Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Anks3 |
A |
G |
16: 4,773,774 (GRCm39) |
M174T |
possibly damaging |
Het |
Arhgap23 |
G |
A |
11: 97,357,304 (GRCm39) |
R934Q |
possibly damaging |
Het |
Atad5 |
T |
C |
11: 79,986,832 (GRCm39) |
S640P |
probably damaging |
Het |
B3galnt2 |
C |
T |
13: 14,155,065 (GRCm39) |
|
probably null |
Het |
B430305J03Rik |
T |
C |
3: 61,271,539 (GRCm39) |
S69G |
unknown |
Het |
Cd163 |
A |
T |
6: 124,295,897 (GRCm39) |
N747I |
possibly damaging |
Het |
Cep126 |
A |
G |
9: 8,099,817 (GRCm39) |
S906P |
probably damaging |
Het |
Cimip2b |
T |
C |
4: 43,428,022 (GRCm39) |
D145G |
possibly damaging |
Het |
Cyp4f39 |
G |
A |
17: 32,705,753 (GRCm39) |
G318R |
probably damaging |
Het |
D630003M21Rik |
C |
T |
2: 158,059,129 (GRCm39) |
G257D |
probably damaging |
Het |
Dcaf10 |
T |
C |
4: 45,342,583 (GRCm39) |
L139P |
probably damaging |
Het |
Dcc |
A |
G |
18: 71,511,895 (GRCm39) |
V840A |
probably benign |
Het |
Dnhd1 |
A |
T |
7: 105,353,174 (GRCm39) |
I2776L |
probably benign |
Het |
Fbxo24 |
G |
T |
5: 137,619,523 (GRCm39) |
F234L |
probably damaging |
Het |
Gm21190 |
T |
C |
5: 15,732,902 (GRCm39) |
|
probably null |
Het |
Grhl3 |
C |
T |
4: 135,273,557 (GRCm39) |
R565Q |
probably damaging |
Het |
Gtf3c1 |
A |
T |
7: 125,244,842 (GRCm39) |
Y1731N |
probably damaging |
Het |
Il1a |
C |
A |
2: 129,146,693 (GRCm39) |
R133S |
probably benign |
Het |
Ipo4 |
C |
T |
14: 55,872,988 (GRCm39) |
R23Q |
probably benign |
Het |
Klc3 |
G |
A |
7: 19,128,814 (GRCm39) |
T481M |
probably benign |
Het |
Map2k6 |
A |
T |
11: 110,383,734 (GRCm39) |
I127F |
|
Het |
Mapk8 |
A |
T |
14: 33,130,068 (GRCm39) |
N63K |
probably damaging |
Het |
Med13l |
T |
C |
5: 118,880,825 (GRCm39) |
W1306R |
probably damaging |
Het |
Megf6 |
C |
A |
4: 154,351,772 (GRCm39) |
Q1162K |
probably benign |
Het |
Myo5b |
A |
G |
18: 74,841,095 (GRCm39) |
E992G |
possibly damaging |
Het |
Ndst4 |
C |
T |
3: 125,508,308 (GRCm39) |
T291M |
probably benign |
Het |
Nek10 |
T |
A |
14: 14,955,503 (GRCm38) |
F838L |
probably benign |
Het |
Nrm |
A |
G |
17: 36,175,476 (GRCm39) |
H194R |
probably damaging |
Het |
Nup188 |
T |
C |
2: 30,230,613 (GRCm39) |
S1384P |
probably benign |
Het |
Olfml2a |
C |
A |
2: 38,850,139 (GRCm39) |
D618E |
probably damaging |
Het |
Or5p78 |
C |
T |
7: 108,212,270 (GRCm39) |
T252I |
probably benign |
Het |
Or8g23 |
A |
G |
9: 38,971,875 (GRCm39) |
L29P |
probably damaging |
Het |
Or8g24 |
G |
A |
9: 38,989,630 (GRCm39) |
S137F |
probably damaging |
Het |
Or9s18 |
A |
C |
13: 65,300,557 (GRCm39) |
N173T |
possibly damaging |
Het |
P2ry1 |
T |
C |
3: 60,911,095 (GRCm39) |
F78S |
possibly damaging |
Het |
Pcdhb18 |
T |
C |
18: 37,624,976 (GRCm39) |
F769L |
probably benign |
Het |
Poc5 |
A |
G |
13: 96,533,304 (GRCm39) |
E144G |
probably damaging |
Het |
Pole |
T |
A |
5: 110,451,769 (GRCm39) |
N870K |
possibly damaging |
Het |
Polr2b |
T |
C |
5: 77,496,966 (GRCm39) |
F1159L |
possibly damaging |
Het |
Pramel32 |
T |
C |
4: 88,546,416 (GRCm39) |
K309E |
possibly damaging |
Het |
Rubcnl |
A |
G |
14: 75,279,793 (GRCm39) |
Y392C |
probably benign |
Het |
Sec31a |
T |
C |
5: 100,533,129 (GRCm39) |
T539A |
probably damaging |
Het |
Serpinh1 |
A |
C |
7: 98,995,563 (GRCm39) |
S340A |
probably damaging |
Het |
Slc1a5 |
T |
A |
7: 16,530,085 (GRCm39) |
|
probably null |
Het |
Soat2 |
A |
G |
15: 102,071,013 (GRCm39) |
D469G |
probably benign |
Het |
Speg |
T |
C |
1: 75,361,479 (GRCm39) |
L70P |
probably damaging |
Het |
Spred2 |
T |
C |
11: 19,874,958 (GRCm39) |
|
probably null |
Het |
Stac2 |
A |
C |
11: 97,933,439 (GRCm39) |
S168A |
probably damaging |
Het |
Stx1a |
T |
A |
5: 135,066,042 (GRCm39) |
D31E |
probably benign |
Het |
Timeless |
C |
T |
10: 128,085,623 (GRCm39) |
T885M |
probably damaging |
Het |
Tmem94 |
G |
T |
11: 115,677,082 (GRCm39) |
R118L |
possibly damaging |
Het |
Tsen34 |
T |
C |
7: 3,698,614 (GRCm39) |
Y253H |
probably damaging |
Het |
Unc13b |
T |
C |
4: 43,173,966 (GRCm39) |
V1598A |
unknown |
Het |
Zfat |
A |
T |
15: 67,976,892 (GRCm39) |
Y1086N |
probably damaging |
Het |
|
Other mutations in Zfp551 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01470:Zfp551
|
APN |
7 |
12,152,468 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01990:Zfp551
|
APN |
7 |
12,156,343 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02511:Zfp551
|
APN |
7 |
12,150,602 (GRCm39) |
missense |
possibly damaging |
0.70 |
R2001:Zfp551
|
UTSW |
7 |
12,150,276 (GRCm39) |
missense |
probably damaging |
1.00 |
R3120:Zfp551
|
UTSW |
7 |
12,149,943 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4256:Zfp551
|
UTSW |
7 |
12,150,318 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4387:Zfp551
|
UTSW |
7 |
12,152,568 (GRCm39) |
missense |
probably damaging |
1.00 |
R5314:Zfp551
|
UTSW |
7 |
12,150,087 (GRCm39) |
nonsense |
probably null |
|
R5536:Zfp551
|
UTSW |
7 |
12,149,488 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5874:Zfp551
|
UTSW |
7 |
12,150,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R6265:Zfp551
|
UTSW |
7 |
12,149,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R6765:Zfp551
|
UTSW |
7 |
12,150,767 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6803:Zfp551
|
UTSW |
7 |
12,151,108 (GRCm39) |
nonsense |
probably null |
|
R6953:Zfp551
|
UTSW |
7 |
12,150,715 (GRCm39) |
nonsense |
probably null |
|
R7334:Zfp551
|
UTSW |
7 |
12,150,681 (GRCm39) |
missense |
probably damaging |
0.97 |
R7502:Zfp551
|
UTSW |
7 |
12,149,725 (GRCm39) |
nonsense |
probably null |
|
R7772:Zfp551
|
UTSW |
7 |
12,152,535 (GRCm39) |
missense |
probably damaging |
0.98 |
R7776:Zfp551
|
UTSW |
7 |
12,152,569 (GRCm39) |
missense |
probably damaging |
1.00 |
R7999:Zfp551
|
UTSW |
7 |
12,151,138 (GRCm39) |
nonsense |
probably null |
|
R8032:Zfp551
|
UTSW |
7 |
12,152,487 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8984:Zfp551
|
UTSW |
7 |
12,156,559 (GRCm39) |
unclassified |
probably benign |
|
R9082:Zfp551
|
UTSW |
7 |
12,151,004 (GRCm39) |
missense |
probably damaging |
1.00 |
|