Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcf1 |
A |
T |
17: 36,270,342 (GRCm39) |
V616E |
possibly damaging |
Het |
Adam21 |
A |
G |
12: 81,605,692 (GRCm39) |
V690A |
probably benign |
Het |
Afg3l1 |
A |
T |
8: 124,228,119 (GRCm39) |
T635S |
probably damaging |
Het |
Ahcyl2 |
T |
A |
6: 29,890,700 (GRCm39) |
M390K |
probably benign |
Het |
Ank3 |
T |
A |
10: 69,734,053 (GRCm39) |
|
probably null |
Het |
Antkmt |
T |
G |
17: 26,010,652 (GRCm39) |
|
probably null |
Het |
Arhgef3 |
A |
T |
14: 27,106,170 (GRCm39) |
K151N |
probably damaging |
Het |
Ccr3 |
T |
G |
9: 123,829,043 (GRCm39) |
F126C |
probably damaging |
Het |
Ccser1 |
A |
G |
6: 61,695,175 (GRCm39) |
D170G |
possibly damaging |
Het |
Celsr2 |
T |
A |
3: 108,310,074 (GRCm39) |
D1552V |
probably damaging |
Het |
Cfap69 |
G |
A |
5: 5,675,820 (GRCm39) |
L265F |
probably damaging |
Het |
Chrna9 |
C |
T |
5: 66,126,533 (GRCm39) |
R92* |
probably null |
Het |
Cog3 |
A |
T |
14: 75,970,394 (GRCm39) |
V341D |
probably damaging |
Het |
Csmd1 |
C |
A |
8: 16,073,779 (GRCm39) |
R2072L |
probably damaging |
Het |
Dbf4 |
G |
T |
5: 8,448,039 (GRCm39) |
H390Q |
probably benign |
Het |
Dcaf4 |
T |
A |
12: 83,579,078 (GRCm39) |
C166S |
possibly damaging |
Het |
Dclk3 |
T |
A |
9: 111,297,110 (GRCm39) |
L218Q |
possibly damaging |
Het |
Dip2b |
T |
A |
15: 100,069,603 (GRCm39) |
W643R |
probably damaging |
Het |
Dip2c |
A |
G |
13: 9,674,008 (GRCm39) |
K1091E |
probably damaging |
Het |
Dis3 |
T |
A |
14: 99,326,340 (GRCm39) |
H415L |
probably damaging |
Het |
Dnah7a |
T |
A |
1: 53,542,737 (GRCm39) |
I2478F |
possibly damaging |
Het |
Dnah8 |
G |
A |
17: 30,967,542 (GRCm39) |
D2585N |
probably benign |
Het |
Doc2a |
T |
C |
7: 126,447,752 (GRCm39) |
|
probably benign |
Het |
Dph5 |
A |
T |
3: 115,693,456 (GRCm39) |
M125L |
probably benign |
Het |
Dst |
A |
T |
1: 34,267,764 (GRCm39) |
T5247S |
possibly damaging |
Het |
Eno4 |
T |
G |
19: 58,952,889 (GRCm39) |
V477G |
possibly damaging |
Het |
Exosc8 |
T |
C |
3: 54,636,711 (GRCm39) |
I207V |
possibly damaging |
Het |
Fat4 |
T |
A |
3: 39,061,352 (GRCm39) |
S4312T |
probably benign |
Het |
Fgfr2 |
T |
C |
7: 129,843,007 (GRCm39) |
D126G |
probably damaging |
Het |
Gcn1 |
A |
T |
5: 115,730,203 (GRCm39) |
D839V |
probably benign |
Het |
Gprin3 |
A |
G |
6: 59,331,158 (GRCm39) |
V383A |
probably benign |
Het |
Gpt |
T |
C |
15: 76,583,040 (GRCm39) |
V361A |
probably benign |
Het |
Hepacam |
G |
A |
9: 37,293,060 (GRCm39) |
C217Y |
probably damaging |
Het |
Hsp90aa1 |
A |
T |
12: 110,660,151 (GRCm39) |
Y382N |
probably damaging |
Het |
Htr2a |
T |
A |
14: 74,879,462 (GRCm39) |
N30K |
probably benign |
Het |
Jhy |
A |
T |
9: 40,872,299 (GRCm39) |
M70K |
possibly damaging |
Het |
Lrrc19 |
T |
C |
4: 94,529,174 (GRCm39) |
Y36C |
probably damaging |
Het |
Madcam1 |
C |
T |
10: 79,501,447 (GRCm39) |
Q171* |
probably null |
Het |
Mcm8 |
G |
A |
2: 132,680,629 (GRCm39) |
M544I |
probably benign |
Het |
Mdga1 |
C |
T |
17: 30,076,580 (GRCm39) |
G64E |
probably damaging |
Het |
Mmp3 |
A |
G |
9: 7,446,994 (GRCm39) |
D58G |
probably benign |
Het |
Ms4a10 |
T |
C |
19: 10,942,132 (GRCm39) |
Y123C |
probably damaging |
Het |
Ms4a4d |
T |
A |
19: 11,535,296 (GRCm39) |
I198K |
probably benign |
Het |
Mthfd1l |
A |
T |
10: 3,930,241 (GRCm39) |
D112V |
probably benign |
Het |
N4bp2l2 |
A |
C |
5: 150,566,606 (GRCm39) |
S567R |
probably benign |
Het |
Ndufaf2 |
A |
G |
13: 108,295,010 (GRCm39) |
Y32H |
probably damaging |
Het |
Nup153 |
T |
A |
13: 46,866,213 (GRCm39) |
K182* |
probably null |
Het |
Or4c100 |
A |
G |
2: 88,356,079 (GRCm39) |
T51A |
probably benign |
Het |
Or52p2 |
A |
G |
7: 102,237,623 (GRCm39) |
F109S |
probably damaging |
Het |
Or5p4 |
T |
A |
7: 107,680,781 (GRCm39) |
V260E |
probably damaging |
Het |
Otoa |
T |
C |
7: 120,754,358 (GRCm39) |
S928P |
probably damaging |
Het |
Oxct2a |
T |
C |
4: 123,216,496 (GRCm39) |
D295G |
probably benign |
Het |
P4ha2 |
C |
A |
11: 54,015,846 (GRCm39) |
T411K |
probably benign |
Het |
Plcg2 |
A |
T |
8: 118,333,822 (GRCm39) |
Q865L |
probably benign |
Het |
Prepl |
G |
T |
17: 85,385,932 (GRCm39) |
T244K |
possibly damaging |
Het |
Ptpro |
A |
T |
6: 137,388,103 (GRCm39) |
K776* |
probably null |
Het |
Rc3h2 |
T |
C |
2: 37,279,844 (GRCm39) |
K462E |
possibly damaging |
Het |
Scn10a |
A |
G |
9: 119,516,940 (GRCm39) |
|
probably null |
Het |
Serpinb1c |
A |
G |
13: 33,066,147 (GRCm39) |
V266A |
probably damaging |
Het |
Slc6a20b |
T |
A |
9: 123,433,861 (GRCm39) |
N326Y |
probably damaging |
Het |
Spcs2 |
C |
T |
7: 99,508,038 (GRCm39) |
G16D |
possibly damaging |
Het |
Spns3 |
T |
C |
11: 72,390,321 (GRCm39) |
D441G |
possibly damaging |
Het |
Srsf4 |
A |
G |
4: 131,618,556 (GRCm39) |
D49G |
probably damaging |
Het |
Tec |
A |
T |
5: 72,917,736 (GRCm39) |
C494* |
probably null |
Het |
Tecpr1 |
A |
T |
5: 144,141,476 (GRCm39) |
Y798N |
probably damaging |
Het |
Tex56 |
A |
T |
13: 35,116,613 (GRCm39) |
T121S |
possibly damaging |
Het |
Tmt1a |
T |
A |
15: 100,202,987 (GRCm39) |
F87Y |
probably benign |
Het |
Trim56 |
C |
T |
5: 137,143,343 (GRCm39) |
E58K |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,626,478 (GRCm39) |
D13146E |
probably damaging |
Het |
Ube2q1 |
A |
T |
3: 89,686,790 (GRCm39) |
K46* |
probably null |
Het |
Ucn |
G |
T |
5: 31,295,842 (GRCm39) |
T8K |
probably benign |
Het |
Usp25 |
T |
C |
16: 76,830,870 (GRCm39) |
|
probably null |
Het |
Usp48 |
A |
T |
4: 137,343,144 (GRCm39) |
Q430L |
probably benign |
Het |
Usp48 |
A |
T |
4: 137,343,145 (GRCm39) |
|
probably null |
Het |
Vill |
A |
T |
9: 118,890,579 (GRCm39) |
D164V |
probably damaging |
Het |
Vmn2r91 |
T |
A |
17: 18,356,751 (GRCm39) |
M806K |
possibly damaging |
Het |
Wdfy4 |
T |
A |
14: 32,750,970 (GRCm39) |
Y2256F |
probably damaging |
Het |
Wsb1 |
A |
G |
11: 79,141,826 (GRCm39) |
S64P |
probably damaging |
Het |
Zc3h11a |
C |
A |
1: 133,552,350 (GRCm39) |
V586F |
probably benign |
Het |
Zc3h12d |
A |
G |
10: 7,729,014 (GRCm39) |
D126G |
probably damaging |
Het |
Zfp296 |
G |
T |
7: 19,313,637 (GRCm39) |
C164F |
possibly damaging |
Het |
Zfp442 |
T |
A |
2: 150,251,635 (GRCm39) |
H89L |
possibly damaging |
Het |
Zfp82 |
T |
A |
7: 29,756,312 (GRCm39) |
|
probably null |
Het |
Zmynd8 |
A |
G |
2: 165,676,871 (GRCm39) |
V249A |
possibly damaging |
Het |
|
Other mutations in Fgfr4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00848:Fgfr4
|
APN |
13 |
55,306,983 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02140:Fgfr4
|
APN |
13 |
55,308,992 (GRCm39) |
missense |
probably benign |
|
IGL02817:Fgfr4
|
APN |
13 |
55,304,481 (GRCm39) |
critical splice donor site |
probably null |
|
interference
|
UTSW |
13 |
55,313,777 (GRCm39) |
missense |
probably damaging |
1.00 |
Modest
|
UTSW |
13 |
55,314,064 (GRCm39) |
missense |
probably damaging |
1.00 |
offense
|
UTSW |
13 |
55,309,328 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0153:Fgfr4
|
UTSW |
13 |
55,309,198 (GRCm39) |
splice site |
probably benign |
|
R0727:Fgfr4
|
UTSW |
13 |
55,304,041 (GRCm39) |
splice site |
probably null |
|
R1646:Fgfr4
|
UTSW |
13 |
55,313,777 (GRCm39) |
missense |
probably damaging |
1.00 |
R1749:Fgfr4
|
UTSW |
13 |
55,315,605 (GRCm39) |
splice site |
probably null |
|
R1993:Fgfr4
|
UTSW |
13 |
55,313,715 (GRCm39) |
missense |
probably damaging |
1.00 |
R2037:Fgfr4
|
UTSW |
13 |
55,315,702 (GRCm39) |
missense |
possibly damaging |
0.51 |
R2152:Fgfr4
|
UTSW |
13 |
55,314,777 (GRCm39) |
missense |
probably damaging |
1.00 |
R2386:Fgfr4
|
UTSW |
13 |
55,315,714 (GRCm39) |
missense |
probably benign |
0.36 |
R3086:Fgfr4
|
UTSW |
13 |
55,315,205 (GRCm39) |
splice site |
probably benign |
|
R3939:Fgfr4
|
UTSW |
13 |
55,304,307 (GRCm39) |
missense |
probably null |
0.96 |
R4255:Fgfr4
|
UTSW |
13 |
55,314,064 (GRCm39) |
missense |
probably damaging |
1.00 |
R4463:Fgfr4
|
UTSW |
13 |
55,304,280 (GRCm39) |
missense |
probably benign |
0.02 |
R4510:Fgfr4
|
UTSW |
13 |
55,309,328 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4511:Fgfr4
|
UTSW |
13 |
55,309,328 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4852:Fgfr4
|
UTSW |
13 |
55,308,969 (GRCm39) |
missense |
possibly damaging |
0.68 |
R5133:Fgfr4
|
UTSW |
13 |
55,307,828 (GRCm39) |
missense |
probably damaging |
1.00 |
R5146:Fgfr4
|
UTSW |
13 |
55,313,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R5380:Fgfr4
|
UTSW |
13 |
55,315,230 (GRCm39) |
missense |
probably damaging |
1.00 |
R5431:Fgfr4
|
UTSW |
13 |
55,304,464 (GRCm39) |
missense |
probably benign |
|
R5927:Fgfr4
|
UTSW |
13 |
55,314,700 (GRCm39) |
missense |
probably damaging |
1.00 |
R6318:Fgfr4
|
UTSW |
13 |
55,313,921 (GRCm39) |
missense |
probably damaging |
1.00 |
R6792:Fgfr4
|
UTSW |
13 |
55,304,711 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7018:Fgfr4
|
UTSW |
13 |
55,314,013 (GRCm39) |
missense |
probably damaging |
0.98 |
R7290:Fgfr4
|
UTSW |
13 |
55,309,262 (GRCm39) |
missense |
probably benign |
0.00 |
R7343:Fgfr4
|
UTSW |
13 |
55,306,968 (GRCm39) |
missense |
probably damaging |
1.00 |
R7808:Fgfr4
|
UTSW |
13 |
55,308,969 (GRCm39) |
missense |
possibly damaging |
0.68 |
R7891:Fgfr4
|
UTSW |
13 |
55,306,964 (GRCm39) |
missense |
probably benign |
0.22 |
R9028:Fgfr4
|
UTSW |
13 |
55,306,967 (GRCm39) |
missense |
probably damaging |
1.00 |
R9144:Fgfr4
|
UTSW |
13 |
55,315,837 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9257:Fgfr4
|
UTSW |
13 |
55,315,974 (GRCm39) |
missense |
unknown |
|
R9399:Fgfr4
|
UTSW |
13 |
55,304,293 (GRCm39) |
missense |
probably damaging |
1.00 |
R9457:Fgfr4
|
UTSW |
13 |
55,308,940 (GRCm39) |
missense |
probably benign |
|
R9553:Fgfr4
|
UTSW |
13 |
55,309,228 (GRCm39) |
missense |
probably damaging |
0.99 |
R9620:Fgfr4
|
UTSW |
13 |
55,308,994 (GRCm39) |
missense |
possibly damaging |
0.68 |
Z1177:Fgfr4
|
UTSW |
13 |
55,313,742 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Fgfr4
|
UTSW |
13 |
55,309,520 (GRCm39) |
missense |
probably damaging |
1.00 |
|