Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abraxas1 |
C |
T |
5: 100,965,827 (GRCm39) |
|
probably null |
Het |
Acsl3 |
A |
G |
1: 78,679,004 (GRCm39) |
D520G |
probably damaging |
Het |
Adgrl3 |
T |
C |
5: 81,796,560 (GRCm39) |
V623A |
probably benign |
Het |
Ak9 |
G |
T |
10: 41,223,218 (GRCm39) |
V454L |
probably damaging |
Het |
Alpk2 |
C |
A |
18: 65,482,558 (GRCm39) |
K483N |
probably damaging |
Het |
Arhgef12 |
T |
C |
9: 42,893,281 (GRCm39) |
Y974C |
probably damaging |
Het |
Armc8 |
C |
T |
9: 99,418,211 (GRCm39) |
|
probably benign |
Het |
Atp2a2 |
C |
T |
5: 122,595,696 (GRCm39) |
|
probably benign |
Het |
Atrn |
T |
C |
2: 130,812,147 (GRCm39) |
|
probably null |
Het |
Caps2 |
T |
A |
10: 112,039,943 (GRCm39) |
|
probably benign |
Het |
Cep97 |
C |
T |
16: 55,735,265 (GRCm39) |
R583H |
probably benign |
Het |
Cog7 |
A |
G |
7: 121,555,363 (GRCm39) |
|
probably benign |
Het |
Commd5 |
T |
A |
15: 76,784,768 (GRCm39) |
V55E |
probably damaging |
Het |
Csmd3 |
A |
T |
15: 47,874,543 (GRCm39) |
D684E |
possibly damaging |
Het |
Ctxn2 |
T |
C |
2: 124,989,376 (GRCm39) |
M1T |
probably null |
Het |
Exph5 |
A |
G |
9: 53,288,775 (GRCm39) |
D1952G |
unknown |
Het |
Fmo2 |
A |
T |
1: 162,704,343 (GRCm39) |
L521Q |
possibly damaging |
Het |
Fryl |
T |
A |
5: 73,222,702 (GRCm39) |
T1960S |
probably damaging |
Het |
G6pd2 |
T |
C |
5: 61,967,017 (GRCm39) |
L264P |
probably damaging |
Het |
Gne |
A |
T |
4: 44,039,033 (GRCm39) |
V647E |
possibly damaging |
Het |
Grb14 |
G |
A |
2: 64,745,071 (GRCm39) |
Q96* |
probably null |
Het |
Gtf3c1 |
A |
G |
7: 125,298,134 (GRCm39) |
F146L |
probably damaging |
Het |
Gvin3 |
C |
A |
7: 106,202,093 (GRCm39) |
V384L |
possibly damaging |
Het |
Irak2 |
A |
G |
6: 113,615,525 (GRCm39) |
Y6C |
probably damaging |
Het |
Kel |
T |
A |
6: 41,679,965 (GRCm39) |
N75I |
probably damaging |
Het |
Lgr4 |
T |
A |
2: 109,842,132 (GRCm39) |
F706I |
possibly damaging |
Het |
Lox |
A |
T |
18: 52,661,955 (GRCm39) |
S149R |
probably benign |
Het |
Lrrc66 |
T |
G |
5: 73,768,287 (GRCm39) |
D218A |
probably benign |
Het |
Luc7l |
C |
T |
17: 26,485,296 (GRCm39) |
R99W |
probably damaging |
Het |
Megf10 |
T |
C |
18: 57,385,968 (GRCm39) |
V327A |
probably benign |
Het |
Mthfd1l |
G |
T |
10: 3,997,976 (GRCm39) |
|
probably null |
Het |
Myh11 |
C |
A |
16: 14,041,883 (GRCm39) |
Q720H |
probably damaging |
Het |
Myh8 |
G |
T |
11: 67,175,358 (GRCm39) |
|
probably null |
Het |
Or5b109 |
A |
T |
19: 13,212,424 (GRCm39) |
D270V |
possibly damaging |
Het |
Pdia3 |
G |
A |
2: 121,262,858 (GRCm39) |
G275S |
probably damaging |
Het |
Pgf |
C |
T |
12: 85,216,159 (GRCm39) |
R153K |
probably benign |
Het |
Pramel12 |
A |
T |
4: 143,144,170 (GRCm39) |
Q172L |
probably damaging |
Het |
Prdm2 |
A |
G |
4: 142,861,835 (GRCm39) |
V485A |
probably damaging |
Het |
Rag1 |
T |
C |
2: 101,473,028 (GRCm39) |
T705A |
probably damaging |
Het |
Rflna |
A |
C |
5: 125,080,774 (GRCm39) |
D48A |
possibly damaging |
Het |
Rnf148 |
A |
T |
6: 23,654,456 (GRCm39) |
I180N |
probably damaging |
Het |
Rtn4 |
T |
A |
11: 29,656,475 (GRCm39) |
S94T |
probably damaging |
Het |
Scn11a |
G |
A |
9: 119,640,226 (GRCm39) |
T223I |
probably benign |
Het |
Scube2 |
T |
A |
7: 109,436,327 (GRCm39) |
|
probably benign |
Het |
Septin14 |
T |
C |
5: 129,774,972 (GRCm39) |
I68V |
probably benign |
Het |
Sil1 |
A |
T |
18: 35,399,910 (GRCm39) |
L365Q |
possibly damaging |
Het |
Sirt1 |
A |
G |
10: 63,157,515 (GRCm39) |
|
probably benign |
Het |
Slc9a1 |
T |
C |
4: 133,147,810 (GRCm39) |
|
probably benign |
Het |
Smpdl3a |
A |
G |
10: 57,687,336 (GRCm39) |
T355A |
probably damaging |
Het |
Syne2 |
T |
C |
12: 76,141,110 (GRCm39) |
I6074T |
probably damaging |
Het |
Thbs2 |
T |
A |
17: 14,900,587 (GRCm39) |
H540L |
probably benign |
Het |
Tsc22d4 |
T |
C |
5: 137,766,283 (GRCm39) |
S450P |
probably benign |
Het |
Tshr |
C |
A |
12: 91,505,000 (GRCm39) |
S54* |
probably null |
Het |
Ubxn4 |
G |
A |
1: 128,190,641 (GRCm39) |
E256K |
probably benign |
Het |
Uncx |
G |
T |
5: 139,529,942 (GRCm39) |
C65F |
probably damaging |
Het |
Vmn1r87 |
A |
T |
7: 12,865,756 (GRCm39) |
M177K |
probably damaging |
Het |
Vmn2r56 |
A |
T |
7: 12,444,235 (GRCm39) |
C466S |
probably benign |
Het |
Wnk1 |
G |
A |
6: 119,925,466 (GRCm39) |
P1831S |
probably damaging |
Het |
Zfp820 |
T |
C |
17: 22,037,901 (GRCm39) |
S476G |
probably benign |
Het |
|
Other mutations in Cep76 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01333:Cep76
|
APN |
18 |
67,773,187 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01344:Cep76
|
APN |
18 |
67,756,467 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02426:Cep76
|
APN |
18 |
67,767,987 (GRCm39) |
missense |
probably benign |
|
IGL02544:Cep76
|
APN |
18 |
67,768,020 (GRCm39) |
splice site |
probably benign |
|
IGL02711:Cep76
|
APN |
18 |
67,771,406 (GRCm39) |
missense |
probably benign |
|
IGL03283:Cep76
|
APN |
18 |
67,773,139 (GRCm39) |
missense |
possibly damaging |
0.76 |
R0117:Cep76
|
UTSW |
18 |
67,759,744 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0450:Cep76
|
UTSW |
18 |
67,767,850 (GRCm39) |
missense |
probably benign |
0.30 |
R0469:Cep76
|
UTSW |
18 |
67,767,850 (GRCm39) |
missense |
probably benign |
0.30 |
R0587:Cep76
|
UTSW |
18 |
67,756,245 (GRCm39) |
nonsense |
probably null |
|
R0667:Cep76
|
UTSW |
18 |
67,767,848 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1508:Cep76
|
UTSW |
18 |
67,756,358 (GRCm39) |
missense |
probably damaging |
1.00 |
R1511:Cep76
|
UTSW |
18 |
67,758,028 (GRCm39) |
missense |
probably benign |
|
R4280:Cep76
|
UTSW |
18 |
67,773,229 (GRCm39) |
missense |
probably benign |
0.39 |
R4355:Cep76
|
UTSW |
18 |
67,759,710 (GRCm39) |
missense |
probably benign |
0.02 |
R4702:Cep76
|
UTSW |
18 |
67,767,968 (GRCm39) |
missense |
possibly damaging |
0.48 |
R4847:Cep76
|
UTSW |
18 |
67,752,639 (GRCm39) |
missense |
probably benign |
0.04 |
R5650:Cep76
|
UTSW |
18 |
67,758,136 (GRCm39) |
missense |
probably damaging |
1.00 |
R5897:Cep76
|
UTSW |
18 |
67,771,398 (GRCm39) |
missense |
probably benign |
0.00 |
R6648:Cep76
|
UTSW |
18 |
67,752,804 (GRCm39) |
missense |
probably benign |
0.27 |
R7193:Cep76
|
UTSW |
18 |
67,774,204 (GRCm39) |
missense |
possibly damaging |
0.70 |
R7822:Cep76
|
UTSW |
18 |
67,774,219 (GRCm39) |
nonsense |
probably null |
|
R7846:Cep76
|
UTSW |
18 |
67,762,975 (GRCm39) |
missense |
probably damaging |
1.00 |
R8870:Cep76
|
UTSW |
18 |
67,773,190 (GRCm39) |
missense |
probably benign |
0.02 |
R8883:Cep76
|
UTSW |
18 |
67,766,540 (GRCm39) |
missense |
probably benign |
0.02 |
R9025:Cep76
|
UTSW |
18 |
67,767,885 (GRCm39) |
missense |
probably damaging |
1.00 |
R9221:Cep76
|
UTSW |
18 |
67,767,977 (GRCm39) |
missense |
probably damaging |
1.00 |
|