Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam1b |
C |
A |
5: 121,640,788 (GRCm39) |
E86* |
probably null |
Het |
Ahnak |
T |
G |
19: 8,984,617 (GRCm39) |
I1967S |
possibly damaging |
Het |
Alox12e |
A |
G |
11: 70,212,600 (GRCm39) |
V83A |
possibly damaging |
Het |
Arhgap20 |
A |
T |
9: 51,754,977 (GRCm39) |
R439S |
probably damaging |
Het |
Arl1 |
A |
G |
10: 88,569,458 (GRCm39) |
I20V |
probably damaging |
Het |
Atad2 |
T |
C |
15: 57,995,628 (GRCm39) |
D93G |
probably benign |
Het |
Btbd7 |
T |
G |
12: 102,804,838 (GRCm39) |
K67N |
probably damaging |
Het |
C130050O18Rik |
A |
G |
5: 139,400,301 (GRCm39) |
N118S |
probably benign |
Het |
Ccz1 |
A |
C |
5: 143,946,120 (GRCm39) |
|
probably benign |
Het |
Cdk19 |
A |
G |
10: 40,355,728 (GRCm39) |
S479G |
unknown |
Het |
Chrd |
A |
G |
16: 20,555,737 (GRCm39) |
T503A |
probably damaging |
Het |
Clca4b |
G |
A |
3: 144,617,827 (GRCm39) |
R759* |
probably null |
Het |
Cpa5 |
G |
T |
6: 30,612,604 (GRCm39) |
M1I |
probably null |
Het |
Cr2 |
A |
T |
1: 194,834,029 (GRCm39) |
I920N |
probably benign |
Het |
Crmp1 |
C |
A |
5: 37,437,947 (GRCm39) |
Y430* |
probably null |
Het |
Dars1 |
A |
T |
1: 128,296,163 (GRCm39) |
V390D |
possibly damaging |
Het |
Dmtn |
A |
G |
14: 70,853,555 (GRCm39) |
S85P |
probably damaging |
Het |
Ermardl1 |
A |
G |
17: 15,242,364 (GRCm39) |
E416G |
unknown |
Het |
Fancm |
C |
A |
12: 65,122,605 (GRCm39) |
D42E |
probably damaging |
Het |
Gabrg3 |
T |
A |
7: 56,423,122 (GRCm39) |
Y192F |
possibly damaging |
Het |
Gpr3 |
A |
T |
4: 132,938,209 (GRCm39) |
Y154* |
probably null |
Het |
Huwe1 |
G |
A |
X: 150,716,084 (GRCm39) |
R4331Q |
unknown |
Het |
Jhy |
A |
T |
9: 40,828,823 (GRCm39) |
V361D |
probably benign |
Het |
Klhl33 |
G |
A |
14: 51,130,322 (GRCm39) |
Q131* |
probably null |
Het |
Lama2 |
A |
T |
10: 27,080,881 (GRCm39) |
C981S |
probably damaging |
Het |
Mks1 |
C |
A |
11: 87,748,041 (GRCm39) |
L225I |
probably damaging |
Het |
Ms4a20 |
A |
T |
19: 11,083,055 (GRCm39) |
Y122N |
probably damaging |
Het |
Nfasc |
T |
A |
1: 132,539,343 (GRCm39) |
S402C |
probably damaging |
Het |
Or2a57 |
T |
C |
6: 43,213,358 (GRCm39) |
I272T |
possibly damaging |
Het |
Or4k50-ps1 |
A |
T |
2: 111,522,517 (GRCm39) |
Y218F |
unknown |
Het |
Or51g2 |
T |
C |
7: 102,622,560 (GRCm39) |
D213G |
probably damaging |
Het |
Pbx4 |
T |
A |
8: 70,316,999 (GRCm39) |
D85E |
possibly damaging |
Het |
Plcd1 |
T |
C |
9: 118,913,709 (GRCm39) |
T50A |
probably damaging |
Het |
Plk5 |
C |
G |
10: 80,193,830 (GRCm39) |
R40G |
probably damaging |
Het |
Psen2 |
C |
A |
1: 180,056,972 (GRCm39) |
E351* |
probably null |
Het |
Rragd |
G |
A |
4: 32,996,083 (GRCm39) |
V143I |
probably damaging |
Het |
Rsph14 |
A |
T |
10: 74,795,423 (GRCm39) |
M254K |
probably damaging |
Het |
Selenoi |
C |
T |
5: 30,437,607 (GRCm39) |
|
probably benign |
Het |
Six6 |
T |
C |
12: 72,986,935 (GRCm39) |
S36P |
|
Het |
Slc12a8 |
T |
C |
16: 33,445,215 (GRCm39) |
S370P |
probably benign |
Het |
Slc25a46 |
A |
G |
18: 31,716,432 (GRCm39) |
Y357H |
probably benign |
Het |
Socs2 |
A |
T |
10: 95,248,948 (GRCm39) |
V55D |
probably damaging |
Het |
Socs6 |
T |
C |
18: 88,888,852 (GRCm39) |
E21G |
probably benign |
Het |
Spata31e4 |
C |
T |
13: 50,857,007 (GRCm39) |
Q882* |
probably null |
Het |
Speg |
A |
T |
1: 75,365,076 (GRCm39) |
T486S |
possibly damaging |
Het |
Spryd3 |
A |
G |
15: 102,027,843 (GRCm39) |
Y235H |
probably damaging |
Het |
Sry |
GCTGCTGGTGGTGGTCATGGAACTGCTGCTTCTGCTGGTGGTGGTCATGGAACTGCTGCTTCTGCTGGTGGTGGTCATGGAACTGCTGCTTCTGCTG |
GCTGCTGGTGGTGGTCATGGAACTGCTGCTTCTGCTGGTGGTGGTCATGGAACTGCTGCTTCTGCTG |
Y: 2,662,638 (GRCm39) |
|
probably benign |
Het |
Stxbp5l |
T |
C |
16: 37,165,473 (GRCm39) |
K82E |
probably damaging |
Het |
Sugt1 |
A |
G |
14: 79,825,155 (GRCm39) |
|
probably benign |
Het |
Synm |
T |
C |
7: 67,384,440 (GRCm39) |
Y1074C |
probably damaging |
Het |
Sytl2 |
A |
G |
7: 90,028,748 (GRCm39) |
T476A |
probably benign |
Het |
Tbc1d1 |
T |
C |
5: 64,414,349 (GRCm39) |
S237P |
probably benign |
Het |
Tbc1d5 |
C |
A |
17: 51,063,692 (GRCm39) |
M629I |
probably damaging |
Het |
Tlr11 |
G |
A |
14: 50,598,749 (GRCm39) |
G245D |
probably damaging |
Het |
Tspan4 |
T |
C |
7: 141,069,577 (GRCm39) |
V59A |
probably benign |
Het |
Tulp4 |
T |
A |
17: 6,283,472 (GRCm39) |
V1167E |
possibly damaging |
Het |
Usp42 |
G |
A |
5: 143,708,906 (GRCm39) |
T204M |
probably damaging |
Het |
Vapb |
A |
G |
2: 173,617,948 (GRCm39) |
K147R |
possibly damaging |
Het |
Vmn1r228 |
T |
C |
17: 20,997,422 (GRCm39) |
D32G |
probably benign |
Het |
Vmn2r33 |
A |
G |
7: 7,554,168 (GRCm39) |
F795S |
probably damaging |
Het |
Vmn2r34 |
A |
T |
7: 7,675,527 (GRCm39) |
N620K |
probably damaging |
Het |
Vwf |
G |
T |
6: 125,643,626 (GRCm39) |
C2389F |
|
Het |
Wdr81 |
T |
C |
11: 75,332,908 (GRCm39) |
E652G |
|
Het |
Wdr81 |
A |
T |
11: 75,343,207 (GRCm39) |
S687T |
probably benign |
Het |
Zcrb1 |
A |
G |
15: 93,285,456 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Ints5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01448:Ints5
|
APN |
19 |
8,872,851 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01915:Ints5
|
APN |
19 |
8,874,357 (GRCm39) |
missense |
probably benign |
|
IGL01993:Ints5
|
APN |
19 |
8,872,829 (GRCm39) |
missense |
probably benign |
|
IGL02264:Ints5
|
APN |
19 |
8,873,076 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02367:Ints5
|
APN |
19 |
8,872,959 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02955:Ints5
|
APN |
19 |
8,875,014 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4449:Ints5
|
UTSW |
19 |
8,874,594 (GRCm39) |
missense |
probably benign |
0.10 |
R0348:Ints5
|
UTSW |
19 |
8,873,114 (GRCm39) |
missense |
probably damaging |
0.97 |
R0379:Ints5
|
UTSW |
19 |
8,874,497 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0617:Ints5
|
UTSW |
19 |
8,873,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R1954:Ints5
|
UTSW |
19 |
8,872,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R2172:Ints5
|
UTSW |
19 |
8,873,646 (GRCm39) |
missense |
possibly damaging |
0.73 |
R2370:Ints5
|
UTSW |
19 |
8,874,143 (GRCm39) |
missense |
probably benign |
|
R3116:Ints5
|
UTSW |
19 |
8,872,136 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4395:Ints5
|
UTSW |
19 |
8,873,808 (GRCm39) |
missense |
probably damaging |
0.96 |
R5390:Ints5
|
UTSW |
19 |
8,873,931 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6868:Ints5
|
UTSW |
19 |
8,874,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R7133:Ints5
|
UTSW |
19 |
8,872,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R7685:Ints5
|
UTSW |
19 |
8,874,168 (GRCm39) |
missense |
probably benign |
0.10 |
R7999:Ints5
|
UTSW |
19 |
8,874,407 (GRCm39) |
missense |
probably benign |
|
R8024:Ints5
|
UTSW |
19 |
8,873,504 (GRCm39) |
missense |
probably damaging |
1.00 |
R8296:Ints5
|
UTSW |
19 |
8,872,484 (GRCm39) |
missense |
probably damaging |
1.00 |
R8672:Ints5
|
UTSW |
19 |
8,873,370 (GRCm39) |
missense |
probably damaging |
1.00 |
R9493:Ints5
|
UTSW |
19 |
8,872,686 (GRCm39) |
missense |
probably damaging |
1.00 |
X0066:Ints5
|
UTSW |
19 |
8,873,595 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Ints5
|
UTSW |
19 |
8,872,337 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Ints5
|
UTSW |
19 |
8,872,299 (GRCm39) |
missense |
probably benign |
0.31 |
|