Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310057J18Rik |
A |
G |
10: 28,849,882 (GRCm39) |
S293P |
probably benign |
Het |
Actn2 |
T |
C |
13: 12,291,376 (GRCm39) |
N676S |
probably benign |
Het |
Amfr |
C |
T |
8: 94,702,776 (GRCm39) |
M463I |
possibly damaging |
Het |
Ankdd1a |
G |
T |
9: 65,411,834 (GRCm39) |
A325D |
probably damaging |
Het |
Apba2 |
A |
G |
7: 64,389,493 (GRCm39) |
D463G |
probably damaging |
Het |
Arid5b |
A |
G |
10: 67,933,637 (GRCm39) |
V755A |
probably damaging |
Het |
Boc |
A |
T |
16: 44,310,533 (GRCm39) |
F796I |
|
Het |
Ccnt1 |
G |
A |
15: 98,463,005 (GRCm39) |
Q56* |
probably null |
Het |
Cd248 |
T |
A |
19: 5,119,383 (GRCm39) |
Y410* |
probably null |
Het |
Chd9 |
T |
A |
8: 91,721,171 (GRCm39) |
N986K |
unknown |
Het |
Col6a6 |
T |
C |
9: 105,661,168 (GRCm39) |
T314A |
probably benign |
Het |
Cpped1 |
A |
G |
16: 11,646,327 (GRCm39) |
F142L |
possibly damaging |
Het |
Csmd1 |
C |
T |
8: 16,050,574 (GRCm39) |
A2221T |
probably damaging |
Het |
Cyp2c69 |
C |
A |
19: 39,831,344 (GRCm39) |
V490L |
probably benign |
Het |
Cyrib |
A |
T |
15: 63,829,438 (GRCm39) |
F23L |
possibly damaging |
Het |
Dcst2 |
T |
C |
3: 89,273,593 (GRCm39) |
F157S |
probably damaging |
Het |
Ddx54 |
G |
T |
5: 120,764,985 (GRCm39) |
R788L |
probably benign |
Het |
Dnah1 |
T |
C |
14: 30,991,343 (GRCm39) |
Y3145C |
probably damaging |
Het |
Dnah14 |
A |
T |
1: 181,534,309 (GRCm39) |
R2320W |
probably damaging |
Het |
Dnai3 |
T |
A |
3: 145,752,295 (GRCm39) |
M794L |
probably benign |
Het |
Emilin2 |
T |
C |
17: 71,581,785 (GRCm39) |
T314A |
probably benign |
Het |
Eml2 |
A |
G |
7: 18,934,515 (GRCm39) |
S405G |
probably benign |
Het |
Ephb2 |
A |
G |
4: 136,498,885 (GRCm39) |
F65L |
probably damaging |
Het |
Fbn2 |
T |
C |
18: 58,199,188 (GRCm39) |
D1360G |
probably benign |
Het |
Fbxo22 |
A |
G |
9: 55,125,754 (GRCm39) |
T206A |
probably benign |
Het |
Filip1l |
A |
G |
16: 57,391,287 (GRCm39) |
E625G |
probably damaging |
Het |
Gen1 |
A |
C |
12: 11,306,849 (GRCm39) |
M172R |
probably damaging |
Het |
Gk5 |
A |
G |
9: 96,001,663 (GRCm39) |
K54E |
probably benign |
Het |
Glis3 |
T |
C |
19: 28,508,802 (GRCm39) |
E394G |
probably benign |
Het |
Helq |
T |
A |
5: 100,939,793 (GRCm39) |
E373D |
probably damaging |
Het |
Ighv1-74 |
A |
G |
12: 115,766,372 (GRCm39) |
F83L |
probably benign |
Het |
Ints15 |
A |
G |
5: 143,297,594 (GRCm39) |
V151A |
probably benign |
Het |
Iqcn |
T |
C |
8: 71,161,397 (GRCm39) |
Y197H |
probably benign |
Het |
Kdm4d |
T |
C |
9: 14,374,454 (GRCm39) |
D468G |
probably benign |
Het |
Kif20b |
A |
G |
19: 34,927,610 (GRCm39) |
I957M |
probably damaging |
Het |
Ldhal6b |
A |
G |
17: 5,468,535 (GRCm39) |
F133S |
possibly damaging |
Het |
Loxhd1 |
T |
C |
18: 77,420,338 (GRCm39) |
Y321H |
possibly damaging |
Het |
Ltbp1 |
A |
T |
17: 75,373,139 (GRCm39) |
M261L |
probably benign |
Het |
Mical2 |
A |
T |
7: 111,919,001 (GRCm39) |
Q430L |
probably benign |
Het |
Mroh4 |
A |
T |
15: 74,479,978 (GRCm39) |
N885K |
possibly damaging |
Het |
Ms4a7 |
A |
G |
19: 11,299,710 (GRCm39) |
Y231H |
probably damaging |
Het |
Msh2 |
G |
T |
17: 88,025,047 (GRCm39) |
V642F |
probably damaging |
Het |
Muc5b |
G |
T |
7: 141,396,385 (GRCm39) |
A166S |
unknown |
Het |
Myo18b |
T |
C |
5: 112,923,154 (GRCm39) |
I1868V |
probably benign |
Het |
Nfatc3 |
T |
C |
8: 106,835,578 (GRCm39) |
S975P |
probably benign |
Het |
Oacyl |
T |
C |
18: 65,831,438 (GRCm39) |
L25P |
probably damaging |
Het |
Or12e10 |
A |
G |
2: 87,640,731 (GRCm39) |
N189S |
probably damaging |
Het |
Or5b109 |
T |
C |
19: 13,212,388 (GRCm39) |
F258S |
probably damaging |
Het |
Or5w15 |
T |
C |
2: 87,568,852 (GRCm39) |
|
probably null |
Het |
Or6c69 |
T |
A |
10: 129,748,156 (GRCm39) |
|
probably benign |
Het |
Or8a1 |
T |
A |
9: 37,642,049 (GRCm39) |
I77F |
probably damaging |
Het |
Patj |
A |
G |
4: 98,304,970 (GRCm39) |
I275V |
possibly damaging |
Het |
Pdcd11 |
G |
A |
19: 47,117,673 (GRCm39) |
R1674Q |
possibly damaging |
Het |
Peg10 |
CCACATCAGGATCCACATCAGGATGCACATCAGCATCAGGATCCCCATCAGGATGCACATCAGGATCCACATCAGGATGCACATCAG |
CCACATCAGGATCCACATCAGGATGCACATCAG |
6: 4,756,398 (GRCm39) |
|
probably benign |
Het |
Phkb |
T |
A |
8: 86,604,759 (GRCm39) |
Y55N |
probably benign |
Het |
Pias4 |
A |
G |
10: 80,993,302 (GRCm39) |
V207A |
possibly damaging |
Het |
Plxna4 |
C |
A |
6: 32,216,455 (GRCm39) |
R540L |
possibly damaging |
Het |
Psapl1 |
G |
A |
5: 36,362,556 (GRCm39) |
V383M |
probably benign |
Het |
Rars1 |
C |
A |
11: 35,725,281 (GRCm39) |
A10S |
probably benign |
Het |
Rhobtb1 |
A |
T |
10: 69,106,610 (GRCm39) |
K454* |
probably null |
Het |
Rmnd1 |
A |
T |
10: 4,364,803 (GRCm39) |
|
probably null |
Het |
Rnf213 |
A |
G |
11: 119,343,401 (GRCm39) |
I3589V |
|
Het |
Sh3bgr |
A |
G |
16: 96,025,681 (GRCm39) |
E189G |
unknown |
Het |
Slc30a3 |
G |
A |
5: 31,245,690 (GRCm39) |
T281I |
probably damaging |
Het |
Smok3c |
T |
A |
5: 138,063,885 (GRCm39) |
D457E |
possibly damaging |
Het |
Stard9 |
C |
A |
2: 120,537,419 (GRCm39) |
Q4274K |
possibly damaging |
Het |
Syne2 |
G |
T |
12: 75,991,853 (GRCm39) |
L1938F |
probably damaging |
Het |
Tmem70 |
C |
A |
1: 16,735,590 (GRCm39) |
T20K |
possibly damaging |
Het |
Tnrc6a |
A |
G |
7: 122,785,813 (GRCm39) |
E1502G |
probably benign |
Het |
Tpp1 |
A |
T |
7: 105,396,704 (GRCm39) |
S438T |
probably benign |
Het |
Tubb2a |
T |
A |
13: 34,259,397 (GRCm39) |
Q131L |
probably damaging |
Het |
Ube2v1 |
A |
G |
2: 167,471,114 (GRCm39) |
S26P |
probably benign |
Het |
Unc13a |
G |
T |
8: 72,113,229 (GRCm39) |
S207R |
possibly damaging |
Het |
Usp35 |
T |
G |
7: 96,969,286 (GRCm39) |
D362A |
probably damaging |
Het |
Utp20 |
A |
G |
10: 88,587,334 (GRCm39) |
I2487T |
probably benign |
Het |
Vmn2r111 |
T |
C |
17: 22,778,032 (GRCm39) |
N549S |
possibly damaging |
Het |
Vmn2r117 |
T |
A |
17: 23,694,359 (GRCm39) |
H496L |
probably benign |
Het |
Vmn2r92 |
C |
T |
17: 18,387,138 (GRCm39) |
A159V |
probably damaging |
Het |
Wiz |
T |
C |
17: 32,578,085 (GRCm39) |
K467E |
probably damaging |
Het |
Zfp534 |
T |
C |
4: 147,759,461 (GRCm39) |
T403A |
probably benign |
Het |
Zswim5 |
T |
C |
4: 116,819,843 (GRCm39) |
L416P |
probably damaging |
Het |
|
Other mutations in Rngtt |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01865:Rngtt
|
APN |
4 |
33,325,157 (GRCm39) |
splice site |
probably benign |
|
IGL01945:Rngtt
|
APN |
4 |
33,339,073 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02104:Rngtt
|
APN |
4 |
33,320,517 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL02505:Rngtt
|
APN |
4 |
33,337,936 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL02679:Rngtt
|
APN |
4 |
33,356,098 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL03309:Rngtt
|
APN |
4 |
33,339,091 (GRCm39) |
missense |
probably damaging |
1.00 |
R0013:Rngtt
|
UTSW |
4 |
33,379,409 (GRCm39) |
missense |
probably benign |
0.01 |
R0626:Rngtt
|
UTSW |
4 |
33,329,598 (GRCm39) |
splice site |
probably null |
|
R0633:Rngtt
|
UTSW |
4 |
33,368,690 (GRCm39) |
missense |
probably damaging |
1.00 |
R1645:Rngtt
|
UTSW |
4 |
33,362,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R1670:Rngtt
|
UTSW |
4 |
33,368,660 (GRCm39) |
missense |
probably benign |
|
R1700:Rngtt
|
UTSW |
4 |
33,330,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R1754:Rngtt
|
UTSW |
4 |
33,329,634 (GRCm39) |
splice site |
probably null |
|
R1809:Rngtt
|
UTSW |
4 |
33,443,614 (GRCm39) |
missense |
probably benign |
0.04 |
R1929:Rngtt
|
UTSW |
4 |
33,500,302 (GRCm39) |
nonsense |
probably null |
|
R2271:Rngtt
|
UTSW |
4 |
33,500,302 (GRCm39) |
nonsense |
probably null |
|
R2844:Rngtt
|
UTSW |
4 |
33,368,678 (GRCm39) |
missense |
probably benign |
|
R3773:Rngtt
|
UTSW |
4 |
33,330,889 (GRCm39) |
missense |
probably damaging |
1.00 |
R4445:Rngtt
|
UTSW |
4 |
33,499,035 (GRCm39) |
missense |
probably benign |
|
R4449:Rngtt
|
UTSW |
4 |
33,330,865 (GRCm39) |
missense |
probably damaging |
1.00 |
R4510:Rngtt
|
UTSW |
4 |
33,339,032 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4511:Rngtt
|
UTSW |
4 |
33,339,032 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4578:Rngtt
|
UTSW |
4 |
33,339,050 (GRCm39) |
missense |
probably benign |
0.30 |
R4610:Rngtt
|
UTSW |
4 |
33,339,133 (GRCm39) |
intron |
probably benign |
|
R4712:Rngtt
|
UTSW |
4 |
33,379,394 (GRCm39) |
missense |
probably benign |
0.00 |
R4888:Rngtt
|
UTSW |
4 |
33,500,335 (GRCm39) |
missense |
unknown |
|
R4911:Rngtt
|
UTSW |
4 |
33,500,292 (GRCm39) |
splice site |
probably null |
|
R5248:Rngtt
|
UTSW |
4 |
33,325,110 (GRCm39) |
nonsense |
probably null |
|
R6429:Rngtt
|
UTSW |
4 |
33,320,606 (GRCm39) |
nonsense |
probably null |
|
R6571:Rngtt
|
UTSW |
4 |
33,379,413 (GRCm39) |
missense |
probably damaging |
1.00 |
R7298:Rngtt
|
UTSW |
4 |
33,362,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R7379:Rngtt
|
UTSW |
4 |
33,498,981 (GRCm39) |
nonsense |
probably null |
|
R8163:Rngtt
|
UTSW |
4 |
33,325,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R8717:Rngtt
|
UTSW |
4 |
33,368,695 (GRCm39) |
missense |
probably damaging |
1.00 |
R9136:Rngtt
|
UTSW |
4 |
33,404,218 (GRCm39) |
missense |
probably damaging |
1.00 |
R9324:Rngtt
|
UTSW |
4 |
33,320,613 (GRCm39) |
nonsense |
probably null |
|
R9749:Rngtt
|
UTSW |
4 |
33,368,618 (GRCm39) |
missense |
possibly damaging |
0.71 |
|