Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
B230217C12Rik |
T |
C |
11: 97,732,086 (GRCm39) |
|
probably benign |
Het |
Cacna1g |
T |
C |
11: 94,317,265 (GRCm39) |
D1498G |
probably damaging |
Het |
Ces3b |
T |
A |
8: 105,811,901 (GRCm39) |
D103E |
possibly damaging |
Het |
Chd5 |
A |
G |
4: 152,440,614 (GRCm39) |
Y158C |
probably damaging |
Het |
Cic |
A |
G |
7: 24,984,662 (GRCm39) |
T1033A |
probably benign |
Het |
Cst13 |
A |
T |
2: 148,672,247 (GRCm39) |
I141F |
possibly damaging |
Het |
Dnah7a |
A |
G |
1: 53,604,855 (GRCm39) |
L1301P |
probably damaging |
Het |
Dnah8 |
T |
A |
17: 30,923,636 (GRCm39) |
F1201L |
probably benign |
Het |
Dok7 |
T |
C |
5: 35,232,633 (GRCm39) |
|
probably benign |
Het |
Dzip3 |
A |
G |
16: 48,774,171 (GRCm39) |
|
probably benign |
Het |
Eml6 |
A |
G |
11: 29,699,877 (GRCm39) |
V1753A |
probably benign |
Het |
Fer1l4 |
A |
G |
2: 155,887,583 (GRCm39) |
F538L |
possibly damaging |
Het |
Fmo2 |
C |
T |
1: 162,704,383 (GRCm39) |
D508N |
probably benign |
Het |
Gabpb1 |
A |
T |
2: 126,472,248 (GRCm39) |
Y351N |
probably damaging |
Het |
Gnaq |
T |
A |
19: 16,312,428 (GRCm39) |
V230E |
probably damaging |
Het |
Gprc5c |
A |
C |
11: 114,757,537 (GRCm39) |
K48Q |
probably damaging |
Het |
Gzmd |
A |
G |
14: 56,369,948 (GRCm39) |
L11P |
unknown |
Het |
Hbq1b |
A |
C |
11: 32,237,581 (GRCm39) |
H123P |
probably damaging |
Het |
Hibadh |
T |
A |
6: 52,533,490 (GRCm39) |
I209F |
probably damaging |
Het |
Il17f |
G |
T |
1: 20,848,177 (GRCm39) |
C100* |
probably null |
Het |
Iqca1 |
C |
A |
1: 90,070,453 (GRCm39) |
G133V |
probably null |
Het |
Itga8 |
A |
T |
2: 12,198,362 (GRCm39) |
V541E |
possibly damaging |
Het |
Klra2 |
A |
T |
6: 131,207,137 (GRCm39) |
Y157* |
probably null |
Het |
Kprp |
T |
C |
3: 92,732,342 (GRCm39) |
Y236C |
unknown |
Het |
Mmp12 |
A |
T |
9: 7,357,827 (GRCm39) |
M414L |
possibly damaging |
Het |
Myh6 |
A |
G |
14: 55,190,735 (GRCm39) |
|
probably benign |
Het |
Nlgn2 |
A |
G |
11: 69,716,823 (GRCm39) |
F573L |
possibly damaging |
Het |
Or10j7 |
C |
T |
1: 173,011,627 (GRCm39) |
A125T |
probably damaging |
Het |
Or4c124 |
A |
G |
2: 89,156,008 (GRCm39) |
V172A |
probably benign |
Het |
Pakap |
T |
A |
4: 57,709,650 (GRCm39) |
D198E |
probably benign |
Het |
Papss1 |
T |
A |
3: 131,305,615 (GRCm39) |
|
probably benign |
Het |
Parp4 |
A |
G |
14: 56,827,408 (GRCm39) |
T181A |
probably benign |
Het |
Piwil2 |
A |
T |
14: 70,646,486 (GRCm39) |
|
probably benign |
Het |
Pla2g12b |
A |
G |
10: 59,239,642 (GRCm39) |
N17S |
probably benign |
Het |
Polr3c |
C |
A |
3: 96,626,627 (GRCm39) |
V266L |
probably damaging |
Het |
Pou3f3 |
A |
G |
1: 42,737,527 (GRCm39) |
T408A |
probably damaging |
Het |
Pskh1 |
A |
G |
8: 106,640,238 (GRCm39) |
Y306C |
probably damaging |
Het |
Rom1 |
T |
A |
19: 8,906,272 (GRCm39) |
D89V |
probably damaging |
Het |
Sell |
T |
A |
1: 163,893,770 (GRCm39) |
|
probably null |
Het |
Sox6 |
A |
G |
7: 115,178,249 (GRCm39) |
|
probably null |
Het |
Speg |
T |
C |
1: 75,400,133 (GRCm39) |
S2527P |
probably damaging |
Het |
Stat3 |
A |
G |
11: 100,784,981 (GRCm39) |
|
probably benign |
Het |
Stra6l |
A |
G |
4: 45,882,797 (GRCm39) |
T503A |
probably benign |
Het |
Tapbp |
A |
G |
17: 34,145,227 (GRCm39) |
T375A |
probably benign |
Het |
Tgm6 |
G |
A |
2: 129,985,342 (GRCm39) |
V382M |
possibly damaging |
Het |
Trappc9 |
A |
T |
15: 72,824,981 (GRCm39) |
|
probably benign |
Het |
Txlnb |
A |
G |
10: 17,675,240 (GRCm39) |
N131S |
possibly damaging |
Het |
Usp19 |
A |
G |
9: 108,372,353 (GRCm39) |
E469G |
probably damaging |
Het |
Vmn2r17 |
T |
A |
5: 109,575,192 (GRCm39) |
|
probably benign |
Het |
Zfp750 |
T |
C |
11: 121,402,838 (GRCm39) |
T637A |
probably benign |
Het |
Zhx2 |
A |
C |
15: 57,686,124 (GRCm39) |
I498L |
probably damaging |
Het |
|
Other mutations in Kifc5b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01337:Kifc5b
|
APN |
17 |
27,143,718 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01886:Kifc5b
|
APN |
17 |
27,151,091 (GRCm39) |
missense |
probably damaging |
0.99 |
FR4449:Kifc5b
|
UTSW |
17 |
27,143,191 (GRCm39) |
missense |
probably benign |
|
R0394:Kifc5b
|
UTSW |
17 |
27,142,056 (GRCm39) |
missense |
probably benign |
0.37 |
R0890:Kifc5b
|
UTSW |
17 |
27,141,996 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1122:Kifc5b
|
UTSW |
17 |
27,143,035 (GRCm39) |
missense |
probably benign |
0.01 |
R1651:Kifc5b
|
UTSW |
17 |
27,144,504 (GRCm39) |
missense |
probably damaging |
1.00 |
R1875:Kifc5b
|
UTSW |
17 |
27,136,264 (GRCm39) |
splice site |
probably null |
|
R1955:Kifc5b
|
UTSW |
17 |
27,145,271 (GRCm39) |
critical splice donor site |
probably null |
|
R2279:Kifc5b
|
UTSW |
17 |
27,144,515 (GRCm39) |
missense |
probably damaging |
0.99 |
R4921:Kifc5b
|
UTSW |
17 |
27,139,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R4949:Kifc5b
|
UTSW |
17 |
27,144,488 (GRCm39) |
missense |
probably damaging |
1.00 |
R5044:Kifc5b
|
UTSW |
17 |
27,143,761 (GRCm39) |
missense |
probably damaging |
1.00 |
R6144:Kifc5b
|
UTSW |
17 |
27,140,826 (GRCm39) |
missense |
probably benign |
0.01 |
R6393:Kifc5b
|
UTSW |
17 |
27,140,816 (GRCm39) |
missense |
probably benign |
0.08 |
R6484:Kifc5b
|
UTSW |
17 |
27,143,746 (GRCm39) |
missense |
probably damaging |
1.00 |
R7075:Kifc5b
|
UTSW |
17 |
27,144,872 (GRCm39) |
missense |
probably benign |
0.30 |
R7385:Kifc5b
|
UTSW |
17 |
27,144,597 (GRCm39) |
missense |
probably damaging |
1.00 |
R7743:Kifc5b
|
UTSW |
17 |
27,143,176 (GRCm39) |
missense |
probably damaging |
1.00 |
R8710:Kifc5b
|
UTSW |
17 |
27,139,880 (GRCm39) |
missense |
probably damaging |
0.98 |
R9661:Kifc5b
|
UTSW |
17 |
27,140,836 (GRCm39) |
critical splice donor site |
probably null |
|
R9765:Kifc5b
|
UTSW |
17 |
27,142,239 (GRCm39) |
missense |
probably damaging |
0.98 |
|