Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abtb2 |
G |
T |
2: 103,397,861 (GRCm39) |
A264S |
probably benign |
Het |
Atosa |
T |
C |
9: 74,911,633 (GRCm39) |
C42R |
probably damaging |
Het |
Atr |
G |
T |
9: 95,744,844 (GRCm39) |
E54* |
probably null |
Het |
Bmp4 |
A |
G |
14: 46,621,456 (GRCm39) |
S363P |
probably damaging |
Het |
Cfap54 |
C |
A |
10: 92,773,590 (GRCm39) |
A2077S |
unknown |
Het |
Chrna7 |
T |
C |
7: 62,755,775 (GRCm39) |
D257G |
probably damaging |
Het |
Chrnd |
C |
T |
1: 87,118,780 (GRCm39) |
R46W |
probably damaging |
Het |
Cntn2 |
A |
G |
1: 132,444,824 (GRCm39) |
I851T |
probably damaging |
Het |
Col3a1 |
T |
A |
1: 45,372,817 (GRCm39) |
I534K |
unknown |
Het |
Cyp3a25 |
A |
T |
5: 145,939,870 (GRCm39) |
L46I |
probably benign |
Het |
Dnah7b |
G |
C |
1: 46,281,302 (GRCm39) |
G2788R |
probably damaging |
Het |
Dnpep |
T |
C |
1: 75,290,074 (GRCm39) |
E301G |
probably damaging |
Het |
Efcab3 |
T |
C |
11: 104,986,690 (GRCm39) |
S30P |
probably benign |
Het |
Elk4 |
A |
G |
1: 131,947,127 (GRCm39) |
I373V |
probably damaging |
Het |
Fam161b |
T |
C |
12: 84,395,420 (GRCm39) |
S508G |
probably damaging |
Het |
Fgf10 |
A |
G |
13: 118,925,659 (GRCm39) |
E146G |
probably benign |
Het |
Fsip2 |
A |
G |
2: 82,823,581 (GRCm39) |
D6438G |
possibly damaging |
Het |
Garin2 |
C |
T |
12: 78,758,982 (GRCm39) |
P101S |
probably benign |
Het |
Gask1b |
T |
A |
3: 79,794,114 (GRCm39) |
L194* |
probably null |
Het |
Gm49355 |
T |
A |
14: 12,296,672 (GRCm38) |
C10* |
probably null |
Het |
Hfm1 |
A |
G |
5: 107,049,569 (GRCm39) |
|
probably null |
Het |
Hivep3 |
T |
C |
4: 119,989,416 (GRCm39) |
S1956P |
probably damaging |
Het |
Hrh2 |
A |
G |
13: 54,375,270 (GRCm39) |
S369G |
unknown |
Het |
Hspg2 |
T |
C |
4: 137,260,872 (GRCm39) |
|
probably null |
Het |
Hsph1 |
T |
C |
5: 149,553,925 (GRCm39) |
Y181C |
probably damaging |
Het |
Kcnh8 |
A |
G |
17: 53,201,145 (GRCm39) |
|
probably null |
Het |
Kctd1 |
C |
T |
18: 15,195,700 (GRCm39) |
E308K |
possibly damaging |
Het |
Kdm8 |
A |
T |
7: 125,060,103 (GRCm39) |
Y335F |
probably damaging |
Het |
Kif2b |
C |
G |
11: 91,467,963 (GRCm39) |
G107R |
probably benign |
Het |
Lama4 |
G |
A |
10: 38,841,729 (GRCm39) |
|
probably benign |
Het |
Lepr |
T |
C |
4: 101,671,961 (GRCm39) |
V995A |
probably benign |
Het |
Mfsd4a |
A |
T |
1: 131,980,131 (GRCm39) |
V375E |
probably damaging |
Het |
Mgl2 |
G |
T |
11: 70,027,869 (GRCm39) |
W359L |
probably damaging |
Het |
Muc5b |
C |
A |
7: 141,414,798 (GRCm39) |
Y2581* |
probably null |
Het |
Or4k47 |
T |
A |
2: 111,451,538 (GRCm39) |
M294L |
probably benign |
Het |
Or52n3 |
A |
T |
7: 104,530,348 (GRCm39) |
K145* |
probably null |
Het |
Otud3 |
C |
T |
4: 138,636,865 (GRCm39) |
V99M |
probably damaging |
Het |
Parvb |
T |
C |
15: 84,187,672 (GRCm39) |
|
probably null |
Het |
Pclo |
C |
A |
5: 14,571,932 (GRCm39) |
P439Q |
possibly damaging |
Het |
Peg10 |
CATCAGGATCCCCATCAGGATGCACATCAGGATCCACATCAGGATGCACATCAGGATC |
CATC |
6: 4,756,431 (GRCm39) |
|
probably benign |
Het |
Pkn1 |
A |
T |
8: 84,419,302 (GRCm39) |
H100Q |
possibly damaging |
Het |
Plce1 |
A |
T |
19: 38,748,581 (GRCm39) |
I1771F |
probably damaging |
Het |
Plxna2 |
G |
T |
1: 194,483,366 (GRCm39) |
R1559L |
possibly damaging |
Het |
Ppp2r3d |
T |
A |
9: 101,003,621 (GRCm39) |
I416L |
possibly damaging |
Het |
Pramel42 |
T |
A |
5: 94,685,610 (GRCm39) |
Y423* |
probably null |
Het |
Robo1 |
C |
A |
16: 72,757,039 (GRCm39) |
C333* |
probably null |
Het |
Ryr2 |
A |
T |
13: 11,898,009 (GRCm39) |
Y129N |
probably damaging |
Het |
Schip1 |
A |
T |
3: 68,525,032 (GRCm39) |
K359M |
probably damaging |
Het |
Schip1 |
G |
T |
3: 68,525,033 (GRCm39) |
K359N |
probably damaging |
Het |
Sh2d2a |
T |
A |
3: 87,755,668 (GRCm39) |
S65T |
possibly damaging |
Het |
Ssrp1 |
G |
A |
2: 84,875,906 (GRCm39) |
M588I |
probably benign |
Het |
Stim2 |
T |
A |
5: 54,273,470 (GRCm39) |
C567S |
probably benign |
Het |
Syne1 |
C |
A |
10: 5,374,295 (GRCm39) |
A171S |
probably benign |
Het |
Tigd3 |
A |
G |
19: 5,943,050 (GRCm39) |
S27P |
probably benign |
Het |
Vipr1 |
C |
A |
9: 121,493,620 (GRCm39) |
Q224K |
probably damaging |
Het |
Vmn1r75 |
T |
A |
7: 11,614,475 (GRCm39) |
M69K |
possibly damaging |
Het |
Vmn2r72 |
T |
G |
7: 85,404,125 (GRCm39) |
D22A |
probably benign |
Het |
Zbtb24 |
G |
A |
10: 41,340,472 (GRCm39) |
V523I |
probably benign |
Het |
Zbtb43 |
A |
G |
2: 33,352,307 (GRCm39) |
F20S |
probably benign |
Het |
|
Other mutations in Nol10 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00916:Nol10
|
APN |
12 |
17,411,130 (GRCm39) |
splice site |
probably benign |
|
R1769:Nol10
|
UTSW |
12 |
17,466,709 (GRCm39) |
splice site |
probably benign |
|
R1884:Nol10
|
UTSW |
12 |
17,418,390 (GRCm39) |
critical splice donor site |
probably null |
|
R1930:Nol10
|
UTSW |
12 |
17,398,555 (GRCm39) |
start codon destroyed |
probably null |
0.99 |
R1931:Nol10
|
UTSW |
12 |
17,398,555 (GRCm39) |
start codon destroyed |
probably null |
0.99 |
R2010:Nol10
|
UTSW |
12 |
17,466,102 (GRCm39) |
missense |
probably benign |
0.00 |
R2037:Nol10
|
UTSW |
12 |
17,411,152 (GRCm39) |
missense |
probably benign |
0.01 |
R2168:Nol10
|
UTSW |
12 |
17,423,585 (GRCm39) |
missense |
probably damaging |
1.00 |
R3729:Nol10
|
UTSW |
12 |
17,474,674 (GRCm39) |
missense |
probably benign |
0.42 |
R3731:Nol10
|
UTSW |
12 |
17,474,674 (GRCm39) |
missense |
probably benign |
0.42 |
R4368:Nol10
|
UTSW |
12 |
17,429,293 (GRCm39) |
missense |
probably damaging |
1.00 |
R4618:Nol10
|
UTSW |
12 |
17,398,562 (GRCm39) |
missense |
probably damaging |
0.98 |
R4736:Nol10
|
UTSW |
12 |
17,405,288 (GRCm39) |
missense |
probably damaging |
1.00 |
R5342:Nol10
|
UTSW |
12 |
17,419,621 (GRCm39) |
splice site |
probably null |
|
R5451:Nol10
|
UTSW |
12 |
17,409,103 (GRCm39) |
nonsense |
probably null |
|
R5536:Nol10
|
UTSW |
12 |
17,466,138 (GRCm39) |
nonsense |
probably null |
|
R5586:Nol10
|
UTSW |
12 |
17,466,829 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6045:Nol10
|
UTSW |
12 |
17,398,479 (GRCm39) |
start gained |
probably benign |
|
R6833:Nol10
|
UTSW |
12 |
17,402,728 (GRCm39) |
missense |
probably benign |
0.03 |
R7039:Nol10
|
UTSW |
12 |
17,479,185 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7251:Nol10
|
UTSW |
12 |
17,452,108 (GRCm39) |
missense |
probably damaging |
1.00 |
R7399:Nol10
|
UTSW |
12 |
17,452,174 (GRCm39) |
missense |
probably damaging |
1.00 |
R7600:Nol10
|
UTSW |
12 |
17,419,481 (GRCm39) |
missense |
probably damaging |
0.99 |
R7650:Nol10
|
UTSW |
12 |
17,412,683 (GRCm39) |
critical splice donor site |
probably null |
|
R7729:Nol10
|
UTSW |
12 |
17,474,676 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7772:Nol10
|
UTSW |
12 |
17,398,586 (GRCm39) |
missense |
probably damaging |
1.00 |
R7869:Nol10
|
UTSW |
12 |
17,408,239 (GRCm39) |
missense |
probably null |
0.93 |
R7972:Nol10
|
UTSW |
12 |
17,402,648 (GRCm39) |
missense |
probably benign |
0.15 |
R8686:Nol10
|
UTSW |
12 |
17,419,772 (GRCm39) |
intron |
probably benign |
|
R8926:Nol10
|
UTSW |
12 |
17,466,871 (GRCm39) |
missense |
probably benign |
0.00 |
R8936:Nol10
|
UTSW |
12 |
17,466,863 (GRCm39) |
missense |
probably benign |
0.08 |
R8966:Nol10
|
UTSW |
12 |
17,419,507 (GRCm39) |
missense |
possibly damaging |
0.64 |
R8994:Nol10
|
UTSW |
12 |
17,402,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R9002:Nol10
|
UTSW |
12 |
17,408,134 (GRCm39) |
missense |
probably damaging |
1.00 |
R9096:Nol10
|
UTSW |
12 |
17,466,199 (GRCm39) |
missense |
probably benign |
|
R9196:Nol10
|
UTSW |
12 |
17,455,316 (GRCm39) |
missense |
probably benign |
0.04 |
R9548:Nol10
|
UTSW |
12 |
17,466,144 (GRCm39) |
missense |
possibly damaging |
0.49 |
Z1177:Nol10
|
UTSW |
12 |
17,409,089 (GRCm39) |
critical splice acceptor site |
probably null |
|
|