Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acbd6 |
T |
C |
1: 155,443,356 (GRCm39) |
S105P |
probably benign |
Het |
Acot12 |
G |
A |
13: 91,931,110 (GRCm39) |
V453M |
probably damaging |
Het |
Actr2 |
C |
T |
11: 20,044,350 (GRCm39) |
M85I |
probably benign |
Het |
Anxa9 |
T |
C |
3: 95,210,379 (GRCm39) |
D62G |
probably benign |
Het |
Arnt |
C |
T |
3: 95,397,954 (GRCm39) |
A599V |
probably benign |
Het |
Ash1l |
A |
G |
3: 88,950,566 (GRCm39) |
E2153G |
probably damaging |
Het |
Asic5 |
A |
T |
3: 81,911,850 (GRCm39) |
T149S |
probably benign |
Het |
Atcay |
G |
A |
10: 81,043,686 (GRCm39) |
T353I |
unknown |
Het |
Aven |
T |
C |
2: 112,455,517 (GRCm39) |
F143L |
probably damaging |
Het |
BB014433 |
GCACACAGCTTTGGAGGTGTACACACCCGGGTTGGGGCCTCTACACACAGCTTTGGAGGTGTACACACCCGGGTTGGGGCCTCTGCACACAGCTTTGG |
GCACACAGCTTTGGAGGTGTACACACCCGGGTTGGGGCCTCTGCACACAGCTTTGG |
8: 15,092,160 (GRCm39) |
|
probably benign |
Het |
BC024139 |
T |
A |
15: 76,009,715 (GRCm39) |
L149F |
probably damaging |
Het |
C3 |
T |
C |
17: 57,532,037 (GRCm39) |
Y228C |
probably damaging |
Het |
Cacna1d |
A |
G |
14: 29,845,316 (GRCm39) |
F640L |
probably benign |
Het |
Ccdc187 |
T |
C |
2: 26,145,930 (GRCm39) |
R1220G |
possibly damaging |
Het |
Cdc42bpb |
G |
A |
12: 111,268,508 (GRCm39) |
Q1231* |
probably null |
Het |
Cdh20 |
T |
A |
1: 104,875,067 (GRCm39) |
V283E |
probably damaging |
Het |
Cep63 |
T |
C |
9: 102,484,533 (GRCm39) |
I241V |
probably benign |
Het |
Dis3 |
A |
G |
14: 99,316,975 (GRCm39) |
V787A |
probably damaging |
Het |
Dock9 |
A |
G |
14: 121,864,775 (GRCm39) |
F727S |
probably damaging |
Het |
Eif5b |
G |
T |
1: 38,057,131 (GRCm39) |
E63* |
probably null |
Het |
Fanca |
A |
G |
8: 124,023,078 (GRCm39) |
V553A |
probably damaging |
Het |
Flacc1 |
C |
T |
1: 58,717,504 (GRCm39) |
A136T |
probably benign |
Het |
Gm37240 |
A |
C |
3: 84,417,196 (GRCm39) |
H174Q |
probably benign |
Het |
Myh2 |
G |
A |
11: 67,072,002 (GRCm39) |
E577K |
possibly damaging |
Het |
Ncoa1 |
C |
T |
12: 4,325,178 (GRCm39) |
V967I |
possibly damaging |
Het |
Nmur2 |
T |
C |
11: 55,931,649 (GRCm39) |
T21A |
probably damaging |
Het |
Nrde2 |
A |
G |
12: 100,110,426 (GRCm39) |
C197R |
probably damaging |
Het |
Or2m12 |
A |
T |
16: 19,104,943 (GRCm39) |
D183E |
probably benign |
Het |
Or2o1 |
C |
A |
11: 49,051,073 (GRCm39) |
C77* |
probably null |
Het |
Or52ad1 |
T |
C |
7: 102,995,569 (GRCm39) |
I189V |
probably benign |
Het |
Or8h7 |
G |
T |
2: 86,720,813 (GRCm39) |
H235Q |
probably benign |
Het |
Pard3b |
C |
T |
1: 62,250,786 (GRCm39) |
R572* |
probably null |
Het |
Pdcd6ip |
T |
C |
9: 113,520,589 (GRCm39) |
S132G |
probably damaging |
Het |
Pdzrn3 |
A |
T |
6: 101,149,235 (GRCm39) |
F364L |
probably benign |
Het |
Pfpl |
G |
C |
19: 12,406,297 (GRCm39) |
E183Q |
probably damaging |
Het |
Pgr |
G |
T |
9: 8,901,532 (GRCm39) |
C355F |
possibly damaging |
Het |
Pkhd1 |
T |
G |
1: 20,188,004 (GRCm39) |
S3435R |
probably damaging |
Het |
Pkhd1l1 |
A |
G |
15: 44,410,284 (GRCm39) |
D2597G |
probably benign |
Het |
Pramel30 |
T |
C |
4: 144,057,095 (GRCm39) |
Y93H |
possibly damaging |
Het |
Prrc2c |
T |
C |
1: 162,508,359 (GRCm39) |
E2410G |
possibly damaging |
Het |
Rpap2 |
C |
G |
5: 107,768,180 (GRCm39) |
S339R |
probably benign |
Het |
Rrp36 |
G |
C |
17: 46,983,492 (GRCm39) |
R69G |
possibly damaging |
Het |
Rrp8 |
T |
C |
7: 105,382,606 (GRCm39) |
T449A |
probably benign |
Het |
Scn3a |
T |
C |
2: 65,366,860 (GRCm39) |
D54G |
probably damaging |
Het |
Serinc2 |
C |
T |
4: 130,152,516 (GRCm39) |
W228* |
probably null |
Het |
Serpinb9g |
A |
G |
13: 33,679,141 (GRCm39) |
K337R |
probably benign |
Het |
Slc28a2b |
A |
T |
2: 122,324,822 (GRCm39) |
K131N |
probably benign |
Het |
Spata31 |
A |
T |
13: 65,070,077 (GRCm39) |
I742F |
probably damaging |
Het |
Speg |
C |
T |
1: 75,399,426 (GRCm39) |
P2291L |
probably benign |
Het |
Ss18l2 |
T |
A |
9: 121,541,666 (GRCm39) |
L61* |
probably null |
Het |
Suco |
C |
T |
1: 161,661,668 (GRCm39) |
R921H |
probably damaging |
Het |
Taok2 |
A |
T |
7: 126,466,008 (GRCm39) |
I910N |
probably damaging |
Het |
Tmem18 |
G |
A |
12: 30,638,557 (GRCm39) |
M106I |
|
Het |
Tob1 |
T |
G |
11: 94,105,234 (GRCm39) |
S257A |
unknown |
Het |
Trim67 |
G |
C |
8: 125,521,497 (GRCm39) |
K286N |
possibly damaging |
Het |
Trmt112 |
A |
G |
19: 6,887,956 (GRCm39) |
N62S |
probably benign |
Het |
Tsc2 |
C |
T |
17: 24,819,308 (GRCm39) |
|
probably null |
Het |
Ttn |
C |
T |
2: 76,715,357 (GRCm39) |
E7912K |
unknown |
Het |
Ube2j1 |
G |
T |
4: 33,040,793 (GRCm39) |
E100* |
probably null |
Het |
Urgcp |
A |
T |
11: 5,667,517 (GRCm39) |
F317I |
possibly damaging |
Het |
Vps9d1 |
A |
T |
8: 123,970,522 (GRCm39) |
D588E |
probably damaging |
Het |
Wdr38 |
A |
T |
2: 38,890,210 (GRCm39) |
T115S |
probably damaging |
Het |
Zfp119a |
G |
A |
17: 56,172,593 (GRCm39) |
Q417* |
probably null |
Het |
Zfp687 |
C |
T |
3: 94,916,442 (GRCm39) |
C860Y |
probably damaging |
Het |
Zmym4 |
T |
C |
4: 126,799,164 (GRCm39) |
N724S |
probably benign |
Het |
|
Other mutations in Kcnc4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00337:Kcnc4
|
APN |
3 |
107,355,189 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00899:Kcnc4
|
APN |
3 |
107,365,779 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01755:Kcnc4
|
APN |
3 |
107,355,491 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01895:Kcnc4
|
APN |
3 |
107,355,534 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02741:Kcnc4
|
APN |
3 |
107,355,294 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03393:Kcnc4
|
APN |
3 |
107,355,243 (GRCm39) |
missense |
possibly damaging |
0.75 |
PIT4151001:Kcnc4
|
UTSW |
3 |
107,366,019 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4378001:Kcnc4
|
UTSW |
3 |
107,354,879 (GRCm39) |
missense |
probably benign |
|
R0158:Kcnc4
|
UTSW |
3 |
107,365,920 (GRCm39) |
missense |
probably benign |
0.21 |
R0415:Kcnc4
|
UTSW |
3 |
107,352,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R0704:Kcnc4
|
UTSW |
3 |
107,355,279 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0747:Kcnc4
|
UTSW |
3 |
107,355,470 (GRCm39) |
missense |
probably damaging |
1.00 |
R1481:Kcnc4
|
UTSW |
3 |
107,355,534 (GRCm39) |
missense |
probably benign |
0.02 |
R1540:Kcnc4
|
UTSW |
3 |
107,352,743 (GRCm39) |
splice site |
probably null |
|
R1602:Kcnc4
|
UTSW |
3 |
107,355,520 (GRCm39) |
missense |
possibly damaging |
0.96 |
R2422:Kcnc4
|
UTSW |
3 |
107,352,863 (GRCm39) |
missense |
probably benign |
0.30 |
R3750:Kcnc4
|
UTSW |
3 |
107,355,506 (GRCm39) |
missense |
probably benign |
0.36 |
R4791:Kcnc4
|
UTSW |
3 |
107,354,859 (GRCm39) |
missense |
probably benign |
0.32 |
R4815:Kcnc4
|
UTSW |
3 |
107,365,582 (GRCm39) |
missense |
probably benign |
0.37 |
R5216:Kcnc4
|
UTSW |
3 |
107,346,757 (GRCm39) |
missense |
probably benign |
|
R5259:Kcnc4
|
UTSW |
3 |
107,355,401 (GRCm39) |
missense |
probably damaging |
1.00 |
R5317:Kcnc4
|
UTSW |
3 |
107,366,055 (GRCm39) |
missense |
probably damaging |
0.98 |
R5474:Kcnc4
|
UTSW |
3 |
107,355,207 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5783:Kcnc4
|
UTSW |
3 |
107,355,188 (GRCm39) |
missense |
possibly damaging |
0.69 |
R5865:Kcnc4
|
UTSW |
3 |
107,365,515 (GRCm39) |
critical splice donor site |
probably null |
|
R6228:Kcnc4
|
UTSW |
3 |
107,355,693 (GRCm39) |
missense |
probably damaging |
0.99 |
R6536:Kcnc4
|
UTSW |
3 |
107,355,512 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7018:Kcnc4
|
UTSW |
3 |
107,366,178 (GRCm39) |
missense |
probably benign |
0.00 |
R7319:Kcnc4
|
UTSW |
3 |
107,366,100 (GRCm39) |
missense |
probably benign |
0.21 |
R7687:Kcnc4
|
UTSW |
3 |
107,365,925 (GRCm39) |
small insertion |
probably benign |
|
R8436:Kcnc4
|
UTSW |
3 |
107,366,084 (GRCm39) |
missense |
probably damaging |
0.96 |
R8707:Kcnc4
|
UTSW |
3 |
107,355,449 (GRCm39) |
missense |
possibly damaging |
0.76 |
R8844:Kcnc4
|
UTSW |
3 |
107,355,396 (GRCm39) |
missense |
probably damaging |
1.00 |
R8868:Kcnc4
|
UTSW |
3 |
107,355,452 (GRCm39) |
missense |
probably damaging |
1.00 |
X0020:Kcnc4
|
UTSW |
3 |
107,354,967 (GRCm39) |
missense |
possibly damaging |
0.90 |
|