Other mutations in this stock |
Total: 87 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd17a |
A |
G |
10: 80,419,737 (GRCm39) |
Y290H |
probably benign |
Het |
Aco2 |
T |
C |
15: 81,788,142 (GRCm39) |
V257A |
probably damaging |
Het |
Adam26a |
C |
A |
8: 44,023,007 (GRCm39) |
C161F |
possibly damaging |
Het |
Adam9 |
G |
A |
8: 25,445,988 (GRCm39) |
P820S |
unknown |
Het |
Adcy4 |
G |
A |
14: 56,010,922 (GRCm39) |
T665M |
probably benign |
Het |
Ahnak |
T |
A |
19: 8,984,188 (GRCm39) |
M1824K |
probably benign |
Het |
Alpi |
T |
C |
1: 87,026,795 (GRCm39) |
N428D |
probably benign |
Het |
Ano5 |
C |
T |
7: 51,196,528 (GRCm39) |
P153L |
probably benign |
Het |
Atp1a1 |
A |
T |
3: 101,489,437 (GRCm39) |
L725* |
probably null |
Het |
Atp8b2 |
G |
A |
3: 89,854,071 (GRCm39) |
T595I |
probably damaging |
Het |
Ccdc66 |
T |
C |
14: 27,220,820 (GRCm39) |
I35V |
possibly damaging |
Het |
Cd163 |
A |
G |
6: 124,284,187 (GRCm39) |
T120A |
probably benign |
Het |
Cmah |
A |
T |
13: 24,640,938 (GRCm39) |
T396S |
possibly damaging |
Het |
Cmya5 |
C |
T |
13: 93,205,820 (GRCm39) |
V3350I |
probably benign |
Het |
Commd9 |
A |
C |
2: 101,731,410 (GRCm39) |
K198N |
probably damaging |
Het |
Cxcr1 |
A |
G |
1: 74,231,773 (GRCm39) |
V83A |
probably benign |
Het |
D630045J12Rik |
A |
G |
6: 38,125,383 (GRCm39) |
S1544P |
probably damaging |
Het |
Ddt |
A |
T |
10: 75,609,048 (GRCm39) |
|
probably null |
Het |
Depdc7 |
A |
G |
2: 104,557,585 (GRCm39) |
S222P |
possibly damaging |
Het |
Ehd2 |
A |
G |
7: 15,684,431 (GRCm39) |
I456T |
probably damaging |
Het |
Epas1 |
A |
T |
17: 87,136,471 (GRCm39) |
M748L |
probably benign |
Het |
Esr1 |
G |
A |
10: 4,806,903 (GRCm39) |
R273H |
probably damaging |
Het |
Fras1 |
G |
A |
5: 96,916,297 (GRCm39) |
D3444N |
probably damaging |
Het |
Hand2 |
A |
G |
8: 57,775,272 (GRCm39) |
R111G |
probably damaging |
Het |
Hecw1 |
A |
T |
13: 14,490,835 (GRCm39) |
V306E |
probably damaging |
Het |
Ift140 |
T |
C |
17: 25,252,089 (GRCm39) |
I312T |
probably benign |
Het |
Ikbke |
A |
T |
1: 131,199,887 (GRCm39) |
L257* |
probably null |
Het |
Kcnk5 |
G |
A |
14: 20,192,349 (GRCm39) |
P271S |
probably benign |
Het |
Lama1 |
T |
C |
17: 68,044,662 (GRCm39) |
V187A |
|
Het |
Lemd2 |
A |
T |
17: 27,412,810 (GRCm39) |
|
probably null |
Het |
Lig3 |
T |
A |
11: 82,679,717 (GRCm39) |
D341E |
probably benign |
Het |
Lpcat1 |
C |
T |
13: 73,643,014 (GRCm39) |
S196L |
probably damaging |
Het |
Lrp1b |
A |
T |
2: 40,567,582 (GRCm39) |
D4048E |
|
Het |
Lrrfip1 |
G |
A |
1: 91,033,005 (GRCm39) |
E158K |
probably damaging |
Het |
Mcm5 |
T |
C |
8: 75,848,220 (GRCm39) |
S490P |
probably damaging |
Het |
Mia3 |
A |
C |
1: 183,147,036 (GRCm39) |
Y73* |
probably null |
Het |
Minar1 |
T |
A |
9: 89,483,888 (GRCm39) |
H503L |
probably benign |
Het |
Msr1 |
A |
T |
8: 40,077,003 (GRCm39) |
N202K |
probably benign |
Het |
N4bp2l2 |
A |
T |
5: 150,585,286 (GRCm39) |
Y231* |
probably null |
Het |
Nbeal2 |
A |
G |
9: 110,482,985 (GRCm39) |
W11R |
probably benign |
Het |
Ncor1 |
T |
C |
11: 62,264,250 (GRCm39) |
E384G |
possibly damaging |
Het |
Neb |
A |
G |
2: 52,137,202 (GRCm39) |
V254A |
|
Het |
Nlrp9b |
T |
C |
7: 19,779,691 (GRCm39) |
S785P |
probably benign |
Het |
Oprd1 |
T |
G |
4: 131,841,092 (GRCm39) |
I289L |
possibly damaging |
Het |
Or4c10 |
G |
T |
2: 89,761,064 (GRCm39) |
D304Y |
probably benign |
Het |
Or4s2 |
A |
G |
2: 88,473,752 (GRCm39) |
I214V |
probably benign |
Het |
Or5m12 |
A |
G |
2: 85,734,447 (GRCm39) |
V317A |
probably benign |
Het |
Or6a2 |
T |
C |
7: 106,600,534 (GRCm39) |
T178A |
probably benign |
Het |
Or6c2 |
T |
A |
10: 129,362,429 (GRCm39) |
F111Y |
possibly damaging |
Het |
Orc1 |
A |
G |
4: 108,445,951 (GRCm39) |
N23S |
probably benign |
Het |
Paip1 |
A |
T |
13: 119,577,356 (GRCm39) |
H149L |
possibly damaging |
Het |
Pdhx |
A |
T |
2: 102,877,099 (GRCm39) |
D103E |
probably benign |
Het |
Pi4ka |
T |
C |
16: 17,109,080 (GRCm39) |
Y1614C |
|
Het |
Pias3 |
ACC |
AC |
3: 96,608,701 (GRCm39) |
|
probably null |
Het |
Pla2g4d |
A |
G |
2: 120,114,620 (GRCm39) |
I37T |
possibly damaging |
Het |
Ppfia1 |
A |
T |
7: 144,059,982 (GRCm39) |
V610D |
probably damaging |
Het |
Pramel41 |
G |
A |
5: 94,596,394 (GRCm39) |
C477Y |
probably damaging |
Het |
Prss1 |
T |
C |
6: 41,439,507 (GRCm39) |
V80A |
probably benign |
Het |
Psph |
G |
A |
5: 129,847,800 (GRCm39) |
R49W |
probably benign |
Het |
Qrich2 |
T |
C |
11: 116,347,080 (GRCm39) |
Y1248C |
possibly damaging |
Het |
Rlbp1 |
T |
A |
7: 79,029,861 (GRCm39) |
Y124F |
probably damaging |
Het |
Scn4a |
T |
A |
11: 106,239,995 (GRCm39) |
E74V |
probably benign |
Het |
Sdk2 |
A |
T |
11: 113,764,039 (GRCm39) |
I249N |
possibly damaging |
Het |
Sgsh |
A |
T |
11: 119,237,378 (GRCm39) |
L412Q |
probably damaging |
Het |
Shank1 |
C |
A |
7: 44,002,452 (GRCm39) |
D1390E |
probably benign |
Het |
Slc12a6 |
A |
G |
2: 112,172,319 (GRCm39) |
D421G |
probably damaging |
Het |
Snx29 |
T |
A |
16: 11,238,649 (GRCm39) |
|
probably null |
Het |
Spata31d1c |
A |
G |
13: 65,183,937 (GRCm39) |
Y493C |
probably damaging |
Het |
Stmn4 |
G |
A |
14: 66,593,727 (GRCm39) |
G40E |
probably damaging |
Het |
Stox2 |
A |
G |
8: 47,656,154 (GRCm39) |
|
probably null |
Het |
Strada |
T |
C |
11: 106,077,830 (GRCm39) |
S45G |
unknown |
Het |
Taco1 |
G |
A |
11: 105,962,774 (GRCm39) |
G154S |
probably benign |
Het |
Tas2r121 |
T |
C |
6: 132,677,505 (GRCm39) |
M156V |
probably benign |
Het |
Tbc1d31 |
A |
G |
15: 57,804,136 (GRCm39) |
S384G |
probably benign |
Het |
Tbc1d9 |
A |
T |
8: 83,966,560 (GRCm39) |
D387V |
probably damaging |
Het |
Tet3 |
A |
G |
6: 83,345,289 (GRCm39) |
L1716P |
probably damaging |
Het |
Thbs1 |
A |
G |
2: 117,943,843 (GRCm39) |
K154E |
possibly damaging |
Het |
Ush2a |
T |
C |
1: 187,999,241 (GRCm39) |
Y184H |
possibly damaging |
Het |
Vmn1r235 |
C |
A |
17: 21,481,713 (GRCm39) |
Q13K |
probably benign |
Het |
Vmn2r15 |
A |
T |
5: 109,440,774 (GRCm39) |
Y361* |
probably null |
Het |
Vmn2r88 |
A |
T |
14: 51,648,315 (GRCm39) |
|
probably null |
Het |
Vps54 |
T |
C |
11: 21,248,831 (GRCm39) |
V460A |
probably benign |
Het |
Wdr64 |
A |
G |
1: 175,613,147 (GRCm39) |
N674S |
possibly damaging |
Het |
Zfp592 |
A |
G |
7: 80,673,390 (GRCm39) |
D118G |
probably benign |
Het |
Zfp763 |
A |
G |
17: 33,237,625 (GRCm39) |
Y507H |
probably benign |
Het |
Zfp934 |
T |
C |
13: 62,640,705 (GRCm39) |
E16G |
probably damaging |
Het |
Zfyve26 |
G |
A |
12: 79,337,731 (GRCm39) |
L94F |
probably damaging |
Het |
|
Other mutations in Pigb |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01391:Pigb
|
APN |
9 |
72,929,573 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01792:Pigb
|
APN |
9 |
72,925,268 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02416:Pigb
|
APN |
9 |
72,924,714 (GRCm39) |
missense |
probably benign |
0.00 |
R2396:Pigb
|
UTSW |
9 |
72,922,553 (GRCm39) |
nonsense |
probably null |
|
R2914:Pigb
|
UTSW |
9 |
72,947,060 (GRCm39) |
splice site |
probably null |
|
R3830:Pigb
|
UTSW |
9 |
72,924,755 (GRCm39) |
missense |
probably benign |
0.03 |
R5048:Pigb
|
UTSW |
9 |
72,936,990 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5158:Pigb
|
UTSW |
9 |
72,929,683 (GRCm39) |
missense |
probably damaging |
1.00 |
R5180:Pigb
|
UTSW |
9 |
72,941,872 (GRCm39) |
missense |
probably damaging |
0.99 |
R5385:Pigb
|
UTSW |
9 |
72,946,827 (GRCm39) |
missense |
probably benign |
0.05 |
R5866:Pigb
|
UTSW |
9 |
72,936,966 (GRCm39) |
missense |
probably damaging |
1.00 |
R7460:Pigb
|
UTSW |
9 |
72,945,957 (GRCm39) |
missense |
probably damaging |
0.99 |
R8005:Pigb
|
UTSW |
9 |
72,922,546 (GRCm39) |
missense |
unknown |
|
R8136:Pigb
|
UTSW |
9 |
72,929,602 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8525:Pigb
|
UTSW |
9 |
72,924,809 (GRCm39) |
missense |
probably damaging |
1.00 |
R8955:Pigb
|
UTSW |
9 |
72,945,983 (GRCm39) |
missense |
probably damaging |
0.99 |
R8988:Pigb
|
UTSW |
9 |
72,929,576 (GRCm39) |
missense |
probably damaging |
1.00 |
R9526:Pigb
|
UTSW |
9 |
72,941,840 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:Pigb
|
UTSW |
9 |
72,941,854 (GRCm39) |
missense |
probably benign |
|
|