Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ano2 |
C |
T |
6: 125,840,499 (GRCm39) |
T390I |
probably damaging |
Het |
Cc2d2b |
T |
C |
19: 40,781,271 (GRCm39) |
V772A |
probably damaging |
Het |
Cd109 |
A |
G |
9: 78,614,834 (GRCm39) |
I1294V |
probably benign |
Het |
Cic |
A |
G |
7: 24,971,403 (GRCm39) |
E378G |
probably damaging |
Het |
Clhc1 |
C |
T |
11: 29,507,778 (GRCm39) |
P175L |
probably benign |
Het |
Clip1 |
T |
C |
5: 123,760,009 (GRCm39) |
E783G |
probably damaging |
Het |
Cnot1 |
A |
G |
8: 96,488,019 (GRCm39) |
Y546H |
probably damaging |
Het |
Cr2 |
T |
C |
1: 194,823,575 (GRCm39) |
T1008A |
probably benign |
Het |
Diaph1 |
T |
C |
18: 38,036,124 (GRCm39) |
T196A |
unknown |
Het |
Entr1 |
T |
C |
2: 26,276,990 (GRCm39) |
N247D |
probably benign |
Het |
Flg2 |
A |
T |
3: 93,108,467 (GRCm39) |
D165V |
probably damaging |
Het |
Fstl1 |
T |
G |
16: 37,649,534 (GRCm39) |
N249K |
probably damaging |
Het |
Gatad2a |
A |
G |
8: 70,364,839 (GRCm39) |
V515A |
probably benign |
Het |
Gbp2b |
A |
T |
3: 142,313,917 (GRCm39) |
D399V |
probably benign |
Het |
Gna14 |
G |
A |
19: 16,586,781 (GRCm39) |
V319I |
probably benign |
Het |
Grip1 |
A |
G |
10: 119,871,256 (GRCm39) |
D661G |
possibly damaging |
Het |
Gtf3c4 |
C |
A |
2: 28,724,126 (GRCm39) |
L535F |
probably damaging |
Het |
Haus8 |
A |
C |
8: 71,715,731 (GRCm39) |
S36A |
probably damaging |
Het |
Hectd4 |
A |
T |
5: 121,448,744 (GRCm39) |
Y364F |
probably benign |
Het |
Hectd4 |
C |
T |
5: 121,472,415 (GRCm39) |
A2717V |
possibly damaging |
Het |
Hsf5 |
C |
T |
11: 87,513,709 (GRCm39) |
T258M |
probably benign |
Het |
Ifi209 |
A |
T |
1: 173,472,235 (GRCm39) |
I359F |
probably damaging |
Het |
Ighmbp2 |
A |
G |
19: 3,324,360 (GRCm39) |
V302A |
probably benign |
Het |
Iqgap3 |
C |
A |
3: 88,016,176 (GRCm39) |
F986L |
probably damaging |
Het |
Itgav |
T |
A |
2: 83,600,451 (GRCm39) |
|
probably null |
Het |
Kcp |
A |
T |
6: 29,497,754 (GRCm39) |
D502E |
probably damaging |
Het |
Kif15 |
T |
C |
9: 122,824,890 (GRCm39) |
|
probably null |
Het |
Lipo2 |
C |
G |
19: 33,723,221 (GRCm39) |
K189N |
possibly damaging |
Het |
Lrch4 |
T |
A |
5: 137,636,218 (GRCm39) |
S390T |
probably benign |
Het |
Mast2 |
G |
T |
4: 116,179,508 (GRCm39) |
H389N |
probably benign |
Het |
Med13 |
A |
G |
11: 86,174,147 (GRCm39) |
Y1784H |
possibly damaging |
Het |
Micu3 |
A |
G |
8: 40,833,751 (GRCm39) |
K462E |
possibly damaging |
Het |
Mrps10 |
T |
C |
17: 47,683,572 (GRCm39) |
|
probably null |
Het |
Msh6 |
T |
C |
17: 88,293,963 (GRCm39) |
L906P |
probably damaging |
Het |
Nphp4 |
A |
G |
4: 152,621,737 (GRCm39) |
E531G |
probably benign |
Het |
Nrp2 |
A |
T |
1: 62,851,726 (GRCm39) |
Y825F |
probably benign |
Het |
Ntn1 |
C |
T |
11: 68,276,712 (GRCm39) |
V79M |
possibly damaging |
Het |
Nxnl2 |
A |
G |
13: 51,325,507 (GRCm39) |
D50G |
probably damaging |
Het |
Or1e16 |
T |
A |
11: 73,286,479 (GRCm39) |
Y123F |
possibly damaging |
Het |
Or2t26 |
T |
C |
11: 49,039,681 (GRCm39) |
M199T |
probably benign |
Het |
Or52h9 |
A |
T |
7: 104,202,530 (GRCm39) |
I135F |
possibly damaging |
Het |
Or52r1c |
T |
A |
7: 102,735,669 (GRCm39) |
C310S |
probably benign |
Het |
Or6c219 |
T |
C |
10: 129,780,990 (GRCm39) |
R314G |
probably benign |
Het |
Or7e176 |
G |
A |
9: 20,171,204 (GRCm39) |
V23I |
probably benign |
Het |
Ppp1r42 |
A |
G |
1: 10,073,674 (GRCm39) |
|
probably benign |
Het |
Ppp4r3a |
A |
T |
12: 101,008,763 (GRCm39) |
N692K |
probably benign |
Het |
Prr11 |
T |
C |
11: 86,994,416 (GRCm39) |
T77A |
possibly damaging |
Het |
Resf1 |
T |
A |
6: 149,228,068 (GRCm39) |
N371K |
probably benign |
Het |
Rrn3 |
A |
G |
16: 13,631,095 (GRCm39) |
I644V |
probably benign |
Het |
Scd4 |
T |
C |
19: 44,322,475 (GRCm39) |
S23P |
probably benign |
Het |
Slc26a2 |
T |
A |
18: 61,335,010 (GRCm39) |
S148C |
probably benign |
Het |
Slc7a8 |
T |
C |
14: 54,995,931 (GRCm39) |
E157G |
probably benign |
Het |
Spi1 |
A |
G |
2: 90,943,666 (GRCm39) |
H70R |
probably benign |
Het |
Styk1 |
CTCTTCATGATTTTCTT |
CTCTT |
6: 131,278,612 (GRCm39) |
|
probably benign |
Het |
Tlr4 |
A |
G |
4: 66,757,912 (GRCm39) |
N235S |
probably benign |
Het |
Trpc6 |
C |
A |
9: 8,643,641 (GRCm39) |
S475R |
probably benign |
Het |
Usp34 |
C |
T |
11: 23,409,182 (GRCm39) |
P2674L |
probably benign |
Het |
Usp48 |
G |
A |
4: 137,341,137 (GRCm39) |
G379D |
probably damaging |
Het |
Vkorc1l1 |
T |
A |
5: 130,011,078 (GRCm39) |
C97* |
probably null |
Het |
Wfikkn2 |
T |
C |
11: 94,129,211 (GRCm39) |
E310G |
probably benign |
Het |
Zfp266 |
T |
A |
9: 20,411,496 (GRCm39) |
N227I |
probably benign |
Het |
Zfp335 |
C |
T |
2: 164,749,347 (GRCm39) |
|
probably null |
Het |
Zfp677 |
T |
A |
17: 21,618,511 (GRCm39) |
C523S |
probably damaging |
Het |
Zrsr2 |
GCTCCTCCTCCTCCTCCT |
GCTCCTCCTCCTCCT |
X: 162,719,750 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Cog7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02023:Cog7
|
APN |
7 |
121,543,000 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02094:Cog7
|
APN |
7 |
121,562,470 (GRCm39) |
missense |
probably benign |
0.21 |
IGL02113:Cog7
|
APN |
7 |
121,524,703 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02151:Cog7
|
APN |
7 |
121,543,031 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02365:Cog7
|
APN |
7 |
121,576,959 (GRCm39) |
missense |
possibly damaging |
0.56 |
IGL02398:Cog7
|
APN |
7 |
121,563,432 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02732:Cog7
|
APN |
7 |
121,522,590 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02887:Cog7
|
APN |
7 |
121,543,067 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0143:Cog7
|
UTSW |
7 |
121,550,387 (GRCm39) |
missense |
probably damaging |
1.00 |
R0446:Cog7
|
UTSW |
7 |
121,536,295 (GRCm39) |
missense |
probably benign |
|
R0521:Cog7
|
UTSW |
7 |
121,540,392 (GRCm39) |
critical splice donor site |
probably null |
|
R0526:Cog7
|
UTSW |
7 |
121,562,494 (GRCm39) |
splice site |
probably null |
|
R0658:Cog7
|
UTSW |
7 |
121,555,363 (GRCm39) |
splice site |
probably benign |
|
R0782:Cog7
|
UTSW |
7 |
121,543,020 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1029:Cog7
|
UTSW |
7 |
121,529,752 (GRCm39) |
critical splice donor site |
probably null |
|
R1419:Cog7
|
UTSW |
7 |
121,555,215 (GRCm39) |
missense |
probably damaging |
0.99 |
R1521:Cog7
|
UTSW |
7 |
121,529,797 (GRCm39) |
missense |
possibly damaging |
0.57 |
R1639:Cog7
|
UTSW |
7 |
121,580,642 (GRCm39) |
missense |
probably damaging |
1.00 |
R2023:Cog7
|
UTSW |
7 |
121,536,193 (GRCm39) |
missense |
probably damaging |
0.99 |
R3896:Cog7
|
UTSW |
7 |
121,540,392 (GRCm39) |
critical splice donor site |
probably benign |
|
R4240:Cog7
|
UTSW |
7 |
121,524,707 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4731:Cog7
|
UTSW |
7 |
121,563,467 (GRCm39) |
missense |
probably benign |
0.00 |
R4732:Cog7
|
UTSW |
7 |
121,563,467 (GRCm39) |
missense |
probably benign |
0.00 |
R4733:Cog7
|
UTSW |
7 |
121,563,467 (GRCm39) |
missense |
probably benign |
0.00 |
R4838:Cog7
|
UTSW |
7 |
121,570,604 (GRCm39) |
missense |
probably damaging |
1.00 |
R5001:Cog7
|
UTSW |
7 |
121,549,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R5237:Cog7
|
UTSW |
7 |
121,550,444 (GRCm39) |
missense |
probably damaging |
1.00 |
R5353:Cog7
|
UTSW |
7 |
121,540,470 (GRCm39) |
splice site |
probably null |
|
R5609:Cog7
|
UTSW |
7 |
121,524,683 (GRCm39) |
missense |
probably benign |
0.12 |
R5964:Cog7
|
UTSW |
7 |
121,555,252 (GRCm39) |
missense |
probably damaging |
0.99 |
R6544:Cog7
|
UTSW |
7 |
121,534,966 (GRCm39) |
missense |
probably damaging |
0.99 |
R6784:Cog7
|
UTSW |
7 |
121,563,516 (GRCm39) |
splice site |
probably null |
|
R7110:Cog7
|
UTSW |
7 |
121,534,999 (GRCm39) |
missense |
probably damaging |
0.98 |
R7212:Cog7
|
UTSW |
7 |
121,576,537 (GRCm39) |
missense |
probably damaging |
0.98 |
R7304:Cog7
|
UTSW |
7 |
121,536,362 (GRCm39) |
missense |
probably benign |
0.04 |
R8185:Cog7
|
UTSW |
7 |
121,576,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R8207:Cog7
|
UTSW |
7 |
121,576,515 (GRCm39) |
missense |
possibly damaging |
0.70 |
R8838:Cog7
|
UTSW |
7 |
121,549,106 (GRCm39) |
missense |
probably damaging |
0.98 |
R9116:Cog7
|
UTSW |
7 |
121,570,561 (GRCm39) |
missense |
probably damaging |
0.99 |
R9582:Cog7
|
UTSW |
7 |
121,536,200 (GRCm39) |
missense |
probably benign |
0.00 |
X0066:Cog7
|
UTSW |
7 |
121,576,847 (GRCm39) |
missense |
probably damaging |
1.00 |
|