Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610008E11Rik |
A |
C |
10: 78,903,573 (GRCm39) |
C248G |
probably damaging |
Het |
4933427D14Rik |
A |
T |
11: 72,059,612 (GRCm39) |
V693E |
possibly damaging |
Het |
Abcc10 |
G |
T |
17: 46,638,735 (GRCm39) |
L42I |
probably damaging |
Het |
Alb |
A |
G |
5: 90,616,449 (GRCm39) |
E318G |
probably benign |
Het |
Alkal2 |
G |
T |
12: 30,934,850 (GRCm39) |
G23V |
probably damaging |
Het |
Aox4 |
T |
A |
1: 58,293,470 (GRCm39) |
C941S |
possibly damaging |
Het |
Aqp9 |
A |
G |
9: 71,045,495 (GRCm39) |
V38A |
probably benign |
Het |
AW209491 |
A |
G |
13: 14,812,349 (GRCm39) |
T401A |
probably damaging |
Het |
Ccdc57 |
C |
T |
11: 120,776,742 (GRCm39) |
A553T |
probably damaging |
Het |
Celf2 |
C |
T |
2: 6,551,914 (GRCm39) |
D522N |
probably benign |
Het |
Cfap210 |
A |
G |
2: 69,612,287 (GRCm39) |
|
probably null |
Het |
Cmpk2 |
A |
G |
12: 26,524,136 (GRCm39) |
N311S |
probably damaging |
Het |
Dcn |
T |
C |
10: 97,330,939 (GRCm39) |
I91T |
probably damaging |
Het |
Defa30 |
G |
A |
8: 21,624,709 (GRCm39) |
V11I |
probably benign |
Het |
Dnmt3a |
T |
A |
12: 3,946,965 (GRCm39) |
V397E |
probably benign |
Het |
Ehhadh |
G |
A |
16: 21,585,053 (GRCm39) |
A276V |
probably benign |
Het |
Fibcd1 |
T |
C |
2: 31,723,791 (GRCm39) |
|
probably benign |
Het |
Gpr156 |
A |
G |
16: 37,818,336 (GRCm39) |
D344G |
probably null |
Het |
H2-T5 |
A |
G |
17: 36,479,154 (GRCm39) |
S32P |
unknown |
Het |
Invs |
G |
T |
4: 48,426,199 (GRCm39) |
R995S |
possibly damaging |
Het |
Itpr3 |
T |
C |
17: 27,325,199 (GRCm39) |
M1264T |
possibly damaging |
Het |
Lzic |
C |
T |
4: 149,572,527 (GRCm39) |
A39V |
probably benign |
Het |
Marchf6 |
A |
G |
15: 31,482,650 (GRCm39) |
L516P |
possibly damaging |
Het |
Mecom |
C |
T |
3: 30,011,529 (GRCm39) |
E591K |
probably benign |
Het |
Mms22l |
T |
C |
4: 24,578,855 (GRCm39) |
I738T |
probably damaging |
Het |
Mroh2b |
G |
A |
15: 4,980,746 (GRCm39) |
W1438* |
probably null |
Het |
Mroh8 |
G |
T |
2: 157,071,879 (GRCm39) |
T542K |
possibly damaging |
Het |
Msl1 |
A |
T |
11: 98,691,074 (GRCm39) |
K416I |
probably damaging |
Het |
Myh15 |
C |
A |
16: 48,940,381 (GRCm39) |
T777N |
probably damaging |
Het |
Or51a10 |
A |
T |
7: 103,698,829 (GRCm39) |
V244E |
probably damaging |
Het |
Or5p5 |
G |
T |
7: 107,414,030 (GRCm39) |
V82F |
possibly damaging |
Het |
Or5p58 |
A |
G |
7: 107,694,450 (GRCm39) |
F109S |
probably benign |
Het |
Or6c70 |
A |
G |
10: 129,709,891 (GRCm39) |
V245A |
probably damaging |
Het |
Pdzk1ip1 |
T |
A |
4: 114,946,323 (GRCm39) |
V61D |
probably benign |
Het |
Plcxd1 |
A |
T |
5: 110,250,180 (GRCm39) |
M212L |
probably benign |
Het |
Pld1 |
A |
G |
3: 28,078,361 (GRCm39) |
T7A |
probably benign |
Het |
Ppm1n |
T |
C |
7: 19,012,302 (GRCm39) |
D310G |
probably damaging |
Het |
Prpf8 |
A |
G |
11: 75,390,641 (GRCm39) |
N1264S |
possibly damaging |
Het |
Pum2 |
T |
A |
12: 8,763,456 (GRCm39) |
N204K |
possibly damaging |
Het |
Recql5 |
G |
A |
11: 115,784,861 (GRCm39) |
T822I |
possibly damaging |
Het |
Rfc1 |
T |
C |
5: 65,436,077 (GRCm39) |
T656A |
probably benign |
Het |
Sacs |
T |
C |
14: 61,427,068 (GRCm39) |
Y159H |
possibly damaging |
Het |
Septin14 |
A |
G |
5: 129,773,194 (GRCm39) |
S148P |
probably damaging |
Het |
Slco1c1 |
T |
A |
6: 141,492,640 (GRCm39) |
M341K |
probably benign |
Het |
Smok2a |
T |
C |
17: 13,445,160 (GRCm39) |
S246P |
probably damaging |
Het |
Spata9 |
C |
A |
13: 76,125,890 (GRCm39) |
S124R |
possibly damaging |
Het |
Sri |
A |
G |
5: 8,113,317 (GRCm39) |
N103D |
probably damaging |
Het |
Sspo |
G |
A |
6: 48,459,622 (GRCm39) |
C3327Y |
probably damaging |
Het |
Trank1 |
A |
G |
9: 111,178,370 (GRCm39) |
M353V |
probably benign |
Het |
Trim80 |
A |
T |
11: 115,332,006 (GRCm39) |
E66V |
probably damaging |
Het |
Txndc16 |
A |
G |
14: 45,448,641 (GRCm39) |
L73P |
probably damaging |
Het |
Ugt2b34 |
T |
A |
5: 87,039,249 (GRCm39) |
M471L |
probably damaging |
Het |
Ush2a |
G |
T |
1: 188,178,899 (GRCm39) |
V1357L |
probably benign |
Het |
Usp15 |
G |
T |
10: 122,959,848 (GRCm39) |
P855T |
|
Het |
Uspl1 |
C |
T |
5: 149,135,491 (GRCm39) |
T290I |
possibly damaging |
Het |
Zbtb2 |
A |
C |
10: 4,319,084 (GRCm39) |
M314R |
probably benign |
Het |
Zcchc2 |
A |
G |
1: 105,959,844 (GRCm39) |
Y1151C |
probably damaging |
Het |
Zmat3 |
T |
C |
3: 32,395,670 (GRCm39) |
Y279C |
probably damaging |
Het |
|
Other mutations in Mical3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00569:Mical3
|
APN |
6 |
120,938,585 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL00718:Mical3
|
APN |
6 |
121,017,410 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL00940:Mical3
|
APN |
6 |
120,999,371 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL00973:Mical3
|
APN |
6 |
120,911,885 (GRCm39) |
splice site |
probably benign |
|
IGL01503:Mical3
|
APN |
6 |
120,935,537 (GRCm39) |
missense |
probably benign |
0.09 |
IGL01991:Mical3
|
APN |
6 |
120,912,172 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02794:Mical3
|
APN |
6 |
120,984,270 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02996:Mical3
|
APN |
6 |
120,935,519 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03105:Mical3
|
APN |
6 |
121,019,199 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03109:Mical3
|
APN |
6 |
120,986,085 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03236:Mical3
|
APN |
6 |
120,946,345 (GRCm39) |
missense |
probably benign |
0.00 |
P0028:Mical3
|
UTSW |
6 |
121,001,650 (GRCm39) |
missense |
probably benign |
0.33 |
R0244:Mical3
|
UTSW |
6 |
120,934,683 (GRCm39) |
missense |
probably benign |
0.00 |
R0494:Mical3
|
UTSW |
6 |
120,936,162 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0586:Mical3
|
UTSW |
6 |
121,006,602 (GRCm39) |
unclassified |
probably benign |
|
R1029:Mical3
|
UTSW |
6 |
120,911,639 (GRCm39) |
missense |
probably benign |
0.02 |
R1263:Mical3
|
UTSW |
6 |
120,929,430 (GRCm39) |
missense |
probably damaging |
0.99 |
R1507:Mical3
|
UTSW |
6 |
121,019,199 (GRCm39) |
missense |
probably benign |
0.36 |
R1527:Mical3
|
UTSW |
6 |
121,001,740 (GRCm39) |
missense |
probably damaging |
0.99 |
R1623:Mical3
|
UTSW |
6 |
121,001,768 (GRCm39) |
missense |
probably damaging |
0.99 |
R1680:Mical3
|
UTSW |
6 |
120,936,604 (GRCm39) |
missense |
probably benign |
0.09 |
R1697:Mical3
|
UTSW |
6 |
120,984,369 (GRCm39) |
missense |
possibly damaging |
0.84 |
R1817:Mical3
|
UTSW |
6 |
121,019,196 (GRCm39) |
missense |
probably benign |
0.06 |
R1875:Mical3
|
UTSW |
6 |
121,019,025 (GRCm39) |
missense |
probably damaging |
1.00 |
R1961:Mical3
|
UTSW |
6 |
120,959,568 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2004:Mical3
|
UTSW |
6 |
120,928,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R2093:Mical3
|
UTSW |
6 |
121,017,347 (GRCm39) |
missense |
probably damaging |
1.00 |
R2141:Mical3
|
UTSW |
6 |
121,008,095 (GRCm39) |
splice site |
probably null |
|
R2142:Mical3
|
UTSW |
6 |
121,008,095 (GRCm39) |
splice site |
probably null |
|
R2257:Mical3
|
UTSW |
6 |
121,010,696 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2404:Mical3
|
UTSW |
6 |
120,936,789 (GRCm39) |
missense |
probably benign |
0.01 |
R2419:Mical3
|
UTSW |
6 |
120,936,884 (GRCm39) |
missense |
probably benign |
|
R2509:Mical3
|
UTSW |
6 |
121,011,118 (GRCm39) |
missense |
probably damaging |
1.00 |
R3784:Mical3
|
UTSW |
6 |
120,998,298 (GRCm39) |
missense |
probably benign |
0.00 |
R4342:Mical3
|
UTSW |
6 |
120,911,799 (GRCm39) |
nonsense |
probably null |
|
R4343:Mical3
|
UTSW |
6 |
120,911,799 (GRCm39) |
nonsense |
probably null |
|
R4579:Mical3
|
UTSW |
6 |
120,935,660 (GRCm39) |
missense |
probably benign |
|
R4603:Mical3
|
UTSW |
6 |
120,911,799 (GRCm39) |
nonsense |
probably null |
|
R4605:Mical3
|
UTSW |
6 |
121,011,041 (GRCm39) |
nonsense |
probably null |
|
R4610:Mical3
|
UTSW |
6 |
120,911,799 (GRCm39) |
nonsense |
probably null |
|
R4611:Mical3
|
UTSW |
6 |
120,911,799 (GRCm39) |
nonsense |
probably null |
|
R4623:Mical3
|
UTSW |
6 |
120,938,586 (GRCm39) |
nonsense |
probably null |
|
R4669:Mical3
|
UTSW |
6 |
120,934,664 (GRCm39) |
missense |
probably damaging |
0.98 |
R4704:Mical3
|
UTSW |
6 |
120,935,649 (GRCm39) |
missense |
probably benign |
0.00 |
R4722:Mical3
|
UTSW |
6 |
121,015,486 (GRCm39) |
missense |
probably benign |
0.00 |
R4863:Mical3
|
UTSW |
6 |
121,010,748 (GRCm39) |
missense |
probably damaging |
0.99 |
R4878:Mical3
|
UTSW |
6 |
120,946,348 (GRCm39) |
missense |
possibly damaging |
0.51 |
R4885:Mical3
|
UTSW |
6 |
120,912,214 (GRCm39) |
missense |
probably damaging |
1.00 |
R4907:Mical3
|
UTSW |
6 |
120,984,259 (GRCm39) |
missense |
probably benign |
0.00 |
R5007:Mical3
|
UTSW |
6 |
121,015,030 (GRCm39) |
missense |
probably damaging |
0.98 |
R5299:Mical3
|
UTSW |
6 |
120,936,473 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5303:Mical3
|
UTSW |
6 |
120,936,941 (GRCm39) |
missense |
probably benign |
|
R5368:Mical3
|
UTSW |
6 |
120,936,434 (GRCm39) |
missense |
probably damaging |
1.00 |
R5955:Mical3
|
UTSW |
6 |
121,010,711 (GRCm39) |
missense |
probably damaging |
0.99 |
R5970:Mical3
|
UTSW |
6 |
120,935,232 (GRCm39) |
nonsense |
probably null |
|
R6000:Mical3
|
UTSW |
6 |
120,998,281 (GRCm39) |
missense |
probably benign |
0.06 |
R6101:Mical3
|
UTSW |
6 |
121,010,671 (GRCm39) |
missense |
probably damaging |
1.00 |
R6195:Mical3
|
UTSW |
6 |
120,993,796 (GRCm39) |
intron |
probably benign |
|
R6210:Mical3
|
UTSW |
6 |
121,017,478 (GRCm39) |
splice site |
probably null |
|
R6225:Mical3
|
UTSW |
6 |
120,935,684 (GRCm39) |
missense |
probably damaging |
0.98 |
R6258:Mical3
|
UTSW |
6 |
120,985,991 (GRCm39) |
missense |
probably damaging |
1.00 |
R6260:Mical3
|
UTSW |
6 |
120,985,991 (GRCm39) |
missense |
probably damaging |
1.00 |
R6349:Mical3
|
UTSW |
6 |
120,936,486 (GRCm39) |
missense |
probably benign |
|
R6352:Mical3
|
UTSW |
6 |
120,929,434 (GRCm39) |
missense |
probably damaging |
0.97 |
R6480:Mical3
|
UTSW |
6 |
121,011,236 (GRCm39) |
missense |
possibly damaging |
0.76 |
R6704:Mical3
|
UTSW |
6 |
120,986,761 (GRCm39) |
intron |
probably benign |
|
R6783:Mical3
|
UTSW |
6 |
120,935,786 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6925:Mical3
|
UTSW |
6 |
120,936,351 (GRCm39) |
missense |
probably benign |
0.05 |
R6960:Mical3
|
UTSW |
6 |
120,935,504 (GRCm39) |
missense |
probably damaging |
1.00 |
R7170:Mical3
|
UTSW |
6 |
120,950,694 (GRCm39) |
splice site |
probably null |
|
R7344:Mical3
|
UTSW |
6 |
121,013,505 (GRCm39) |
nonsense |
probably null |
|
R7414:Mical3
|
UTSW |
6 |
121,011,074 (GRCm39) |
missense |
probably damaging |
1.00 |
R7455:Mical3
|
UTSW |
6 |
120,935,705 (GRCm39) |
missense |
probably damaging |
1.00 |
R7649:Mical3
|
UTSW |
6 |
120,911,909 (GRCm39) |
missense |
probably damaging |
1.00 |
R8236:Mical3
|
UTSW |
6 |
120,989,504 (GRCm39) |
missense |
|
|
R8286:Mical3
|
UTSW |
6 |
120,998,149 (GRCm39) |
missense |
possibly damaging |
0.68 |
R8328:Mical3
|
UTSW |
6 |
120,912,138 (GRCm39) |
missense |
probably damaging |
0.98 |
R8354:Mical3
|
UTSW |
6 |
120,950,381 (GRCm39) |
missense |
probably damaging |
0.99 |
R8511:Mical3
|
UTSW |
6 |
121,015,513 (GRCm39) |
missense |
possibly damaging |
0.78 |
R8687:Mical3
|
UTSW |
6 |
120,936,438 (GRCm39) |
missense |
probably benign |
0.19 |
R8728:Mical3
|
UTSW |
6 |
120,950,514 (GRCm39) |
missense |
probably damaging |
0.99 |
R8925:Mical3
|
UTSW |
6 |
120,984,325 (GRCm39) |
missense |
probably benign |
0.00 |
R8927:Mical3
|
UTSW |
6 |
120,984,325 (GRCm39) |
missense |
probably benign |
0.00 |
R8986:Mical3
|
UTSW |
6 |
120,991,822 (GRCm39) |
missense |
|
|
R9026:Mical3
|
UTSW |
6 |
120,986,848 (GRCm39) |
splice site |
probably benign |
|
R9415:Mical3
|
UTSW |
6 |
120,934,712 (GRCm39) |
missense |
probably damaging |
1.00 |
R9515:Mical3
|
UTSW |
6 |
121,001,758 (GRCm39) |
missense |
probably damaging |
1.00 |
R9720:Mical3
|
UTSW |
6 |
120,935,238 (GRCm39) |
missense |
probably damaging |
0.99 |
R9777:Mical3
|
UTSW |
6 |
120,959,529 (GRCm39) |
missense |
possibly damaging |
0.91 |
U24488:Mical3
|
UTSW |
6 |
120,978,457 (GRCm39) |
missense |
possibly damaging |
0.90 |
Z1177:Mical3
|
UTSW |
6 |
120,936,689 (GRCm39) |
missense |
possibly damaging |
0.71 |
Z1190:Mical3
|
UTSW |
6 |
120,998,319 (GRCm39) |
critical splice acceptor site |
probably null |
|
|