Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ankrd44 |
T |
C |
1: 54,792,087 (GRCm39) |
H316R |
probably damaging |
Het |
Arfgef2 |
G |
A |
2: 166,709,275 (GRCm39) |
M1117I |
probably damaging |
Het |
Cdc42bpg |
A |
G |
19: 6,360,881 (GRCm39) |
D213G |
probably damaging |
Het |
Cfap69 |
G |
A |
5: 5,696,979 (GRCm39) |
P106S |
probably damaging |
Het |
Chkb |
A |
T |
15: 89,312,987 (GRCm39) |
L30H |
probably damaging |
Het |
Clstn3 |
G |
A |
6: 124,415,781 (GRCm39) |
Q634* |
probably null |
Het |
Efcab15 |
T |
C |
11: 103,091,754 (GRCm39) |
Q42R |
probably damaging |
Het |
Esrra |
C |
A |
19: 6,890,100 (GRCm39) |
W98C |
probably damaging |
Het |
Ganab |
A |
G |
19: 8,892,058 (GRCm39) |
|
probably benign |
Het |
Gcnt3 |
G |
T |
9: 69,941,739 (GRCm39) |
H276Q |
probably benign |
Het |
Gm16506 |
A |
G |
14: 43,961,630 (GRCm39) |
Y206H |
probably benign |
Het |
Gvin3 |
C |
T |
7: 106,202,258 (GRCm39) |
|
noncoding transcript |
Het |
Hkdc1 |
T |
A |
10: 62,229,638 (GRCm39) |
N680Y |
probably damaging |
Het |
Ighe |
A |
C |
12: 113,235,011 (GRCm39) |
L383R |
unknown |
Het |
Lgals9 |
T |
G |
11: 78,863,977 (GRCm39) |
D56A |
probably damaging |
Het |
Marveld3 |
G |
A |
8: 110,688,705 (GRCm39) |
T12I |
possibly damaging |
Het |
Nab2 |
A |
T |
10: 127,500,972 (GRCm39) |
L40Q |
probably damaging |
Het |
Naip6 |
T |
C |
13: 100,439,798 (GRCm39) |
E323G |
probably benign |
Het |
Nubpl |
T |
A |
12: 52,317,853 (GRCm39) |
V182E |
possibly damaging |
Het |
Or2ag15 |
A |
G |
7: 106,340,706 (GRCm39) |
V145A |
probably benign |
Het |
Or4c11 |
T |
A |
2: 88,695,864 (GRCm39) |
M305K |
probably benign |
Het |
Or6b3 |
A |
G |
1: 92,438,974 (GRCm39) |
Y259H |
probably damaging |
Het |
Peg3 |
A |
G |
7: 6,714,652 (GRCm39) |
I190T |
probably damaging |
Het |
Plcl1 |
G |
A |
1: 55,735,555 (GRCm39) |
V299M |
possibly damaging |
Het |
Ppp4r1 |
G |
A |
17: 66,120,522 (GRCm39) |
E219K |
probably damaging |
Het |
Sh3d19 |
G |
A |
3: 86,005,492 (GRCm39) |
A280T |
probably benign |
Het |
Srebf2 |
A |
G |
15: 82,061,663 (GRCm39) |
I370V |
probably benign |
Het |
Tfb2m |
A |
G |
1: 179,359,695 (GRCm39) |
|
probably benign |
Het |
Ttll7 |
T |
G |
3: 146,615,354 (GRCm39) |
S273A |
possibly damaging |
Het |
Unc79 |
A |
G |
12: 103,074,944 (GRCm39) |
N1401D |
probably damaging |
Het |
Vmn2r115 |
T |
A |
17: 23,578,755 (GRCm39) |
S743T |
probably damaging |
Het |
Zfand4 |
G |
A |
6: 116,291,830 (GRCm39) |
R588Q |
probably benign |
Het |
|
Other mutations in Cit |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00321:Cit
|
APN |
5 |
115,984,524 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00482:Cit
|
APN |
5 |
116,076,814 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01317:Cit
|
APN |
5 |
116,046,775 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01335:Cit
|
APN |
5 |
116,046,889 (GRCm39) |
splice site |
probably benign |
|
IGL01447:Cit
|
APN |
5 |
116,011,902 (GRCm39) |
splice site |
probably benign |
|
IGL01537:Cit
|
APN |
5 |
116,071,913 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01621:Cit
|
APN |
5 |
116,130,662 (GRCm39) |
splice site |
probably benign |
|
IGL02010:Cit
|
APN |
5 |
116,014,006 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02538:Cit
|
APN |
5 |
116,125,048 (GRCm39) |
nonsense |
probably null |
|
IGL02607:Cit
|
APN |
5 |
115,997,268 (GRCm39) |
missense |
probably benign |
|
IGL02720:Cit
|
APN |
5 |
116,133,511 (GRCm39) |
missense |
probably benign |
0.26 |
IGL02725:Cit
|
APN |
5 |
116,123,532 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02967:Cit
|
APN |
5 |
116,083,896 (GRCm39) |
missense |
probably benign |
0.11 |
IGL02973:Cit
|
APN |
5 |
116,144,058 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL03383:Cit
|
APN |
5 |
116,011,904 (GRCm39) |
splice site |
probably benign |
|
PIT4514001:Cit
|
UTSW |
5 |
116,135,913 (GRCm39) |
critical splice donor site |
probably null |
|
R0206:Cit
|
UTSW |
5 |
116,132,089 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0206:Cit
|
UTSW |
5 |
116,132,089 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0226:Cit
|
UTSW |
5 |
116,122,899 (GRCm39) |
missense |
probably damaging |
0.99 |
R0320:Cit
|
UTSW |
5 |
116,117,504 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0401:Cit
|
UTSW |
5 |
116,123,538 (GRCm39) |
missense |
probably benign |
0.06 |
R0480:Cit
|
UTSW |
5 |
116,071,452 (GRCm39) |
splice site |
probably benign |
|
R0609:Cit
|
UTSW |
5 |
116,012,002 (GRCm39) |
missense |
probably damaging |
0.98 |
R0737:Cit
|
UTSW |
5 |
116,084,978 (GRCm39) |
missense |
probably damaging |
1.00 |
R1238:Cit
|
UTSW |
5 |
115,989,280 (GRCm39) |
missense |
probably benign |
0.30 |
R1503:Cit
|
UTSW |
5 |
116,011,959 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1551:Cit
|
UTSW |
5 |
116,083,901 (GRCm39) |
missense |
probably benign |
0.00 |
R1602:Cit
|
UTSW |
5 |
116,135,789 (GRCm39) |
missense |
probably damaging |
1.00 |
R1720:Cit
|
UTSW |
5 |
116,105,956 (GRCm39) |
missense |
probably damaging |
0.98 |
R1854:Cit
|
UTSW |
5 |
116,011,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R1886:Cit
|
UTSW |
5 |
116,071,545 (GRCm39) |
missense |
probably damaging |
1.00 |
R2024:Cit
|
UTSW |
5 |
116,143,899 (GRCm39) |
missense |
probably damaging |
0.97 |
R2024:Cit
|
UTSW |
5 |
116,085,983 (GRCm39) |
missense |
probably damaging |
0.97 |
R2048:Cit
|
UTSW |
5 |
116,024,872 (GRCm39) |
splice site |
probably null |
|
R2128:Cit
|
UTSW |
5 |
116,123,566 (GRCm39) |
missense |
possibly damaging |
0.63 |
R2192:Cit
|
UTSW |
5 |
116,106,068 (GRCm39) |
missense |
probably benign |
0.00 |
R2244:Cit
|
UTSW |
5 |
116,064,564 (GRCm39) |
missense |
probably damaging |
1.00 |
R2518:Cit
|
UTSW |
5 |
116,125,105 (GRCm39) |
missense |
probably damaging |
0.99 |
R2679:Cit
|
UTSW |
5 |
116,107,174 (GRCm39) |
missense |
probably benign |
0.00 |
R2898:Cit
|
UTSW |
5 |
116,012,037 (GRCm39) |
splice site |
probably null |
|
R2908:Cit
|
UTSW |
5 |
116,119,735 (GRCm39) |
missense |
probably benign |
0.00 |
R3079:Cit
|
UTSW |
5 |
116,063,545 (GRCm39) |
missense |
probably damaging |
0.97 |
R3779:Cit
|
UTSW |
5 |
115,997,400 (GRCm39) |
missense |
probably benign |
0.01 |
R4081:Cit
|
UTSW |
5 |
116,086,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R4494:Cit
|
UTSW |
5 |
116,012,043 (GRCm39) |
missense |
probably damaging |
1.00 |
R4610:Cit
|
UTSW |
5 |
116,132,146 (GRCm39) |
missense |
probably benign |
0.01 |
R4757:Cit
|
UTSW |
5 |
116,135,608 (GRCm39) |
missense |
probably damaging |
1.00 |
R4788:Cit
|
UTSW |
5 |
116,071,565 (GRCm39) |
missense |
probably damaging |
1.00 |
R4816:Cit
|
UTSW |
5 |
116,046,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R4890:Cit
|
UTSW |
5 |
116,126,182 (GRCm39) |
intron |
probably benign |
|
R4899:Cit
|
UTSW |
5 |
116,001,087 (GRCm39) |
missense |
possibly damaging |
0.60 |
R4928:Cit
|
UTSW |
5 |
116,123,856 (GRCm39) |
missense |
probably benign |
0.00 |
R5073:Cit
|
UTSW |
5 |
116,084,902 (GRCm39) |
missense |
probably benign |
0.24 |
R5151:Cit
|
UTSW |
5 |
116,117,894 (GRCm39) |
missense |
probably damaging |
1.00 |
R5154:Cit
|
UTSW |
5 |
116,126,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R5222:Cit
|
UTSW |
5 |
116,090,602 (GRCm39) |
missense |
probably benign |
0.03 |
R5814:Cit
|
UTSW |
5 |
116,117,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R5935:Cit
|
UTSW |
5 |
116,063,598 (GRCm39) |
intron |
probably benign |
|
R5946:Cit
|
UTSW |
5 |
116,135,593 (GRCm39) |
missense |
probably damaging |
1.00 |
R6051:Cit
|
UTSW |
5 |
115,984,464 (GRCm39) |
missense |
probably benign |
|
R6289:Cit
|
UTSW |
5 |
116,144,385 (GRCm39) |
makesense |
probably null |
|
R6298:Cit
|
UTSW |
5 |
116,086,124 (GRCm39) |
missense |
probably damaging |
1.00 |
R6362:Cit
|
UTSW |
5 |
116,024,735 (GRCm39) |
missense |
probably benign |
0.01 |
R6545:Cit
|
UTSW |
5 |
115,984,493 (GRCm39) |
missense |
probably null |
0.00 |
R6761:Cit
|
UTSW |
5 |
116,046,734 (GRCm39) |
missense |
probably damaging |
1.00 |
R6798:Cit
|
UTSW |
5 |
116,064,585 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6814:Cit
|
UTSW |
5 |
116,023,022 (GRCm39) |
missense |
probably damaging |
1.00 |
R6825:Cit
|
UTSW |
5 |
116,119,833 (GRCm39) |
missense |
probably damaging |
0.99 |
R6845:Cit
|
UTSW |
5 |
116,122,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R6983:Cit
|
UTSW |
5 |
116,132,150 (GRCm39) |
missense |
probably damaging |
1.00 |
R7164:Cit
|
UTSW |
5 |
116,123,846 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7359:Cit
|
UTSW |
5 |
116,064,633 (GRCm39) |
missense |
probably damaging |
1.00 |
R7597:Cit
|
UTSW |
5 |
116,024,740 (GRCm39) |
nonsense |
probably null |
|
R7729:Cit
|
UTSW |
5 |
116,122,881 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7763:Cit
|
UTSW |
5 |
116,125,060 (GRCm39) |
missense |
probably benign |
0.01 |
R7786:Cit
|
UTSW |
5 |
116,001,077 (GRCm39) |
missense |
probably benign |
0.00 |
R7799:Cit
|
UTSW |
5 |
116,001,027 (GRCm39) |
missense |
probably benign |
0.00 |
R8060:Cit
|
UTSW |
5 |
116,046,786 (GRCm39) |
missense |
probably benign |
0.00 |
R8068:Cit
|
UTSW |
5 |
116,120,294 (GRCm39) |
missense |
probably benign |
0.03 |
R8068:Cit
|
UTSW |
5 |
116,090,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R8122:Cit
|
UTSW |
5 |
116,107,069 (GRCm39) |
missense |
probably damaging |
1.00 |
R8177:Cit
|
UTSW |
5 |
116,126,218 (GRCm39) |
missense |
probably benign |
0.18 |
R8178:Cit
|
UTSW |
5 |
116,107,131 (GRCm39) |
missense |
probably damaging |
1.00 |
R8265:Cit
|
UTSW |
5 |
116,126,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R8359:Cit
|
UTSW |
5 |
116,122,603 (GRCm39) |
splice site |
probably null |
|
R8397:Cit
|
UTSW |
5 |
116,024,856 (GRCm39) |
missense |
probably benign |
|
R8489:Cit
|
UTSW |
5 |
116,083,962 (GRCm39) |
critical splice donor site |
probably null |
|
R8784:Cit
|
UTSW |
5 |
115,984,442 (GRCm39) |
nonsense |
probably null |
|
R8798:Cit
|
UTSW |
5 |
116,107,102 (GRCm39) |
missense |
probably damaging |
0.99 |
R8882:Cit
|
UTSW |
5 |
116,001,089 (GRCm39) |
missense |
probably benign |
0.04 |
R8984:Cit
|
UTSW |
5 |
116,064,534 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9091:Cit
|
UTSW |
5 |
115,984,161 (GRCm39) |
intron |
probably benign |
|
R9127:Cit
|
UTSW |
5 |
116,074,896 (GRCm39) |
nonsense |
probably null |
|
R9204:Cit
|
UTSW |
5 |
116,126,498 (GRCm39) |
missense |
probably damaging |
0.99 |
R9212:Cit
|
UTSW |
5 |
116,013,952 (GRCm39) |
missense |
possibly damaging |
0.75 |
R9279:Cit
|
UTSW |
5 |
116,065,970 (GRCm39) |
missense |
probably damaging |
1.00 |
R9288:Cit
|
UTSW |
5 |
116,123,512 (GRCm39) |
missense |
probably damaging |
1.00 |
R9377:Cit
|
UTSW |
5 |
116,084,914 (GRCm39) |
missense |
probably benign |
0.04 |
R9520:Cit
|
UTSW |
5 |
116,079,954 (GRCm39) |
nonsense |
probably null |
|
Z1088:Cit
|
UTSW |
5 |
116,123,592 (GRCm39) |
missense |
possibly damaging |
0.62 |
Z1176:Cit
|
UTSW |
5 |
116,124,662 (GRCm39) |
missense |
probably damaging |
1.00 |
|