| Other mutations in this stock |
Total: 52 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4932442E05Rik |
T |
A |
10: 118,697,371 (GRCm39) |
W210R |
possibly damaging |
Het |
| Aknad1 |
T |
C |
3: 108,659,217 (GRCm39) |
M77T |
probably benign |
Het |
| Aox1 |
A |
T |
1: 58,393,469 (GRCm39) |
I1210F |
possibly damaging |
Het |
| Brd8 |
A |
T |
18: 34,747,858 (GRCm39) |
|
probably benign |
Het |
| Cdh23 |
T |
C |
10: 60,139,292 (GRCm39) |
D3307G |
probably benign |
Het |
| Chsy1 |
T |
C |
7: 65,821,058 (GRCm39) |
I431T |
probably damaging |
Het |
| Cobl |
A |
G |
11: 12,204,980 (GRCm39) |
|
probably benign |
Het |
| Col28a1 |
T |
C |
6: 8,158,134 (GRCm39) |
D308G |
probably damaging |
Het |
| Csmd3 |
A |
G |
15: 48,048,700 (GRCm39) |
Y568H |
probably damaging |
Het |
| Dmrt3 |
T |
C |
19: 25,599,947 (GRCm39) |
I264T |
probably damaging |
Het |
| Dusp22 |
G |
T |
13: 30,880,235 (GRCm39) |
C52F |
probably damaging |
Het |
| Fbxw22 |
A |
C |
9: 109,212,993 (GRCm39) |
M318R |
probably damaging |
Het |
| Ffar4 |
C |
T |
19: 38,102,295 (GRCm39) |
T310M |
probably damaging |
Het |
| Glt6d1 |
T |
A |
2: 25,684,505 (GRCm39) |
Y167F |
probably benign |
Het |
| Hydin |
T |
A |
8: 111,217,421 (GRCm39) |
Y1436* |
probably null |
Het |
| Il12a |
G |
A |
3: 68,598,888 (GRCm39) |
C2Y |
possibly damaging |
Het |
| Inpp5a |
T |
C |
7: 139,034,006 (GRCm39) |
Y38H |
possibly damaging |
Het |
| Jmy |
A |
C |
13: 93,596,159 (GRCm39) |
L490R |
probably damaging |
Het |
| Kif26a |
T |
A |
12: 112,143,262 (GRCm39) |
L1172H |
probably benign |
Het |
| Kmo |
A |
T |
1: 175,482,668 (GRCm39) |
M331L |
probably benign |
Het |
| Lonp1 |
G |
A |
17: 56,923,026 (GRCm39) |
T627M |
probably damaging |
Het |
| Lrrc41 |
T |
C |
4: 115,950,331 (GRCm39) |
|
probably null |
Het |
| Mast4 |
A |
T |
13: 102,874,123 (GRCm39) |
S1556R |
probably damaging |
Het |
| Mmel1 |
A |
G |
4: 154,976,408 (GRCm39) |
N490S |
probably benign |
Het |
| Mpped2 |
A |
G |
2: 106,614,158 (GRCm39) |
D164G |
probably damaging |
Het |
| Nap1l1 |
A |
G |
10: 111,328,760 (GRCm39) |
T230A |
probably benign |
Het |
| Nrap |
C |
A |
19: 56,338,741 (GRCm39) |
A913S |
probably damaging |
Het |
| Nudt16 |
G |
T |
9: 105,008,707 (GRCm39) |
Q65K |
probably benign |
Het |
| Or1e23 |
C |
A |
11: 73,407,462 (GRCm39) |
A188S |
probably benign |
Het |
| Or5ac17 |
T |
G |
16: 59,036,792 (GRCm39) |
L61F |
probably benign |
Het |
| Or5ac19 |
T |
A |
16: 59,089,213 (GRCm39) |
K272N |
probably benign |
Het |
| Or5al5 |
T |
A |
2: 85,962,012 (GRCm39) |
|
probably benign |
Het |
| Or6c76b |
T |
A |
10: 129,692,671 (GRCm39) |
C95S |
probably benign |
Het |
| Parp14 |
A |
G |
16: 35,678,970 (GRCm39) |
F333L |
probably benign |
Het |
| Pi4ka |
G |
T |
16: 17,115,124 (GRCm39) |
Q1422K |
probably benign |
Het |
| Polr3c |
T |
C |
3: 96,620,836 (GRCm39) |
E494G |
probably damaging |
Het |
| Prss42 |
C |
A |
9: 110,627,411 (GRCm39) |
P49Q |
probably benign |
Het |
| Ptpra |
C |
T |
2: 130,385,997 (GRCm39) |
T568I |
probably damaging |
Het |
| Ring1 |
T |
C |
17: 34,242,294 (GRCm39) |
D71G |
probably damaging |
Het |
| Siae |
T |
A |
9: 37,542,782 (GRCm39) |
S193T |
probably damaging |
Het |
| Slf2 |
T |
C |
19: 44,961,706 (GRCm39) |
|
probably null |
Het |
| Spinkl |
T |
A |
18: 44,307,639 (GRCm39) |
K7N |
possibly damaging |
Het |
| Tbk1 |
G |
A |
10: 121,407,888 (GRCm39) |
R82* |
probably null |
Het |
| Tcf12 |
T |
C |
9: 71,829,930 (GRCm39) |
|
probably null |
Het |
| Tcl1b5 |
G |
A |
12: 105,145,214 (GRCm39) |
M59I |
probably benign |
Het |
| Thumpd3 |
C |
A |
6: 113,043,806 (GRCm39) |
T407K |
probably damaging |
Het |
| Timm29 |
T |
C |
9: 21,505,031 (GRCm39) |
V233A |
probably damaging |
Het |
| Tns3 |
A |
G |
11: 8,469,192 (GRCm39) |
|
probably benign |
Het |
| Ubash3b |
T |
C |
9: 40,937,543 (GRCm39) |
|
probably benign |
Het |
| Ugdh |
G |
T |
5: 65,580,031 (GRCm39) |
T253K |
probably benign |
Het |
| Zfp143 |
T |
A |
7: 109,671,416 (GRCm39) |
|
probably benign |
Het |
| Zfp738 |
A |
G |
13: 67,831,563 (GRCm39) |
|
probably benign |
Het |
|
| Other mutations in Fn1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00236:Fn1
|
APN |
1 |
71,692,032 (GRCm39) |
missense |
probably benign |
0.28 |
|
IGL00402:Fn1
|
APN |
1 |
71,680,322 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL00946:Fn1
|
APN |
1 |
71,684,699 (GRCm39) |
splice site |
probably benign |
|
|
IGL01311:Fn1
|
APN |
1 |
71,667,299 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01338:Fn1
|
APN |
1 |
71,665,369 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL01353:Fn1
|
APN |
1 |
71,626,098 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01674:Fn1
|
APN |
1 |
71,645,900 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01701:Fn1
|
APN |
1 |
71,669,012 (GRCm39) |
splice site |
probably benign |
|
|
IGL01788:Fn1
|
APN |
1 |
71,652,996 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02186:Fn1
|
APN |
1 |
71,677,693 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02398:Fn1
|
APN |
1 |
71,657,829 (GRCm39) |
splice site |
probably null |
|
|
IGL02425:Fn1
|
APN |
1 |
71,680,302 (GRCm39) |
splice site |
probably benign |
|
|
IGL02516:Fn1
|
APN |
1 |
71,676,482 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
IGL02593:Fn1
|
APN |
1 |
71,641,591 (GRCm39) |
missense |
probably benign |
|
|
IGL02651:Fn1
|
APN |
1 |
71,636,835 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
IGL02681:Fn1
|
APN |
1 |
71,658,641 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02890:Fn1
|
APN |
1 |
71,637,531 (GRCm39) |
critical splice donor site |
probably null |
|
|
IGL02929:Fn1
|
APN |
1 |
71,634,821 (GRCm39) |
critical splice donor site |
probably null |
|
|
IGL03036:Fn1
|
APN |
1 |
71,668,932 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03088:Fn1
|
APN |
1 |
71,653,197 (GRCm39) |
splice site |
probably null |
|
|
IGL03142:Fn1
|
APN |
1 |
71,676,455 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03172:Fn1
|
APN |
1 |
71,680,421 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL03184:Fn1
|
APN |
1 |
71,648,656 (GRCm39) |
missense |
probably benign |
0.02 |
|
IGL03212:Fn1
|
APN |
1 |
71,680,484 (GRCm39) |
nonsense |
probably null |
|
|
IGL03246:Fn1
|
APN |
1 |
71,663,455 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
IGL03367:Fn1
|
APN |
1 |
71,636,712 (GRCm39) |
missense |
probably benign |
0.27 |
|
depth
|
UTSW |
1 |
71,647,072 (GRCm39) |
missense |
probably damaging |
1.00 |
|
flooded
|
UTSW |
1 |
71,636,675 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0684_Fn1_062
|
UTSW |
1 |
71,634,968 (GRCm39) |
splice site |
probably null |
|
|
series
|
UTSW |
1 |
71,634,945 (GRCm39) |
missense |
probably damaging |
1.00 |
|
PIT4514001:Fn1
|
UTSW |
1 |
71,667,615 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0008:Fn1
|
UTSW |
1 |
71,634,879 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R0112:Fn1
|
UTSW |
1 |
71,648,812 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0138:Fn1
|
UTSW |
1 |
71,663,269 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
R0383:Fn1
|
UTSW |
1 |
71,636,844 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0386:Fn1
|
UTSW |
1 |
71,634,945 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0648:Fn1
|
UTSW |
1 |
71,636,744 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R0684:Fn1
|
UTSW |
1 |
71,634,968 (GRCm39) |
splice site |
probably null |
|
|
R1054:Fn1
|
UTSW |
1 |
71,625,373 (GRCm39) |
makesense |
probably null |
|
|
R1183:Fn1
|
UTSW |
1 |
71,625,404 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R1405:Fn1
|
UTSW |
1 |
71,681,237 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1405:Fn1
|
UTSW |
1 |
71,681,237 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1414:Fn1
|
UTSW |
1 |
71,640,462 (GRCm39) |
splice site |
probably benign |
|
|
R1677:Fn1
|
UTSW |
1 |
71,636,814 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1773:Fn1
|
UTSW |
1 |
71,676,542 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1830:Fn1
|
UTSW |
1 |
71,663,418 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1987:Fn1
|
UTSW |
1 |
71,690,784 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1989:Fn1
|
UTSW |
1 |
71,690,784 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2068:Fn1
|
UTSW |
1 |
71,639,598 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2113:Fn1
|
UTSW |
1 |
71,665,323 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2145:Fn1
|
UTSW |
1 |
71,645,163 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2246:Fn1
|
UTSW |
1 |
71,667,694 (GRCm39) |
missense |
probably benign |
0.10 |
|
R2273:Fn1
|
UTSW |
1 |
71,653,102 (GRCm39) |
missense |
probably null |
1.00 |
|
R2274:Fn1
|
UTSW |
1 |
71,653,102 (GRCm39) |
missense |
probably null |
1.00 |
|
R2275:Fn1
|
UTSW |
1 |
71,653,102 (GRCm39) |
missense |
probably null |
1.00 |
|
R2303:Fn1
|
UTSW |
1 |
71,653,195 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
R2379:Fn1
|
UTSW |
1 |
71,688,443 (GRCm39) |
nonsense |
probably null |
|
|
R2382:Fn1
|
UTSW |
1 |
71,687,278 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2567:Fn1
|
UTSW |
1 |
71,636,895 (GRCm39) |
nonsense |
probably null |
|
|
R2864:Fn1
|
UTSW |
1 |
71,641,578 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3154:Fn1
|
UTSW |
1 |
71,632,242 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3837:Fn1
|
UTSW |
1 |
71,692,314 (GRCm39) |
splice site |
probably null |
|
|
R3844:Fn1
|
UTSW |
1 |
71,648,733 (GRCm39) |
missense |
possibly damaging |
0.61 |
|
R3886:Fn1
|
UTSW |
1 |
71,679,465 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3887:Fn1
|
UTSW |
1 |
71,679,465 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3888:Fn1
|
UTSW |
1 |
71,679,465 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3889:Fn1
|
UTSW |
1 |
71,679,465 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3905:Fn1
|
UTSW |
1 |
71,647,072 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3906:Fn1
|
UTSW |
1 |
71,647,072 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3907:Fn1
|
UTSW |
1 |
71,647,072 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3909:Fn1
|
UTSW |
1 |
71,647,072 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4611:Fn1
|
UTSW |
1 |
71,663,337 (GRCm39) |
nonsense |
probably null |
|
|
R4724:Fn1
|
UTSW |
1 |
71,687,307 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
R4732:Fn1
|
UTSW |
1 |
71,641,671 (GRCm39) |
splice site |
probably null |
|
|
R4733:Fn1
|
UTSW |
1 |
71,641,671 (GRCm39) |
splice site |
probably null |
|
|
R4756:Fn1
|
UTSW |
1 |
71,629,967 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4809:Fn1
|
UTSW |
1 |
71,691,959 (GRCm39) |
intron |
probably benign |
|
|
R4839:Fn1
|
UTSW |
1 |
71,681,242 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4915:Fn1
|
UTSW |
1 |
71,634,968 (GRCm39) |
splice site |
probably null |
|
|
R4917:Fn1
|
UTSW |
1 |
71,634,968 (GRCm39) |
splice site |
probably null |
|
|
R4918:Fn1
|
UTSW |
1 |
71,634,968 (GRCm39) |
splice site |
probably null |
|
|
R5002:Fn1
|
UTSW |
1 |
71,668,887 (GRCm39) |
missense |
possibly damaging |
0.48 |
|
R5015:Fn1
|
UTSW |
1 |
71,665,336 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5022:Fn1
|
UTSW |
1 |
71,663,338 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5109:Fn1
|
UTSW |
1 |
71,688,394 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5267:Fn1
|
UTSW |
1 |
71,668,863 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5323:Fn1
|
UTSW |
1 |
71,636,591 (GRCm39) |
missense |
probably benign |
0.09 |
|
R5333:Fn1
|
UTSW |
1 |
71,663,339 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5631:Fn1
|
UTSW |
1 |
71,629,355 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5644:Fn1
|
UTSW |
1 |
71,666,409 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5754:Fn1
|
UTSW |
1 |
71,639,481 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5807:Fn1
|
UTSW |
1 |
71,687,218 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6053:Fn1
|
UTSW |
1 |
71,638,449 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6133:Fn1
|
UTSW |
1 |
71,636,886 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6186:Fn1
|
UTSW |
1 |
71,676,449 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6270:Fn1
|
UTSW |
1 |
71,676,434 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6332:Fn1
|
UTSW |
1 |
71,667,230 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6431:Fn1
|
UTSW |
1 |
71,687,003 (GRCm39) |
splice site |
probably null |
|
|
R6571:Fn1
|
UTSW |
1 |
71,665,349 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6596:Fn1
|
UTSW |
1 |
71,648,641 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6862:Fn1
|
UTSW |
1 |
71,653,066 (GRCm39) |
missense |
probably benign |
0.43 |
|
R6898:Fn1
|
UTSW |
1 |
71,639,572 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6984:Fn1
|
UTSW |
1 |
71,665,238 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7107:Fn1
|
UTSW |
1 |
71,666,408 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7121:Fn1
|
UTSW |
1 |
71,639,697 (GRCm39) |
intron |
probably benign |
|
|
R7127:Fn1
|
UTSW |
1 |
71,636,703 (GRCm39) |
missense |
probably benign |
0.16 |
|
R7194:Fn1
|
UTSW |
1 |
71,641,482 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7274:Fn1
|
UTSW |
1 |
71,667,272 (GRCm39) |
missense |
probably benign |
|
|
R7285:Fn1
|
UTSW |
1 |
71,676,498 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7426:Fn1
|
UTSW |
1 |
71,688,384 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7453:Fn1
|
UTSW |
1 |
71,630,039 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7508:Fn1
|
UTSW |
1 |
71,636,675 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7724:Fn1
|
UTSW |
1 |
71,642,894 (GRCm39) |
missense |
probably benign |
0.02 |
|
R7848:Fn1
|
UTSW |
1 |
71,689,760 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7992:Fn1
|
UTSW |
1 |
71,638,825 (GRCm39) |
missense |
probably benign |
0.34 |
|
R8036:Fn1
|
UTSW |
1 |
71,629,310 (GRCm39) |
nonsense |
probably null |
|
|
R8077:Fn1
|
UTSW |
1 |
71,651,761 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8175:Fn1
|
UTSW |
1 |
71,638,824 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8177:Fn1
|
UTSW |
1 |
71,648,746 (GRCm39) |
missense |
probably benign |
|
|
R8212:Fn1
|
UTSW |
1 |
71,682,064 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8322:Fn1
|
UTSW |
1 |
71,667,618 (GRCm39) |
missense |
probably benign |
0.04 |
|
R8745:Fn1
|
UTSW |
1 |
71,676,528 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8780:Fn1
|
UTSW |
1 |
71,682,308 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8805:Fn1
|
UTSW |
1 |
71,644,239 (GRCm39) |
missense |
probably benign |
0.27 |
|
R8927:Fn1
|
UTSW |
1 |
71,638,535 (GRCm39) |
missense |
probably benign |
0.16 |
|
R8928:Fn1
|
UTSW |
1 |
71,638,535 (GRCm39) |
missense |
probably benign |
0.16 |
|
R8928:Fn1
|
UTSW |
1 |
71,641,777 (GRCm39) |
intron |
probably benign |
|
|
R8989:Fn1
|
UTSW |
1 |
71,663,446 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R8991:Fn1
|
UTSW |
1 |
71,676,491 (GRCm39) |
missense |
probably benign |
0.05 |
|
R9095:Fn1
|
UTSW |
1 |
71,647,149 (GRCm39) |
missense |
probably null |
0.02 |
|
R9455:Fn1
|
UTSW |
1 |
71,647,112 (GRCm39) |
missense |
probably benign |
|
|
R9589:Fn1
|
UTSW |
1 |
71,668,941 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9631:Fn1
|
UTSW |
1 |
71,625,387 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9645:Fn1
|
UTSW |
1 |
71,667,629 (GRCm39) |
missense |
probably benign |
0.35 |
|
R9723:Fn1
|
UTSW |
1 |
71,663,369 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
X0023:Fn1
|
UTSW |
1 |
71,637,532 (GRCm39) |
critical splice donor site |
probably null |
|
|
Z1088:Fn1
|
UTSW |
1 |
71,688,451 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1176:Fn1
|
UTSW |
1 |
71,636,570 (GRCm39) |
missense |
probably benign |
0.10 |
|
Incidental Mutation