Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700017N19Rik |
T |
C |
10: 100,430,498 (GRCm39) |
F52L |
possibly damaging |
Het |
Abca16 |
T |
C |
7: 120,126,308 (GRCm39) |
C1156R |
possibly damaging |
Het |
Abcg3 |
A |
C |
5: 105,084,483 (GRCm39) |
S571A |
probably benign |
Het |
Abi3 |
C |
A |
11: 95,724,503 (GRCm39) |
L259F |
unknown |
Het |
Adam19 |
A |
T |
11: 46,027,149 (GRCm39) |
D594V |
probably damaging |
Het |
Adam34 |
C |
T |
8: 44,104,076 (GRCm39) |
S523N |
probably damaging |
Het |
Adam6b |
G |
T |
12: 113,454,176 (GRCm39) |
C331F |
probably benign |
Het |
Adamts14 |
A |
T |
10: 61,106,829 (GRCm39) |
V97E |
probably damaging |
Het |
Adipor1 |
T |
C |
1: 134,355,878 (GRCm39) |
Y226H |
probably damaging |
Het |
Alox12e |
T |
C |
11: 70,212,261 (GRCm39) |
Y139C |
probably damaging |
Het |
Ankrd53 |
A |
G |
6: 83,740,692 (GRCm39) |
D160G |
possibly damaging |
Het |
Ap1m1 |
A |
T |
8: 73,003,606 (GRCm39) |
Y94F |
probably damaging |
Het |
Arhgef28 |
A |
C |
13: 98,078,983 (GRCm39) |
D1314E |
probably benign |
Het |
Bicc1 |
A |
G |
10: 70,863,772 (GRCm39) |
I90T |
probably benign |
Het |
Celf6 |
A |
G |
9: 59,485,833 (GRCm39) |
D58G |
probably damaging |
Het |
Cfap74 |
T |
C |
4: 155,549,054 (GRCm39) |
S38P |
unknown |
Het |
Cps1 |
A |
G |
1: 67,234,342 (GRCm39) |
I910V |
probably benign |
Het |
Cracdl |
C |
T |
1: 37,663,592 (GRCm39) |
A769T |
possibly damaging |
Het |
Crybg2 |
C |
T |
4: 133,816,620 (GRCm39) |
Q1353* |
probably null |
Het |
Cyp4f39 |
T |
C |
17: 32,705,982 (GRCm39) |
Y358H |
probably damaging |
Het |
Dcp1a |
T |
A |
14: 30,241,132 (GRCm39) |
I314N |
probably damaging |
Het |
Dgki |
A |
C |
6: 37,126,489 (GRCm39) |
W164G |
probably damaging |
Het |
Dnah8 |
A |
G |
17: 30,932,029 (GRCm39) |
I1466V |
probably benign |
Het |
Efcab6 |
T |
A |
15: 83,763,676 (GRCm39) |
R1219W |
probably damaging |
Het |
Faap24 |
A |
T |
7: 35,094,494 (GRCm39) |
F102Y |
probably damaging |
Het |
Fam186a |
T |
C |
15: 99,838,244 (GRCm39) |
T2667A |
probably benign |
Het |
Frem1 |
C |
T |
4: 82,877,653 (GRCm39) |
G1308D |
probably damaging |
Het |
Hectd1 |
T |
C |
12: 51,816,047 (GRCm39) |
T1347A |
probably benign |
Het |
Hipk3 |
A |
T |
2: 104,267,376 (GRCm39) |
H620Q |
probably benign |
Het |
Hpd |
A |
G |
5: 123,310,052 (GRCm39) |
S391P |
probably benign |
Het |
Ino80 |
A |
G |
2: 119,275,965 (GRCm39) |
V437A |
probably benign |
Het |
Itgax |
G |
T |
7: 127,741,152 (GRCm39) |
G785C |
probably damaging |
Het |
Kcnk18 |
C |
T |
19: 59,223,266 (GRCm39) |
T137I |
probably damaging |
Het |
Kif16b |
A |
G |
2: 142,542,589 (GRCm39) |
F236L |
probably benign |
Het |
Lamb1 |
T |
C |
12: 31,337,457 (GRCm39) |
M396T |
probably damaging |
Het |
Lrfn5 |
C |
A |
12: 61,886,540 (GRCm39) |
N109K |
probably damaging |
Het |
Lrrc15 |
T |
A |
16: 30,093,006 (GRCm39) |
N111I |
probably damaging |
Het |
Lrrk2 |
A |
T |
15: 91,671,251 (GRCm39) |
I2011F |
possibly damaging |
Het |
Lsr |
A |
G |
7: 30,658,285 (GRCm39) |
I336T |
probably damaging |
Het |
Mettl21e |
T |
A |
1: 44,250,351 (GRCm39) |
R18S |
probably benign |
Het |
Mrpl22 |
T |
C |
11: 58,068,047 (GRCm39) |
L115P |
probably damaging |
Het |
N4bp2 |
T |
A |
5: 65,948,035 (GRCm39) |
S222T |
probably benign |
Het |
Nat2 |
A |
G |
8: 67,954,522 (GRCm39) |
T211A |
probably benign |
Het |
Nbeal1 |
T |
A |
1: 60,350,247 (GRCm39) |
I2432N |
probably damaging |
Het |
Neb |
A |
G |
2: 52,112,783 (GRCm39) |
I1158T |
|
Het |
Nrip3 |
C |
T |
7: 109,362,793 (GRCm39) |
E164K |
probably damaging |
Het |
Obox6 |
G |
A |
7: 15,568,742 (GRCm39) |
Q45* |
probably null |
Het |
Ola1 |
T |
C |
2: 73,033,784 (GRCm39) |
N44D |
probably benign |
Het |
Or1x6 |
C |
T |
11: 50,939,207 (GRCm39) |
T91M |
probably benign |
Het |
Or2y1c |
T |
C |
11: 49,361,509 (GRCm39) |
F177S |
probably damaging |
Het |
Or5b111 |
A |
T |
19: 13,291,100 (GRCm39) |
M183K |
probably damaging |
Het |
Or5d39 |
A |
T |
2: 87,980,255 (GRCm39) |
I36N |
possibly damaging |
Het |
Or5p81 |
A |
T |
7: 108,267,516 (GRCm39) |
N298Y |
probably damaging |
Het |
Or6ae1 |
A |
G |
7: 139,742,771 (GRCm39) |
F31L |
probably benign |
Het |
Or8b51 |
T |
A |
9: 38,568,915 (GRCm39) |
M258L |
probably benign |
Het |
Pde10a |
A |
G |
17: 9,197,816 (GRCm39) |
K753R |
|
Het |
Phldb1 |
T |
C |
9: 44,627,839 (GRCm39) |
D202G |
probably damaging |
Het |
Pik3cb |
T |
C |
9: 98,955,789 (GRCm39) |
N376S |
probably benign |
Het |
Plekhh2 |
A |
G |
17: 84,874,130 (GRCm39) |
N472D |
probably damaging |
Het |
Ppp4r4 |
T |
A |
12: 103,567,811 (GRCm39) |
F708Y |
probably benign |
Het |
Rnf157 |
A |
G |
11: 116,303,576 (GRCm39) |
V12A |
probably benign |
Het |
Saa3 |
T |
C |
7: 46,364,494 (GRCm39) |
I11V |
probably benign |
Het |
Sar1b |
C |
T |
11: 51,670,573 (GRCm39) |
T39I |
probably damaging |
Het |
Scn10a |
A |
T |
9: 119,445,869 (GRCm39) |
L1428Q |
possibly damaging |
Het |
Sema3f |
A |
G |
9: 107,565,454 (GRCm39) |
I213T |
unknown |
Het |
Serpina3m |
C |
T |
12: 104,360,085 (GRCm39) |
Q386* |
probably null |
Het |
Sh3gl3 |
G |
A |
7: 81,909,370 (GRCm39) |
G26R |
probably damaging |
Het |
Shq1 |
T |
C |
6: 100,550,633 (GRCm39) |
E435G |
probably damaging |
Het |
Sidt2 |
G |
T |
9: 45,864,495 (GRCm39) |
A78E |
probably benign |
Het |
Sin3b |
A |
G |
8: 73,477,187 (GRCm39) |
Y818C |
probably damaging |
Het |
Smarca2 |
C |
T |
19: 26,656,498 (GRCm39) |
L825F |
possibly damaging |
Het |
Srgn |
T |
A |
10: 62,330,884 (GRCm39) |
M74L |
probably benign |
Het |
Tbc1d22b |
A |
C |
17: 29,813,747 (GRCm39) |
D360A |
possibly damaging |
Het |
Tbx4 |
A |
G |
11: 85,803,128 (GRCm39) |
R335G |
probably damaging |
Het |
Tmem144 |
T |
C |
3: 79,734,200 (GRCm39) |
N168D |
probably benign |
Het |
Trip11 |
G |
A |
12: 101,859,957 (GRCm39) |
Q307* |
probably null |
Het |
Ttyh2 |
T |
C |
11: 114,598,516 (GRCm39) |
Y296H |
probably damaging |
Het |
Vmn1r236 |
G |
T |
17: 21,507,043 (GRCm39) |
V54F |
probably benign |
Het |
Xrra1 |
A |
C |
7: 99,561,088 (GRCm39) |
H443P |
probably benign |
Het |
Zc3h12a |
T |
C |
4: 125,014,852 (GRCm39) |
T211A |
probably damaging |
Het |
Zfp386 |
T |
G |
12: 116,023,330 (GRCm39) |
D349E |
probably benign |
Het |
Zkscan16 |
T |
A |
4: 58,956,577 (GRCm39) |
H286Q |
probably benign |
Het |
Znrf2 |
C |
T |
6: 54,861,788 (GRCm39) |
P233L |
probably damaging |
Het |
|
Other mutations in Sall2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01587:Sall2
|
APN |
14 |
52,552,028 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02152:Sall2
|
APN |
14 |
52,552,971 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02318:Sall2
|
APN |
14 |
52,553,022 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02933:Sall2
|
APN |
14 |
52,550,484 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03165:Sall2
|
APN |
14 |
52,551,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R1079:Sall2
|
UTSW |
14 |
52,550,660 (GRCm39) |
missense |
probably benign |
0.13 |
R1295:Sall2
|
UTSW |
14 |
52,551,182 (GRCm39) |
missense |
probably damaging |
1.00 |
R1674:Sall2
|
UTSW |
14 |
52,551,293 (GRCm39) |
missense |
probably damaging |
1.00 |
R1840:Sall2
|
UTSW |
14 |
52,551,182 (GRCm39) |
missense |
probably damaging |
1.00 |
R1989:Sall2
|
UTSW |
14 |
52,551,896 (GRCm39) |
missense |
probably damaging |
1.00 |
R2339:Sall2
|
UTSW |
14 |
52,550,813 (GRCm39) |
missense |
probably damaging |
1.00 |
R3407:Sall2
|
UTSW |
14 |
52,565,561 (GRCm39) |
missense |
probably benign |
0.03 |
R3870:Sall2
|
UTSW |
14 |
52,551,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R3895:Sall2
|
UTSW |
14 |
52,551,504 (GRCm39) |
missense |
probably damaging |
0.99 |
R4059:Sall2
|
UTSW |
14 |
52,552,028 (GRCm39) |
missense |
probably damaging |
1.00 |
R4272:Sall2
|
UTSW |
14 |
52,551,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R4273:Sall2
|
UTSW |
14 |
52,551,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R4275:Sall2
|
UTSW |
14 |
52,551,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R4289:Sall2
|
UTSW |
14 |
52,551,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R4503:Sall2
|
UTSW |
14 |
52,550,916 (GRCm39) |
missense |
probably benign |
|
R4592:Sall2
|
UTSW |
14 |
52,551,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R4611:Sall2
|
UTSW |
14 |
52,551,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R4615:Sall2
|
UTSW |
14 |
52,550,207 (GRCm39) |
missense |
probably benign |
0.20 |
R4640:Sall2
|
UTSW |
14 |
52,552,616 (GRCm39) |
missense |
probably damaging |
0.99 |
R4693:Sall2
|
UTSW |
14 |
52,551,935 (GRCm39) |
missense |
probably damaging |
1.00 |
R4921:Sall2
|
UTSW |
14 |
52,552,850 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5007:Sall2
|
UTSW |
14 |
52,551,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R5015:Sall2
|
UTSW |
14 |
52,553,112 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5079:Sall2
|
UTSW |
14 |
52,552,211 (GRCm39) |
missense |
probably damaging |
1.00 |
R5419:Sall2
|
UTSW |
14 |
52,550,586 (GRCm39) |
missense |
probably damaging |
1.00 |
R5849:Sall2
|
UTSW |
14 |
52,551,704 (GRCm39) |
missense |
probably benign |
0.13 |
R6229:Sall2
|
UTSW |
14 |
52,550,648 (GRCm39) |
missense |
probably benign |
|
R6397:Sall2
|
UTSW |
14 |
52,552,610 (GRCm39) |
missense |
probably damaging |
1.00 |
R6422:Sall2
|
UTSW |
14 |
52,550,181 (GRCm39) |
makesense |
probably null |
|
R6456:Sall2
|
UTSW |
14 |
52,551,051 (GRCm39) |
nonsense |
probably null |
|
R6456:Sall2
|
UTSW |
14 |
52,551,050 (GRCm39) |
missense |
probably damaging |
1.00 |
R6786:Sall2
|
UTSW |
14 |
52,552,078 (GRCm39) |
missense |
probably damaging |
1.00 |
R7293:Sall2
|
UTSW |
14 |
52,551,868 (GRCm39) |
nonsense |
probably null |
|
R7496:Sall2
|
UTSW |
14 |
52,553,018 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7792:Sall2
|
UTSW |
14 |
52,553,521 (GRCm39) |
missense |
probably damaging |
1.00 |
R8324:Sall2
|
UTSW |
14 |
52,550,343 (GRCm39) |
missense |
probably benign |
0.30 |
R9017:Sall2
|
UTSW |
14 |
52,550,719 (GRCm39) |
missense |
possibly damaging |
0.51 |
R9149:Sall2
|
UTSW |
14 |
52,550,673 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9362:Sall2
|
UTSW |
14 |
52,550,601 (GRCm39) |
nonsense |
probably null |
|
R9571:Sall2
|
UTSW |
14 |
52,551,830 (GRCm39) |
missense |
probably damaging |
1.00 |
R9574:Sall2
|
UTSW |
14 |
52,551,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R9648:Sall2
|
UTSW |
14 |
52,551,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R9694:Sall2
|
UTSW |
14 |
52,552,124 (GRCm39) |
missense |
possibly damaging |
0.63 |
|