Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Accsl |
A |
G |
2: 93,696,253 (GRCm39) |
V119A |
possibly damaging |
Het |
Adamts12 |
T |
A |
15: 11,311,331 (GRCm39) |
M1196K |
probably benign |
Het |
Adgre1 |
T |
A |
17: 57,718,024 (GRCm39) |
C345* |
probably null |
Het |
Adrb2 |
T |
C |
18: 62,312,078 (GRCm39) |
E249G |
probably benign |
Het |
Amdhd1 |
T |
A |
10: 93,360,291 (GRCm39) |
I423F |
probably benign |
Het |
Ankhd1 |
A |
G |
18: 36,727,867 (GRCm39) |
N501S |
probably damaging |
Het |
Bltp2 |
T |
C |
11: 78,179,858 (GRCm39) |
V2127A |
probably damaging |
Het |
Cd180 |
T |
A |
13: 102,841,821 (GRCm39) |
I289N |
probably damaging |
Het |
Cox6a2 |
A |
G |
7: 127,805,103 (GRCm39) |
I60T |
possibly damaging |
Het |
Dnajc6 |
C |
T |
4: 101,471,483 (GRCm39) |
|
probably null |
Het |
Dpp6 |
G |
A |
5: 27,674,409 (GRCm39) |
E179K |
probably benign |
Het |
Fasn |
G |
A |
11: 120,704,562 (GRCm39) |
T1341I |
possibly damaging |
Het |
Fat1 |
C |
T |
8: 45,404,620 (GRCm39) |
T457I |
probably benign |
Het |
Filip1l |
A |
T |
16: 57,392,096 (GRCm39) |
|
probably null |
Het |
Gje1 |
A |
T |
10: 14,592,413 (GRCm39) |
I123N |
probably damaging |
Het |
Gli3 |
A |
G |
13: 15,894,874 (GRCm39) |
T683A |
probably damaging |
Het |
Gm29326 |
C |
A |
7: 29,260,833 (GRCm39) |
|
noncoding transcript |
Het |
Gm5460 |
A |
G |
14: 33,765,909 (GRCm39) |
|
probably benign |
Het |
Hspa4 |
C |
T |
11: 53,153,200 (GRCm39) |
S739N |
probably benign |
Het |
Ighv1-42 |
T |
A |
12: 114,900,885 (GRCm39) |
I67F |
probably damaging |
Het |
Iqgap1 |
A |
G |
7: 80,402,041 (GRCm39) |
V408A |
probably benign |
Het |
Kdm7a |
A |
T |
6: 39,147,198 (GRCm39) |
W250R |
probably damaging |
Het |
Kif5a |
A |
G |
10: 127,078,565 (GRCm39) |
I360T |
possibly damaging |
Het |
Maml1 |
T |
C |
11: 50,148,992 (GRCm39) |
N916S |
probably benign |
Het |
Mier2 |
A |
T |
10: 79,384,184 (GRCm39) |
|
probably benign |
Het |
Mpst |
A |
T |
15: 78,294,474 (GRCm39) |
T69S |
probably benign |
Het |
Nlk |
C |
A |
11: 78,477,763 (GRCm39) |
V327F |
probably damaging |
Het |
Nme5 |
A |
T |
18: 34,711,730 (GRCm39) |
S4T |
probably benign |
Het |
Notch2 |
A |
G |
3: 98,045,711 (GRCm39) |
I1625M |
possibly damaging |
Het |
Nup210l |
T |
C |
3: 90,088,859 (GRCm39) |
|
probably null |
Het |
Oas1d |
A |
G |
5: 121,057,111 (GRCm39) |
E239G |
probably damaging |
Het |
Olfm4 |
T |
C |
14: 80,243,761 (GRCm39) |
S110P |
probably damaging |
Het |
Or52e2 |
T |
C |
7: 102,804,772 (GRCm39) |
M61V |
probably benign |
Het |
Parn |
T |
A |
16: 13,384,567 (GRCm39) |
I499F |
probably damaging |
Het |
Ppargc1a |
G |
A |
5: 51,653,068 (GRCm39) |
Q165* |
probably null |
Het |
Ppp1r12b |
T |
A |
1: 134,814,244 (GRCm39) |
E353V |
probably damaging |
Het |
Prkdc |
A |
G |
16: 15,603,842 (GRCm39) |
Q2952R |
possibly damaging |
Het |
Prkdc |
G |
T |
16: 15,603,843 (GRCm39) |
Q2952H |
probably benign |
Het |
Qars1 |
G |
T |
9: 108,392,185 (GRCm39) |
E143* |
probably null |
Het |
Reln |
A |
G |
5: 22,134,132 (GRCm39) |
Y2599H |
probably damaging |
Het |
Rnf123 |
T |
C |
9: 107,939,041 (GRCm39) |
E803G |
probably damaging |
Het |
Rnf141 |
G |
A |
7: 110,436,405 (GRCm39) |
Q8* |
probably null |
Het |
Rnf167 |
A |
G |
11: 70,540,952 (GRCm39) |
I193V |
probably benign |
Het |
Rprd2 |
A |
T |
3: 95,694,622 (GRCm39) |
M137K |
probably benign |
Het |
Rtf1 |
T |
G |
2: 119,559,226 (GRCm39) |
|
probably benign |
Het |
Serpina1d |
T |
A |
12: 103,731,055 (GRCm39) |
R308* |
probably null |
Het |
Smg7 |
T |
C |
1: 152,719,030 (GRCm39) |
Y899C |
probably benign |
Het |
Tbr1 |
C |
A |
2: 61,635,336 (GRCm39) |
H95Q |
possibly damaging |
Het |
Tcf19 |
A |
T |
17: 35,825,380 (GRCm39) |
|
probably null |
Het |
Timm44 |
T |
A |
8: 4,317,692 (GRCm39) |
R210W |
probably damaging |
Het |
Trnau1ap |
C |
A |
4: 132,041,331 (GRCm39) |
E194* |
probably null |
Het |
Trp63 |
G |
A |
16: 25,639,192 (GRCm39) |
G127S |
probably damaging |
Het |
Trrap |
C |
T |
5: 144,735,200 (GRCm39) |
A989V |
probably benign |
Het |
Ttn |
T |
C |
2: 76,600,326 (GRCm39) |
D18988G |
probably damaging |
Het |
Tubb4b-ps1 |
T |
A |
5: 7,229,952 (GRCm39) |
|
probably benign |
Het |
Vmn1r77 |
G |
A |
7: 11,775,223 (GRCm39) |
|
probably null |
Het |
Vmn1r80 |
A |
G |
7: 11,927,181 (GRCm39) |
Y97C |
probably benign |
Het |
Vmn2r77 |
G |
A |
7: 86,451,224 (GRCm39) |
C370Y |
probably damaging |
Het |
Xntrpc |
C |
A |
7: 101,733,492 (GRCm39) |
A147D |
probably damaging |
Het |
Zc3h4 |
C |
T |
7: 16,159,702 (GRCm39) |
S424F |
unknown |
Het |
Zcwpw1 |
T |
A |
5: 137,808,376 (GRCm39) |
S275T |
probably damaging |
Het |
Zfp979 |
C |
T |
4: 147,699,808 (GRCm39) |
C44Y |
probably damaging |
Het |
Zscan20 |
T |
C |
4: 128,479,587 (GRCm39) |
H968R |
probably damaging |
Het |
Zswim3 |
T |
C |
2: 164,662,297 (GRCm39) |
V259A |
probably damaging |
Het |
Zzz3 |
T |
G |
3: 152,133,696 (GRCm39) |
D251E |
possibly damaging |
Het |
|
Other mutations in Chst5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01146:Chst5
|
APN |
8 |
112,617,314 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02634:Chst5
|
APN |
8 |
112,617,477 (GRCm39) |
missense |
probably damaging |
1.00 |
R0606:Chst5
|
UTSW |
8 |
112,617,551 (GRCm39) |
missense |
probably benign |
0.05 |
R1552:Chst5
|
UTSW |
8 |
112,616,912 (GRCm39) |
missense |
probably damaging |
0.99 |
R2094:Chst5
|
UTSW |
8 |
112,617,176 (GRCm39) |
missense |
probably benign |
0.01 |
R3769:Chst5
|
UTSW |
8 |
112,616,513 (GRCm39) |
missense |
possibly damaging |
0.67 |
R4135:Chst5
|
UTSW |
8 |
112,616,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R4872:Chst5
|
UTSW |
8 |
112,617,192 (GRCm39) |
missense |
possibly damaging |
0.61 |
R5658:Chst5
|
UTSW |
8 |
112,617,422 (GRCm39) |
missense |
probably damaging |
1.00 |
R5759:Chst5
|
UTSW |
8 |
112,616,842 (GRCm39) |
missense |
probably benign |
0.25 |
R5893:Chst5
|
UTSW |
8 |
112,616,828 (GRCm39) |
missense |
probably damaging |
1.00 |
R6657:Chst5
|
UTSW |
8 |
112,616,906 (GRCm39) |
missense |
probably benign |
0.00 |
R6731:Chst5
|
UTSW |
8 |
112,616,676 (GRCm39) |
missense |
probably benign |
0.00 |
R7406:Chst5
|
UTSW |
8 |
112,617,245 (GRCm39) |
missense |
probably benign |
0.00 |
R7535:Chst5
|
UTSW |
8 |
112,616,795 (GRCm39) |
missense |
probably damaging |
1.00 |
R7727:Chst5
|
UTSW |
8 |
112,617,557 (GRCm39) |
missense |
probably benign |
0.25 |
R7835:Chst5
|
UTSW |
8 |
112,617,234 (GRCm39) |
missense |
probably damaging |
1.00 |
R7843:Chst5
|
UTSW |
8 |
112,617,204 (GRCm39) |
missense |
probably benign |
0.00 |
R8257:Chst5
|
UTSW |
8 |
112,617,092 (GRCm39) |
missense |
probably damaging |
1.00 |
R8324:Chst5
|
UTSW |
8 |
112,617,140 (GRCm39) |
missense |
probably benign |
0.06 |
R8444:Chst5
|
UTSW |
8 |
112,617,395 (GRCm39) |
missense |
probably damaging |
1.00 |
R8458:Chst5
|
UTSW |
8 |
112,617,422 (GRCm39) |
missense |
probably damaging |
1.00 |
R9001:Chst5
|
UTSW |
8 |
112,616,534 (GRCm39) |
missense |
probably benign |
|
R9223:Chst5
|
UTSW |
8 |
112,617,492 (GRCm39) |
missense |
probably benign |
0.13 |
R9517:Chst5
|
UTSW |
8 |
112,616,652 (GRCm39) |
missense |
possibly damaging |
0.76 |
|