Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
T |
C |
11: 9,247,527 (GRCm39) |
F2425L |
probably benign |
Het |
Adgre4 |
A |
T |
17: 56,121,188 (GRCm39) |
Y418F |
probably benign |
Het |
Adra1a |
G |
T |
14: 66,875,322 (GRCm39) |
C99F |
probably damaging |
Het |
Aox3 |
C |
A |
1: 58,197,431 (GRCm39) |
H592Q |
probably benign |
Het |
Cacna1f |
A |
G |
X: 7,495,644 (GRCm39) |
|
probably null |
Het |
Cacna2d2 |
T |
A |
9: 107,342,753 (GRCm39) |
I100N |
probably damaging |
Het |
Cblif |
A |
T |
19: 11,729,596 (GRCm39) |
N185I |
probably damaging |
Het |
Ccr9 |
T |
A |
9: 123,608,911 (GRCm39) |
C198S |
probably damaging |
Het |
Cdc45 |
C |
T |
16: 18,617,479 (GRCm39) |
M200I |
probably benign |
Het |
Col4a3 |
T |
A |
1: 82,647,913 (GRCm39) |
C475S |
unknown |
Het |
Csnk2a2 |
T |
C |
8: 96,203,859 (GRCm39) |
D100G |
possibly damaging |
Het |
Cstf2t |
G |
A |
19: 31,061,277 (GRCm39) |
G271E |
possibly damaging |
Het |
Fbxw22 |
T |
C |
9: 109,214,160 (GRCm39) |
R219G |
probably damaging |
Het |
Homez |
A |
G |
14: 55,095,559 (GRCm39) |
F50L |
probably damaging |
Het |
Hspa4l |
C |
T |
3: 40,707,657 (GRCm39) |
Q81* |
probably null |
Het |
Ifi202b |
T |
C |
1: 173,799,875 (GRCm39) |
D202G |
possibly damaging |
Het |
Inava |
T |
C |
1: 136,144,173 (GRCm39) |
|
probably null |
Het |
Or13a24 |
A |
G |
7: 140,154,684 (GRCm39) |
Y206C |
probably benign |
Het |
Or4a27 |
T |
G |
2: 88,559,739 (GRCm39) |
D68A |
probably damaging |
Het |
Or51h5 |
T |
A |
7: 102,577,723 (GRCm39) |
V296E |
possibly damaging |
Het |
P2rx1 |
A |
T |
11: 72,900,410 (GRCm39) |
|
probably null |
Het |
Phactr4 |
A |
G |
4: 132,104,483 (GRCm39) |
|
probably benign |
Het |
Pus10 |
C |
T |
11: 23,675,574 (GRCm39) |
T482I |
probably damaging |
Het |
Scyl2 |
G |
T |
10: 89,488,871 (GRCm39) |
Y206* |
probably null |
Het |
Sell |
G |
A |
1: 163,896,632 (GRCm39) |
|
probably null |
Het |
Slfn10-ps |
C |
T |
11: 82,921,090 (GRCm39) |
|
noncoding transcript |
Het |
Ssh2 |
T |
C |
11: 77,307,233 (GRCm39) |
|
probably benign |
Het |
Tas2r117 |
A |
G |
6: 132,779,963 (GRCm39) |
M34V |
probably benign |
Het |
Vmn2r103 |
A |
T |
17: 19,993,631 (GRCm39) |
T3S |
probably benign |
Het |
Vmn2r73 |
A |
T |
7: 85,522,084 (GRCm39) |
I85K |
probably damaging |
Het |
Vps13b |
T |
C |
15: 35,770,887 (GRCm39) |
V2110A |
possibly damaging |
Het |
Zfp13 |
C |
T |
17: 23,795,072 (GRCm39) |
A493T |
probably benign |
Het |
Zfp518a |
G |
A |
19: 40,903,061 (GRCm39) |
G997R |
probably damaging |
Het |
Zfp592 |
G |
A |
7: 80,673,746 (GRCm39) |
G237R |
probably damaging |
Het |
Zkscan7 |
A |
G |
9: 122,717,950 (GRCm39) |
E115G |
probably damaging |
Het |
Zranb3 |
G |
A |
1: 127,943,829 (GRCm39) |
T306M |
probably benign |
Het |
|
Other mutations in Mansc1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00519:Mansc1
|
APN |
6 |
134,587,769 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL01141:Mansc1
|
APN |
6 |
134,598,748 (GRCm39) |
missense |
probably benign |
0.21 |
IGL01447:Mansc1
|
APN |
6 |
134,594,289 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01582:Mansc1
|
APN |
6 |
134,598,836 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02121:Mansc1
|
APN |
6 |
134,598,800 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02214:Mansc1
|
APN |
6 |
134,587,323 (GRCm39) |
missense |
probably benign |
0.39 |
IGL02699:Mansc1
|
APN |
6 |
134,587,317 (GRCm39) |
missense |
probably benign |
0.34 |
R0266:Mansc1
|
UTSW |
6 |
134,587,670 (GRCm39) |
missense |
probably benign |
0.08 |
R0730:Mansc1
|
UTSW |
6 |
134,594,424 (GRCm39) |
splice site |
probably benign |
|
R0849:Mansc1
|
UTSW |
6 |
134,587,670 (GRCm39) |
missense |
probably benign |
0.08 |
R2015:Mansc1
|
UTSW |
6 |
134,587,274 (GRCm39) |
missense |
possibly damaging |
0.77 |
R3874:Mansc1
|
UTSW |
6 |
134,587,146 (GRCm39) |
missense |
possibly damaging |
0.62 |
R4886:Mansc1
|
UTSW |
6 |
134,587,625 (GRCm39) |
missense |
probably benign |
0.01 |
R5864:Mansc1
|
UTSW |
6 |
134,587,816 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5932:Mansc1
|
UTSW |
6 |
134,587,478 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7233:Mansc1
|
UTSW |
6 |
134,598,806 (GRCm39) |
missense |
probably damaging |
0.98 |
R7576:Mansc1
|
UTSW |
6 |
134,587,674 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7858:Mansc1
|
UTSW |
6 |
134,587,377 (GRCm39) |
missense |
probably benign |
0.23 |
R7981:Mansc1
|
UTSW |
6 |
134,587,274 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8775:Mansc1
|
UTSW |
6 |
134,587,631 (GRCm39) |
missense |
probably benign |
0.10 |
R8775-TAIL:Mansc1
|
UTSW |
6 |
134,587,631 (GRCm39) |
missense |
probably benign |
0.10 |
R9130:Mansc1
|
UTSW |
6 |
134,586,951 (GRCm39) |
missense |
probably damaging |
1.00 |
R9761:Mansc1
|
UTSW |
6 |
134,587,004 (GRCm39) |
missense |
probably damaging |
1.00 |
|