Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A530084C06Rik |
G |
T |
13: 31,742,978 (GRCm39) |
R92S |
unknown |
Het |
Acaca |
A |
G |
11: 84,263,465 (GRCm39) |
I2029V |
probably benign |
Het |
Anks1b |
A |
C |
10: 90,784,446 (GRCm39) |
D1138A |
probably damaging |
Het |
Atr |
T |
A |
9: 95,829,171 (GRCm39) |
V2508E |
probably damaging |
Het |
C4b |
C |
T |
17: 34,948,373 (GRCm39) |
|
probably null |
Het |
Calhm4 |
G |
A |
10: 33,919,904 (GRCm39) |
T121M |
possibly damaging |
Het |
Cd46 |
A |
T |
1: 194,765,927 (GRCm39) |
M146K |
probably null |
Het |
Chp1 |
A |
G |
2: 119,391,226 (GRCm39) |
I28V |
probably benign |
Het |
Chrnb1 |
T |
A |
11: 69,683,699 (GRCm39) |
R216W |
probably damaging |
Het |
Clmn |
G |
A |
12: 104,748,371 (GRCm39) |
T392M |
probably benign |
Het |
Cracd |
A |
G |
5: 77,005,367 (GRCm39) |
E576G |
unknown |
Het |
Dcxr |
A |
C |
11: 120,617,279 (GRCm39) |
L88R |
probably benign |
Het |
Dedd |
C |
T |
1: 171,166,478 (GRCm39) |
P138L |
probably benign |
Het |
Degs1 |
A |
G |
1: 182,107,263 (GRCm39) |
S35P |
probably damaging |
Het |
Ehmt1 |
T |
C |
2: 24,705,792 (GRCm39) |
D851G |
possibly damaging |
Het |
Fam117b |
A |
G |
1: 60,020,693 (GRCm39) |
D521G |
probably damaging |
Het |
Gm6882 |
A |
G |
7: 21,161,577 (GRCm39) |
V97A |
probably damaging |
Het |
Hgs |
A |
T |
11: 120,365,128 (GRCm39) |
Q172L |
probably damaging |
Het |
Hormad2 |
T |
C |
11: 4,296,662 (GRCm39) |
Q274R |
probably benign |
Het |
Igkv8-19 |
C |
T |
6: 70,318,383 (GRCm39) |
|
probably benign |
Het |
Ikbkb |
T |
C |
8: 23,161,757 (GRCm39) |
N377S |
probably benign |
Het |
Intu |
G |
A |
3: 40,608,683 (GRCm39) |
G232S |
probably damaging |
Het |
Lypd9 |
C |
A |
11: 58,338,304 (GRCm39) |
M29I |
probably benign |
Het |
Mov10 |
A |
G |
3: 104,704,381 (GRCm39) |
S806P |
possibly damaging |
Het |
Mrgprb1 |
A |
G |
7: 48,097,331 (GRCm39) |
F194L |
probably benign |
Het |
Notch3 |
A |
T |
17: 32,377,596 (GRCm39) |
I160K |
probably benign |
Het |
Nup155 |
C |
G |
15: 8,138,937 (GRCm39) |
S3W |
probably damaging |
Het |
Or4k41 |
A |
G |
2: 111,279,967 (GRCm39) |
I161V |
probably benign |
Het |
Or8s5 |
A |
G |
15: 98,237,967 (GRCm39) |
I301T |
probably damaging |
Het |
Plxdc1 |
A |
T |
11: 97,846,977 (GRCm39) |
F147L |
possibly damaging |
Het |
Ppfia1 |
T |
C |
7: 144,106,173 (GRCm39) |
D33G |
possibly damaging |
Het |
Prdm11 |
G |
A |
2: 92,810,999 (GRCm39) |
A200V |
probably damaging |
Het |
Qrich2 |
A |
T |
11: 116,347,455 (GRCm39) |
I1123K |
unknown |
Het |
Rgs1 |
A |
G |
1: 144,124,215 (GRCm39) |
|
probably null |
Het |
Skint7 |
T |
A |
4: 111,841,337 (GRCm39) |
V259E |
probably benign |
Het |
Slc25a3 |
A |
T |
10: 90,953,904 (GRCm39) |
|
probably null |
Het |
Slc28a2b |
A |
T |
2: 122,317,161 (GRCm39) |
R7S |
probably null |
Het |
Slco1a6 |
A |
T |
6: 142,091,481 (GRCm39) |
I73N |
probably damaging |
Het |
Sltm |
C |
G |
9: 70,493,955 (GRCm39) |
P802R |
possibly damaging |
Het |
Smc4 |
CTA |
CTATA |
3: 68,925,400 (GRCm39) |
|
probably benign |
Het |
Spock2 |
G |
A |
10: 59,962,002 (GRCm39) |
D206N |
probably damaging |
Het |
Stard3nl |
T |
G |
13: 19,552,008 (GRCm39) |
R185S |
probably damaging |
Het |
Supt16 |
A |
G |
14: 52,434,556 (GRCm39) |
Y18H |
probably benign |
Het |
Synpo |
G |
A |
18: 60,736,500 (GRCm39) |
T482I |
probably damaging |
Het |
Tcstv7b |
G |
A |
13: 120,702,376 (GRCm39) |
W57* |
probably null |
Het |
Trim59 |
T |
A |
3: 68,945,259 (GRCm39) |
H27L |
probably damaging |
Het |
Trpv2 |
G |
A |
11: 62,481,832 (GRCm39) |
|
probably null |
Het |
Tyw5 |
A |
T |
1: 57,432,644 (GRCm39) |
D117E |
probably benign |
Het |
Usp17la |
T |
C |
7: 104,510,354 (GRCm39) |
Y320H |
probably damaging |
Het |
Usp31 |
T |
C |
7: 121,258,185 (GRCm39) |
D694G |
probably damaging |
Het |
Vmn1r159 |
T |
A |
7: 22,542,448 (GRCm39) |
T195S |
probably damaging |
Het |
Vmn2r57 |
C |
T |
7: 41,074,513 (GRCm39) |
V517M |
possibly damaging |
Het |
Yipf1 |
A |
G |
4: 107,176,193 (GRCm39) |
N29S |
probably benign |
Het |
Zfp954 |
A |
T |
7: 7,118,823 (GRCm39) |
F240L |
possibly damaging |
Het |
|
Other mutations in Tmc6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00763:Tmc6
|
APN |
11 |
117,669,872 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02637:Tmc6
|
APN |
11 |
117,658,416 (GRCm39) |
missense |
possibly damaging |
0.94 |
PIT4520001:Tmc6
|
UTSW |
11 |
117,663,556 (GRCm39) |
missense |
possibly damaging |
0.55 |
R0140:Tmc6
|
UTSW |
11 |
117,657,077 (GRCm39) |
unclassified |
probably benign |
|
R0149:Tmc6
|
UTSW |
11 |
117,660,274 (GRCm39) |
missense |
probably damaging |
1.00 |
R0437:Tmc6
|
UTSW |
11 |
117,669,087 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1566:Tmc6
|
UTSW |
11 |
117,660,262 (GRCm39) |
missense |
probably damaging |
0.99 |
R2011:Tmc6
|
UTSW |
11 |
117,660,232 (GRCm39) |
missense |
probably damaging |
1.00 |
R2012:Tmc6
|
UTSW |
11 |
117,660,232 (GRCm39) |
missense |
probably damaging |
1.00 |
R2169:Tmc6
|
UTSW |
11 |
117,659,932 (GRCm39) |
missense |
probably damaging |
1.00 |
R2568:Tmc6
|
UTSW |
11 |
117,663,646 (GRCm39) |
missense |
probably benign |
0.08 |
R3853:Tmc6
|
UTSW |
11 |
117,663,884 (GRCm39) |
nonsense |
probably null |
|
R4049:Tmc6
|
UTSW |
11 |
117,669,087 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4655:Tmc6
|
UTSW |
11 |
117,663,868 (GRCm39) |
missense |
possibly damaging |
0.62 |
R4708:Tmc6
|
UTSW |
11 |
117,659,774 (GRCm39) |
missense |
probably benign |
0.00 |
R5001:Tmc6
|
UTSW |
11 |
117,661,610 (GRCm39) |
missense |
probably benign |
0.28 |
R5115:Tmc6
|
UTSW |
11 |
117,666,014 (GRCm39) |
missense |
probably damaging |
0.98 |
R5551:Tmc6
|
UTSW |
11 |
117,660,271 (GRCm39) |
missense |
probably damaging |
1.00 |
R5667:Tmc6
|
UTSW |
11 |
117,666,441 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5671:Tmc6
|
UTSW |
11 |
117,666,441 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5763:Tmc6
|
UTSW |
11 |
117,660,259 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6137:Tmc6
|
UTSW |
11 |
117,667,154 (GRCm39) |
missense |
probably damaging |
1.00 |
R6354:Tmc6
|
UTSW |
11 |
117,665,062 (GRCm39) |
missense |
probably benign |
0.32 |
R6418:Tmc6
|
UTSW |
11 |
117,661,326 (GRCm39) |
missense |
probably damaging |
0.99 |
R6868:Tmc6
|
UTSW |
11 |
117,665,143 (GRCm39) |
missense |
probably benign |
0.01 |
R7006:Tmc6
|
UTSW |
11 |
117,665,083 (GRCm39) |
missense |
probably damaging |
0.96 |
R7208:Tmc6
|
UTSW |
11 |
117,667,151 (GRCm39) |
missense |
probably benign |
0.41 |
R7210:Tmc6
|
UTSW |
11 |
117,666,670 (GRCm39) |
missense |
possibly damaging |
0.59 |
R8802:Tmc6
|
UTSW |
11 |
117,665,901 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8959:Tmc6
|
UTSW |
11 |
117,661,293 (GRCm39) |
critical splice donor site |
probably null |
|
R9002:Tmc6
|
UTSW |
11 |
117,661,308 (GRCm39) |
missense |
probably damaging |
1.00 |
R9621:Tmc6
|
UTSW |
11 |
117,669,995 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Tmc6
|
UTSW |
11 |
117,669,573 (GRCm39) |
missense |
probably damaging |
0.98 |
|