Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb4 |
T |
G |
5: 8,984,203 (GRCm39) |
S644R |
probably benign |
Het |
Adra2a |
A |
G |
19: 54,034,659 (GRCm39) |
E5G |
probably benign |
Het |
Ankrd1 |
A |
T |
19: 36,092,922 (GRCm39) |
V201D |
possibly damaging |
Het |
Ano9 |
A |
T |
7: 140,683,114 (GRCm39) |
V598E |
probably damaging |
Het |
Apob |
T |
A |
12: 8,051,885 (GRCm39) |
M1150K |
possibly damaging |
Het |
BC005624 |
A |
T |
2: 30,864,032 (GRCm39) |
I187N |
probably damaging |
Het |
Bltp3b |
C |
T |
10: 89,651,968 (GRCm39) |
T1381I |
probably benign |
Het |
Ccl9 |
T |
C |
11: 83,467,257 (GRCm39) |
E31G |
probably benign |
Het |
Cnnm4 |
T |
A |
1: 36,511,019 (GRCm39) |
D82E |
probably benign |
Het |
Coq10b |
T |
C |
1: 55,092,013 (GRCm39) |
|
probably benign |
Het |
Cplane1 |
T |
G |
15: 8,233,241 (GRCm39) |
F1189V |
probably damaging |
Het |
Cyb561 |
T |
C |
11: 105,830,935 (GRCm39) |
N50S |
probably benign |
Het |
Dctn4 |
G |
T |
18: 60,679,348 (GRCm39) |
A223S |
probably benign |
Het |
Dysf |
A |
G |
6: 84,114,380 (GRCm39) |
Y1223C |
probably damaging |
Het |
Eed |
C |
T |
7: 89,630,022 (GRCm39) |
|
probably benign |
Het |
Eef1g |
T |
A |
19: 8,954,738 (GRCm39) |
V305E |
probably benign |
Het |
Eif4ebp2 |
C |
A |
10: 61,270,772 (GRCm39) |
A86S |
probably benign |
Het |
Ermp1 |
T |
C |
19: 29,609,788 (GRCm39) |
|
probably null |
Het |
Hid1 |
T |
C |
11: 115,249,821 (GRCm39) |
Y198C |
probably damaging |
Het |
Hoxd1 |
C |
A |
2: 74,593,816 (GRCm39) |
A124E |
probably benign |
Het |
Hyal5 |
G |
A |
6: 24,891,347 (GRCm39) |
C387Y |
probably damaging |
Het |
Il11 |
A |
G |
7: 4,778,999 (GRCm39) |
S103P |
probably damaging |
Het |
Lgalsl2 |
A |
T |
7: 5,362,507 (GRCm39) |
K46M |
probably damaging |
Het |
Lmtk3 |
A |
C |
7: 45,436,327 (GRCm39) |
I128L |
possibly damaging |
Het |
Lrrc4b |
G |
T |
7: 44,094,316 (GRCm39) |
|
probably benign |
Het |
Magel2 |
T |
A |
7: 62,028,116 (GRCm39) |
I340N |
possibly damaging |
Het |
Mfsd14a |
A |
T |
3: 116,442,200 (GRCm39) |
F71I |
possibly damaging |
Het |
Mgarp |
A |
G |
3: 51,296,487 (GRCm39) |
S172P |
probably benign |
Het |
Mug1 |
T |
C |
6: 121,847,611 (GRCm39) |
|
probably null |
Het |
Naa15 |
G |
T |
3: 51,370,688 (GRCm39) |
E651* |
probably null |
Het |
Ndfip2 |
T |
C |
14: 105,529,675 (GRCm39) |
V168A |
probably benign |
Het |
Neb |
C |
A |
2: 52,113,373 (GRCm39) |
|
probably null |
Het |
Nfil3 |
A |
G |
13: 53,121,968 (GRCm39) |
V312A |
possibly damaging |
Het |
Nrap |
T |
C |
19: 56,338,729 (GRCm39) |
I953V |
probably benign |
Het |
Ntrk1 |
T |
A |
3: 87,687,041 (GRCm39) |
K706* |
probably null |
Het |
Nuf2 |
A |
T |
1: 169,352,898 (GRCm39) |
F36I |
probably benign |
Het |
Or51h7 |
T |
A |
7: 102,591,125 (GRCm39) |
T220S |
possibly damaging |
Het |
Or5aq7 |
T |
C |
2: 86,937,861 (GRCm39) |
Y290C |
probably damaging |
Het |
Pcdh8 |
T |
G |
14: 80,006,101 (GRCm39) |
T821P |
possibly damaging |
Het |
Ppl |
C |
T |
16: 4,906,725 (GRCm39) |
R1190H |
probably damaging |
Het |
Ptch2 |
C |
A |
4: 116,962,224 (GRCm39) |
|
probably null |
Het |
Ptdss1 |
A |
G |
13: 67,081,719 (GRCm39) |
I50V |
probably benign |
Het |
Pth2r |
G |
T |
1: 65,390,722 (GRCm39) |
W292L |
probably damaging |
Het |
Ptprd |
G |
A |
4: 75,900,881 (GRCm39) |
T825M |
probably damaging |
Het |
Ptprk |
T |
C |
10: 28,449,385 (GRCm39) |
Y987H |
probably damaging |
Het |
Qser1 |
T |
C |
2: 104,606,579 (GRCm39) |
E1470G |
probably damaging |
Het |
Rab11fip3 |
T |
C |
17: 26,287,232 (GRCm39) |
E307G |
possibly damaging |
Het |
Rims2 |
A |
G |
15: 39,544,475 (GRCm39) |
Y1484C |
probably damaging |
Het |
Rock1 |
A |
T |
18: 10,097,651 (GRCm39) |
|
probably null |
Het |
Slc15a1 |
T |
A |
14: 121,718,145 (GRCm39) |
K245* |
probably null |
Het |
Snx11 |
T |
A |
11: 96,660,032 (GRCm39) |
E219V |
possibly damaging |
Het |
Sox21 |
C |
A |
14: 118,472,729 (GRCm39) |
E107* |
probably null |
Het |
Spink5 |
T |
A |
18: 44,132,888 (GRCm39) |
H501Q |
probably benign |
Het |
Stard5 |
C |
T |
7: 83,285,984 (GRCm39) |
T103M |
probably damaging |
Het |
Stfa2l1 |
A |
T |
16: 35,977,203 (GRCm39) |
|
probably benign |
Het |
Sult1c2 |
A |
C |
17: 54,271,076 (GRCm39) |
V185G |
probably damaging |
Het |
Svs5 |
A |
G |
2: 164,079,500 (GRCm39) |
S136P |
possibly damaging |
Het |
Sytl3 |
T |
A |
17: 6,982,774 (GRCm39) |
|
probably null |
Het |
Tc2n |
C |
T |
12: 101,619,112 (GRCm39) |
V349I |
possibly damaging |
Het |
Tln1 |
A |
G |
4: 43,554,309 (GRCm39) |
V271A |
probably benign |
Het |
Tmem260 |
T |
A |
14: 48,746,519 (GRCm39) |
S446R |
probably benign |
Het |
Trim30a |
T |
C |
7: 104,084,802 (GRCm39) |
D136G |
probably benign |
Het |
Ulk4 |
A |
T |
9: 120,873,885 (GRCm39) |
I1182N |
possibly damaging |
Het |
Unc50 |
T |
G |
1: 37,476,377 (GRCm39) |
I179S |
possibly damaging |
Het |
Upb1 |
T |
A |
10: 75,248,667 (GRCm39) |
Y57* |
probably null |
Het |
Usp34 |
C |
T |
11: 23,396,614 (GRCm39) |
T2349I |
|
Het |
Vmn1r71 |
A |
G |
7: 10,482,277 (GRCm39) |
V137A |
possibly damaging |
Het |
Vmn1r85 |
T |
C |
7: 12,818,698 (GRCm39) |
I149V |
probably benign |
Het |
Vmn2r118 |
A |
G |
17: 55,900,242 (GRCm39) |
L554P |
probably damaging |
Het |
Wdr4 |
C |
G |
17: 31,718,782 (GRCm39) |
|
probably null |
Het |
Zbbx |
A |
T |
3: 74,985,781 (GRCm39) |
S424T |
possibly damaging |
Het |
Zfp207 |
C |
G |
11: 80,282,726 (GRCm39) |
P246A |
probably damaging |
Het |
Zfp414 |
T |
A |
17: 33,848,962 (GRCm39) |
Y65* |
probably null |
Het |
Zfp600 |
T |
A |
4: 146,133,523 (GRCm39) |
N730K |
probably benign |
Het |
Zfp827 |
T |
C |
8: 79,912,979 (GRCm39) |
L1073P |
probably damaging |
Het |
Zgrf1 |
T |
A |
3: 127,357,080 (GRCm39) |
Y769N |
probably damaging |
Het |
Zup1 |
A |
T |
10: 33,795,315 (GRCm39) |
I547N |
unknown |
Het |
|
Other mutations in Zfp986 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
FR4548:Zfp986
|
UTSW |
4 |
145,625,928 (GRCm39) |
missense |
probably benign |
0.01 |
PIT4142001:Zfp986
|
UTSW |
4 |
145,625,513 (GRCm39) |
missense |
probably benign |
|
R0126:Zfp986
|
UTSW |
4 |
145,625,513 (GRCm39) |
missense |
probably benign |
|
R1835:Zfp986
|
UTSW |
4 |
145,625,805 (GRCm39) |
missense |
probably benign |
0.00 |
R3926:Zfp986
|
UTSW |
4 |
145,619,090 (GRCm39) |
splice site |
probably benign |
|
R4287:Zfp986
|
UTSW |
4 |
145,619,088 (GRCm39) |
critical splice donor site |
probably null |
|
R4401:Zfp986
|
UTSW |
4 |
145,625,513 (GRCm39) |
missense |
probably benign |
|
R6517:Zfp986
|
UTSW |
4 |
145,625,870 (GRCm39) |
missense |
probably benign |
0.30 |
R8108:Zfp986
|
UTSW |
4 |
145,625,875 (GRCm39) |
missense |
probably benign |
0.02 |
R8738:Zfp986
|
UTSW |
4 |
145,625,550 (GRCm39) |
missense |
probably benign |
0.04 |
R9153:Zfp986
|
UTSW |
4 |
145,626,030 (GRCm39) |
missense |
probably damaging |
1.00 |
R9210:Zfp986
|
UTSW |
4 |
145,625,798 (GRCm39) |
missense |
probably benign |
0.01 |
R9212:Zfp986
|
UTSW |
4 |
145,625,798 (GRCm39) |
missense |
probably benign |
0.01 |
R9235:Zfp986
|
UTSW |
4 |
145,625,759 (GRCm39) |
missense |
probably benign |
0.09 |
R9326:Zfp986
|
UTSW |
4 |
145,626,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R9691:Zfp986
|
UTSW |
4 |
145,626,070 (GRCm39) |
missense |
probably benign |
0.25 |
|