Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adnp2 |
T |
C |
18: 80,171,692 (GRCm39) |
T906A |
probably damaging |
Het |
Akap13 |
A |
G |
7: 75,347,141 (GRCm39) |
S1731G |
probably damaging |
Het |
Apbb2 |
A |
G |
5: 66,465,044 (GRCm39) |
V650A |
probably benign |
Het |
Appl1 |
A |
G |
14: 26,681,427 (GRCm39) |
|
probably benign |
Het |
Avpr1b |
T |
G |
1: 131,527,885 (GRCm39) |
V136G |
probably damaging |
Het |
C6 |
T |
C |
15: 4,811,378 (GRCm39) |
F409L |
probably benign |
Het |
Cdk20 |
A |
G |
13: 64,584,124 (GRCm39) |
|
probably benign |
Het |
Cenpf |
T |
C |
1: 189,385,381 (GRCm39) |
K2300E |
possibly damaging |
Het |
Cfap57 |
C |
T |
4: 118,457,993 (GRCm39) |
R399Q |
probably damaging |
Het |
Cimap3 |
G |
T |
3: 105,904,523 (GRCm39) |
|
probably null |
Het |
Cnnm1 |
A |
T |
19: 43,460,375 (GRCm39) |
S706C |
probably benign |
Het |
Cr1l |
T |
C |
1: 194,812,189 (GRCm39) |
I45V |
possibly damaging |
Het |
D130043K22Rik |
A |
T |
13: 25,083,779 (GRCm39) |
R1081S |
probably damaging |
Het |
Ddx60 |
A |
T |
8: 62,416,774 (GRCm39) |
H573L |
probably null |
Het |
Eif5b |
T |
C |
1: 38,084,787 (GRCm39) |
L878S |
probably damaging |
Het |
Ets1 |
T |
C |
9: 32,644,235 (GRCm39) |
|
probably benign |
Het |
Evi5 |
A |
G |
5: 107,912,573 (GRCm39) |
L696P |
probably damaging |
Het |
Fbh1 |
C |
A |
2: 11,762,334 (GRCm39) |
E12* |
probably null |
Het |
Gabpb1 |
C |
A |
2: 126,495,520 (GRCm39) |
M77I |
possibly damaging |
Het |
Glul |
T |
A |
1: 153,782,222 (GRCm39) |
N152K |
probably benign |
Het |
Gm45234 |
T |
C |
6: 124,723,394 (GRCm39) |
Y613C |
probably damaging |
Het |
Gm5611 |
A |
G |
9: 16,941,647 (GRCm39) |
|
noncoding transcript |
Het |
Gpr156 |
T |
A |
16: 37,808,953 (GRCm39) |
I225K |
probably damaging |
Het |
Herc4 |
T |
C |
10: 63,126,461 (GRCm39) |
|
probably benign |
Het |
Iqsec3 |
C |
T |
6: 121,387,580 (GRCm39) |
V720M |
probably damaging |
Het |
Itgam |
A |
T |
7: 127,715,939 (GRCm39) |
H1104L |
possibly damaging |
Het |
Itgb3 |
T |
A |
11: 104,534,791 (GRCm39) |
D549E |
probably damaging |
Het |
Kctd7 |
A |
T |
5: 130,176,976 (GRCm39) |
M76L |
probably damaging |
Het |
Kdm3b |
T |
G |
18: 34,962,284 (GRCm39) |
N1523K |
probably damaging |
Het |
Map3k12 |
T |
A |
15: 102,412,186 (GRCm39) |
E318D |
probably damaging |
Het |
Mc1r |
T |
C |
8: 124,134,789 (GRCm39) |
Y181H |
probably damaging |
Het |
Mex3c |
G |
A |
18: 73,706,703 (GRCm39) |
A197T |
unknown |
Het |
Mvk |
A |
G |
5: 114,584,353 (GRCm39) |
D71G |
probably benign |
Het |
Ndufb3 |
T |
A |
1: 58,634,912 (GRCm39) |
L88* |
probably null |
Het |
Or56a4 |
A |
G |
7: 104,806,667 (GRCm39) |
V74A |
probably benign |
Het |
Or5p55 |
A |
G |
7: 107,567,144 (GRCm39) |
D180G |
probably damaging |
Het |
Pramel17 |
T |
A |
4: 101,694,201 (GRCm39) |
R227S |
possibly damaging |
Het |
Psmg2 |
G |
A |
18: 67,786,293 (GRCm39) |
V218I |
probably benign |
Het |
Slc5a3 |
C |
T |
16: 91,876,000 (GRCm39) |
Q686* |
probably null |
Het |
Vmn2r75 |
T |
C |
7: 85,797,681 (GRCm39) |
I711V |
probably benign |
Het |
Vps13c |
T |
A |
9: 67,863,063 (GRCm39) |
H3026Q |
probably benign |
Het |
Zfp354c |
A |
G |
11: 50,708,732 (GRCm39) |
S22P |
possibly damaging |
Het |
|
Other mutations in Ccdc121rt3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00904:Ccdc121rt3
|
APN |
5 |
112,502,994 (GRCm39) |
nonsense |
probably null |
|
IGL01464:Ccdc121rt3
|
APN |
5 |
112,503,399 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0508:Ccdc121rt3
|
UTSW |
5 |
112,502,685 (GRCm39) |
missense |
probably damaging |
0.99 |
R1466:Ccdc121rt3
|
UTSW |
5 |
112,502,630 (GRCm39) |
missense |
probably benign |
0.00 |
R1466:Ccdc121rt3
|
UTSW |
5 |
112,502,630 (GRCm39) |
missense |
probably benign |
0.00 |
R1473:Ccdc121rt3
|
UTSW |
5 |
112,502,415 (GRCm39) |
missense |
probably benign |
0.45 |
R1474:Ccdc121rt3
|
UTSW |
5 |
112,503,642 (GRCm39) |
missense |
probably benign |
|
R1584:Ccdc121rt3
|
UTSW |
5 |
112,502,630 (GRCm39) |
missense |
probably benign |
0.00 |
R2032:Ccdc121rt3
|
UTSW |
5 |
112,502,978 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2422:Ccdc121rt3
|
UTSW |
5 |
112,502,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R4795:Ccdc121rt3
|
UTSW |
5 |
112,503,165 (GRCm39) |
missense |
possibly damaging |
0.65 |
R4796:Ccdc121rt3
|
UTSW |
5 |
112,503,165 (GRCm39) |
missense |
possibly damaging |
0.65 |
R5306:Ccdc121rt3
|
UTSW |
5 |
112,502,910 (GRCm39) |
missense |
probably benign |
0.41 |
R5997:Ccdc121rt3
|
UTSW |
5 |
112,502,874 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6915:Ccdc121rt3
|
UTSW |
5 |
112,502,523 (GRCm39) |
missense |
probably damaging |
1.00 |
R7022:Ccdc121rt3
|
UTSW |
5 |
112,503,395 (GRCm39) |
missense |
probably benign |
|
R7702:Ccdc121rt3
|
UTSW |
5 |
112,503,063 (GRCm39) |
missense |
probably benign |
0.27 |
R7721:Ccdc121rt3
|
UTSW |
5 |
112,503,383 (GRCm39) |
missense |
probably benign |
|
R8037:Ccdc121rt3
|
UTSW |
5 |
112,502,882 (GRCm39) |
missense |
probably benign |
0.23 |
R8114:Ccdc121rt3
|
UTSW |
5 |
112,503,563 (GRCm39) |
missense |
probably benign |
|
R8380:Ccdc121rt3
|
UTSW |
5 |
112,503,191 (GRCm39) |
missense |
probably benign |
0.01 |
R8914:Ccdc121rt3
|
UTSW |
5 |
112,503,087 (GRCm39) |
missense |
probably damaging |
0.98 |
R9067:Ccdc121rt3
|
UTSW |
5 |
112,502,706 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9140:Ccdc121rt3
|
UTSW |
5 |
112,502,723 (GRCm39) |
missense |
probably damaging |
1.00 |
R9322:Ccdc121rt3
|
UTSW |
5 |
112,503,272 (GRCm39) |
missense |
probably damaging |
0.99 |
R9690:Ccdc121rt3
|
UTSW |
5 |
112,503,300 (GRCm39) |
missense |
probably benign |
|
R9786:Ccdc121rt3
|
UTSW |
5 |
112,502,939 (GRCm39) |
missense |
probably benign |
|
Z1177:Ccdc121rt3
|
UTSW |
5 |
112,502,784 (GRCm39) |
missense |
probably damaging |
0.98 |
|