Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca2 |
G |
A |
2: 25,323,371 (GRCm39) |
R113Q |
probably benign |
Het |
Aip |
G |
A |
19: 4,166,010 (GRCm39) |
P147L |
possibly damaging |
Het |
Anapc1 |
A |
C |
2: 128,448,957 (GRCm39) |
|
probably benign |
Het |
Arhgap42 |
C |
T |
9: 9,046,518 (GRCm39) |
V240I |
possibly damaging |
Het |
Axdnd1 |
T |
C |
1: 156,176,528 (GRCm39) |
E684G |
probably damaging |
Het |
BC005624 |
G |
A |
2: 30,871,869 (GRCm39) |
R2W |
probably benign |
Het |
Cd177 |
T |
G |
7: 24,457,495 (GRCm39) |
Q182P |
probably damaging |
Het |
Cdca5 |
G |
A |
19: 6,140,399 (GRCm39) |
E187K |
possibly damaging |
Het |
Chmp1a |
T |
C |
8: 123,934,839 (GRCm39) |
Q39R |
probably benign |
Het |
Dab2ip |
A |
G |
2: 35,617,511 (GRCm39) |
I1079V |
probably damaging |
Het |
Dip2c |
A |
T |
13: 9,556,712 (GRCm39) |
E85D |
possibly damaging |
Het |
Elmo2 |
A |
T |
2: 165,137,472 (GRCm39) |
S497R |
possibly damaging |
Het |
Ephb6 |
C |
T |
6: 41,592,507 (GRCm39) |
A339V |
possibly damaging |
Het |
Foxred1 |
T |
C |
9: 35,121,435 (GRCm39) |
K38E |
probably damaging |
Het |
Frem2 |
T |
A |
3: 53,555,342 (GRCm39) |
T1732S |
probably damaging |
Het |
Fto |
A |
G |
8: 92,393,068 (GRCm39) |
|
probably benign |
Het |
Gm17430 |
T |
A |
18: 9,726,528 (GRCm39) |
Q48L |
probably damaging |
Het |
Gng2 |
A |
G |
14: 19,925,882 (GRCm39) |
I70T |
probably damaging |
Het |
Gtf2a2 |
A |
G |
9: 69,922,575 (GRCm39) |
|
probably benign |
Het |
Invs |
A |
G |
4: 48,396,284 (GRCm39) |
D263G |
probably damaging |
Het |
Itga2b |
C |
T |
11: 102,352,157 (GRCm39) |
V475M |
probably damaging |
Het |
Kansl1l |
A |
G |
1: 66,809,374 (GRCm39) |
|
probably benign |
Het |
Klhl25 |
T |
C |
7: 75,516,440 (GRCm39) |
F449L |
possibly damaging |
Het |
Lamb1 |
T |
A |
12: 31,316,755 (GRCm39) |
C83S |
probably damaging |
Het |
Loxl4 |
G |
T |
19: 42,587,154 (GRCm39) |
T648K |
probably damaging |
Het |
Lrit2 |
T |
C |
14: 36,790,962 (GRCm39) |
F214L |
possibly damaging |
Het |
N4bp2 |
T |
G |
5: 65,965,437 (GRCm39) |
L1162R |
probably damaging |
Het |
Naa40 |
A |
T |
19: 7,207,373 (GRCm39) |
I117N |
probably benign |
Het |
Ncapd3 |
T |
C |
9: 27,006,054 (GRCm39) |
S1492P |
probably benign |
Het |
Nf2 |
T |
A |
11: 4,766,146 (GRCm39) |
D128V |
probably benign |
Het |
Nox4 |
T |
C |
7: 87,010,001 (GRCm39) |
S401P |
probably benign |
Het |
Nt5c1b |
T |
C |
12: 10,427,171 (GRCm39) |
V323A |
probably damaging |
Het |
Or52a33 |
C |
T |
7: 103,288,463 (GRCm39) |
V295I |
probably benign |
Het |
Or52s19 |
T |
A |
7: 103,007,576 (GRCm39) |
H275L |
probably damaging |
Het |
Or5b118 |
G |
A |
19: 13,449,242 (GRCm39) |
V303I |
probably benign |
Het |
Pcdhb14 |
T |
C |
18: 37,581,803 (GRCm39) |
V303A |
probably benign |
Het |
Pde8a |
C |
A |
7: 80,863,713 (GRCm39) |
H17Q |
probably benign |
Het |
Pfkl |
C |
T |
10: 77,824,558 (GRCm39) |
V716I |
probably benign |
Het |
Phc3 |
G |
A |
3: 30,990,732 (GRCm39) |
S495L |
possibly damaging |
Het |
Psg18 |
A |
G |
7: 18,080,527 (GRCm39) |
|
probably benign |
Het |
Rcc2 |
T |
G |
4: 140,439,449 (GRCm39) |
N175K |
possibly damaging |
Het |
Rhot2 |
G |
A |
17: 26,059,032 (GRCm39) |
T276I |
probably benign |
Het |
Rnase9 |
A |
T |
14: 51,276,445 (GRCm39) |
Y178N |
probably benign |
Het |
Sema4b |
T |
C |
7: 79,868,697 (GRCm39) |
C297R |
probably damaging |
Het |
Slc35d2 |
T |
C |
13: 64,266,227 (GRCm39) |
|
probably null |
Het |
Sptlc3 |
A |
T |
2: 139,389,126 (GRCm39) |
N169Y |
probably damaging |
Het |
Srsf9 |
T |
G |
5: 115,469,524 (GRCm39) |
M29R |
probably benign |
Het |
Syne2 |
T |
A |
12: 75,927,065 (GRCm39) |
|
probably null |
Het |
Tgm5 |
A |
G |
2: 120,916,141 (GRCm39) |
|
probably null |
Het |
Thbs2 |
A |
T |
17: 14,901,692 (GRCm39) |
|
probably null |
Het |
Trak2 |
T |
C |
1: 58,958,432 (GRCm39) |
E283G |
probably damaging |
Het |
Trbv21 |
A |
G |
6: 41,179,792 (GRCm39) |
Y36C |
probably damaging |
Het |
Trpm7 |
A |
T |
2: 126,664,531 (GRCm39) |
Y949* |
probably null |
Het |
Ubqln5 |
T |
C |
7: 103,778,161 (GRCm39) |
D221G |
possibly damaging |
Het |
Ubxn4 |
T |
A |
1: 128,187,262 (GRCm39) |
V85D |
possibly damaging |
Het |
Vmn1r172 |
T |
A |
7: 23,359,600 (GRCm39) |
W162R |
probably benign |
Het |
Vrk2 |
A |
G |
11: 26,484,314 (GRCm39) |
|
probably benign |
Het |
Zc3h8 |
A |
C |
2: 128,771,824 (GRCm39) |
D276E |
probably benign |
Het |
Zfp369 |
C |
T |
13: 65,445,092 (GRCm39) |
T745I |
possibly damaging |
Het |
Zfp608 |
T |
C |
18: 55,031,978 (GRCm39) |
K654R |
probably damaging |
Het |
|
Other mutations in Stip1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01325:Stip1
|
APN |
19 |
6,998,464 (GRCm39) |
unclassified |
probably benign |
|
IGL02506:Stip1
|
APN |
19 |
7,012,857 (GRCm39) |
splice site |
probably benign |
|
IGL02515:Stip1
|
APN |
19 |
6,999,487 (GRCm39) |
missense |
probably benign |
0.23 |
IGL03009:Stip1
|
APN |
19 |
6,998,489 (GRCm39) |
missense |
probably damaging |
1.00 |
Whisp
|
UTSW |
19 |
6,999,178 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1768:Stip1
|
UTSW |
19 |
6,999,165 (GRCm39) |
missense |
probably damaging |
1.00 |
R3081:Stip1
|
UTSW |
19 |
7,013,016 (GRCm39) |
missense |
probably benign |
0.42 |
R4530:Stip1
|
UTSW |
19 |
7,013,026 (GRCm39) |
missense |
probably benign |
0.04 |
R4965:Stip1
|
UTSW |
19 |
7,012,938 (GRCm39) |
missense |
probably benign |
0.41 |
R5638:Stip1
|
UTSW |
19 |
7,009,883 (GRCm39) |
missense |
probably damaging |
1.00 |
R5776:Stip1
|
UTSW |
19 |
6,999,393 (GRCm39) |
critical splice donor site |
probably null |
|
R7064:Stip1
|
UTSW |
19 |
7,012,925 (GRCm39) |
missense |
probably benign |
0.18 |
R7096:Stip1
|
UTSW |
19 |
6,999,178 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7109:Stip1
|
UTSW |
19 |
6,999,178 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7111:Stip1
|
UTSW |
19 |
6,999,178 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7116:Stip1
|
UTSW |
19 |
6,999,178 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7117:Stip1
|
UTSW |
19 |
6,999,178 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7127:Stip1
|
UTSW |
19 |
6,999,178 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7129:Stip1
|
UTSW |
19 |
6,999,178 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7130:Stip1
|
UTSW |
19 |
6,999,178 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7132:Stip1
|
UTSW |
19 |
6,999,178 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7776:Stip1
|
UTSW |
19 |
6,999,141 (GRCm39) |
missense |
probably benign |
0.06 |
R8293:Stip1
|
UTSW |
19 |
7,011,618 (GRCm39) |
missense |
probably benign |
|
R8924:Stip1
|
UTSW |
19 |
7,002,687 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Stip1
|
UTSW |
19 |
6,999,676 (GRCm39) |
missense |
probably null |
1.00 |
|