Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2210408I21Rik |
C |
A |
13: 77,480,471 (GRCm39) |
P1167Q |
probably damaging |
Het |
Adcy10 |
A |
T |
1: 165,378,867 (GRCm39) |
Q885H |
probably damaging |
Het |
Alkal2 |
C |
T |
12: 30,940,055 (GRCm39) |
L139F |
probably damaging |
Het |
Ankrd17 |
A |
T |
5: 90,441,062 (GRCm39) |
M439K |
probably benign |
Het |
Arl11 |
C |
A |
14: 61,548,422 (GRCm39) |
Y77* |
probably null |
Het |
Bcas3 |
T |
C |
11: 85,449,973 (GRCm39) |
Y669H |
probably benign |
Het |
Bpifb3 |
C |
T |
2: 153,764,516 (GRCm39) |
A136V |
probably benign |
Het |
Ccne2 |
A |
G |
4: 11,202,279 (GRCm39) |
T345A |
probably benign |
Het |
Ciz1 |
T |
C |
2: 32,254,286 (GRCm39) |
S76P |
probably benign |
Het |
Clip4 |
A |
T |
17: 72,107,800 (GRCm39) |
K94* |
probably null |
Het |
Cthrc1 |
G |
A |
15: 38,947,866 (GRCm39) |
R195H |
probably damaging |
Het |
Ddx31 |
T |
C |
2: 28,730,816 (GRCm39) |
|
probably benign |
Het |
Elf2 |
T |
A |
3: 51,174,188 (GRCm39) |
D113V |
possibly damaging |
Het |
Esrrb |
A |
G |
12: 86,535,324 (GRCm39) |
N155S |
probably benign |
Het |
Flnb |
A |
G |
14: 7,887,624 (GRCm38) |
D478G |
probably benign |
Het |
Galm |
T |
A |
17: 80,435,215 (GRCm39) |
L24H |
probably damaging |
Het |
Gask1b |
T |
C |
3: 79,816,078 (GRCm39) |
S363P |
possibly damaging |
Het |
Gon4l |
G |
A |
3: 88,802,314 (GRCm39) |
G975D |
possibly damaging |
Het |
Hspbp1 |
T |
G |
7: 4,667,783 (GRCm39) |
M237L |
probably benign |
Het |
Ighv1-62-1 |
A |
T |
12: 115,350,367 (GRCm39) |
M100K |
probably damaging |
Het |
Ipo8 |
A |
T |
6: 148,676,575 (GRCm39) |
D971E |
possibly damaging |
Het |
Itgax |
C |
T |
7: 127,732,979 (GRCm39) |
A286V |
probably damaging |
Het |
Jpt2 |
T |
C |
17: 25,179,578 (GRCm39) |
Q3R |
probably benign |
Het |
Katnip |
A |
C |
7: 125,396,867 (GRCm39) |
R309S |
probably benign |
Het |
Klrg2 |
A |
C |
6: 38,613,838 (GRCm39) |
L55R |
probably damaging |
Het |
Lrp6 |
T |
A |
6: 134,433,141 (GRCm39) |
M1397L |
probably benign |
Het |
Lrrc31 |
T |
A |
3: 30,733,328 (GRCm39) |
Q462L |
probably benign |
Het |
Lyg2 |
T |
A |
1: 37,949,054 (GRCm39) |
I103F |
probably damaging |
Het |
Map10 |
T |
C |
8: 126,396,664 (GRCm39) |
V19A |
probably damaging |
Het |
Map1b |
T |
A |
13: 99,569,323 (GRCm39) |
M1133L |
unknown |
Het |
Mrgpra4 |
A |
G |
7: 47,631,481 (GRCm39) |
V40A |
probably benign |
Het |
Myh1 |
G |
A |
11: 67,099,967 (GRCm39) |
G626R |
probably benign |
Het |
Myo9a |
T |
C |
9: 59,687,030 (GRCm39) |
V45A |
probably benign |
Het |
Ncdn |
A |
G |
4: 126,638,905 (GRCm39) |
F638S |
possibly damaging |
Het |
Ncs1 |
T |
A |
2: 31,174,213 (GRCm39) |
M121K |
probably damaging |
Het |
Nf1 |
T |
C |
11: 79,437,180 (GRCm39) |
V16A |
probably damaging |
Het |
Nktr |
T |
A |
9: 121,579,317 (GRCm39) |
D1128E |
unknown |
Het |
Nup205 |
T |
G |
6: 35,191,269 (GRCm39) |
L1000R |
probably damaging |
Het |
Obscn |
T |
C |
11: 58,925,921 (GRCm39) |
E5604G |
probably damaging |
Het |
Or1p4-ps1 |
T |
A |
11: 74,208,534 (GRCm39) |
S228T |
unknown |
Het |
Or2p2 |
T |
C |
13: 21,257,220 (GRCm39) |
N84D |
probably damaging |
Het |
Or4a68 |
A |
G |
2: 89,270,209 (GRCm39) |
V138A |
probably benign |
Het |
Or4c35 |
G |
T |
2: 89,808,715 (GRCm39) |
A198S |
possibly damaging |
Het |
Or51ah3 |
G |
T |
7: 103,209,816 (GRCm39) |
C44F |
probably benign |
Het |
Or5b96 |
A |
T |
19: 12,867,560 (GRCm39) |
V127E |
probably damaging |
Het |
Or7g12 |
A |
G |
9: 18,899,812 (GRCm39) |
H176R |
possibly damaging |
Het |
Ovch2 |
T |
A |
7: 107,392,462 (GRCm39) |
I294F |
probably damaging |
Het |
Ovch2 |
A |
T |
7: 107,393,251 (GRCm39) |
C207* |
probably null |
Het |
P3h2 |
T |
A |
16: 25,801,467 (GRCm39) |
Y397F |
possibly damaging |
Het |
Pappa |
A |
T |
4: 65,123,166 (GRCm39) |
I834F |
possibly damaging |
Het |
Pcdha11 |
T |
C |
18: 37,140,716 (GRCm39) |
S782P |
probably benign |
Het |
Pex1 |
T |
C |
5: 3,681,614 (GRCm39) |
V980A |
probably benign |
Het |
Pik3c2a |
G |
T |
7: 115,951,112 (GRCm39) |
L1258I |
probably damaging |
Het |
Pmp22 |
T |
A |
11: 63,049,239 (GRCm39) |
*161R |
probably null |
Het |
Ppp1r26 |
T |
A |
2: 28,341,192 (GRCm39) |
M274K |
probably benign |
Het |
Ppp6r2 |
T |
C |
15: 89,167,275 (GRCm39) |
V830A |
probably benign |
Het |
Pramel34 |
T |
C |
5: 93,785,660 (GRCm39) |
T207A |
possibly damaging |
Het |
Prss1 |
T |
A |
6: 41,439,520 (GRCm39) |
N84K |
probably benign |
Het |
Rab3il1 |
G |
A |
19: 10,004,141 (GRCm39) |
A18T |
probably damaging |
Het |
Sbf2 |
A |
T |
7: 109,929,069 (GRCm39) |
S1471T |
probably damaging |
Het |
Setdb1 |
T |
A |
3: 95,263,371 (GRCm39) |
D45V |
probably damaging |
Het |
Sik3 |
G |
T |
9: 46,089,811 (GRCm39) |
V275L |
probably benign |
Het |
Skint6 |
C |
A |
4: 112,846,149 (GRCm39) |
M659I |
probably benign |
Het |
Slc24a1 |
T |
A |
9: 64,835,985 (GRCm39) |
D714V |
unknown |
Het |
Slc26a5 |
T |
A |
5: 22,018,880 (GRCm39) |
D653V |
probably damaging |
Het |
Snrnp27 |
A |
T |
6: 86,653,196 (GRCm39) |
C141S |
probably benign |
Het |
Stradb |
A |
G |
1: 59,033,478 (GRCm39) |
I380M |
probably benign |
Het |
Sult1e1 |
T |
C |
5: 87,735,501 (GRCm39) |
Y59C |
probably benign |
Het |
Tas2r122 |
C |
T |
6: 132,688,702 (GRCm39) |
A64T |
probably benign |
Het |
Tep1 |
C |
T |
14: 51,074,589 (GRCm39) |
C1812Y |
probably damaging |
Het |
Tln2 |
C |
A |
9: 67,128,693 (GRCm39) |
E1465D |
possibly damaging |
Het |
Trio |
A |
T |
15: 27,905,311 (GRCm39) |
C152S |
unknown |
Het |
Tro |
G |
A |
X: 149,438,555 (GRCm39) |
S34L |
unknown |
Het |
Vmn1r15 |
A |
G |
6: 57,235,123 (GRCm39) |
|
probably benign |
Het |
Vmn1r19 |
A |
G |
6: 57,381,436 (GRCm39) |
|
probably benign |
Het |
Vmn1r75 |
A |
G |
7: 11,614,630 (GRCm39) |
T121A |
possibly damaging |
Het |
Vmn2r32 |
A |
G |
7: 7,477,669 (GRCm39) |
F241L |
probably damaging |
Het |
Vmn2r66 |
A |
G |
7: 84,654,893 (GRCm39) |
L472P |
probably damaging |
Het |
Ylpm1 |
G |
T |
12: 85,043,566 (GRCm39) |
W101C |
unknown |
Het |
Zdbf2 |
C |
A |
1: 63,347,272 (GRCm39) |
H1884N |
probably benign |
Het |
Zfp1005 |
T |
A |
2: 150,109,624 (GRCm39) |
C105S |
possibly damaging |
Het |
|
Other mutations in Abtb3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00666:Abtb3
|
APN |
10 |
85,465,080 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL01143:Abtb3
|
APN |
10 |
85,490,335 (GRCm39) |
splice site |
probably benign |
|
IGL01365:Abtb3
|
APN |
10 |
85,469,680 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL01409:Abtb3
|
APN |
10 |
85,494,029 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL01531:Abtb3
|
APN |
10 |
85,465,069 (GRCm39) |
splice site |
probably benign |
|
IGL01593:Abtb3
|
APN |
10 |
85,490,339 (GRCm39) |
splice site |
probably benign |
|
IGL01751:Abtb3
|
APN |
10 |
85,490,366 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01752:Abtb3
|
APN |
10 |
85,490,366 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02041:Abtb3
|
APN |
10 |
85,223,418 (GRCm39) |
missense |
unknown |
|
IGL02486:Abtb3
|
APN |
10 |
85,476,419 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02597:Abtb3
|
APN |
10 |
85,469,665 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02957:Abtb3
|
APN |
10 |
85,467,150 (GRCm39) |
splice site |
probably benign |
|
IGL02957:Abtb3
|
APN |
10 |
85,469,701 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02967:Abtb3
|
APN |
10 |
85,469,646 (GRCm39) |
missense |
probably benign |
0.11 |
IGL02975:Abtb3
|
APN |
10 |
85,467,207 (GRCm39) |
missense |
probably benign |
0.16 |
IGL03078:Abtb3
|
APN |
10 |
85,468,027 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03130:Abtb3
|
APN |
10 |
85,224,347 (GRCm39) |
splice site |
probably null |
|
IGL03335:Abtb3
|
APN |
10 |
85,494,222 (GRCm39) |
utr 3 prime |
probably benign |
|
R0024:Abtb3
|
UTSW |
10 |
85,223,311 (GRCm39) |
missense |
unknown |
|
R0599:Abtb3
|
UTSW |
10 |
85,494,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R0655:Abtb3
|
UTSW |
10 |
85,481,390 (GRCm39) |
missense |
probably damaging |
1.00 |
R0660:Abtb3
|
UTSW |
10 |
85,224,234 (GRCm39) |
missense |
possibly damaging |
0.65 |
R0664:Abtb3
|
UTSW |
10 |
85,224,234 (GRCm39) |
missense |
possibly damaging |
0.65 |
R1155:Abtb3
|
UTSW |
10 |
85,465,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R1244:Abtb3
|
UTSW |
10 |
85,223,227 (GRCm39) |
missense |
unknown |
|
R1389:Abtb3
|
UTSW |
10 |
85,476,460 (GRCm39) |
missense |
possibly damaging |
0.76 |
R1418:Abtb3
|
UTSW |
10 |
85,481,442 (GRCm39) |
missense |
probably damaging |
1.00 |
R1703:Abtb3
|
UTSW |
10 |
85,223,248 (GRCm39) |
missense |
unknown |
|
R1957:Abtb3
|
UTSW |
10 |
85,469,563 (GRCm39) |
missense |
probably damaging |
1.00 |
R2519:Abtb3
|
UTSW |
10 |
85,487,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R3716:Abtb3
|
UTSW |
10 |
85,397,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R3915:Abtb3
|
UTSW |
10 |
85,468,134 (GRCm39) |
missense |
probably damaging |
1.00 |
R4738:Abtb3
|
UTSW |
10 |
85,463,112 (GRCm39) |
nonsense |
probably null |
|
R4782:Abtb3
|
UTSW |
10 |
85,490,414 (GRCm39) |
missense |
probably damaging |
1.00 |
R4846:Abtb3
|
UTSW |
10 |
85,465,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R4887:Abtb3
|
UTSW |
10 |
85,223,242 (GRCm39) |
missense |
unknown |
|
R4960:Abtb3
|
UTSW |
10 |
85,487,526 (GRCm39) |
missense |
probably benign |
0.34 |
R5224:Abtb3
|
UTSW |
10 |
85,481,386 (GRCm39) |
small deletion |
probably benign |
|
R5341:Abtb3
|
UTSW |
10 |
85,223,236 (GRCm39) |
missense |
unknown |
|
R5713:Abtb3
|
UTSW |
10 |
85,487,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R6046:Abtb3
|
UTSW |
10 |
85,223,947 (GRCm39) |
missense |
unknown |
|
R6461:Abtb3
|
UTSW |
10 |
85,476,428 (GRCm39) |
missense |
probably damaging |
1.00 |
R6809:Abtb3
|
UTSW |
10 |
85,467,240 (GRCm39) |
missense |
probably benign |
0.01 |
R7069:Abtb3
|
UTSW |
10 |
85,223,520 (GRCm39) |
missense |
unknown |
|
R7130:Abtb3
|
UTSW |
10 |
85,223,419 (GRCm39) |
missense |
unknown |
|
R7202:Abtb3
|
UTSW |
10 |
85,223,629 (GRCm39) |
missense |
unknown |
|
R7275:Abtb3
|
UTSW |
10 |
85,490,346 (GRCm39) |
missense |
probably damaging |
1.00 |
R7489:Abtb3
|
UTSW |
10 |
85,463,079 (GRCm39) |
missense |
probably damaging |
1.00 |
R7743:Abtb3
|
UTSW |
10 |
85,460,813 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7873:Abtb3
|
UTSW |
10 |
85,466,989 (GRCm39) |
missense |
possibly damaging |
0.74 |
R8155:Abtb3
|
UTSW |
10 |
85,476,473 (GRCm39) |
critical splice donor site |
probably null |
|
R8306:Abtb3
|
UTSW |
10 |
85,434,409 (GRCm39) |
nonsense |
probably null |
|
R8891:Abtb3
|
UTSW |
10 |
85,223,958 (GRCm39) |
missense |
unknown |
|
R9068:Abtb3
|
UTSW |
10 |
85,223,762 (GRCm39) |
missense |
unknown |
|
R9800:Abtb3
|
UTSW |
10 |
85,224,079 (GRCm39) |
missense |
unknown |
|
X0020:Abtb3
|
UTSW |
10 |
85,467,216 (GRCm39) |
missense |
possibly damaging |
0.86 |
Z1088:Abtb3
|
UTSW |
10 |
85,223,721 (GRCm39) |
missense |
probably benign |
0.23 |
|