Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb1b |
T |
C |
5: 8,903,468 (GRCm39) |
F1040L |
probably damaging |
Het |
Adamts7 |
A |
G |
9: 90,075,745 (GRCm39) |
N1201S |
probably benign |
Het |
Ahnak |
C |
T |
19: 8,983,089 (GRCm39) |
P1458S |
probably damaging |
Het |
Akap6 |
T |
C |
12: 53,187,707 (GRCm39) |
V1707A |
probably benign |
Het |
Akr1c21 |
T |
A |
13: 4,631,263 (GRCm39) |
V266E |
probably damaging |
Het |
Arap2 |
A |
C |
5: 62,833,361 (GRCm39) |
C894G |
probably damaging |
Het |
Atp2a2 |
T |
C |
5: 122,604,901 (GRCm39) |
D426G |
possibly damaging |
Het |
Azi2 |
A |
T |
9: 117,884,909 (GRCm39) |
Q132L |
possibly damaging |
Het |
Carmil1 |
C |
T |
13: 24,283,032 (GRCm39) |
D91N |
probably damaging |
Het |
Cnot7 |
A |
T |
8: 40,960,494 (GRCm39) |
|
probably null |
Het |
Cntnap5b |
A |
G |
1: 100,202,086 (GRCm39) |
E311G |
probably benign |
Het |
Csmd1 |
A |
G |
8: 16,283,036 (GRCm39) |
V640A |
probably benign |
Het |
Cst7 |
T |
C |
2: 150,417,647 (GRCm39) |
S31P |
probably benign |
Het |
Cyp7b1 |
T |
A |
3: 18,151,530 (GRCm39) |
I228L |
probably benign |
Het |
Ddx28 |
G |
A |
8: 106,736,921 (GRCm39) |
T379I |
probably benign |
Het |
Drd1 |
T |
A |
13: 54,207,600 (GRCm39) |
I205F |
probably damaging |
Het |
Fsd1l |
A |
G |
4: 53,647,664 (GRCm39) |
|
probably null |
Het |
Fubp1 |
T |
A |
3: 151,925,841 (GRCm39) |
Y264* |
probably null |
Het |
Gbp5 |
T |
A |
3: 142,212,680 (GRCm39) |
|
probably null |
Het |
Gm7094 |
A |
G |
1: 21,342,958 (GRCm39) |
|
noncoding transcript |
Het |
Gpr55 |
A |
G |
1: 85,868,858 (GRCm39) |
V241A |
probably benign |
Het |
Impa1 |
C |
T |
3: 10,394,020 (GRCm39) |
A16T |
probably damaging |
Het |
Llgl2 |
T |
C |
11: 115,735,680 (GRCm39) |
L92P |
probably damaging |
Het |
Ltbp2 |
T |
A |
12: 84,833,132 (GRCm39) |
Q1472L |
probably benign |
Het |
Lyplal1 |
A |
T |
1: 185,820,943 (GRCm39) |
M168K |
probably benign |
Het |
Macc1 |
A |
T |
12: 119,410,815 (GRCm39) |
R528* |
probably null |
Het |
Mdm1 |
T |
A |
10: 118,002,585 (GRCm39) |
D635E |
probably damaging |
Het |
Miox |
C |
T |
15: 89,220,477 (GRCm39) |
L189F |
possibly damaging |
Het |
Mrpl23 |
C |
T |
7: 142,088,851 (GRCm39) |
R69W |
probably damaging |
Het |
Ncoa6 |
TGC |
TGCGC |
2: 155,250,211 (GRCm39) |
|
probably null |
Het |
Nr0b2 |
A |
G |
4: 133,281,049 (GRCm39) |
Q105R |
probably damaging |
Het |
Or8b53 |
T |
A |
9: 38,667,484 (GRCm39) |
S167T |
probably benign |
Het |
Otog |
G |
A |
7: 45,953,655 (GRCm39) |
V2638M |
probably damaging |
Het |
Pcdhb14 |
A |
T |
18: 37,581,542 (GRCm39) |
|
probably null |
Het |
Plxna1 |
A |
G |
6: 89,310,001 (GRCm39) |
W1055R |
probably damaging |
Het |
Pramel22 |
T |
A |
4: 143,381,081 (GRCm39) |
H314L |
probably benign |
Het |
Prdm1 |
C |
T |
10: 44,316,087 (GRCm39) |
R716Q |
probably damaging |
Het |
Proser1 |
C |
A |
3: 53,388,038 (GRCm39) |
Q909K |
possibly damaging |
Het |
Pus10 |
T |
A |
11: 23,617,358 (GRCm39) |
C24S |
probably damaging |
Het |
Rpl27 |
T |
A |
11: 101,336,146 (GRCm39) |
F69I |
possibly damaging |
Het |
Sctr |
A |
T |
1: 119,983,124 (GRCm39) |
I325F |
probably damaging |
Het |
Slc49a4 |
G |
A |
16: 35,539,684 (GRCm39) |
T379I |
possibly damaging |
Het |
Slc5a3 |
G |
A |
16: 91,874,581 (GRCm39) |
V213I |
possibly damaging |
Het |
Spib |
G |
T |
7: 44,179,324 (GRCm39) |
D28E |
probably damaging |
Het |
Spic |
T |
C |
10: 88,511,579 (GRCm39) |
S226G |
possibly damaging |
Het |
Tet1 |
T |
A |
10: 62,676,058 (GRCm39) |
T673S |
probably benign |
Het |
Tph1 |
A |
G |
7: 46,297,020 (GRCm39) |
F392L |
probably damaging |
Het |
Ttc28 |
T |
C |
5: 111,373,500 (GRCm39) |
S979P |
probably benign |
Het |
Unc79 |
T |
C |
12: 103,122,812 (GRCm39) |
L2110P |
probably damaging |
Het |
Vmn1r28 |
G |
A |
6: 58,242,702 (GRCm39) |
A182T |
probably benign |
Het |
Zfp467 |
T |
C |
6: 48,415,615 (GRCm39) |
T346A |
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 |
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 |
|
R2213: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 |
|