Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930447C04Rik |
A |
T |
12: 72,956,502 (GRCm39) |
Y199* |
probably null |
Het |
Adhfe1 |
A |
T |
1: 9,637,029 (GRCm39) |
I394F |
probably benign |
Het |
Arhgap26 |
G |
T |
18: 39,379,893 (GRCm39) |
R485L |
probably damaging |
Het |
Atat1 |
T |
A |
17: 36,212,467 (GRCm39) |
N231I |
probably damaging |
Het |
B4galnt2 |
T |
C |
11: 95,760,100 (GRCm39) |
N309S |
probably benign |
Het |
Bank1 |
A |
T |
3: 135,772,134 (GRCm39) |
F499I |
probably damaging |
Het |
Bcl9l |
A |
G |
9: 44,416,365 (GRCm39) |
D146G |
possibly damaging |
Het |
Bglap3 |
A |
T |
3: 88,283,671 (GRCm39) |
|
probably benign |
Het |
Bscl2 |
C |
A |
19: 8,825,344 (GRCm39) |
T376K |
probably benign |
Het |
Cercam |
A |
T |
2: 29,761,033 (GRCm39) |
|
probably null |
Het |
Clec4f |
C |
T |
6: 83,633,012 (GRCm39) |
M1I |
probably null |
Het |
Clec4n |
A |
T |
6: 123,209,066 (GRCm39) |
I14F |
probably benign |
Het |
Cmya5 |
T |
C |
13: 93,227,093 (GRCm39) |
E2665G |
probably damaging |
Het |
Cog4 |
T |
A |
8: 111,578,915 (GRCm39) |
|
probably null |
Het |
Cubn |
A |
G |
2: 13,352,856 (GRCm39) |
F1961L |
probably benign |
Het |
Cyp4a29 |
A |
T |
4: 115,104,196 (GRCm39) |
H88L |
probably benign |
Het |
Dhdh |
A |
G |
7: 45,128,530 (GRCm39) |
L216P |
probably damaging |
Het |
Dpp6 |
T |
C |
5: 27,871,509 (GRCm39) |
F544S |
probably damaging |
Het |
Dthd1 |
C |
T |
5: 63,045,549 (GRCm39) |
T771I |
probably benign |
Het |
Emc10 |
A |
G |
7: 44,142,612 (GRCm39) |
|
probably null |
Het |
Fgg |
A |
T |
3: 82,920,072 (GRCm39) |
T284S |
probably benign |
Het |
Gask1a |
C |
T |
9: 121,794,784 (GRCm39) |
R313W |
probably damaging |
Het |
Gm3002 |
T |
A |
14: 3,824,737 (GRCm38) |
N24K |
probably damaging |
Het |
Gm8674 |
G |
A |
13: 50,056,034 (GRCm39) |
|
noncoding transcript |
Het |
Gpr63 |
G |
A |
4: 25,008,368 (GRCm39) |
W364* |
probably null |
Het |
Hcn4 |
C |
G |
9: 58,767,111 (GRCm39) |
P891A |
unknown |
Het |
Hcrtr1 |
A |
T |
4: 130,024,792 (GRCm39) |
F365I |
possibly damaging |
Het |
Hmcn2 |
A |
G |
2: 31,244,176 (GRCm39) |
|
probably null |
Het |
Hoxc5 |
T |
A |
15: 102,923,786 (GRCm39) |
L194H |
probably damaging |
Het |
Ifna11 |
A |
G |
4: 88,738,287 (GRCm39) |
N31S |
probably null |
Het |
Ikbke |
GCC |
G |
1: 131,203,004 (GRCm39) |
|
probably null |
Het |
Iqgap2 |
A |
T |
13: 95,766,514 (GRCm39) |
D1496E |
probably benign |
Het |
Kif28 |
G |
T |
1: 179,536,007 (GRCm39) |
Q556K |
probably damaging |
Het |
Klhl42 |
C |
T |
6: 147,009,502 (GRCm39) |
T447I |
possibly damaging |
Het |
Lrp1b |
A |
C |
2: 41,678,986 (GRCm39) |
D35E |
probably damaging |
Het |
Lsm14b |
A |
G |
2: 179,675,692 (GRCm39) |
|
probably benign |
Het |
Map3k1 |
T |
C |
13: 111,909,272 (GRCm39) |
E226G |
probably damaging |
Het |
Map3k14 |
T |
A |
11: 103,130,357 (GRCm39) |
N187Y |
probably benign |
Het |
Mcm6 |
A |
T |
1: 128,263,586 (GRCm39) |
V645E |
probably damaging |
Het |
Mdh1b |
G |
T |
1: 63,759,022 (GRCm39) |
P190Q |
probably damaging |
Het |
Meiob |
T |
G |
17: 25,037,353 (GRCm39) |
L77R |
probably damaging |
Het |
Mrgpra3 |
A |
T |
7: 47,239,267 (GRCm39) |
F220I |
probably benign |
Het |
Mrtfa |
C |
A |
15: 80,929,476 (GRCm39) |
|
probably benign |
Het |
Mtor |
T |
A |
4: 148,575,817 (GRCm39) |
S1324T |
possibly damaging |
Het |
Myot |
T |
A |
18: 44,487,995 (GRCm39) |
D437E |
possibly damaging |
Het |
Ncoa6 |
G |
T |
2: 155,263,252 (GRCm39) |
T394K |
possibly damaging |
Het |
Nf1 |
T |
A |
11: 79,456,379 (GRCm39) |
|
probably null |
Het |
Nup210 |
T |
A |
6: 91,013,451 (GRCm39) |
T1190S |
possibly damaging |
Het |
Odf1 |
T |
A |
15: 38,226,652 (GRCm39) |
I184N |
probably damaging |
Het |
Or10d1 |
C |
T |
9: 39,484,054 (GRCm39) |
C167Y |
probably damaging |
Het |
Or13d1 |
T |
C |
4: 52,970,960 (GRCm39) |
V113A |
possibly damaging |
Het |
Or1n1b |
A |
G |
2: 36,780,719 (GRCm39) |
I47T |
probably damaging |
Het |
Or5k15 |
G |
T |
16: 58,709,957 (GRCm39) |
Q209K |
possibly damaging |
Het |
Padi1 |
A |
G |
4: 140,572,901 (GRCm39) |
V21A |
probably benign |
Het |
Pdzrn3 |
C |
T |
6: 101,128,551 (GRCm39) |
R705H |
probably damaging |
Het |
Pik3cb |
T |
C |
9: 98,987,685 (GRCm39) |
I18V |
probably benign |
Het |
Pmpca |
T |
C |
2: 26,280,320 (GRCm39) |
S117P |
probably damaging |
Het |
Poteg |
T |
A |
8: 27,985,009 (GRCm39) |
|
probably benign |
Het |
Pramel32 |
T |
C |
4: 88,547,432 (GRCm39) |
T80A |
probably damaging |
Het |
Rab30 |
G |
A |
7: 92,478,771 (GRCm39) |
R72H |
probably damaging |
Het |
Ramp2 |
T |
A |
11: 101,138,383 (GRCm39) |
|
probably null |
Het |
Rbks |
G |
A |
5: 31,781,876 (GRCm39) |
T308I |
probably damaging |
Het |
Rnf112 |
A |
G |
11: 61,343,752 (GRCm39) |
|
probably benign |
Het |
Rnf38 |
G |
A |
4: 44,152,460 (GRCm39) |
P3S |
probably damaging |
Het |
Sec16a |
A |
G |
2: 26,302,883 (GRCm39) |
S2344P |
probably benign |
Het |
Slc16a8 |
C |
T |
15: 79,137,084 (GRCm39) |
V109M |
possibly damaging |
Het |
Slc28a1 |
A |
T |
7: 80,791,757 (GRCm39) |
T308S |
possibly damaging |
Het |
Slc39a3 |
T |
C |
10: 80,867,453 (GRCm39) |
T98A |
possibly damaging |
Het |
Smarcc2 |
T |
C |
10: 128,319,049 (GRCm39) |
F731L |
probably damaging |
Het |
Smc4 |
A |
G |
3: 68,925,572 (GRCm39) |
|
probably benign |
Het |
Sparcl1 |
T |
G |
5: 104,240,776 (GRCm39) |
D216A |
probably damaging |
Het |
Speg |
G |
A |
1: 75,364,513 (GRCm39) |
R192H |
probably damaging |
Het |
Sspo |
T |
C |
6: 48,441,539 (GRCm39) |
L1892P |
probably damaging |
Het |
Tacc2 |
A |
G |
7: 130,225,678 (GRCm39) |
N807D |
probably damaging |
Het |
Teddm1a |
A |
T |
1: 153,767,979 (GRCm39) |
K148* |
probably null |
Het |
Tex15 |
T |
A |
8: 34,064,498 (GRCm39) |
D1309E |
probably benign |
Het |
Thbs1 |
A |
T |
2: 117,945,259 (GRCm39) |
E277D |
probably benign |
Het |
Ticrr |
G |
A |
7: 79,310,158 (GRCm39) |
R24Q |
probably damaging |
Het |
Tigd4 |
A |
G |
3: 84,502,460 (GRCm39) |
E459G |
probably benign |
Het |
Tln2 |
C |
A |
9: 67,262,407 (GRCm39) |
A615S |
probably damaging |
Het |
Tmprss5 |
T |
C |
9: 49,026,817 (GRCm39) |
V410A |
probably damaging |
Het |
Tnrc6a |
G |
T |
7: 122,789,095 (GRCm39) |
W1638L |
probably damaging |
Het |
Tpr |
A |
G |
1: 150,285,810 (GRCm39) |
D424G |
probably damaging |
Het |
Trim34a |
A |
T |
7: 103,910,271 (GRCm39) |
K358* |
probably null |
Het |
Tssk5 |
T |
A |
15: 76,258,856 (GRCm39) |
D10V |
possibly damaging |
Het |
Usp35 |
A |
C |
7: 96,962,782 (GRCm39) |
L470R |
probably damaging |
Het |
Usp42 |
T |
C |
5: 143,701,119 (GRCm39) |
D968G |
possibly damaging |
Het |
Utrn |
A |
G |
10: 12,331,164 (GRCm39) |
V2924A |
probably damaging |
Het |
Wdtc1 |
C |
A |
4: 133,021,654 (GRCm39) |
A627S |
probably damaging |
Het |
Xrra1 |
A |
G |
7: 99,555,730 (GRCm39) |
T366A |
probably damaging |
Het |
Zfp712 |
T |
A |
13: 67,188,773 (GRCm39) |
K585* |
probably null |
Het |
Zfp97 |
T |
A |
17: 17,365,393 (GRCm39) |
N297K |
probably damaging |
Het |
Zfp97 |
G |
T |
17: 17,364,938 (GRCm39) |
E146* |
probably null |
Het |
|
Other mutations in Styxl2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00706:Styxl2
|
APN |
1 |
165,928,121 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00973:Styxl2
|
APN |
1 |
165,927,027 (GRCm39) |
missense |
probably benign |
|
IGL01331:Styxl2
|
APN |
1 |
165,935,749 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01466:Styxl2
|
APN |
1 |
165,928,073 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01572:Styxl2
|
APN |
1 |
165,927,941 (GRCm39) |
missense |
probably benign |
0.18 |
IGL01906:Styxl2
|
APN |
1 |
165,927,092 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01974:Styxl2
|
APN |
1 |
165,928,105 (GRCm39) |
nonsense |
probably null |
|
IGL02112:Styxl2
|
APN |
1 |
165,927,240 (GRCm39) |
nonsense |
probably null |
|
IGL02805:Styxl2
|
APN |
1 |
165,926,630 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03343:Styxl2
|
APN |
1 |
165,927,017 (GRCm39) |
missense |
probably benign |
0.00 |
R0116:Styxl2
|
UTSW |
1 |
165,927,270 (GRCm39) |
missense |
probably benign |
0.19 |
R0367:Styxl2
|
UTSW |
1 |
165,928,332 (GRCm39) |
missense |
probably benign |
0.05 |
R0499:Styxl2
|
UTSW |
1 |
165,926,670 (GRCm39) |
missense |
probably benign |
0.00 |
R0542:Styxl2
|
UTSW |
1 |
165,928,853 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1312:Styxl2
|
UTSW |
1 |
165,926,860 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1572:Styxl2
|
UTSW |
1 |
165,927,024 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1598:Styxl2
|
UTSW |
1 |
165,937,828 (GRCm39) |
missense |
probably benign |
0.10 |
R1858:Styxl2
|
UTSW |
1 |
165,928,415 (GRCm39) |
missense |
possibly damaging |
0.87 |
R2021:Styxl2
|
UTSW |
1 |
165,928,392 (GRCm39) |
missense |
probably benign |
0.00 |
R2970:Styxl2
|
UTSW |
1 |
165,926,798 (GRCm39) |
missense |
probably benign |
0.04 |
R3727:Styxl2
|
UTSW |
1 |
165,927,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R4041:Styxl2
|
UTSW |
1 |
165,927,680 (GRCm39) |
missense |
probably benign |
0.01 |
R4245:Styxl2
|
UTSW |
1 |
165,928,685 (GRCm39) |
missense |
probably damaging |
1.00 |
R4955:Styxl2
|
UTSW |
1 |
165,935,661 (GRCm39) |
missense |
probably damaging |
1.00 |
R5040:Styxl2
|
UTSW |
1 |
165,927,914 (GRCm39) |
missense |
probably benign |
0.17 |
R5342:Styxl2
|
UTSW |
1 |
165,937,819 (GRCm39) |
missense |
probably benign |
0.01 |
R5467:Styxl2
|
UTSW |
1 |
165,939,599 (GRCm39) |
critical splice donor site |
probably null |
|
R5742:Styxl2
|
UTSW |
1 |
165,927,023 (GRCm39) |
missense |
probably benign |
0.00 |
R6222:Styxl2
|
UTSW |
1 |
165,926,214 (GRCm39) |
missense |
probably benign |
0.26 |
R6239:Styxl2
|
UTSW |
1 |
165,926,388 (GRCm39) |
missense |
probably damaging |
1.00 |
R6531:Styxl2
|
UTSW |
1 |
165,937,615 (GRCm39) |
splice site |
probably null |
|
R6586:Styxl2
|
UTSW |
1 |
165,928,454 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6958:Styxl2
|
UTSW |
1 |
165,935,565 (GRCm39) |
missense |
probably damaging |
1.00 |
R7006:Styxl2
|
UTSW |
1 |
165,926,663 (GRCm39) |
missense |
probably benign |
|
R7111:Styxl2
|
UTSW |
1 |
165,954,723 (GRCm39) |
missense |
possibly damaging |
0.66 |
R7310:Styxl2
|
UTSW |
1 |
165,926,300 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7312:Styxl2
|
UTSW |
1 |
165,954,676 (GRCm39) |
missense |
probably damaging |
0.99 |
R7378:Styxl2
|
UTSW |
1 |
165,939,632 (GRCm39) |
nonsense |
probably null |
|
R7398:Styxl2
|
UTSW |
1 |
165,928,044 (GRCm39) |
missense |
probably damaging |
1.00 |
R7442:Styxl2
|
UTSW |
1 |
165,928,584 (GRCm39) |
missense |
probably benign |
0.01 |
R7569:Styxl2
|
UTSW |
1 |
165,935,604 (GRCm39) |
missense |
probably damaging |
1.00 |
R7920:Styxl2
|
UTSW |
1 |
165,927,465 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7954:Styxl2
|
UTSW |
1 |
165,926,849 (GRCm39) |
missense |
probably benign |
0.05 |
R7972:Styxl2
|
UTSW |
1 |
165,926,708 (GRCm39) |
missense |
probably damaging |
1.00 |
R8186:Styxl2
|
UTSW |
1 |
165,927,648 (GRCm39) |
missense |
probably damaging |
1.00 |
R8354:Styxl2
|
UTSW |
1 |
165,935,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R8454:Styxl2
|
UTSW |
1 |
165,935,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R8535:Styxl2
|
UTSW |
1 |
165,928,730 (GRCm39) |
missense |
probably benign |
0.01 |
R9419:Styxl2
|
UTSW |
1 |
165,927,755 (GRCm39) |
missense |
probably damaging |
1.00 |
R9493:Styxl2
|
UTSW |
1 |
165,926,410 (GRCm39) |
missense |
probably damaging |
1.00 |
R9694:Styxl2
|
UTSW |
1 |
165,928,654 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Styxl2
|
UTSW |
1 |
165,926,852 (GRCm39) |
missense |
probably damaging |
1.00 |
|