Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca17 |
G |
A |
17: 24,483,318 (GRCm39) |
R1713C |
unknown |
Het |
Ano6 |
C |
T |
15: 95,846,298 (GRCm39) |
T512I |
probably damaging |
Het |
Ap3s1 |
T |
C |
18: 46,887,505 (GRCm39) |
V46A |
probably benign |
Het |
Art2a |
C |
A |
7: 101,204,413 (GRCm39) |
V42F |
probably damaging |
Het |
Asph |
C |
T |
4: 9,531,960 (GRCm39) |
V386M |
probably benign |
Het |
B4galnt4 |
T |
A |
7: 140,644,643 (GRCm39) |
D179E |
probably benign |
Het |
Bbx |
T |
C |
16: 50,071,730 (GRCm39) |
I232V |
probably benign |
Het |
C1ql2 |
A |
G |
1: 120,269,321 (GRCm39) |
I159V |
probably benign |
Het |
Ccar1 |
A |
G |
10: 62,612,496 (GRCm39) |
V223A |
possibly damaging |
Het |
Cd2ap |
A |
T |
17: 43,136,802 (GRCm39) |
L277I |
probably benign |
Het |
Cfap44 |
G |
A |
16: 44,250,255 (GRCm39) |
E778K |
probably benign |
Het |
Chd3 |
A |
T |
11: 69,240,063 (GRCm39) |
D1626E |
probably benign |
Het |
Crocc |
C |
T |
4: 140,769,032 (GRCm39) |
G505S |
probably benign |
Het |
Crocc |
T |
A |
4: 140,773,851 (GRCm39) |
Q72L |
probably damaging |
Het |
Drosha |
T |
C |
15: 12,834,156 (GRCm39) |
|
probably benign |
Het |
Eps8l1 |
T |
A |
7: 4,474,296 (GRCm39) |
S256T |
possibly damaging |
Het |
F830045P16Rik |
A |
G |
2: 129,316,310 (GRCm39) |
V133A |
probably damaging |
Het |
Fermt2 |
A |
T |
14: 45,697,338 (GRCm39) |
M671K |
possibly damaging |
Het |
Fhdc1 |
G |
A |
3: 84,353,336 (GRCm39) |
L630F |
probably benign |
Het |
Gon4l |
T |
C |
3: 88,807,306 (GRCm39) |
S1667P |
probably damaging |
Het |
Greb1l |
A |
C |
18: 10,557,340 (GRCm39) |
K1780T |
probably damaging |
Het |
H2-Q10 |
C |
T |
17: 35,781,026 (GRCm39) |
T8M |
probably benign |
Het |
Hmcn2 |
A |
T |
2: 31,324,725 (GRCm39) |
T4215S |
probably benign |
Het |
I0C0044D17Rik |
G |
A |
4: 98,708,576 (GRCm39) |
|
probably benign |
Het |
Ifi204 |
A |
G |
1: 173,579,223 (GRCm39) |
F541L |
probably benign |
Het |
Igkv6-17 |
C |
T |
6: 70,348,764 (GRCm39) |
A45V |
probably damaging |
Het |
Intu |
G |
A |
3: 40,608,524 (GRCm39) |
A161T |
probably damaging |
Het |
Kcnmb2 |
A |
G |
3: 32,233,141 (GRCm39) |
Y73C |
probably damaging |
Het |
Lrit1 |
T |
C |
14: 36,776,945 (GRCm39) |
F22L |
probably benign |
Het |
Lrp1b |
A |
T |
2: 41,174,156 (GRCm39) |
C699* |
probably null |
Het |
Lrrc8d |
A |
G |
5: 105,959,992 (GRCm39) |
D134G |
probably benign |
Het |
Map1b |
T |
C |
13: 99,567,645 (GRCm39) |
D1692G |
unknown |
Het |
Met |
C |
T |
6: 17,491,967 (GRCm39) |
S243F |
probably damaging |
Het |
Mlph |
C |
A |
1: 90,855,882 (GRCm39) |
H96Q |
probably damaging |
Het |
Mycbp2 |
A |
T |
14: 103,372,582 (GRCm39) |
V4088D |
probably damaging |
Het |
Nampt |
T |
A |
12: 32,898,658 (GRCm39) |
S425T |
probably damaging |
Het |
Nts |
G |
A |
10: 102,320,856 (GRCm39) |
H78Y |
probably benign |
Het |
Nxf1 |
A |
G |
19: 8,745,151 (GRCm39) |
E467G |
possibly damaging |
Het |
Olfml2a |
C |
A |
2: 38,841,155 (GRCm39) |
D230E |
probably benign |
Het |
Or4b13 |
C |
A |
2: 90,082,771 (GRCm39) |
C187F |
probably benign |
Het |
Or52n2c |
C |
T |
7: 104,574,599 (GRCm39) |
R124H |
probably benign |
Het |
Pcsk5 |
A |
G |
19: 17,432,045 (GRCm39) |
|
probably null |
Het |
Pde5a |
C |
A |
3: 122,618,574 (GRCm39) |
T629K |
probably benign |
Het |
Plcb3 |
G |
T |
19: 6,940,202 (GRCm39) |
R462S |
possibly damaging |
Het |
Pnpla6 |
T |
A |
8: 3,574,156 (GRCm39) |
M469K |
probably benign |
Het |
Pram1 |
A |
T |
17: 33,860,386 (GRCm39) |
K318* |
probably null |
Het |
Prkd1 |
T |
C |
12: 50,388,826 (GRCm39) |
R906G |
probably benign |
Het |
Ptprh |
T |
A |
7: 4,576,361 (GRCm39) |
T300S |
possibly damaging |
Het |
Rdh16f2 |
A |
G |
10: 127,712,743 (GRCm39) |
Y247C |
probably benign |
Het |
Rimbp3 |
A |
G |
16: 17,028,781 (GRCm39) |
E735G |
probably damaging |
Het |
Sall3 |
G |
A |
18: 81,017,470 (GRCm39) |
P153S |
possibly damaging |
Het |
Samd4b |
T |
A |
7: 28,123,056 (GRCm39) |
M1L |
possibly damaging |
Het |
Septin12 |
T |
C |
16: 4,810,127 (GRCm39) |
E136G |
probably damaging |
Het |
Shpk |
A |
T |
11: 73,104,270 (GRCm39) |
K140* |
probably null |
Het |
Sidt1 |
G |
T |
16: 44,079,829 (GRCm39) |
F608L |
probably benign |
Het |
Skint5 |
A |
G |
4: 113,347,842 (GRCm39) |
Y1300H |
probably benign |
Het |
Slc22a28 |
G |
A |
19: 8,094,386 (GRCm39) |
P212S |
probably benign |
Het |
Slc22a5 |
A |
T |
11: 53,758,359 (GRCm39) |
F480L |
possibly damaging |
Het |
Slc35e2 |
C |
T |
4: 155,694,483 (GRCm39) |
P10L |
probably benign |
Het |
Slc3a1 |
C |
T |
17: 85,335,951 (GRCm39) |
P31L |
probably benign |
Het |
Slc4a7 |
T |
C |
14: 14,793,964 (GRCm38) |
V1074A |
possibly damaging |
Het |
Snx2 |
C |
T |
18: 53,342,697 (GRCm39) |
Q254* |
probably null |
Het |
Sox30 |
G |
A |
11: 45,882,769 (GRCm39) |
V600I |
probably benign |
Het |
Svil |
T |
G |
18: 5,106,724 (GRCm39) |
V1855G |
probably damaging |
Het |
Tdpoz9 |
A |
G |
3: 93,957,408 (GRCm39) |
F7L |
probably benign |
Het |
Tdrd7 |
A |
G |
4: 46,005,486 (GRCm39) |
T431A |
probably benign |
Het |
Tenm2 |
A |
T |
11: 36,054,544 (GRCm39) |
|
probably null |
Het |
Tigar |
A |
G |
6: 127,068,164 (GRCm39) |
S85P |
probably benign |
Het |
Tnr |
A |
C |
1: 159,740,254 (GRCm39) |
M1143L |
probably benign |
Het |
Trio |
G |
T |
15: 27,891,465 (GRCm39) |
Q429K |
possibly damaging |
Het |
Urb1 |
T |
C |
16: 90,585,985 (GRCm39) |
I452M |
probably benign |
Het |
Vax1 |
C |
A |
19: 59,157,036 (GRCm39) |
R99L |
unknown |
Het |
Xab2 |
A |
T |
8: 3,663,051 (GRCm39) |
I510N |
possibly damaging |
Het |
Zbtb34 |
A |
T |
2: 33,301,842 (GRCm39) |
I233K |
possibly damaging |
Het |
Zbtb47 |
A |
G |
9: 121,592,598 (GRCm39) |
E306G |
probably benign |
Het |
Zfp27 |
A |
G |
7: 29,593,727 (GRCm39) |
F746S |
probably damaging |
Het |
Zfp719 |
C |
T |
7: 43,239,050 (GRCm39) |
Q213* |
probably null |
Het |
Zswim6 |
T |
C |
13: 107,865,112 (GRCm39) |
|
noncoding transcript |
Het |
|
Other mutations in Uroc1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00963:Uroc1
|
APN |
6 |
90,315,810 (GRCm39) |
missense |
probably benign |
|
IGL01015:Uroc1
|
APN |
6 |
90,335,883 (GRCm39) |
splice site |
probably benign |
|
IGL01386:Uroc1
|
APN |
6 |
90,323,747 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01449:Uroc1
|
APN |
6 |
90,315,635 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01514:Uroc1
|
APN |
6 |
90,340,082 (GRCm39) |
splice site |
probably benign |
|
IGL02060:Uroc1
|
APN |
6 |
90,315,237 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02247:Uroc1
|
APN |
6 |
90,324,910 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02256:Uroc1
|
APN |
6 |
90,323,669 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL02886:Uroc1
|
APN |
6 |
90,323,811 (GRCm39) |
splice site |
probably benign |
|
IGL03087:Uroc1
|
APN |
6 |
90,340,085 (GRCm39) |
splice site |
probably benign |
|
PIT4651001:Uroc1
|
UTSW |
6 |
90,340,095 (GRCm39) |
nonsense |
probably null |
|
R0034:Uroc1
|
UTSW |
6 |
90,322,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R0245:Uroc1
|
UTSW |
6 |
90,321,179 (GRCm39) |
missense |
probably damaging |
1.00 |
R0402:Uroc1
|
UTSW |
6 |
90,324,284 (GRCm39) |
missense |
probably damaging |
1.00 |
R0570:Uroc1
|
UTSW |
6 |
90,315,546 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0729:Uroc1
|
UTSW |
6 |
90,313,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R1471:Uroc1
|
UTSW |
6 |
90,321,153 (GRCm39) |
missense |
probably damaging |
1.00 |
R1782:Uroc1
|
UTSW |
6 |
90,313,901 (GRCm39) |
missense |
probably damaging |
1.00 |
R1866:Uroc1
|
UTSW |
6 |
90,338,506 (GRCm39) |
missense |
probably benign |
0.03 |
R1983:Uroc1
|
UTSW |
6 |
90,322,351 (GRCm39) |
missense |
probably damaging |
1.00 |
R2086:Uroc1
|
UTSW |
6 |
90,321,096 (GRCm39) |
missense |
probably damaging |
1.00 |
R2321:Uroc1
|
UTSW |
6 |
90,324,229 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3720:Uroc1
|
UTSW |
6 |
90,323,337 (GRCm39) |
missense |
probably damaging |
1.00 |
R3874:Uroc1
|
UTSW |
6 |
90,338,494 (GRCm39) |
nonsense |
probably null |
|
R4628:Uroc1
|
UTSW |
6 |
90,332,310 (GRCm39) |
missense |
probably damaging |
0.99 |
R4810:Uroc1
|
UTSW |
6 |
90,340,135 (GRCm39) |
missense |
probably damaging |
1.00 |
R4820:Uroc1
|
UTSW |
6 |
90,334,600 (GRCm39) |
critical splice donor site |
probably null |
|
R4838:Uroc1
|
UTSW |
6 |
90,326,174 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4880:Uroc1
|
UTSW |
6 |
90,334,519 (GRCm39) |
missense |
probably damaging |
1.00 |
R4964:Uroc1
|
UTSW |
6 |
90,322,376 (GRCm39) |
missense |
probably damaging |
0.98 |
R4966:Uroc1
|
UTSW |
6 |
90,322,376 (GRCm39) |
missense |
probably damaging |
0.98 |
R5468:Uroc1
|
UTSW |
6 |
90,315,586 (GRCm39) |
missense |
probably benign |
0.45 |
R5592:Uroc1
|
UTSW |
6 |
90,332,326 (GRCm39) |
missense |
probably damaging |
0.99 |
R5698:Uroc1
|
UTSW |
6 |
90,324,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R5789:Uroc1
|
UTSW |
6 |
90,321,179 (GRCm39) |
missense |
probably damaging |
1.00 |
R5853:Uroc1
|
UTSW |
6 |
90,323,738 (GRCm39) |
missense |
probably damaging |
0.99 |
R6883:Uroc1
|
UTSW |
6 |
90,315,574 (GRCm39) |
nonsense |
probably null |
|
R7374:Uroc1
|
UTSW |
6 |
90,315,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R7394:Uroc1
|
UTSW |
6 |
90,322,315 (GRCm39) |
missense |
probably damaging |
1.00 |
R7427:Uroc1
|
UTSW |
6 |
90,323,344 (GRCm39) |
missense |
possibly damaging |
0.56 |
R8224:Uroc1
|
UTSW |
6 |
90,321,049 (GRCm39) |
splice site |
probably null |
|
R8376:Uroc1
|
UTSW |
6 |
90,314,697 (GRCm39) |
missense |
probably damaging |
0.99 |
R8807:Uroc1
|
UTSW |
6 |
90,328,110 (GRCm39) |
missense |
probably damaging |
1.00 |
R8857:Uroc1
|
UTSW |
6 |
90,334,510 (GRCm39) |
missense |
possibly damaging |
0.74 |
R9418:Uroc1
|
UTSW |
6 |
90,313,880 (GRCm39) |
missense |
probably benign |
0.00 |
R9440:Uroc1
|
UTSW |
6 |
90,322,353 (GRCm39) |
missense |
possibly damaging |
0.94 |
X0021:Uroc1
|
UTSW |
6 |
90,321,132 (GRCm39) |
missense |
probably benign |
0.40 |
|