Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110038F14Rik |
CGGG |
CGGGGGG |
15: 76,833,863 (GRCm39) |
|
probably benign |
Het |
Abca17 |
A |
T |
17: 24,486,690 (GRCm39) |
C1446S |
probably damaging |
Het |
Asb16 |
C |
A |
11: 102,167,582 (GRCm39) |
A316E |
possibly damaging |
Het |
Axdnd1 |
C |
T |
1: 156,204,114 (GRCm39) |
V384I |
possibly damaging |
Het |
BC024139 |
A |
T |
15: 76,009,461 (GRCm39) |
L207* |
probably null |
Het |
Bcl3 |
T |
G |
7: 19,543,552 (GRCm39) |
S305R |
probably damaging |
Het |
Cachd1 |
T |
C |
4: 100,634,555 (GRCm39) |
V77A |
probably benign |
Het |
Cd101 |
C |
T |
3: 100,936,764 (GRCm39) |
|
probably null |
Het |
Cela1 |
T |
C |
15: 100,583,048 (GRCm39) |
N64S |
probably benign |
Het |
Cep128 |
T |
C |
12: 91,256,372 (GRCm39) |
D366G |
probably benign |
Het |
Col12a1 |
A |
G |
9: 79,604,823 (GRCm39) |
V675A |
probably benign |
Het |
Copg1 |
A |
G |
6: 87,870,800 (GRCm39) |
Y201C |
probably damaging |
Het |
Cyp24a1 |
T |
C |
2: 170,329,837 (GRCm39) |
R372G |
probably benign |
Het |
Dcaf1 |
A |
C |
9: 106,729,161 (GRCm39) |
I567L |
probably benign |
Het |
Dcn |
A |
G |
10: 97,342,536 (GRCm39) |
D164G |
probably benign |
Het |
Dnase2a |
T |
A |
8: 85,635,951 (GRCm39) |
H113Q |
probably benign |
Het |
Espl1 |
T |
C |
15: 102,207,448 (GRCm39) |
V304A |
probably benign |
Het |
Fam193a |
A |
G |
5: 34,600,716 (GRCm39) |
D315G |
possibly damaging |
Het |
Fkbp8 |
T |
A |
8: 70,983,685 (GRCm39) |
|
probably null |
Het |
Foxp4 |
T |
A |
17: 48,188,884 (GRCm39) |
T321S |
probably null |
Het |
Fut10 |
A |
G |
8: 31,726,328 (GRCm39) |
N361S |
probably damaging |
Het |
Gyg1 |
A |
T |
3: 20,205,286 (GRCm39) |
V94D |
probably damaging |
Het |
Has2 |
T |
C |
15: 56,531,974 (GRCm39) |
K247R |
probably damaging |
Het |
Helz2 |
G |
T |
2: 180,873,878 (GRCm39) |
D2205E |
probably benign |
Het |
Hps6 |
T |
A |
19: 45,993,409 (GRCm39) |
S449T |
probably benign |
Het |
Ints10 |
T |
C |
8: 69,247,323 (GRCm39) |
Y64H |
probably damaging |
Het |
Kalrn |
T |
C |
16: 34,177,331 (GRCm39) |
H278R |
probably damaging |
Het |
Klhdc8a |
T |
C |
1: 132,231,548 (GRCm39) |
V280A |
possibly damaging |
Het |
Klk1b5 |
A |
G |
7: 43,869,549 (GRCm39) |
M210V |
probably benign |
Het |
Kmt2c |
G |
A |
5: 25,578,434 (GRCm39) |
A614V |
probably benign |
Het |
Lck |
T |
A |
4: 129,451,879 (GRCm39) |
I45F |
probably benign |
Het |
Lin7a |
A |
C |
10: 107,247,920 (GRCm39) |
E75A |
probably damaging |
Het |
Lrp1 |
A |
T |
10: 127,414,542 (GRCm39) |
C1070S |
probably damaging |
Het |
Mapk8ip3 |
G |
T |
17: 25,133,557 (GRCm39) |
N289K |
probably benign |
Het |
Mbtps1 |
T |
C |
8: 120,249,232 (GRCm39) |
D686G |
probably benign |
Het |
Mknk1 |
T |
A |
4: 115,730,428 (GRCm39) |
C178* |
probably null |
Het |
Mtmr6 |
A |
G |
14: 60,534,184 (GRCm39) |
N474S |
probably damaging |
Het |
Mvb12b |
A |
G |
2: 33,730,169 (GRCm39) |
|
probably null |
Het |
Myh6 |
T |
C |
14: 55,182,131 (GRCm39) |
K1759R |
probably damaging |
Het |
Nfatc1 |
T |
C |
18: 80,678,746 (GRCm39) |
K881E |
possibly damaging |
Het |
Nlrp10 |
A |
G |
7: 108,526,248 (GRCm39) |
F30S |
probably damaging |
Het |
Nop14 |
G |
T |
5: 34,807,672 (GRCm39) |
A430E |
possibly damaging |
Het |
Ntn4 |
C |
T |
10: 93,543,215 (GRCm39) |
R314W |
probably damaging |
Het |
Or1j18 |
A |
T |
2: 36,624,854 (GRCm39) |
I174F |
probably damaging |
Het |
Or4c107 |
A |
G |
2: 88,789,211 (GRCm39) |
I134V |
probably damaging |
Het |
Or4c108 |
A |
G |
2: 88,803,482 (GRCm39) |
V251A |
probably benign |
Het |
Or6c205 |
A |
G |
10: 129,086,463 (GRCm39) |
E20G |
probably benign |
Het |
Or6c88 |
A |
T |
10: 129,407,217 (GRCm39) |
Q231L |
probably damaging |
Het |
Or7g17 |
A |
T |
9: 18,768,782 (GRCm39) |
Y287F |
possibly damaging |
Het |
Osbpl7 |
C |
A |
11: 96,949,954 (GRCm39) |
S378R |
probably damaging |
Het |
Otof |
A |
T |
5: 30,529,067 (GRCm39) |
Y1775* |
probably null |
Het |
Parp16 |
T |
C |
9: 65,122,876 (GRCm39) |
S46P |
possibly damaging |
Het |
Pdlim2 |
C |
T |
14: 70,402,228 (GRCm39) |
R296H |
probably damaging |
Het |
Pi16 |
A |
T |
17: 29,538,361 (GRCm39) |
Q58L |
possibly damaging |
Het |
Pld3 |
C |
A |
7: 27,238,877 (GRCm39) |
M190I |
probably benign |
Het |
Plscr4 |
T |
G |
9: 92,372,099 (GRCm39) |
I290S |
probably damaging |
Het |
Ppip5k2 |
T |
C |
1: 97,651,531 (GRCm39) |
D928G |
possibly damaging |
Het |
Ppp1r13l |
T |
A |
7: 19,102,536 (GRCm39) |
L15Q |
probably damaging |
Het |
Prorp |
T |
A |
12: 55,351,117 (GRCm39) |
I142N |
possibly damaging |
Het |
Ptpn14 |
C |
A |
1: 189,571,699 (GRCm39) |
S263R |
possibly damaging |
Het |
Sema7a |
G |
A |
9: 57,862,182 (GRCm39) |
V178I |
possibly damaging |
Het |
Sesn2 |
A |
T |
4: 132,224,381 (GRCm39) |
Y342* |
probably null |
Het |
Shroom3 |
G |
T |
5: 93,090,945 (GRCm39) |
V1151F |
probably damaging |
Het |
Sltm |
A |
G |
9: 70,450,314 (GRCm39) |
N38S |
possibly damaging |
Het |
Smg1 |
T |
C |
7: 117,753,845 (GRCm39) |
|
probably benign |
Het |
Spsb1 |
A |
T |
4: 149,991,367 (GRCm39) |
V67E |
probably damaging |
Het |
Suox |
A |
G |
10: 128,506,408 (GRCm39) |
V540A |
possibly damaging |
Het |
Tbc1d12 |
T |
A |
19: 38,899,529 (GRCm39) |
I483N |
probably damaging |
Het |
Tbcb |
A |
T |
7: 29,923,924 (GRCm39) |
D198E |
possibly damaging |
Het |
Tbce |
T |
C |
13: 14,194,294 (GRCm39) |
K122E |
probably benign |
Het |
Tcap |
T |
A |
11: 98,275,205 (GRCm39) |
L113H |
probably damaging |
Het |
Thsd7a |
A |
T |
6: 12,321,040 (GRCm39) |
I1545N |
probably damaging |
Het |
Tmed10 |
T |
C |
12: 85,421,277 (GRCm39) |
T55A |
possibly damaging |
Het |
Tmem268 |
T |
A |
4: 63,498,180 (GRCm39) |
V200D |
probably damaging |
Het |
Tmem45b |
A |
C |
9: 31,342,651 (GRCm39) |
I50M |
probably damaging |
Het |
Trp53bp2 |
T |
C |
1: 182,286,468 (GRCm39) |
W1103R |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,594,377 (GRCm39) |
V20524M |
probably damaging |
Het |
Vmn1r59 |
A |
G |
7: 5,457,553 (GRCm39) |
V69A |
probably benign |
Het |
Vmn2r10 |
A |
T |
5: 109,149,861 (GRCm39) |
Y394* |
probably null |
Het |
Zfp212 |
T |
C |
6: 47,908,475 (GRCm39) |
S485P |
probably benign |
Het |
Zfp512b |
A |
T |
2: 181,227,528 (GRCm39) |
C776S |
probably damaging |
Het |
Zfp518b |
A |
G |
5: 38,829,084 (GRCm39) |
Y974H |
probably damaging |
Het |
|
Other mutations in Ulk2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01599:Ulk2
|
APN |
11 |
61,682,262 (GRCm39) |
nonsense |
probably null |
|
IGL02044:Ulk2
|
APN |
11 |
61,672,465 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02185:Ulk2
|
APN |
11 |
61,672,886 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03036:Ulk2
|
APN |
11 |
61,725,660 (GRCm39) |
missense |
probably damaging |
1.00 |
BB007:Ulk2
|
UTSW |
11 |
61,682,258 (GRCm39) |
critical splice donor site |
probably null |
|
BB009:Ulk2
|
UTSW |
11 |
61,698,916 (GRCm39) |
missense |
probably benign |
|
BB017:Ulk2
|
UTSW |
11 |
61,682,258 (GRCm39) |
critical splice donor site |
probably null |
|
BB019:Ulk2
|
UTSW |
11 |
61,698,916 (GRCm39) |
missense |
probably benign |
|
R0207:Ulk2
|
UTSW |
11 |
61,668,611 (GRCm39) |
missense |
probably benign |
0.42 |
R0362:Ulk2
|
UTSW |
11 |
61,678,412 (GRCm39) |
missense |
probably benign |
|
R0657:Ulk2
|
UTSW |
11 |
61,698,880 (GRCm39) |
splice site |
probably benign |
|
R1076:Ulk2
|
UTSW |
11 |
61,710,135 (GRCm39) |
missense |
probably damaging |
1.00 |
R1144:Ulk2
|
UTSW |
11 |
61,690,886 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1573:Ulk2
|
UTSW |
11 |
61,670,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R1583:Ulk2
|
UTSW |
11 |
61,674,371 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1619:Ulk2
|
UTSW |
11 |
61,672,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R1757:Ulk2
|
UTSW |
11 |
61,732,165 (GRCm39) |
splice site |
probably benign |
|
R1883:Ulk2
|
UTSW |
11 |
61,721,438 (GRCm39) |
missense |
probably damaging |
1.00 |
R1966:Ulk2
|
UTSW |
11 |
61,710,297 (GRCm39) |
splice site |
probably null |
|
R2177:Ulk2
|
UTSW |
11 |
61,682,335 (GRCm39) |
missense |
probably benign |
0.01 |
R2416:Ulk2
|
UTSW |
11 |
61,672,865 (GRCm39) |
missense |
probably damaging |
1.00 |
R2509:Ulk2
|
UTSW |
11 |
61,678,340 (GRCm39) |
missense |
probably benign |
0.00 |
R2847:Ulk2
|
UTSW |
11 |
61,715,555 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4736:Ulk2
|
UTSW |
11 |
61,724,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R4997:Ulk2
|
UTSW |
11 |
61,689,982 (GRCm39) |
missense |
probably benign |
0.00 |
R5081:Ulk2
|
UTSW |
11 |
61,694,488 (GRCm39) |
missense |
probably damaging |
1.00 |
R5190:Ulk2
|
UTSW |
11 |
61,672,537 (GRCm39) |
missense |
probably benign |
|
R5346:Ulk2
|
UTSW |
11 |
61,725,740 (GRCm39) |
missense |
probably damaging |
1.00 |
R5348:Ulk2
|
UTSW |
11 |
61,674,439 (GRCm39) |
missense |
probably benign |
|
R5520:Ulk2
|
UTSW |
11 |
61,698,970 (GRCm39) |
missense |
probably damaging |
1.00 |
R5954:Ulk2
|
UTSW |
11 |
61,694,622 (GRCm39) |
splice site |
probably benign |
|
R6153:Ulk2
|
UTSW |
11 |
61,672,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R6223:Ulk2
|
UTSW |
11 |
61,678,330 (GRCm39) |
nonsense |
probably null |
|
R7204:Ulk2
|
UTSW |
11 |
61,674,457 (GRCm39) |
missense |
probably benign |
0.11 |
R7205:Ulk2
|
UTSW |
11 |
61,725,657 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7259:Ulk2
|
UTSW |
11 |
61,672,909 (GRCm39) |
missense |
probably damaging |
1.00 |
R7353:Ulk2
|
UTSW |
11 |
61,710,174 (GRCm39) |
missense |
probably damaging |
1.00 |
R7734:Ulk2
|
UTSW |
11 |
61,744,127 (GRCm39) |
nonsense |
probably null |
|
R7797:Ulk2
|
UTSW |
11 |
61,672,928 (GRCm39) |
missense |
probably benign |
0.06 |
R7808:Ulk2
|
UTSW |
11 |
61,745,378 (GRCm39) |
missense |
probably damaging |
1.00 |
R7930:Ulk2
|
UTSW |
11 |
61,682,258 (GRCm39) |
critical splice donor site |
probably null |
|
R7932:Ulk2
|
UTSW |
11 |
61,698,916 (GRCm39) |
missense |
probably benign |
|
R8882:Ulk2
|
UTSW |
11 |
61,698,887 (GRCm39) |
critical splice donor site |
probably null |
|
R8909:Ulk2
|
UTSW |
11 |
61,690,380 (GRCm39) |
missense |
probably benign |
|
R9704:Ulk2
|
UTSW |
11 |
61,716,694 (GRCm39) |
missense |
probably damaging |
1.00 |
X0028:Ulk2
|
UTSW |
11 |
61,690,394 (GRCm39) |
missense |
probably benign |
0.00 |
|