Other mutations in this stock |
Total: 87 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700102P08Rik |
T |
A |
9: 108,270,809 (GRCm39) |
D124E |
possibly damaging |
Het |
Aarsd1 |
T |
C |
11: 101,302,227 (GRCm39) |
T278A |
probably benign |
Het |
Acacb |
T |
A |
5: 114,357,020 (GRCm39) |
L1317Q |
probably damaging |
Het |
Acsf3 |
T |
C |
8: 123,510,741 (GRCm39) |
V293A |
probably damaging |
Het |
Adora3 |
A |
C |
3: 105,812,152 (GRCm39) |
N13H |
possibly damaging |
Het |
Aen |
A |
T |
7: 78,557,073 (GRCm39) |
D307V |
probably damaging |
Het |
Ahnak |
G |
A |
19: 8,993,343 (GRCm39) |
D4876N |
probably damaging |
Het |
Ap2b1 |
T |
A |
11: 83,281,561 (GRCm39) |
N822K |
probably damaging |
Het |
Arhgdia |
T |
C |
11: 120,470,244 (GRCm39) |
D143G |
probably benign |
Het |
Bcl9 |
G |
T |
3: 97,122,713 (GRCm39) |
R29S |
probably benign |
Het |
Bhmt2 |
T |
A |
13: 93,798,998 (GRCm39) |
K274N |
probably benign |
Het |
Brip1 |
C |
A |
11: 86,029,641 (GRCm39) |
G631V |
probably damaging |
Het |
Cacna1i |
A |
G |
15: 80,243,145 (GRCm39) |
E434G |
probably damaging |
Het |
Ccdc81 |
T |
C |
7: 89,515,819 (GRCm39) |
E620G |
possibly damaging |
Het |
Cdhr18 |
A |
C |
14: 13,828,607 (GRCm38) |
Y718D |
probably damaging |
Het |
Cfap299 |
A |
G |
5: 98,949,690 (GRCm39) |
N208S |
probably benign |
Het |
Cit |
A |
G |
5: 116,071,545 (GRCm39) |
Y584C |
probably damaging |
Het |
Crebl2 |
T |
C |
6: 134,828,059 (GRCm39) |
M77T |
probably benign |
Het |
Dach2 |
G |
A |
X: 112,208,305 (GRCm39) |
G61D |
probably benign |
Het |
Ddx4 |
A |
T |
13: 112,759,199 (GRCm39) |
D237E |
probably damaging |
Het |
Dgcr8 |
A |
G |
16: 18,096,218 (GRCm39) |
I490T |
possibly damaging |
Het |
Dmxl1 |
G |
A |
18: 49,992,202 (GRCm39) |
R316H |
probably benign |
Het |
Dnah17 |
T |
A |
11: 117,998,987 (GRCm39) |
I929F |
possibly damaging |
Het |
Eif3f |
A |
G |
7: 108,539,958 (GRCm39) |
T289A |
probably benign |
Het |
Ercc5 |
A |
T |
1: 44,215,136 (GRCm39) |
K890* |
probably null |
Het |
Esrp2 |
A |
T |
8: 106,860,489 (GRCm39) |
V247E |
probably damaging |
Het |
Evpl |
C |
T |
11: 116,118,402 (GRCm39) |
G735E |
probably damaging |
Het |
Ezhip |
GTCATCATCATCATC |
GTCATCATCATCATCATC |
X: 5,994,645 (GRCm39) |
|
probably benign |
Het |
Fbxl21 |
A |
G |
13: 56,674,906 (GRCm39) |
I60V |
probably benign |
Het |
Frem3 |
A |
G |
8: 81,340,514 (GRCm39) |
I936V |
probably benign |
Het |
Fsd1l |
T |
C |
4: 53,696,984 (GRCm39) |
|
probably null |
Het |
Gad1-ps |
T |
C |
10: 99,281,444 (GRCm39) |
|
noncoding transcript |
Het |
Gbp2b |
A |
G |
3: 142,314,063 (GRCm39) |
T448A |
probably benign |
Het |
Gfus |
G |
T |
15: 75,798,838 (GRCm39) |
T123N |
possibly damaging |
Het |
Gmppa |
T |
C |
1: 75,419,152 (GRCm39) |
V353A |
probably damaging |
Het |
Hmcn1 |
T |
C |
1: 150,453,046 (GRCm39) |
E5423G |
probably benign |
Het |
Hmgxb3 |
A |
G |
18: 61,270,473 (GRCm39) |
|
probably null |
Het |
Krt12 |
T |
C |
11: 99,309,402 (GRCm39) |
D286G |
probably damaging |
Het |
Krt75 |
A |
T |
15: 101,479,532 (GRCm39) |
M266K |
probably damaging |
Het |
Ksr1 |
C |
A |
11: 78,911,204 (GRCm39) |
V11F |
probably null |
Het |
Lag3 |
T |
C |
6: 124,886,402 (GRCm39) |
N184D |
probably damaging |
Het |
Lsm10 |
C |
G |
4: 125,991,741 (GRCm39) |
D32E |
probably benign |
Het |
Mettl5 |
A |
G |
2: 69,711,149 (GRCm39) |
V123A |
probably damaging |
Het |
Mfrp |
A |
G |
9: 44,014,785 (GRCm39) |
D274G |
possibly damaging |
Het |
Mgat3 |
A |
G |
15: 80,095,820 (GRCm39) |
I216V |
probably benign |
Het |
Mkrn3 |
G |
A |
7: 62,068,486 (GRCm39) |
A435V |
probably benign |
Het |
Mob3a |
G |
A |
10: 80,527,068 (GRCm39) |
Q86* |
probably null |
Het |
Mplkipl1 |
A |
G |
19: 61,164,136 (GRCm39) |
F100L |
probably damaging |
Het |
Mttp |
A |
T |
3: 137,798,376 (GRCm39) |
V840D |
probably damaging |
Het |
Nadk2 |
A |
C |
15: 9,103,446 (GRCm39) |
N308H |
possibly damaging |
Het |
Ncoa7 |
T |
C |
10: 30,524,448 (GRCm39) |
N823S |
possibly damaging |
Het |
Nlk |
T |
A |
11: 78,477,754 (GRCm39) |
I330F |
probably damaging |
Het |
Ofcc1 |
T |
C |
13: 40,360,100 (GRCm39) |
S310G |
possibly damaging |
Het |
Or5p57 |
T |
C |
7: 107,665,985 (GRCm39) |
N7D |
probably benign |
Het |
Or5p73 |
A |
T |
7: 108,064,947 (GRCm39) |
M139L |
probably benign |
Het |
Orc2 |
T |
C |
1: 58,510,247 (GRCm39) |
|
probably null |
Het |
Orc3 |
A |
G |
4: 34,584,829 (GRCm39) |
Y459H |
probably damaging |
Het |
Pah |
T |
A |
10: 87,364,190 (GRCm39) |
N30K |
possibly damaging |
Het |
Pcsk4 |
T |
C |
10: 80,164,794 (GRCm39) |
K74E |
probably benign |
Het |
Pdlim7 |
C |
T |
13: 55,653,981 (GRCm39) |
G212D |
probably benign |
Het |
Pfkm |
A |
G |
15: 98,025,627 (GRCm39) |
N547S |
probably damaging |
Het |
Por |
A |
G |
5: 135,763,128 (GRCm39) |
E546G |
probably damaging |
Het |
Ppp1r13l |
T |
C |
7: 19,111,496 (GRCm39) |
S774P |
probably damaging |
Het |
Prdm1 |
T |
A |
10: 44,315,754 (GRCm39) |
D794V |
probably damaging |
Het |
Prdx5 |
A |
G |
19: 6,885,558 (GRCm39) |
I32T |
probably benign |
Het |
Prlhr |
G |
T |
19: 60,455,932 (GRCm39) |
C211* |
probably null |
Het |
Ripk3 |
C |
T |
14: 56,025,694 (GRCm39) |
|
probably null |
Het |
Rmnd5b |
G |
A |
11: 51,518,465 (GRCm39) |
A137V |
probably damaging |
Het |
Rwdd2b |
A |
T |
16: 87,234,013 (GRCm39) |
F72I |
probably benign |
Het |
Scml4 |
A |
G |
10: 42,788,223 (GRCm39) |
Y51C |
probably damaging |
Het |
Septin1 |
A |
G |
7: 126,813,937 (GRCm39) |
|
probably benign |
Het |
Serpinb9h |
C |
T |
13: 33,588,203 (GRCm39) |
R263C |
possibly damaging |
Het |
Slc30a10 |
T |
A |
1: 185,195,061 (GRCm39) |
I291N |
probably damaging |
Het |
Slc7a9 |
T |
G |
7: 35,152,827 (GRCm39) |
C20W |
possibly damaging |
Het |
Slc7a9 |
G |
C |
7: 35,152,828 (GRCm39) |
A21P |
probably damaging |
Het |
Slco1b2 |
A |
T |
6: 141,628,951 (GRCm39) |
Y551F |
probably damaging |
Het |
Sra1 |
T |
C |
18: 36,801,830 (GRCm39) |
M87V |
probably benign |
Het |
Syvn1 |
T |
C |
19: 6,099,257 (GRCm39) |
S169P |
possibly damaging |
Het |
Tmc7 |
A |
T |
7: 118,160,310 (GRCm39) |
F176I |
possibly damaging |
Het |
Tmem62 |
A |
T |
2: 120,817,151 (GRCm39) |
I236F |
probably damaging |
Het |
Trip4 |
T |
A |
9: 65,782,163 (GRCm39) |
I190F |
probably null |
Het |
Trpa1 |
T |
C |
1: 14,959,649 (GRCm39) |
D679G |
probably benign |
Het |
Ttc22 |
T |
A |
4: 106,494,063 (GRCm39) |
|
probably null |
Het |
Ttn |
A |
T |
2: 76,641,587 (GRCm39) |
L5176Q |
possibly damaging |
Het |
Tyrp1 |
T |
A |
4: 80,759,043 (GRCm39) |
|
probably null |
Het |
Usp36 |
A |
T |
11: 118,163,784 (GRCm39) |
Y255N |
probably damaging |
Het |
Zfp944 |
A |
T |
17: 22,558,960 (GRCm39) |
Y96N |
probably benign |
Het |
|
Other mutations in Ubap2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01011:Ubap2
|
APN |
4 |
41,195,328 (GRCm39) |
splice site |
probably benign |
|
IGL01109:Ubap2
|
APN |
4 |
41,195,155 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01354:Ubap2
|
APN |
4 |
41,207,005 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01563:Ubap2
|
APN |
4 |
41,195,998 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01602:Ubap2
|
APN |
4 |
41,227,237 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01605:Ubap2
|
APN |
4 |
41,227,237 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01688:Ubap2
|
APN |
4 |
41,226,308 (GRCm39) |
missense |
probably benign |
|
IGL01733:Ubap2
|
APN |
4 |
41,195,862 (GRCm39) |
unclassified |
probably benign |
|
IGL01896:Ubap2
|
APN |
4 |
41,202,362 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL01942:Ubap2
|
APN |
4 |
41,251,608 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02095:Ubap2
|
APN |
4 |
41,229,709 (GRCm39) |
missense |
probably benign |
|
R0608:Ubap2
|
UTSW |
4 |
41,218,319 (GRCm39) |
missense |
probably benign |
0.10 |
R0938:Ubap2
|
UTSW |
4 |
41,202,304 (GRCm39) |
missense |
probably damaging |
1.00 |
R1449:Ubap2
|
UTSW |
4 |
41,209,351 (GRCm39) |
critical splice donor site |
probably null |
|
R1484:Ubap2
|
UTSW |
4 |
41,235,593 (GRCm39) |
missense |
probably damaging |
1.00 |
R1548:Ubap2
|
UTSW |
4 |
41,199,872 (GRCm39) |
missense |
probably benign |
0.12 |
R1549:Ubap2
|
UTSW |
4 |
41,199,872 (GRCm39) |
missense |
probably benign |
0.12 |
R1604:Ubap2
|
UTSW |
4 |
41,199,872 (GRCm39) |
missense |
probably benign |
0.12 |
R1607:Ubap2
|
UTSW |
4 |
41,199,872 (GRCm39) |
missense |
probably benign |
0.12 |
R1739:Ubap2
|
UTSW |
4 |
41,206,849 (GRCm39) |
missense |
probably benign |
0.00 |
R1772:Ubap2
|
UTSW |
4 |
41,202,380 (GRCm39) |
missense |
probably benign |
0.02 |
R1862:Ubap2
|
UTSW |
4 |
41,221,607 (GRCm39) |
missense |
probably benign |
|
R1869:Ubap2
|
UTSW |
4 |
41,233,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R1887:Ubap2
|
UTSW |
4 |
41,199,872 (GRCm39) |
missense |
probably benign |
0.12 |
R2063:Ubap2
|
UTSW |
4 |
41,199,872 (GRCm39) |
missense |
probably benign |
0.12 |
R2064:Ubap2
|
UTSW |
4 |
41,199,872 (GRCm39) |
missense |
probably benign |
0.12 |
R2065:Ubap2
|
UTSW |
4 |
41,199,872 (GRCm39) |
missense |
probably benign |
0.12 |
R2066:Ubap2
|
UTSW |
4 |
41,199,872 (GRCm39) |
missense |
probably benign |
0.12 |
R2095:Ubap2
|
UTSW |
4 |
41,206,901 (GRCm39) |
missense |
possibly damaging |
0.68 |
R2214:Ubap2
|
UTSW |
4 |
41,199,714 (GRCm39) |
critical splice donor site |
probably null |
|
R2215:Ubap2
|
UTSW |
4 |
41,196,483 (GRCm39) |
splice site |
probably null |
|
R2318:Ubap2
|
UTSW |
4 |
41,251,542 (GRCm39) |
missense |
probably damaging |
0.99 |
R3755:Ubap2
|
UTSW |
4 |
41,195,482 (GRCm39) |
missense |
probably damaging |
1.00 |
R4620:Ubap2
|
UTSW |
4 |
41,233,698 (GRCm39) |
missense |
probably damaging |
1.00 |
R4717:Ubap2
|
UTSW |
4 |
41,218,333 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4756:Ubap2
|
UTSW |
4 |
41,211,771 (GRCm39) |
missense |
probably damaging |
1.00 |
R4942:Ubap2
|
UTSW |
4 |
41,245,461 (GRCm39) |
intron |
probably benign |
|
R5344:Ubap2
|
UTSW |
4 |
41,251,578 (GRCm39) |
missense |
possibly damaging |
0.46 |
R5763:Ubap2
|
UTSW |
4 |
41,195,809 (GRCm39) |
missense |
probably damaging |
1.00 |
R5851:Ubap2
|
UTSW |
4 |
41,206,268 (GRCm39) |
nonsense |
probably null |
|
R5951:Ubap2
|
UTSW |
4 |
41,205,753 (GRCm39) |
splice site |
probably null |
|
R6178:Ubap2
|
UTSW |
4 |
41,206,981 (GRCm39) |
missense |
probably benign |
|
R6489:Ubap2
|
UTSW |
4 |
41,203,574 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6520:Ubap2
|
UTSW |
4 |
41,195,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R6652:Ubap2
|
UTSW |
4 |
41,196,743 (GRCm39) |
missense |
possibly damaging |
0.68 |
R6702:Ubap2
|
UTSW |
4 |
41,227,210 (GRCm39) |
small insertion |
probably benign |
|
R6736:Ubap2
|
UTSW |
4 |
41,227,224 (GRCm39) |
small insertion |
probably benign |
|
R6736:Ubap2
|
UTSW |
4 |
41,227,210 (GRCm39) |
small insertion |
probably benign |
|
R6860:Ubap2
|
UTSW |
4 |
41,233,631 (GRCm39) |
missense |
probably damaging |
1.00 |
R7007:Ubap2
|
UTSW |
4 |
41,206,221 (GRCm39) |
missense |
probably damaging |
0.97 |
R7048:Ubap2
|
UTSW |
4 |
41,196,033 (GRCm39) |
missense |
possibly damaging |
0.49 |
R7121:Ubap2
|
UTSW |
4 |
41,205,550 (GRCm39) |
missense |
probably benign |
0.00 |
R7371:Ubap2
|
UTSW |
4 |
41,195,779 (GRCm39) |
missense |
probably benign |
0.16 |
R7378:Ubap2
|
UTSW |
4 |
41,235,515 (GRCm39) |
critical splice donor site |
probably null |
|
R7695:Ubap2
|
UTSW |
4 |
41,211,740 (GRCm39) |
missense |
probably damaging |
0.98 |
R7811:Ubap2
|
UTSW |
4 |
41,211,710 (GRCm39) |
missense |
probably benign |
0.22 |
R7828:Ubap2
|
UTSW |
4 |
41,221,615 (GRCm39) |
missense |
probably benign |
0.00 |
R7838:Ubap2
|
UTSW |
4 |
41,233,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R8016:Ubap2
|
UTSW |
4 |
41,195,201 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8790:Ubap2
|
UTSW |
4 |
41,209,351 (GRCm39) |
critical splice donor site |
probably null |
|
R8817:Ubap2
|
UTSW |
4 |
41,223,425 (GRCm39) |
missense |
possibly damaging |
0.66 |
R9379:Ubap2
|
UTSW |
4 |
41,216,630 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9470:Ubap2
|
UTSW |
4 |
41,195,434 (GRCm39) |
missense |
possibly damaging |
0.64 |
R9536:Ubap2
|
UTSW |
4 |
41,195,661 (GRCm39) |
missense |
probably benign |
0.01 |
X0061:Ubap2
|
UTSW |
4 |
41,196,507 (GRCm39) |
missense |
probably damaging |
1.00 |
|