Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Agbl2 |
A |
G |
2: 90,627,891 (GRCm39) |
E232G |
probably damaging |
Het |
Atf7 |
A |
G |
15: 102,442,670 (GRCm39) |
S480P |
probably benign |
Het |
Cdk14 |
A |
G |
5: 5,245,325 (GRCm39) |
I166T |
possibly damaging |
Het |
Cdk5rap2 |
G |
T |
4: 70,267,393 (GRCm39) |
F358L |
probably benign |
Het |
Cplane1 |
T |
C |
15: 8,223,928 (GRCm39) |
L897P |
possibly damaging |
Het |
Dennd5b |
C |
T |
6: 148,946,102 (GRCm39) |
R503Q |
probably damaging |
Het |
Dnajc10 |
T |
A |
2: 80,171,159 (GRCm39) |
C480S |
probably damaging |
Het |
Drc7 |
A |
G |
8: 95,785,711 (GRCm39) |
D189G |
probably damaging |
Het |
Engase |
G |
A |
11: 118,372,121 (GRCm39) |
V138M |
probably damaging |
Het |
Esyt3 |
C |
A |
9: 99,220,840 (GRCm39) |
R121L |
probably damaging |
Het |
Frem1 |
T |
G |
4: 82,858,918 (GRCm39) |
I1516L |
probably benign |
Het |
Gatad2b |
T |
A |
3: 90,258,724 (GRCm39) |
I249N |
probably damaging |
Het |
Grk6 |
T |
C |
13: 55,602,219 (GRCm39) |
S383P |
probably benign |
Het |
Hectd1 |
C |
T |
12: 51,874,134 (GRCm39) |
|
probably null |
Het |
Hipk2 |
A |
G |
6: 38,795,579 (GRCm39) |
L230P |
probably damaging |
Het |
Hivep1 |
A |
T |
13: 42,310,814 (GRCm39) |
Q1018L |
probably benign |
Het |
Itgad |
T |
C |
7: 127,797,550 (GRCm39) |
F927S |
probably benign |
Het |
Itgb3bp |
A |
G |
4: 99,702,335 (GRCm39) |
V3A |
probably damaging |
Het |
Kcnh7 |
G |
T |
2: 62,618,031 (GRCm39) |
A486D |
possibly damaging |
Het |
Krt1c |
T |
C |
15: 101,723,522 (GRCm39) |
T318A |
probably benign |
Het |
Ndrg1 |
A |
G |
15: 66,818,377 (GRCm39) |
F77S |
probably damaging |
Het |
Nlrp4c |
T |
A |
7: 6,068,708 (GRCm39) |
L203* |
probably null |
Het |
Nos1 |
T |
A |
5: 118,085,496 (GRCm39) |
C1275S |
probably damaging |
Het |
Or14a256 |
T |
C |
7: 86,264,900 (GRCm39) |
S318G |
probably null |
Het |
Or4a69 |
A |
G |
2: 89,313,458 (GRCm39) |
V7A |
possibly damaging |
Het |
Or5an9 |
T |
C |
19: 12,187,242 (GRCm39) |
I104T |
possibly damaging |
Het |
Or5d39 |
T |
C |
2: 87,979,716 (GRCm39) |
T216A |
possibly damaging |
Het |
Or5j3 |
T |
A |
2: 86,128,564 (GRCm39) |
S135T |
probably benign |
Het |
Or8b12b |
A |
T |
9: 37,684,437 (GRCm39) |
N161Y |
possibly damaging |
Het |
Pip4k2b |
T |
C |
11: 97,623,542 (GRCm39) |
M67V |
possibly damaging |
Het |
Polq |
C |
A |
16: 36,909,715 (GRCm39) |
Y2366* |
probably null |
Het |
Prg3 |
T |
C |
2: 84,819,097 (GRCm39) |
S8P |
probably benign |
Het |
Prl7c1 |
A |
T |
13: 27,962,952 (GRCm39) |
L17* |
probably null |
Het |
Prl8a8 |
A |
T |
13: 27,695,479 (GRCm39) |
S51R |
probably damaging |
Het |
Pttg1 |
G |
C |
11: 43,311,976 (GRCm39) |
P160A |
probably benign |
Het |
Rbfox1 |
C |
A |
16: 7,170,867 (GRCm39) |
R276S |
possibly damaging |
Het |
Rnase2a |
T |
G |
14: 51,492,988 (GRCm39) |
M126L |
probably benign |
Het |
Secisbp2 |
A |
T |
13: 51,810,943 (GRCm39) |
K202* |
probably null |
Het |
Sema6c |
A |
G |
3: 95,076,156 (GRCm39) |
H236R |
possibly damaging |
Het |
Septin12 |
A |
G |
16: 4,809,857 (GRCm39) |
L181P |
probably damaging |
Het |
Shc3 |
A |
T |
13: 51,585,241 (GRCm39) |
V458D |
possibly damaging |
Het |
Tecta |
A |
G |
9: 42,278,239 (GRCm39) |
Y1090H |
probably benign |
Het |
Thsd7a |
A |
T |
6: 12,379,429 (GRCm39) |
N998K |
|
Het |
Tmem131l |
A |
T |
3: 83,826,766 (GRCm39) |
S1184T |
possibly damaging |
Het |
Tnfsf15 |
T |
C |
4: 63,647,887 (GRCm39) |
D251G |
probably damaging |
Het |
Ttyh3 |
T |
C |
5: 140,615,540 (GRCm39) |
E348G |
probably benign |
Het |
Unc5c |
T |
C |
3: 141,439,665 (GRCm39) |
L186P |
probably damaging |
Het |
Vmn2r37 |
A |
T |
7: 9,219,045 (GRCm39) |
N446K |
probably damaging |
Het |
Vmn2r63 |
T |
C |
7: 42,577,959 (GRCm39) |
D193G |
possibly damaging |
Het |
Vmn2r85 |
A |
T |
10: 130,262,376 (GRCm39) |
M121K |
probably benign |
Het |
Vmn2r88 |
A |
G |
14: 51,651,253 (GRCm39) |
D189G |
|
Het |
Vwc2l |
C |
A |
1: 70,768,252 (GRCm39) |
C105* |
probably null |
Het |
Wdr72 |
T |
A |
9: 74,055,597 (GRCm39) |
D275E |
probably damaging |
Het |
Zfhx4 |
A |
T |
3: 5,467,549 (GRCm39) |
D2594V |
probably damaging |
Het |
Zfp174 |
C |
T |
16: 3,672,269 (GRCm39) |
H273Y |
probably benign |
Het |
Zwilch |
A |
G |
9: 64,068,658 (GRCm39) |
S203P |
probably damaging |
Het |
|
Other mutations in Cytip |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01635:Cytip
|
APN |
2 |
58,038,243 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01670:Cytip
|
APN |
2 |
58,023,785 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02184:Cytip
|
APN |
2 |
58,023,750 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02271:Cytip
|
APN |
2 |
58,023,872 (GRCm39) |
nonsense |
probably null |
|
IGL02468:Cytip
|
APN |
2 |
58,024,025 (GRCm39) |
missense |
probably benign |
0.08 |
R0079:Cytip
|
UTSW |
2 |
58,050,006 (GRCm39) |
missense |
probably benign |
0.37 |
R0304:Cytip
|
UTSW |
2 |
58,038,258 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0612:Cytip
|
UTSW |
2 |
58,024,202 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1448:Cytip
|
UTSW |
2 |
58,035,192 (GRCm39) |
missense |
probably damaging |
1.00 |
R1822:Cytip
|
UTSW |
2 |
58,024,158 (GRCm39) |
missense |
probably benign |
0.00 |
R1954:Cytip
|
UTSW |
2 |
58,038,265 (GRCm39) |
missense |
possibly damaging |
0.75 |
R4401:Cytip
|
UTSW |
2 |
58,023,947 (GRCm39) |
missense |
probably benign |
0.01 |
R4578:Cytip
|
UTSW |
2 |
58,050,024 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5101:Cytip
|
UTSW |
2 |
58,037,911 (GRCm39) |
missense |
probably damaging |
1.00 |
R7703:Cytip
|
UTSW |
2 |
58,037,920 (GRCm39) |
missense |
probably damaging |
1.00 |
R7966:Cytip
|
UTSW |
2 |
58,037,944 (GRCm39) |
missense |
probably damaging |
1.00 |
R8492:Cytip
|
UTSW |
2 |
58,027,869 (GRCm39) |
critical splice donor site |
probably null |
|
R8711:Cytip
|
UTSW |
2 |
58,041,135 (GRCm39) |
missense |
probably damaging |
0.99 |
R8862:Cytip
|
UTSW |
2 |
58,037,887 (GRCm39) |
missense |
probably benign |
0.25 |
R9548:Cytip
|
UTSW |
2 |
58,041,141 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:Cytip
|
UTSW |
2 |
58,024,049 (GRCm39) |
missense |
probably damaging |
1.00 |
|