Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts8 |
C |
A |
9: 30,864,766 (GRCm39) |
P419H |
probably damaging |
Het |
Adgra3 |
C |
T |
5: 50,118,792 (GRCm39) |
V919I |
probably benign |
Het |
Akap12 |
G |
A |
10: 4,303,213 (GRCm39) |
V113I |
probably damaging |
Het |
Akr1d1 |
T |
A |
6: 37,513,043 (GRCm39) |
I113K |
probably benign |
Het |
Alx3 |
A |
T |
3: 107,511,680 (GRCm39) |
I230F |
probably damaging |
Het |
Apob |
A |
T |
12: 8,052,219 (GRCm39) |
D1220V |
probably damaging |
Het |
Ascc3 |
T |
C |
10: 50,721,796 (GRCm39) |
L2083P |
probably damaging |
Het |
Atp10b |
A |
G |
11: 43,116,373 (GRCm39) |
I907V |
probably benign |
Het |
B4galnt3 |
G |
T |
6: 120,271,384 (GRCm39) |
S46* |
probably null |
Het |
Bfsp1 |
A |
C |
2: 143,673,755 (GRCm39) |
|
probably null |
Het |
Cant1 |
G |
A |
11: 118,302,291 (GRCm39) |
R9W |
possibly damaging |
Het |
Ccdc88a |
A |
T |
11: 29,413,370 (GRCm39) |
H636L |
probably benign |
Het |
Cfi |
G |
A |
3: 129,652,464 (GRCm39) |
R297H |
probably benign |
Het |
Cherp |
T |
A |
8: 73,216,263 (GRCm39) |
Q749L |
|
Het |
Clec10a |
A |
G |
11: 70,060,604 (GRCm39) |
D153G |
probably benign |
Het |
Cnga1 |
T |
C |
5: 72,769,723 (GRCm39) |
K99E |
probably benign |
Het |
Cyp2r1 |
A |
T |
7: 114,162,002 (GRCm39) |
V64D |
probably damaging |
Het |
Dact3 |
T |
A |
7: 16,609,443 (GRCm39) |
W32R |
probably damaging |
Het |
Dennd4c |
T |
C |
4: 86,692,753 (GRCm39) |
C88R |
probably damaging |
Het |
Dock8 |
A |
T |
19: 25,135,782 (GRCm39) |
D1200V |
probably damaging |
Het |
Drosha |
C |
G |
15: 12,926,329 (GRCm39) |
S1262W |
probably damaging |
Het |
Dtnb |
T |
C |
12: 3,823,611 (GRCm39) |
M592T |
possibly damaging |
Het |
Eef2k |
T |
A |
7: 120,491,215 (GRCm39) |
V567E |
probably benign |
Het |
Fem1b |
A |
G |
9: 62,718,449 (GRCm39) |
S47P |
probably damaging |
Het |
Fryl |
T |
C |
5: 73,180,019 (GRCm39) |
E2864G |
probably benign |
Het |
Fscn2 |
A |
G |
11: 120,258,152 (GRCm39) |
N358S |
possibly damaging |
Het |
Fsip2 |
T |
C |
2: 82,818,894 (GRCm39) |
S4876P |
possibly damaging |
Het |
Ggh |
C |
G |
4: 20,049,833 (GRCm39) |
S88C |
probably damaging |
Het |
Grhl2 |
T |
C |
15: 37,328,603 (GRCm39) |
Y410H |
probably damaging |
Het |
Gucy2c |
C |
T |
6: 136,686,742 (GRCm39) |
G831D |
probably damaging |
Het |
Hars1 |
A |
T |
18: 36,904,194 (GRCm39) |
D228E |
probably benign |
Het |
Hdhd5 |
T |
C |
6: 120,498,257 (GRCm39) |
D114G |
possibly damaging |
Het |
Kcna2 |
A |
G |
3: 107,011,884 (GRCm39) |
Y155C |
probably benign |
Het |
Klc1 |
A |
G |
12: 111,751,879 (GRCm39) |
K441R |
probably benign |
Het |
Kmt2a |
A |
G |
9: 44,759,041 (GRCm39) |
L936P |
probably damaging |
Het |
Map3k6 |
T |
C |
4: 132,979,238 (GRCm39) |
V1197A |
probably benign |
Het |
Mthfsd |
C |
T |
8: 121,825,525 (GRCm39) |
A349T |
probably benign |
Het |
Mtmr7 |
G |
A |
8: 41,050,427 (GRCm39) |
R123W |
probably damaging |
Het |
Muc16 |
G |
A |
9: 18,566,747 (GRCm39) |
T1924I |
unknown |
Het |
Muc16 |
T |
A |
9: 18,553,427 (GRCm39) |
I4289F |
probably benign |
Het |
Mybpc3 |
A |
C |
2: 90,950,832 (GRCm39) |
D220A |
probably damaging |
Het |
Neb |
A |
T |
2: 52,146,587 (GRCm39) |
|
probably null |
Het |
Nectin2 |
A |
G |
7: 19,464,544 (GRCm39) |
W287R |
probably damaging |
Het |
Nipsnap1 |
A |
T |
11: 4,834,089 (GRCm39) |
T114S |
probably damaging |
Het |
Olfml2b |
A |
T |
1: 170,477,402 (GRCm39) |
K179I |
possibly damaging |
Het |
Or4a80 |
G |
T |
2: 89,582,665 (GRCm39) |
P169H |
probably damaging |
Het |
Pcnt |
T |
C |
10: 76,235,773 (GRCm39) |
M1403V |
probably benign |
Het |
Phf7 |
T |
C |
14: 30,960,386 (GRCm39) |
D284G |
probably benign |
Het |
Pias3 |
A |
G |
3: 96,609,534 (GRCm39) |
T319A |
possibly damaging |
Het |
Pik3ip1 |
A |
T |
11: 3,283,558 (GRCm39) |
I189F |
probably damaging |
Het |
Pik3r1 |
T |
A |
13: 101,825,914 (GRCm39) |
T371S |
probably damaging |
Het |
Prmt7 |
A |
G |
8: 106,964,018 (GRCm39) |
D304G |
probably benign |
Het |
Prpf6 |
T |
C |
2: 181,294,248 (GRCm39) |
V818A |
probably benign |
Het |
Pstpip2 |
A |
G |
18: 77,959,305 (GRCm39) |
E185G |
probably damaging |
Het |
Ptprz1 |
T |
G |
6: 22,999,895 (GRCm39) |
F662V |
possibly damaging |
Het |
Rasgrp3 |
T |
C |
17: 75,803,411 (GRCm39) |
F70L |
probably benign |
Het |
Rcor1 |
A |
T |
12: 111,034,271 (GRCm39) |
|
probably null |
Het |
Rnasel |
A |
G |
1: 153,630,306 (GRCm39) |
K274R |
probably benign |
Het |
Rsbn1l |
G |
A |
5: 21,101,455 (GRCm39) |
T695I |
probably benign |
Het |
Rsf1 |
GGCG |
GGCGACGGCCGCG |
7: 97,229,113 (GRCm39) |
|
probably benign |
Het |
Sema3a |
T |
C |
5: 13,611,787 (GRCm39) |
V351A |
probably benign |
Het |
Serpina12 |
A |
G |
12: 104,004,587 (GRCm39) |
L15P |
unknown |
Het |
Siah1a |
G |
A |
8: 87,451,840 (GRCm39) |
R215C |
probably benign |
Het |
Sin3a |
T |
A |
9: 57,011,210 (GRCm39) |
V489D |
possibly damaging |
Het |
Slc22a17 |
A |
G |
14: 55,149,575 (GRCm39) |
I208T |
probably benign |
Het |
Slc36a4 |
G |
A |
9: 15,645,511 (GRCm39) |
V313M |
possibly damaging |
Het |
Sod1 |
T |
A |
16: 90,023,114 (GRCm39) |
L145* |
probably null |
Het |
Svep1 |
T |
C |
4: 58,053,260 (GRCm39) |
N3362D |
possibly damaging |
Het |
Taf4b |
T |
C |
18: 14,946,602 (GRCm39) |
L475P |
probably damaging |
Het |
Telo2 |
G |
T |
17: 25,329,795 (GRCm39) |
T239K |
probably benign |
Het |
Trmt11 |
T |
G |
10: 30,436,870 (GRCm39) |
D290A |
probably damaging |
Het |
Trpc4 |
A |
T |
3: 54,225,516 (GRCm39) |
D955V |
possibly damaging |
Het |
Trpv6 |
T |
C |
6: 41,603,101 (GRCm39) |
N257S |
probably benign |
Het |
Usp12 |
T |
C |
5: 146,731,430 (GRCm39) |
T15A |
probably benign |
Het |
Vars2 |
G |
T |
17: 35,971,672 (GRCm39) |
Q526K |
probably damaging |
Het |
Vipas39 |
A |
G |
12: 87,310,677 (GRCm39) |
|
probably null |
Het |
Zfp689 |
A |
T |
7: 127,044,010 (GRCm39) |
C207S |
probably damaging |
Het |
Zfpl1 |
C |
A |
19: 6,134,432 (GRCm39) |
E18* |
probably null |
Het |
|
Other mutations in Nol9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00770:Nol9
|
APN |
4 |
152,136,472 (GRCm39) |
missense |
probably benign |
0.38 |
IGL00774:Nol9
|
APN |
4 |
152,136,472 (GRCm39) |
missense |
probably benign |
0.38 |
IGL00885:Nol9
|
APN |
4 |
152,126,057 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01125:Nol9
|
APN |
4 |
152,131,066 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01368:Nol9
|
APN |
4 |
152,142,848 (GRCm39) |
missense |
probably benign |
|
IGL01759:Nol9
|
APN |
4 |
152,130,500 (GRCm39) |
intron |
probably benign |
|
IGL01983:Nol9
|
APN |
4 |
152,130,494 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02185:Nol9
|
APN |
4 |
152,142,368 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02869:Nol9
|
APN |
4 |
152,131,030 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02967:Nol9
|
APN |
4 |
152,125,559 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0401:Nol9
|
UTSW |
4 |
152,137,062 (GRCm39) |
missense |
probably benign |
0.00 |
R3721:Nol9
|
UTSW |
4 |
152,124,163 (GRCm39) |
missense |
probably benign |
0.07 |
R4429:Nol9
|
UTSW |
4 |
152,125,631 (GRCm39) |
missense |
probably damaging |
1.00 |
R4460:Nol9
|
UTSW |
4 |
152,142,293 (GRCm39) |
missense |
probably damaging |
1.00 |
R4837:Nol9
|
UTSW |
4 |
152,136,552 (GRCm39) |
intron |
probably benign |
|
R5137:Nol9
|
UTSW |
4 |
152,130,428 (GRCm39) |
missense |
probably damaging |
1.00 |
R5698:Nol9
|
UTSW |
4 |
152,135,031 (GRCm39) |
missense |
probably damaging |
0.98 |
R6190:Nol9
|
UTSW |
4 |
152,125,691 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6317:Nol9
|
UTSW |
4 |
152,125,514 (GRCm39) |
missense |
probably damaging |
1.00 |
R6372:Nol9
|
UTSW |
4 |
152,130,452 (GRCm39) |
missense |
probably damaging |
1.00 |
R6525:Nol9
|
UTSW |
4 |
152,123,906 (GRCm39) |
missense |
probably damaging |
0.98 |
R6551:Nol9
|
UTSW |
4 |
152,136,325 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6580:Nol9
|
UTSW |
4 |
152,136,218 (GRCm39) |
missense |
probably benign |
0.00 |
R8143:Nol9
|
UTSW |
4 |
152,125,559 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9018:Nol9
|
UTSW |
4 |
152,123,918 (GRCm39) |
missense |
probably damaging |
0.99 |
R9428:Nol9
|
UTSW |
4 |
152,124,109 (GRCm39) |
missense |
probably benign |
0.00 |
R9578:Nol9
|
UTSW |
4 |
152,125,706 (GRCm39) |
missense |
probably benign |
0.00 |
|