Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930451I11Rik |
A |
T |
7: 126,429,809 (GRCm39) |
|
probably null |
Het |
Alox5 |
A |
C |
6: 116,397,241 (GRCm39) |
Y314* |
probably null |
Het |
Ap4e1 |
T |
C |
2: 126,906,871 (GRCm39) |
S1044P |
probably benign |
Het |
Ash2l |
A |
G |
8: 26,312,796 (GRCm39) |
V391A |
possibly damaging |
Het |
B4galnt4 |
A |
G |
7: 140,647,145 (GRCm39) |
T326A |
probably benign |
Het |
Ccm2 |
T |
A |
11: 6,544,239 (GRCm39) |
I345N |
probably damaging |
Het |
Cntnap3 |
G |
A |
13: 64,896,373 (GRCm39) |
H1034Y |
probably benign |
Het |
Cpsf1 |
A |
G |
15: 76,483,696 (GRCm39) |
L849S |
probably damaging |
Het |
Ctrb1 |
A |
G |
8: 112,413,296 (GRCm39) |
S239P |
probably damaging |
Het |
Dennd1b |
T |
A |
1: 139,096,683 (GRCm39) |
|
probably benign |
Het |
Dnah17 |
A |
G |
11: 117,957,258 (GRCm39) |
I2773T |
probably damaging |
Het |
Eif2b2 |
T |
A |
12: 85,272,817 (GRCm39) |
F267L |
probably damaging |
Het |
Fcrl2 |
A |
G |
3: 87,170,983 (GRCm39) |
|
probably benign |
Het |
Furin |
G |
T |
7: 80,046,712 (GRCm39) |
D181E |
possibly damaging |
Het |
Gm29106 |
T |
A |
1: 118,128,317 (GRCm39) |
C670S |
probably damaging |
Het |
Gm6309 |
A |
T |
5: 146,105,300 (GRCm39) |
D204E |
possibly damaging |
Het |
Hsf2 |
T |
A |
10: 57,380,739 (GRCm39) |
I191N |
probably damaging |
Het |
Hspa12a |
T |
C |
19: 58,788,124 (GRCm39) |
D566G |
probably benign |
Het |
Igf1 |
G |
C |
10: 87,700,722 (GRCm39) |
V49L |
probably damaging |
Het |
Igfbpl1 |
C |
T |
4: 45,826,663 (GRCm39) |
C44Y |
probably damaging |
Het |
Letm1 |
G |
A |
5: 33,939,851 (GRCm39) |
R16C |
probably benign |
Het |
Lypd8l |
T |
A |
11: 58,499,314 (GRCm39) |
Y168F |
probably benign |
Het |
Marf1 |
A |
G |
16: 13,956,384 (GRCm39) |
V819A |
probably damaging |
Het |
Mfsd4b4 |
A |
T |
10: 39,767,948 (GRCm39) |
S428T |
probably benign |
Het |
Myo1d |
T |
C |
11: 80,565,783 (GRCm39) |
I347M |
probably benign |
Het |
Myo9b |
A |
G |
8: 71,743,463 (GRCm39) |
I175V |
probably damaging |
Het |
Naip5 |
A |
T |
13: 100,359,922 (GRCm39) |
V438E |
probably damaging |
Het |
Nup205 |
T |
A |
6: 35,185,044 (GRCm39) |
V768E |
possibly damaging |
Het |
Or4k6 |
A |
T |
14: 50,475,567 (GRCm39) |
Y258* |
probably null |
Het |
Or9g4b |
T |
A |
2: 85,616,726 (GRCm39) |
Y290* |
probably null |
Het |
Pcdh15 |
C |
T |
10: 74,481,821 (GRCm39) |
H1651Y |
possibly damaging |
Het |
Pdgfra |
A |
T |
5: 75,334,055 (GRCm39) |
Q376L |
possibly damaging |
Het |
Pign |
T |
C |
1: 105,481,622 (GRCm39) |
I791M |
probably benign |
Het |
Pik3c2b |
T |
G |
1: 132,994,041 (GRCm39) |
S2A |
possibly damaging |
Het |
Pip5k1a |
A |
T |
3: 94,975,558 (GRCm39) |
I304K |
probably damaging |
Het |
Pkdrej |
A |
T |
15: 85,702,054 (GRCm39) |
L1294* |
probably null |
Het |
Pprc1 |
T |
C |
19: 46,052,872 (GRCm39) |
S797P |
probably damaging |
Het |
Prob1 |
A |
G |
18: 35,787,321 (GRCm39) |
V311A |
probably benign |
Het |
Prune2 |
C |
A |
19: 16,977,385 (GRCm39) |
T40K |
probably damaging |
Het |
Rif1 |
T |
G |
2: 52,002,703 (GRCm39) |
D2052E |
probably benign |
Het |
Sall1 |
A |
G |
8: 89,759,519 (GRCm39) |
V195A |
probably damaging |
Het |
Scfd1 |
T |
C |
12: 51,474,729 (GRCm39) |
|
probably null |
Het |
Sidt2 |
A |
T |
9: 45,864,148 (GRCm39) |
N123K |
probably benign |
Het |
Slc22a6 |
G |
A |
19: 8,599,460 (GRCm39) |
A320T |
probably benign |
Het |
Slc25a10 |
A |
G |
11: 120,388,973 (GRCm39) |
H279R |
probably benign |
Het |
Slc35b4 |
A |
G |
6: 34,135,556 (GRCm39) |
V252A |
probably benign |
Het |
Slc46a3 |
T |
C |
5: 147,823,150 (GRCm39) |
T231A |
probably benign |
Het |
Stxbp1 |
T |
A |
2: 32,691,905 (GRCm39) |
H429L |
probably damaging |
Het |
Tas2r134 |
C |
T |
2: 51,517,782 (GRCm39) |
T87I |
probably benign |
Het |
Tcstv6 |
A |
G |
13: 120,307,666 (GRCm39) |
D20G |
possibly damaging |
Het |
Tdpoz2 |
A |
T |
3: 93,559,582 (GRCm39) |
L130H |
probably damaging |
Het |
Tmem69 |
T |
C |
4: 116,411,921 (GRCm39) |
|
probably null |
Het |
Ung |
G |
T |
5: 114,269,398 (GRCm39) |
A37S |
probably benign |
Het |
Vdac1 |
T |
C |
11: 52,277,200 (GRCm39) |
Y237H |
probably damaging |
Het |
Vgll4 |
T |
C |
6: 114,898,328 (GRCm39) |
Y11C |
probably damaging |
Het |
Vmn1r24 |
A |
G |
6: 57,933,437 (GRCm39) |
I27T |
probably benign |
Het |
Zfp280b |
T |
A |
10: 75,875,522 (GRCm39) |
M467K |
probably benign |
Het |
Zkscan4 |
A |
G |
13: 21,668,535 (GRCm39) |
I329V |
probably damaging |
Het |
|
Other mutations in Tmppe |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01823:Tmppe
|
APN |
9 |
114,234,175 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02274:Tmppe
|
APN |
9 |
114,234,499 (GRCm39) |
missense |
probably benign |
|
IGL02349:Tmppe
|
APN |
9 |
114,234,268 (GRCm39) |
missense |
probably benign |
|
R0201:Tmppe
|
UTSW |
9 |
114,233,707 (GRCm39) |
frame shift |
probably null |
|
R1668:Tmppe
|
UTSW |
9 |
114,233,968 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2206:Tmppe
|
UTSW |
9 |
114,234,640 (GRCm39) |
missense |
probably benign |
|
R5026:Tmppe
|
UTSW |
9 |
114,234,887 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5054:Tmppe
|
UTSW |
9 |
114,235,026 (GRCm39) |
missense |
probably benign |
0.41 |
R5118:Tmppe
|
UTSW |
9 |
114,234,549 (GRCm39) |
missense |
probably benign |
0.02 |
R5623:Tmppe
|
UTSW |
9 |
114,234,964 (GRCm39) |
missense |
possibly damaging |
0.59 |
R6307:Tmppe
|
UTSW |
9 |
114,233,812 (GRCm39) |
missense |
probably benign |
0.00 |
R6502:Tmppe
|
UTSW |
9 |
114,234,720 (GRCm39) |
missense |
probably damaging |
1.00 |
R6597:Tmppe
|
UTSW |
9 |
114,234,312 (GRCm39) |
missense |
probably benign |
0.00 |
R6627:Tmppe
|
UTSW |
9 |
114,234,553 (GRCm39) |
missense |
probably damaging |
1.00 |
R6888:Tmppe
|
UTSW |
9 |
114,233,769 (GRCm39) |
missense |
probably damaging |
1.00 |
R7032:Tmppe
|
UTSW |
9 |
114,234,858 (GRCm39) |
missense |
probably damaging |
1.00 |
R7141:Tmppe
|
UTSW |
9 |
114,234,036 (GRCm39) |
missense |
probably benign |
0.00 |
R7642:Tmppe
|
UTSW |
9 |
114,233,862 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8894:Tmppe
|
UTSW |
9 |
114,230,260 (GRCm39) |
start gained |
probably benign |
|
R9101:Tmppe
|
UTSW |
9 |
114,234,309 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1088:Tmppe
|
UTSW |
9 |
114,234,145 (GRCm39) |
missense |
probably benign |
0.01 |
|