Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca7 |
G |
T |
10: 79,833,701 (GRCm39) |
|
probably null |
Het |
Abcb4 |
A |
T |
5: 8,997,328 (GRCm39) |
I936F |
probably benign |
Het |
Adnp2 |
G |
T |
18: 80,171,863 (GRCm39) |
L849I |
probably benign |
Het |
Atf7ip |
T |
C |
6: 136,576,692 (GRCm39) |
S1032P |
probably benign |
Het |
Atr |
A |
C |
9: 95,747,720 (GRCm39) |
D334A |
probably benign |
Het |
Atrip |
A |
T |
9: 108,889,347 (GRCm39) |
D20E |
probably damaging |
Het |
Atxn7 |
T |
A |
14: 14,096,268 (GRCm38) |
C43* |
probably null |
Het |
Cfap65 |
C |
A |
1: 74,943,215 (GRCm39) |
Q1603H |
possibly damaging |
Het |
Cpne5 |
T |
C |
17: 29,383,687 (GRCm39) |
I327V |
probably benign |
Het |
Ctsa |
T |
C |
2: 164,676,070 (GRCm39) |
S41P |
possibly damaging |
Het |
Cyp4x1 |
A |
T |
4: 114,965,994 (GRCm39) |
L444Q |
probably damaging |
Het |
Dchs1 |
C |
A |
7: 105,405,248 (GRCm39) |
M2431I |
probably benign |
Het |
Ddi1 |
T |
A |
9: 6,266,003 (GRCm39) |
H122L |
probably benign |
Het |
Defa21 |
C |
T |
8: 21,515,664 (GRCm39) |
P21S |
probably damaging |
Het |
Ect2 |
A |
G |
3: 27,201,149 (GRCm39) |
V77A |
probably damaging |
Het |
Ermap |
C |
A |
4: 119,045,445 (GRCm39) |
|
probably benign |
Het |
Gcnt3 |
T |
A |
9: 69,941,512 (GRCm39) |
D352V |
probably damaging |
Het |
Gys2 |
A |
G |
6: 142,395,181 (GRCm39) |
M428T |
possibly damaging |
Het |
Igtp |
T |
A |
11: 58,097,508 (GRCm39) |
N226K |
probably damaging |
Het |
Itpr2 |
T |
A |
6: 146,142,694 (GRCm39) |
H1675L |
probably benign |
Het |
Lipo4 |
G |
A |
19: 33,476,647 (GRCm39) |
P367L |
possibly damaging |
Het |
Lzts3 |
T |
C |
2: 130,476,686 (GRCm39) |
*587W |
probably null |
Het |
Mast3 |
T |
A |
8: 71,233,251 (GRCm39) |
K300* |
probably null |
Het |
Mepce |
G |
A |
5: 137,783,534 (GRCm39) |
T264I |
possibly damaging |
Het |
Mif4gd |
A |
T |
11: 115,500,372 (GRCm39) |
I62N |
probably damaging |
Het |
Or14a260 |
C |
T |
7: 85,984,852 (GRCm39) |
V251I |
probably benign |
Het |
Or7e175 |
T |
A |
9: 20,049,383 (GRCm39) |
*324K |
probably null |
Het |
Palm3 |
A |
G |
8: 84,756,015 (GRCm39) |
K509R |
probably benign |
Het |
Pde11a |
T |
C |
2: 75,859,647 (GRCm39) |
T821A |
probably damaging |
Het |
Pik3r5 |
A |
G |
11: 68,384,087 (GRCm39) |
|
probably benign |
Het |
Pkhd1 |
T |
C |
1: 20,271,092 (GRCm39) |
T3154A |
probably benign |
Het |
Ptprs |
A |
G |
17: 56,732,534 (GRCm39) |
Y438H |
probably damaging |
Het |
Rdh8 |
T |
A |
9: 20,734,025 (GRCm39) |
D70E |
probably benign |
Het |
Scn2a |
A |
T |
2: 65,544,111 (GRCm39) |
I831L |
possibly damaging |
Het |
Selenoo |
A |
G |
15: 88,980,921 (GRCm39) |
H420R |
probably benign |
Het |
Slc22a16 |
T |
C |
10: 40,446,677 (GRCm39) |
|
probably benign |
Het |
Slc5a1 |
A |
G |
5: 33,302,632 (GRCm39) |
T208A |
probably benign |
Het |
Sparc |
T |
C |
11: 55,296,062 (GRCm39) |
M121V |
probably benign |
Het |
Sstr1 |
G |
T |
12: 58,260,417 (GRCm39) |
A347S |
probably benign |
Het |
Stab1 |
C |
A |
14: 30,879,402 (GRCm39) |
V693F |
probably benign |
Het |
Tnn |
A |
G |
1: 159,972,681 (GRCm39) |
V307A |
probably benign |
Het |
Trmt1 |
A |
G |
8: 85,417,382 (GRCm39) |
|
probably benign |
Het |
Ttc3 |
T |
C |
16: 94,243,760 (GRCm39) |
S1255P |
probably benign |
Het |
Ube2ql1 |
A |
C |
13: 69,887,276 (GRCm39) |
S62A |
unknown |
Het |
Vmn2r84 |
T |
A |
10: 130,221,809 (GRCm39) |
M804L |
probably damaging |
Het |
Vps13a |
T |
C |
19: 16,617,403 (GRCm39) |
T3002A |
probably damaging |
Het |
Vps50 |
A |
G |
6: 3,562,306 (GRCm39) |
E467G |
probably damaging |
Het |
|
Other mutations in Fancm |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00158:Fancm
|
APN |
12 |
65,122,510 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL00489:Fancm
|
APN |
12 |
65,152,967 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00529:Fancm
|
APN |
12 |
65,177,191 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL00898:Fancm
|
APN |
12 |
65,152,774 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01805:Fancm
|
APN |
12 |
65,160,635 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01986:Fancm
|
APN |
12 |
65,173,429 (GRCm39) |
nonsense |
probably null |
|
IGL02026:Fancm
|
APN |
12 |
65,152,508 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02069:Fancm
|
APN |
12 |
65,122,685 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02103:Fancm
|
APN |
12 |
65,142,558 (GRCm39) |
missense |
probably benign |
0.38 |
IGL02133:Fancm
|
APN |
12 |
65,153,249 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02400:Fancm
|
APN |
12 |
65,160,589 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02478:Fancm
|
APN |
12 |
65,123,864 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02479:Fancm
|
APN |
12 |
65,153,259 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02563:Fancm
|
APN |
12 |
65,139,236 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02606:Fancm
|
APN |
12 |
65,122,913 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02731:Fancm
|
APN |
12 |
65,135,079 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02809:Fancm
|
APN |
12 |
65,168,441 (GRCm39) |
missense |
possibly damaging |
0.54 |
IGL02953:Fancm
|
APN |
12 |
65,168,740 (GRCm39) |
missense |
probably benign |
0.27 |
IGL03066:Fancm
|
APN |
12 |
65,171,888 (GRCm39) |
nonsense |
probably null |
|
IGL03073:Fancm
|
APN |
12 |
65,148,406 (GRCm39) |
missense |
probably damaging |
1.00 |
Fancypants
|
UTSW |
12 |
65,153,235 (GRCm39) |
missense |
probably damaging |
1.00 |
Mylord
|
UTSW |
12 |
65,163,197 (GRCm39) |
nonsense |
probably null |
|
R0041_fancm_712
|
UTSW |
12 |
65,153,217 (GRCm39) |
nonsense |
probably null |
|
R7172_Fancm_370
|
UTSW |
12 |
65,152,828 (GRCm39) |
missense |
possibly damaging |
0.95 |
BB005:Fancm
|
UTSW |
12 |
65,152,898 (GRCm39) |
missense |
unknown |
|
BB015:Fancm
|
UTSW |
12 |
65,152,898 (GRCm39) |
missense |
unknown |
|
PIT4131001:Fancm
|
UTSW |
12 |
65,152,196 (GRCm39) |
missense |
probably benign |
0.03 |
R0041:Fancm
|
UTSW |
12 |
65,153,217 (GRCm39) |
nonsense |
probably null |
|
R0041:Fancm
|
UTSW |
12 |
65,153,217 (GRCm39) |
nonsense |
probably null |
|
R0125:Fancm
|
UTSW |
12 |
65,168,730 (GRCm39) |
missense |
possibly damaging |
0.68 |
R0201:Fancm
|
UTSW |
12 |
65,148,406 (GRCm39) |
missense |
probably damaging |
1.00 |
R0360:Fancm
|
UTSW |
12 |
65,122,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R0491:Fancm
|
UTSW |
12 |
65,152,835 (GRCm39) |
missense |
probably benign |
0.32 |
R0557:Fancm
|
UTSW |
12 |
65,165,216 (GRCm39) |
critical splice donor site |
probably null |
|
R0617:Fancm
|
UTSW |
12 |
65,144,091 (GRCm39) |
nonsense |
probably null |
|
R1201:Fancm
|
UTSW |
12 |
65,153,542 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1353:Fancm
|
UTSW |
12 |
65,134,944 (GRCm39) |
missense |
probably damaging |
1.00 |
R1456:Fancm
|
UTSW |
12 |
65,165,125 (GRCm39) |
missense |
possibly damaging |
0.48 |
R1468:Fancm
|
UTSW |
12 |
65,146,067 (GRCm39) |
missense |
probably damaging |
1.00 |
R1468:Fancm
|
UTSW |
12 |
65,146,067 (GRCm39) |
missense |
probably damaging |
1.00 |
R1521:Fancm
|
UTSW |
12 |
65,168,478 (GRCm39) |
missense |
probably benign |
0.25 |
R1530:Fancm
|
UTSW |
12 |
65,139,264 (GRCm39) |
critical splice donor site |
probably null |
|
R1559:Fancm
|
UTSW |
12 |
65,140,463 (GRCm39) |
missense |
probably benign |
0.00 |
R1632:Fancm
|
UTSW |
12 |
65,177,105 (GRCm39) |
missense |
probably damaging |
1.00 |
R1681:Fancm
|
UTSW |
12 |
65,152,430 (GRCm39) |
missense |
probably benign |
0.03 |
R1919:Fancm
|
UTSW |
12 |
65,152,294 (GRCm39) |
missense |
possibly damaging |
0.48 |
R1969:Fancm
|
UTSW |
12 |
65,148,466 (GRCm39) |
missense |
probably benign |
0.09 |
R1971:Fancm
|
UTSW |
12 |
65,148,466 (GRCm39) |
missense |
probably benign |
0.09 |
R2117:Fancm
|
UTSW |
12 |
65,123,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R2510:Fancm
|
UTSW |
12 |
65,160,544 (GRCm39) |
splice site |
probably benign |
|
R2909:Fancm
|
UTSW |
12 |
65,171,630 (GRCm39) |
missense |
probably damaging |
1.00 |
R3155:Fancm
|
UTSW |
12 |
65,163,195 (GRCm39) |
missense |
probably benign |
0.32 |
R3405:Fancm
|
UTSW |
12 |
65,122,546 (GRCm39) |
missense |
probably benign |
0.00 |
R4133:Fancm
|
UTSW |
12 |
65,167,304 (GRCm39) |
missense |
probably benign |
0.44 |
R4308:Fancm
|
UTSW |
12 |
65,173,305 (GRCm39) |
missense |
probably benign |
0.14 |
R4602:Fancm
|
UTSW |
12 |
65,171,718 (GRCm39) |
missense |
probably benign |
0.12 |
R4653:Fancm
|
UTSW |
12 |
65,129,828 (GRCm39) |
missense |
probably damaging |
0.99 |
R4702:Fancm
|
UTSW |
12 |
65,168,826 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4719:Fancm
|
UTSW |
12 |
65,168,480 (GRCm39) |
missense |
possibly damaging |
0.64 |
R4885:Fancm
|
UTSW |
12 |
65,149,417 (GRCm39) |
nonsense |
probably null |
|
R4896:Fancm
|
UTSW |
12 |
65,122,605 (GRCm39) |
missense |
probably damaging |
1.00 |
R4908:Fancm
|
UTSW |
12 |
65,141,645 (GRCm39) |
missense |
probably benign |
0.28 |
R4921:Fancm
|
UTSW |
12 |
65,123,915 (GRCm39) |
missense |
probably benign |
0.19 |
R4922:Fancm
|
UTSW |
12 |
65,153,666 (GRCm39) |
critical splice donor site |
probably null |
|
R4948:Fancm
|
UTSW |
12 |
65,137,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R5103:Fancm
|
UTSW |
12 |
65,152,632 (GRCm39) |
missense |
probably damaging |
0.99 |
R5577:Fancm
|
UTSW |
12 |
65,177,185 (GRCm39) |
utr 3 prime |
probably benign |
|
R5631:Fancm
|
UTSW |
12 |
65,160,617 (GRCm39) |
missense |
probably damaging |
0.97 |
R5741:Fancm
|
UTSW |
12 |
65,148,389 (GRCm39) |
missense |
probably benign |
0.01 |
R6137:Fancm
|
UTSW |
12 |
65,177,156 (GRCm39) |
missense |
probably damaging |
1.00 |
R6167:Fancm
|
UTSW |
12 |
65,141,669 (GRCm39) |
missense |
probably benign |
0.42 |
R6242:Fancm
|
UTSW |
12 |
65,163,216 (GRCm39) |
missense |
probably benign |
0.01 |
R6242:Fancm
|
UTSW |
12 |
65,163,223 (GRCm39) |
missense |
probably benign |
0.00 |
R6281:Fancm
|
UTSW |
12 |
65,135,044 (GRCm39) |
missense |
probably damaging |
1.00 |
R6325:Fancm
|
UTSW |
12 |
65,171,826 (GRCm39) |
missense |
probably damaging |
1.00 |
R6434:Fancm
|
UTSW |
12 |
65,123,942 (GRCm39) |
missense |
probably damaging |
1.00 |
R6493:Fancm
|
UTSW |
12 |
65,144,262 (GRCm39) |
missense |
probably benign |
0.04 |
R6542:Fancm
|
UTSW |
12 |
65,144,203 (GRCm39) |
missense |
probably damaging |
1.00 |
R6645:Fancm
|
UTSW |
12 |
65,152,874 (GRCm39) |
missense |
probably damaging |
0.99 |
R6878:Fancm
|
UTSW |
12 |
65,163,197 (GRCm39) |
nonsense |
probably null |
|
R7171:Fancm
|
UTSW |
12 |
65,148,394 (GRCm39) |
missense |
probably damaging |
0.99 |
R7172:Fancm
|
UTSW |
12 |
65,152,828 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7498:Fancm
|
UTSW |
12 |
65,146,165 (GRCm39) |
missense |
probably benign |
0.01 |
R7585:Fancm
|
UTSW |
12 |
65,153,021 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7610:Fancm
|
UTSW |
12 |
65,152,454 (GRCm39) |
missense |
probably damaging |
1.00 |
R7722:Fancm
|
UTSW |
12 |
65,153,235 (GRCm39) |
missense |
probably damaging |
1.00 |
R7740:Fancm
|
UTSW |
12 |
65,173,321 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7867:Fancm
|
UTSW |
12 |
65,165,173 (GRCm39) |
missense |
probably benign |
0.12 |
R7867:Fancm
|
UTSW |
12 |
65,163,240 (GRCm39) |
critical splice donor site |
probably null |
|
R7882:Fancm
|
UTSW |
12 |
65,173,568 (GRCm39) |
missense |
probably benign |
0.12 |
R7928:Fancm
|
UTSW |
12 |
65,152,898 (GRCm39) |
missense |
unknown |
|
R8230:Fancm
|
UTSW |
12 |
65,149,424 (GRCm39) |
missense |
probably benign |
0.17 |
R8470:Fancm
|
UTSW |
12 |
65,171,931 (GRCm39) |
missense |
probably damaging |
1.00 |
R8553:Fancm
|
UTSW |
12 |
65,173,469 (GRCm39) |
missense |
possibly damaging |
0.62 |
R8695:Fancm
|
UTSW |
12 |
65,171,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R8817:Fancm
|
UTSW |
12 |
65,167,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R8878:Fancm
|
UTSW |
12 |
65,173,522 (GRCm39) |
missense |
probably damaging |
1.00 |
R9027:Fancm
|
UTSW |
12 |
65,122,605 (GRCm39) |
missense |
probably damaging |
1.00 |
R9223:Fancm
|
UTSW |
12 |
65,149,358 (GRCm39) |
missense |
probably benign |
0.12 |
R9280:Fancm
|
UTSW |
12 |
65,153,612 (GRCm39) |
missense |
probably benign |
0.16 |
R9487:Fancm
|
UTSW |
12 |
65,153,388 (GRCm39) |
nonsense |
probably null |
|
R9562:Fancm
|
UTSW |
12 |
65,168,494 (GRCm39) |
missense |
probably damaging |
1.00 |
R9565:Fancm
|
UTSW |
12 |
65,168,494 (GRCm39) |
missense |
probably damaging |
1.00 |
R9575:Fancm
|
UTSW |
12 |
65,152,314 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9664:Fancm
|
UTSW |
12 |
65,137,758 (GRCm39) |
missense |
probably benign |
0.08 |
Z1176:Fancm
|
UTSW |
12 |
65,141,700 (GRCm39) |
missense |
probably benign |
0.16 |
|