Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd16a |
T |
C |
17: 35,320,063 (GRCm39) |
|
probably null |
Het |
Adsl |
T |
C |
15: 80,851,968 (GRCm39) |
|
probably null |
Het |
Arhgap32 |
T |
C |
9: 32,172,241 (GRCm39) |
S1674P |
probably benign |
Het |
Cd244a |
T |
G |
1: 171,405,447 (GRCm39) |
D277E |
probably benign |
Het |
Ceacam23 |
C |
T |
7: 17,620,149 (GRCm39) |
L18F |
possibly damaging |
Het |
Ces1a |
A |
G |
8: 93,751,932 (GRCm39) |
Y401H |
probably damaging |
Het |
Chd9 |
G |
T |
8: 91,763,134 (GRCm39) |
V2320F |
possibly damaging |
Het |
Chrd |
A |
G |
16: 20,557,325 (GRCm39) |
E670G |
possibly damaging |
Het |
Ckap2 |
A |
G |
8: 22,666,992 (GRCm39) |
S290P |
probably benign |
Het |
Cluap1 |
T |
A |
16: 3,751,680 (GRCm39) |
|
probably null |
Het |
Col15a1 |
C |
T |
4: 47,257,184 (GRCm39) |
T325M |
probably damaging |
Het |
Cplane1 |
T |
C |
15: 8,230,636 (GRCm39) |
I971T |
possibly damaging |
Het |
Dnah5 |
T |
C |
15: 28,304,745 (GRCm39) |
F1652S |
probably damaging |
Het |
Dok6 |
T |
C |
18: 89,319,320 (GRCm39) |
Q312R |
probably benign |
Het |
Glis1 |
C |
A |
4: 107,484,740 (GRCm39) |
H600N |
possibly damaging |
Het |
Hivep1 |
A |
G |
13: 42,309,704 (GRCm39) |
D648G |
probably benign |
Het |
Kif22 |
A |
T |
7: 126,632,052 (GRCm39) |
|
probably null |
Het |
Lmtk3 |
A |
G |
7: 45,443,504 (GRCm39) |
D729G |
possibly damaging |
Het |
Mapk8ip3 |
G |
A |
17: 25,123,761 (GRCm39) |
P587L |
probably damaging |
Het |
Muc4 |
G |
C |
16: 32,753,919 (GRCm38) |
R1265P |
probably benign |
Het |
Myt1l |
A |
G |
12: 29,960,800 (GRCm39) |
K1038E |
unknown |
Het |
Nf1 |
T |
A |
11: 79,426,863 (GRCm39) |
|
probably null |
Het |
Nom1 |
T |
C |
5: 29,656,163 (GRCm39) |
S843P |
possibly damaging |
Het |
Or1e33 |
A |
G |
11: 73,738,045 (GRCm39) |
I302T |
probably benign |
Het |
Pex14 |
A |
G |
4: 149,048,021 (GRCm39) |
|
probably benign |
Het |
Ptcd1 |
T |
C |
5: 145,091,531 (GRCm39) |
T523A |
possibly damaging |
Het |
Rasip1 |
T |
C |
7: 45,282,159 (GRCm39) |
V554A |
possibly damaging |
Het |
Ric3 |
A |
T |
7: 108,653,570 (GRCm39) |
|
probably null |
Het |
Skint4 |
G |
A |
4: 111,944,221 (GRCm39) |
C11Y |
probably damaging |
Het |
Smr2 |
G |
A |
5: 88,256,631 (GRCm39) |
R103H |
probably benign |
Het |
Sobp |
T |
C |
10: 43,034,020 (GRCm39) |
Y102C |
probably damaging |
Het |
Taar7f |
T |
A |
10: 23,926,473 (GRCm39) |
F356I |
probably damaging |
Het |
Tbcd |
T |
C |
11: 121,496,097 (GRCm39) |
V1044A |
possibly damaging |
Het |
Tecpr1 |
C |
G |
5: 144,149,408 (GRCm39) |
V340L |
probably damaging |
Het |
Tle3 |
A |
G |
9: 61,281,295 (GRCm39) |
I22V |
probably damaging |
Het |
Trim30a |
G |
A |
7: 104,084,851 (GRCm39) |
R120* |
probably null |
Het |
Trim72 |
A |
G |
7: 127,607,164 (GRCm39) |
D231G |
probably benign |
Het |
Vmn2r59 |
T |
A |
7: 41,695,648 (GRCm39) |
N255Y |
probably benign |
Het |
Vps13a |
T |
C |
19: 16,617,403 (GRCm39) |
T3002A |
probably damaging |
Het |
Wnt7a |
A |
T |
6: 91,343,324 (GRCm39) |
|
probably null |
Het |
Zfp51 |
C |
T |
17: 21,685,178 (GRCm39) |
Q598* |
probably null |
Het |
Zfp617 |
A |
T |
8: 72,683,003 (GRCm39) |
N51I |
probably damaging |
Het |
Zic1 |
A |
G |
9: 91,246,875 (GRCm39) |
S66P |
probably damaging |
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 |
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 |
R8294:Zfp977
|
UTSW |
7 |
42,229,689 (GRCm39) |
missense |
probably benign |
|
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 |
|
|