Other mutations in this stock |
Total: 29 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrg6 |
T |
C |
10: 14,316,147 (GRCm39) |
|
probably null |
Het |
Alcam |
T |
A |
16: 52,115,380 (GRCm39) |
|
probably benign |
Het |
Aspm |
C |
A |
1: 139,406,429 (GRCm39) |
A1772E |
probably damaging |
Het |
Bag6 |
T |
A |
17: 35,363,627 (GRCm39) |
D770E |
probably damaging |
Het |
Baz2b |
A |
T |
2: 59,788,019 (GRCm39) |
Y724* |
probably null |
Het |
Ccdc178 |
A |
T |
18: 21,977,968 (GRCm39) |
I833N |
probably benign |
Het |
Ccdc28a |
C |
A |
10: 18,106,261 (GRCm39) |
V22F |
possibly damaging |
Het |
Cmya5 |
T |
C |
13: 93,229,628 (GRCm39) |
N1820S |
probably benign |
Het |
Fgfrl1 |
G |
A |
5: 108,853,753 (GRCm39) |
G287S |
probably damaging |
Het |
Galntl6 |
G |
A |
8: 58,310,574 (GRCm39) |
P376S |
probably damaging |
Het |
Gm21985 |
A |
G |
2: 112,168,342 (GRCm39) |
|
probably benign |
Het |
Hck |
A |
G |
2: 152,992,939 (GRCm39) |
E482G |
possibly damaging |
Het |
Kcna3 |
C |
T |
3: 106,944,472 (GRCm39) |
S245L |
probably benign |
Het |
Mcc |
T |
C |
18: 44,582,283 (GRCm39) |
M798V |
possibly damaging |
Het |
Nlrp9c |
T |
C |
7: 26,084,013 (GRCm39) |
Y522C |
probably benign |
Het |
Ofcc1 |
C |
A |
13: 40,433,967 (GRCm39) |
S46I |
probably damaging |
Het |
Pdgfra |
A |
G |
5: 75,324,340 (GRCm39) |
D65G |
probably benign |
Het |
Phf24 |
A |
C |
4: 42,933,905 (GRCm39) |
T59P |
possibly damaging |
Het |
Pik3cg |
A |
G |
12: 32,255,148 (GRCm39) |
Y280H |
probably damaging |
Het |
Pkd1l1 |
C |
A |
11: 8,784,773 (GRCm39) |
|
probably null |
Het |
Plcd4 |
C |
A |
1: 74,591,274 (GRCm39) |
T223N |
probably damaging |
Het |
Polr1b |
G |
A |
2: 128,967,829 (GRCm39) |
G1074D |
probably damaging |
Het |
Pou2f3 |
T |
C |
9: 43,040,188 (GRCm39) |
T367A |
probably damaging |
Het |
Prkdc |
T |
A |
16: 15,617,790 (GRCm39) |
M3207K |
possibly damaging |
Het |
Rb1cc1 |
T |
C |
1: 6,319,730 (GRCm39) |
S1050P |
probably damaging |
Het |
Sf3b3 |
G |
A |
8: 111,540,383 (GRCm39) |
R1013* |
probably null |
Het |
Svep1 |
T |
C |
4: 58,068,988 (GRCm39) |
T2933A |
possibly damaging |
Het |
Vwf |
A |
G |
6: 125,635,835 (GRCm39) |
R289G |
unknown |
Het |
Zfp263 |
T |
C |
16: 3,563,710 (GRCm39) |
S155P |
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 |
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 |
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 |
|