Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca15 |
T |
C |
7: 119,944,592 (GRCm39) |
V409A |
probably damaging |
Het |
Abtb1 |
A |
G |
6: 88,815,240 (GRCm39) |
F297L |
probably damaging |
Het |
Adam22 |
C |
A |
5: 8,140,182 (GRCm39) |
G202W |
probably damaging |
Het |
Adgrg3 |
G |
A |
8: 95,766,492 (GRCm39) |
V388I |
probably benign |
Het |
Adnp |
T |
C |
2: 168,026,108 (GRCm39) |
T396A |
probably benign |
Het |
Ank2 |
T |
C |
3: 126,753,417 (GRCm39) |
Q288R |
probably damaging |
Het |
Bdp1 |
T |
C |
13: 100,234,109 (GRCm39) |
|
probably null |
Het |
Cdc45 |
C |
T |
16: 18,614,647 (GRCm39) |
R205H |
probably damaging |
Het |
Ceacam23 |
T |
G |
7: 17,643,067 (GRCm39) |
H492Q |
probably damaging |
Het |
Cfap210 |
T |
C |
2: 69,617,602 (GRCm39) |
T60A |
possibly damaging |
Het |
Cntnap5c |
A |
T |
17: 58,666,249 (GRCm39) |
E1093V |
probably benign |
Het |
Cplx3 |
A |
T |
9: 57,518,360 (GRCm39) |
L343Q |
probably damaging |
Het |
Dmrta1 |
A |
C |
4: 89,580,284 (GRCm39) |
N415H |
probably damaging |
Het |
Dnaaf5 |
T |
A |
5: 139,138,617 (GRCm39) |
V266E |
probably damaging |
Het |
Dot1l |
A |
G |
10: 80,620,471 (GRCm39) |
Q511R |
possibly damaging |
Het |
Ehmt1 |
A |
G |
2: 24,774,207 (GRCm39) |
V201A |
probably damaging |
Het |
Fancg |
A |
G |
4: 43,003,019 (GRCm39) |
F613L |
probably benign |
Het |
Fbxo10 |
A |
T |
4: 45,042,036 (GRCm39) |
I731N |
possibly damaging |
Het |
Fchsd1 |
C |
T |
18: 38,092,926 (GRCm39) |
|
probably benign |
Het |
Ighv1-74 |
A |
G |
12: 115,766,501 (GRCm39) |
S39P |
probably damaging |
Het |
Kbtbd11 |
A |
G |
8: 15,078,589 (GRCm39) |
D396G |
possibly damaging |
Het |
Klc1 |
A |
G |
12: 111,762,055 (GRCm39) |
K575R |
possibly damaging |
Het |
Mki67 |
A |
T |
7: 135,302,559 (GRCm39) |
V825E |
probably damaging |
Het |
Mus81 |
T |
C |
19: 5,533,522 (GRCm39) |
K489R |
possibly damaging |
Het |
Myog |
A |
G |
1: 134,218,064 (GRCm39) |
K91E |
probably damaging |
Het |
Nfil3 |
A |
T |
13: 53,121,656 (GRCm39) |
V416E |
probably damaging |
Het |
Nup160 |
G |
T |
2: 90,563,176 (GRCm39) |
E1314* |
probably null |
Het |
Nwd2 |
C |
T |
5: 63,963,415 (GRCm39) |
Q1000* |
probably null |
Het |
Or4g17 |
T |
C |
2: 111,210,179 (GRCm39) |
V278A |
possibly damaging |
Het |
Or4k35 |
T |
G |
2: 111,100,655 (GRCm39) |
D19A |
probably benign |
Het |
Or6c66b |
A |
C |
10: 129,377,134 (GRCm39) |
M243L |
probably benign |
Het |
Or6c75 |
T |
A |
10: 129,337,383 (GRCm39) |
V210E |
probably damaging |
Het |
Ppp4r4 |
T |
A |
12: 103,573,147 (GRCm39) |
|
probably null |
Het |
Pramel16 |
A |
T |
4: 143,675,665 (GRCm39) |
I387N |
possibly damaging |
Het |
Psg27 |
C |
A |
7: 18,290,958 (GRCm39) |
R415L |
probably benign |
Het |
Ptprr |
T |
A |
10: 116,024,324 (GRCm39) |
S212T |
probably benign |
Het |
Ramp3 |
T |
C |
11: 6,624,888 (GRCm39) |
F61L |
probably damaging |
Het |
Rap1gds1 |
A |
G |
3: 138,664,389 (GRCm39) |
L322P |
probably damaging |
Het |
Rnf5 |
A |
G |
17: 34,820,562 (GRCm39) |
F175S |
probably benign |
Het |
Sema4a |
G |
A |
3: 88,344,343 (GRCm39) |
S636F |
probably damaging |
Het |
Sfrp2 |
A |
G |
3: 83,676,708 (GRCm39) |
D193G |
probably damaging |
Het |
Slc26a5 |
T |
C |
5: 22,052,258 (GRCm39) |
S24G |
probably damaging |
Het |
Slco1a8 |
A |
T |
6: 141,918,058 (GRCm39) |
F606Y |
probably benign |
Het |
Spg21 |
A |
G |
9: 65,376,084 (GRCm39) |
I31V |
probably benign |
Het |
Utrn |
A |
T |
10: 12,603,513 (GRCm39) |
D627E |
probably damaging |
Het |
Vmn2r103 |
A |
T |
17: 20,013,296 (GRCm39) |
N139I |
probably benign |
Het |
Vps35l |
T |
C |
7: 118,412,799 (GRCm39) |
I629T |
probably damaging |
Het |
Washc5 |
A |
T |
15: 59,217,377 (GRCm39) |
|
probably null |
Het |
Zfp667 |
T |
C |
7: 6,308,466 (GRCm39) |
I378T |
probably benign |
Het |
Zfp949 |
A |
C |
9: 88,449,236 (GRCm39) |
T14P |
possibly damaging |
Het |
|
Other mutations in Tmem45a2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00925:Tmem45a2
|
APN |
16 |
56,865,618 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01121:Tmem45a2
|
APN |
16 |
56,861,153 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL01481:Tmem45a2
|
APN |
16 |
56,867,375 (GRCm39) |
missense |
probably benign |
0.00 |
R0230:Tmem45a2
|
UTSW |
16 |
56,867,359 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0633:Tmem45a2
|
UTSW |
16 |
56,869,777 (GRCm39) |
missense |
probably benign |
0.03 |
R0850:Tmem45a2
|
UTSW |
16 |
56,865,732 (GRCm39) |
missense |
probably benign |
0.00 |
R1164:Tmem45a2
|
UTSW |
16 |
56,869,789 (GRCm39) |
missense |
probably damaging |
0.99 |
R1874:Tmem45a2
|
UTSW |
16 |
56,867,447 (GRCm39) |
missense |
possibly damaging |
0.86 |
R3938:Tmem45a2
|
UTSW |
16 |
56,859,398 (GRCm39) |
missense |
probably benign |
|
R4084:Tmem45a2
|
UTSW |
16 |
56,891,387 (GRCm39) |
missense |
probably benign |
|
R5309:Tmem45a2
|
UTSW |
16 |
56,859,370 (GRCm39) |
missense |
possibly damaging |
0.70 |
R6866:Tmem45a2
|
UTSW |
16 |
56,867,386 (GRCm39) |
missense |
probably damaging |
0.97 |
R9055:Tmem45a2
|
UTSW |
16 |
56,861,115 (GRCm39) |
missense |
probably benign |
0.42 |
R9286:Tmem45a2
|
UTSW |
16 |
56,867,332 (GRCm39) |
missense |
probably damaging |
1.00 |
|