Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930453N24Rik |
A |
G |
16: 64,591,135 (GRCm39) |
V31A |
possibly damaging |
Het |
Adss2 |
A |
G |
1: 177,597,527 (GRCm39) |
Y378H |
probably damaging |
Het |
Aldh1a1 |
T |
A |
19: 20,608,150 (GRCm39) |
V324D |
probably damaging |
Het |
Ankrd33b |
A |
G |
15: 31,297,903 (GRCm39) |
S285P |
probably damaging |
Het |
Arel1 |
C |
T |
12: 84,981,371 (GRCm39) |
G269S |
probably damaging |
Het |
Arhgap44 |
A |
G |
11: 65,053,463 (GRCm39) |
M1T |
probably null |
Het |
Arpin |
C |
T |
7: 79,577,983 (GRCm39) |
V149I |
probably benign |
Het |
Arpp21 |
A |
G |
9: 112,014,720 (GRCm39) |
L28P |
possibly damaging |
Het |
Ccr8 |
G |
A |
9: 119,923,133 (GRCm39) |
V83I |
probably damaging |
Het |
Cnksr1 |
T |
C |
4: 133,963,508 (GRCm39) |
E58G |
probably damaging |
Het |
Dctn2 |
T |
A |
10: 127,114,084 (GRCm39) |
H341Q |
probably damaging |
Het |
Ddx21 |
C |
A |
10: 62,428,825 (GRCm39) |
A362S |
possibly damaging |
Het |
Dnajc1 |
C |
T |
2: 18,289,586 (GRCm39) |
V274I |
probably benign |
Het |
Dock3 |
A |
C |
9: 106,870,763 (GRCm39) |
C550W |
probably damaging |
Het |
Dst |
T |
C |
1: 34,220,676 (GRCm39) |
L2160S |
probably damaging |
Het |
Duox1 |
T |
A |
2: 122,168,163 (GRCm39) |
M1096K |
probably benign |
Het |
Dync2h1 |
A |
T |
9: 7,148,659 (GRCm39) |
D928E |
probably benign |
Het |
E030025P04Rik |
C |
T |
11: 109,030,454 (GRCm39) |
|
probably null |
Het |
Eid2b |
T |
C |
7: 27,977,591 (GRCm39) |
M129T |
possibly damaging |
Het |
Fnip2 |
G |
A |
3: 79,407,717 (GRCm39) |
S288F |
possibly damaging |
Het |
Grm4 |
G |
T |
17: 27,653,737 (GRCm39) |
R738S |
probably benign |
Het |
Gsto2 |
A |
G |
19: 47,864,884 (GRCm39) |
D139G |
probably benign |
Het |
Herc2 |
T |
A |
7: 55,772,112 (GRCm39) |
V1097E |
probably benign |
Het |
Impg1 |
G |
A |
9: 80,312,040 (GRCm39) |
A181V |
probably benign |
Het |
Irs2 |
G |
T |
8: 11,057,289 (GRCm39) |
S381* |
probably null |
Het |
Itprid1 |
C |
T |
6: 55,955,470 (GRCm39) |
T1026I |
probably benign |
Het |
Lrrd1 |
A |
C |
5: 3,908,819 (GRCm39) |
D697A |
possibly damaging |
Het |
Nat10 |
A |
G |
2: 103,573,460 (GRCm39) |
S346P |
probably damaging |
Het |
Ncapg2 |
G |
A |
12: 116,388,273 (GRCm39) |
R319H |
probably damaging |
Het |
Nid1 |
A |
G |
13: 13,652,894 (GRCm39) |
Y568C |
probably damaging |
Het |
Noc2l |
G |
A |
4: 156,325,130 (GRCm39) |
C325Y |
probably damaging |
Het |
Or12e9 |
A |
T |
2: 87,202,161 (GRCm39) |
D95V |
possibly damaging |
Het |
Or1e17 |
C |
A |
11: 73,831,744 (GRCm39) |
S224Y |
possibly damaging |
Het |
Pde2a |
G |
T |
7: 101,144,891 (GRCm39) |
V169F |
possibly damaging |
Het |
Pon3 |
T |
C |
6: 5,221,586 (GRCm39) |
K348R |
probably benign |
Het |
Ppp6c |
A |
G |
2: 39,090,052 (GRCm39) |
|
probably null |
Het |
Prrc2b |
G |
A |
2: 32,103,600 (GRCm39) |
G1026D |
probably benign |
Het |
Psg22 |
A |
T |
7: 18,460,816 (GRCm39) |
T482S |
possibly damaging |
Het |
Rdh19 |
G |
A |
10: 127,692,740 (GRCm39) |
V136M |
probably damaging |
Het |
Sbf2 |
T |
A |
7: 109,940,535 (GRCm39) |
N1275I |
probably benign |
Het |
Sema4c |
T |
C |
1: 36,592,395 (GRCm39) |
N182D |
probably damaging |
Het |
Slc7a12 |
T |
A |
3: 14,570,491 (GRCm39) |
H414Q |
probably damaging |
Het |
Slitrk5 |
A |
G |
14: 111,916,702 (GRCm39) |
I109V |
probably damaging |
Het |
Spag17 |
C |
T |
3: 100,010,793 (GRCm39) |
P2096S |
probably benign |
Het |
Steap1 |
T |
A |
5: 5,786,459 (GRCm39) |
D326V |
probably damaging |
Het |
Tacr1 |
C |
T |
6: 82,380,847 (GRCm39) |
T86I |
probably damaging |
Het |
Tenm4 |
C |
T |
7: 96,545,352 (GRCm39) |
T2493I |
probably damaging |
Het |
Tom1 |
C |
T |
8: 75,785,076 (GRCm39) |
R303C |
probably damaging |
Het |
Trav7n-4 |
T |
A |
14: 53,329,200 (GRCm39) |
I70N |
possibly damaging |
Het |
Utrn |
A |
C |
10: 12,560,275 (GRCm39) |
V1338G |
probably benign |
Het |
Vipr1 |
G |
A |
9: 121,471,993 (GRCm39) |
|
probably null |
Het |
Vmn1r122 |
A |
T |
7: 20,867,271 (GRCm39) |
H261Q |
probably benign |
Het |
Vmn1r40 |
G |
T |
6: 89,691,235 (GRCm39) |
L17F |
probably benign |
Het |
Vmn2r54 |
A |
G |
7: 12,366,283 (GRCm39) |
V217A |
probably benign |
Het |
Vmn2r55 |
C |
A |
7: 12,385,782 (GRCm39) |
G733* |
probably null |
Het |
Vmn2r98 |
A |
T |
17: 19,286,777 (GRCm39) |
N425I |
probably benign |
Het |
Vps51 |
C |
T |
19: 6,126,345 (GRCm39) |
V136I |
unknown |
Het |
Zfp184 |
T |
C |
13: 22,144,411 (GRCm39) |
C706R |
probably damaging |
Het |
|
Other mutations in Tet2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00341:Tet2
|
APN |
3 |
133,193,846 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL00401:Tet2
|
APN |
3 |
133,172,643 (GRCm39) |
missense |
possibly damaging |
0.72 |
IGL01528:Tet2
|
APN |
3 |
133,186,059 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL02053:Tet2
|
APN |
3 |
133,194,284 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL02142:Tet2
|
APN |
3 |
133,185,900 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL02512:Tet2
|
APN |
3 |
133,175,069 (GRCm39) |
missense |
probably benign |
0.05 |
IGL03148:Tet2
|
APN |
3 |
133,187,124 (GRCm39) |
missense |
probably benign |
0.18 |
IGL03182:Tet2
|
APN |
3 |
133,177,159 (GRCm39) |
nonsense |
probably null |
|
IGL03371:Tet2
|
APN |
3 |
133,173,312 (GRCm39) |
missense |
possibly damaging |
0.71 |
P0022:Tet2
|
UTSW |
3 |
133,192,654 (GRCm39) |
missense |
probably benign |
0.01 |
P0023:Tet2
|
UTSW |
3 |
133,192,654 (GRCm39) |
missense |
probably benign |
0.01 |
P0031:Tet2
|
UTSW |
3 |
133,185,963 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0012:Tet2
|
UTSW |
3 |
133,182,319 (GRCm39) |
missense |
probably damaging |
0.98 |
R0012:Tet2
|
UTSW |
3 |
133,182,319 (GRCm39) |
missense |
probably damaging |
0.98 |
R0463:Tet2
|
UTSW |
3 |
133,192,427 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0522:Tet2
|
UTSW |
3 |
133,172,565 (GRCm39) |
missense |
probably damaging |
0.98 |
R0593:Tet2
|
UTSW |
3 |
133,193,870 (GRCm39) |
missense |
probably benign |
0.00 |
R0600:Tet2
|
UTSW |
3 |
133,173,486 (GRCm39) |
missense |
probably benign |
0.01 |
R0600:Tet2
|
UTSW |
3 |
133,173,363 (GRCm39) |
missense |
probably benign |
0.00 |
R0698:Tet2
|
UTSW |
3 |
133,173,145 (GRCm39) |
missense |
probably benign |
0.32 |
R0723:Tet2
|
UTSW |
3 |
133,173,045 (GRCm39) |
missense |
probably benign |
|
R0726:Tet2
|
UTSW |
3 |
133,173,945 (GRCm39) |
missense |
probably benign |
|
R0747:Tet2
|
UTSW |
3 |
133,173,231 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1006:Tet2
|
UTSW |
3 |
133,182,362 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1382:Tet2
|
UTSW |
3 |
133,182,376 (GRCm39) |
missense |
probably damaging |
1.00 |
R1455:Tet2
|
UTSW |
3 |
133,179,406 (GRCm39) |
missense |
possibly damaging |
0.51 |
R1550:Tet2
|
UTSW |
3 |
133,175,280 (GRCm39) |
missense |
probably benign |
0.32 |
R1647:Tet2
|
UTSW |
3 |
133,191,641 (GRCm39) |
missense |
probably benign |
|
R1662:Tet2
|
UTSW |
3 |
133,172,613 (GRCm39) |
missense |
possibly damaging |
0.96 |
R1727:Tet2
|
UTSW |
3 |
133,193,051 (GRCm39) |
missense |
probably damaging |
0.98 |
R1738:Tet2
|
UTSW |
3 |
133,187,148 (GRCm39) |
missense |
probably benign |
0.08 |
R1749:Tet2
|
UTSW |
3 |
133,185,892 (GRCm39) |
critical splice donor site |
probably null |
|
R1869:Tet2
|
UTSW |
3 |
133,187,202 (GRCm39) |
splice site |
probably null |
|
R1887:Tet2
|
UTSW |
3 |
133,193,094 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1937:Tet2
|
UTSW |
3 |
133,194,399 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1939:Tet2
|
UTSW |
3 |
133,194,399 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1940:Tet2
|
UTSW |
3 |
133,194,399 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1997:Tet2
|
UTSW |
3 |
133,192,350 (GRCm39) |
nonsense |
probably null |
|
R2082:Tet2
|
UTSW |
3 |
133,191,488 (GRCm39) |
missense |
possibly damaging |
0.96 |
R2084:Tet2
|
UTSW |
3 |
133,193,528 (GRCm39) |
missense |
possibly damaging |
0.68 |
R2215:Tet2
|
UTSW |
3 |
133,192,362 (GRCm39) |
missense |
probably benign |
0.03 |
R2321:Tet2
|
UTSW |
3 |
133,192,100 (GRCm39) |
missense |
possibly damaging |
0.53 |
R2873:Tet2
|
UTSW |
3 |
133,192,715 (GRCm39) |
missense |
probably damaging |
1.00 |
R3439:Tet2
|
UTSW |
3 |
133,172,592 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3783:Tet2
|
UTSW |
3 |
133,185,124 (GRCm39) |
missense |
possibly damaging |
0.53 |
R3894:Tet2
|
UTSW |
3 |
133,175,238 (GRCm39) |
missense |
possibly damaging |
0.86 |
R3916:Tet2
|
UTSW |
3 |
133,191,816 (GRCm39) |
missense |
possibly damaging |
0.53 |
R3966:Tet2
|
UTSW |
3 |
133,193,418 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4457:Tet2
|
UTSW |
3 |
133,191,324 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4633:Tet2
|
UTSW |
3 |
133,191,310 (GRCm39) |
missense |
probably benign |
0.33 |
R4646:Tet2
|
UTSW |
3 |
133,193,843 (GRCm39) |
missense |
probably benign |
0.02 |
R4647:Tet2
|
UTSW |
3 |
133,193,843 (GRCm39) |
missense |
probably benign |
0.02 |
R4648:Tet2
|
UTSW |
3 |
133,193,843 (GRCm39) |
missense |
probably benign |
0.02 |
R4691:Tet2
|
UTSW |
3 |
133,191,844 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4805:Tet2
|
UTSW |
3 |
133,173,076 (GRCm39) |
missense |
probably benign |
0.32 |
R4829:Tet2
|
UTSW |
3 |
133,182,381 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4901:Tet2
|
UTSW |
3 |
133,172,805 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4975:Tet2
|
UTSW |
3 |
133,192,520 (GRCm39) |
unclassified |
probably benign |
|
R5004:Tet2
|
UTSW |
3 |
133,193,140 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5075:Tet2
|
UTSW |
3 |
133,192,667 (GRCm39) |
missense |
probably benign |
|
R5137:Tet2
|
UTSW |
3 |
133,182,326 (GRCm39) |
missense |
probably benign |
0.32 |
R5324:Tet2
|
UTSW |
3 |
133,191,674 (GRCm39) |
missense |
probably benign |
0.00 |
R5590:Tet2
|
UTSW |
3 |
133,182,241 (GRCm39) |
splice site |
probably null |
|
R5854:Tet2
|
UTSW |
3 |
133,193,646 (GRCm39) |
missense |
probably damaging |
0.98 |
R5856:Tet2
|
UTSW |
3 |
133,192,401 (GRCm39) |
missense |
probably benign |
0.01 |
R5865:Tet2
|
UTSW |
3 |
133,192,860 (GRCm39) |
missense |
probably benign |
0.08 |
R5879:Tet2
|
UTSW |
3 |
133,193,721 (GRCm39) |
missense |
possibly damaging |
0.96 |
R5935:Tet2
|
UTSW |
3 |
133,194,296 (GRCm39) |
missense |
possibly damaging |
0.68 |
R6012:Tet2
|
UTSW |
3 |
133,172,542 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6075:Tet2
|
UTSW |
3 |
133,177,196 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6181:Tet2
|
UTSW |
3 |
133,193,520 (GRCm39) |
nonsense |
probably null |
|
R6188:Tet2
|
UTSW |
3 |
133,186,087 (GRCm39) |
missense |
probably benign |
0.18 |
R6339:Tet2
|
UTSW |
3 |
133,192,178 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6612:Tet2
|
UTSW |
3 |
133,193,096 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6923:Tet2
|
UTSW |
3 |
133,185,102 (GRCm39) |
critical splice donor site |
probably null |
|
R6934:Tet2
|
UTSW |
3 |
133,188,998 (GRCm39) |
critical splice donor site |
probably null |
|
R7076:Tet2
|
UTSW |
3 |
133,172,784 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7155:Tet2
|
UTSW |
3 |
133,175,352 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7184:Tet2
|
UTSW |
3 |
133,179,391 (GRCm39) |
missense |
probably damaging |
0.98 |
R7200:Tet2
|
UTSW |
3 |
133,192,953 (GRCm39) |
missense |
probably benign |
0.18 |
R7459:Tet2
|
UTSW |
3 |
133,186,050 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7504:Tet2
|
UTSW |
3 |
133,193,100 (GRCm39) |
missense |
probably benign |
0.33 |
R7524:Tet2
|
UTSW |
3 |
133,185,990 (GRCm39) |
missense |
probably benign |
0.33 |
R7613:Tet2
|
UTSW |
3 |
133,172,509 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7653:Tet2
|
UTSW |
3 |
133,192,146 (GRCm39) |
missense |
probably benign |
0.18 |
R7691:Tet2
|
UTSW |
3 |
133,192,610 (GRCm39) |
missense |
probably damaging |
0.98 |
R7770:Tet2
|
UTSW |
3 |
133,186,056 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7807:Tet2
|
UTSW |
3 |
133,192,302 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7813:Tet2
|
UTSW |
3 |
133,179,404 (GRCm39) |
missense |
probably benign |
0.06 |
R7978:Tet2
|
UTSW |
3 |
133,193,426 (GRCm39) |
missense |
possibly damaging |
0.96 |
R8055:Tet2
|
UTSW |
3 |
133,173,753 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8164:Tet2
|
UTSW |
3 |
133,172,895 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8236:Tet2
|
UTSW |
3 |
133,193,547 (GRCm39) |
missense |
probably benign |
0.00 |
R8755:Tet2
|
UTSW |
3 |
133,194,039 (GRCm39) |
missense |
probably damaging |
0.99 |
R8962:Tet2
|
UTSW |
3 |
133,193,804 (GRCm39) |
missense |
probably benign |
0.22 |
R9009:Tet2
|
UTSW |
3 |
133,193,360 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9014:Tet2
|
UTSW |
3 |
133,172,949 (GRCm39) |
missense |
probably damaging |
0.99 |
R9128:Tet2
|
UTSW |
3 |
133,175,374 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9166:Tet2
|
UTSW |
3 |
133,173,933 (GRCm39) |
missense |
probably damaging |
1.00 |
R9190:Tet2
|
UTSW |
3 |
133,187,147 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9360:Tet2
|
UTSW |
3 |
133,192,903 (GRCm39) |
missense |
possibly damaging |
0.72 |
R9471:Tet2
|
UTSW |
3 |
133,191,680 (GRCm39) |
missense |
probably damaging |
1.00 |
R9488:Tet2
|
UTSW |
3 |
133,193,103 (GRCm39) |
missense |
probably benign |
0.18 |
R9534:Tet2
|
UTSW |
3 |
133,173,689 (GRCm39) |
nonsense |
probably null |
|
R9557:Tet2
|
UTSW |
3 |
133,191,566 (GRCm39) |
missense |
probably benign |
|
R9621:Tet2
|
UTSW |
3 |
133,193,767 (GRCm39) |
nonsense |
probably null |
|
R9644:Tet2
|
UTSW |
3 |
133,193,064 (GRCm39) |
nonsense |
probably null |
|
R9719:Tet2
|
UTSW |
3 |
133,191,803 (GRCm39) |
missense |
possibly damaging |
0.86 |
X0021:Tet2
|
UTSW |
3 |
133,192,056 (GRCm39) |
missense |
possibly damaging |
0.85 |
X0066:Tet2
|
UTSW |
3 |
133,194,134 (GRCm39) |
missense |
possibly damaging |
0.95 |
|