Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9830107B12Rik |
A |
T |
17: 48,439,174 (GRCm39) |
Y127* |
probably null |
Het |
Abcb5 |
C |
T |
12: 118,836,525 (GRCm39) |
V1129I |
possibly damaging |
Het |
Abcc2 |
A |
G |
19: 43,795,519 (GRCm39) |
D425G |
probably damaging |
Het |
Adamts15 |
T |
A |
9: 30,833,322 (GRCm39) |
D71V |
probably damaging |
Het |
Add1 |
A |
G |
5: 34,774,049 (GRCm39) |
H435R |
possibly damaging |
Het |
Akr1c19 |
A |
G |
13: 4,292,591 (GRCm39) |
N204S |
probably benign |
Het |
Ankub1 |
C |
A |
3: 57,597,837 (GRCm39) |
R44S |
possibly damaging |
Het |
Ano3 |
T |
A |
2: 110,496,801 (GRCm39) |
N783Y |
probably damaging |
Het |
Bbs9 |
A |
G |
9: 22,425,359 (GRCm39) |
M138V |
probably benign |
Het |
Ccdc18 |
G |
A |
5: 108,345,661 (GRCm39) |
E936K |
possibly damaging |
Het |
Cit |
T |
G |
5: 116,126,218 (GRCm39) |
L1604V |
probably benign |
Het |
Col2a1 |
T |
A |
15: 97,874,654 (GRCm39) |
S1396C |
unknown |
Het |
Col3a1 |
G |
C |
1: 45,374,924 (GRCm39) |
G653R |
unknown |
Het |
Col6a1 |
T |
C |
10: 76,560,863 (GRCm39) |
E45G |
probably damaging |
Het |
Col9a3 |
T |
A |
2: 180,249,450 (GRCm39) |
F271I |
probably damaging |
Het |
Cyp2g1 |
C |
A |
7: 26,518,578 (GRCm39) |
D364E |
probably damaging |
Het |
Dmbt1 |
T |
A |
7: 130,708,162 (GRCm39) |
V1457D |
possibly damaging |
Het |
Dnah17 |
A |
T |
11: 118,019,753 (GRCm39) |
I98N |
possibly damaging |
Het |
Dyrk1b |
T |
A |
7: 27,882,601 (GRCm39) |
M222K |
possibly damaging |
Het |
Epha8 |
T |
C |
4: 136,672,974 (GRCm39) |
D270G |
probably benign |
Het |
Fbxw17 |
T |
C |
13: 50,579,660 (GRCm39) |
L159P |
probably damaging |
Het |
Fgl2 |
G |
A |
5: 21,578,307 (GRCm39) |
|
probably null |
Het |
Fn1 |
T |
C |
1: 71,648,746 (GRCm39) |
I1479V |
probably benign |
Het |
Gm11939 |
A |
T |
11: 99,450,124 (GRCm39) |
S57T |
possibly damaging |
Het |
Gm9195 |
C |
T |
14: 72,697,977 (GRCm39) |
A1268T |
possibly damaging |
Het |
Gnpda1 |
A |
G |
18: 38,466,348 (GRCm39) |
W90R |
possibly damaging |
Het |
Igkv5-43 |
T |
A |
6: 69,800,445 (GRCm39) |
R81W |
probably damaging |
Het |
Mapk3 |
T |
A |
7: 126,362,937 (GRCm39) |
W230R |
probably null |
Het |
Mplkip |
A |
G |
13: 17,870,205 (GRCm39) |
S46G |
probably benign |
Het |
Mrs2 |
T |
C |
13: 25,188,961 (GRCm39) |
T118A |
probably benign |
Het |
Mst1r |
T |
A |
9: 107,784,784 (GRCm39) |
H147Q |
probably damaging |
Het |
Muc5ac |
G |
C |
7: 141,361,068 (GRCm39) |
G1460R |
probably damaging |
Het |
Myorg |
G |
T |
4: 41,497,568 (GRCm39) |
Y687* |
probably null |
Het |
Naip1 |
T |
C |
13: 100,563,911 (GRCm39) |
H418R |
probably benign |
Het |
Ncapg |
A |
G |
5: 45,851,095 (GRCm39) |
T763A |
probably benign |
Het |
Nr6a1 |
T |
C |
2: 38,619,510 (GRCm39) |
I462V |
probably benign |
Het |
Nudcd3 |
T |
C |
11: 6,143,460 (GRCm39) |
D70G |
possibly damaging |
Het |
Nup210 |
A |
G |
6: 90,991,470 (GRCm39) |
S1858P |
probably benign |
Het |
Or12e13 |
T |
A |
2: 87,663,512 (GRCm39) |
I43N |
probably benign |
Het |
Or5aq1 |
C |
A |
2: 86,966,294 (GRCm39) |
V124L |
possibly damaging |
Het |
Or6a2 |
G |
C |
7: 106,600,663 (GRCm39) |
L135V |
probably damaging |
Het |
Or6c205 |
A |
G |
10: 129,086,790 (GRCm39) |
H129R |
probably benign |
Het |
Or8k33 |
T |
A |
2: 86,383,623 (GRCm39) |
I282F |
noncoding transcript |
Het |
Pde4dip |
T |
C |
3: 97,674,848 (GRCm39) |
T23A |
probably damaging |
Het |
Pex6 |
A |
G |
17: 47,024,988 (GRCm39) |
Q347R |
probably benign |
Het |
Rbm27 |
A |
G |
18: 42,457,175 (GRCm39) |
K694R |
probably damaging |
Het |
Rnf40 |
T |
G |
7: 127,195,322 (GRCm39) |
D549E |
probably benign |
Het |
Rpl22 |
A |
G |
4: 152,411,968 (GRCm39) |
K15E |
probably damaging |
Het |
Rsph6a |
T |
A |
7: 18,808,164 (GRCm39) |
D697E |
unknown |
Het |
Sec23b |
C |
T |
2: 144,427,543 (GRCm39) |
P590L |
probably benign |
Het |
Semp2l1 |
T |
C |
1: 32,585,457 (GRCm39) |
E151G |
probably benign |
Het |
Slc17a7 |
T |
A |
7: 44,824,356 (GRCm39) |
M524K |
probably benign |
Het |
Slc28a1 |
G |
A |
7: 80,814,164 (GRCm39) |
D454N |
probably benign |
Het |
Slc6a13 |
C |
T |
6: 121,301,987 (GRCm39) |
R190* |
probably null |
Het |
Slc7a9 |
G |
A |
7: 35,155,558 (GRCm39) |
V257I |
probably benign |
Het |
Slco1a6 |
T |
A |
6: 142,047,460 (GRCm39) |
M377L |
probably damaging |
Het |
Slit3 |
A |
G |
11: 35,469,919 (GRCm39) |
E307G |
probably damaging |
Het |
Smchd1 |
A |
G |
17: 71,697,448 (GRCm39) |
M1164T |
probably benign |
Het |
Stk4 |
T |
C |
2: 163,930,777 (GRCm39) |
I126T |
probably damaging |
Het |
Syndig1 |
A |
T |
2: 149,741,788 (GRCm39) |
S125C |
probably damaging |
Het |
Synm |
T |
C |
7: 67,383,813 (GRCm39) |
D1283G |
probably benign |
Het |
Tmprss6 |
T |
C |
15: 78,349,327 (GRCm39) |
M73V |
probably benign |
Het |
Tmprss9 |
A |
G |
10: 80,730,882 (GRCm39) |
I803V |
probably benign |
Het |
Tmx4 |
A |
T |
2: 134,485,822 (GRCm39) |
V35E |
probably damaging |
Het |
Topbp1 |
T |
G |
9: 103,197,740 (GRCm39) |
S440A |
probably benign |
Het |
Twf1 |
T |
C |
15: 94,482,276 (GRCm39) |
I157V |
possibly damaging |
Het |
Vmn1r205 |
T |
C |
13: 22,776,415 (GRCm39) |
N229S |
probably benign |
Het |
Vmn1r27 |
T |
A |
6: 58,192,759 (GRCm39) |
I82L |
probably benign |
Het |
Vmn2r112 |
A |
G |
17: 22,822,594 (GRCm39) |
N424S |
possibly damaging |
Het |
Vmn2r68 |
A |
T |
7: 84,871,422 (GRCm39) |
Y620* |
probably null |
Het |
Zfp51 |
A |
G |
17: 21,684,129 (GRCm39) |
D248G |
probably benign |
Het |
|
Other mutations in Fmnl1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00424:Fmnl1
|
APN |
11 |
103,088,166 (GRCm39) |
nonsense |
probably null |
|
IGL00972:Fmnl1
|
APN |
11 |
103,071,781 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01406:Fmnl1
|
APN |
11 |
103,085,516 (GRCm39) |
unclassified |
probably benign |
|
IGL01417:Fmnl1
|
APN |
11 |
103,087,520 (GRCm39) |
unclassified |
probably benign |
|
IGL01599:Fmnl1
|
APN |
11 |
103,077,482 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02151:Fmnl1
|
APN |
11 |
103,083,598 (GRCm39) |
missense |
probably benign |
0.38 |
IGL02324:Fmnl1
|
APN |
11 |
103,070,364 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02812:Fmnl1
|
APN |
11 |
103,087,592 (GRCm39) |
unclassified |
probably benign |
|
IGL03369:Fmnl1
|
APN |
11 |
103,088,008 (GRCm39) |
splice site |
probably null |
|
archetypal
|
UTSW |
11 |
103,077,453 (GRCm39) |
missense |
probably damaging |
1.00 |
contractual
|
UTSW |
11 |
103,071,741 (GRCm39) |
missense |
probably damaging |
1.00 |
stylistic
|
UTSW |
11 |
103,084,562 (GRCm39) |
critical splice donor site |
probably null |
|
R0077:Fmnl1
|
UTSW |
11 |
103,080,795 (GRCm39) |
missense |
probably damaging |
1.00 |
R0241:Fmnl1
|
UTSW |
11 |
103,072,996 (GRCm39) |
critical splice donor site |
probably null |
|
R0241:Fmnl1
|
UTSW |
11 |
103,072,996 (GRCm39) |
critical splice donor site |
probably null |
|
R0413:Fmnl1
|
UTSW |
11 |
103,084,889 (GRCm39) |
splice site |
probably benign |
|
R1170:Fmnl1
|
UTSW |
11 |
103,088,196 (GRCm39) |
missense |
probably benign |
0.02 |
R1389:Fmnl1
|
UTSW |
11 |
103,077,535 (GRCm39) |
splice site |
probably null |
|
R1794:Fmnl1
|
UTSW |
11 |
103,087,973 (GRCm39) |
missense |
probably benign |
0.00 |
R2082:Fmnl1
|
UTSW |
11 |
103,082,851 (GRCm39) |
missense |
probably damaging |
1.00 |
R2105:Fmnl1
|
UTSW |
11 |
103,085,518 (GRCm39) |
missense |
probably benign |
0.39 |
R3611:Fmnl1
|
UTSW |
11 |
103,085,591 (GRCm39) |
unclassified |
probably benign |
|
R3883:Fmnl1
|
UTSW |
11 |
103,072,940 (GRCm39) |
missense |
probably damaging |
1.00 |
R3893:Fmnl1
|
UTSW |
11 |
103,087,583 (GRCm39) |
unclassified |
probably benign |
|
R4658:Fmnl1
|
UTSW |
11 |
103,088,520 (GRCm39) |
missense |
probably damaging |
1.00 |
R4689:Fmnl1
|
UTSW |
11 |
103,084,562 (GRCm39) |
critical splice donor site |
probably null |
|
R4812:Fmnl1
|
UTSW |
11 |
103,089,390 (GRCm39) |
unclassified |
probably benign |
|
R4996:Fmnl1
|
UTSW |
11 |
103,073,482 (GRCm39) |
missense |
possibly damaging |
0.58 |
R5646:Fmnl1
|
UTSW |
11 |
103,087,338 (GRCm39) |
unclassified |
probably benign |
|
R5702:Fmnl1
|
UTSW |
11 |
103,076,491 (GRCm39) |
missense |
probably damaging |
1.00 |
R5850:Fmnl1
|
UTSW |
11 |
103,086,111 (GRCm39) |
unclassified |
probably benign |
|
R5903:Fmnl1
|
UTSW |
11 |
103,062,270 (GRCm39) |
splice site |
probably null |
|
R6254:Fmnl1
|
UTSW |
11 |
103,087,141 (GRCm39) |
unclassified |
probably benign |
|
R6958:Fmnl1
|
UTSW |
11 |
103,062,140 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R7030:Fmnl1
|
UTSW |
11 |
103,085,600 (GRCm39) |
unclassified |
probably benign |
|
R7133:Fmnl1
|
UTSW |
11 |
103,072,610 (GRCm39) |
critical splice donor site |
probably null |
|
R7171:Fmnl1
|
UTSW |
11 |
103,081,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R7224:Fmnl1
|
UTSW |
11 |
103,073,595 (GRCm39) |
critical splice donor site |
probably null |
|
R7282:Fmnl1
|
UTSW |
11 |
103,087,091 (GRCm39) |
missense |
unknown |
|
R7448:Fmnl1
|
UTSW |
11 |
103,077,453 (GRCm39) |
missense |
probably damaging |
1.00 |
R7463:Fmnl1
|
UTSW |
11 |
103,083,954 (GRCm39) |
missense |
probably damaging |
1.00 |
R7831:Fmnl1
|
UTSW |
11 |
103,088,999 (GRCm39) |
missense |
unknown |
|
R7862:Fmnl1
|
UTSW |
11 |
103,071,756 (GRCm39) |
missense |
probably damaging |
1.00 |
R7973:Fmnl1
|
UTSW |
11 |
103,061,984 (GRCm39) |
start gained |
probably benign |
|
R8273:Fmnl1
|
UTSW |
11 |
103,077,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R8345:Fmnl1
|
UTSW |
11 |
103,077,440 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8507:Fmnl1
|
UTSW |
11 |
103,084,859 (GRCm39) |
missense |
unknown |
|
R8921:Fmnl1
|
UTSW |
11 |
103,087,967 (GRCm39) |
missense |
unknown |
|
R8946:Fmnl1
|
UTSW |
11 |
103,071,741 (GRCm39) |
missense |
probably damaging |
1.00 |
R8968:Fmnl1
|
UTSW |
11 |
103,077,444 (GRCm39) |
small deletion |
probably benign |
|
R9114:Fmnl1
|
UTSW |
11 |
103,087,327 (GRCm39) |
missense |
unknown |
|
R9696:Fmnl1
|
UTSW |
11 |
103,086,297 (GRCm39) |
missense |
unknown |
|
|