Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abl1 |
T |
A |
2: 31,680,811 (GRCm39) |
S368T |
probably damaging |
Het |
Acmsd |
A |
G |
1: 127,657,172 (GRCm39) |
|
probably benign |
Het |
Arid3b |
A |
T |
9: 57,703,495 (GRCm39) |
S445T |
probably benign |
Het |
Brinp1 |
A |
G |
4: 68,759,591 (GRCm39) |
V91A |
probably benign |
Het |
Ccne1 |
A |
G |
7: 37,805,702 (GRCm39) |
|
probably null |
Het |
Col3a1 |
A |
T |
1: 45,366,973 (GRCm39) |
I249F |
unknown |
Het |
Crybg3 |
T |
C |
16: 59,377,688 (GRCm39) |
I1189V |
probably benign |
Het |
Cyp2d34 |
A |
T |
15: 82,500,964 (GRCm39) |
D389E |
probably benign |
Het |
D130043K22Rik |
A |
C |
13: 25,077,360 (GRCm39) |
I998L |
probably damaging |
Het |
Dgkq |
A |
G |
5: 108,803,056 (GRCm39) |
I298T |
possibly damaging |
Het |
Dnah17 |
T |
C |
11: 117,971,550 (GRCm39) |
E2161G |
probably damaging |
Het |
Dnajc25 |
T |
C |
4: 59,017,824 (GRCm39) |
|
probably null |
Het |
Dpp9 |
G |
A |
17: 56,496,405 (GRCm39) |
R768* |
probably null |
Het |
Dusp6 |
T |
A |
10: 99,100,740 (GRCm39) |
N245K |
probably damaging |
Het |
Eea1 |
C |
A |
10: 95,831,493 (GRCm39) |
H195N |
probably benign |
Het |
Efhc1 |
A |
G |
1: 21,059,744 (GRCm39) |
E598G |
probably benign |
Het |
Epb41l1 |
T |
C |
2: 156,376,682 (GRCm39) |
V809A |
probably damaging |
Het |
Gas8 |
T |
A |
8: 124,245,690 (GRCm39) |
M1K |
probably null |
Het |
Gcm1 |
G |
A |
9: 77,971,961 (GRCm39) |
V301I |
probably benign |
Het |
Gm11554 |
T |
A |
11: 99,695,085 (GRCm39) |
S43C |
unknown |
Het |
Gm7298 |
A |
G |
6: 121,758,912 (GRCm39) |
I1177V |
probably benign |
Het |
Gm8011 |
A |
G |
14: 42,285,918 (GRCm39) |
T27A |
|
Het |
Hmcn1 |
A |
G |
1: 150,522,421 (GRCm39) |
I3493T |
probably benign |
Het |
Insrr |
T |
G |
3: 87,716,039 (GRCm39) |
I578S |
probably damaging |
Het |
Kif13b |
A |
G |
14: 64,994,972 (GRCm39) |
D908G |
probably null |
Het |
Lhcgr |
G |
C |
17: 89,079,474 (GRCm39) |
Q71E |
probably benign |
Het |
Lrrc7 |
C |
A |
3: 157,997,595 (GRCm39) |
E156* |
probably null |
Het |
Lrrc9 |
A |
G |
12: 72,547,590 (GRCm39) |
D1255G |
probably damaging |
Het |
Mcidas |
A |
G |
13: 113,133,416 (GRCm39) |
N116D |
probably benign |
Het |
Mmp7 |
A |
G |
9: 7,697,594 (GRCm39) |
N210D |
probably damaging |
Het |
Morc3 |
A |
G |
16: 93,671,748 (GRCm39) |
D926G |
probably damaging |
Het |
Mrgpra9 |
A |
G |
7: 46,885,385 (GRCm39) |
I94T |
possibly damaging |
Het |
Muc16 |
C |
A |
9: 18,549,038 (GRCm39) |
V5752F |
possibly damaging |
Het |
Myo16 |
A |
T |
8: 10,612,183 (GRCm39) |
D1276V |
unknown |
Het |
Nlrc4 |
T |
G |
17: 74,753,537 (GRCm39) |
E282A |
probably damaging |
Het |
Nos2 |
T |
A |
11: 78,827,297 (GRCm39) |
Y227* |
probably null |
Het |
Obox5 |
A |
C |
7: 15,492,713 (GRCm39) |
M223L |
probably benign |
Het |
Or10ak13 |
C |
A |
4: 118,638,896 (GRCm39) |
L295F |
possibly damaging |
Het |
Pygm |
G |
A |
19: 6,435,966 (GRCm39) |
R139H |
probably damaging |
Het |
Ranbp2 |
C |
A |
10: 58,303,099 (GRCm39) |
P789T |
probably damaging |
Het |
Riok2 |
T |
G |
17: 17,607,501 (GRCm39) |
S350A |
probably benign |
Het |
Rnf214 |
C |
T |
9: 45,778,845 (GRCm39) |
V445I |
possibly damaging |
Het |
Skida1 |
C |
T |
2: 18,051,083 (GRCm39) |
V603I |
unknown |
Het |
Skint6 |
T |
A |
4: 112,755,335 (GRCm39) |
R747S |
probably benign |
Het |
Slc24a5 |
G |
A |
2: 124,927,694 (GRCm39) |
W331* |
probably null |
Het |
Slc5a10 |
A |
T |
11: 61,564,405 (GRCm39) |
C525S |
probably benign |
Het |
Styxl2 |
A |
G |
1: 165,928,044 (GRCm39) |
S523P |
probably damaging |
Het |
Sult2b1 |
T |
C |
7: 45,380,718 (GRCm39) |
Y288C |
probably damaging |
Het |
Tagln3 |
G |
T |
16: 45,543,440 (GRCm39) |
N67K |
probably damaging |
Het |
Trav21-dv12 |
A |
T |
14: 54,114,162 (GRCm39) |
H94L |
probably benign |
Het |
Tshz2 |
A |
G |
2: 169,726,094 (GRCm39) |
E230G |
probably damaging |
Het |
Usb1 |
T |
A |
8: 96,071,931 (GRCm39) |
H210Q |
probably damaging |
Het |
Vill |
C |
T |
9: 118,899,716 (GRCm39) |
P767L |
probably benign |
Het |
Vmn2r94 |
A |
T |
17: 18,477,603 (GRCm39) |
N269K |
probably benign |
Het |
Zfp764l1 |
C |
T |
7: 126,992,496 (GRCm39) |
C38Y |
probably null |
Het |
|
Other mutations in Lrrc34 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02502:Lrrc34
|
APN |
3 |
30,699,394 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02738:Lrrc34
|
APN |
3 |
30,685,441 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL02985:Lrrc34
|
APN |
3 |
30,690,444 (GRCm39) |
missense |
probably benign |
0.32 |
IGL02999:Lrrc34
|
APN |
3 |
30,688,782 (GRCm39) |
missense |
probably damaging |
0.99 |
R0367:Lrrc34
|
UTSW |
3 |
30,684,142 (GRCm39) |
missense |
probably benign |
0.08 |
R0761:Lrrc34
|
UTSW |
3 |
30,685,425 (GRCm39) |
splice site |
probably null |
|
R1426:Lrrc34
|
UTSW |
3 |
30,697,728 (GRCm39) |
unclassified |
probably benign |
|
R1980:Lrrc34
|
UTSW |
3 |
30,696,890 (GRCm39) |
missense |
probably benign |
0.33 |
R2215:Lrrc34
|
UTSW |
3 |
30,697,678 (GRCm39) |
missense |
probably benign |
0.03 |
R2414:Lrrc34
|
UTSW |
3 |
30,688,711 (GRCm39) |
missense |
probably benign |
0.00 |
R4379:Lrrc34
|
UTSW |
3 |
30,685,524 (GRCm39) |
missense |
probably damaging |
1.00 |
R5214:Lrrc34
|
UTSW |
3 |
30,690,397 (GRCm39) |
nonsense |
probably null |
|
R5418:Lrrc34
|
UTSW |
3 |
30,696,923 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5662:Lrrc34
|
UTSW |
3 |
30,685,473 (GRCm39) |
missense |
probably benign |
0.03 |
R6736:Lrrc34
|
UTSW |
3 |
30,679,008 (GRCm39) |
missense |
probably benign |
0.03 |
R6809:Lrrc34
|
UTSW |
3 |
30,688,749 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6941:Lrrc34
|
UTSW |
3 |
30,678,969 (GRCm39) |
missense |
probably benign |
0.01 |
R7017:Lrrc34
|
UTSW |
3 |
30,699,465 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7080:Lrrc34
|
UTSW |
3 |
30,688,705 (GRCm39) |
missense |
probably damaging |
0.96 |
R7139:Lrrc34
|
UTSW |
3 |
30,679,036 (GRCm39) |
missense |
probably benign |
0.22 |
R7191:Lrrc34
|
UTSW |
3 |
30,679,027 (GRCm39) |
missense |
possibly damaging |
0.61 |
R7662:Lrrc34
|
UTSW |
3 |
30,697,452 (GRCm39) |
missense |
probably benign |
0.16 |
R7707:Lrrc34
|
UTSW |
3 |
30,679,041 (GRCm39) |
missense |
probably benign |
0.00 |
R7945:Lrrc34
|
UTSW |
3 |
30,696,886 (GRCm39) |
critical splice donor site |
probably null |
|
R8799:Lrrc34
|
UTSW |
3 |
30,678,979 (GRCm39) |
missense |
probably benign |
0.06 |
R9764:Lrrc34
|
UTSW |
3 |
30,697,467 (GRCm39) |
missense |
probably damaging |
1.00 |
|