Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl4fm1 |
A |
C |
4: 144,255,567 (GRCm39) |
D329A |
probably damaging |
Het |
Abcc12 |
T |
A |
8: 87,264,962 (GRCm39) |
H661L |
probably damaging |
Het |
Abcg4 |
A |
G |
9: 44,186,672 (GRCm39) |
Y491H |
probably damaging |
Het |
Acsbg2 |
C |
G |
17: 57,154,710 (GRCm39) |
A481P |
probably damaging |
Het |
Aknad1 |
T |
A |
3: 108,688,501 (GRCm39) |
C610S |
probably benign |
Het |
Ang4 |
G |
T |
14: 52,001,860 (GRCm39) |
Y29* |
probably null |
Het |
Aqp11 |
A |
T |
7: 97,375,896 (GRCm39) |
I251N |
possibly damaging |
Het |
Arid1a |
G |
T |
4: 133,418,487 (GRCm39) |
T1032K |
unknown |
Het |
Atg16l1 |
T |
C |
1: 87,717,187 (GRCm39) |
V538A |
probably benign |
Het |
Bbs1 |
C |
T |
19: 4,956,042 (GRCm39) |
A44T |
probably damaging |
Het |
Bpifa3 |
A |
C |
2: 153,980,070 (GRCm39) |
H234P |
probably damaging |
Het |
Btbd9 |
A |
T |
17: 30,749,188 (GRCm39) |
V42E |
probably damaging |
Het |
Carmil3 |
C |
G |
14: 55,730,333 (GRCm39) |
S15R |
probably damaging |
Het |
Casp8ap2 |
A |
G |
4: 32,640,185 (GRCm39) |
D413G |
probably damaging |
Het |
Cfap44 |
T |
A |
16: 44,241,583 (GRCm39) |
F651L |
probably benign |
Het |
Clcn3 |
A |
T |
8: 61,386,104 (GRCm39) |
|
probably benign |
Het |
Crip3 |
A |
G |
17: 46,741,920 (GRCm39) |
K136E |
probably damaging |
Het |
Ctr9 |
G |
A |
7: 110,643,154 (GRCm39) |
A509T |
possibly damaging |
Het |
D930020B18Rik |
T |
C |
10: 121,525,726 (GRCm39) |
S367P |
probably damaging |
Het |
Dhrs11 |
A |
T |
11: 84,713,976 (GRCm39) |
L125H |
probably damaging |
Het |
Dst |
C |
T |
1: 34,228,200 (GRCm39) |
P1606L |
probably damaging |
Het |
Efcab7 |
A |
T |
4: 99,758,834 (GRCm39) |
|
probably benign |
Het |
Eif2ak4 |
A |
C |
2: 118,293,202 (GRCm39) |
S1253R |
probably damaging |
Het |
Emc1 |
A |
G |
4: 139,098,320 (GRCm39) |
D767G |
probably damaging |
Het |
Fads1 |
G |
A |
19: 10,164,261 (GRCm39) |
|
probably benign |
Het |
Fbxw26 |
T |
C |
9: 109,547,079 (GRCm39) |
T449A |
probably benign |
Het |
Frrs1 |
T |
C |
3: 116,690,437 (GRCm39) |
F27L |
probably damaging |
Het |
Fry |
T |
C |
5: 150,374,563 (GRCm39) |
S2358P |
possibly damaging |
Het |
Gas6 |
A |
C |
8: 13,520,344 (GRCm39) |
L448R |
probably damaging |
Het |
Hikeshi |
T |
C |
7: 89,569,412 (GRCm39) |
|
probably benign |
Het |
Ifngr1 |
C |
T |
10: 19,485,197 (GRCm39) |
R399* |
probably null |
Het |
Itga2 |
G |
A |
13: 115,007,032 (GRCm39) |
S432L |
possibly damaging |
Het |
Knl1 |
C |
T |
2: 118,933,030 (GRCm39) |
T2063I |
possibly damaging |
Het |
Lyzl6 |
A |
G |
11: 103,527,697 (GRCm39) |
V9A |
probably benign |
Het |
Macf1 |
A |
T |
4: 123,382,107 (GRCm39) |
|
probably benign |
Het |
Myo6 |
T |
C |
9: 80,190,816 (GRCm39) |
V789A |
possibly damaging |
Het |
Myo9b |
A |
T |
8: 71,786,412 (GRCm39) |
R693W |
probably damaging |
Het |
Nasp |
A |
G |
4: 116,462,968 (GRCm39) |
|
probably benign |
Het |
Nr1i3 |
T |
C |
1: 171,044,900 (GRCm39) |
F247L |
probably damaging |
Het |
Plekhs1 |
T |
G |
19: 56,466,948 (GRCm39) |
S260A |
probably damaging |
Het |
Rpl21-ps6 |
T |
C |
17: 56,222,536 (GRCm39) |
|
noncoding transcript |
Het |
Rtcb |
A |
T |
10: 85,785,315 (GRCm39) |
|
probably benign |
Het |
Sppl2a |
T |
A |
2: 126,755,213 (GRCm39) |
|
probably null |
Het |
Suco |
A |
T |
1: 161,673,154 (GRCm39) |
|
probably null |
Het |
Tnn |
T |
A |
1: 159,932,498 (GRCm39) |
T1075S |
probably benign |
Het |
Traf3 |
T |
A |
12: 111,209,912 (GRCm39) |
C169* |
probably null |
Het |
Ucp3 |
G |
T |
7: 100,134,250 (GRCm39) |
V288L |
probably benign |
Het |
Vmn1r73 |
A |
T |
7: 11,490,997 (GRCm39) |
T272S |
probably benign |
Het |
Vmn2r115 |
G |
A |
17: 23,565,252 (GRCm39) |
E380K |
probably benign |
Het |
Vmn2r3 |
T |
A |
3: 64,182,787 (GRCm39) |
N304I |
probably damaging |
Het |
Xylt1 |
G |
T |
7: 117,233,928 (GRCm39) |
G485V |
probably damaging |
Het |
Yars1 |
A |
G |
4: 129,090,981 (GRCm39) |
T130A |
probably benign |
Het |
Zfp652 |
A |
T |
11: 95,644,295 (GRCm39) |
R205* |
probably null |
Het |
|
Other mutations in Ulk3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0164:Ulk3
|
UTSW |
9 |
57,497,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R0164:Ulk3
|
UTSW |
9 |
57,497,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R0334:Ulk3
|
UTSW |
9 |
57,501,510 (GRCm39) |
unclassified |
probably benign |
|
R0391:Ulk3
|
UTSW |
9 |
57,502,115 (GRCm39) |
missense |
probably benign |
|
R1635:Ulk3
|
UTSW |
9 |
57,500,443 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2696:Ulk3
|
UTSW |
9 |
57,497,724 (GRCm39) |
missense |
possibly damaging |
0.63 |
R3689:Ulk3
|
UTSW |
9 |
57,501,077 (GRCm39) |
missense |
probably benign |
0.44 |
R4151:Ulk3
|
UTSW |
9 |
57,499,650 (GRCm39) |
missense |
possibly damaging |
0.64 |
R4502:Ulk3
|
UTSW |
9 |
57,500,512 (GRCm39) |
missense |
probably damaging |
1.00 |
R4586:Ulk3
|
UTSW |
9 |
57,501,593 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4746:Ulk3
|
UTSW |
9 |
57,500,201 (GRCm39) |
missense |
probably benign |
|
R5034:Ulk3
|
UTSW |
9 |
57,501,047 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5288:Ulk3
|
UTSW |
9 |
57,498,023 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5385:Ulk3
|
UTSW |
9 |
57,498,023 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5386:Ulk3
|
UTSW |
9 |
57,498,023 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7480:Ulk3
|
UTSW |
9 |
57,498,523 (GRCm39) |
nonsense |
probably null |
|
R7581:Ulk3
|
UTSW |
9 |
57,499,325 (GRCm39) |
missense |
probably damaging |
1.00 |
R8848:Ulk3
|
UTSW |
9 |
57,496,890 (GRCm39) |
missense |
probably benign |
|
R8976:Ulk3
|
UTSW |
9 |
57,502,220 (GRCm39) |
unclassified |
probably benign |
|
R9002:Ulk3
|
UTSW |
9 |
57,500,542 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Ulk3
|
UTSW |
9 |
57,496,828 (GRCm39) |
unclassified |
probably benign |
|
|