Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930407I10Rik |
A |
G |
15: 81,947,617 (GRCm39) |
K505E |
possibly damaging |
Het |
Abcb1b |
A |
T |
5: 8,874,245 (GRCm39) |
N390I |
possibly damaging |
Het |
Apob |
A |
T |
12: 8,056,077 (GRCm39) |
M1520L |
probably benign |
Het |
Atg4c |
C |
T |
4: 99,123,400 (GRCm39) |
R396* |
probably null |
Het |
Atp2a3 |
G |
A |
11: 72,871,442 (GRCm39) |
V648M |
probably damaging |
Het |
Blm |
T |
C |
7: 80,162,733 (GRCm39) |
D203G |
probably benign |
Het |
Csrnp3 |
A |
T |
2: 65,779,363 (GRCm39) |
D13V |
probably damaging |
Het |
Dnajc10 |
A |
T |
2: 80,147,735 (GRCm39) |
|
probably benign |
Het |
Dst |
A |
G |
1: 34,250,253 (GRCm39) |
Y1729C |
probably damaging |
Het |
Dynlt2b |
G |
A |
16: 32,238,660 (GRCm39) |
A12T |
possibly damaging |
Het |
Ecsit |
T |
C |
9: 21,985,987 (GRCm39) |
Y213C |
probably damaging |
Het |
Fer |
A |
G |
17: 64,385,880 (GRCm39) |
K654R |
probably damaging |
Het |
Hdac9 |
G |
T |
12: 34,439,428 (GRCm39) |
A383E |
probably damaging |
Het |
Hltf |
T |
A |
3: 20,130,660 (GRCm39) |
S293T |
probably benign |
Het |
Hydin |
T |
A |
8: 111,254,648 (GRCm39) |
D2359E |
probably benign |
Het |
Inf2 |
A |
G |
12: 112,571,222 (GRCm39) |
|
probably benign |
Het |
Kcns2 |
A |
G |
15: 34,839,504 (GRCm39) |
N289S |
possibly damaging |
Het |
Meioc |
T |
C |
11: 102,559,227 (GRCm39) |
S50P |
probably damaging |
Het |
Mocs1 |
G |
T |
17: 49,761,764 (GRCm39) |
E619D |
probably benign |
Het |
Nfatc2 |
A |
G |
2: 168,361,371 (GRCm39) |
|
probably benign |
Het |
Or51i1 |
T |
A |
7: 103,671,105 (GRCm39) |
N140I |
possibly damaging |
Het |
Pag1 |
A |
T |
3: 9,758,896 (GRCm39) |
H407Q |
probably benign |
Het |
Plaat1 |
A |
G |
16: 29,036,501 (GRCm39) |
I46M |
possibly damaging |
Het |
Plcb3 |
G |
A |
19: 6,943,533 (GRCm39) |
A122V |
probably damaging |
Het |
Pld4 |
C |
T |
12: 112,734,535 (GRCm39) |
T432I |
probably damaging |
Het |
Psd3 |
T |
G |
8: 68,574,179 (GRCm39) |
M1L |
probably benign |
Het |
Rasgrp2 |
C |
A |
19: 6,452,531 (GRCm39) |
L35I |
probably damaging |
Het |
Ripor2 |
T |
C |
13: 24,885,052 (GRCm39) |
L390P |
probably damaging |
Het |
Rpgrip1 |
A |
T |
14: 52,349,631 (GRCm39) |
E6D |
probably benign |
Het |
Ryr3 |
A |
T |
2: 112,672,244 (GRCm39) |
L1409Q |
probably damaging |
Het |
Slc6a5 |
A |
G |
7: 49,601,250 (GRCm39) |
T684A |
probably benign |
Het |
Smpd4 |
G |
T |
16: 17,458,930 (GRCm39) |
|
probably null |
Het |
Snx18 |
T |
C |
13: 113,753,725 (GRCm39) |
S403G |
probably damaging |
Het |
Spsb4 |
G |
T |
9: 96,878,160 (GRCm39) |
H54Q |
probably damaging |
Het |
Ssrp1 |
A |
G |
2: 84,871,072 (GRCm39) |
Y236C |
probably damaging |
Het |
Tenm3 |
C |
T |
8: 48,751,843 (GRCm39) |
S982N |
probably damaging |
Het |
Tet1 |
A |
G |
10: 62,675,749 (GRCm39) |
S776P |
probably damaging |
Het |
Tln1 |
G |
A |
4: 43,534,744 (GRCm39) |
P2166S |
probably benign |
Het |
Ufl1 |
T |
A |
4: 25,279,350 (GRCm39) |
Q83L |
possibly damaging |
Het |
Unc80 |
A |
T |
1: 66,693,188 (GRCm39) |
K2458* |
probably null |
Het |
Ush2a |
A |
T |
1: 188,460,467 (GRCm39) |
Y2576F |
probably benign |
Het |
Xrcc6 |
C |
A |
15: 81,913,305 (GRCm39) |
|
probably null |
Het |
Zbtb48 |
A |
G |
4: 152,106,064 (GRCm39) |
F380L |
probably damaging |
Het |
|
Other mutations in Zfp534 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
PIT1430001:Zfp534
|
UTSW |
4 |
147,759,917 (GRCm39) |
missense |
probably benign |
|
PIT1430001:Zfp534
|
UTSW |
4 |
147,759,880 (GRCm39) |
missense |
probably benign |
|
PIT4142001:Zfp534
|
UTSW |
4 |
147,762,770 (GRCm39) |
missense |
probably benign |
0.13 |
PIT4142001:Zfp534
|
UTSW |
4 |
147,760,031 (GRCm39) |
missense |
probably benign |
|
R0765:Zfp534
|
UTSW |
4 |
147,758,693 (GRCm39) |
missense |
probably damaging |
0.99 |
R4368:Zfp534
|
UTSW |
4 |
147,760,015 (GRCm39) |
missense |
probably benign |
0.15 |
R4660:Zfp534
|
UTSW |
4 |
147,759,175 (GRCm39) |
missense |
probably benign |
0.00 |
R4816:Zfp534
|
UTSW |
4 |
147,758,743 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5520:Zfp534
|
UTSW |
4 |
147,759,887 (GRCm39) |
missense |
possibly damaging |
0.58 |
R5577:Zfp534
|
UTSW |
4 |
147,759,173 (GRCm39) |
missense |
probably damaging |
1.00 |
R6154:Zfp534
|
UTSW |
4 |
147,759,145 (GRCm39) |
missense |
probably benign |
0.18 |
R6374:Zfp534
|
UTSW |
4 |
147,759,299 (GRCm39) |
missense |
probably benign |
0.44 |
R6610:Zfp534
|
UTSW |
4 |
147,758,947 (GRCm39) |
missense |
probably benign |
|
R6764:Zfp534
|
UTSW |
4 |
147,759,175 (GRCm39) |
missense |
probably benign |
0.00 |
R6803:Zfp534
|
UTSW |
4 |
147,758,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R6866:Zfp534
|
UTSW |
4 |
147,758,938 (GRCm39) |
missense |
probably benign |
0.18 |
R7027:Zfp534
|
UTSW |
4 |
147,759,667 (GRCm39) |
missense |
possibly damaging |
0.58 |
R7260:Zfp534
|
UTSW |
4 |
147,759,461 (GRCm39) |
missense |
probably benign |
0.03 |
R7455:Zfp534
|
UTSW |
4 |
147,759,212 (GRCm39) |
missense |
probably damaging |
1.00 |
R9128:Zfp534
|
UTSW |
4 |
147,760,082 (GRCm39) |
nonsense |
probably null |
|
R9199:Zfp534
|
UTSW |
4 |
147,760,439 (GRCm39) |
missense |
probably benign |
0.00 |
R9292:Zfp534
|
UTSW |
4 |
147,759,095 (GRCm39) |
missense |
probably damaging |
1.00 |
R9340:Zfp534
|
UTSW |
4 |
147,758,698 (GRCm39) |
missense |
possibly damaging |
0.48 |
R9475:Zfp534
|
UTSW |
4 |
147,766,731 (GRCm39) |
missense |
probably benign |
0.21 |
R9730:Zfp534
|
UTSW |
4 |
147,759,378 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Zfp534
|
UTSW |
4 |
147,758,684 (GRCm39) |
makesense |
probably null |
|
|