Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700034J05Rik |
T |
A |
6: 146,854,813 (GRCm39) |
K76N |
possibly damaging |
Het |
Agxt |
A |
G |
1: 93,063,425 (GRCm39) |
E109G |
probably damaging |
Het |
Alcam |
T |
C |
16: 52,109,299 (GRCm39) |
T325A |
probably benign |
Het |
Bco1 |
C |
A |
8: 117,840,178 (GRCm39) |
S232Y |
probably benign |
Het |
Cacna1c |
A |
T |
6: 118,652,884 (GRCm39) |
V763D |
probably damaging |
Het |
Ccdc15 |
T |
C |
9: 37,215,628 (GRCm39) |
D618G |
probably damaging |
Het |
Cimip1 |
A |
G |
2: 173,364,496 (GRCm39) |
M14V |
probably benign |
Het |
Col6a5 |
T |
C |
9: 105,783,312 (GRCm39) |
N1603S |
unknown |
Het |
Cyp4v3 |
A |
G |
8: 45,761,411 (GRCm39) |
|
probably null |
Het |
Eml5 |
A |
T |
12: 98,810,346 (GRCm39) |
V870E |
probably damaging |
Het |
Epn2 |
A |
G |
11: 61,410,497 (GRCm39) |
V512A |
probably damaging |
Het |
Farp2 |
A |
G |
1: 93,504,185 (GRCm39) |
R321G |
probably damaging |
Het |
Garin3 |
G |
T |
11: 46,297,379 (GRCm39) |
V228L |
probably damaging |
Het |
Gprasp1 |
T |
C |
X: 134,701,552 (GRCm39) |
S582P |
probably damaging |
Het |
Grhl2 |
T |
C |
15: 37,291,821 (GRCm39) |
V303A |
probably damaging |
Het |
Grik1 |
A |
T |
16: 87,743,444 (GRCm39) |
F594L |
probably damaging |
Het |
Hivep1 |
A |
G |
13: 42,309,925 (GRCm39) |
K722E |
probably benign |
Het |
Htr5b |
G |
A |
1: 121,455,564 (GRCm39) |
R119C |
probably damaging |
Het |
Ifit2 |
T |
C |
19: 34,551,737 (GRCm39) |
S426P |
probably benign |
Het |
Kif13a |
T |
C |
13: 46,978,698 (GRCm39) |
Y234C |
probably damaging |
Het |
Mios |
T |
A |
6: 8,222,598 (GRCm39) |
F511I |
probably benign |
Het |
Mtfmt |
T |
C |
9: 65,346,849 (GRCm39) |
W148R |
probably damaging |
Het |
Myo1c |
C |
A |
11: 75,552,400 (GRCm39) |
T391N |
probably benign |
Het |
Nlrp1a |
A |
T |
11: 71,004,339 (GRCm39) |
L710* |
probably null |
Het |
Nlrp1b |
A |
G |
11: 71,052,506 (GRCm39) |
I971T |
probably damaging |
Het |
Nup43 |
A |
G |
10: 7,549,358 (GRCm39) |
D171G |
probably damaging |
Het |
Or5b12b |
A |
G |
19: 12,861,305 (GRCm39) |
E20G |
probably benign |
Het |
P2rx7 |
T |
C |
5: 122,811,719 (GRCm39) |
|
probably benign |
Het |
Pgap6 |
T |
A |
17: 26,338,473 (GRCm39) |
Y512N |
probably benign |
Het |
Poli |
C |
T |
18: 70,656,363 (GRCm39) |
G155R |
probably damaging |
Het |
Rad9b |
T |
C |
5: 122,471,405 (GRCm39) |
S220G |
possibly damaging |
Het |
Rgn |
C |
T |
X: 20,416,700 (GRCm39) |
S28L |
probably damaging |
Het |
Tcp11l2 |
G |
A |
10: 84,440,932 (GRCm39) |
|
probably null |
Het |
Tenm4 |
G |
A |
7: 96,353,344 (GRCm39) |
V379I |
possibly damaging |
Het |
Thsd7a |
A |
T |
6: 12,343,264 (GRCm39) |
C1118S |
probably damaging |
Het |
Trpm7 |
A |
G |
2: 126,667,664 (GRCm39) |
Y776H |
probably damaging |
Het |
Trpv4 |
T |
C |
5: 114,774,418 (GRCm39) |
N222S |
probably benign |
Het |
Tut1 |
C |
T |
19: 8,941,403 (GRCm39) |
R397C |
probably damaging |
Het |
Vmn1r72 |
T |
A |
7: 11,403,672 (GRCm39) |
T259S |
probably benign |
Het |
Wdr17 |
A |
G |
8: 55,149,423 (GRCm39) |
S2P |
possibly damaging |
Het |
|
Other mutations in Apol7c |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01112:Apol7c
|
APN |
15 |
77,410,637 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01653:Apol7c
|
APN |
15 |
77,410,500 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02169:Apol7c
|
APN |
15 |
77,410,616 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL02262:Apol7c
|
APN |
15 |
77,410,013 (GRCm39) |
missense |
probably benign |
0.20 |
IGL02645:Apol7c
|
APN |
15 |
77,413,083 (GRCm39) |
missense |
probably benign |
0.19 |
IGL02934:Apol7c
|
APN |
15 |
77,410,318 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL03127:Apol7c
|
APN |
15 |
77,410,106 (GRCm39) |
missense |
probably benign |
0.16 |
R0130:Apol7c
|
UTSW |
15 |
77,410,562 (GRCm39) |
missense |
possibly damaging |
0.52 |
R0659:Apol7c
|
UTSW |
15 |
77,410,473 (GRCm39) |
missense |
probably damaging |
0.99 |
R1638:Apol7c
|
UTSW |
15 |
77,410,418 (GRCm39) |
missense |
probably damaging |
0.97 |
R1980:Apol7c
|
UTSW |
15 |
77,410,244 (GRCm39) |
missense |
probably benign |
0.16 |
R4366:Apol7c
|
UTSW |
15 |
77,410,589 (GRCm39) |
missense |
probably benign |
0.07 |
R4466:Apol7c
|
UTSW |
15 |
77,410,664 (GRCm39) |
missense |
probably benign |
0.00 |
R4624:Apol7c
|
UTSW |
15 |
77,410,595 (GRCm39) |
missense |
probably damaging |
1.00 |
R4629:Apol7c
|
UTSW |
15 |
77,410,595 (GRCm39) |
missense |
probably damaging |
1.00 |
R4706:Apol7c
|
UTSW |
15 |
77,409,923 (GRCm39) |
missense |
probably benign |
0.05 |
R5367:Apol7c
|
UTSW |
15 |
77,410,347 (GRCm39) |
missense |
probably damaging |
1.00 |
R5586:Apol7c
|
UTSW |
15 |
77,410,599 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6239:Apol7c
|
UTSW |
15 |
77,410,631 (GRCm39) |
missense |
probably benign |
0.28 |
R6860:Apol7c
|
UTSW |
15 |
77,410,274 (GRCm39) |
missense |
probably benign |
0.02 |
R7179:Apol7c
|
UTSW |
15 |
77,409,843 (GRCm39) |
missense |
probably benign |
0.01 |
R7234:Apol7c
|
UTSW |
15 |
77,409,875 (GRCm39) |
nonsense |
probably null |
|
R7513:Apol7c
|
UTSW |
15 |
77,409,911 (GRCm39) |
missense |
possibly damaging |
0.51 |
R7779:Apol7c
|
UTSW |
15 |
77,409,946 (GRCm39) |
missense |
probably damaging |
0.98 |
R8499:Apol7c
|
UTSW |
15 |
77,410,280 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9335:Apol7c
|
UTSW |
15 |
77,409,889 (GRCm39) |
missense |
probably benign |
0.00 |
R9354:Apol7c
|
UTSW |
15 |
77,410,112 (GRCm39) |
missense |
possibly damaging |
0.51 |
|