Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700024G13Rik |
A |
T |
14: 32,099,901 (GRCm39) |
I42N |
possibly damaging |
Het |
Adarb2 |
T |
A |
13: 8,253,287 (GRCm39) |
S11T |
unknown |
Het |
Adgrg1 |
C |
T |
8: 95,738,438 (GRCm39) |
Q644* |
probably null |
Het |
Akr1c18 |
T |
G |
13: 4,195,252 (GRCm39) |
I69L |
probably benign |
Het |
Anxa9 |
C |
T |
3: 95,207,884 (GRCm39) |
V219I |
probably benign |
Het |
Aqp9 |
T |
C |
9: 71,045,385 (GRCm39) |
T101A |
probably benign |
Het |
Arhgef1 |
C |
T |
7: 24,613,057 (GRCm39) |
R251W |
probably damaging |
Het |
Arl13b |
T |
A |
16: 62,627,007 (GRCm39) |
E231D |
possibly damaging |
Het |
Atosa |
C |
T |
9: 74,916,241 (GRCm39) |
A280V |
probably benign |
Het |
Bcl2l11 |
C |
T |
2: 128,000,176 (GRCm39) |
A173V |
probably benign |
Het |
Ccni |
A |
T |
5: 93,335,933 (GRCm39) |
|
probably null |
Het |
Cdh18 |
A |
G |
15: 23,474,485 (GRCm39) |
E785G |
probably benign |
Het |
Cdk4 |
A |
G |
10: 126,900,849 (GRCm39) |
Y167C |
probably benign |
Het |
Clip1 |
A |
C |
5: 123,768,466 (GRCm39) |
V757G |
possibly damaging |
Het |
Ctsc |
T |
C |
7: 87,930,616 (GRCm39) |
V65A |
possibly damaging |
Het |
Cuedc2 |
G |
A |
19: 46,320,427 (GRCm39) |
S48L |
probably damaging |
Het |
Cyp39a1 |
T |
A |
17: 43,978,510 (GRCm39) |
M4K |
possibly damaging |
Het |
Dgcr8 |
T |
C |
16: 18,074,577 (GRCm39) |
S733G |
probably benign |
Het |
Dnhd1 |
T |
C |
7: 105,363,488 (GRCm39) |
S4017P |
probably damaging |
Het |
Ehbp1 |
A |
G |
11: 22,096,694 (GRCm39) |
I255T |
probably benign |
Het |
Fam83e |
T |
C |
7: 45,371,687 (GRCm39) |
V28A |
probably benign |
Het |
Fanci |
A |
G |
7: 79,054,936 (GRCm39) |
|
probably benign |
Het |
Fat1 |
C |
T |
8: 45,478,567 (GRCm39) |
Q2538* |
probably null |
Het |
Fshr |
A |
G |
17: 89,508,009 (GRCm39) |
F11S |
unknown |
Het |
Gab1 |
G |
T |
8: 81,515,388 (GRCm39) |
P310Q |
probably damaging |
Het |
Galnt18 |
A |
G |
7: 111,215,699 (GRCm39) |
|
probably benign |
Het |
Gm28042 |
C |
A |
2: 119,869,370 (GRCm39) |
P355Q |
probably damaging |
Het |
H2-DMa |
A |
G |
17: 34,357,116 (GRCm39) |
T205A |
possibly damaging |
Het |
Hnf4g |
A |
T |
3: 3,718,011 (GRCm39) |
D420V |
probably benign |
Het |
Ift70b |
T |
C |
2: 75,767,760 (GRCm39) |
K331R |
probably benign |
Het |
Il1b |
A |
G |
2: 129,207,989 (GRCm39) |
V164A |
probably damaging |
Het |
Irf4 |
C |
A |
13: 30,941,485 (GRCm39) |
H279Q |
probably benign |
Het |
Loxhd1 |
A |
G |
18: 77,409,364 (GRCm39) |
T203A |
possibly damaging |
Het |
Lsamp |
C |
T |
16: 41,775,682 (GRCm39) |
P178S |
probably damaging |
Het |
Mcm6 |
T |
C |
1: 128,277,155 (GRCm39) |
S223G |
possibly damaging |
Het |
Misp |
G |
T |
10: 79,661,777 (GRCm39) |
V65L |
possibly damaging |
Het |
Mov10 |
A |
G |
3: 104,706,912 (GRCm39) |
V666A |
probably benign |
Het |
Mycbp2 |
A |
T |
14: 103,485,194 (GRCm39) |
D1102E |
probably damaging |
Het |
Myef2 |
G |
T |
2: 124,939,860 (GRCm39) |
|
probably null |
Het |
Myo1e |
T |
A |
9: 70,303,216 (GRCm39) |
I1079N |
probably damaging |
Het |
Nisch |
G |
T |
14: 30,899,228 (GRCm39) |
|
probably benign |
Het |
Obox7 |
T |
C |
7: 14,399,346 (GRCm39) |
S191P |
probably benign |
Het |
Or11h7 |
T |
C |
14: 50,891,465 (GRCm39) |
V257A |
probably benign |
Het |
Or13p10 |
A |
G |
4: 118,523,385 (GRCm39) |
I224V |
probably damaging |
Het |
Or14c40 |
C |
T |
7: 86,313,331 (GRCm39) |
L154F |
probably benign |
Het |
Or1j11 |
G |
A |
2: 36,311,658 (GRCm39) |
V83M |
probably benign |
Het |
Or5w14 |
A |
T |
2: 87,541,422 (GRCm39) |
V276D |
possibly damaging |
Het |
Or7d9 |
A |
G |
9: 20,197,873 (GRCm39) |
R301G |
probably damaging |
Het |
Phf1 |
T |
C |
17: 27,156,333 (GRCm39) |
S492P |
possibly damaging |
Het |
Phyh |
A |
T |
2: 4,943,164 (GRCm39) |
N337I |
probably damaging |
Het |
Poteg |
A |
T |
8: 27,985,060 (GRCm39) |
|
probably benign |
Het |
Prag1 |
G |
T |
8: 36,571,500 (GRCm39) |
K694N |
probably damaging |
Het |
Proser2 |
C |
T |
2: 6,107,870 (GRCm39) |
E49K |
probably damaging |
Het |
Pskh1 |
T |
C |
8: 106,656,389 (GRCm39) |
V355A |
possibly damaging |
Het |
Psmc2 |
T |
C |
5: 22,004,549 (GRCm39) |
V182A |
possibly damaging |
Het |
Rbfox1 |
A |
G |
16: 7,124,333 (GRCm39) |
|
probably benign |
Het |
Slc26a7 |
A |
T |
4: 14,621,221 (GRCm39) |
I55K |
possibly damaging |
Het |
Slc5a8 |
G |
A |
10: 88,761,648 (GRCm39) |
|
probably null |
Het |
Slitrk3 |
T |
C |
3: 72,957,672 (GRCm39) |
R367G |
probably damaging |
Het |
Snrnp40 |
C |
G |
4: 130,271,836 (GRCm39) |
|
probably null |
Het |
Spata31 |
A |
G |
13: 65,068,953 (GRCm39) |
E367G |
probably benign |
Het |
Srrm3 |
A |
T |
5: 135,863,892 (GRCm39) |
|
probably null |
Het |
Ssmem1 |
T |
C |
6: 30,517,507 (GRCm39) |
S6P |
probably damaging |
Het |
Swap70 |
A |
G |
7: 109,821,034 (GRCm39) |
D6G |
probably benign |
Het |
Syt1 |
T |
C |
10: 108,419,776 (GRCm39) |
E295G |
probably damaging |
Het |
Tap2 |
A |
T |
17: 34,424,927 (GRCm39) |
I192F |
possibly damaging |
Het |
Tgoln1 |
C |
T |
6: 72,591,068 (GRCm39) |
R348H |
probably damaging |
Het |
Tln2 |
C |
T |
9: 67,134,389 (GRCm39) |
V1373I |
possibly damaging |
Het |
Tmc2 |
A |
G |
2: 130,089,854 (GRCm39) |
D613G |
possibly damaging |
Het |
Tmem62 |
T |
A |
2: 120,837,483 (GRCm39) |
Y597N |
probably benign |
Het |
Vmn2r92 |
T |
C |
17: 18,372,198 (GRCm39) |
S3P |
probably benign |
Het |
Wdfy3 |
A |
T |
5: 102,089,313 (GRCm39) |
I627N |
probably damaging |
Het |
Zfhx4 |
T |
C |
3: 5,478,076 (GRCm39) |
S3564P |
probably damaging |
Het |
Zfp467 |
T |
G |
6: 48,416,013 (GRCm39) |
E213A |
possibly damaging |
Het |
Zfp746 |
T |
G |
6: 48,041,411 (GRCm39) |
K437N |
probably damaging |
Het |
Zfp853 |
A |
G |
5: 143,274,840 (GRCm39) |
|
probably benign |
Het |
Zranb1 |
T |
A |
7: 132,551,496 (GRCm39) |
V49D |
probably benign |
Het |
|
Other mutations in Trhr2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03070:Trhr2
|
APN |
8 |
123,085,342 (GRCm39) |
missense |
probably benign |
|
IGL03387:Trhr2
|
APN |
8 |
123,085,220 (GRCm39) |
intron |
probably benign |
|
IGL03408:Trhr2
|
APN |
8 |
123,085,534 (GRCm39) |
missense |
probably damaging |
1.00 |
R0546:Trhr2
|
UTSW |
8 |
123,085,228 (GRCm39) |
critical splice donor site |
probably null |
|
R1135:Trhr2
|
UTSW |
8 |
123,085,372 (GRCm39) |
missense |
probably damaging |
1.00 |
R1377:Trhr2
|
UTSW |
8 |
123,087,327 (GRCm39) |
missense |
probably damaging |
1.00 |
R2055:Trhr2
|
UTSW |
8 |
123,085,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R4030:Trhr2
|
UTSW |
8 |
123,087,438 (GRCm39) |
start codon destroyed |
probably null |
0.01 |
R4998:Trhr2
|
UTSW |
8 |
123,085,511 (GRCm39) |
missense |
probably benign |
0.04 |
R5074:Trhr2
|
UTSW |
8 |
123,084,110 (GRCm39) |
missense |
probably benign |
0.01 |
R6175:Trhr2
|
UTSW |
8 |
123,084,118 (GRCm39) |
missense |
probably damaging |
0.99 |
R7048:Trhr2
|
UTSW |
8 |
123,085,418 (GRCm39) |
missense |
probably damaging |
1.00 |
R7168:Trhr2
|
UTSW |
8 |
123,087,276 (GRCm39) |
missense |
probably damaging |
1.00 |
R7185:Trhr2
|
UTSW |
8 |
123,087,396 (GRCm39) |
missense |
probably benign |
0.26 |
R7284:Trhr2
|
UTSW |
8 |
123,087,114 (GRCm39) |
missense |
probably damaging |
1.00 |
R7314:Trhr2
|
UTSW |
8 |
123,085,489 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7644:Trhr2
|
UTSW |
8 |
123,084,061 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7891:Trhr2
|
UTSW |
8 |
123,084,083 (GRCm39) |
missense |
probably damaging |
0.99 |
R8715:Trhr2
|
UTSW |
8 |
123,085,619 (GRCm39) |
missense |
probably damaging |
1.00 |
R8840:Trhr2
|
UTSW |
8 |
123,085,621 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Trhr2
|
UTSW |
8 |
123,085,534 (GRCm39) |
missense |
probably damaging |
1.00 |
|