Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrg6 |
A |
G |
10: 14,296,349 (GRCm39) |
I1045T |
probably damaging |
Het |
Ankrd22 |
T |
C |
19: 34,143,181 (GRCm39) |
|
probably benign |
Het |
Bahcc1 |
A |
G |
11: 120,163,760 (GRCm39) |
D686G |
probably damaging |
Het |
Carns1 |
A |
G |
19: 4,216,569 (GRCm39) |
|
probably benign |
Het |
Cc2d1b |
C |
T |
4: 108,483,333 (GRCm39) |
L306F |
probably benign |
Het |
Ccdc153 |
A |
G |
9: 44,157,129 (GRCm39) |
E135G |
probably damaging |
Het |
Ccne1 |
T |
C |
7: 37,802,224 (GRCm39) |
D148G |
probably damaging |
Het |
Cfap57 |
A |
T |
4: 118,471,947 (GRCm39) |
M144K |
probably damaging |
Het |
Chd6 |
A |
G |
2: 160,826,552 (GRCm39) |
V1049A |
probably damaging |
Het |
Cpne9 |
A |
G |
6: 113,279,034 (GRCm39) |
D476G |
probably benign |
Het |
Dna2 |
T |
C |
10: 62,797,504 (GRCm39) |
|
probably null |
Het |
Eif4h |
T |
C |
5: 134,656,459 (GRCm39) |
D77G |
probably benign |
Het |
Fhl2 |
C |
T |
1: 43,167,562 (GRCm39) |
R177Q |
probably benign |
Het |
Fxyd5 |
C |
T |
7: 30,732,404 (GRCm39) |
R176H |
possibly damaging |
Het |
G6pd2 |
A |
G |
5: 61,966,735 (GRCm39) |
E170G |
probably damaging |
Het |
Haus3 |
A |
G |
5: 34,323,668 (GRCm39) |
I314T |
possibly damaging |
Het |
Igkv4-54 |
A |
G |
6: 69,608,862 (GRCm39) |
V41A |
probably damaging |
Het |
Lsr |
T |
C |
7: 30,657,838 (GRCm39) |
D442G |
probably damaging |
Het |
Mecom |
T |
C |
3: 30,015,183 (GRCm39) |
I847V |
probably damaging |
Het |
Mia2 |
C |
T |
12: 59,235,277 (GRCm39) |
R1326* |
probably null |
Het |
Myo15a |
C |
A |
11: 60,393,195 (GRCm39) |
H2240N |
probably damaging |
Het |
Or1e17 |
A |
G |
11: 73,831,942 (GRCm39) |
Y290C |
probably damaging |
Het |
Or4f62 |
A |
T |
2: 111,986,589 (GRCm39) |
I98F |
possibly damaging |
Het |
Osgep |
T |
A |
14: 51,153,314 (GRCm39) |
|
probably benign |
Het |
Pcnt |
G |
A |
10: 76,248,417 (GRCm39) |
Q901* |
probably null |
Het |
Pgm3 |
T |
C |
9: 86,437,431 (GRCm39) |
E481G |
possibly damaging |
Het |
Plch1 |
T |
A |
3: 63,605,899 (GRCm39) |
D1326V |
probably benign |
Het |
Rabgap1l |
T |
C |
1: 160,299,623 (GRCm39) |
D590G |
possibly damaging |
Het |
Rapsn |
A |
G |
2: 90,873,584 (GRCm39) |
M244V |
probably benign |
Het |
Rcbtb2 |
T |
A |
14: 73,405,543 (GRCm39) |
Y299* |
probably null |
Het |
Slc8a1 |
A |
T |
17: 81,715,752 (GRCm39) |
D760E |
probably benign |
Het |
Smim23 |
C |
A |
11: 32,774,424 (GRCm39) |
|
probably null |
Het |
Sva |
A |
G |
6: 42,017,069 (GRCm39) |
T59A |
unknown |
Het |
Tacc2 |
T |
A |
7: 130,225,809 (GRCm39) |
D831E |
probably benign |
Het |
Tasor2 |
T |
C |
13: 3,635,154 (GRCm39) |
N551S |
probably benign |
Het |
Tg |
G |
T |
15: 66,629,735 (GRCm39) |
W472L |
probably damaging |
Het |
Tmem231 |
A |
G |
8: 112,640,664 (GRCm39) |
V283A |
probably benign |
Het |
Traf4 |
A |
T |
11: 78,051,061 (GRCm39) |
I365N |
possibly damaging |
Het |
Usf3 |
G |
A |
16: 44,039,459 (GRCm39) |
S1313N |
probably benign |
Het |
Vangl1 |
G |
A |
3: 102,070,611 (GRCm39) |
|
probably benign |
Het |
Wdr70 |
T |
C |
15: 8,111,980 (GRCm39) |
S88G |
probably benign |
Het |
|
Other mutations in Kidins220 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00551:Kidins220
|
APN |
12 |
25,088,559 (GRCm39) |
splice site |
probably benign |
|
IGL00959:Kidins220
|
APN |
12 |
25,101,132 (GRCm39) |
missense |
possibly damaging |
0.74 |
IGL00978:Kidins220
|
APN |
12 |
25,107,473 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01144:Kidins220
|
APN |
12 |
25,060,925 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01326:Kidins220
|
APN |
12 |
25,088,498 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01545:Kidins220
|
APN |
12 |
25,090,459 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL01802:Kidins220
|
APN |
12 |
25,044,999 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01875:Kidins220
|
APN |
12 |
25,107,728 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02160:Kidins220
|
APN |
12 |
25,054,110 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02383:Kidins220
|
APN |
12 |
25,047,332 (GRCm39) |
splice site |
probably benign |
|
IGL02673:Kidins220
|
APN |
12 |
25,044,991 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03345:Kidins220
|
APN |
12 |
25,053,044 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03379:Kidins220
|
APN |
12 |
25,058,447 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03412:Kidins220
|
APN |
12 |
25,049,344 (GRCm39) |
missense |
probably damaging |
1.00 |
P0043:Kidins220
|
UTSW |
12 |
25,058,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R0011:Kidins220
|
UTSW |
12 |
25,049,351 (GRCm39) |
missense |
probably damaging |
0.99 |
R0011:Kidins220
|
UTSW |
12 |
25,049,351 (GRCm39) |
missense |
probably damaging |
0.99 |
R0269:Kidins220
|
UTSW |
12 |
25,090,511 (GRCm39) |
missense |
probably damaging |
0.98 |
R0280:Kidins220
|
UTSW |
12 |
25,060,140 (GRCm39) |
missense |
probably damaging |
1.00 |
R0334:Kidins220
|
UTSW |
12 |
25,058,068 (GRCm39) |
missense |
probably damaging |
1.00 |
R1601:Kidins220
|
UTSW |
12 |
25,055,087 (GRCm39) |
missense |
probably benign |
0.35 |
R1778:Kidins220
|
UTSW |
12 |
25,063,445 (GRCm39) |
splice site |
probably benign |
|
R1808:Kidins220
|
UTSW |
12 |
25,053,008 (GRCm39) |
missense |
probably benign |
0.00 |
R1855:Kidins220
|
UTSW |
12 |
25,106,590 (GRCm39) |
missense |
probably damaging |
1.00 |
R1965:Kidins220
|
UTSW |
12 |
25,044,905 (GRCm39) |
missense |
probably damaging |
1.00 |
R1982:Kidins220
|
UTSW |
12 |
25,101,193 (GRCm39) |
missense |
probably benign |
0.01 |
R2069:Kidins220
|
UTSW |
12 |
25,037,005 (GRCm39) |
splice site |
probably benign |
|
R2101:Kidins220
|
UTSW |
12 |
25,107,422 (GRCm39) |
missense |
probably damaging |
1.00 |
R2124:Kidins220
|
UTSW |
12 |
25,091,302 (GRCm39) |
critical splice donor site |
probably null |
|
R2371:Kidins220
|
UTSW |
12 |
25,107,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R2405:Kidins220
|
UTSW |
12 |
25,061,508 (GRCm39) |
missense |
probably damaging |
0.99 |
R3522:Kidins220
|
UTSW |
12 |
25,040,757 (GRCm39) |
missense |
probably damaging |
1.00 |
R3877:Kidins220
|
UTSW |
12 |
25,051,564 (GRCm39) |
splice site |
probably benign |
|
R3915:Kidins220
|
UTSW |
12 |
25,103,957 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4023:Kidins220
|
UTSW |
12 |
25,107,143 (GRCm39) |
splice site |
probably null |
|
R4287:Kidins220
|
UTSW |
12 |
25,106,845 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4476:Kidins220
|
UTSW |
12 |
25,061,000 (GRCm39) |
missense |
probably damaging |
1.00 |
R4495:Kidins220
|
UTSW |
12 |
25,088,301 (GRCm39) |
splice site |
probably null |
|
R4627:Kidins220
|
UTSW |
12 |
25,107,041 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4807:Kidins220
|
UTSW |
12 |
25,107,284 (GRCm39) |
missense |
probably damaging |
1.00 |
R4899:Kidins220
|
UTSW |
12 |
25,063,442 (GRCm39) |
critical splice donor site |
probably null |
|
R4960:Kidins220
|
UTSW |
12 |
25,042,259 (GRCm39) |
nonsense |
probably null |
|
R5118:Kidins220
|
UTSW |
12 |
25,042,296 (GRCm39) |
missense |
probably damaging |
1.00 |
R5183:Kidins220
|
UTSW |
12 |
25,101,125 (GRCm39) |
missense |
probably benign |
0.17 |
R5238:Kidins220
|
UTSW |
12 |
25,053,009 (GRCm39) |
missense |
probably benign |
0.31 |
R5580:Kidins220
|
UTSW |
12 |
25,097,896 (GRCm39) |
missense |
probably benign |
0.00 |
R5707:Kidins220
|
UTSW |
12 |
25,063,390 (GRCm39) |
missense |
probably damaging |
1.00 |
R5813:Kidins220
|
UTSW |
12 |
25,107,139 (GRCm39) |
nonsense |
probably null |
|
R6131:Kidins220
|
UTSW |
12 |
25,042,313 (GRCm39) |
splice site |
probably null |
|
R6146:Kidins220
|
UTSW |
12 |
25,102,812 (GRCm39) |
missense |
probably damaging |
1.00 |
R6151:Kidins220
|
UTSW |
12 |
25,106,908 (GRCm39) |
missense |
possibly damaging |
0.65 |
R6160:Kidins220
|
UTSW |
12 |
25,047,310 (GRCm39) |
missense |
probably damaging |
1.00 |
R6187:Kidins220
|
UTSW |
12 |
25,101,307 (GRCm39) |
splice site |
probably null |
|
R6289:Kidins220
|
UTSW |
12 |
25,106,615 (GRCm39) |
missense |
probably damaging |
1.00 |
R6321:Kidins220
|
UTSW |
12 |
25,107,533 (GRCm39) |
missense |
probably benign |
0.09 |
R6450:Kidins220
|
UTSW |
12 |
25,107,190 (GRCm39) |
missense |
probably benign |
|
R6513:Kidins220
|
UTSW |
12 |
25,088,434 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6652:Kidins220
|
UTSW |
12 |
25,060,059 (GRCm39) |
splice site |
probably null |
|
R6711:Kidins220
|
UTSW |
12 |
25,048,750 (GRCm39) |
missense |
probably damaging |
0.96 |
R6858:Kidins220
|
UTSW |
12 |
25,058,542 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7102:Kidins220
|
UTSW |
12 |
25,107,662 (GRCm39) |
missense |
probably benign |
0.00 |
R7112:Kidins220
|
UTSW |
12 |
25,054,018 (GRCm39) |
missense |
probably damaging |
1.00 |
R7139:Kidins220
|
UTSW |
12 |
25,044,820 (GRCm39) |
missense |
probably damaging |
1.00 |
R7140:Kidins220
|
UTSW |
12 |
25,086,623 (GRCm39) |
missense |
probably damaging |
1.00 |
R7271:Kidins220
|
UTSW |
12 |
25,061,570 (GRCm39) |
missense |
probably benign |
0.21 |
R7361:Kidins220
|
UTSW |
12 |
25,106,999 (GRCm39) |
missense |
probably benign |
0.01 |
R7509:Kidins220
|
UTSW |
12 |
25,032,360 (GRCm39) |
missense |
probably damaging |
0.98 |
R7510:Kidins220
|
UTSW |
12 |
25,042,268 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7783:Kidins220
|
UTSW |
12 |
25,038,555 (GRCm39) |
missense |
probably damaging |
1.00 |
R7796:Kidins220
|
UTSW |
12 |
25,032,350 (GRCm39) |
missense |
probably damaging |
0.96 |
R7831:Kidins220
|
UTSW |
12 |
25,111,230 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8074:Kidins220
|
UTSW |
12 |
25,107,715 (GRCm39) |
missense |
probably benign |
0.29 |
R8214:Kidins220
|
UTSW |
12 |
25,044,854 (GRCm39) |
missense |
probably damaging |
1.00 |
R8304:Kidins220
|
UTSW |
12 |
25,107,127 (GRCm39) |
missense |
probably benign |
0.01 |
R8313:Kidins220
|
UTSW |
12 |
25,054,110 (GRCm39) |
missense |
probably damaging |
1.00 |
R8346:Kidins220
|
UTSW |
12 |
25,086,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R8392:Kidins220
|
UTSW |
12 |
25,040,727 (GRCm39) |
missense |
probably damaging |
1.00 |
R8482:Kidins220
|
UTSW |
12 |
25,090,527 (GRCm39) |
missense |
probably benign |
0.00 |
R8722:Kidins220
|
UTSW |
12 |
25,051,593 (GRCm39) |
missense |
probably benign |
|
R8831:Kidins220
|
UTSW |
12 |
25,086,454 (GRCm39) |
missense |
possibly damaging |
0.70 |
R8960:Kidins220
|
UTSW |
12 |
25,106,914 (GRCm39) |
missense |
probably benign |
0.05 |
R9193:Kidins220
|
UTSW |
12 |
25,036,966 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9267:Kidins220
|
UTSW |
12 |
25,038,558 (GRCm39) |
missense |
probably benign |
0.29 |
R9303:Kidins220
|
UTSW |
12 |
25,107,110 (GRCm39) |
missense |
probably benign |
0.36 |
R9343:Kidins220
|
UTSW |
12 |
25,058,078 (GRCm39) |
missense |
probably damaging |
1.00 |
R9526:Kidins220
|
UTSW |
12 |
25,088,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R9644:Kidins220
|
UTSW |
12 |
25,061,018 (GRCm39) |
missense |
probably damaging |
1.00 |
R9655:Kidins220
|
UTSW |
12 |
25,047,295 (GRCm39) |
missense |
probably damaging |
1.00 |
R9664:Kidins220
|
UTSW |
12 |
25,106,895 (GRCm39) |
missense |
probably benign |
0.39 |
|