Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc10 |
A |
T |
17: 46,623,359 (GRCm39) |
V851E |
probably benign |
Het |
Adam28 |
A |
G |
14: 68,870,620 (GRCm39) |
I351T |
probably benign |
Het |
Agrp |
G |
T |
8: 106,293,467 (GRCm39) |
T106K |
probably damaging |
Het |
Anpep |
C |
T |
7: 79,488,004 (GRCm39) |
E518K |
probably benign |
Het |
Ap2a1 |
T |
C |
7: 44,556,369 (GRCm39) |
E285G |
probably damaging |
Het |
Arfgef1 |
A |
C |
1: 10,243,480 (GRCm39) |
I1023R |
probably damaging |
Het |
Atp2c2 |
G |
A |
8: 120,451,833 (GRCm39) |
V133I |
probably benign |
Het |
Bpifb6 |
A |
G |
2: 153,753,403 (GRCm39) |
T401A |
possibly damaging |
Het |
Capn3 |
G |
A |
2: 120,320,170 (GRCm39) |
V283M |
possibly damaging |
Het |
Chd6 |
A |
T |
2: 160,823,587 (GRCm39) |
V1261E |
probably damaging |
Het |
Col22a1 |
C |
T |
15: 71,878,636 (GRCm39) |
A174T |
probably damaging |
Het |
Crnn |
T |
C |
3: 93,054,198 (GRCm39) |
V27A |
probably benign |
Het |
Dclk2 |
C |
T |
3: 86,712,946 (GRCm39) |
R503Q |
possibly damaging |
Het |
Dgkd |
T |
C |
1: 87,859,766 (GRCm39) |
|
probably null |
Het |
Diaph3 |
A |
G |
14: 87,203,996 (GRCm39) |
L554P |
probably damaging |
Het |
Ephb4 |
A |
T |
5: 137,358,696 (GRCm39) |
H293L |
probably benign |
Het |
Erbin |
G |
T |
13: 103,975,957 (GRCm39) |
H646N |
probably damaging |
Het |
Faiml |
T |
C |
9: 99,116,511 (GRCm39) |
N60D |
probably benign |
Het |
Fem1al |
A |
G |
11: 29,774,723 (GRCm39) |
S245P |
probably benign |
Het |
Flot1 |
A |
G |
17: 36,135,552 (GRCm39) |
E102G |
probably damaging |
Het |
Fryl |
G |
A |
5: 73,190,204 (GRCm39) |
|
probably benign |
Het |
Gad1-ps |
A |
T |
10: 99,281,386 (GRCm39) |
|
noncoding transcript |
Het |
Gtf3c3 |
A |
G |
1: 54,473,371 (GRCm39) |
S81P |
probably damaging |
Het |
Hs1bp3 |
C |
T |
12: 8,371,690 (GRCm39) |
Q91* |
probably null |
Het |
Igf1r |
T |
C |
7: 67,819,661 (GRCm39) |
C324R |
probably damaging |
Het |
Il23r |
G |
A |
6: 67,443,275 (GRCm39) |
T276I |
probably damaging |
Het |
Ip6k1 |
G |
A |
9: 107,918,195 (GRCm39) |
E77K |
possibly damaging |
Het |
Kctd1 |
A |
T |
18: 15,196,263 (GRCm39) |
|
probably benign |
Het |
Kmt2b |
A |
T |
7: 30,285,275 (GRCm39) |
M539K |
possibly damaging |
Het |
Man2b1 |
T |
A |
8: 85,820,563 (GRCm39) |
F617I |
probably damaging |
Het |
Med15 |
G |
A |
16: 17,473,570 (GRCm39) |
|
probably benign |
Het |
Myo9b |
A |
G |
8: 71,806,691 (GRCm39) |
K1543R |
probably damaging |
Het |
N4bp2 |
A |
G |
5: 65,948,165 (GRCm39) |
Y265C |
probably benign |
Het |
N4bp2l2 |
A |
T |
5: 150,585,424 (GRCm39) |
N185K |
probably benign |
Het |
Nkx2-1 |
A |
G |
12: 56,580,529 (GRCm39) |
M137T |
probably benign |
Het |
Or51q1c |
A |
G |
7: 103,653,270 (GRCm39) |
T269A |
probably benign |
Het |
Prickle2 |
A |
T |
6: 92,353,574 (GRCm39) |
Y631N |
probably damaging |
Het |
Ptpro |
A |
G |
6: 137,377,643 (GRCm39) |
T698A |
probably benign |
Het |
Rapgef3 |
T |
C |
15: 97,648,059 (GRCm39) |
I690V |
probably benign |
Het |
Rnf44 |
G |
A |
13: 54,830,005 (GRCm39) |
R271W |
probably damaging |
Het |
Rundc3a |
GAGCC |
GAGCCAGCC |
11: 102,291,739 (GRCm39) |
|
probably null |
Het |
Ryr2 |
A |
G |
13: 11,805,153 (GRCm39) |
Y904H |
probably damaging |
Het |
Suz12 |
T |
C |
11: 79,912,922 (GRCm39) |
L322P |
probably damaging |
Het |
Tnfsf13 |
G |
A |
11: 69,575,973 (GRCm39) |
A38V |
probably benign |
Het |
Topbp1 |
G |
A |
9: 103,186,044 (GRCm39) |
R62H |
probably benign |
Het |
Tor1aip1 |
G |
T |
1: 155,906,180 (GRCm39) |
|
probably null |
Het |
Trpv4 |
A |
T |
5: 114,771,215 (GRCm39) |
V438E |
probably damaging |
Het |
Tsku |
A |
T |
7: 98,001,386 (GRCm39) |
V315E |
possibly damaging |
Het |
Vmn1r170 |
A |
G |
7: 23,305,759 (GRCm39) |
I54V |
probably damaging |
Het |
Vmn1r71 |
T |
C |
7: 10,482,196 (GRCm39) |
D98G |
probably benign |
Het |
Wdfy3 |
A |
T |
5: 102,096,795 (GRCm39) |
D334E |
probably damaging |
Het |
Zfhx3 |
T |
A |
8: 109,682,494 (GRCm39) |
F3311Y |
unknown |
Het |
Zswim9 |
A |
G |
7: 13,003,482 (GRCm39) |
S123P |
probably damaging |
Het |
|
Other mutations in Ttc38 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00899:Ttc38
|
APN |
15 |
85,728,663 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL01596:Ttc38
|
APN |
15 |
85,720,274 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL03221:Ttc38
|
APN |
15 |
85,718,742 (GRCm39) |
missense |
probably benign |
0.00 |
hairy
|
UTSW |
15 |
85,735,802 (GRCm39) |
splice site |
probably null |
|
Stubble
|
UTSW |
15 |
85,728,716 (GRCm39) |
nonsense |
probably null |
|
PIT4431001:Ttc38
|
UTSW |
15 |
85,720,328 (GRCm39) |
missense |
probably benign |
|
R0040:Ttc38
|
UTSW |
15 |
85,725,690 (GRCm39) |
missense |
probably damaging |
1.00 |
R0040:Ttc38
|
UTSW |
15 |
85,725,690 (GRCm39) |
missense |
probably damaging |
1.00 |
R0081:Ttc38
|
UTSW |
15 |
85,740,673 (GRCm39) |
missense |
probably benign |
0.04 |
R0143:Ttc38
|
UTSW |
15 |
85,737,920 (GRCm39) |
missense |
possibly damaging |
0.51 |
R0764:Ttc38
|
UTSW |
15 |
85,730,604 (GRCm39) |
splice site |
probably benign |
|
R1837:Ttc38
|
UTSW |
15 |
85,735,764 (GRCm39) |
missense |
probably damaging |
1.00 |
R2069:Ttc38
|
UTSW |
15 |
85,722,989 (GRCm39) |
missense |
probably damaging |
1.00 |
R2086:Ttc38
|
UTSW |
15 |
85,722,928 (GRCm39) |
missense |
probably benign |
|
R2151:Ttc38
|
UTSW |
15 |
85,735,802 (GRCm39) |
splice site |
probably null |
|
R2228:Ttc38
|
UTSW |
15 |
85,728,704 (GRCm39) |
missense |
probably benign |
0.01 |
R4641:Ttc38
|
UTSW |
15 |
85,728,659 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4705:Ttc38
|
UTSW |
15 |
85,737,164 (GRCm39) |
missense |
probably benign |
0.00 |
R4721:Ttc38
|
UTSW |
15 |
85,722,947 (GRCm39) |
missense |
probably benign |
|
R5037:Ttc38
|
UTSW |
15 |
85,728,741 (GRCm39) |
missense |
probably benign |
0.16 |
R6208:Ttc38
|
UTSW |
15 |
85,725,698 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6454:Ttc38
|
UTSW |
15 |
85,723,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R7326:Ttc38
|
UTSW |
15 |
85,737,062 (GRCm39) |
missense |
probably benign |
0.00 |
R7809:Ttc38
|
UTSW |
15 |
85,722,939 (GRCm39) |
missense |
possibly damaging |
0.65 |
R8195:Ttc38
|
UTSW |
15 |
85,728,716 (GRCm39) |
nonsense |
probably null |
|
R9042:Ttc38
|
UTSW |
15 |
85,720,310 (GRCm39) |
missense |
probably benign |
0.00 |
R9631:Ttc38
|
UTSW |
15 |
85,728,659 (GRCm39) |
missense |
possibly damaging |
0.87 |
|