Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akr1c12 |
T |
C |
13: 4,326,247 (GRCm39) |
D78G |
probably damaging |
Het |
Anxa1 |
C |
T |
19: 20,360,239 (GRCm39) |
R124H |
probably damaging |
Het |
Arhgef4 |
G |
A |
1: 34,846,230 (GRCm39) |
|
probably null |
Het |
C87436 |
G |
A |
6: 86,422,455 (GRCm39) |
V10I |
probably benign |
Het |
Ces1a |
G |
T |
8: 93,751,853 (GRCm39) |
P427Q |
probably damaging |
Het |
Cpm |
T |
C |
10: 117,495,744 (GRCm39) |
Y78H |
probably damaging |
Het |
Csmd3 |
G |
A |
15: 47,683,843 (GRCm39) |
T1663I |
possibly damaging |
Het |
Cul7 |
T |
C |
17: 46,962,398 (GRCm39) |
F10L |
probably damaging |
Het |
Cyp2j5 |
T |
C |
4: 96,547,852 (GRCm39) |
N130S |
probably benign |
Het |
Dclk1 |
G |
A |
3: 55,387,854 (GRCm39) |
C100Y |
probably damaging |
Het |
Ddb1 |
T |
C |
19: 10,585,691 (GRCm39) |
L135P |
probably damaging |
Het |
Dixdc1 |
A |
G |
9: 50,613,245 (GRCm39) |
S211P |
probably benign |
Het |
Dnah12 |
G |
T |
14: 26,460,485 (GRCm39) |
K970N |
probably benign |
Het |
Eps15 |
A |
G |
4: 109,218,417 (GRCm39) |
K391E |
probably damaging |
Het |
Fabp9 |
A |
G |
3: 10,259,860 (GRCm39) |
V51A |
probably damaging |
Het |
Flg |
T |
C |
3: 93,200,335 (GRCm39) |
|
probably benign |
Het |
Fscb |
A |
T |
12: 64,520,890 (GRCm39) |
I192N |
possibly damaging |
Het |
Galntl5 |
A |
G |
5: 25,422,527 (GRCm39) |
I333V |
probably benign |
Het |
Gcnt3 |
A |
T |
9: 69,941,989 (GRCm39) |
V193E |
probably benign |
Het |
Gle1 |
T |
C |
2: 29,839,313 (GRCm39) |
F535S |
probably damaging |
Het |
Gpr87 |
A |
T |
3: 59,086,465 (GRCm39) |
S347T |
probably damaging |
Het |
Gstm2 |
C |
T |
3: 107,893,409 (GRCm39) |
R18H |
probably damaging |
Het |
H1f7 |
T |
A |
15: 98,154,219 (GRCm39) |
Q310L |
unknown |
Het |
Haus6 |
C |
T |
4: 86,500,229 (GRCm39) |
E927K |
possibly damaging |
Het |
Hunk |
A |
G |
16: 90,229,505 (GRCm39) |
N122S |
probably damaging |
Het |
Itih4 |
T |
A |
14: 30,612,670 (GRCm39) |
V232E |
probably damaging |
Het |
Jag1 |
G |
T |
2: 136,931,812 (GRCm39) |
D586E |
probably benign |
Het |
Klk1b1 |
T |
C |
7: 43,619,905 (GRCm39) |
S155P |
probably damaging |
Het |
Lama1 |
G |
T |
17: 68,084,029 (GRCm39) |
G1424* |
probably null |
Het |
Lrp1 |
T |
A |
10: 127,376,571 (GRCm39) |
N4279I |
probably damaging |
Het |
Lrrc43 |
G |
A |
5: 123,641,640 (GRCm39) |
V525I |
possibly damaging |
Het |
Lrrc4c |
G |
A |
2: 97,460,816 (GRCm39) |
V481M |
probably benign |
Het |
Mecr |
T |
A |
4: 131,581,126 (GRCm39) |
|
probably null |
Het |
Megf10 |
T |
A |
18: 57,421,081 (GRCm39) |
Y906* |
probably null |
Het |
Mpdz |
A |
G |
4: 81,228,409 (GRCm39) |
F1319L |
probably damaging |
Het |
Mtf2 |
A |
G |
5: 108,248,780 (GRCm39) |
E364G |
possibly damaging |
Het |
Nelfe |
T |
A |
17: 35,072,859 (GRCm39) |
D160E |
probably benign |
Het |
Nin |
A |
G |
12: 70,092,128 (GRCm39) |
L727P |
probably damaging |
Het |
Npat |
A |
G |
9: 53,463,681 (GRCm39) |
T155A |
probably benign |
Het |
Nup58 |
T |
C |
14: 60,476,945 (GRCm39) |
D242G |
probably benign |
Het |
Or4a78 |
A |
T |
2: 89,497,891 (GRCm39) |
L113Q |
probably damaging |
Het |
Pnlip |
T |
C |
19: 58,662,202 (GRCm39) |
V116A |
probably benign |
Het |
Prl7a2 |
T |
A |
13: 27,849,051 (GRCm39) |
L79F |
probably benign |
Het |
Rbm25 |
A |
T |
12: 83,722,856 (GRCm39) |
I760L |
probably benign |
Het |
Rbms3 |
A |
T |
9: 116,788,534 (GRCm39) |
|
probably null |
Het |
Rif1 |
GCCACCA |
GCCA |
2: 52,000,336 (GRCm39) |
|
probably benign |
Het |
Rps10 |
C |
A |
17: 27,849,473 (GRCm39) |
|
probably benign |
Het |
Slc35e4 |
T |
C |
11: 3,863,159 (GRCm39) |
E10G |
possibly damaging |
Het |
Smad2 |
A |
T |
18: 76,437,697 (GRCm39) |
T434S |
probably damaging |
Het |
Sox30 |
C |
T |
11: 45,875,679 (GRCm39) |
S477F |
probably damaging |
Het |
Speer4a3 |
G |
T |
5: 26,158,175 (GRCm39) |
T59K |
probably benign |
Het |
Stat4 |
A |
T |
1: 52,053,014 (GRCm39) |
D65V |
probably damaging |
Het |
Strip2 |
A |
G |
6: 29,931,147 (GRCm39) |
D366G |
probably damaging |
Het |
Syngap1 |
C |
A |
17: 27,172,043 (GRCm39) |
R84S |
probably damaging |
Het |
Synpo2l |
A |
G |
14: 20,710,734 (GRCm39) |
Y629H |
probably damaging |
Het |
Taf4 |
A |
T |
2: 179,577,683 (GRCm39) |
|
probably null |
Het |
Ttc21a |
A |
G |
9: 119,769,527 (GRCm39) |
H68R |
probably benign |
Het |
Txndc8 |
T |
A |
4: 57,984,199 (GRCm39) |
Q144L |
probably benign |
Het |
Tyr |
T |
G |
7: 87,142,086 (GRCm39) |
Q158P |
probably damaging |
Het |
Uchl3 |
T |
A |
14: 101,904,106 (GRCm39) |
|
probably null |
Het |
Vwa5b1 |
T |
C |
4: 138,332,123 (GRCm39) |
K298R |
probably benign |
Het |
Wrn |
T |
C |
8: 33,747,043 (GRCm39) |
N891S |
probably benign |
Het |
Ylpm1 |
A |
G |
12: 85,116,492 (GRCm39) |
S2125G |
probably benign |
Het |
|
Other mutations in Flnb |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01017:Flnb
|
APN |
14 |
7,917,390 (GRCm38) |
splice site |
probably benign |
|
IGL01063:Flnb
|
APN |
14 |
7,926,518 (GRCm38) |
splice site |
probably benign |
|
IGL01135:Flnb
|
APN |
14 |
7,909,736 (GRCm38) |
missense |
probably benign |
|
IGL01139:Flnb
|
APN |
14 |
7,945,989 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01364:Flnb
|
APN |
14 |
7,934,562 (GRCm38) |
critical splice acceptor site |
probably null |
|
IGL01417:Flnb
|
APN |
14 |
7,905,513 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL01505:Flnb
|
APN |
14 |
7,902,003 (GRCm38) |
critical splice donor site |
probably null |
|
IGL01560:Flnb
|
APN |
14 |
7,893,829 (GRCm38) |
missense |
probably benign |
0.07 |
IGL01621:Flnb
|
APN |
14 |
7,950,470 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01656:Flnb
|
APN |
14 |
7,902,010 (GRCm38) |
splice site |
probably benign |
|
IGL01889:Flnb
|
APN |
14 |
7,935,967 (GRCm38) |
missense |
possibly damaging |
0.85 |
IGL01987:Flnb
|
APN |
14 |
7,922,748 (GRCm38) |
critical splice donor site |
probably null |
|
IGL02322:Flnb
|
APN |
14 |
7,894,676 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02496:Flnb
|
APN |
14 |
7,930,919 (GRCm38) |
splice site |
probably benign |
|
IGL02752:Flnb
|
APN |
14 |
7,917,338 (GRCm38) |
missense |
probably benign |
|
IGL03001:Flnb
|
APN |
14 |
7,934,680 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL03076:Flnb
|
APN |
14 |
7,901,988 (GRCm38) |
missense |
probably benign |
0.01 |
IGL03085:Flnb
|
APN |
14 |
7,882,211 (GRCm38) |
missense |
probably benign |
|
IGL03170:Flnb
|
APN |
14 |
7,818,261 (GRCm38) |
missense |
possibly damaging |
0.90 |
IGL03373:Flnb
|
APN |
14 |
7,890,867 (GRCm38) |
critical splice donor site |
probably null |
|
Boomerang
|
UTSW |
14 |
7,901,945 (GRCm38) |
missense |
probably damaging |
1.00 |
Queensland
|
UTSW |
14 |
7,927,352 (GRCm38) |
missense |
probably damaging |
1.00 |
R3437_Flnb_252
|
UTSW |
14 |
7,942,057 (GRCm38) |
missense |
probably damaging |
0.97 |
R8441_Flnb_221
|
UTSW |
14 |
7,896,488 (GRCm38) |
missense |
probably benign |
0.15 |
Rhodelinda
|
UTSW |
14 |
7,887,682 (GRCm38) |
splice site |
probably benign |
|
saul
|
UTSW |
14 |
7,889,183 (GRCm38) |
missense |
probably damaging |
0.99 |
Xerxes
|
UTSW |
14 |
7,867,551 (GRCm38) |
missense |
probably damaging |
1.00 |
R0068:Flnb
|
UTSW |
14 |
7,915,290 (GRCm38) |
missense |
possibly damaging |
0.49 |
R0068:Flnb
|
UTSW |
14 |
7,915,290 (GRCm38) |
missense |
possibly damaging |
0.49 |
R0084:Flnb
|
UTSW |
14 |
7,935,979 (GRCm38) |
missense |
probably benign |
|
R0128:Flnb
|
UTSW |
14 |
7,901,951 (GRCm38) |
missense |
probably damaging |
0.99 |
R0130:Flnb
|
UTSW |
14 |
7,901,951 (GRCm38) |
missense |
probably damaging |
0.99 |
R0148:Flnb
|
UTSW |
14 |
7,939,077 (GRCm38) |
missense |
probably benign |
0.01 |
R0166:Flnb
|
UTSW |
14 |
7,896,115 (GRCm38) |
missense |
probably damaging |
1.00 |
R0376:Flnb
|
UTSW |
14 |
7,946,014 (GRCm38) |
critical splice donor site |
probably null |
|
R0547:Flnb
|
UTSW |
14 |
7,912,943 (GRCm38) |
splice site |
probably null |
|
R0612:Flnb
|
UTSW |
14 |
7,887,682 (GRCm38) |
splice site |
probably benign |
|
R0656:Flnb
|
UTSW |
14 |
7,927,352 (GRCm38) |
missense |
probably damaging |
1.00 |
R0691:Flnb
|
UTSW |
14 |
7,890,810 (GRCm38) |
missense |
probably benign |
0.16 |
R1241:Flnb
|
UTSW |
14 |
7,896,503 (GRCm38) |
missense |
probably benign |
0.06 |
R1572:Flnb
|
UTSW |
14 |
7,883,908 (GRCm38) |
missense |
probably damaging |
0.97 |
R1682:Flnb
|
UTSW |
14 |
7,913,121 (GRCm38) |
missense |
probably benign |
0.04 |
R1807:Flnb
|
UTSW |
14 |
7,934,645 (GRCm38) |
missense |
probably benign |
0.26 |
R1848:Flnb
|
UTSW |
14 |
7,892,113 (GRCm38) |
missense |
probably damaging |
1.00 |
R1959:Flnb
|
UTSW |
14 |
7,884,735 (GRCm38) |
nonsense |
probably null |
|
R2078:Flnb
|
UTSW |
14 |
7,927,466 (GRCm38) |
missense |
probably damaging |
1.00 |
R2132:Flnb
|
UTSW |
14 |
7,873,376 (GRCm38) |
missense |
probably benign |
0.04 |
R2209:Flnb
|
UTSW |
14 |
7,905,507 (GRCm38) |
nonsense |
probably null |
|
R2212:Flnb
|
UTSW |
14 |
7,881,652 (GRCm38) |
small deletion |
probably benign |
|
R2363:Flnb
|
UTSW |
14 |
7,945,950 (GRCm38) |
missense |
possibly damaging |
0.95 |
R2415:Flnb
|
UTSW |
14 |
7,929,932 (GRCm38) |
missense |
probably benign |
0.07 |
R2983:Flnb
|
UTSW |
14 |
7,882,250 (GRCm38) |
missense |
probably damaging |
1.00 |
R3001:Flnb
|
UTSW |
14 |
7,907,162 (GRCm38) |
missense |
probably benign |
0.22 |
R3002:Flnb
|
UTSW |
14 |
7,907,162 (GRCm38) |
missense |
probably benign |
0.22 |
R3436:Flnb
|
UTSW |
14 |
7,942,057 (GRCm38) |
missense |
probably damaging |
0.97 |
R3437:Flnb
|
UTSW |
14 |
7,942,057 (GRCm38) |
missense |
probably damaging |
0.97 |
R3778:Flnb
|
UTSW |
14 |
7,915,353 (GRCm38) |
missense |
probably benign |
0.06 |
R3783:Flnb
|
UTSW |
14 |
7,889,236 (GRCm38) |
missense |
probably benign |
0.04 |
R4162:Flnb
|
UTSW |
14 |
7,915,374 (GRCm38) |
missense |
possibly damaging |
0.81 |
R4163:Flnb
|
UTSW |
14 |
7,915,374 (GRCm38) |
missense |
possibly damaging |
0.81 |
R4164:Flnb
|
UTSW |
14 |
7,915,374 (GRCm38) |
missense |
possibly damaging |
0.81 |
R4356:Flnb
|
UTSW |
14 |
7,922,700 (GRCm38) |
missense |
probably benign |
|
R4369:Flnb
|
UTSW |
14 |
7,942,216 (GRCm38) |
missense |
probably benign |
|
R4783:Flnb
|
UTSW |
14 |
7,905,701 (GRCm38) |
missense |
probably benign |
0.12 |
R4785:Flnb
|
UTSW |
14 |
7,905,701 (GRCm38) |
missense |
probably benign |
0.12 |
R4790:Flnb
|
UTSW |
14 |
7,905,661 (GRCm38) |
missense |
probably benign |
0.34 |
R4828:Flnb
|
UTSW |
14 |
7,919,238 (GRCm38) |
missense |
probably benign |
0.13 |
R4882:Flnb
|
UTSW |
14 |
7,929,936 (GRCm38) |
missense |
possibly damaging |
0.56 |
R5002:Flnb
|
UTSW |
14 |
7,945,882 (GRCm38) |
missense |
probably damaging |
1.00 |
R5058:Flnb
|
UTSW |
14 |
7,924,262 (GRCm38) |
nonsense |
probably null |
|
R5184:Flnb
|
UTSW |
14 |
7,901,945 (GRCm38) |
missense |
probably damaging |
1.00 |
R5186:Flnb
|
UTSW |
14 |
7,909,748 (GRCm38) |
missense |
probably damaging |
1.00 |
R5395:Flnb
|
UTSW |
14 |
7,883,881 (GRCm38) |
missense |
probably benign |
0.02 |
R5421:Flnb
|
UTSW |
14 |
7,926,494 (GRCm38) |
missense |
probably damaging |
1.00 |
R5667:Flnb
|
UTSW |
14 |
7,890,843 (GRCm38) |
missense |
probably benign |
0.00 |
R5671:Flnb
|
UTSW |
14 |
7,890,843 (GRCm38) |
missense |
probably benign |
0.00 |
R5714:Flnb
|
UTSW |
14 |
7,929,073 (GRCm38) |
missense |
probably damaging |
1.00 |
R5860:Flnb
|
UTSW |
14 |
7,931,135 (GRCm38) |
missense |
probably damaging |
1.00 |
R5892:Flnb
|
UTSW |
14 |
7,907,183 (GRCm38) |
missense |
probably damaging |
1.00 |
R5924:Flnb
|
UTSW |
14 |
7,890,765 (GRCm38) |
missense |
probably benign |
0.00 |
R6131:Flnb
|
UTSW |
14 |
7,894,635 (GRCm38) |
missense |
possibly damaging |
0.79 |
R6244:Flnb
|
UTSW |
14 |
7,892,092 (GRCm38) |
missense |
probably damaging |
1.00 |
R6489:Flnb
|
UTSW |
14 |
7,867,551 (GRCm38) |
missense |
probably damaging |
1.00 |
R6582:Flnb
|
UTSW |
14 |
7,892,275 (GRCm38) |
critical splice donor site |
probably null |
|
R6586:Flnb
|
UTSW |
14 |
7,929,138 (GRCm38) |
missense |
possibly damaging |
0.93 |
R6611:Flnb
|
UTSW |
14 |
7,915,318 (GRCm38) |
missense |
probably damaging |
1.00 |
R6626:Flnb
|
UTSW |
14 |
7,929,012 (GRCm38) |
missense |
probably damaging |
1.00 |
R6700:Flnb
|
UTSW |
14 |
7,892,189 (GRCm38) |
missense |
probably damaging |
0.99 |
R6738:Flnb
|
UTSW |
14 |
7,904,536 (GRCm38) |
missense |
probably benign |
0.01 |
R6864:Flnb
|
UTSW |
14 |
7,905,640 (GRCm38) |
missense |
possibly damaging |
0.84 |
R6916:Flnb
|
UTSW |
14 |
7,907,171 (GRCm38) |
missense |
probably damaging |
0.99 |
R7117:Flnb
|
UTSW |
14 |
7,894,214 (GRCm38) |
missense |
probably benign |
0.02 |
R7164:Flnb
|
UTSW |
14 |
7,915,944 (GRCm38) |
splice site |
probably null |
|
R7328:Flnb
|
UTSW |
14 |
7,894,660 (GRCm38) |
nonsense |
probably null |
|
R7328:Flnb
|
UTSW |
14 |
7,883,788 (GRCm38) |
missense |
possibly damaging |
0.95 |
R7687:Flnb
|
UTSW |
14 |
7,924,224 (GRCm38) |
missense |
probably damaging |
1.00 |
R7716:Flnb
|
UTSW |
14 |
7,917,274 (GRCm38) |
missense |
possibly damaging |
0.64 |
R7763:Flnb
|
UTSW |
14 |
7,926,478 (GRCm38) |
missense |
probably benign |
0.00 |
R7821:Flnb
|
UTSW |
14 |
7,939,113 (GRCm38) |
missense |
probably benign |
0.00 |
R7921:Flnb
|
UTSW |
14 |
7,933,800 (GRCm38) |
missense |
possibly damaging |
0.57 |
R8008:Flnb
|
UTSW |
14 |
7,892,155 (GRCm38) |
missense |
probably damaging |
1.00 |
R8075:Flnb
|
UTSW |
14 |
7,913,048 (GRCm38) |
missense |
probably benign |
0.00 |
R8084:Flnb
|
UTSW |
14 |
7,907,243 (GRCm38) |
missense |
probably benign |
0.00 |
R8259:Flnb
|
UTSW |
14 |
7,889,183 (GRCm38) |
missense |
probably damaging |
0.99 |
R8441:Flnb
|
UTSW |
14 |
7,896,488 (GRCm38) |
missense |
probably benign |
0.15 |
R8493:Flnb
|
UTSW |
14 |
7,869,822 (GRCm38) |
missense |
probably damaging |
0.97 |
R8508:Flnb
|
UTSW |
14 |
7,950,394 (GRCm38) |
missense |
probably damaging |
0.98 |
R8531:Flnb
|
UTSW |
14 |
7,929,939 (GRCm38) |
missense |
probably damaging |
1.00 |
R8812:Flnb
|
UTSW |
14 |
7,887,624 (GRCm38) |
missense |
probably benign |
0.06 |
R8814:Flnb
|
UTSW |
14 |
7,927,409 (GRCm38) |
missense |
probably damaging |
1.00 |
R8825:Flnb
|
UTSW |
14 |
7,887,566 (GRCm38) |
missense |
probably damaging |
1.00 |
R8868:Flnb
|
UTSW |
14 |
7,908,671 (GRCm38) |
missense |
probably benign |
0.02 |
R8955:Flnb
|
UTSW |
14 |
7,904,688 (GRCm38) |
nonsense |
probably null |
|
R8955:Flnb
|
UTSW |
14 |
7,892,874 (GRCm38) |
missense |
probably damaging |
1.00 |
R8976:Flnb
|
UTSW |
14 |
7,901,882 (GRCm38) |
critical splice acceptor site |
probably null |
|
R9055:Flnb
|
UTSW |
14 |
7,908,553 (GRCm38) |
missense |
probably benign |
0.00 |
R9148:Flnb
|
UTSW |
14 |
7,817,996 (GRCm38) |
start gained |
probably benign |
|
R9179:Flnb
|
UTSW |
14 |
7,887,541 (GRCm38) |
nonsense |
probably null |
|
R9180:Flnb
|
UTSW |
14 |
7,818,219 (GRCm38) |
missense |
probably damaging |
1.00 |
R9189:Flnb
|
UTSW |
14 |
7,892,976 (GRCm38) |
missense |
possibly damaging |
0.90 |
R9286:Flnb
|
UTSW |
14 |
7,873,414 (GRCm38) |
missense |
probably damaging |
0.98 |
R9288:Flnb
|
UTSW |
14 |
7,904,498 (GRCm38) |
missense |
probably benign |
0.43 |
R9354:Flnb
|
UTSW |
14 |
7,818,411 (GRCm38) |
missense |
probably benign |
0.13 |
R9484:Flnb
|
UTSW |
14 |
7,929,004 (GRCm38) |
missense |
probably benign |
0.06 |
R9505:Flnb
|
UTSW |
14 |
7,904,665 (GRCm38) |
missense |
probably benign |
|
R9525:Flnb
|
UTSW |
14 |
7,905,481 (GRCm38) |
missense |
probably damaging |
1.00 |
R9621:Flnb
|
UTSW |
14 |
7,926,421 (GRCm38) |
missense |
probably damaging |
0.99 |
R9630:Flnb
|
UTSW |
14 |
7,926,438 (GRCm38) |
nonsense |
probably null |
|
R9739:Flnb
|
UTSW |
14 |
7,935,954 (GRCm38) |
nonsense |
probably null |
|
R9760:Flnb
|
UTSW |
14 |
7,929,846 (GRCm38) |
missense |
probably damaging |
0.98 |
X0066:Flnb
|
UTSW |
14 |
7,908,636 (GRCm38) |
missense |
probably damaging |
1.00 |
Z1088:Flnb
|
UTSW |
14 |
7,905,871 (GRCm38) |
missense |
probably benign |
0.04 |
Z1176:Flnb
|
UTSW |
14 |
7,942,066 (GRCm38) |
missense |
probably benign |
0.25 |
|