Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1810009J06Rik |
T |
C |
6: 40,943,663 (GRCm39) |
I109T |
probably damaging |
Het |
2200002D01Rik |
CCTTCTCCTTCTTCTCCTTCTTCTCCTTCTTCTCCATCTTCTCCTTCTTC |
CCTTCTCCTTCTTCTCCTTCTTCTCCATCTTCTCCTTCTTC |
7: 28,947,048 (GRCm39) |
|
probably benign |
Het |
Abca8b |
T |
G |
11: 109,858,498 (GRCm39) |
Q568P |
probably damaging |
Het |
Add3 |
A |
G |
19: 53,221,499 (GRCm39) |
T204A |
probably damaging |
Het |
Afg3l2 |
C |
A |
18: 67,567,262 (GRCm39) |
R196L |
possibly damaging |
Het |
Agps |
T |
A |
2: 75,742,024 (GRCm39) |
|
probably null |
Het |
Akap9 |
A |
G |
5: 4,011,852 (GRCm39) |
S852G |
possibly damaging |
Het |
Aoc1 |
A |
G |
6: 48,883,102 (GRCm39) |
D326G |
probably benign |
Het |
Cecr2 |
A |
G |
6: 120,739,229 (GRCm39) |
T1319A |
probably benign |
Het |
Cenpo |
C |
T |
12: 4,266,686 (GRCm39) |
V141I |
probably benign |
Het |
Clca4b |
A |
G |
3: 144,631,845 (GRCm39) |
L220S |
possibly damaging |
Het |
Dicer1 |
A |
G |
12: 104,670,991 (GRCm39) |
L1017P |
probably damaging |
Het |
Ero1b |
T |
G |
13: 12,589,728 (GRCm39) |
C44G |
probably damaging |
Het |
Ffar2 |
A |
T |
7: 30,518,929 (GRCm39) |
W204R |
probably benign |
Het |
Fmo3 |
T |
A |
1: 162,796,281 (GRCm39) |
E97V |
probably benign |
Het |
Gcnt4 |
G |
T |
13: 97,083,634 (GRCm39) |
R310L |
possibly damaging |
Het |
Gm7298 |
A |
G |
6: 121,744,541 (GRCm39) |
I520V |
probably benign |
Het |
Gmpr |
T |
C |
13: 45,699,471 (GRCm39) |
L327P |
probably damaging |
Het |
Grid2 |
T |
A |
6: 64,677,506 (GRCm39) |
H108Q |
unknown |
Het |
Hmcn2 |
G |
T |
2: 31,301,917 (GRCm39) |
L2935F |
probably damaging |
Het |
Hnf1b |
T |
C |
11: 83,779,986 (GRCm39) |
S440P |
probably benign |
Het |
Hsph1 |
A |
T |
5: 149,543,395 (GRCm39) |
Y644N |
probably damaging |
Het |
Igf2r |
A |
G |
17: 12,924,646 (GRCm39) |
I1057T |
possibly damaging |
Het |
Igfn1 |
T |
C |
1: 135,906,001 (GRCm39) |
E269G |
probably damaging |
Het |
Igkv14-126 |
A |
G |
6: 67,873,352 (GRCm39) |
T27A |
possibly damaging |
Het |
Inhca |
A |
T |
9: 103,158,252 (GRCm39) |
Y103N |
probably benign |
Het |
Kcnj15 |
A |
G |
16: 95,097,556 (GRCm39) |
R393G |
unknown |
Het |
Lamb1 |
A |
G |
12: 31,348,863 (GRCm39) |
T632A |
probably damaging |
Het |
Lrrk2 |
T |
C |
15: 91,607,407 (GRCm39) |
L590P |
probably damaging |
Het |
Mrm3 |
A |
G |
11: 76,138,286 (GRCm39) |
T225A |
possibly damaging |
Het |
Mthfd1l |
A |
G |
10: 4,053,335 (GRCm39) |
T895A |
possibly damaging |
Het |
Myh1 |
G |
A |
11: 67,110,631 (GRCm39) |
|
probably null |
Het |
Naip2 |
T |
A |
13: 100,298,354 (GRCm39) |
K561* |
probably null |
Het |
Necab2 |
C |
T |
8: 120,173,923 (GRCm39) |
P44S |
probably benign |
Het |
Nrde2 |
T |
C |
12: 100,092,477 (GRCm39) |
S1126G |
probably benign |
Het |
Nup210l |
C |
T |
3: 90,107,173 (GRCm39) |
P1570L |
probably benign |
Het |
Or14j6 |
A |
G |
17: 38,214,962 (GRCm39) |
H175R |
probably benign |
Het |
Or8c17 |
T |
A |
9: 38,179,926 (GRCm39) |
V31E |
possibly damaging |
Het |
Pecam1 |
T |
G |
11: 106,581,947 (GRCm39) |
D333A |
probably benign |
Het |
Prss27 |
T |
C |
17: 24,257,141 (GRCm39) |
|
probably benign |
Het |
Rapgef2 |
T |
C |
3: 79,082,300 (GRCm39) |
E100G |
probably damaging |
Het |
Rnft2 |
A |
G |
5: 118,340,982 (GRCm39) |
F299L |
probably damaging |
Het |
Rptor |
A |
G |
11: 119,562,152 (GRCm39) |
N105S |
possibly damaging |
Het |
S100a7l2 |
T |
C |
3: 90,997,698 (GRCm39) |
T6A |
unknown |
Het |
Scgb2b3 |
T |
A |
7: 31,059,642 (GRCm39) |
H44L |
probably benign |
Het |
Slc22a17 |
A |
T |
14: 55,147,139 (GRCm39) |
V53D |
possibly damaging |
Het |
Slc39a14 |
G |
A |
14: 70,547,569 (GRCm39) |
T298M |
probably benign |
Het |
Sorbs1 |
G |
A |
19: 40,315,324 (GRCm39) |
T496M |
probably damaging |
Het |
Spata31e1 |
G |
C |
13: 49,939,052 (GRCm39) |
T886S |
unknown |
Het |
Taar8a |
T |
C |
10: 23,952,753 (GRCm39) |
V119A |
probably benign |
Het |
Tas1r3 |
T |
C |
4: 155,945,059 (GRCm39) |
T721A |
possibly damaging |
Het |
Tm7sf3 |
C |
T |
6: 146,525,179 (GRCm39) |
D89N |
possibly damaging |
Het |
Tmie |
A |
T |
9: 110,696,651 (GRCm39) |
C77S |
probably damaging |
Het |
Tpp2 |
T |
A |
1: 43,999,369 (GRCm39) |
I381K |
probably damaging |
Het |
Ttn |
G |
C |
2: 76,776,822 (GRCm39) |
A1526G |
unknown |
Het |
Vmn2r12 |
T |
A |
5: 109,234,452 (GRCm39) |
M587L |
probably benign |
Het |
Zeb2 |
G |
T |
2: 44,888,912 (GRCm39) |
H344Q |
probably damaging |
Het |
Zfp292 |
A |
G |
4: 34,810,800 (GRCm39) |
I753T |
probably damaging |
Het |
Zfp442 |
A |
T |
2: 150,250,676 (GRCm39) |
C409S |
unknown |
Het |
Zfp947 |
G |
A |
17: 22,364,384 (GRCm39) |
T430I |
possibly damaging |
Het |
|
Other mutations in Zfp677 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00481:Zfp677
|
APN |
17 |
21,617,930 (GRCm39) |
missense |
probably benign |
0.33 |
IGL01973:Zfp677
|
APN |
17 |
21,617,169 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02206:Zfp677
|
APN |
17 |
21,613,499 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03240:Zfp677
|
APN |
17 |
21,617,135 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03409:Zfp677
|
APN |
17 |
21,617,107 (GRCm39) |
missense |
probably damaging |
1.00 |
R0622:Zfp677
|
UTSW |
17 |
21,617,962 (GRCm39) |
missense |
probably benign |
0.04 |
R0972:Zfp677
|
UTSW |
17 |
21,618,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R1519:Zfp677
|
UTSW |
17 |
21,617,499 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2155:Zfp677
|
UTSW |
17 |
21,617,970 (GRCm39) |
missense |
probably benign |
0.01 |
R2316:Zfp677
|
UTSW |
17 |
21,617,582 (GRCm39) |
missense |
probably benign |
0.38 |
R2866:Zfp677
|
UTSW |
17 |
21,617,518 (GRCm39) |
nonsense |
probably null |
|
R2989:Zfp677
|
UTSW |
17 |
21,617,114 (GRCm39) |
missense |
probably benign |
0.11 |
R3955:Zfp677
|
UTSW |
17 |
21,618,079 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4075:Zfp677
|
UTSW |
17 |
21,618,421 (GRCm39) |
missense |
probably damaging |
1.00 |
R4134:Zfp677
|
UTSW |
17 |
21,618,043 (GRCm39) |
missense |
probably benign |
0.01 |
R4229:Zfp677
|
UTSW |
17 |
21,618,544 (GRCm39) |
missense |
probably damaging |
1.00 |
R4729:Zfp677
|
UTSW |
17 |
21,617,680 (GRCm39) |
missense |
possibly damaging |
0.51 |
R4843:Zfp677
|
UTSW |
17 |
21,612,788 (GRCm39) |
missense |
probably benign |
0.23 |
R5023:Zfp677
|
UTSW |
17 |
21,618,056 (GRCm39) |
missense |
probably damaging |
1.00 |
R5316:Zfp677
|
UTSW |
17 |
21,617,410 (GRCm39) |
missense |
probably damaging |
0.99 |
R5420:Zfp677
|
UTSW |
17 |
21,618,175 (GRCm39) |
missense |
probably damaging |
1.00 |
R5694:Zfp677
|
UTSW |
17 |
21,618,021 (GRCm39) |
missense |
probably damaging |
0.99 |
R5837:Zfp677
|
UTSW |
17 |
21,617,648 (GRCm39) |
missense |
probably damaging |
1.00 |
R5888:Zfp677
|
UTSW |
17 |
21,618,520 (GRCm39) |
missense |
probably damaging |
1.00 |
R6007:Zfp677
|
UTSW |
17 |
21,617,918 (GRCm39) |
missense |
probably damaging |
1.00 |
R6119:Zfp677
|
UTSW |
17 |
21,618,070 (GRCm39) |
missense |
possibly damaging |
0.55 |
R6190:Zfp677
|
UTSW |
17 |
21,617,530 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6518:Zfp677
|
UTSW |
17 |
21,618,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R7198:Zfp677
|
UTSW |
17 |
21,618,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R7391:Zfp677
|
UTSW |
17 |
21,618,653 (GRCm39) |
missense |
possibly damaging |
0.56 |
R7801:Zfp677
|
UTSW |
17 |
21,618,277 (GRCm39) |
missense |
probably damaging |
1.00 |
R7808:Zfp677
|
UTSW |
17 |
21,617,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R8202:Zfp677
|
UTSW |
17 |
21,613,535 (GRCm39) |
missense |
probably damaging |
1.00 |
R8206:Zfp677
|
UTSW |
17 |
21,612,717 (GRCm39) |
splice site |
probably null |
|
R8885:Zfp677
|
UTSW |
17 |
21,618,350 (GRCm39) |
missense |
probably benign |
|
R8965:Zfp677
|
UTSW |
17 |
21,617,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R9062:Zfp677
|
UTSW |
17 |
21,612,815 (GRCm39) |
critical splice donor site |
probably null |
|
R9167:Zfp677
|
UTSW |
17 |
21,613,460 (GRCm39) |
missense |
probably damaging |
1.00 |
R9638:Zfp677
|
UTSW |
17 |
21,618,056 (GRCm39) |
missense |
probably damaging |
1.00 |
R9752:Zfp677
|
UTSW |
17 |
21,618,511 (GRCm39) |
missense |
probably damaging |
1.00 |
RF003:Zfp677
|
UTSW |
17 |
21,617,704 (GRCm39) |
missense |
probably damaging |
1.00 |
|