Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ankrd35 |
A |
G |
3: 96,590,623 (GRCm39) |
E303G |
possibly damaging |
Het |
Atosa |
A |
G |
9: 74,932,954 (GRCm39) |
T974A |
probably damaging |
Het |
C2cd5 |
T |
C |
6: 142,995,954 (GRCm39) |
T389A |
possibly damaging |
Het |
Catsperb |
T |
A |
12: 101,542,075 (GRCm39) |
Y592N |
possibly damaging |
Het |
Cfap91 |
A |
G |
16: 38,154,173 (GRCm39) |
F124S |
possibly damaging |
Het |
Cnot9 |
T |
C |
1: 74,567,952 (GRCm39) |
V280A |
probably benign |
Het |
Cyld |
A |
G |
8: 89,473,561 (GRCm39) |
I927V |
possibly damaging |
Het |
Etfdh |
A |
T |
3: 79,512,251 (GRCm39) |
S490T |
probably benign |
Het |
Fance |
C |
T |
17: 28,545,068 (GRCm39) |
R150C |
probably benign |
Het |
Far1 |
A |
G |
7: 113,153,425 (GRCm39) |
K353E |
probably benign |
Het |
Fbn1 |
T |
C |
2: 125,174,283 (GRCm39) |
I1858V |
probably damaging |
Het |
Frem1 |
T |
C |
4: 82,874,492 (GRCm39) |
K1359E |
probably benign |
Het |
Ghdc |
T |
G |
11: 100,659,928 (GRCm39) |
E273A |
possibly damaging |
Het |
Gpt |
A |
G |
15: 76,582,170 (GRCm39) |
D209G |
probably benign |
Het |
Hspb7 |
T |
C |
4: 141,149,862 (GRCm39) |
F83L |
probably benign |
Het |
Itga7 |
A |
G |
10: 128,778,804 (GRCm39) |
I306M |
probably benign |
Het |
Itgb5 |
A |
G |
16: 33,719,612 (GRCm39) |
E261G |
probably benign |
Het |
Kcnj14 |
G |
T |
7: 45,469,424 (GRCm39) |
A27E |
possibly damaging |
Het |
Kif13b |
A |
G |
14: 64,979,760 (GRCm39) |
H470R |
probably damaging |
Het |
Macroh2a1 |
A |
T |
13: 56,252,268 (GRCm39) |
N108K |
probably damaging |
Het |
Morc3 |
T |
C |
16: 93,638,271 (GRCm39) |
F18L |
probably damaging |
Het |
Mrgprb8 |
T |
A |
7: 48,038,565 (GRCm39) |
C79S |
possibly damaging |
Het |
Mroh2b |
T |
A |
15: 4,947,832 (GRCm39) |
M549K |
probably benign |
Het |
Msl1 |
T |
C |
11: 98,695,673 (GRCm39) |
V563A |
probably damaging |
Het |
Nwd1 |
C |
T |
8: 73,388,814 (GRCm39) |
R81W |
probably damaging |
Het |
Or5b124 |
A |
T |
19: 13,610,507 (GRCm39) |
I11F |
possibly damaging |
Het |
Or5b124 |
C |
T |
19: 13,610,952 (GRCm39) |
A159V |
probably benign |
Het |
Phf2 |
C |
A |
13: 48,967,341 (GRCm39) |
|
probably null |
Het |
Pjvk |
T |
G |
2: 76,480,562 (GRCm39) |
|
probably null |
Het |
Rgl2 |
A |
G |
17: 34,150,739 (GRCm39) |
T66A |
probably benign |
Het |
Rsf1 |
ATGGCG |
ATGGCGACGGTGGCG |
7: 97,229,111 (GRCm39) |
|
probably benign |
Het |
Rtkn |
G |
T |
6: 83,122,944 (GRCm39) |
E67D |
probably damaging |
Het |
Serpinb9 |
T |
A |
13: 33,192,807 (GRCm39) |
F121L |
possibly damaging |
Het |
Slc34a1 |
G |
A |
13: 23,999,053 (GRCm39) |
V149I |
probably benign |
Het |
Sobp |
A |
G |
10: 42,898,599 (GRCm39) |
S329P |
probably damaging |
Het |
Syne1 |
A |
T |
10: 5,375,678 (GRCm39) |
L138Q |
probably damaging |
Het |
Tfr2 |
T |
A |
5: 137,578,519 (GRCm39) |
V449D |
probably damaging |
Het |
Tmem151b |
T |
C |
17: 45,856,711 (GRCm39) |
Y243C |
probably damaging |
Het |
Trank1 |
T |
C |
9: 111,220,940 (GRCm39) |
V2559A |
probably benign |
Het |
Trim35 |
T |
C |
14: 66,546,654 (GRCm39) |
Y474H |
probably damaging |
Het |
Uso1 |
A |
T |
5: 92,335,126 (GRCm39) |
L495F |
probably damaging |
Het |
Wdr24 |
A |
G |
17: 26,045,395 (GRCm39) |
I377V |
probably benign |
Het |
Xpo5 |
T |
A |
17: 46,546,883 (GRCm39) |
V878D |
possibly damaging |
Het |
Zfc3h1 |
A |
G |
10: 115,256,574 (GRCm39) |
I1515V |
probably benign |
Het |
Zfp384 |
T |
G |
6: 125,001,896 (GRCm39) |
|
probably null |
Het |
Zfp704 |
G |
T |
3: 9,508,946 (GRCm39) |
P416T |
probably benign |
Het |
Zfr |
C |
T |
15: 12,146,331 (GRCm39) |
A294V |
unknown |
Het |
|
Other mutations in Zfp319 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01611:Zfp319
|
APN |
8 |
96,055,540 (GRCm39) |
missense |
probably benign |
0.11 |
IGL02478:Zfp319
|
APN |
8 |
96,055,721 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02563:Zfp319
|
APN |
8 |
96,050,362 (GRCm39) |
unclassified |
probably benign |
|
IGL02622:Zfp319
|
APN |
8 |
96,055,589 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02945:Zfp319
|
APN |
8 |
96,050,446 (GRCm39) |
unclassified |
probably benign |
|
Lanky
|
UTSW |
8 |
96,054,733 (GRCm39) |
frame shift |
probably null |
|
R0894:Zfp319
|
UTSW |
8 |
96,056,250 (GRCm39) |
unclassified |
probably benign |
|
R1898:Zfp319
|
UTSW |
8 |
96,055,417 (GRCm39) |
missense |
probably damaging |
1.00 |
R1937:Zfp319
|
UTSW |
8 |
96,055,199 (GRCm39) |
missense |
probably damaging |
1.00 |
R2127:Zfp319
|
UTSW |
8 |
96,050,391 (GRCm39) |
unclassified |
probably benign |
|
R2157:Zfp319
|
UTSW |
8 |
96,054,659 (GRCm39) |
missense |
probably damaging |
1.00 |
R2256:Zfp319
|
UTSW |
8 |
96,055,129 (GRCm39) |
missense |
possibly damaging |
0.47 |
R3547:Zfp319
|
UTSW |
8 |
96,055,445 (GRCm39) |
missense |
probably damaging |
0.96 |
R4665:Zfp319
|
UTSW |
8 |
96,052,201 (GRCm39) |
unclassified |
probably benign |
|
R5174:Zfp319
|
UTSW |
8 |
96,054,797 (GRCm39) |
splice site |
probably null |
|
R5249:Zfp319
|
UTSW |
8 |
96,055,099 (GRCm39) |
missense |
probably benign |
0.00 |
R5478:Zfp319
|
UTSW |
8 |
96,052,193 (GRCm39) |
unclassified |
probably benign |
|
R5623:Zfp319
|
UTSW |
8 |
96,052,199 (GRCm39) |
unclassified |
probably benign |
|
R7175:Zfp319
|
UTSW |
8 |
96,055,410 (GRCm39) |
missense |
probably damaging |
1.00 |
R7271:Zfp319
|
UTSW |
8 |
96,058,471 (GRCm39) |
unclassified |
probably benign |
|
R8303:Zfp319
|
UTSW |
8 |
96,055,765 (GRCm39) |
missense |
probably damaging |
1.00 |
R8734:Zfp319
|
UTSW |
8 |
96,054,938 (GRCm39) |
missense |
possibly damaging |
0.51 |
R9443:Zfp319
|
UTSW |
8 |
96,054,922 (GRCm39) |
missense |
probably benign |
0.00 |
R9550:Zfp319
|
UTSW |
8 |
96,055,025 (GRCm39) |
missense |
probably benign |
0.06 |
|