Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca4 |
T |
C |
3: 121,897,217 (GRCm39) |
V632A |
possibly damaging |
Het |
Abcf2 |
CAT |
CATAAT |
5: 24,781,589 (GRCm39) |
|
probably benign |
Het |
Acat2 |
T |
C |
17: 13,175,243 (GRCm39) |
I79V |
probably benign |
Het |
Arid3a |
A |
T |
10: 79,786,535 (GRCm39) |
|
silent |
Het |
Cecr2 |
C |
T |
6: 120,710,747 (GRCm39) |
A154V |
probably damaging |
Het |
Cog3 |
A |
C |
14: 75,954,619 (GRCm39) |
L650R |
probably damaging |
Het |
Col12a1 |
A |
T |
9: 79,606,594 (GRCm39) |
F610I |
possibly damaging |
Het |
Col24a1 |
A |
G |
3: 145,186,844 (GRCm39) |
D1215G |
probably null |
Het |
Ctsh |
C |
G |
9: 89,950,489 (GRCm39) |
A219G |
possibly damaging |
Het |
Dnah10 |
C |
T |
5: 124,859,410 (GRCm39) |
L2126F |
probably damaging |
Het |
Dock10 |
A |
G |
1: 80,488,079 (GRCm39) |
V2028A |
possibly damaging |
Het |
Ece1 |
T |
C |
4: 137,675,931 (GRCm39) |
V435A |
possibly damaging |
Het |
Epha8 |
G |
T |
4: 136,665,897 (GRCm39) |
L420M |
probably damaging |
Het |
H4c1 |
A |
G |
13: 23,944,957 (GRCm39) |
F62L |
probably damaging |
Het |
Hk1 |
T |
G |
10: 62,131,624 (GRCm39) |
I245L |
probably benign |
Het |
Hyal6 |
A |
C |
6: 24,734,378 (GRCm39) |
K104Q |
possibly damaging |
Het |
Kalrn |
T |
C |
16: 33,853,954 (GRCm39) |
I2017V |
probably benign |
Het |
Khdc4 |
C |
T |
3: 88,603,915 (GRCm39) |
A244V |
probably damaging |
Het |
Krt72 |
A |
T |
15: 101,694,472 (GRCm39) |
L141Q |
probably damaging |
Het |
Map3k4 |
C |
A |
17: 12,537,500 (GRCm39) |
A6S |
unknown |
Het |
Muc6 |
T |
C |
7: 141,217,263 (GRCm39) |
Y2470C |
possibly damaging |
Het |
Nrip1 |
A |
G |
16: 76,089,418 (GRCm39) |
V713A |
probably damaging |
Het |
Or10q1b |
A |
G |
19: 13,683,010 (GRCm39) |
D273G |
probably benign |
Het |
Or11g26 |
A |
G |
14: 50,753,083 (GRCm39) |
T141A |
possibly damaging |
Het |
Or2ah1 |
T |
A |
2: 85,653,531 (GRCm39) |
I72N |
probably damaging |
Het |
Or6aa1 |
T |
C |
7: 86,044,487 (GRCm39) |
Y73C |
probably damaging |
Het |
Paip1 |
C |
T |
13: 119,587,300 (GRCm39) |
T304I |
possibly damaging |
Het |
Pde4dip |
A |
G |
3: 97,674,694 (GRCm39) |
L74P |
probably damaging |
Het |
Prkch |
T |
A |
12: 73,806,484 (GRCm39) |
L577H |
probably damaging |
Het |
Rp1 |
A |
G |
1: 4,416,220 (GRCm39) |
S1631P |
probably benign |
Het |
Rph3a |
A |
G |
5: 121,099,429 (GRCm39) |
F154S |
probably damaging |
Het |
S1pr5 |
A |
G |
9: 21,156,300 (GRCm39) |
V42A |
possibly damaging |
Het |
Scaper |
G |
A |
9: 55,517,280 (GRCm39) |
L1052F |
possibly damaging |
Het |
Slc44a2 |
G |
T |
9: 21,259,643 (GRCm39) |
V597F |
probably damaging |
Het |
Srsf1 |
T |
A |
11: 87,939,467 (GRCm39) |
S116T |
probably benign |
Het |
Ssh2 |
A |
G |
11: 77,345,027 (GRCm39) |
D1004G |
probably benign |
Het |
St3gal5 |
T |
A |
6: 72,074,816 (GRCm39) |
D25E |
|
Het |
Syt17 |
A |
T |
7: 118,009,228 (GRCm39) |
Y327N |
probably damaging |
Het |
T |
T |
A |
17: 8,653,364 (GRCm39) |
M1K |
probably null |
Het |
Tmem201 |
A |
T |
4: 149,815,554 (GRCm39) |
I132N |
possibly damaging |
Het |
Tmprss15 |
A |
T |
16: 78,868,176 (GRCm39) |
C211S |
probably benign |
Het |
Trim36 |
T |
C |
18: 46,331,588 (GRCm39) |
D7G |
probably benign |
Het |
Trip11 |
T |
A |
12: 101,811,160 (GRCm39) |
K1863N |
possibly damaging |
Het |
Vmn2r13 |
A |
T |
5: 109,322,978 (GRCm39) |
S104T |
probably benign |
Het |
|
Other mutations in Zfp977 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01350:Zfp977
|
APN |
7 |
42,230,090 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01541:Zfp977
|
APN |
7 |
42,230,156 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02034:Zfp977
|
APN |
7 |
42,230,136 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02678:Zfp977
|
APN |
7 |
42,232,419 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02684:Zfp977
|
APN |
7 |
42,232,439 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03178:Zfp977
|
APN |
7 |
42,232,072 (GRCm39) |
missense |
probably damaging |
0.99 |
R0707:Zfp977
|
UTSW |
7 |
42,229,958 (GRCm39) |
missense |
probably damaging |
1.00 |
R1640:Zfp977
|
UTSW |
7 |
42,229,530 (GRCm39) |
missense |
probably damaging |
0.99 |
R1668:Zfp977
|
UTSW |
7 |
42,230,070 (GRCm39) |
missense |
probably benign |
0.03 |
R1993:Zfp977
|
UTSW |
7 |
42,229,409 (GRCm39) |
missense |
probably benign |
0.00 |
R3151:Zfp977
|
UTSW |
7 |
42,229,870 (GRCm39) |
missense |
probably benign |
0.00 |
R4587:Zfp977
|
UTSW |
7 |
42,229,614 (GRCm39) |
missense |
probably damaging |
0.98 |
R4678:Zfp977
|
UTSW |
7 |
42,229,437 (GRCm39) |
missense |
probably benign |
0.04 |
R6073:Zfp977
|
UTSW |
7 |
42,230,165 (GRCm39) |
missense |
probably benign |
0.34 |
R7054:Zfp977
|
UTSW |
7 |
42,229,786 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7436:Zfp977
|
UTSW |
7 |
42,229,884 (GRCm39) |
missense |
probably benign |
|
R7500:Zfp977
|
UTSW |
7 |
42,229,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R8418:Zfp977
|
UTSW |
7 |
42,229,410 (GRCm39) |
missense |
probably benign |
|
R8439:Zfp977
|
UTSW |
7 |
42,230,102 (GRCm39) |
missense |
probably benign |
0.03 |
R8995:Zfp977
|
UTSW |
7 |
42,232,072 (GRCm39) |
missense |
probably damaging |
1.00 |
R9005:Zfp977
|
UTSW |
7 |
42,230,082 (GRCm39) |
missense |
probably benign |
0.04 |
R9369:Zfp977
|
UTSW |
7 |
42,229,518 (GRCm39) |
missense |
probably damaging |
0.99 |
X0023:Zfp977
|
UTSW |
7 |
42,229,543 (GRCm39) |
nonsense |
probably null |
|
|