Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8b |
T |
A |
11: 109,844,423 (GRCm39) |
E931D |
possibly damaging |
Het |
Aebp1 |
C |
T |
11: 5,817,911 (GRCm39) |
T62I |
possibly damaging |
Het |
Babam2 |
A |
T |
5: 31,977,964 (GRCm39) |
E139V |
possibly damaging |
Het |
Bclaf1 |
C |
T |
10: 20,198,809 (GRCm39) |
R67* |
probably null |
Het |
Bcr |
C |
A |
10: 75,012,248 (GRCm39) |
T51K |
probably benign |
Het |
Best3 |
T |
A |
10: 116,840,322 (GRCm39) |
C251S |
probably damaging |
Het |
Birc6 |
A |
G |
17: 74,955,153 (GRCm39) |
M3457V |
probably benign |
Het |
C87436 |
C |
A |
6: 86,422,957 (GRCm39) |
T177K |
possibly damaging |
Het |
Cabin1 |
T |
A |
10: 75,561,394 (GRCm39) |
T1036S |
probably benign |
Het |
Catsperg2 |
C |
A |
7: 29,412,442 (GRCm39) |
V383L |
possibly damaging |
Het |
Ccdc182 |
C |
T |
11: 88,185,165 (GRCm39) |
Q82* |
probably null |
Het |
Ccl9 |
T |
C |
11: 83,466,700 (GRCm39) |
T76A |
probably damaging |
Het |
Cdc16 |
G |
T |
8: 13,831,399 (GRCm39) |
C544F |
possibly damaging |
Het |
Cdh18 |
A |
C |
15: 23,474,302 (GRCm39) |
D724A |
possibly damaging |
Het |
Cdip1 |
G |
A |
16: 4,587,946 (GRCm39) |
P6S |
probably damaging |
Het |
Col12a1 |
A |
G |
9: 79,537,842 (GRCm39) |
V2542A |
probably damaging |
Het |
Dnajc13 |
G |
T |
9: 104,061,814 (GRCm39) |
T1380K |
possibly damaging |
Het |
Dsg4 |
T |
A |
18: 20,598,226 (GRCm39) |
S715T |
possibly damaging |
Het |
Dync2h1 |
G |
T |
9: 6,955,986 (GRCm39) |
T4132K |
probably benign |
Het |
Egfem1 |
A |
T |
3: 29,711,419 (GRCm39) |
|
probably null |
Het |
Etl4 |
G |
T |
2: 20,785,826 (GRCm39) |
V716L |
probably damaging |
Het |
Exoc3l2 |
A |
G |
7: 19,213,957 (GRCm39) |
E461G |
unknown |
Het |
Fam135b |
A |
G |
15: 71,320,518 (GRCm39) |
|
probably null |
Het |
Flrt3 |
G |
T |
2: 140,502,836 (GRCm39) |
P264Q |
possibly damaging |
Het |
Fmn2 |
G |
C |
1: 174,330,019 (GRCm39) |
E136D |
unknown |
Het |
Fosl2 |
A |
G |
5: 32,304,217 (GRCm39) |
I51V |
probably benign |
Het |
Foxm1 |
A |
G |
6: 128,347,998 (GRCm39) |
T307A |
probably damaging |
Het |
Garem1 |
T |
C |
18: 21,281,408 (GRCm39) |
D316G |
possibly damaging |
Het |
Gm14403 |
A |
T |
2: 177,200,345 (GRCm39) |
H97L |
probably damaging |
Het |
Gm5616 |
A |
G |
9: 48,361,890 (GRCm39) |
|
noncoding transcript |
Het |
Hkdc1 |
T |
C |
10: 62,229,589 (GRCm39) |
D696G |
probably benign |
Het |
Igkv1-88 |
C |
A |
6: 68,839,432 (GRCm39) |
W60L |
probably damaging |
Het |
Iqgap3 |
G |
A |
3: 87,998,899 (GRCm39) |
W333* |
probably null |
Het |
Itgb4 |
C |
T |
11: 115,874,983 (GRCm39) |
R447W |
probably benign |
Het |
Kcnk3 |
G |
T |
5: 30,780,014 (GRCm39) |
V355L |
probably benign |
Het |
Kmt5c |
A |
C |
7: 4,749,790 (GRCm39) |
K436T |
probably damaging |
Het |
Lynx1 |
T |
C |
15: 74,623,264 (GRCm39) |
Y56C |
possibly damaging |
Het |
Lypd5 |
T |
C |
7: 24,052,462 (GRCm39) |
S149P |
probably damaging |
Het |
Map3k21 |
A |
T |
8: 126,638,169 (GRCm39) |
N252Y |
probably damaging |
Het |
Mgat2 |
T |
C |
12: 69,232,454 (GRCm39) |
W343R |
probably damaging |
Het |
Misp |
T |
G |
10: 79,663,728 (GRCm39) |
Y567* |
probably null |
Het |
Mrgprb1 |
A |
T |
7: 48,097,568 (GRCm39) |
S115T |
probably benign |
Het |
Muc16 |
A |
C |
9: 18,558,442 (GRCm39) |
I2617R |
unknown |
Het |
Myo19 |
T |
A |
11: 84,790,226 (GRCm39) |
V394E |
probably damaging |
Het |
Myo9b |
T |
A |
8: 71,801,040 (GRCm39) |
L1065Q |
probably benign |
Het |
Nap1l1 |
A |
G |
10: 111,331,229 (GRCm39) |
D405G |
possibly damaging |
Het |
Napb |
A |
T |
2: 148,542,411 (GRCm39) |
|
probably null |
Het |
Nbas |
A |
G |
12: 13,443,431 (GRCm39) |
Y1162C |
probably benign |
Het |
Nfam1 |
A |
T |
15: 82,917,325 (GRCm39) |
L36Q |
probably damaging |
Het |
Nrros |
T |
C |
16: 31,963,411 (GRCm39) |
D202G |
probably damaging |
Het |
Or51k1 |
T |
G |
7: 103,661,117 (GRCm39) |
H264P |
probably damaging |
Het |
Or7a39 |
T |
G |
10: 78,715,787 (GRCm39) |
Y260* |
probably null |
Het |
Osgin2 |
T |
C |
4: 15,998,908 (GRCm39) |
E238G |
probably benign |
Het |
Papss2 |
A |
G |
19: 32,616,636 (GRCm39) |
T221A |
probably benign |
Het |
Pcdhga12 |
A |
C |
18: 37,901,084 (GRCm39) |
K639Q |
probably damaging |
Het |
Pkhd1l1 |
T |
A |
15: 44,352,900 (GRCm39) |
|
probably null |
Het |
Pmepa1 |
A |
G |
2: 173,076,105 (GRCm39) |
S83P |
possibly damaging |
Het |
Pnp |
G |
A |
14: 51,188,000 (GRCm39) |
V118M |
probably damaging |
Het |
Ppat |
T |
C |
5: 77,063,112 (GRCm39) |
T500A |
probably benign |
Het |
Pramel22 |
C |
A |
4: 143,381,034 (GRCm39) |
V330F |
probably damaging |
Het |
Rab11fip4 |
A |
G |
11: 79,581,601 (GRCm39) |
N532S |
probably benign |
Het |
Rbm25 |
A |
G |
12: 83,718,725 (GRCm39) |
D499G |
probably damaging |
Het |
Rnf139 |
A |
G |
15: 58,770,687 (GRCm39) |
I237M |
possibly damaging |
Het |
Rrp15 |
C |
T |
1: 186,471,952 (GRCm39) |
S85N |
possibly damaging |
Het |
Slirp |
A |
G |
12: 87,490,784 (GRCm39) |
T29A |
probably damaging |
Het |
Sltm |
G |
C |
9: 70,494,086 (GRCm39) |
E828Q |
probably damaging |
Het |
Spindoc |
A |
G |
19: 7,351,960 (GRCm39) |
I129T |
probably damaging |
Het |
Spire1 |
T |
A |
18: 67,630,386 (GRCm39) |
|
probably null |
Het |
Styx |
A |
G |
14: 45,605,909 (GRCm39) |
T138A |
probably benign |
Het |
Sv2c |
A |
T |
13: 96,112,571 (GRCm39) |
L642* |
probably null |
Het |
Taf7 |
T |
C |
18: 37,776,498 (GRCm39) |
E23G |
probably damaging |
Het |
Tcp10a |
A |
T |
17: 7,612,425 (GRCm39) |
T406S |
possibly damaging |
Het |
Tnrc6b |
T |
A |
15: 80,765,017 (GRCm39) |
S840T |
probably benign |
Het |
Tns3 |
A |
G |
11: 8,442,245 (GRCm39) |
I706T |
probably damaging |
Het |
Tpsab1 |
A |
G |
17: 25,564,346 (GRCm39) |
V36A |
probably benign |
Het |
Trafd1 |
T |
A |
5: 121,511,342 (GRCm39) |
D492V |
probably damaging |
Het |
Trp53 |
A |
G |
11: 69,478,244 (GRCm39) |
E51G |
probably benign |
Het |
Vdr |
C |
T |
15: 97,755,477 (GRCm39) |
A349T |
probably benign |
Het |
Vmn2r59 |
T |
C |
7: 41,695,491 (GRCm39) |
D307G |
probably benign |
Het |
Zfp365 |
C |
A |
10: 67,733,437 (GRCm39) |
V252F |
probably damaging |
Het |
Zfp830 |
T |
A |
11: 82,655,803 (GRCm39) |
N202K |
probably benign |
Het |
|
Other mutations in Sidt1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00709:Sidt1
|
APN |
16 |
44,082,374 (GRCm39) |
splice site |
probably benign |
|
IGL01103:Sidt1
|
APN |
16 |
44,063,906 (GRCm39) |
nonsense |
probably null |
|
IGL01725:Sidt1
|
APN |
16 |
44,104,645 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02000:Sidt1
|
APN |
16 |
44,106,732 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02266:Sidt1
|
APN |
16 |
44,075,348 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02309:Sidt1
|
APN |
16 |
44,075,343 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02898:Sidt1
|
APN |
16 |
44,102,858 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0282:Sidt1
|
UTSW |
16 |
44,102,249 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0525:Sidt1
|
UTSW |
16 |
44,079,809 (GRCm39) |
missense |
possibly damaging |
0.64 |
R0927:Sidt1
|
UTSW |
16 |
44,063,895 (GRCm39) |
missense |
probably benign |
0.00 |
R1806:Sidt1
|
UTSW |
16 |
44,102,234 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1911:Sidt1
|
UTSW |
16 |
44,102,234 (GRCm39) |
missense |
possibly damaging |
0.81 |
R3843:Sidt1
|
UTSW |
16 |
44,104,587 (GRCm39) |
missense |
probably benign |
0.04 |
R3848:Sidt1
|
UTSW |
16 |
44,076,322 (GRCm39) |
intron |
probably benign |
|
R4023:Sidt1
|
UTSW |
16 |
44,102,249 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4026:Sidt1
|
UTSW |
16 |
44,102,249 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4495:Sidt1
|
UTSW |
16 |
44,102,841 (GRCm39) |
missense |
probably damaging |
1.00 |
R4603:Sidt1
|
UTSW |
16 |
44,075,389 (GRCm39) |
missense |
probably damaging |
0.98 |
R4707:Sidt1
|
UTSW |
16 |
44,090,221 (GRCm39) |
nonsense |
probably null |
|
R5322:Sidt1
|
UTSW |
16 |
44,101,985 (GRCm39) |
intron |
probably benign |
|
R5921:Sidt1
|
UTSW |
16 |
44,094,098 (GRCm39) |
splice site |
probably benign |
|
R5980:Sidt1
|
UTSW |
16 |
44,083,675 (GRCm39) |
nonsense |
probably null |
|
R6063:Sidt1
|
UTSW |
16 |
44,079,829 (GRCm39) |
missense |
probably benign |
0.01 |
R6337:Sidt1
|
UTSW |
16 |
44,121,298 (GRCm39) |
splice site |
probably null |
|
R6392:Sidt1
|
UTSW |
16 |
44,111,657 (GRCm39) |
missense |
possibly damaging |
0.47 |
R6855:Sidt1
|
UTSW |
16 |
44,065,706 (GRCm39) |
missense |
probably null |
1.00 |
R7092:Sidt1
|
UTSW |
16 |
44,120,192 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7099:Sidt1
|
UTSW |
16 |
44,063,860 (GRCm39) |
missense |
probably damaging |
1.00 |
R7448:Sidt1
|
UTSW |
16 |
44,106,763 (GRCm39) |
nonsense |
probably null |
|
R7574:Sidt1
|
UTSW |
16 |
44,079,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R8265:Sidt1
|
UTSW |
16 |
44,088,250 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8379:Sidt1
|
UTSW |
16 |
44,106,755 (GRCm39) |
missense |
probably benign |
0.14 |
R8460:Sidt1
|
UTSW |
16 |
44,107,705 (GRCm39) |
nonsense |
probably null |
|
R8480:Sidt1
|
UTSW |
16 |
44,065,529 (GRCm39) |
missense |
probably damaging |
1.00 |
R8762:Sidt1
|
UTSW |
16 |
44,152,707 (GRCm39) |
missense |
probably benign |
0.16 |
R8954:Sidt1
|
UTSW |
16 |
44,082,390 (GRCm39) |
missense |
probably benign |
0.04 |
R8974:Sidt1
|
UTSW |
16 |
44,101,980 (GRCm39) |
makesense |
probably null |
|
R9362:Sidt1
|
UTSW |
16 |
44,078,316 (GRCm39) |
missense |
possibly damaging |
0.96 |
R9451:Sidt1
|
UTSW |
16 |
44,075,392 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9669:Sidt1
|
UTSW |
16 |
44,102,243 (GRCm39) |
missense |
probably damaging |
1.00 |
R9737:Sidt1
|
UTSW |
16 |
44,102,243 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Sidt1
|
UTSW |
16 |
44,079,845 (GRCm39) |
missense |
possibly damaging |
0.90 |
Z1191:Sidt1
|
UTSW |
16 |
44,078,294 (GRCm39) |
critical splice donor site |
probably null |
|
|