Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aldh8a1 |
T |
A |
10: 21,265,032 (GRCm39) |
S220T |
probably benign |
Het |
Ankrd66 |
A |
G |
17: 43,845,811 (GRCm39) |
V192A |
probably benign |
Het |
Aoc1l3 |
A |
G |
6: 48,965,774 (GRCm39) |
Y594C |
probably damaging |
Het |
Atp1a2 |
A |
G |
1: 172,103,494 (GRCm39) |
Y1009H |
probably benign |
Het |
Bptf |
A |
C |
11: 106,935,411 (GRCm39) |
M142R |
probably damaging |
Het |
Brwd1 |
C |
T |
16: 95,845,703 (GRCm39) |
R740Q |
probably damaging |
Het |
C3 |
A |
G |
17: 57,531,169 (GRCm39) |
M339T |
probably benign |
Het |
Catsperg1 |
A |
G |
7: 28,897,772 (GRCm39) |
|
probably null |
Het |
Cep295nl |
T |
A |
11: 118,224,446 (GRCm39) |
K133* |
probably null |
Het |
Copg2 |
A |
T |
6: 30,793,786 (GRCm39) |
|
probably benign |
Het |
Coro7 |
A |
T |
16: 4,488,402 (GRCm39) |
D89E |
probably damaging |
Het |
Cyp2t4 |
G |
A |
7: 26,854,717 (GRCm39) |
V66M |
possibly damaging |
Het |
Ddx54 |
G |
T |
5: 120,765,209 (GRCm39) |
R826L |
probably damaging |
Het |
Dlg4 |
G |
T |
11: 69,922,065 (GRCm39) |
K162N |
probably damaging |
Het |
Dna2 |
T |
A |
10: 62,790,072 (GRCm39) |
L185H |
probably benign |
Het |
Dock9 |
C |
T |
14: 121,787,601 (GRCm39) |
|
probably benign |
Het |
Efcab8 |
G |
C |
2: 153,646,861 (GRCm39) |
V397L |
unknown |
Het |
Etl4 |
A |
G |
2: 20,813,926 (GRCm39) |
I1322V |
probably benign |
Het |
Exd1 |
T |
C |
2: 119,355,064 (GRCm39) |
K284E |
possibly damaging |
Het |
Flnc |
A |
G |
6: 29,445,462 (GRCm39) |
T786A |
probably damaging |
Het |
Gm29106 |
A |
C |
1: 118,127,644 (GRCm39) |
E445D |
possibly damaging |
Het |
Gm5592 |
T |
C |
7: 40,935,876 (GRCm39) |
L126P |
probably damaging |
Het |
Grep1 |
A |
G |
17: 23,936,187 (GRCm39) |
Y19H |
unknown |
Het |
Gtf3c2 |
T |
G |
5: 31,325,773 (GRCm39) |
T389P |
probably damaging |
Het |
Hhipl1 |
C |
A |
12: 108,294,100 (GRCm39) |
R669S |
probably benign |
Het |
Hivep1 |
A |
G |
13: 42,337,252 (GRCm39) |
T2444A |
probably benign |
Het |
Hspg2 |
A |
G |
4: 137,238,380 (GRCm39) |
E289G |
probably damaging |
Het |
Htatip2 |
C |
A |
7: 49,408,987 (GRCm39) |
T9K |
unknown |
Het |
Ifngr1 |
T |
C |
10: 19,483,041 (GRCm39) |
V265A |
possibly damaging |
Het |
Ift140 |
A |
G |
17: 25,252,925 (GRCm39) |
N359D |
probably benign |
Het |
Mat1a |
A |
G |
14: 40,836,803 (GRCm39) |
R178G |
probably damaging |
Het |
Mknk2 |
C |
T |
10: 80,505,496 (GRCm39) |
R154H |
probably benign |
Het |
Myh14 |
C |
T |
7: 44,273,743 (GRCm39) |
|
probably null |
Het |
Myof |
A |
G |
19: 37,966,096 (GRCm39) |
|
probably null |
Het |
Nfe2l1 |
G |
T |
11: 96,718,453 (GRCm39) |
D27E |
probably damaging |
Het |
Or1ad6 |
A |
G |
11: 50,859,950 (GRCm39) |
Y35C |
|
Het |
Or4a15 |
A |
T |
2: 89,193,243 (GRCm39) |
C177S |
probably damaging |
Het |
Or4k51 |
T |
C |
2: 111,585,218 (GRCm39) |
V208A |
probably benign |
Het |
Or5p61 |
A |
G |
7: 107,758,468 (GRCm39) |
V204A |
probably benign |
Het |
Or8s5 |
A |
G |
15: 98,238,144 (GRCm39) |
V242A |
possibly damaging |
Het |
Plec |
C |
A |
15: 76,067,987 (GRCm39) |
Q1139H |
unknown |
Het |
Plxna2 |
T |
A |
1: 194,326,692 (GRCm39) |
S209T |
probably benign |
Het |
Plxnd1 |
T |
C |
6: 115,940,277 (GRCm39) |
E1369G |
possibly damaging |
Het |
Psd3 |
T |
C |
8: 68,363,487 (GRCm39) |
I3V |
unknown |
Het |
Pwp1 |
T |
A |
10: 85,714,428 (GRCm39) |
F195L |
probably damaging |
Het |
Rab3ip |
C |
T |
10: 116,775,354 (GRCm39) |
M1I |
probably null |
Het |
Rad54l2 |
T |
C |
9: 106,585,488 (GRCm39) |
K759R |
probably benign |
Het |
Rims2 |
G |
T |
15: 39,300,724 (GRCm39) |
V344L |
probably damaging |
Het |
Robo1 |
G |
A |
16: 72,803,718 (GRCm39) |
R1088Q |
probably benign |
Het |
Rtf2 |
A |
G |
2: 172,282,745 (GRCm39) |
|
probably benign |
Het |
Serhl |
A |
C |
15: 82,987,167 (GRCm39) |
K131N |
possibly damaging |
Het |
Sidt1 |
T |
A |
16: 44,075,392 (GRCm39) |
|
probably null |
Het |
Slc27a1 |
T |
A |
8: 72,032,808 (GRCm39) |
Y248* |
probably null |
Het |
Slitrk3 |
T |
A |
3: 72,958,616 (GRCm39) |
E52V |
possibly damaging |
Het |
Snx2 |
T |
C |
18: 53,343,415 (GRCm39) |
V271A |
probably benign |
Het |
Snx9 |
C |
A |
17: 5,949,768 (GRCm39) |
P156Q |
probably damaging |
Het |
Spag6 |
C |
A |
2: 18,715,369 (GRCm39) |
Y71* |
probably null |
Het |
Speer4a3 |
T |
A |
5: 26,156,569 (GRCm39) |
K137* |
probably null |
Het |
Speg |
A |
G |
1: 75,394,377 (GRCm39) |
D1724G |
probably damaging |
Het |
Thoc2l |
C |
A |
5: 104,668,644 (GRCm39) |
S1055R |
probably benign |
Het |
Ticam2 |
A |
G |
18: 46,693,766 (GRCm39) |
I107T |
probably damaging |
Het |
Tm7sf3 |
C |
T |
6: 146,525,179 (GRCm39) |
D89N |
possibly damaging |
Het |
Tmem268 |
G |
A |
4: 63,488,256 (GRCm39) |
V135M |
probably benign |
Het |
Toporsl |
A |
G |
4: 52,611,663 (GRCm39) |
T519A |
possibly damaging |
Het |
Trim43b |
G |
A |
9: 88,973,608 (GRCm39) |
L42F |
possibly damaging |
Het |
Ttf2 |
A |
C |
3: 100,852,089 (GRCm39) |
V1019G |
probably damaging |
Het |
Ugt3a1 |
A |
G |
15: 9,292,158 (GRCm39) |
D97G |
probably benign |
Het |
Uncx |
A |
G |
5: 139,532,475 (GRCm39) |
N180S |
probably damaging |
Het |
Vmn2r23 |
A |
G |
6: 123,710,352 (GRCm39) |
T552A |
probably damaging |
Het |
Vmn2r51 |
A |
T |
7: 9,833,816 (GRCm39) |
H407Q |
probably damaging |
Het |
Wdfy4 |
C |
T |
14: 32,855,518 (GRCm39) |
E699K |
|
Het |
Wdr95 |
A |
G |
5: 149,504,165 (GRCm39) |
T324A |
probably benign |
Het |
|
Other mutations in Syt7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01956:Syt7
|
APN |
19 |
10,420,755 (GRCm39) |
missense |
probably benign |
0.03 |
R0412:Syt7
|
UTSW |
19 |
10,421,444 (GRCm39) |
nonsense |
probably null |
|
R1068:Syt7
|
UTSW |
19 |
10,421,375 (GRCm39) |
missense |
probably benign |
0.01 |
R1793:Syt7
|
UTSW |
19 |
10,421,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R1955:Syt7
|
UTSW |
19 |
10,395,402 (GRCm39) |
missense |
probably damaging |
1.00 |
R2049:Syt7
|
UTSW |
19 |
10,416,577 (GRCm39) |
missense |
probably benign |
0.28 |
R2170:Syt7
|
UTSW |
19 |
10,416,744 (GRCm39) |
missense |
probably damaging |
1.00 |
R2911:Syt7
|
UTSW |
19 |
10,420,799 (GRCm39) |
missense |
probably benign |
0.00 |
R3694:Syt7
|
UTSW |
19 |
10,413,000 (GRCm39) |
missense |
possibly damaging |
0.69 |
R4330:Syt7
|
UTSW |
19 |
10,399,162 (GRCm39) |
missense |
probably damaging |
1.00 |
R4573:Syt7
|
UTSW |
19 |
10,416,576 (GRCm39) |
nonsense |
probably null |
|
R4691:Syt7
|
UTSW |
19 |
10,403,845 (GRCm39) |
missense |
probably damaging |
0.98 |
R4732:Syt7
|
UTSW |
19 |
10,420,288 (GRCm39) |
missense |
probably damaging |
1.00 |
R4733:Syt7
|
UTSW |
19 |
10,420,288 (GRCm39) |
missense |
probably damaging |
1.00 |
R4811:Syt7
|
UTSW |
19 |
10,412,931 (GRCm39) |
missense |
probably damaging |
0.98 |
R5067:Syt7
|
UTSW |
19 |
10,420,222 (GRCm39) |
missense |
possibly damaging |
0.58 |
R5069:Syt7
|
UTSW |
19 |
10,416,601 (GRCm39) |
missense |
probably benign |
0.00 |
R5071:Syt7
|
UTSW |
19 |
10,420,792 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5372:Syt7
|
UTSW |
19 |
10,403,985 (GRCm39) |
missense |
probably damaging |
1.00 |
R5830:Syt7
|
UTSW |
19 |
10,399,151 (GRCm39) |
missense |
probably damaging |
1.00 |
R5979:Syt7
|
UTSW |
19 |
10,420,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R6737:Syt7
|
UTSW |
19 |
10,421,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R6833:Syt7
|
UTSW |
19 |
10,421,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R6843:Syt7
|
UTSW |
19 |
10,399,135 (GRCm39) |
missense |
probably damaging |
1.00 |
R7010:Syt7
|
UTSW |
19 |
10,395,354 (GRCm39) |
missense |
probably benign |
0.16 |
R7078:Syt7
|
UTSW |
19 |
10,412,963 (GRCm39) |
missense |
probably benign |
0.14 |
R7206:Syt7
|
UTSW |
19 |
10,395,337 (GRCm39) |
missense |
probably damaging |
1.00 |
R9116:Syt7
|
UTSW |
19 |
10,421,373 (GRCm39) |
missense |
probably damaging |
1.00 |
R9582:Syt7
|
UTSW |
19 |
10,416,780 (GRCm39) |
missense |
probably damaging |
1.00 |
R9610:Syt7
|
UTSW |
19 |
10,421,459 (GRCm39) |
missense |
probably benign |
0.06 |
Z1176:Syt7
|
UTSW |
19 |
10,420,774 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Syt7
|
UTSW |
19 |
10,403,857 (GRCm39) |
missense |
probably benign |
0.03 |
|