Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca12 |
T |
C |
1: 71,356,383 (GRCm39) |
N608S |
probably benign |
Het |
Actg1 |
T |
C |
11: 120,237,784 (GRCm39) |
N7S |
probably damaging |
Het |
Adamtsl3 |
T |
A |
7: 82,225,262 (GRCm39) |
L357Q |
probably benign |
Het |
Ahnak |
A |
T |
19: 8,987,995 (GRCm39) |
Q3093L |
possibly damaging |
Het |
Ankrd16 |
T |
A |
2: 11,794,692 (GRCm39) |
V359E |
probably benign |
Het |
Ankrd40 |
T |
C |
11: 94,230,550 (GRCm39) |
|
probably benign |
Het |
Ano10 |
G |
A |
9: 122,101,625 (GRCm39) |
Q49* |
probably null |
Het |
Aoah |
A |
T |
13: 21,099,129 (GRCm39) |
D236V |
probably damaging |
Het |
Bin1 |
T |
C |
18: 32,552,983 (GRCm39) |
|
probably null |
Het |
Braf |
T |
C |
6: 39,665,221 (GRCm39) |
D49G |
probably benign |
Het |
Brsk1 |
A |
T |
7: 4,707,265 (GRCm39) |
R273W |
probably damaging |
Het |
C2cd3 |
T |
A |
7: 100,109,049 (GRCm39) |
M2259K |
possibly damaging |
Het |
Cabp1 |
T |
C |
5: 115,313,531 (GRCm39) |
N43D |
possibly damaging |
Het |
Ccar2 |
T |
A |
14: 70,379,951 (GRCm39) |
Q412L |
possibly damaging |
Het |
Cd4 |
T |
C |
6: 124,843,583 (GRCm39) |
T443A |
possibly damaging |
Het |
Cdh23 |
T |
A |
10: 60,140,627 (GRCm39) |
I3206F |
possibly damaging |
Het |
Ceacam9 |
A |
T |
7: 16,459,122 (GRCm39) |
|
probably null |
Het |
Chid1 |
T |
C |
7: 141,093,749 (GRCm39) |
D289G |
probably damaging |
Het |
Chmp6 |
T |
A |
11: 119,809,469 (GRCm39) |
L196Q |
probably damaging |
Het |
Cog8 |
A |
G |
8: 107,775,757 (GRCm39) |
S536P |
probably benign |
Het |
Dmxl2 |
A |
T |
9: 54,323,960 (GRCm39) |
S1141R |
probably damaging |
Het |
Dnah7a |
T |
G |
1: 53,701,657 (GRCm39) |
Y166S |
probably damaging |
Het |
Dnah7b |
G |
T |
1: 46,226,523 (GRCm39) |
W1318L |
probably damaging |
Het |
Ecd |
A |
G |
14: 20,387,098 (GRCm39) |
F212S |
probably damaging |
Het |
Entpd6 |
A |
T |
2: 150,605,564 (GRCm39) |
S265C |
probably damaging |
Het |
Epb41l2 |
A |
G |
10: 25,360,206 (GRCm39) |
T523A |
possibly damaging |
Het |
Focad |
T |
C |
4: 88,262,819 (GRCm39) |
S939P |
unknown |
Het |
Gjb3 |
A |
T |
4: 127,220,280 (GRCm39) |
V84D |
probably damaging |
Het |
Gm572 |
A |
T |
4: 148,739,301 (GRCm39) |
E43V |
possibly damaging |
Het |
Gm6185 |
T |
A |
1: 161,052,178 (GRCm39) |
|
noncoding transcript |
Het |
Gria1 |
T |
A |
11: 57,201,522 (GRCm39) |
C787S |
probably damaging |
Het |
Grpel2 |
A |
G |
18: 61,849,024 (GRCm39) |
L162P |
probably damaging |
Het |
Herc1 |
A |
G |
9: 66,393,408 (GRCm39) |
T4096A |
probably benign |
Het |
Hook3 |
A |
T |
8: 26,600,785 (GRCm39) |
M41K |
probably damaging |
Het |
Ifit1bl1 |
T |
C |
19: 34,571,293 (GRCm39) |
Y388C |
probably damaging |
Het |
Ighv3-4 |
A |
G |
12: 114,217,382 (GRCm39) |
Y70H |
probably benign |
Het |
Itm2c |
T |
C |
1: 85,834,213 (GRCm39) |
L176P |
probably damaging |
Het |
Lmtk3 |
G |
A |
7: 45,443,836 (GRCm39) |
|
probably benign |
Het |
Macf1 |
G |
A |
4: 123,333,287 (GRCm39) |
T2376I |
possibly damaging |
Het |
Map1a |
T |
G |
2: 121,138,019 (GRCm39) |
S2660A |
possibly damaging |
Het |
Nbeal1 |
A |
T |
1: 60,276,338 (GRCm39) |
K693M |
probably damaging |
Het |
Ndufa13 |
T |
A |
8: 70,347,920 (GRCm39) |
R49* |
probably null |
Het |
Neb |
T |
A |
2: 52,094,892 (GRCm39) |
T1115S |
possibly damaging |
Het |
Nvl |
C |
T |
1: 180,932,720 (GRCm39) |
R699H |
probably damaging |
Het |
Or10w1 |
A |
G |
19: 13,632,296 (GRCm39) |
I163V |
probably benign |
Het |
Or5d47 |
A |
T |
2: 87,804,364 (GRCm39) |
I215N |
probably damaging |
Het |
Or8b53 |
A |
G |
9: 38,667,041 (GRCm39) |
D19G |
probably benign |
Het |
Or8d2b |
A |
T |
9: 38,789,195 (GRCm39) |
H241L |
possibly damaging |
Het |
Piezo1 |
G |
T |
8: 123,213,557 (GRCm39) |
D1779E |
probably benign |
Het |
Prl8a9 |
A |
G |
13: 27,745,560 (GRCm39) |
S77P |
probably damaging |
Het |
Prune2 |
A |
T |
19: 17,176,506 (GRCm39) |
I2904F |
probably damaging |
Het |
Retreg1 |
T |
A |
15: 25,970,214 (GRCm39) |
S151T |
probably damaging |
Het |
Rnf213 |
A |
G |
11: 119,327,590 (GRCm39) |
D1859G |
probably damaging |
Het |
Rnf39 |
T |
C |
17: 37,256,426 (GRCm39) |
F173L |
probably benign |
Het |
Rspry1 |
T |
A |
8: 95,376,931 (GRCm39) |
N371K |
probably damaging |
Het |
Samd9l |
T |
A |
6: 3,375,284 (GRCm39) |
D659V |
possibly damaging |
Het |
Sez6 |
T |
A |
11: 77,859,815 (GRCm39) |
F378Y |
probably damaging |
Het |
Slc22a19 |
G |
A |
19: 7,651,737 (GRCm39) |
T490M |
probably benign |
Het |
Slit2 |
A |
T |
5: 48,414,147 (GRCm39) |
N917I |
probably damaging |
Het |
Smg1 |
T |
A |
7: 117,792,768 (GRCm39) |
|
probably benign |
Het |
Tes |
T |
C |
6: 17,096,339 (GRCm39) |
V24A |
probably benign |
Het |
Tial1 |
C |
T |
7: 128,050,120 (GRCm39) |
E82K |
probably damaging |
Het |
Tmem94 |
G |
A |
11: 115,683,930 (GRCm39) |
C750Y |
probably damaging |
Het |
Tmppe |
T |
A |
9: 114,234,887 (GRCm39) |
N395K |
possibly damaging |
Het |
Tnn |
T |
C |
1: 159,973,707 (GRCm39) |
H220R |
probably benign |
Het |
Trappc10 |
T |
C |
10: 78,040,122 (GRCm39) |
T610A |
possibly damaging |
Het |
Trmt1l |
T |
A |
1: 151,316,627 (GRCm39) |
M196K |
probably damaging |
Het |
Trpv4 |
T |
C |
5: 114,760,715 (GRCm39) |
*872W |
probably null |
Het |
Ttn |
T |
C |
2: 76,579,353 (GRCm39) |
T23847A |
probably benign |
Het |
Ube4b |
T |
A |
4: 149,445,022 (GRCm39) |
L440F |
probably damaging |
Het |
Ugt1a5 |
C |
G |
1: 88,093,963 (GRCm39) |
R64G |
probably benign |
Het |
Unc13c |
T |
A |
9: 73,838,185 (GRCm39) |
T889S |
possibly damaging |
Het |
Vmn1r215 |
C |
T |
13: 23,260,449 (GRCm39) |
T163I |
probably benign |
Het |
Vmn2r16 |
T |
A |
5: 109,508,722 (GRCm39) |
Y483* |
probably null |
Het |
Wdr47 |
T |
A |
3: 108,525,838 (GRCm39) |
C120* |
probably null |
Het |
Zc3h6 |
G |
A |
2: 128,859,229 (GRCm39) |
V1087I |
probably benign |
Het |
Zfp423 |
T |
C |
8: 88,507,302 (GRCm39) |
H889R |
probably damaging |
Het |
Zfp825 |
G |
T |
13: 74,629,196 (GRCm39) |
H107N |
probably benign |
Het |
Zfp945 |
T |
C |
17: 23,069,859 (GRCm39) |
H680R |
probably damaging |
Het |
|
Other mutations in Mmrn2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01523:Mmrn2
|
APN |
14 |
34,125,174 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02529:Mmrn2
|
APN |
14 |
34,120,570 (GRCm39) |
missense |
possibly damaging |
0.74 |
IGL02590:Mmrn2
|
APN |
14 |
34,121,224 (GRCm39) |
nonsense |
probably null |
|
P0037:Mmrn2
|
UTSW |
14 |
34,125,022 (GRCm39) |
missense |
probably damaging |
1.00 |
R0323:Mmrn2
|
UTSW |
14 |
34,119,991 (GRCm39) |
missense |
probably damaging |
0.97 |
R0499:Mmrn2
|
UTSW |
14 |
34,119,913 (GRCm39) |
missense |
probably damaging |
1.00 |
R1073:Mmrn2
|
UTSW |
14 |
34,118,251 (GRCm39) |
critical splice donor site |
probably null |
|
R1422:Mmrn2
|
UTSW |
14 |
34,118,196 (GRCm39) |
missense |
probably damaging |
1.00 |
R1455:Mmrn2
|
UTSW |
14 |
34,121,089 (GRCm39) |
missense |
probably benign |
0.00 |
R1584:Mmrn2
|
UTSW |
14 |
34,097,642 (GRCm39) |
missense |
probably benign |
0.19 |
R1702:Mmrn2
|
UTSW |
14 |
34,119,871 (GRCm39) |
missense |
probably benign |
0.34 |
R1919:Mmrn2
|
UTSW |
14 |
34,119,600 (GRCm39) |
missense |
probably benign |
0.10 |
R1961:Mmrn2
|
UTSW |
14 |
34,120,432 (GRCm39) |
splice site |
probably null |
|
R2267:Mmrn2
|
UTSW |
14 |
34,121,449 (GRCm39) |
missense |
probably benign |
0.41 |
R2268:Mmrn2
|
UTSW |
14 |
34,121,449 (GRCm39) |
missense |
probably benign |
0.41 |
R2516:Mmrn2
|
UTSW |
14 |
34,120,759 (GRCm39) |
missense |
probably benign |
0.12 |
R2571:Mmrn2
|
UTSW |
14 |
34,124,896 (GRCm39) |
missense |
probably damaging |
0.99 |
R2696:Mmrn2
|
UTSW |
14 |
34,120,372 (GRCm39) |
missense |
probably damaging |
1.00 |
R2892:Mmrn2
|
UTSW |
14 |
34,118,587 (GRCm39) |
missense |
probably benign |
0.01 |
R2919:Mmrn2
|
UTSW |
14 |
34,124,879 (GRCm39) |
missense |
possibly damaging |
0.72 |
R3611:Mmrn2
|
UTSW |
14 |
34,120,632 (GRCm39) |
missense |
probably benign |
0.00 |
R3898:Mmrn2
|
UTSW |
14 |
34,121,517 (GRCm39) |
splice site |
probably null |
|
R3899:Mmrn2
|
UTSW |
14 |
34,121,517 (GRCm39) |
splice site |
probably null |
|
R3900:Mmrn2
|
UTSW |
14 |
34,121,517 (GRCm39) |
splice site |
probably null |
|
R4363:Mmrn2
|
UTSW |
14 |
34,119,934 (GRCm39) |
missense |
probably damaging |
0.99 |
R4392:Mmrn2
|
UTSW |
14 |
34,119,573 (GRCm39) |
missense |
probably damaging |
1.00 |
R4510:Mmrn2
|
UTSW |
14 |
34,125,016 (GRCm39) |
missense |
possibly damaging |
0.67 |
R4511:Mmrn2
|
UTSW |
14 |
34,125,016 (GRCm39) |
missense |
possibly damaging |
0.67 |
R4993:Mmrn2
|
UTSW |
14 |
34,118,355 (GRCm39) |
missense |
probably damaging |
1.00 |
R5263:Mmrn2
|
UTSW |
14 |
34,121,541 (GRCm39) |
missense |
probably benign |
|
R5478:Mmrn2
|
UTSW |
14 |
34,118,539 (GRCm39) |
missense |
probably benign |
0.11 |
R5606:Mmrn2
|
UTSW |
14 |
34,119,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R6059:Mmrn2
|
UTSW |
14 |
34,119,548 (GRCm39) |
nonsense |
probably null |
|
R6279:Mmrn2
|
UTSW |
14 |
34,119,614 (GRCm39) |
missense |
probably benign |
|
R6300:Mmrn2
|
UTSW |
14 |
34,119,614 (GRCm39) |
missense |
probably benign |
|
R6938:Mmrn2
|
UTSW |
14 |
34,120,671 (GRCm39) |
missense |
probably benign |
0.22 |
R7491:Mmrn2
|
UTSW |
14 |
34,121,374 (GRCm39) |
missense |
probably damaging |
1.00 |
R7607:Mmrn2
|
UTSW |
14 |
34,120,897 (GRCm39) |
missense |
possibly damaging |
0.58 |
R7979:Mmrn2
|
UTSW |
14 |
34,118,138 (GRCm39) |
nonsense |
probably null |
|
R7999:Mmrn2
|
UTSW |
14 |
34,119,879 (GRCm39) |
missense |
probably benign |
0.30 |
R8113:Mmrn2
|
UTSW |
14 |
34,119,593 (GRCm39) |
missense |
probably benign |
0.39 |
R9063:Mmrn2
|
UTSW |
14 |
34,120,567 (GRCm39) |
missense |
probably benign |
0.04 |
R9092:Mmrn2
|
UTSW |
14 |
34,118,587 (GRCm39) |
missense |
probably benign |
0.00 |
R9180:Mmrn2
|
UTSW |
14 |
34,121,158 (GRCm39) |
missense |
probably benign |
0.07 |
R9327:Mmrn2
|
UTSW |
14 |
34,097,473 (GRCm39) |
unclassified |
probably benign |
|
R9476:Mmrn2
|
UTSW |
14 |
34,120,407 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9510:Mmrn2
|
UTSW |
14 |
34,120,407 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9606:Mmrn2
|
UTSW |
14 |
34,119,654 (GRCm39) |
missense |
possibly damaging |
0.58 |
X0064:Mmrn2
|
UTSW |
14 |
34,121,109 (GRCm39) |
missense |
probably benign |
|
|