Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl4fm5 |
T |
G |
4: 144,504,191 (GRCm39) |
Q320P |
probably damaging |
Het |
Adamtsl2 |
G |
A |
2: 26,994,055 (GRCm39) |
|
probably benign |
Het |
Adgrl3 |
T |
A |
5: 81,657,568 (GRCm39) |
|
probably benign |
Het |
Angptl3 |
A |
G |
4: 98,919,480 (GRCm39) |
Q80R |
probably benign |
Het |
Atmin |
G |
A |
8: 117,684,019 (GRCm39) |
V560M |
probably benign |
Het |
Bbx |
A |
G |
16: 50,045,023 (GRCm39) |
S513P |
probably benign |
Het |
Cacng8 |
C |
A |
7: 3,459,746 (GRCm39) |
Y112* |
probably null |
Het |
Catsperg2 |
A |
G |
7: 29,405,006 (GRCm39) |
|
probably null |
Het |
Ccdc12 |
A |
C |
9: 110,540,203 (GRCm39) |
T131P |
probably damaging |
Het |
Cdh23 |
G |
A |
10: 60,143,306 (GRCm39) |
A3005V |
possibly damaging |
Het |
Cep95 |
A |
T |
11: 106,704,624 (GRCm39) |
H493L |
probably benign |
Het |
Cntnap1 |
A |
G |
11: 101,068,137 (GRCm39) |
T50A |
probably benign |
Het |
Cyp3a16 |
T |
A |
5: 145,377,304 (GRCm39) |
I428F |
probably damaging |
Het |
Dnhd1 |
G |
T |
7: 105,301,091 (GRCm39) |
L149F |
probably damaging |
Het |
Dop1b |
T |
A |
16: 93,557,196 (GRCm39) |
V497E |
probably damaging |
Het |
Erich3 |
A |
T |
3: 154,404,308 (GRCm39) |
N55I |
|
Het |
Fbxw26 |
A |
T |
9: 109,550,962 (GRCm39) |
|
probably benign |
Het |
Gm4841 |
A |
G |
18: 60,403,895 (GRCm39) |
I66T |
probably damaging |
Het |
Gp5 |
G |
A |
16: 30,127,094 (GRCm39) |
L527F |
probably damaging |
Het |
Gpatch2l |
G |
A |
12: 86,290,883 (GRCm39) |
G22D |
probably benign |
Het |
Isg20l2 |
T |
A |
3: 87,838,991 (GRCm39) |
D67E |
probably benign |
Het |
Itgae |
G |
A |
11: 73,012,752 (GRCm39) |
V695I |
probably benign |
Het |
Itpr2 |
A |
T |
6: 146,256,174 (GRCm39) |
N1006K |
probably benign |
Het |
Iws1 |
G |
A |
18: 32,213,213 (GRCm39) |
E214K |
possibly damaging |
Het |
Lama3 |
C |
T |
18: 12,583,541 (GRCm39) |
Q710* |
probably null |
Het |
Loxhd1 |
C |
T |
18: 77,501,826 (GRCm39) |
A1715V |
probably damaging |
Het |
Map3k20 |
C |
T |
2: 72,228,755 (GRCm39) |
Q325* |
probably null |
Het |
Med1 |
A |
T |
11: 98,046,366 (GRCm39) |
S1477T |
unknown |
Het |
Mr1 |
T |
A |
1: 155,013,274 (GRCm39) |
H101L |
probably benign |
Het |
Mtor |
T |
A |
4: 148,543,537 (GRCm39) |
S405T |
probably benign |
Het |
Nme9 |
G |
C |
9: 99,338,321 (GRCm39) |
|
probably null |
Het |
Nom1 |
T |
A |
5: 29,647,532 (GRCm39) |
I589N |
probably damaging |
Het |
Nr6a1 |
A |
T |
2: 38,638,890 (GRCm39) |
D148E |
probably damaging |
Het |
Nup160 |
T |
C |
2: 90,548,375 (GRCm39) |
V1006A |
possibly damaging |
Het |
Or2ag1b |
A |
T |
7: 106,288,416 (GRCm39) |
I174N |
possibly damaging |
Het |
Or2aj4 |
A |
G |
16: 19,385,357 (GRCm39) |
I92T |
probably damaging |
Het |
Or4d10b |
A |
T |
19: 12,036,273 (GRCm39) |
L281Q |
probably damaging |
Het |
Or5d37 |
T |
A |
2: 87,924,278 (GRCm39) |
M1L |
probably benign |
Het |
Or6c200-ps1 |
G |
A |
10: 128,869,821 (GRCm39) |
P297S |
probably damaging |
Het |
Phyhd1 |
G |
T |
2: 30,156,879 (GRCm39) |
G7* |
probably null |
Het |
Pla2g4e |
T |
C |
2: 120,004,730 (GRCm39) |
|
probably benign |
Het |
Ppfia3 |
A |
G |
7: 45,011,222 (GRCm39) |
C3R |
probably damaging |
Het |
Pramel1 |
T |
C |
4: 143,123,769 (GRCm39) |
V148A |
probably benign |
Het |
Ptpdc1 |
A |
T |
13: 48,740,167 (GRCm39) |
D421E |
probably benign |
Het |
Rapgef2 |
A |
T |
3: 79,000,010 (GRCm39) |
D579E |
probably damaging |
Het |
Rbpj |
T |
G |
5: 53,810,724 (GRCm39) |
V448G |
probably damaging |
Het |
Rif1 |
T |
C |
2: 51,998,564 (GRCm39) |
V1067A |
probably benign |
Het |
Scfd1 |
A |
T |
12: 51,439,024 (GRCm39) |
N162I |
probably benign |
Het |
Sh2b1 |
TGGGGACCAGCTCAGCCACGGGGACCAGCTC |
TGGGGACCAGCTCAGCCACGGGGACCAGCTCAGCCACGGGGACCAGCTC |
7: 126,066,742 (GRCm39) |
|
probably benign |
Het |
Sp110 |
A |
T |
1: 85,507,363 (GRCm39) |
|
probably null |
Het |
Sparcl1 |
A |
T |
5: 104,236,345 (GRCm39) |
C469* |
probably null |
Het |
Srebf2 |
G |
A |
15: 82,066,357 (GRCm39) |
R635Q |
probably benign |
Het |
Stard7 |
T |
G |
2: 127,132,956 (GRCm39) |
S250A |
probably damaging |
Het |
Stxbp5l |
A |
C |
16: 37,028,442 (GRCm39) |
Y540* |
probably null |
Het |
Tlr5 |
T |
C |
1: 182,801,377 (GRCm39) |
V227A |
probably benign |
Het |
Tnik |
G |
T |
3: 28,593,570 (GRCm39) |
S142I |
unknown |
Het |
Trim6 |
A |
G |
7: 103,882,116 (GRCm39) |
T482A |
probably damaging |
Het |
Tssk5 |
A |
G |
15: 76,257,168 (GRCm39) |
I238T |
probably benign |
Het |
Ugt2b35 |
A |
G |
5: 87,156,140 (GRCm39) |
T411A |
probably benign |
Het |
Zc2hc1b |
C |
A |
10: 13,043,562 (GRCm39) |
R111L |
probably benign |
Het |
Zfp266 |
A |
T |
9: 20,411,300 (GRCm39) |
C292* |
probably null |
Het |
|
Other mutations in Tmem132b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01397:Tmem132b
|
APN |
5 |
125,775,792 (GRCm39) |
missense |
probably benign |
|
IGL01518:Tmem132b
|
APN |
5 |
125,855,855 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02542:Tmem132b
|
APN |
5 |
125,699,558 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02652:Tmem132b
|
APN |
5 |
125,864,639 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02671:Tmem132b
|
APN |
5 |
125,855,791 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02951:Tmem132b
|
APN |
5 |
125,864,611 (GRCm39) |
missense |
probably damaging |
0.99 |
R0456:Tmem132b
|
UTSW |
5 |
125,864,788 (GRCm39) |
missense |
probably damaging |
0.99 |
R0462:Tmem132b
|
UTSW |
5 |
125,862,990 (GRCm39) |
missense |
probably damaging |
1.00 |
R0724:Tmem132b
|
UTSW |
5 |
125,860,485 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1137:Tmem132b
|
UTSW |
5 |
125,860,606 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1168:Tmem132b
|
UTSW |
5 |
125,864,083 (GRCm39) |
missense |
probably damaging |
0.99 |
R1418:Tmem132b
|
UTSW |
5 |
125,715,313 (GRCm39) |
missense |
probably benign |
0.01 |
R1689:Tmem132b
|
UTSW |
5 |
125,864,678 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1744:Tmem132b
|
UTSW |
5 |
125,855,908 (GRCm39) |
critical splice donor site |
probably null |
|
R1835:Tmem132b
|
UTSW |
5 |
125,862,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R2016:Tmem132b
|
UTSW |
5 |
125,700,080 (GRCm39) |
missense |
probably benign |
|
R2033:Tmem132b
|
UTSW |
5 |
125,826,353 (GRCm39) |
missense |
probably damaging |
0.98 |
R2097:Tmem132b
|
UTSW |
5 |
125,715,272 (GRCm39) |
missense |
probably damaging |
0.99 |
R2114:Tmem132b
|
UTSW |
5 |
125,699,615 (GRCm39) |
missense |
probably damaging |
1.00 |
R2116:Tmem132b
|
UTSW |
5 |
125,699,615 (GRCm39) |
missense |
probably damaging |
1.00 |
R2117:Tmem132b
|
UTSW |
5 |
125,699,615 (GRCm39) |
missense |
probably damaging |
1.00 |
R2870:Tmem132b
|
UTSW |
5 |
125,715,332 (GRCm39) |
missense |
probably benign |
|
R2870:Tmem132b
|
UTSW |
5 |
125,715,332 (GRCm39) |
missense |
probably benign |
|
R3807:Tmem132b
|
UTSW |
5 |
125,864,644 (GRCm39) |
missense |
probably damaging |
1.00 |
R4825:Tmem132b
|
UTSW |
5 |
125,860,497 (GRCm39) |
missense |
probably benign |
|
R5149:Tmem132b
|
UTSW |
5 |
125,699,989 (GRCm39) |
missense |
probably damaging |
0.99 |
R5484:Tmem132b
|
UTSW |
5 |
125,864,797 (GRCm39) |
missense |
probably damaging |
1.00 |
R5623:Tmem132b
|
UTSW |
5 |
125,700,416 (GRCm39) |
missense |
probably damaging |
0.99 |
R5624:Tmem132b
|
UTSW |
5 |
125,699,710 (GRCm39) |
missense |
probably benign |
0.04 |
R5775:Tmem132b
|
UTSW |
5 |
125,715,394 (GRCm39) |
critical splice donor site |
probably null |
|
R7012:Tmem132b
|
UTSW |
5 |
125,775,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R7142:Tmem132b
|
UTSW |
5 |
125,699,737 (GRCm39) |
missense |
probably damaging |
1.00 |
R7308:Tmem132b
|
UTSW |
5 |
125,864,710 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7414:Tmem132b
|
UTSW |
5 |
125,864,555 (GRCm39) |
missense |
probably damaging |
1.00 |
R7452:Tmem132b
|
UTSW |
5 |
125,715,332 (GRCm39) |
missense |
probably benign |
|
R7650:Tmem132b
|
UTSW |
5 |
125,864,074 (GRCm39) |
missense |
probably benign |
0.04 |
R8111:Tmem132b
|
UTSW |
5 |
125,699,857 (GRCm39) |
missense |
probably benign |
0.00 |
R8326:Tmem132b
|
UTSW |
5 |
125,864,618 (GRCm39) |
missense |
probably damaging |
1.00 |
R8525:Tmem132b
|
UTSW |
5 |
125,715,380 (GRCm39) |
missense |
probably benign |
0.01 |
R8900:Tmem132b
|
UTSW |
5 |
125,855,884 (GRCm39) |
missense |
probably damaging |
0.96 |
R9147:Tmem132b
|
UTSW |
5 |
125,864,167 (GRCm39) |
missense |
probably damaging |
1.00 |
R9148:Tmem132b
|
UTSW |
5 |
125,864,167 (GRCm39) |
missense |
probably damaging |
1.00 |
R9179:Tmem132b
|
UTSW |
5 |
125,700,115 (GRCm39) |
missense |
probably benign |
0.02 |
R9215:Tmem132b
|
UTSW |
5 |
125,864,180 (GRCm39) |
missense |
probably damaging |
0.99 |
R9231:Tmem132b
|
UTSW |
5 |
125,860,531 (GRCm39) |
missense |
probably damaging |
1.00 |
R9311:Tmem132b
|
UTSW |
5 |
125,863,029 (GRCm39) |
missense |
possibly damaging |
0.56 |
R9436:Tmem132b
|
UTSW |
5 |
125,775,633 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9484:Tmem132b
|
UTSW |
5 |
125,860,420 (GRCm39) |
missense |
probably damaging |
0.98 |
R9775:Tmem132b
|
UTSW |
5 |
125,864,566 (GRCm39) |
missense |
probably benign |
0.07 |
Z1176:Tmem132b
|
UTSW |
5 |
125,864,950 (GRCm39) |
missense |
possibly damaging |
0.51 |
|