Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
T |
A |
11: 9,240,421 (GRCm39) |
N761K |
possibly damaging |
Het |
Abi2 |
A |
G |
1: 60,476,362 (GRCm39) |
I145V |
probably benign |
Het |
Ampd2 |
C |
A |
3: 107,987,432 (GRCm39) |
V134L |
probably benign |
Het |
Atf7ip2 |
T |
A |
16: 10,059,522 (GRCm39) |
V354E |
possibly damaging |
Het |
Bglap |
T |
C |
3: 88,290,958 (GRCm39) |
Y91C |
probably damaging |
Het |
Cacna1e |
A |
T |
1: 154,341,538 (GRCm39) |
S1219T |
probably damaging |
Het |
Ccng2 |
C |
G |
5: 93,421,202 (GRCm39) |
S237R |
probably benign |
Het |
Cd177 |
A |
G |
7: 24,449,800 (GRCm39) |
C562R |
probably damaging |
Het |
Cfap57 |
C |
T |
4: 118,472,128 (GRCm39) |
V84I |
probably benign |
Het |
Chd7 |
T |
A |
4: 8,862,485 (GRCm39) |
|
probably null |
Het |
Dyrk3 |
A |
G |
1: 131,057,543 (GRCm39) |
V210A |
probably damaging |
Het |
Eif3c |
C |
A |
7: 126,158,066 (GRCm39) |
G297W |
probably damaging |
Het |
Eml1 |
A |
G |
12: 108,482,863 (GRCm39) |
H494R |
probably benign |
Het |
Enpp2 |
A |
T |
15: 54,764,629 (GRCm39) |
|
probably null |
Het |
Fbxw21 |
C |
A |
9: 108,986,720 (GRCm39) |
C53F |
possibly damaging |
Het |
Fndc3a |
C |
A |
14: 72,799,156 (GRCm39) |
G609V |
possibly damaging |
Het |
Grid1 |
A |
G |
14: 35,172,036 (GRCm39) |
D514G |
probably damaging |
Het |
Gxylt2 |
T |
C |
6: 100,760,278 (GRCm39) |
V271A |
probably damaging |
Het |
Hes1 |
A |
G |
16: 29,884,997 (GRCm39) |
K74R |
probably damaging |
Het |
Igsf9 |
A |
G |
1: 172,319,752 (GRCm39) |
N349S |
probably benign |
Het |
Isx |
T |
A |
8: 75,600,285 (GRCm39) |
I6N |
possibly damaging |
Het |
Kcnb1 |
A |
T |
2: 167,030,251 (GRCm39) |
F98Y |
probably damaging |
Het |
Kif1b |
G |
C |
4: 149,321,532 (GRCm39) |
T1129R |
possibly damaging |
Het |
Klra10 |
T |
A |
6: 130,249,724 (GRCm39) |
|
probably null |
Het |
Mcm10 |
A |
T |
2: 4,996,253 (GRCm39) |
L870Q |
probably damaging |
Het |
Mettl16 |
T |
A |
11: 74,693,829 (GRCm39) |
I280K |
probably benign |
Het |
Mre11a |
G |
A |
9: 14,721,128 (GRCm39) |
R349Q |
possibly damaging |
Het |
Mrpl10 |
C |
T |
11: 96,935,402 (GRCm39) |
T34I |
probably damaging |
Het |
Muc16 |
T |
A |
9: 18,496,392 (GRCm39) |
|
probably null |
Het |
Myt1l |
T |
C |
12: 29,877,548 (GRCm39) |
C400R |
unknown |
Het |
Nbr1 |
C |
T |
11: 101,460,210 (GRCm39) |
T402M |
probably damaging |
Het |
Ndufs1 |
A |
G |
1: 63,200,099 (GRCm39) |
M271T |
possibly damaging |
Het |
Or10q1 |
A |
G |
19: 13,727,419 (GRCm39) |
*316W |
probably null |
Het |
Or4c29 |
C |
T |
2: 88,740,003 (GRCm39) |
V245I |
possibly damaging |
Het |
Or51f23c-ps1 |
G |
T |
7: 102,431,597 (GRCm39) |
V305L |
probably benign |
Het |
Pakap |
T |
C |
4: 57,709,519 (GRCm39) |
S155P |
probably damaging |
Het |
Pced1a |
C |
T |
2: 130,263,972 (GRCm39) |
D227N |
probably damaging |
Het |
Phf21b |
A |
G |
15: 84,689,070 (GRCm39) |
I152T |
probably damaging |
Het |
Pla2g4a |
A |
G |
1: 149,736,853 (GRCm39) |
V430A |
probably benign |
Het |
Plbd1 |
T |
C |
6: 136,594,244 (GRCm39) |
E335G |
probably benign |
Het |
Plce1 |
G |
A |
19: 38,608,899 (GRCm39) |
V403M |
possibly damaging |
Het |
Pnpla6 |
T |
A |
8: 3,581,677 (GRCm39) |
N642K |
probably benign |
Het |
Ptprb |
T |
C |
10: 116,113,389 (GRCm39) |
I123T |
probably benign |
Het |
Rab3il1 |
T |
A |
19: 10,005,641 (GRCm39) |
|
probably null |
Het |
Ranbp3 |
C |
T |
17: 57,015,219 (GRCm39) |
T307M |
possibly damaging |
Het |
Rasgrp2 |
T |
C |
19: 6,455,031 (GRCm39) |
S254P |
probably damaging |
Het |
Rgl3 |
T |
C |
9: 21,898,866 (GRCm39) |
K191R |
probably benign |
Het |
Rnf223 |
G |
A |
4: 156,216,982 (GRCm39) |
R119H |
probably benign |
Het |
Sapcd2 |
C |
T |
2: 25,263,508 (GRCm39) |
P217S |
unknown |
Het |
Setd7 |
C |
T |
3: 51,434,261 (GRCm39) |
|
probably null |
Het |
Sh3bp1 |
A |
C |
15: 78,794,209 (GRCm39) |
T526P |
possibly damaging |
Het |
Slc17a4 |
C |
A |
13: 24,085,767 (GRCm39) |
W382L |
probably benign |
Het |
Slc26a3 |
A |
T |
12: 31,513,464 (GRCm39) |
|
probably null |
Het |
Tmem129 |
A |
G |
5: 33,811,732 (GRCm39) |
L356P |
probably damaging |
Het |
Xirp1 |
T |
A |
9: 119,845,912 (GRCm39) |
R990S |
possibly damaging |
Het |
Zfp950 |
A |
C |
19: 61,116,010 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Trib1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01140:Trib1
|
APN |
15 |
59,523,476 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01648:Trib1
|
APN |
15 |
59,526,350 (GRCm39) |
missense |
probably benign |
0.38 |
IGL02267:Trib1
|
APN |
15 |
59,523,449 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03018:Trib1
|
APN |
15 |
59,526,333 (GRCm39) |
missense |
probably damaging |
1.00 |
Dibble
|
UTSW |
15 |
59,526,324 (GRCm39) |
missense |
probably damaging |
1.00 |
lawrence
|
UTSW |
15 |
59,521,264 (GRCm39) |
missense |
probably benign |
|
Topcat
|
UTSW |
15 |
59,523,487 (GRCm39) |
nonsense |
probably null |
|
R1994:Trib1
|
UTSW |
15 |
59,521,192 (GRCm39) |
missense |
possibly damaging |
0.70 |
R2073:Trib1
|
UTSW |
15 |
59,526,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R2407:Trib1
|
UTSW |
15 |
59,526,449 (GRCm39) |
missense |
probably benign |
0.00 |
R3709:Trib1
|
UTSW |
15 |
59,526,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R5759:Trib1
|
UTSW |
15 |
59,526,350 (GRCm39) |
missense |
probably benign |
|
R5986:Trib1
|
UTSW |
15 |
59,526,451 (GRCm39) |
splice site |
probably null |
|
R6083:Trib1
|
UTSW |
15 |
59,526,324 (GRCm39) |
missense |
probably damaging |
1.00 |
R6084:Trib1
|
UTSW |
15 |
59,526,324 (GRCm39) |
missense |
probably damaging |
1.00 |
R6086:Trib1
|
UTSW |
15 |
59,526,324 (GRCm39) |
missense |
probably damaging |
1.00 |
R6112:Trib1
|
UTSW |
15 |
59,523,487 (GRCm39) |
nonsense |
probably null |
|
R6113:Trib1
|
UTSW |
15 |
59,523,487 (GRCm39) |
nonsense |
probably null |
|
R6316:Trib1
|
UTSW |
15 |
59,521,264 (GRCm39) |
missense |
probably benign |
|
R7288:Trib1
|
UTSW |
15 |
59,526,471 (GRCm39) |
missense |
probably benign |
|
R7663:Trib1
|
UTSW |
15 |
59,523,562 (GRCm39) |
missense |
probably damaging |
1.00 |
R8061:Trib1
|
UTSW |
15 |
59,523,404 (GRCm39) |
missense |
probably damaging |
0.97 |
|