Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam3 |
T |
A |
8: 25,204,274 (GRCm39) |
K178I |
possibly damaging |
Het |
Adarb1 |
T |
A |
10: 77,131,539 (GRCm39) |
H650L |
possibly damaging |
Het |
Alms1 |
G |
T |
6: 85,578,234 (GRCm39) |
L187F |
possibly damaging |
Het |
Ano3 |
T |
A |
2: 110,601,376 (GRCm39) |
N294I |
probably damaging |
Het |
Asb3 |
T |
A |
11: 31,031,460 (GRCm39) |
M360K |
probably benign |
Het |
Atp6v0d2 |
T |
C |
4: 19,890,834 (GRCm39) |
I109V |
probably benign |
Het |
C9 |
A |
T |
15: 6,526,430 (GRCm39) |
|
probably null |
Het |
Calcr |
A |
T |
6: 3,687,468 (GRCm39) |
I510N |
probably benign |
Het |
Cdc5l |
G |
A |
17: 45,744,500 (GRCm39) |
|
probably benign |
Het |
Cdca3 |
T |
A |
6: 124,809,172 (GRCm39) |
I104N |
probably benign |
Het |
Chpt1 |
C |
T |
10: 88,339,446 (GRCm39) |
|
probably null |
Het |
Chrna5 |
A |
G |
9: 54,911,919 (GRCm39) |
I240V |
probably benign |
Het |
Dhx29 |
T |
C |
13: 113,081,612 (GRCm39) |
V412A |
possibly damaging |
Het |
Dnah11 |
T |
A |
12: 118,024,148 (GRCm39) |
M1868L |
probably damaging |
Het |
Dock6 |
A |
G |
9: 21,742,418 (GRCm39) |
V269A |
probably benign |
Het |
Eif4b |
T |
C |
15: 101,990,443 (GRCm39) |
S16P |
probably benign |
Het |
Eppk1 |
G |
A |
15: 75,994,526 (GRCm39) |
T785I |
probably benign |
Het |
Ezh2 |
T |
C |
6: 47,531,141 (GRCm39) |
Y181C |
possibly damaging |
Het |
Fem1c |
T |
C |
18: 46,657,561 (GRCm39) |
Y51C |
probably damaging |
Het |
Garin5a |
A |
T |
7: 44,150,405 (GRCm39) |
E199V |
probably damaging |
Het |
Glt8d2 |
T |
C |
10: 82,496,644 (GRCm39) |
N138S |
probably damaging |
Het |
Gltp |
A |
G |
5: 114,808,470 (GRCm39) |
*210Q |
probably null |
Het |
Gm10318 |
T |
A |
10: 77,689,102 (GRCm39) |
V123D |
unknown |
Het |
Gm5134 |
C |
T |
10: 75,821,943 (GRCm39) |
T259I |
probably benign |
Het |
Gm6526 |
T |
A |
14: 43,988,309 (GRCm39) |
C187S |
probably benign |
Het |
Golga2 |
T |
A |
2: 32,189,287 (GRCm39) |
S273T |
probably damaging |
Het |
Gulo |
T |
C |
14: 66,234,348 (GRCm39) |
E238G |
probably benign |
Het |
Htt |
G |
A |
5: 35,012,019 (GRCm39) |
V1565M |
probably damaging |
Het |
Inpp5d |
A |
T |
1: 87,625,191 (GRCm39) |
D457V |
possibly damaging |
Het |
Itpk1 |
C |
T |
12: 102,572,347 (GRCm39) |
|
probably null |
Het |
Kif20a |
T |
C |
18: 34,762,228 (GRCm39) |
C414R |
possibly damaging |
Het |
Klra3 |
T |
C |
6: 130,300,602 (GRCm39) |
I256V |
probably damaging |
Het |
Klrb1a |
T |
C |
6: 128,597,239 (GRCm39) |
T60A |
probably benign |
Het |
Kmt2d |
T |
C |
15: 98,741,283 (GRCm39) |
K4592E |
unknown |
Het |
Lama3 |
T |
C |
18: 12,583,460 (GRCm39) |
C683R |
probably damaging |
Het |
Lhcgr |
A |
G |
17: 89,050,446 (GRCm39) |
I360T |
probably damaging |
Het |
Lmod2 |
G |
A |
6: 24,604,182 (GRCm39) |
V386I |
possibly damaging |
Het |
Med29 |
T |
C |
7: 28,086,308 (GRCm39) |
I167V |
possibly damaging |
Het |
Mis18bp1 |
T |
A |
12: 65,205,337 (GRCm39) |
|
probably benign |
Het |
Mtus2 |
A |
G |
5: 148,013,464 (GRCm39) |
K86E |
possibly damaging |
Het |
Ndst4 |
T |
A |
3: 125,232,211 (GRCm39) |
L260Q |
probably damaging |
Het |
Neurod2 |
T |
C |
11: 98,218,444 (GRCm39) |
Y240C |
probably damaging |
Het |
Nsd1 |
T |
C |
13: 55,458,313 (GRCm39) |
V2142A |
possibly damaging |
Het |
Or10ag55-ps1 |
T |
A |
2: 87,115,491 (GRCm39) |
S286T |
probably damaging |
Het |
Or10c1 |
G |
T |
17: 37,522,355 (GRCm39) |
R130S |
possibly damaging |
Het |
Or1q1 |
C |
T |
2: 36,887,290 (GRCm39) |
A156V |
probably damaging |
Het |
Or6p1 |
T |
A |
1: 174,258,641 (GRCm39) |
S216T |
probably benign |
Het |
Pcm1 |
T |
A |
8: 41,728,168 (GRCm39) |
S542T |
probably damaging |
Het |
Pde7a |
C |
T |
3: 19,285,167 (GRCm39) |
G340D |
probably benign |
Het |
Phkb |
T |
G |
8: 86,604,798 (GRCm39) |
C68G |
probably null |
Het |
Ppif |
A |
G |
14: 25,695,921 (GRCm39) |
T73A |
possibly damaging |
Het |
Prkacb |
T |
C |
3: 146,463,475 (GRCm39) |
E79G |
probably damaging |
Het |
Ptprz1 |
G |
T |
6: 22,959,650 (GRCm39) |
W49L |
probably damaging |
Het |
Ring1 |
T |
C |
17: 34,240,420 (GRCm39) |
E386G |
possibly damaging |
Het |
Rp1 |
A |
G |
1: 4,212,833 (GRCm39) |
|
probably null |
Het |
Rrm2 |
T |
C |
12: 24,760,446 (GRCm39) |
Y177H |
probably damaging |
Het |
Rsf1 |
CGGC |
CGGCGGCGGAGGC |
7: 97,229,139 (GRCm39) |
|
probably benign |
Het |
Scn4b |
T |
A |
9: 45,060,639 (GRCm39) |
I180N |
probably damaging |
Het |
Slc22a12 |
A |
G |
19: 6,586,765 (GRCm39) |
|
probably null |
Het |
Spa17 |
C |
T |
9: 37,518,921 (GRCm39) |
A73T |
probably damaging |
Het |
Ssh3 |
C |
T |
19: 4,312,437 (GRCm39) |
R636Q |
probably benign |
Het |
Sugp2 |
C |
A |
8: 70,712,370 (GRCm39) |
T995K |
probably damaging |
Het |
Sumo3 |
T |
A |
10: 77,442,792 (GRCm39) |
V4E |
unknown |
Het |
Svil |
C |
A |
18: 5,062,370 (GRCm39) |
Q810K |
probably damaging |
Het |
Tbr1 |
C |
T |
2: 61,635,077 (GRCm39) |
P9L |
probably benign |
Het |
Ttll9 |
A |
G |
2: 152,818,136 (GRCm39) |
H42R |
probably benign |
Het |
Usb1 |
T |
C |
8: 96,070,685 (GRCm39) |
Y204H |
probably damaging |
Het |
Vcpip1 |
A |
G |
1: 9,815,948 (GRCm39) |
Y812H |
probably benign |
Het |
Vmn2r15 |
T |
C |
5: 109,445,224 (GRCm39) |
R67G |
possibly damaging |
Het |
Wdr64 |
A |
T |
1: 175,622,658 (GRCm39) |
I802L |
probably benign |
Het |
Xndc1 |
T |
C |
7: 101,725,114 (GRCm39) |
S100P |
probably damaging |
Het |
Xpot |
T |
C |
10: 121,447,392 (GRCm39) |
I128V |
probably benign |
Het |
Xrn1 |
C |
T |
9: 95,927,632 (GRCm39) |
S1472F |
possibly damaging |
Het |
Zscan12 |
A |
T |
13: 21,547,938 (GRCm39) |
Y40F |
possibly damaging |
Het |
|
Other mutations in Tmem26 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00155:Tmem26
|
APN |
10 |
68,611,184 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00471:Tmem26
|
APN |
10 |
68,614,511 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL01301:Tmem26
|
APN |
10 |
68,614,436 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01567:Tmem26
|
APN |
10 |
68,587,061 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02487:Tmem26
|
APN |
10 |
68,614,563 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02713:Tmem26
|
APN |
10 |
68,587,125 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02828:Tmem26
|
APN |
10 |
68,611,215 (GRCm39) |
critical splice donor site |
probably null |
|
ANU18:Tmem26
|
UTSW |
10 |
68,614,436 (GRCm39) |
missense |
probably damaging |
1.00 |
P0027:Tmem26
|
UTSW |
10 |
68,614,548 (GRCm39) |
missense |
probably benign |
0.00 |
R1415:Tmem26
|
UTSW |
10 |
68,614,491 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1649:Tmem26
|
UTSW |
10 |
68,587,103 (GRCm39) |
missense |
probably damaging |
1.00 |
R3871:Tmem26
|
UTSW |
10 |
68,614,562 (GRCm39) |
missense |
probably benign |
0.01 |
R5072:Tmem26
|
UTSW |
10 |
68,611,178 (GRCm39) |
missense |
probably damaging |
1.00 |
R5239:Tmem26
|
UTSW |
10 |
68,587,096 (GRCm39) |
missense |
probably damaging |
0.97 |
R6053:Tmem26
|
UTSW |
10 |
68,584,314 (GRCm39) |
missense |
probably benign |
0.00 |
R6607:Tmem26
|
UTSW |
10 |
68,614,543 (GRCm39) |
missense |
probably benign |
0.00 |
R6710:Tmem26
|
UTSW |
10 |
68,559,884 (GRCm39) |
missense |
probably damaging |
1.00 |
R7378:Tmem26
|
UTSW |
10 |
68,559,922 (GRCm39) |
critical splice donor site |
probably null |
|
R9276:Tmem26
|
UTSW |
10 |
68,614,488 (GRCm39) |
missense |
possibly damaging |
0.58 |
R9303:Tmem26
|
UTSW |
10 |
68,559,816 (GRCm39) |
nonsense |
probably null |
|
R9305:Tmem26
|
UTSW |
10 |
68,559,816 (GRCm39) |
nonsense |
probably null |
|
R9661:Tmem26
|
UTSW |
10 |
68,559,838 (GRCm39) |
missense |
probably damaging |
1.00 |
T0722:Tmem26
|
UTSW |
10 |
68,614,548 (GRCm39) |
missense |
probably benign |
0.00 |
X0003:Tmem26
|
UTSW |
10 |
68,614,548 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Tmem26
|
UTSW |
10 |
68,559,793 (GRCm39) |
missense |
probably damaging |
1.00 |
|