Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700049A03Rik |
T |
A |
12: 71,217,440 (GRCm39) |
M803K |
probably benign |
Het |
4930590J08Rik |
C |
A |
6: 91,894,038 (GRCm39) |
N218K |
probably damaging |
Het |
Abcc2 |
G |
A |
19: 43,807,836 (GRCm39) |
V826M |
possibly damaging |
Het |
Abcg2 |
T |
C |
6: 58,651,792 (GRCm39) |
S395P |
probably damaging |
Het |
Adam1b |
C |
T |
5: 121,640,010 (GRCm39) |
G345D |
probably damaging |
Het |
Alx4 |
T |
A |
2: 93,505,773 (GRCm39) |
C292S |
probably benign |
Het |
Amd2 |
C |
A |
10: 35,586,627 (GRCm39) |
C310F |
possibly damaging |
Het |
BC051665 |
A |
T |
13: 60,931,989 (GRCm39) |
S137T |
possibly damaging |
Het |
Bmp1 |
A |
G |
14: 70,727,469 (GRCm39) |
F705L |
possibly damaging |
Het |
Coil |
C |
T |
11: 88,863,552 (GRCm39) |
|
probably benign |
Het |
Col6a6 |
G |
A |
9: 105,609,462 (GRCm39) |
P1609S |
probably benign |
Het |
Cpt1b |
A |
T |
15: 89,303,066 (GRCm39) |
F633I |
probably damaging |
Het |
Dcun1d2 |
A |
T |
8: 13,311,406 (GRCm39) |
D194E |
probably benign |
Het |
Defb4 |
A |
G |
8: 19,248,752 (GRCm39) |
R2G |
possibly damaging |
Het |
Dll4 |
T |
C |
2: 119,162,897 (GRCm39) |
V506A |
probably benign |
Het |
Dop1b |
A |
G |
16: 93,558,942 (GRCm39) |
S563G |
probably benign |
Het |
Dpp7 |
C |
A |
2: 25,242,460 (GRCm39) |
G498W |
probably damaging |
Het |
Fam210a |
A |
T |
18: 68,409,020 (GRCm39) |
S97T |
possibly damaging |
Het |
Fgg |
A |
T |
3: 82,920,246 (GRCm39) |
N342Y |
probably damaging |
Het |
Gimap6 |
T |
G |
6: 48,684,995 (GRCm39) |
R30S |
probably benign |
Het |
Gm10840 |
T |
C |
11: 106,051,959 (GRCm39) |
V95A |
unknown |
Het |
Herc3 |
T |
A |
6: 58,853,796 (GRCm39) |
I614N |
probably damaging |
Het |
Kdr |
A |
T |
5: 76,097,556 (GRCm39) |
S1233R |
possibly damaging |
Het |
Lrp1 |
C |
G |
10: 127,443,843 (GRCm39) |
Q141H |
possibly damaging |
Het |
Magi2 |
A |
T |
5: 20,866,344 (GRCm39) |
K1078N |
probably damaging |
Het |
Meioc |
A |
T |
11: 102,570,783 (GRCm39) |
E838V |
probably damaging |
Het |
Mmp20 |
A |
G |
9: 7,628,302 (GRCm39) |
K17E |
probably benign |
Het |
Mtor |
C |
T |
4: 148,608,957 (GRCm39) |
R1538W |
probably damaging |
Het |
Notch2 |
C |
T |
3: 98,005,424 (GRCm39) |
T296I |
probably damaging |
Het |
Nup98 |
T |
C |
7: 101,784,171 (GRCm39) |
S1054G |
probably benign |
Het |
Or10ac1 |
T |
C |
6: 42,515,534 (GRCm39) |
T141A |
probably damaging |
Het |
Or2a12 |
T |
C |
6: 42,904,578 (GRCm39) |
C138R |
probably damaging |
Het |
Or5b109 |
A |
C |
19: 13,212,216 (GRCm39) |
I201L |
probably benign |
Het |
Or6f1 |
T |
C |
7: 85,970,941 (GRCm39) |
Y73C |
probably damaging |
Het |
Pipox |
C |
A |
11: 77,774,001 (GRCm39) |
W205L |
probably damaging |
Het |
Plin4 |
T |
G |
17: 56,410,828 (GRCm39) |
T1068P |
probably benign |
Het |
Pou6f2 |
A |
G |
13: 18,414,149 (GRCm39) |
S209P |
unknown |
Het |
Ptpdc1 |
T |
C |
13: 48,736,632 (GRCm39) |
T713A |
probably benign |
Het |
Rgsl1 |
T |
C |
1: 153,701,716 (GRCm39) |
Y246C |
possibly damaging |
Het |
Rnf19b |
C |
T |
4: 128,969,446 (GRCm39) |
A354V |
probably damaging |
Het |
Rsph4a |
A |
G |
10: 33,785,126 (GRCm39) |
T346A |
probably benign |
Het |
Rsrc2 |
T |
C |
5: 123,883,135 (GRCm39) |
T16A |
unknown |
Het |
Scrn3 |
T |
C |
2: 73,148,768 (GRCm39) |
V113A |
possibly damaging |
Het |
Scrn3 |
T |
A |
2: 73,161,347 (GRCm39) |
I311K |
possibly damaging |
Het |
Sfmbt1 |
T |
C |
14: 30,506,148 (GRCm39) |
|
probably null |
Het |
Sin3a |
A |
G |
9: 57,002,740 (GRCm39) |
I211V |
possibly damaging |
Het |
Strn3 |
T |
C |
12: 51,680,491 (GRCm39) |
T370A |
probably benign |
Het |
Sulf1 |
T |
G |
1: 12,918,395 (GRCm39) |
N786K |
probably damaging |
Het |
Taf1b |
T |
A |
12: 24,597,118 (GRCm39) |
Y352* |
probably null |
Het |
Tas2r120 |
T |
A |
6: 132,634,297 (GRCm39) |
N126K |
probably benign |
Het |
Tjap1 |
C |
A |
17: 46,572,432 (GRCm39) |
R68L |
probably benign |
Het |
Tnfsf12 |
C |
T |
11: 69,586,230 (GRCm39) |
R66Q |
probably benign |
Het |
Traj45 |
A |
G |
14: 54,410,303 (GRCm39) |
D6G |
|
Het |
Trappc9 |
T |
C |
15: 72,824,943 (GRCm39) |
T541A |
probably benign |
Het |
Ttc29 |
A |
C |
8: 79,052,106 (GRCm39) |
E329A |
probably benign |
Het |
Vmn1r117 |
T |
G |
7: 20,617,160 (GRCm39) |
D296A |
possibly damaging |
Het |
Vmn1r203 |
A |
G |
13: 22,708,765 (GRCm39) |
N182S |
probably benign |
Het |
Vps53 |
C |
A |
11: 76,007,999 (GRCm39) |
R287L |
probably damaging |
Het |
Vwce |
G |
A |
19: 10,641,946 (GRCm39) |
E891K |
possibly damaging |
Het |
Zfp608 |
T |
C |
18: 55,079,783 (GRCm39) |
N334S |
possibly damaging |
Het |
Zfp648 |
A |
G |
1: 154,080,687 (GRCm39) |
H282R |
probably damaging |
Het |
|
Other mutations in Fastkd1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00163:Fastkd1
|
APN |
2 |
69,537,893 (GRCm39) |
missense |
probably benign |
0.02 |
IGL00702:Fastkd1
|
APN |
2 |
69,538,889 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00960:Fastkd1
|
APN |
2 |
69,524,997 (GRCm39) |
splice site |
probably benign |
|
IGL01154:Fastkd1
|
APN |
2 |
69,520,404 (GRCm39) |
splice site |
probably null |
|
IGL01463:Fastkd1
|
APN |
2 |
69,520,405 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01913:Fastkd1
|
APN |
2 |
69,538,845 (GRCm39) |
splice site |
probably benign |
|
IGL01977:Fastkd1
|
APN |
2 |
69,524,932 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL02408:Fastkd1
|
APN |
2 |
69,532,945 (GRCm39) |
missense |
probably benign |
|
IGL02715:Fastkd1
|
APN |
2 |
69,542,469 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03411:Fastkd1
|
APN |
2 |
69,537,703 (GRCm39) |
missense |
probably damaging |
0.99 |
R0541:Fastkd1
|
UTSW |
2 |
69,532,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R0612:Fastkd1
|
UTSW |
2 |
69,542,727 (GRCm39) |
missense |
probably benign |
0.03 |
R1170:Fastkd1
|
UTSW |
2 |
69,538,993 (GRCm39) |
splice site |
probably benign |
|
R1499:Fastkd1
|
UTSW |
2 |
69,538,982 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1586:Fastkd1
|
UTSW |
2 |
69,542,492 (GRCm39) |
missense |
probably benign |
0.43 |
R1698:Fastkd1
|
UTSW |
2 |
69,532,813 (GRCm39) |
missense |
probably benign |
0.22 |
R2172:Fastkd1
|
UTSW |
2 |
69,530,477 (GRCm39) |
missense |
probably damaging |
1.00 |
R2240:Fastkd1
|
UTSW |
2 |
69,527,297 (GRCm39) |
missense |
probably benign |
0.01 |
R2327:Fastkd1
|
UTSW |
2 |
69,535,872 (GRCm39) |
nonsense |
probably null |
|
R2897:Fastkd1
|
UTSW |
2 |
69,532,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R4120:Fastkd1
|
UTSW |
2 |
69,537,654 (GRCm39) |
missense |
probably damaging |
0.98 |
R4544:Fastkd1
|
UTSW |
2 |
69,542,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R4546:Fastkd1
|
UTSW |
2 |
69,542,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R4798:Fastkd1
|
UTSW |
2 |
69,521,651 (GRCm39) |
missense |
probably benign |
0.38 |
R4993:Fastkd1
|
UTSW |
2 |
69,533,084 (GRCm39) |
missense |
probably damaging |
0.99 |
R5284:Fastkd1
|
UTSW |
2 |
69,542,532 (GRCm39) |
missense |
probably benign |
0.01 |
R5668:Fastkd1
|
UTSW |
2 |
69,537,725 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6869:Fastkd1
|
UTSW |
2 |
69,533,104 (GRCm39) |
missense |
probably benign |
0.02 |
R6870:Fastkd1
|
UTSW |
2 |
69,538,958 (GRCm39) |
missense |
probably benign |
0.05 |
R7062:Fastkd1
|
UTSW |
2 |
69,534,666 (GRCm39) |
missense |
possibly damaging |
0.74 |
R7576:Fastkd1
|
UTSW |
2 |
69,524,988 (GRCm39) |
missense |
probably damaging |
1.00 |
R7644:Fastkd1
|
UTSW |
2 |
69,527,184 (GRCm39) |
splice site |
probably null |
|
R7971:Fastkd1
|
UTSW |
2 |
69,537,703 (GRCm39) |
missense |
probably benign |
0.19 |
R8336:Fastkd1
|
UTSW |
2 |
69,542,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R8403:Fastkd1
|
UTSW |
2 |
69,517,425 (GRCm39) |
nonsense |
probably null |
|
R8422:Fastkd1
|
UTSW |
2 |
69,532,778 (GRCm39) |
missense |
probably damaging |
1.00 |
R9041:Fastkd1
|
UTSW |
2 |
69,532,715 (GRCm39) |
missense |
probably benign |
|
|