Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Bean1 |
T |
C |
8: 104,941,786 (GRCm39) |
S211P |
probably damaging |
Het |
Bltp1 |
T |
C |
3: 36,949,460 (GRCm39) |
S369P |
possibly damaging |
Het |
Camta1 |
A |
G |
4: 151,229,177 (GRCm39) |
S552P |
possibly damaging |
Het |
Cdh11 |
T |
C |
8: 103,400,594 (GRCm39) |
T125A |
possibly damaging |
Het |
Cdk5rap2 |
A |
T |
4: 70,194,952 (GRCm39) |
|
probably null |
Het |
Cenpc1 |
A |
G |
5: 86,195,446 (GRCm39) |
S108P |
possibly damaging |
Het |
Cfap20dc |
A |
T |
14: 8,536,609 (GRCm38) |
D199E |
probably damaging |
Het |
Cfap44 |
T |
A |
16: 44,294,227 (GRCm39) |
Y224* |
probably null |
Het |
Cfap46 |
G |
A |
7: 139,239,998 (GRCm39) |
|
probably benign |
Het |
Cntrl |
G |
A |
2: 35,017,993 (GRCm39) |
V468I |
probably benign |
Het |
Col6a6 |
C |
T |
9: 105,576,148 (GRCm39) |
V2071I |
possibly damaging |
Het |
D7Ertd443e |
C |
G |
7: 133,895,057 (GRCm39) |
Q591H |
probably damaging |
Het |
Dchs1 |
C |
T |
7: 105,404,059 (GRCm39) |
V2828M |
probably damaging |
Het |
Dzank1 |
T |
A |
2: 144,352,042 (GRCm39) |
|
probably benign |
Het |
Elmo1 |
C |
T |
13: 20,467,084 (GRCm39) |
T235I |
probably benign |
Het |
Elp3 |
A |
T |
14: 65,785,326 (GRCm39) |
F492I |
possibly damaging |
Het |
Espl1 |
A |
G |
15: 102,231,671 (GRCm39) |
S90G |
probably benign |
Het |
Fbxl20 |
T |
C |
11: 97,986,061 (GRCm39) |
|
probably benign |
Het |
Gm10722 |
T |
C |
9: 3,000,937 (GRCm39) |
C6R |
probably benign |
Het |
Got1 |
T |
C |
19: 43,493,280 (GRCm39) |
Y243C |
probably damaging |
Het |
Hipk1 |
G |
T |
3: 103,657,688 (GRCm39) |
H799N |
probably damaging |
Het |
Kif21a |
A |
T |
15: 90,855,345 (GRCm39) |
M673K |
probably benign |
Het |
Lama3 |
T |
A |
18: 12,628,415 (GRCm39) |
D1502E |
probably damaging |
Het |
Limk1 |
A |
G |
5: 134,705,640 (GRCm39) |
|
probably benign |
Het |
Myo5b |
A |
G |
18: 74,758,745 (GRCm39) |
Y242C |
probably damaging |
Het |
Naa12 |
G |
A |
18: 80,254,791 (GRCm39) |
M28I |
probably benign |
Het |
Ncbp1 |
T |
C |
4: 46,157,824 (GRCm39) |
V354A |
probably damaging |
Het |
Ncoa2 |
T |
C |
1: 13,217,130 (GRCm39) |
D1380G |
probably damaging |
Het |
Ntng1 |
A |
G |
3: 109,842,329 (GRCm39) |
I148T |
probably damaging |
Het |
Oas1d |
A |
T |
5: 121,057,233 (GRCm39) |
T280S |
probably damaging |
Het |
Or1e29 |
C |
T |
11: 73,667,866 (GRCm39) |
G96S |
probably benign |
Het |
Or4c15b |
T |
A |
2: 89,113,187 (GRCm39) |
M118L |
probably benign |
Het |
Pax7 |
T |
G |
4: 139,508,104 (GRCm39) |
D307A |
probably benign |
Het |
Pdxdc1 |
G |
A |
16: 13,656,210 (GRCm39) |
Q621* |
probably null |
Het |
Rab29 |
A |
T |
1: 131,795,469 (GRCm39) |
Y27F |
possibly damaging |
Het |
Rab3gap2 |
G |
A |
1: 184,999,265 (GRCm39) |
V991I |
probably benign |
Het |
Ric1 |
A |
G |
19: 29,548,165 (GRCm39) |
T278A |
probably benign |
Het |
Rufy4 |
T |
C |
1: 74,186,822 (GRCm39) |
C537R |
probably damaging |
Het |
Slc47a1 |
T |
C |
11: 61,235,339 (GRCm39) |
H498R |
probably benign |
Het |
Spmip6 |
T |
C |
4: 41,517,200 (GRCm39) |
|
probably benign |
Het |
Tas2r116 |
T |
C |
6: 132,833,113 (GRCm39) |
L238P |
probably damaging |
Het |
Tigd5 |
A |
T |
15: 75,782,364 (GRCm39) |
R252* |
probably null |
Het |
Tlr6 |
A |
G |
5: 65,112,247 (GRCm39) |
F220S |
possibly damaging |
Het |
Tmem106b |
C |
T |
6: 13,075,098 (GRCm39) |
T95I |
probably damaging |
Het |
Ubqlnl |
C |
T |
7: 103,798,925 (GRCm39) |
V191M |
probably benign |
Het |
Vmn1r174 |
A |
G |
7: 23,453,768 (GRCm39) |
I145V |
probably benign |
Het |
Vps26a |
T |
C |
10: 62,304,124 (GRCm39) |
M116V |
probably damaging |
Het |
|
Other mutations in Coq7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01639:Coq7
|
APN |
7 |
118,124,527 (GRCm39) |
missense |
probably damaging |
0.98 |
R0309:Coq7
|
UTSW |
7 |
118,128,940 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0628:Coq7
|
UTSW |
7 |
118,128,867 (GRCm39) |
missense |
probably damaging |
1.00 |
R1459:Coq7
|
UTSW |
7 |
118,109,260 (GRCm39) |
missense |
unknown |
|
R1535:Coq7
|
UTSW |
7 |
118,128,897 (GRCm39) |
missense |
possibly damaging |
0.48 |
R1612:Coq7
|
UTSW |
7 |
118,109,134 (GRCm39) |
missense |
unknown |
|
R2519:Coq7
|
UTSW |
7 |
118,109,371 (GRCm39) |
missense |
unknown |
|
R4095:Coq7
|
UTSW |
7 |
118,126,701 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4972:Coq7
|
UTSW |
7 |
118,109,340 (GRCm39) |
missense |
unknown |
|
R5183:Coq7
|
UTSW |
7 |
118,127,490 (GRCm39) |
intron |
probably benign |
|
R5579:Coq7
|
UTSW |
7 |
118,116,558 (GRCm39) |
missense |
unknown |
|
R5619:Coq7
|
UTSW |
7 |
118,126,709 (GRCm39) |
splice site |
probably benign |
|
R5789:Coq7
|
UTSW |
7 |
118,128,929 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6530:Coq7
|
UTSW |
7 |
118,124,558 (GRCm39) |
missense |
probably benign |
0.01 |
R6911:Coq7
|
UTSW |
7 |
118,109,385 (GRCm39) |
missense |
unknown |
|
R7212:Coq7
|
UTSW |
7 |
118,109,271 (GRCm39) |
missense |
unknown |
|
R7248:Coq7
|
UTSW |
7 |
118,128,897 (GRCm39) |
missense |
probably benign |
0.42 |
R7361:Coq7
|
UTSW |
7 |
118,128,798 (GRCm39) |
missense |
probably benign |
0.15 |
R7781:Coq7
|
UTSW |
7 |
118,125,111 (GRCm39) |
missense |
probably damaging |
1.00 |
R8039:Coq7
|
UTSW |
7 |
118,132,469 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8796:Coq7
|
UTSW |
7 |
118,126,640 (GRCm39) |
missense |
probably damaging |
0.96 |
R9166:Coq7
|
UTSW |
7 |
118,109,365 (GRCm39) |
missense |
unknown |
|
RF001:Coq7
|
UTSW |
7 |
118,132,405 (GRCm39) |
missense |
probably benign |
0.05 |
Z1177:Coq7
|
UTSW |
7 |
118,109,372 (GRCm39) |
missense |
unknown |
|
|