Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acaca |
T |
A |
11: 84,152,450 (GRCm39) |
Y866N |
probably damaging |
Het |
Adam24 |
G |
C |
8: 41,132,632 (GRCm39) |
W33C |
probably benign |
Het |
Adgrl2 |
A |
T |
3: 148,564,599 (GRCm39) |
V327E |
probably damaging |
Het |
Aqp7 |
T |
A |
4: 41,045,329 (GRCm39) |
N17I |
probably benign |
Het |
Bicra |
T |
A |
7: 15,713,658 (GRCm39) |
Q848L |
probably benign |
Het |
C4b |
T |
C |
17: 34,960,846 (GRCm39) |
E240G |
possibly damaging |
Het |
Ccni |
T |
C |
5: 93,335,620 (GRCm39) |
S173G |
probably benign |
Het |
Clca3a2 |
T |
A |
3: 144,508,842 (GRCm39) |
N50I |
probably damaging |
Het |
Dcaf7 |
A |
G |
11: 105,945,622 (GRCm39) |
T324A |
probably benign |
Het |
Dnah12 |
G |
A |
14: 26,492,929 (GRCm39) |
R1230H |
probably benign |
Het |
Dsg4 |
G |
A |
18: 20,584,813 (GRCm39) |
V176M |
probably damaging |
Het |
Ect2l |
A |
G |
10: 18,039,141 (GRCm39) |
I339T |
probably damaging |
Het |
Edc4 |
A |
T |
8: 106,612,126 (GRCm39) |
I138F |
probably damaging |
Het |
Ercc6l2 |
T |
A |
13: 63,992,409 (GRCm39) |
V401E |
probably damaging |
Het |
Gm3269 |
T |
A |
14: 16,033,003 (GRCm39) |
V260D |
possibly damaging |
Het |
Gm4076 |
C |
T |
13: 85,275,269 (GRCm39) |
|
noncoding transcript |
Het |
Gm4922 |
A |
T |
10: 18,660,244 (GRCm39) |
N159K |
probably benign |
Het |
Gm5134 |
G |
T |
10: 75,836,281 (GRCm39) |
A421S |
probably benign |
Het |
Hrc |
G |
C |
7: 44,985,757 (GRCm39) |
E303Q |
possibly damaging |
Het |
Ipo4 |
A |
G |
14: 55,870,560 (GRCm39) |
V288A |
probably benign |
Het |
Kng2 |
A |
G |
16: 22,830,745 (GRCm39) |
|
probably null |
Het |
Lrfn1 |
T |
C |
7: 28,159,479 (GRCm39) |
L466P |
possibly damaging |
Het |
Magi1 |
T |
A |
6: 93,676,610 (GRCm39) |
K916N |
probably damaging |
Het |
Mms19 |
T |
C |
19: 41,938,237 (GRCm39) |
T720A |
probably benign |
Het |
Muc5b |
A |
G |
7: 141,415,072 (GRCm39) |
T2673A |
possibly damaging |
Het |
Myo15a |
C |
T |
11: 60,400,489 (GRCm39) |
A1767V |
possibly damaging |
Het |
Npas2 |
A |
T |
1: 39,326,643 (GRCm39) |
M43L |
probably benign |
Het |
Nup43 |
A |
G |
10: 7,550,778 (GRCm39) |
D216G |
possibly damaging |
Het |
Or1e19 |
T |
C |
11: 73,316,678 (GRCm39) |
I44V |
probably benign |
Het |
Orc4 |
G |
A |
2: 48,827,501 (GRCm39) |
P31S |
probably benign |
Het |
Pcdhga6 |
G |
T |
18: 37,841,270 (GRCm39) |
R330L |
probably benign |
Het |
Pear1 |
A |
G |
3: 87,665,439 (GRCm39) |
F145L |
probably benign |
Het |
Pgap1 |
A |
G |
1: 54,569,302 (GRCm39) |
S355P |
possibly damaging |
Het |
Prr14l |
A |
T |
5: 32,985,963 (GRCm39) |
|
probably null |
Het |
Ptpn12 |
T |
C |
5: 21,194,047 (GRCm39) |
K742E |
possibly damaging |
Het |
Ryr1 |
T |
A |
7: 28,756,422 (GRCm39) |
Q3464L |
probably damaging |
Het |
Sema4c |
G |
C |
1: 36,592,804 (GRCm39) |
T138S |
probably benign |
Het |
Slc4a2 |
C |
T |
5: 24,635,099 (GRCm39) |
T168M |
probably benign |
Het |
Slco1a7 |
T |
C |
6: 141,654,322 (GRCm39) |
K647E |
probably benign |
Het |
Spice1 |
G |
T |
16: 44,178,232 (GRCm39) |
S85I |
probably damaging |
Het |
Thrb |
T |
A |
14: 17,963,214 (GRCm38) |
I59N |
probably damaging |
Het |
Trav7-1 |
A |
G |
14: 52,892,756 (GRCm39) |
D103G |
probably damaging |
Het |
Ubap2l |
G |
T |
3: 89,922,758 (GRCm39) |
T766N |
unknown |
Het |
Zfp692 |
C |
T |
11: 58,200,254 (GRCm39) |
T170I |
possibly damaging |
Het |
Zfp759 |
T |
C |
13: 67,287,031 (GRCm39) |
V194A |
probably benign |
Het |
|
Other mutations in Zfp704 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00848:Zfp704
|
APN |
3 |
9,630,299 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL03288:Zfp704
|
APN |
3 |
9,504,951 (GRCm39) |
splice site |
probably benign |
|
R0265:Zfp704
|
UTSW |
3 |
9,630,217 (GRCm39) |
missense |
probably damaging |
1.00 |
R0524:Zfp704
|
UTSW |
3 |
9,674,424 (GRCm39) |
missense |
unknown |
|
R1466:Zfp704
|
UTSW |
3 |
9,512,408 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1466:Zfp704
|
UTSW |
3 |
9,512,408 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1647:Zfp704
|
UTSW |
3 |
9,536,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R1648:Zfp704
|
UTSW |
3 |
9,536,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R1865:Zfp704
|
UTSW |
3 |
9,539,551 (GRCm39) |
splice site |
probably benign |
|
R1912:Zfp704
|
UTSW |
3 |
9,674,418 (GRCm39) |
missense |
unknown |
|
R2109:Zfp704
|
UTSW |
3 |
9,539,585 (GRCm39) |
missense |
probably damaging |
1.00 |
R2566:Zfp704
|
UTSW |
3 |
9,674,553 (GRCm39) |
missense |
unknown |
|
R4495:Zfp704
|
UTSW |
3 |
9,536,137 (GRCm39) |
missense |
probably benign |
0.01 |
R6165:Zfp704
|
UTSW |
3 |
9,508,946 (GRCm39) |
missense |
probably benign |
0.00 |
R6682:Zfp704
|
UTSW |
3 |
9,630,253 (GRCm39) |
missense |
probably benign |
0.11 |
R7057:Zfp704
|
UTSW |
3 |
9,535,977 (GRCm39) |
missense |
probably damaging |
1.00 |
R7348:Zfp704
|
UTSW |
3 |
9,539,658 (GRCm39) |
missense |
probably damaging |
1.00 |
R7758:Zfp704
|
UTSW |
3 |
9,509,282 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7858:Zfp704
|
UTSW |
3 |
9,509,217 (GRCm39) |
critical splice donor site |
probably null |
|
R8104:Zfp704
|
UTSW |
3 |
9,630,301 (GRCm39) |
missense |
probably benign |
0.03 |
R8373:Zfp704
|
UTSW |
3 |
9,674,502 (GRCm39) |
missense |
unknown |
|
R8877:Zfp704
|
UTSW |
3 |
9,674,416 (GRCm39) |
missense |
unknown |
|
R9136:Zfp704
|
UTSW |
3 |
9,509,324 (GRCm39) |
missense |
probably benign |
0.03 |
Z1176:Zfp704
|
UTSW |
3 |
9,536,104 (GRCm39) |
missense |
probably damaging |
1.00 |
|