Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9630041A04Rik |
C |
A |
9: 101,820,193 (GRCm39) |
D204E |
possibly damaging |
Het |
Aldh3a2 |
A |
G |
11: 61,156,037 (GRCm39) |
S80P |
probably benign |
Het |
Bcl6b |
A |
T |
11: 70,117,400 (GRCm39) |
Y407* |
probably null |
Het |
Ccn2 |
T |
C |
10: 24,471,856 (GRCm39) |
V49A |
probably benign |
Het |
Cel |
TTA |
TTATA |
2: 28,449,441 (GRCm39) |
|
probably null |
Het |
Cerkl |
A |
T |
2: 79,171,674 (GRCm39) |
C395S |
probably damaging |
Het |
Chst5 |
C |
A |
8: 112,617,492 (GRCm39) |
V43L |
probably benign |
Het |
Clip1 |
A |
T |
5: 123,784,337 (GRCm39) |
F271I |
probably damaging |
Het |
Clspn |
A |
G |
4: 126,484,411 (GRCm39) |
T1190A |
possibly damaging |
Het |
Col20a1 |
A |
T |
2: 180,648,528 (GRCm39) |
E938D |
probably damaging |
Het |
Dmrta2 |
G |
A |
4: 109,839,779 (GRCm39) |
V509M |
probably damaging |
Het |
Dnah7b |
T |
A |
1: 46,361,420 (GRCm39) |
M3440K |
probably benign |
Het |
Erlin1 |
A |
G |
19: 44,029,184 (GRCm39) |
|
probably null |
Het |
Fam24b |
A |
G |
7: 130,927,869 (GRCm39) |
S107P |
probably benign |
Het |
Fbxo11 |
A |
T |
17: 88,323,124 (GRCm39) |
D12E |
|
Het |
Fbxw13 |
T |
C |
9: 109,024,116 (GRCm39) |
D39G |
probably damaging |
Het |
Gabrb3 |
T |
G |
7: 57,466,152 (GRCm39) |
L322R |
probably damaging |
Het |
Gm5239 |
A |
T |
18: 35,669,672 (GRCm39) |
I13F |
possibly damaging |
Het |
Heatr1 |
A |
G |
13: 12,419,802 (GRCm39) |
Y375C |
probably benign |
Het |
Helq |
A |
T |
5: 100,946,303 (GRCm39) |
S13T |
possibly damaging |
Het |
Helz |
A |
G |
11: 107,509,918 (GRCm39) |
T514A |
probably benign |
Het |
Hook3 |
A |
G |
8: 26,522,552 (GRCm39) |
V32A |
|
Het |
Htra4 |
A |
G |
8: 25,527,048 (GRCm39) |
I249T |
possibly damaging |
Het |
Htt |
G |
T |
5: 35,062,692 (GRCm39) |
V2809L |
probably benign |
Het |
Ifi203 |
T |
A |
1: 173,765,437 (GRCm39) |
I46F |
probably benign |
Het |
Kcna2 |
A |
T |
3: 107,012,306 (GRCm39) |
I296F |
possibly damaging |
Het |
Kndc1 |
A |
G |
7: 139,501,357 (GRCm39) |
E882G |
possibly damaging |
Het |
Krtap16-1 |
A |
T |
11: 99,876,071 (GRCm39) |
D444E |
probably benign |
Het |
Lrrtm3 |
ATTTT |
ATTTTT |
10: 63,925,035 (GRCm39) |
|
probably null |
Het |
Mdga2 |
C |
T |
12: 66,615,634 (GRCm39) |
D658N |
possibly damaging |
Het |
Mkrn1 |
T |
C |
6: 39,378,183 (GRCm39) |
K316R |
possibly damaging |
Het |
Mmd2 |
C |
T |
5: 142,553,666 (GRCm39) |
C165Y |
probably damaging |
Het |
Mpdz |
A |
G |
4: 81,202,867 (GRCm39) |
F1843L |
probably damaging |
Het |
Mrc2 |
G |
A |
11: 105,220,093 (GRCm39) |
R338Q |
probably damaging |
Het |
Naip5 |
C |
T |
13: 100,364,184 (GRCm39) |
R372H |
probably benign |
Het |
Nav2 |
C |
A |
7: 49,202,599 (GRCm39) |
S1461Y |
probably damaging |
Het |
Nol8 |
T |
A |
13: 49,814,738 (GRCm39) |
V282D |
possibly damaging |
Het |
Nup98 |
C |
A |
7: 101,834,167 (GRCm39) |
G265V |
possibly damaging |
Het |
Or1ak2 |
T |
C |
2: 36,827,911 (GRCm39) |
F260S |
probably damaging |
Het |
Or2d3b |
A |
G |
7: 106,513,980 (GRCm39) |
T192A |
possibly damaging |
Het |
Or2h15 |
C |
T |
17: 38,442,012 (GRCm39) |
E24K |
possibly damaging |
Het |
Or4f58 |
T |
A |
2: 111,851,517 (GRCm39) |
K227N |
possibly damaging |
Het |
Or4f62 |
T |
A |
2: 111,986,473 (GRCm39) |
M59K |
possibly damaging |
Het |
Or8k18 |
G |
T |
2: 86,085,544 (GRCm39) |
F164L |
possibly damaging |
Het |
Otogl |
T |
A |
10: 107,690,205 (GRCm39) |
E888D |
probably damaging |
Het |
Pcdhgc4 |
A |
G |
18: 37,948,685 (GRCm39) |
I34V |
possibly damaging |
Het |
Ppp1r12b |
T |
C |
1: 134,807,376 (GRCm39) |
R417G |
probably benign |
Het |
Rtn4 |
A |
G |
11: 29,656,778 (GRCm39) |
S311G |
probably benign |
Het |
Serinc3 |
A |
G |
2: 163,478,812 (GRCm39) |
V105A |
probably benign |
Het |
Serpina3f |
A |
G |
12: 104,183,444 (GRCm39) |
D102G |
possibly damaging |
Het |
Sik3 |
A |
G |
9: 46,066,772 (GRCm39) |
I184V |
probably damaging |
Het |
Spopfm2 |
A |
C |
3: 94,082,950 (GRCm39) |
L287R |
probably damaging |
Het |
Tex35 |
A |
T |
1: 156,935,436 (GRCm39) |
C21S |
probably benign |
Het |
Tfap2b |
T |
C |
1: 19,282,649 (GRCm39) |
|
probably null |
Het |
Thbs4 |
C |
T |
13: 92,897,998 (GRCm39) |
C607Y |
probably damaging |
Het |
Tmem144 |
A |
T |
3: 79,734,964 (GRCm39) |
N151K |
probably benign |
Het |
Tomm70a |
T |
A |
16: 56,963,166 (GRCm39) |
M395K |
probably benign |
Het |
Trim43b |
A |
C |
9: 88,967,663 (GRCm39) |
H324Q |
probably benign |
Het |
Vmn2r116 |
A |
T |
17: 23,620,141 (GRCm39) |
Y625F |
probably damaging |
Het |
Yipf3 |
A |
T |
17: 46,559,798 (GRCm39) |
N38I |
probably damaging |
Het |
Zfp804b |
T |
A |
5: 6,821,496 (GRCm39) |
E522D |
probably benign |
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 |
R4588:Fancm
|
UTSW |
12 |
65,165,215 (GRCm39) |
critical splice donor site |
probably null |
|
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 |
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 |
|