Other mutations in this stock |
Total: 30 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921539E11Rik |
C |
T |
4: 103,094,127 (GRCm39) |
|
probably null |
Het |
Alox12b |
C |
A |
11: 69,059,647 (GRCm39) |
Y566* |
probably null |
Het |
Chl1 |
T |
A |
6: 103,667,220 (GRCm39) |
S403R |
probably damaging |
Het |
Cpa5 |
T |
A |
6: 30,626,363 (GRCm39) |
D241E |
probably damaging |
Het |
Crebbp |
C |
T |
16: 3,937,670 (GRCm39) |
A698T |
possibly damaging |
Het |
Cyp2t4 |
C |
A |
7: 26,855,213 (GRCm39) |
C121* |
probably null |
Het |
Dkkl1 |
C |
A |
7: 44,859,882 (GRCm39) |
R56L |
possibly damaging |
Het |
Ebf3 |
A |
G |
7: 136,802,889 (GRCm39) |
V387A |
probably damaging |
Het |
Efcab3 |
T |
C |
11: 104,784,609 (GRCm39) |
M2797T |
probably benign |
Het |
Fer1l5 |
A |
G |
1: 36,450,466 (GRCm39) |
T1212A |
probably damaging |
Het |
Galnt16 |
T |
A |
12: 80,565,944 (GRCm39) |
M1K |
probably null |
Het |
Gm5800 |
A |
G |
14: 51,953,595 (GRCm39) |
S7P |
possibly damaging |
Het |
Gstp1 |
T |
A |
19: 4,085,510 (GRCm39) |
H199L |
probably benign |
Het |
Herc1 |
T |
C |
9: 66,345,026 (GRCm39) |
S1940P |
probably benign |
Het |
Igkv8-24 |
C |
T |
6: 70,194,365 (GRCm39) |
W14* |
probably null |
Het |
Iqcd |
C |
A |
5: 120,738,556 (GRCm39) |
Q125K |
probably benign |
Het |
Lpin2 |
T |
A |
17: 71,553,413 (GRCm39) |
D812E |
probably damaging |
Het |
Ltb4r2 |
T |
A |
14: 55,999,962 (GRCm39) |
|
probably null |
Het |
Morc2a |
T |
C |
11: 3,622,376 (GRCm39) |
|
probably null |
Het |
Myh1 |
A |
T |
11: 67,099,890 (GRCm39) |
N600I |
possibly damaging |
Het |
Nedd9 |
T |
A |
13: 41,465,584 (GRCm39) |
K685N |
probably damaging |
Het |
Or10aa3 |
A |
G |
1: 173,878,535 (GRCm39) |
I199V |
probably benign |
Het |
Otogl |
A |
C |
10: 107,698,165 (GRCm39) |
V735G |
probably damaging |
Het |
Pcnx1 |
T |
A |
12: 81,964,656 (GRCm39) |
Y274* |
probably null |
Het |
Pias1 |
A |
T |
9: 62,826,706 (GRCm39) |
I252N |
probably damaging |
Het |
Satb2 |
G |
T |
1: 56,884,880 (GRCm39) |
S348* |
probably null |
Het |
Sfxn1 |
T |
A |
13: 54,247,048 (GRCm39) |
V180D |
probably damaging |
Het |
Slc35g3 |
A |
T |
11: 69,651,109 (GRCm39) |
V314D |
probably damaging |
Het |
Tmem200c |
C |
A |
17: 69,149,101 (GRCm39) |
D561E |
probably benign |
Het |
Usp53 |
T |
A |
3: 122,757,935 (GRCm39) |
Q69L |
probably benign |
Het |
|
Other mutations in Pitpnm3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01818:Pitpnm3
|
APN |
11 |
72,003,077 (GRCm39) |
splice site |
probably benign |
|
IGL01871:Pitpnm3
|
APN |
11 |
71,946,964 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02058:Pitpnm3
|
APN |
11 |
72,010,965 (GRCm39) |
missense |
probably benign |
0.31 |
IGL02267:Pitpnm3
|
APN |
11 |
71,962,274 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02370:Pitpnm3
|
APN |
11 |
71,942,684 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02613:Pitpnm3
|
APN |
11 |
71,948,898 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02835:Pitpnm3
|
APN |
11 |
71,952,292 (GRCm39) |
splice site |
probably benign |
|
IGL02946:Pitpnm3
|
APN |
11 |
71,983,378 (GRCm39) |
missense |
probably benign |
0.08 |
IGL02989:Pitpnm3
|
APN |
11 |
72,011,012 (GRCm39) |
splice site |
probably benign |
|
IGL03173:Pitpnm3
|
APN |
11 |
71,983,389 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03357:Pitpnm3
|
APN |
11 |
71,961,716 (GRCm39) |
nonsense |
probably null |
|
Frank
|
UTSW |
11 |
71,961,222 (GRCm39) |
missense |
probably benign |
|
Mickey
|
UTSW |
11 |
71,961,790 (GRCm39) |
missense |
probably damaging |
1.00 |
Stuart
|
UTSW |
11 |
71,942,755 (GRCm39) |
missense |
probably null |
0.99 |
R0102:Pitpnm3
|
UTSW |
11 |
71,947,072 (GRCm39) |
missense |
probably damaging |
1.00 |
R0193:Pitpnm3
|
UTSW |
11 |
71,961,318 (GRCm39) |
splice site |
probably benign |
|
R0964:Pitpnm3
|
UTSW |
11 |
71,949,296 (GRCm39) |
missense |
probably damaging |
1.00 |
R1475:Pitpnm3
|
UTSW |
11 |
71,965,453 (GRCm39) |
missense |
probably damaging |
1.00 |
R1566:Pitpnm3
|
UTSW |
11 |
71,949,785 (GRCm39) |
splice site |
probably null |
|
R1951:Pitpnm3
|
UTSW |
11 |
71,965,450 (GRCm39) |
missense |
possibly damaging |
0.88 |
R3915:Pitpnm3
|
UTSW |
11 |
72,003,110 (GRCm39) |
missense |
probably damaging |
1.00 |
R4192:Pitpnm3
|
UTSW |
11 |
71,942,785 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4278:Pitpnm3
|
UTSW |
11 |
71,965,342 (GRCm39) |
missense |
probably damaging |
1.00 |
R4928:Pitpnm3
|
UTSW |
11 |
71,953,998 (GRCm39) |
missense |
probably damaging |
1.00 |
R5543:Pitpnm3
|
UTSW |
11 |
71,947,023 (GRCm39) |
missense |
probably damaging |
0.99 |
R5626:Pitpnm3
|
UTSW |
11 |
72,003,158 (GRCm39) |
missense |
probably benign |
0.04 |
R5635:Pitpnm3
|
UTSW |
11 |
71,957,986 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5958:Pitpnm3
|
UTSW |
11 |
72,003,193 (GRCm39) |
splice site |
probably null |
|
R6531:Pitpnm3
|
UTSW |
11 |
71,962,313 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6764:Pitpnm3
|
UTSW |
11 |
71,942,059 (GRCm39) |
missense |
probably damaging |
1.00 |
R6912:Pitpnm3
|
UTSW |
11 |
71,961,222 (GRCm39) |
missense |
probably benign |
|
R7132:Pitpnm3
|
UTSW |
11 |
71,942,102 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7307:Pitpnm3
|
UTSW |
11 |
71,961,790 (GRCm39) |
missense |
probably damaging |
1.00 |
R7561:Pitpnm3
|
UTSW |
11 |
71,942,008 (GRCm39) |
missense |
probably benign |
0.02 |
R7771:Pitpnm3
|
UTSW |
11 |
71,952,314 (GRCm39) |
nonsense |
probably null |
|
R8099:Pitpnm3
|
UTSW |
11 |
71,961,144 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8753:Pitpnm3
|
UTSW |
11 |
71,942,704 (GRCm39) |
missense |
probably benign |
0.01 |
R8817:Pitpnm3
|
UTSW |
11 |
71,941,894 (GRCm39) |
missense |
possibly damaging |
0.74 |
R8987:Pitpnm3
|
UTSW |
11 |
72,003,132 (GRCm39) |
missense |
probably damaging |
1.00 |
R9054:Pitpnm3
|
UTSW |
11 |
71,947,017 (GRCm39) |
missense |
probably damaging |
0.97 |
R9450:Pitpnm3
|
UTSW |
11 |
71,952,412 (GRCm39) |
missense |
possibly damaging |
0.50 |
R9508:Pitpnm3
|
UTSW |
11 |
72,003,121 (GRCm39) |
missense |
probably damaging |
1.00 |
R9606:Pitpnm3
|
UTSW |
11 |
71,955,069 (GRCm39) |
missense |
probably benign |
0.02 |
R9740:Pitpnm3
|
UTSW |
11 |
71,947,102 (GRCm39) |
missense |
probably benign |
0.34 |
X0018:Pitpnm3
|
UTSW |
11 |
71,962,266 (GRCm39) |
missense |
probably benign |
0.42 |
X0062:Pitpnm3
|
UTSW |
11 |
71,957,934 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1186:Pitpnm3
|
UTSW |
11 |
72,010,969 (GRCm39) |
missense |
probably benign |
|
Z1186:Pitpnm3
|
UTSW |
11 |
71,954,955 (GRCm39) |
missense |
probably benign |
|
Z1187:Pitpnm3
|
UTSW |
11 |
72,010,969 (GRCm39) |
missense |
probably benign |
|
Z1187:Pitpnm3
|
UTSW |
11 |
71,954,955 (GRCm39) |
missense |
probably benign |
|
Z1188:Pitpnm3
|
UTSW |
11 |
72,010,969 (GRCm39) |
missense |
probably benign |
|
Z1188:Pitpnm3
|
UTSW |
11 |
71,954,955 (GRCm39) |
missense |
probably benign |
|
Z1189:Pitpnm3
|
UTSW |
11 |
72,010,969 (GRCm39) |
missense |
probably benign |
|
Z1189:Pitpnm3
|
UTSW |
11 |
71,954,955 (GRCm39) |
missense |
probably benign |
|
Z1190:Pitpnm3
|
UTSW |
11 |
72,010,969 (GRCm39) |
missense |
probably benign |
|
Z1190:Pitpnm3
|
UTSW |
11 |
71,954,955 (GRCm39) |
missense |
probably benign |
|
Z1191:Pitpnm3
|
UTSW |
11 |
72,010,969 (GRCm39) |
missense |
probably benign |
|
Z1191:Pitpnm3
|
UTSW |
11 |
71,954,955 (GRCm39) |
missense |
probably benign |
|
Z1192:Pitpnm3
|
UTSW |
11 |
72,010,969 (GRCm39) |
missense |
probably benign |
|
Z1192:Pitpnm3
|
UTSW |
11 |
71,954,955 (GRCm39) |
missense |
probably benign |
|
|