Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930550C14Rik |
A |
T |
9: 53,339,456 (GRCm39) |
E106D |
probably damaging |
Het |
A830018L16Rik |
A |
T |
1: 11,868,718 (GRCm39) |
N333Y |
probably damaging |
Het |
Abca4 |
T |
A |
3: 121,917,309 (GRCm39) |
M1007K |
possibly damaging |
Het |
Accsl |
T |
A |
2: 93,687,343 (GRCm39) |
I495F |
probably damaging |
Het |
Acsl3 |
T |
C |
1: 78,674,182 (GRCm39) |
S373P |
possibly damaging |
Het |
Akap11 |
G |
A |
14: 78,752,336 (GRCm39) |
T179I |
probably damaging |
Het |
Ankmy1 |
T |
C |
1: 92,816,187 (GRCm39) |
K309R |
possibly damaging |
Het |
Apaf1 |
A |
T |
10: 90,859,673 (GRCm39) |
I824N |
probably damaging |
Het |
Apc2 |
T |
A |
10: 80,148,488 (GRCm39) |
C1152S |
probably damaging |
Het |
Arhgap17 |
C |
A |
7: 122,899,727 (GRCm39) |
W409L |
probably damaging |
Het |
Arhgef15 |
T |
C |
11: 68,845,796 (GRCm39) |
I19V |
unknown |
Het |
Arnt |
C |
A |
3: 95,397,936 (GRCm39) |
P573H |
probably damaging |
Het |
Arvcf |
G |
A |
16: 18,223,882 (GRCm39) |
G932R |
probably damaging |
Het |
Atg4a-ps |
C |
T |
3: 103,553,044 (GRCm39) |
W99* |
probably null |
Het |
Atp13a5 |
T |
A |
16: 29,056,004 (GRCm39) |
D1052V |
probably benign |
Het |
Atp2b4 |
T |
C |
1: 133,642,797 (GRCm39) |
T1103A |
probably damaging |
Het |
B4galnt4 |
C |
A |
7: 140,647,335 (GRCm39) |
Q362K |
possibly damaging |
Het |
Cd320 |
T |
A |
17: 34,066,491 (GRCm39) |
N90K |
probably benign |
Het |
Cep170b |
A |
T |
12: 112,698,502 (GRCm39) |
I87F |
probably damaging |
Het |
Coq3 |
T |
G |
4: 21,900,486 (GRCm39) |
C238G |
probably benign |
Het |
Cpa5 |
A |
T |
6: 30,614,044 (GRCm39) |
Q62L |
probably benign |
Het |
Ctsg |
A |
T |
14: 56,339,110 (GRCm39) |
C49* |
probably null |
Het |
Cul9 |
T |
C |
17: 46,819,489 (GRCm39) |
T2000A |
probably damaging |
Het |
Dedd |
C |
T |
1: 171,167,790 (GRCm39) |
P155S |
probably benign |
Het |
Dnah1 |
A |
G |
14: 30,997,565 (GRCm39) |
S2598P |
probably damaging |
Het |
Dnah14 |
C |
T |
1: 181,433,459 (GRCm39) |
P379S |
possibly damaging |
Het |
Dync2h1 |
A |
T |
9: 7,165,703 (GRCm39) |
S519R |
probably benign |
Het |
Eea1 |
A |
G |
10: 95,874,660 (GRCm39) |
S1192G |
probably benign |
Het |
Eif5b |
T |
C |
1: 38,084,760 (GRCm39) |
I869T |
probably damaging |
Het |
Elavl4 |
C |
A |
4: 110,112,651 (GRCm39) |
|
probably benign |
Het |
Eml2 |
G |
A |
7: 18,935,088 (GRCm39) |
V432I |
probably damaging |
Het |
Ets2 |
G |
A |
16: 95,520,037 (GRCm39) |
R421H |
probably damaging |
Het |
Exoc3l2 |
G |
A |
7: 19,203,635 (GRCm39) |
A76T |
possibly damaging |
Het |
Fam89b |
T |
C |
19: 5,778,757 (GRCm39) |
Y144C |
probably damaging |
Het |
Greb1 |
T |
C |
12: 16,749,580 (GRCm39) |
E1082G |
probably damaging |
Het |
Gtf3a |
A |
T |
5: 146,890,798 (GRCm39) |
|
probably null |
Het |
Hoxc12 |
C |
A |
15: 102,845,524 (GRCm39) |
F79L |
possibly damaging |
Het |
Hspb8 |
G |
T |
5: 116,547,491 (GRCm39) |
L164I |
probably damaging |
Het |
Ina |
C |
T |
19: 47,003,564 (GRCm39) |
A124V |
probably benign |
Het |
Inhbb |
T |
A |
1: 119,345,411 (GRCm39) |
I293F |
probably damaging |
Het |
Itpr3 |
A |
G |
17: 27,314,449 (GRCm39) |
Y633C |
possibly damaging |
Het |
Jag2 |
C |
T |
12: 112,872,949 (GRCm39) |
V1102I |
probably benign |
Het |
Kalrn |
A |
T |
16: 33,796,361 (GRCm39) |
F1138Y |
probably benign |
Het |
Large2 |
T |
A |
2: 92,200,853 (GRCm39) |
|
probably benign |
Het |
Lats2 |
A |
G |
14: 57,959,966 (GRCm39) |
S177P |
probably benign |
Het |
Lims2 |
G |
A |
18: 32,087,515 (GRCm39) |
R124H |
possibly damaging |
Het |
Lrp2 |
T |
A |
2: 69,313,787 (GRCm39) |
T2315S |
probably benign |
Het |
Lrrc4c |
A |
C |
2: 97,459,391 (GRCm39) |
T6P |
probably benign |
Het |
Lrrk2 |
T |
C |
15: 91,626,469 (GRCm39) |
L1171S |
possibly damaging |
Het |
Man2b2 |
A |
T |
5: 36,978,378 (GRCm39) |
M302K |
probably damaging |
Het |
Mocos |
G |
A |
18: 24,834,542 (GRCm39) |
G860R |
possibly damaging |
Het |
Mylk3 |
T |
A |
8: 86,085,571 (GRCm39) |
D258V |
possibly damaging |
Het |
Nkx1-2 |
C |
T |
7: 132,201,240 (GRCm39) |
D6N |
probably damaging |
Het |
Nrp2 |
A |
G |
1: 62,758,176 (GRCm39) |
N54S |
possibly damaging |
Het |
Nt5el |
T |
C |
13: 105,256,473 (GRCm39) |
I514T |
possibly damaging |
Het |
Or2d2 |
A |
G |
7: 106,727,848 (GRCm39) |
F251L |
probably benign |
Het |
Pacsin1 |
A |
T |
17: 27,926,879 (GRCm39) |
T195S |
probably benign |
Het |
Pank4 |
T |
C |
4: 155,056,693 (GRCm39) |
|
probably null |
Het |
Pdgfra |
A |
T |
5: 75,327,180 (GRCm39) |
M126L |
probably benign |
Het |
Podxl |
T |
A |
6: 31,505,432 (GRCm39) |
T204S |
probably benign |
Het |
Pole |
G |
A |
5: 110,484,240 (GRCm39) |
D2175N |
probably damaging |
Het |
Pramel16 |
C |
T |
4: 143,677,267 (GRCm39) |
G104E |
probably benign |
Het |
Prkdc |
A |
G |
16: 15,587,749 (GRCm39) |
K2545E |
probably benign |
Het |
Prodh |
T |
C |
16: 17,897,849 (GRCm39) |
I183V |
probably benign |
Het |
Ptch1 |
T |
C |
13: 63,691,422 (GRCm39) |
D277G |
possibly damaging |
Het |
Rapgef5 |
G |
A |
12: 117,684,988 (GRCm39) |
V246M |
probably damaging |
Het |
Rubcnl |
A |
G |
14: 75,269,834 (GRCm39) |
N164S |
probably benign |
Het |
Samd4 |
A |
T |
14: 47,290,419 (GRCm39) |
L175F |
probably damaging |
Het |
Scart1 |
G |
A |
7: 139,808,642 (GRCm39) |
G851D |
probably damaging |
Het |
Scimp |
C |
A |
11: 70,688,893 (GRCm39) |
W41L |
possibly damaging |
Het |
Scn3a |
T |
A |
2: 65,291,843 (GRCm39) |
K1634N |
possibly damaging |
Het |
Spta1 |
A |
G |
1: 174,030,888 (GRCm39) |
R957G |
probably benign |
Het |
Sptlc3 |
T |
A |
2: 139,478,692 (GRCm39) |
N550K |
probably benign |
Het |
Srebf1 |
T |
C |
11: 60,094,361 (GRCm39) |
N609D |
probably null |
Het |
Styxl1 |
A |
T |
5: 135,776,664 (GRCm39) |
L164H |
probably benign |
Het |
Synpo2l |
A |
T |
14: 20,710,702 (GRCm39) |
D865E |
probably damaging |
Het |
Tnfsf15 |
T |
C |
4: 63,663,267 (GRCm39) |
M19V |
probably damaging |
Het |
Trappc8 |
G |
C |
18: 20,970,132 (GRCm39) |
R953G |
probably benign |
Het |
Trav13-1 |
A |
G |
14: 53,782,800 (GRCm39) |
N50S |
probably benign |
Het |
Trim12a |
T |
C |
7: 103,955,241 (GRCm39) |
K161E |
probably benign |
Het |
Vipr1 |
C |
A |
9: 121,493,640 (GRCm39) |
N230K |
probably damaging |
Het |
Xirp1 |
A |
T |
9: 119,847,557 (GRCm39) |
V3E |
probably damaging |
Het |
Zfp768 |
A |
G |
7: 126,943,892 (GRCm39) |
F82L |
probably benign |
Het |
|
Other mutations in Adam7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00667:Adam7
|
APN |
14 |
68,759,387 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL01418:Adam7
|
APN |
14 |
68,762,655 (GRCm39) |
missense |
probably benign |
|
IGL01934:Adam7
|
APN |
14 |
68,770,048 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02655:Adam7
|
APN |
14 |
68,754,060 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02669:Adam7
|
APN |
14 |
68,745,343 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4445001:Adam7
|
UTSW |
14 |
68,747,197 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0195:Adam7
|
UTSW |
14 |
68,765,076 (GRCm39) |
splice site |
probably benign |
|
R0277:Adam7
|
UTSW |
14 |
68,748,306 (GRCm39) |
splice site |
probably null |
|
R0362:Adam7
|
UTSW |
14 |
68,747,105 (GRCm39) |
splice site |
probably benign |
|
R0440:Adam7
|
UTSW |
14 |
68,748,305 (GRCm39) |
splice site |
probably null |
|
R0927:Adam7
|
UTSW |
14 |
68,754,133 (GRCm39) |
missense |
probably damaging |
1.00 |
R1172:Adam7
|
UTSW |
14 |
68,752,370 (GRCm39) |
missense |
probably damaging |
1.00 |
R1270:Adam7
|
UTSW |
14 |
68,765,118 (GRCm39) |
missense |
probably damaging |
0.98 |
R1299:Adam7
|
UTSW |
14 |
68,763,748 (GRCm39) |
splice site |
probably benign |
|
R1527:Adam7
|
UTSW |
14 |
68,738,970 (GRCm39) |
missense |
probably benign |
0.04 |
R1543:Adam7
|
UTSW |
14 |
68,759,371 (GRCm39) |
splice site |
probably benign |
|
R1731:Adam7
|
UTSW |
14 |
68,762,805 (GRCm39) |
missense |
probably damaging |
1.00 |
R1732:Adam7
|
UTSW |
14 |
68,735,899 (GRCm39) |
missense |
probably benign |
0.00 |
R1921:Adam7
|
UTSW |
14 |
68,750,074 (GRCm39) |
missense |
possibly damaging |
0.55 |
R2062:Adam7
|
UTSW |
14 |
68,742,610 (GRCm39) |
missense |
probably benign |
0.09 |
R2156:Adam7
|
UTSW |
14 |
68,748,792 (GRCm39) |
missense |
probably benign |
0.02 |
R2353:Adam7
|
UTSW |
14 |
68,742,537 (GRCm39) |
missense |
probably benign |
0.01 |
R2697:Adam7
|
UTSW |
14 |
68,752,232 (GRCm39) |
nonsense |
probably null |
|
R4080:Adam7
|
UTSW |
14 |
68,757,988 (GRCm39) |
missense |
probably benign |
0.05 |
R4775:Adam7
|
UTSW |
14 |
68,745,361 (GRCm39) |
missense |
probably benign |
0.41 |
R5202:Adam7
|
UTSW |
14 |
68,745,305 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6006:Adam7
|
UTSW |
14 |
68,748,845 (GRCm39) |
missense |
probably damaging |
1.00 |
R6087:Adam7
|
UTSW |
14 |
68,748,206 (GRCm39) |
missense |
probably damaging |
1.00 |
R6417:Adam7
|
UTSW |
14 |
68,742,070 (GRCm39) |
missense |
probably benign |
0.37 |
R6672:Adam7
|
UTSW |
14 |
68,742,151 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6756:Adam7
|
UTSW |
14 |
68,762,728 (GRCm39) |
missense |
probably benign |
0.00 |
R6777:Adam7
|
UTSW |
14 |
68,762,784 (GRCm39) |
missense |
probably damaging |
1.00 |
R6913:Adam7
|
UTSW |
14 |
68,771,100 (GRCm39) |
missense |
probably benign |
0.22 |
R7127:Adam7
|
UTSW |
14 |
68,752,218 (GRCm39) |
critical splice donor site |
probably null |
|
R7209:Adam7
|
UTSW |
14 |
68,767,268 (GRCm39) |
missense |
probably damaging |
1.00 |
R7399:Adam7
|
UTSW |
14 |
68,741,915 (GRCm39) |
splice site |
probably null |
|
R7675:Adam7
|
UTSW |
14 |
68,737,302 (GRCm39) |
missense |
probably benign |
0.07 |
R7788:Adam7
|
UTSW |
14 |
68,750,094 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7868:Adam7
|
UTSW |
14 |
68,770,090 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8135:Adam7
|
UTSW |
14 |
68,754,022 (GRCm39) |
missense |
probably damaging |
1.00 |
R8281:Adam7
|
UTSW |
14 |
68,745,334 (GRCm39) |
missense |
possibly damaging |
0.65 |
R8507:Adam7
|
UTSW |
14 |
68,763,773 (GRCm39) |
missense |
probably damaging |
1.00 |
R9049:Adam7
|
UTSW |
14 |
68,762,674 (GRCm39) |
missense |
probably benign |
0.01 |
R9240:Adam7
|
UTSW |
14 |
68,747,208 (GRCm39) |
missense |
probably benign |
0.02 |
R9429:Adam7
|
UTSW |
14 |
68,771,080 (GRCm39) |
missense |
probably null |
|
R9744:Adam7
|
UTSW |
14 |
68,742,583 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Adam7
|
UTSW |
14 |
68,765,150 (GRCm39) |
missense |
probably benign |
0.26 |
|