm39) |
|
probably benign |
Het |
Grik3 |
T |
C |
4: 125,550,166 (GRCm39) |
L397P |
probably damaging |
Het |
Hectd4 |
A |
G |
5: 121,419,936 (GRCm39) |
N627S |
possibly damaging |
Het |
Hecw2 |
C |
T |
1: 53,952,507 (GRCm39) |
V909I |
probably benign |
Het |
Hsd17b12 |
A |
T |
2: 93,945,397 (GRCm39) |
M75K |
probably damaging |
Het |
Htt |
C |
T |
5: 34,977,633 (GRCm39) |
T809I |
probably benign |
Het |
Itih1 |
A |
G |
14: 30,655,381 (GRCm39) |
S609P |
probably damaging |
Het |
Klk1b9 |
T |
A |
7: 43,629,666 (GRCm39) |
C234S |
probably damaging |
Het |
Lrrc37a |
A |
G |
11: 103,389,536 (GRCm39) |
L1963P |
probably benign |
Het |
Lypd3 |
C |
A |
7: 24,337,932 (GRCm39) |
H99Q |
probably damaging |
Het |
Mdn1 |
C |
A |
4: 32,751,390 (GRCm39) |
H4593Q |
probably damaging |
Het |
Mroh1 |
A |
G |
15: 76,297,126 (GRCm39) |
S325G |
probably benign |
Het |
Muc5ac |
G |
A |
7: 141,372,609 (GRCm39) |
G3452R |
probably damaging |
Het |
Myrfl |
A |
T |
10: 116,612,696 (GRCm39) |
D884E |
probably damaging |
Het |
Nbeal1 |
T |
A |
1: 60,274,370 (GRCm39) |
H260Q |
probably damaging |
Het |
Ngef |
A |
G |
1: 87,408,883 (GRCm39) |
L519P |
probably damaging |
Het |
Or5ac20 |
A |
G |
16: 59,104,194 (GRCm39) |
L222P |
probably damaging |
Het |
Or5b102 |
T |
A |
19: 13,041,307 (GRCm39) |
C177* |
probably null |
Het |
Or5w1b |
A |
T |
2: 87,475,960 (GRCm39) |
F169Y |
probably damaging |
Het |
Pcca |
A |
G |
14: 122,854,260 (GRCm39) |
K184R |
probably benign |
Het |
Pkd1l3 |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
8: 110,350,827 (GRCm39) |
|
probably benign |
Het |
Ppp6r1 |
A |
T |
7: 4,644,289 (GRCm39) |
V379E |
probably benign |
Het |
Prkca |
A |
T |
11: 107,842,286 (GRCm39) |
|
probably benign |
Het |
Prune2 |
A |
G |
19: 17,100,442 (GRCm39) |
E1982G |
probably damaging |
Het |
Rad21l |
T |
C |
2: 151,509,838 (GRCm39) |
T88A |
probably benign |
Het |
Rpgrip1l |
T |
C |
8: 91,979,212 (GRCm39) |
|
probably benign |
Het |
Sec62 |
T |
C |
3: 30,864,177 (GRCm39) |
|
probably null |
Het |
Slc22a19 |
C |
T |
19: 7,670,086 (GRCm39) |
R256Q |
possibly damaging |
Het |
Slc43a2 |
G |
T |
11: 75,434,192 (GRCm39) |
|
probably null |
Het |
Smarcd3 |
T |
C |
5: 24,803,792 (GRCm39) |
M30V |
probably benign |
Het |
Tes3-ps |
T |
A |
13: 49,647,356 (GRCm39) |
D77E |
probably benign |
Het |
Thbs3 |
G |
A |
3: 89,131,937 (GRCm39) |
|
probably benign |
Het |
Trpm2 |
A |
T |
10: 77,768,128 (GRCm39) |
N790K |
probably benign |
Het |
Ttc13 |
A |
T |
8: 125,405,816 (GRCm39) |
N492K |
possibly damaging |
Het |
Tyms |
T |
C |
5: 30,278,360 (GRCm39) |
|
probably benign |
Het |
Whamm |
A |
T |
7: 81,234,933 (GRCm39) |
K333* |
probably null |
Het |
Ydjc |
A |
G |
16: 16,968,732 (GRCm39) |
I224V |
probably benign |
Het |
Zc3hav1 |
C |
T |
6: 38,313,416 (GRCm39) |
D210N |
possibly damaging |
Het |
Zfp735 |
G |
A |
11: 73,581,127 (GRCm39) |
E55K |
possibly damaging |
Het |
|
Other mutations in Ttc39c |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00976:Ttc39c
|
APN |
18 |
12,817,952 (GRCm39) |
splice site |
probably benign |
|
IGL02323:Ttc39c
|
APN |
18 |
12,869,800 (GRCm39) |
missense |
probably null |
0.79 |
R1628:Ttc39c
|
UTSW |
18 |
12,867,936 (GRCm39) |
splice site |
probably benign |
|
R1771:Ttc39c
|
UTSW |
18 |
12,817,881 (GRCm39) |
splice site |
probably null |
|
R2002:Ttc39c
|
UTSW |
18 |
12,830,935 (GRCm39) |
splice site |
probably null |
|
R4162:Ttc39c
|
UTSW |
18 |
12,857,994 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4344:Ttc39c
|
UTSW |
18 |
12,861,667 (GRCm39) |
splice site |
probably null |
|
R4484:Ttc39c
|
UTSW |
18 |
12,863,126 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4752:Ttc39c
|
UTSW |
18 |
12,861,782 (GRCm39) |
missense |
probably benign |
0.05 |
R4872:Ttc39c
|
UTSW |
18 |
12,820,173 (GRCm39) |
intron |
probably benign |
|
R4912:Ttc39c
|
UTSW |
18 |
12,867,951 (GRCm39) |
missense |
probably benign |
0.00 |
R4946:Ttc39c
|
UTSW |
18 |
12,857,999 (GRCm39) |
nonsense |
probably null |
|
R5036:Ttc39c
|
UTSW |
18 |
12,820,138 (GRCm39) |
critical splice donor site |
probably null |
|
R5439:Ttc39c
|
UTSW |
18 |
12,828,428 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5726:Ttc39c
|
UTSW |
18 |
12,830,992 (GRCm39) |
missense |
probably damaging |
1.00 |
R7213:Ttc39c
|
UTSW |
18 |
12,820,138 (GRCm39) |
critical splice donor site |
probably null |
|
R7400:Ttc39c
|
UTSW |
18 |
12,776,856 (GRCm39) |
intron |
probably benign |
|
R7413:Ttc39c
|
UTSW |
18 |
12,861,746 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7567:Ttc39c
|
UTSW |
18 |
12,822,936 (GRCm39) |
missense |
probably benign |
0.01 |
R7979:Ttc39c
|
UTSW |
18 |
12,866,022 (GRCm39) |
missense |
probably benign |
|
R8824:Ttc39c
|
UTSW |
18 |
12,820,003 (GRCm39) |
splice site |
probably benign |
|
R8827:Ttc39c
|
UTSW |
18 |
12,828,436 (GRCm39) |
missense |
probably benign |
|
R8855:Ttc39c
|
UTSW |
18 |
12,831,003 (GRCm39) |
missense |
probably benign |
0.30 |
R8866:Ttc39c
|
UTSW |
18 |
12,831,003 (GRCm39) |
missense |
probably benign |
0.30 |
R8996:Ttc39c
|
UTSW |
18 |
12,820,136 (GRCm39) |
missense |
probably benign |
0.00 |
R9349:Ttc39c
|
UTSW |
18 |
12,822,932 (GRCm39) |
nonsense |
probably null |
|
R9356:Ttc39c
|
UTSW |
18 |
12,853,102 (GRCm39) |
critical splice donor site |
probably null |
|
R9797:Ttc39c
|
UTSW |
18 |
12,828,542 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Ttc39c
|
UTSW |
18 |
12,820,020 (GRCm39) |
missense |
possibly damaging |
0.90 |
|