Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8b |
A |
T |
11: 109,871,708 (GRCm39) |
M90K |
probably damaging |
Het |
Actn2 |
T |
C |
13: 12,303,516 (GRCm39) |
D428G |
probably damaging |
Het |
Arrb1 |
T |
C |
7: 99,243,836 (GRCm39) |
V262A |
probably damaging |
Het |
Bok |
A |
G |
1: 93,622,661 (GRCm39) |
I102V |
|
Het |
C87436 |
T |
A |
6: 86,439,567 (GRCm39) |
F419L |
probably damaging |
Het |
Capn15 |
A |
G |
17: 26,192,141 (GRCm39) |
C34R |
probably benign |
Het |
Ccdc8 |
T |
A |
7: 16,728,800 (GRCm39) |
Y96* |
probably null |
Het |
Cd274 |
T |
A |
19: 29,357,771 (GRCm39) |
C154* |
probably null |
Het |
Cfap251 |
A |
G |
5: 123,418,082 (GRCm39) |
|
probably benign |
Het |
Ckap4 |
A |
T |
10: 84,369,402 (GRCm39) |
L110Q |
probably damaging |
Het |
Col26a1 |
A |
T |
5: 136,777,202 (GRCm39) |
D335E |
probably benign |
Het |
Crybg1 |
C |
T |
10: 43,874,844 (GRCm39) |
V755I |
probably benign |
Het |
Dhx38 |
A |
T |
8: 110,282,783 (GRCm39) |
Y628N |
probably damaging |
Het |
Dnah12 |
A |
T |
14: 26,492,325 (GRCm39) |
K1155M |
probably benign |
Het |
Ei24 |
A |
G |
9: 36,697,270 (GRCm39) |
F153L |
probably damaging |
Het |
Erg |
T |
A |
16: 95,178,188 (GRCm39) |
E246D |
probably benign |
Het |
Exoc6b |
T |
C |
6: 84,982,000 (GRCm39) |
N99D |
possibly damaging |
Het |
Fam222b |
G |
T |
11: 78,046,020 (GRCm39) |
R527L |
probably damaging |
Het |
Fam83h |
T |
C |
15: 75,875,135 (GRCm39) |
Y734C |
probably damaging |
Het |
Fbxo43 |
T |
C |
15: 36,162,619 (GRCm39) |
E196G |
possibly damaging |
Het |
Gata5 |
G |
A |
2: 179,976,131 (GRCm39) |
P11L |
possibly damaging |
Het |
Gbp3 |
A |
T |
3: 142,271,048 (GRCm39) |
S151C |
probably benign |
Het |
Gli3 |
T |
C |
13: 15,901,320 (GRCm39) |
L1569P |
probably damaging |
Het |
Helz |
G |
A |
11: 107,523,041 (GRCm39) |
V742M |
probably damaging |
Het |
Ifi27l2b |
A |
T |
12: 103,418,114 (GRCm39) |
N175K |
unknown |
Het |
Itga1 |
A |
T |
13: 115,185,856 (GRCm39) |
Y49N |
probably damaging |
Het |
Kcnk2 |
T |
C |
1: 188,991,072 (GRCm39) |
T167A |
probably damaging |
Het |
Kirrel2 |
T |
A |
7: 30,147,642 (GRCm39) |
T669S |
probably benign |
Het |
Krt9 |
TCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCC |
TCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCC |
11: 100,079,903 (GRCm39) |
|
probably benign |
Het |
Lrit2 |
A |
T |
14: 36,790,812 (GRCm39) |
T164S |
possibly damaging |
Het |
Lrriq1 |
A |
G |
10: 103,051,864 (GRCm39) |
V296A |
probably damaging |
Het |
Malsu1 |
C |
T |
6: 49,050,731 (GRCm39) |
|
probably benign |
Het |
Moxd1 |
G |
A |
10: 24,155,762 (GRCm39) |
V289I |
probably damaging |
Het |
Nfs1 |
C |
T |
2: 155,968,934 (GRCm39) |
G380E |
probably damaging |
Het |
Nol4l |
C |
A |
2: 153,312,630 (GRCm39) |
R226L |
probably damaging |
Het |
Nsmaf |
CAAACTTTTAAACTT |
CAAACTT |
4: 6,416,543 (GRCm39) |
|
probably null |
Het |
Nup98 |
T |
A |
7: 101,844,173 (GRCm39) |
N54I |
probably damaging |
Het |
Or7g21 |
C |
T |
9: 19,032,890 (GRCm39) |
P210L |
probably benign |
Het |
Or8g22 |
A |
T |
9: 38,958,026 (GRCm39) |
C230S |
probably benign |
Het |
Or8g53 |
A |
G |
9: 39,683,514 (GRCm39) |
I194T |
|
Het |
Otoa |
T |
A |
7: 120,739,055 (GRCm39) |
F755I |
probably benign |
Het |
P4htm |
A |
T |
9: 108,460,911 (GRCm39) |
M187K |
probably benign |
Het |
Phldb3 |
C |
T |
7: 24,323,727 (GRCm39) |
R453C |
probably benign |
Het |
Pkd1l1 |
C |
T |
11: 8,922,986 (GRCm39) |
A94T |
|
Het |
Pkp1 |
A |
G |
1: 135,805,429 (GRCm39) |
F669S |
probably benign |
Het |
Prl8a2 |
C |
G |
13: 27,536,793 (GRCm39) |
Y138* |
probably null |
Het |
Prl8a2 |
T |
A |
13: 27,536,794 (GRCm39) |
Y139N |
probably benign |
Het |
Rtn4r |
T |
A |
16: 17,969,068 (GRCm39) |
N165K |
probably benign |
Het |
Scaper |
G |
T |
9: 55,669,616 (GRCm39) |
D353E |
probably damaging |
Het |
Scn4a |
G |
T |
11: 106,211,000 (GRCm39) |
D1672E |
probably damaging |
Het |
She |
A |
G |
3: 89,739,078 (GRCm39) |
S90G |
probably benign |
Het |
Shmt2 |
A |
T |
10: 127,355,962 (GRCm39) |
D130E |
possibly damaging |
Het |
Slc2a12 |
T |
A |
10: 22,569,923 (GRCm39) |
I538K |
possibly damaging |
Het |
Snx29 |
T |
A |
16: 11,478,435 (GRCm39) |
W322R |
probably damaging |
Het |
Spp1 |
A |
G |
5: 104,588,387 (GRCm39) |
D263G |
probably benign |
Het |
Srek1ip1 |
T |
C |
13: 104,973,964 (GRCm39) |
S124P |
possibly damaging |
Het |
Tcp10b |
C |
T |
17: 13,280,656 (GRCm39) |
|
probably benign |
Het |
Thap12 |
T |
C |
7: 98,364,600 (GRCm39) |
F256S |
probably damaging |
Het |
Tpte |
T |
C |
8: 22,845,497 (GRCm39) |
Y516H |
|
Het |
Trem1 |
C |
A |
17: 48,544,271 (GRCm39) |
Q99K |
possibly damaging |
Het |
Umodl1 |
C |
T |
17: 31,178,147 (GRCm39) |
P41L |
probably benign |
Het |
Zfand1 |
A |
T |
3: 10,406,148 (GRCm39) |
M181K |
probably damaging |
Het |
Zfp292 |
T |
C |
4: 34,809,228 (GRCm39) |
E1277G |
possibly damaging |
Het |
Zfp458 |
G |
T |
13: 67,405,696 (GRCm39) |
P248T |
probably damaging |
Het |
Zfp667 |
T |
A |
7: 6,308,322 (GRCm39) |
M330K |
probably benign |
Het |
Zfp827 |
A |
G |
8: 79,917,107 (GRCm39) |
T561A |
|
Het |
Zfp947 |
C |
T |
17: 22,364,855 (GRCm39) |
G273D |
probably benign |
Het |
|
Other mutations in Upp2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00863:Upp2
|
APN |
2 |
58,680,076 (GRCm39) |
missense |
probably benign |
0.43 |
IGL01716:Upp2
|
APN |
2 |
58,680,058 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02069:Upp2
|
APN |
2 |
58,661,429 (GRCm39) |
splice site |
probably benign |
|
IGL02349:Upp2
|
APN |
2 |
58,667,898 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03072:Upp2
|
APN |
2 |
58,645,435 (GRCm39) |
critical splice donor site |
probably null |
|
R0815:Upp2
|
UTSW |
2 |
58,661,568 (GRCm39) |
missense |
probably benign |
0.00 |
R1164:Upp2
|
UTSW |
2 |
58,653,716 (GRCm39) |
missense |
probably damaging |
1.00 |
R1400:Upp2
|
UTSW |
2 |
58,680,118 (GRCm39) |
missense |
probably damaging |
1.00 |
R1553:Upp2
|
UTSW |
2 |
58,680,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R1581:Upp2
|
UTSW |
2 |
58,664,177 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1674:Upp2
|
UTSW |
2 |
58,680,076 (GRCm39) |
missense |
probably benign |
0.43 |
R1702:Upp2
|
UTSW |
2 |
58,661,562 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1902:Upp2
|
UTSW |
2 |
58,661,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R2351:Upp2
|
UTSW |
2 |
58,653,674 (GRCm39) |
splice site |
probably null |
|
R3011:Upp2
|
UTSW |
2 |
58,680,107 (GRCm39) |
missense |
probably damaging |
0.97 |
R3622:Upp2
|
UTSW |
2 |
58,680,128 (GRCm39) |
missense |
possibly damaging |
0.83 |
R3623:Upp2
|
UTSW |
2 |
58,680,128 (GRCm39) |
missense |
possibly damaging |
0.83 |
R3731:Upp2
|
UTSW |
2 |
58,645,379 (GRCm39) |
missense |
probably benign |
0.02 |
R4257:Upp2
|
UTSW |
2 |
58,670,106 (GRCm39) |
missense |
probably damaging |
1.00 |
R4296:Upp2
|
UTSW |
2 |
58,668,021 (GRCm39) |
missense |
probably damaging |
1.00 |
R4768:Upp2
|
UTSW |
2 |
58,667,907 (GRCm39) |
missense |
probably damaging |
0.99 |
R5116:Upp2
|
UTSW |
2 |
58,661,554 (GRCm39) |
missense |
probably damaging |
1.00 |
R5638:Upp2
|
UTSW |
2 |
58,680,107 (GRCm39) |
missense |
probably damaging |
0.97 |
R7100:Upp2
|
UTSW |
2 |
58,681,817 (GRCm39) |
missense |
probably benign |
|
R7421:Upp2
|
UTSW |
2 |
58,661,586 (GRCm39) |
missense |
possibly damaging |
0.49 |
R7727:Upp2
|
UTSW |
2 |
58,664,160 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7840:Upp2
|
UTSW |
2 |
58,664,127 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8033:Upp2
|
UTSW |
2 |
58,670,071 (GRCm39) |
missense |
probably damaging |
1.00 |
R8359:Upp2
|
UTSW |
2 |
58,667,955 (GRCm39) |
missense |
probably benign |
0.05 |
R8461:Upp2
|
UTSW |
2 |
58,670,068 (GRCm39) |
missense |
probably benign |
0.02 |
R8510:Upp2
|
UTSW |
2 |
58,670,118 (GRCm39) |
missense |
probably damaging |
1.00 |
R8956:Upp2
|
UTSW |
2 |
58,457,454 (GRCm39) |
unclassified |
probably benign |
|
R9086:Upp2
|
UTSW |
2 |
58,680,177 (GRCm39) |
nonsense |
probably null |
|
R9130:Upp2
|
UTSW |
2 |
58,668,020 (GRCm39) |
missense |
probably damaging |
1.00 |
R9159:Upp2
|
UTSW |
2 |
58,667,996 (GRCm39) |
missense |
probably damaging |
1.00 |
R9209:Upp2
|
UTSW |
2 |
58,668,022 (GRCm39) |
nonsense |
probably null |
|
R9215:Upp2
|
UTSW |
2 |
58,670,065 (GRCm39) |
missense |
probably damaging |
1.00 |
R9293:Upp2
|
UTSW |
2 |
58,457,443 (GRCm39) |
missense |
unknown |
|
R9343:Upp2
|
UTSW |
2 |
58,645,339 (GRCm39) |
start gained |
probably benign |
|
Z1177:Upp2
|
UTSW |
2 |
58,670,074 (GRCm39) |
missense |
probably damaging |
1.00 |
|