Other mutations in this stock |
Total: 98 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adtrp |
T |
C |
13: 41,920,941 (GRCm39) |
T88A |
probably damaging |
Het |
Afap1l1 |
A |
G |
18: 61,889,976 (GRCm39) |
S87P |
probably benign |
Het |
Ankrd27 |
A |
G |
7: 35,303,125 (GRCm39) |
K196R |
probably benign |
Het |
Apoe |
G |
A |
7: 19,431,005 (GRCm39) |
T79M |
probably damaging |
Het |
Arrdc3 |
T |
A |
13: 81,032,011 (GRCm39) |
Y81* |
probably null |
Het |
Arrdc3 |
T |
A |
13: 81,039,194 (GRCm39) |
I75N |
probably damaging |
Het |
Asah2 |
T |
A |
19: 31,981,131 (GRCm39) |
K629* |
probably null |
Het |
Ass1 |
A |
T |
2: 31,404,831 (GRCm39) |
N371Y |
probably damaging |
Het |
C130074G19Rik |
A |
G |
1: 184,615,119 (GRCm39) |
S24P |
probably benign |
Het |
C87436 |
A |
G |
6: 86,423,265 (GRCm39) |
|
probably benign |
Het |
Calcrl |
T |
C |
2: 84,203,618 (GRCm39) |
D54G |
probably benign |
Het |
Clcn2 |
T |
C |
16: 20,529,140 (GRCm39) |
N367S |
probably null |
Het |
Cnot1 |
G |
T |
8: 96,487,969 (GRCm39) |
D562E |
probably damaging |
Het |
Commd6 |
G |
A |
14: 101,877,709 (GRCm39) |
|
probably benign |
Het |
Cox6a2 |
G |
A |
7: 127,805,212 (GRCm39) |
|
probably benign |
Het |
Cp |
T |
A |
3: 20,022,287 (GRCm39) |
Y230N |
probably damaging |
Het |
Dclre1c |
T |
C |
2: 3,439,032 (GRCm39) |
V64A |
probably damaging |
Het |
Eng |
T |
C |
2: 32,567,692 (GRCm39) |
V110A |
probably damaging |
Het |
Esyt3 |
T |
C |
9: 99,220,860 (GRCm39) |
I114M |
possibly damaging |
Het |
Fam83h |
A |
T |
15: 75,875,811 (GRCm39) |
Y509N |
probably damaging |
Het |
Fat2 |
A |
T |
11: 55,202,075 (GRCm39) |
L333H |
probably damaging |
Het |
Fbxo21 |
A |
G |
5: 118,146,078 (GRCm39) |
N567S |
possibly damaging |
Het |
Fcsk |
T |
C |
8: 111,610,865 (GRCm39) |
|
probably benign |
Het |
Fn1 |
A |
T |
1: 71,634,879 (GRCm39) |
L1964Q |
probably damaging |
Het |
Gorasp1 |
G |
T |
9: 119,757,312 (GRCm39) |
S353R |
possibly damaging |
Het |
Grk2 |
C |
T |
19: 4,337,262 (GRCm39) |
E646K |
probably damaging |
Het |
Hoxc11 |
T |
C |
15: 102,863,397 (GRCm39) |
V146A |
probably damaging |
Het |
Igf2bp2 |
T |
C |
16: 21,894,841 (GRCm39) |
T301A |
probably benign |
Het |
Il11 |
T |
C |
7: 4,776,658 (GRCm39) |
S111G |
probably benign |
Het |
Ist1 |
A |
T |
8: 110,403,418 (GRCm39) |
I273K |
probably benign |
Het |
Kdm2b |
G |
A |
5: 123,019,806 (GRCm39) |
S738L |
probably benign |
Het |
Lrp2 |
T |
A |
2: 69,346,895 (GRCm39) |
N784Y |
probably benign |
Het |
Lrp6 |
T |
C |
6: 134,462,716 (GRCm39) |
E648G |
probably damaging |
Het |
Mapk15 |
G |
A |
15: 75,870,103 (GRCm39) |
E408K |
probably benign |
Het |
Mdn1 |
T |
A |
4: 32,718,317 (GRCm39) |
F2191I |
possibly damaging |
Het |
Metrn |
C |
A |
17: 26,015,479 (GRCm39) |
V79F |
possibly damaging |
Het |
Mtbp |
T |
A |
15: 55,449,889 (GRCm39) |
|
probably benign |
Het |
Myh11 |
C |
A |
16: 14,041,883 (GRCm39) |
Q720H |
probably damaging |
Het |
Myo3a |
T |
A |
2: 22,469,753 (GRCm39) |
I508N |
probably damaging |
Het |
Nat9 |
A |
T |
11: 115,075,941 (GRCm39) |
Y27N |
probably damaging |
Het |
Ncapg2 |
T |
C |
12: 116,393,455 (GRCm39) |
F553S |
probably damaging |
Het |
Nipsnap3b |
T |
A |
4: 53,015,112 (GRCm39) |
L53Q |
probably damaging |
Het |
Nlrp3 |
A |
T |
11: 59,449,274 (GRCm39) |
H852L |
probably benign |
Het |
Or2d3b |
A |
G |
7: 106,514,226 (GRCm39) |
I274V |
probably benign |
Het |
Or2t6 |
T |
A |
14: 14,176,092 (GRCm38) |
|
probably benign |
Het |
Or4a78 |
T |
A |
2: 89,497,428 (GRCm39) |
K267N |
probably damaging |
Het |
Or52e3 |
A |
T |
7: 102,869,558 (GRCm39) |
D211V |
probably damaging |
Het |
Or52e3 |
G |
A |
7: 102,869,584 (GRCm39) |
A220T |
probably benign |
Het |
Or5b122 |
A |
G |
19: 13,563,240 (GRCm39) |
I191V |
probably benign |
Het |
Pax9 |
A |
G |
12: 56,756,528 (GRCm39) |
T289A |
probably benign |
Het |
Pcyt2 |
A |
T |
11: 120,506,695 (GRCm39) |
I53N |
possibly damaging |
Het |
Pdlim4 |
C |
T |
11: 53,945,875 (GRCm39) |
V327M |
probably damaging |
Het |
Pdzph1 |
T |
A |
17: 59,229,756 (GRCm39) |
|
probably benign |
Het |
Plekhm2 |
C |
T |
4: 141,369,704 (GRCm39) |
|
probably benign |
Het |
Ppt1 |
T |
C |
4: 122,742,216 (GRCm39) |
|
probably benign |
Het |
Prdm1 |
C |
T |
10: 44,317,675 (GRCm39) |
E398K |
probably damaging |
Het |
Prep |
T |
C |
10: 44,991,174 (GRCm39) |
V280A |
probably benign |
Het |
Prkdc |
T |
A |
16: 15,526,565 (GRCm39) |
|
probably benign |
Het |
Proser3 |
G |
A |
7: 30,239,563 (GRCm39) |
R514C |
probably damaging |
Het |
Ptk7 |
G |
A |
17: 46,883,688 (GRCm39) |
|
probably benign |
Het |
Rbm45 |
T |
C |
2: 76,208,742 (GRCm39) |
Y293H |
probably damaging |
Het |
Rnf213 |
A |
C |
11: 119,355,878 (GRCm39) |
E4108A |
possibly damaging |
Het |
Sdk2 |
A |
G |
11: 113,747,581 (GRCm39) |
L643P |
probably damaging |
Het |
Sec24d |
C |
A |
3: 123,144,525 (GRCm39) |
|
probably benign |
Het |
Sh2d3c |
C |
G |
2: 32,643,033 (GRCm39) |
H587D |
probably damaging |
Het |
Slc1a1 |
G |
A |
19: 28,878,884 (GRCm39) |
G208S |
probably benign |
Het |
Slc35b4 |
A |
T |
6: 34,135,452 (GRCm39) |
Y287N |
probably damaging |
Het |
Slc46a2 |
T |
A |
4: 59,914,544 (GRCm39) |
L126F |
probably damaging |
Het |
Slc4a8 |
T |
C |
15: 100,698,374 (GRCm39) |
M621T |
possibly damaging |
Het |
Slc9b2 |
T |
A |
3: 135,042,269 (GRCm39) |
V516D |
possibly damaging |
Het |
Slco1a6 |
T |
A |
6: 142,102,948 (GRCm39) |
|
probably benign |
Het |
Sncg |
C |
T |
14: 34,096,495 (GRCm39) |
V15I |
probably benign |
Het |
Srgap2 |
T |
C |
1: 131,283,302 (GRCm39) |
T260A |
probably damaging |
Het |
Stk10 |
T |
A |
11: 32,537,305 (GRCm39) |
|
probably benign |
Het |
Taf5 |
A |
G |
19: 47,064,301 (GRCm39) |
S415G |
possibly damaging |
Het |
Tdp1 |
C |
T |
12: 99,921,217 (GRCm39) |
|
probably benign |
Het |
Tdp2 |
T |
G |
13: 25,025,333 (GRCm39) |
|
probably null |
Het |
Tgfbi |
T |
A |
13: 56,777,587 (GRCm39) |
I357N |
probably benign |
Het |
Tmem116 |
A |
G |
5: 121,633,159 (GRCm39) |
T178A |
probably damaging |
Het |
Tnrc6a |
G |
A |
7: 122,769,617 (GRCm39) |
R469H |
probably benign |
Het |
Top2a |
A |
T |
11: 98,893,729 (GRCm39) |
L1055* |
probably null |
Het |
Tox |
T |
A |
4: 6,842,411 (GRCm39) |
M40L |
probably benign |
Het |
Trib2 |
A |
T |
12: 15,859,930 (GRCm39) |
H110Q |
probably benign |
Het |
Trpa1 |
A |
G |
1: 14,973,439 (GRCm39) |
I293T |
possibly damaging |
Het |
Trpv2 |
A |
G |
11: 62,481,086 (GRCm39) |
Y395C |
probably damaging |
Het |
Ubn2 |
T |
A |
6: 38,411,535 (GRCm39) |
|
probably null |
Het |
Ubr4 |
C |
T |
4: 139,157,487 (GRCm39) |
T2348M |
probably damaging |
Het |
Ubxn4 |
G |
A |
1: 128,190,641 (GRCm39) |
E256K |
probably benign |
Het |
Vmn1r33 |
C |
A |
6: 66,589,510 (GRCm39) |
G15* |
probably null |
Het |
Vmn1r37 |
T |
A |
6: 66,708,769 (GRCm39) |
S95T |
probably benign |
Het |
Vmn2r57 |
A |
G |
7: 41,050,076 (GRCm39) |
C558R |
probably damaging |
Het |
Vnn1 |
T |
C |
10: 23,774,500 (GRCm39) |
|
probably null |
Het |
Vps13c |
T |
C |
9: 67,826,544 (GRCm39) |
V1395A |
probably benign |
Het |
Vwa7 |
A |
G |
17: 35,238,781 (GRCm39) |
I290V |
probably benign |
Het |
Wdr93 |
A |
G |
7: 79,408,221 (GRCm39) |
E234G |
probably damaging |
Het |
Zfp385b |
A |
T |
2: 77,246,291 (GRCm39) |
S245R |
probably benign |
Het |
Zfp942 |
A |
T |
17: 22,147,319 (GRCm39) |
C437S |
probably damaging |
Het |
Zfyve9 |
T |
A |
4: 108,575,902 (GRCm39) |
E393V |
possibly damaging |
Het |
|
Other mutations in 4930579F01Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00335:4930579F01Rik
|
APN |
3 |
137,891,959 (GRCm39) |
intron |
probably benign |
|
IGL02121:4930579F01Rik
|
APN |
3 |
137,870,134 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02424:4930579F01Rik
|
APN |
3 |
137,880,466 (GRCm39) |
splice site |
probably benign |
|
R0008:4930579F01Rik
|
UTSW |
3 |
137,882,346 (GRCm39) |
missense |
possibly damaging |
0.67 |
R0373:4930579F01Rik
|
UTSW |
3 |
137,879,343 (GRCm39) |
missense |
probably damaging |
0.96 |
R1082:4930579F01Rik
|
UTSW |
3 |
137,879,332 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1163:4930579F01Rik
|
UTSW |
3 |
137,882,271 (GRCm39) |
missense |
probably damaging |
1.00 |
R1538:4930579F01Rik
|
UTSW |
3 |
137,889,517 (GRCm39) |
missense |
probably damaging |
1.00 |
R2151:4930579F01Rik
|
UTSW |
3 |
137,882,217 (GRCm39) |
critical splice donor site |
probably null |
|
R2364:4930579F01Rik
|
UTSW |
3 |
137,871,584 (GRCm39) |
missense |
probably benign |
0.00 |
R3978:4930579F01Rik
|
UTSW |
3 |
137,889,435 (GRCm39) |
missense |
probably benign |
0.01 |
R4108:4930579F01Rik
|
UTSW |
3 |
137,889,431 (GRCm39) |
missense |
probably benign |
0.14 |
R5812:4930579F01Rik
|
UTSW |
3 |
137,882,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R5960:4930579F01Rik
|
UTSW |
3 |
137,889,528 (GRCm39) |
missense |
possibly damaging |
0.58 |
R6329:4930579F01Rik
|
UTSW |
3 |
137,879,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R6599:4930579F01Rik
|
UTSW |
3 |
137,882,250 (GRCm39) |
missense |
probably benign |
0.00 |
R6862:4930579F01Rik
|
UTSW |
3 |
137,891,949 (GRCm39) |
intron |
probably benign |
|
R6897:4930579F01Rik
|
UTSW |
3 |
137,889,534 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7092:4930579F01Rik
|
UTSW |
3 |
137,889,506 (GRCm39) |
missense |
probably benign |
0.08 |
R7919:4930579F01Rik
|
UTSW |
3 |
137,885,311 (GRCm39) |
missense |
probably damaging |
1.00 |
R8381:4930579F01Rik
|
UTSW |
3 |
137,879,282 (GRCm39) |
critical splice donor site |
probably null |
|
R9024:4930579F01Rik
|
UTSW |
3 |
137,891,923 (GRCm39) |
missense |
unknown |
|
R9180:4930579F01Rik
|
UTSW |
3 |
137,889,470 (GRCm39) |
missense |
probably benign |
0.05 |
|