Other mutations in this stock |
Total: 76 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9930012K11Rik |
A |
T |
14: 70,394,238 (GRCm39) |
M179K |
probably benign |
Het |
A030003K21Rik |
A |
G |
1: 82,920,787 (GRCm39) |
V86A |
unknown |
Het |
AC133488.1 |
A |
T |
16: 18,440,075 (GRCm39) |
V363E |
probably benign |
Het |
Adamts16 |
A |
G |
13: 70,901,408 (GRCm39) |
S890P |
probably benign |
Het |
Adgrf4 |
A |
G |
17: 42,973,293 (GRCm39) |
V685A |
probably benign |
Het |
Aff1 |
T |
A |
5: 103,990,131 (GRCm39) |
M867K |
possibly damaging |
Het |
Apba3 |
T |
A |
10: 81,106,867 (GRCm39) |
S225T |
|
Het |
Aplp1 |
T |
A |
7: 30,141,775 (GRCm39) |
T228S |
probably benign |
Het |
Arhgap18 |
A |
G |
10: 26,730,886 (GRCm39) |
D188G |
probably benign |
Het |
BC024063 |
T |
A |
10: 81,944,906 (GRCm39) |
S175R |
possibly damaging |
Het |
Bloc1s6 |
T |
G |
2: 122,580,548 (GRCm39) |
S2R |
probably damaging |
Het |
Cd209b |
A |
G |
8: 3,974,245 (GRCm39) |
I119T |
possibly damaging |
Het |
Cdk8 |
T |
C |
5: 146,168,549 (GRCm39) |
V16A |
probably damaging |
Het |
Cep295 |
A |
G |
9: 15,252,904 (GRCm39) |
M308T |
probably benign |
Het |
Cfap53 |
T |
A |
18: 74,416,272 (GRCm39) |
Y2N |
probably damaging |
Het |
Col28a1 |
T |
A |
6: 8,014,993 (GRCm39) |
D804V |
probably damaging |
Het |
Csta3 |
G |
A |
16: 36,038,069 (GRCm39) |
V69I |
probably benign |
Het |
Cyp2c40 |
A |
T |
19: 39,762,317 (GRCm39) |
D443E |
probably damaging |
Het |
Cyp2d9 |
A |
G |
15: 82,338,572 (GRCm39) |
D202G |
possibly damaging |
Het |
Dchs1 |
G |
A |
7: 105,415,126 (GRCm39) |
A686V |
probably benign |
Het |
Egf |
A |
T |
3: 129,472,026 (GRCm39) |
N1199K |
probably benign |
Het |
Eva1a |
A |
G |
6: 82,068,855 (GRCm39) |
R61G |
possibly damaging |
Het |
Exoc6 |
T |
A |
19: 37,597,478 (GRCm39) |
D626E |
probably benign |
Het |
Exosc10 |
T |
C |
4: 148,663,916 (GRCm39) |
|
probably null |
Het |
Firrm |
A |
G |
1: 163,814,514 (GRCm39) |
I143T |
probably damaging |
Het |
Gm12888 |
T |
C |
4: 121,176,600 (GRCm39) |
Q67R |
probably null |
Het |
Gm16485 |
A |
G |
9: 8,972,319 (GRCm39) |
S62G |
unknown |
Het |
Gng4 |
T |
C |
13: 13,999,896 (GRCm39) |
I55T |
probably damaging |
Het |
Gpihbp1 |
A |
G |
15: 75,469,830 (GRCm39) |
S182G |
possibly damaging |
Het |
Hax1 |
T |
C |
3: 89,903,127 (GRCm39) |
R251G |
probably damaging |
Het |
Igf2bp2 |
G |
A |
16: 21,900,502 (GRCm39) |
T213I |
probably damaging |
Het |
Il23a |
T |
A |
10: 128,133,427 (GRCm39) |
K66* |
probably null |
Het |
Itga2 |
A |
T |
13: 115,014,298 (GRCm39) |
L210* |
probably null |
Het |
Ltbp2 |
G |
A |
12: 84,837,864 (GRCm39) |
P1192L |
probably benign |
Het |
Matr3 |
T |
A |
18: 35,712,355 (GRCm39) |
M389K |
possibly damaging |
Het |
Mettl15 |
T |
C |
2: 108,923,444 (GRCm39) |
D326G |
probably damaging |
Het |
Mta1 |
T |
A |
12: 113,100,025 (GRCm39) |
V645E |
probably damaging |
Het |
Muc5ac |
T |
C |
7: 141,363,529 (GRCm39) |
I2280T |
unknown |
Het |
Naa15 |
T |
A |
3: 51,358,802 (GRCm39) |
N362K |
probably benign |
Het |
Necab2 |
T |
C |
8: 120,189,303 (GRCm39) |
Y158H |
probably damaging |
Het |
Nphp3 |
T |
A |
9: 103,897,980 (GRCm39) |
L523Q |
probably damaging |
Het |
Nphs1 |
T |
G |
7: 30,165,026 (GRCm39) |
F540V |
possibly damaging |
Het |
Or2av9 |
A |
G |
11: 58,381,350 (GRCm39) |
V77A |
probably damaging |
Het |
Or2k2 |
A |
G |
4: 58,785,320 (GRCm39) |
I134T |
probably benign |
Het |
Or5p55 |
A |
T |
7: 107,567,524 (GRCm39) |
R307* |
probably null |
Het |
Ppa1 |
A |
T |
10: 61,496,784 (GRCm39) |
I91F |
probably damaging |
Het |
Prdm6 |
C |
A |
18: 53,598,019 (GRCm39) |
A127D |
unknown |
Het |
Prdm8 |
T |
C |
5: 98,334,175 (GRCm39) |
F581L |
probably damaging |
Het |
Rbbp6 |
T |
C |
7: 122,589,428 (GRCm39) |
I372T |
probably damaging |
Het |
Rnf144b |
A |
G |
13: 47,396,348 (GRCm39) |
I228M |
probably damaging |
Het |
Rsf1 |
CG |
CGACGGCGGGG |
7: 97,229,115 (GRCm39) |
|
probably benign |
Het |
Setd2 |
T |
C |
9: 110,374,385 (GRCm39) |
|
probably null |
Het |
Sez6l |
T |
C |
5: 112,613,824 (GRCm39) |
H441R |
possibly damaging |
Het |
Shbg |
G |
A |
11: 69,506,430 (GRCm39) |
L327F |
probably benign |
Het |
Sik3 |
C |
T |
9: 46,123,539 (GRCm39) |
Q1113* |
probably null |
Het |
Smad2 |
T |
A |
18: 76,395,573 (GRCm39) |
I4N |
possibly damaging |
Het |
Spata31h1 |
G |
A |
10: 82,118,524 (GRCm39) |
R4829* |
probably null |
Het |
Sult2b1 |
T |
A |
7: 45,391,534 (GRCm39) |
E84V |
probably damaging |
Het |
Tbc1d8 |
A |
G |
1: 39,444,474 (GRCm39) |
Y162H |
|
Het |
Tedc2 |
A |
G |
17: 24,436,705 (GRCm39) |
L308P |
probably damaging |
Het |
Tmem120b |
T |
A |
5: 123,242,566 (GRCm39) |
N181K |
possibly damaging |
Het |
Tmem229b |
T |
G |
12: 79,011,448 (GRCm39) |
N161T |
possibly damaging |
Het |
Tmem43 |
A |
C |
6: 91,459,291 (GRCm39) |
D254A |
probably benign |
Het |
Trpv6 |
T |
C |
6: 41,603,074 (GRCm39) |
D266G |
probably benign |
Het |
Tspan9 |
A |
G |
6: 127,943,717 (GRCm39) |
I102T |
possibly damaging |
Het |
Ung |
A |
G |
5: 114,270,166 (GRCm39) |
|
probably benign |
Het |
Upp2 |
C |
T |
2: 58,667,996 (GRCm39) |
H230Y |
probably damaging |
Het |
Vmn1r184 |
G |
A |
7: 25,966,545 (GRCm39) |
S97N |
possibly damaging |
Het |
Vmn2r73 |
A |
T |
7: 85,521,931 (GRCm39) |
V136E |
possibly damaging |
Het |
Wdr20rt |
T |
C |
12: 65,272,918 (GRCm39) |
V127A |
probably damaging |
Het |
Yme1l1 |
T |
A |
2: 23,063,058 (GRCm39) |
F210I |
probably damaging |
Het |
Yrdc |
T |
C |
4: 124,747,811 (GRCm39) |
|
probably null |
Het |
Zfhx4 |
G |
T |
3: 5,464,312 (GRCm39) |
R1515L |
probably damaging |
Het |
Zfhx4 |
C |
T |
3: 5,466,217 (GRCm39) |
P2150L |
probably damaging |
Het |
Zfp267 |
C |
A |
3: 36,219,902 (GRCm39) |
H642N |
possibly damaging |
Het |
Zfp988 |
C |
T |
4: 147,416,450 (GRCm39) |
P295S |
possibly damaging |
Het |
|
Other mutations in Tmc5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01484:Tmc5
|
APN |
7 |
118,256,010 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01601:Tmc5
|
APN |
7 |
118,223,047 (GRCm39) |
unclassified |
probably benign |
|
IGL01633:Tmc5
|
APN |
7 |
118,222,809 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01845:Tmc5
|
APN |
7 |
118,251,733 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02148:Tmc5
|
APN |
7 |
118,244,547 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02638:Tmc5
|
APN |
7 |
118,226,456 (GRCm39) |
missense |
probably benign |
0.36 |
IGL02890:Tmc5
|
APN |
7 |
118,244,653 (GRCm39) |
splice site |
probably benign |
|
hipster
|
UTSW |
7 |
118,265,834 (GRCm39) |
critical splice donor site |
probably null |
|
F5426:Tmc5
|
UTSW |
7 |
118,222,546 (GRCm39) |
missense |
probably benign |
|
PIT4802001:Tmc5
|
UTSW |
7 |
118,271,449 (GRCm39) |
missense |
probably benign |
|
R0068:Tmc5
|
UTSW |
7 |
118,233,460 (GRCm39) |
missense |
probably benign |
0.44 |
R0470:Tmc5
|
UTSW |
7 |
118,239,154 (GRCm39) |
missense |
possibly damaging |
0.68 |
R0520:Tmc5
|
UTSW |
7 |
118,265,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R0786:Tmc5
|
UTSW |
7 |
118,226,433 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1263:Tmc5
|
UTSW |
7 |
118,266,093 (GRCm39) |
missense |
probably damaging |
1.00 |
R1269:Tmc5
|
UTSW |
7 |
118,265,816 (GRCm39) |
missense |
probably benign |
0.30 |
R1486:Tmc5
|
UTSW |
7 |
118,272,655 (GRCm39) |
missense |
probably benign |
0.02 |
R1702:Tmc5
|
UTSW |
7 |
118,271,462 (GRCm39) |
missense |
probably benign |
0.00 |
R2188:Tmc5
|
UTSW |
7 |
118,254,178 (GRCm39) |
missense |
probably damaging |
1.00 |
R3508:Tmc5
|
UTSW |
7 |
118,244,618 (GRCm39) |
missense |
probably benign |
0.01 |
R3893:Tmc5
|
UTSW |
7 |
118,244,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R3927:Tmc5
|
UTSW |
7 |
118,251,878 (GRCm39) |
nonsense |
probably null |
|
R4171:Tmc5
|
UTSW |
7 |
118,248,810 (GRCm39) |
missense |
probably damaging |
0.99 |
R4279:Tmc5
|
UTSW |
7 |
118,273,886 (GRCm39) |
makesense |
probably null |
|
R4554:Tmc5
|
UTSW |
7 |
118,269,956 (GRCm39) |
missense |
probably benign |
0.16 |
R4555:Tmc5
|
UTSW |
7 |
118,269,956 (GRCm39) |
missense |
probably benign |
0.16 |
R4557:Tmc5
|
UTSW |
7 |
118,269,956 (GRCm39) |
missense |
probably benign |
0.16 |
R4833:Tmc5
|
UTSW |
7 |
118,228,052 (GRCm39) |
missense |
probably benign |
0.11 |
R4845:Tmc5
|
UTSW |
7 |
118,241,604 (GRCm39) |
missense |
probably damaging |
1.00 |
R4852:Tmc5
|
UTSW |
7 |
118,244,562 (GRCm39) |
missense |
probably benign |
0.32 |
R5087:Tmc5
|
UTSW |
7 |
118,244,609 (GRCm39) |
missense |
possibly damaging |
0.68 |
R5214:Tmc5
|
UTSW |
7 |
118,247,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R5723:Tmc5
|
UTSW |
7 |
118,271,416 (GRCm39) |
missense |
probably damaging |
1.00 |
R5739:Tmc5
|
UTSW |
7 |
118,265,834 (GRCm39) |
critical splice donor site |
probably null |
|
R5882:Tmc5
|
UTSW |
7 |
118,254,142 (GRCm39) |
missense |
probably damaging |
0.99 |
R5946:Tmc5
|
UTSW |
7 |
118,269,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R6244:Tmc5
|
UTSW |
7 |
118,233,437 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6360:Tmc5
|
UTSW |
7 |
118,233,189 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R6375:Tmc5
|
UTSW |
7 |
118,256,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R6458:Tmc5
|
UTSW |
7 |
118,244,539 (GRCm39) |
missense |
probably damaging |
1.00 |
R6566:Tmc5
|
UTSW |
7 |
118,247,067 (GRCm39) |
missense |
probably damaging |
1.00 |
R6681:Tmc5
|
UTSW |
7 |
118,268,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R7202:Tmc5
|
UTSW |
7 |
118,239,179 (GRCm39) |
missense |
possibly damaging |
0.49 |
R7227:Tmc5
|
UTSW |
7 |
118,269,889 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7410:Tmc5
|
UTSW |
7 |
118,222,820 (GRCm39) |
nonsense |
probably null |
|
R7562:Tmc5
|
UTSW |
7 |
118,222,549 (GRCm39) |
missense |
probably benign |
0.10 |
R7808:Tmc5
|
UTSW |
7 |
118,268,440 (GRCm39) |
missense |
probably damaging |
1.00 |
R8560:Tmc5
|
UTSW |
7 |
118,268,514 (GRCm39) |
missense |
probably damaging |
1.00 |
R8682:Tmc5
|
UTSW |
7 |
118,269,925 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8778:Tmc5
|
UTSW |
7 |
118,222,816 (GRCm39) |
missense |
unknown |
|
R8832:Tmc5
|
UTSW |
7 |
118,222,332 (GRCm39) |
missense |
probably benign |
0.06 |
R9026:Tmc5
|
UTSW |
7 |
118,241,594 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9064:Tmc5
|
UTSW |
7 |
118,233,270 (GRCm39) |
missense |
probably benign |
0.01 |
R9258:Tmc5
|
UTSW |
7 |
118,222,501 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Tmc5
|
UTSW |
7 |
118,222,979 (GRCm39) |
missense |
probably damaging |
1.00 |
|