Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930449I24Rik |
T |
A |
5: 146,441,750 (GRCm39) |
V299E |
probably damaging |
Het |
Adgrb3 |
T |
C |
1: 25,170,377 (GRCm39) |
I767V |
probably benign |
Het |
Ahnak2 |
G |
A |
12: 112,739,410 (GRCm39) |
T748I |
probably damaging |
Het |
Aoc3 |
T |
A |
11: 101,222,279 (GRCm39) |
L129M |
probably damaging |
Het |
Arhgef7 |
T |
A |
8: 11,874,667 (GRCm39) |
M540K |
possibly damaging |
Het |
Bod1l |
T |
A |
5: 41,974,009 (GRCm39) |
K2435M |
probably damaging |
Het |
Col11a1 |
A |
G |
3: 113,946,368 (GRCm39) |
|
probably null |
Het |
Creb5 |
G |
T |
6: 53,662,454 (GRCm39) |
M250I |
possibly damaging |
Het |
Dnase1l1 |
C |
T |
X: 73,320,644 (GRCm39) |
|
probably null |
Homo |
Dock10 |
A |
G |
1: 80,544,514 (GRCm39) |
I557T |
probably benign |
Het |
Efcab2 |
G |
A |
1: 178,264,969 (GRCm39) |
A12T |
probably benign |
Het |
Ehd1 |
A |
G |
19: 6,344,474 (GRCm39) |
N245D |
probably benign |
Het |
Erich3 |
T |
A |
3: 154,468,066 (GRCm39) |
D839E |
possibly damaging |
Het |
Fam13b |
T |
C |
18: 34,620,075 (GRCm39) |
T270A |
possibly damaging |
Het |
Fat2 |
A |
T |
11: 55,200,131 (GRCm39) |
L981Q |
probably damaging |
Het |
Fgfrl1 |
G |
A |
5: 108,852,838 (GRCm39) |
W89* |
probably null |
Het |
Fgfrl1 |
G |
T |
5: 108,852,839 (GRCm39) |
W89C |
probably damaging |
Het |
Gm10770 |
G |
A |
2: 150,021,569 (GRCm39) |
P11S |
probably damaging |
Het |
Gm10801 |
TC |
TCGGC |
2: 98,494,151 (GRCm39) |
|
probably benign |
Het |
Hdac3 |
A |
G |
18: 38,077,986 (GRCm39) |
V190A |
possibly damaging |
Het |
Htr1a |
A |
G |
13: 105,581,936 (GRCm39) |
N392S |
probably damaging |
Het |
Ift43 |
A |
G |
12: 86,185,592 (GRCm39) |
M59V |
probably benign |
Het |
Jakmip2 |
T |
C |
18: 43,699,014 (GRCm39) |
T482A |
probably damaging |
Het |
Myo1c |
C |
T |
11: 75,562,461 (GRCm39) |
P918S |
probably benign |
Het |
Nme8 |
A |
T |
13: 19,875,140 (GRCm39) |
|
probably null |
Het |
Or5h26 |
A |
G |
16: 58,988,209 (GRCm39) |
I99T |
probably benign |
Het |
Peg10 |
CCAACAACAACAACAACAACAACA |
CCAACAACAACAACAACAACA |
6: 4,754,276 (GRCm39) |
|
probably benign |
Het |
Plec |
A |
G |
15: 76,058,015 (GRCm39) |
F3996S |
probably damaging |
Het |
Ppfia4 |
A |
T |
1: 134,237,417 (GRCm39) |
Y961N |
probably damaging |
Het |
Rag1 |
G |
A |
2: 101,474,629 (GRCm39) |
P171L |
probably damaging |
Het |
Rbm24 |
A |
T |
13: 46,572,468 (GRCm39) |
|
probably benign |
Het |
Rsf1 |
A |
AAGGCGACGG |
7: 97,229,111 (GRCm39) |
|
probably null |
Het |
Rxfp3 |
T |
C |
15: 11,035,956 (GRCm39) |
Y472C |
probably damaging |
Het |
Sash1 |
T |
A |
10: 8,615,949 (GRCm39) |
I638F |
probably damaging |
Het |
Sh3glb2 |
G |
A |
2: 30,240,631 (GRCm39) |
R145W |
probably damaging |
Het |
Ston2 |
G |
T |
12: 91,614,870 (GRCm39) |
P513T |
probably damaging |
Het |
Sycp2 |
A |
G |
2: 178,022,721 (GRCm39) |
M470T |
probably damaging |
Het |
Syt10 |
C |
A |
15: 89,698,574 (GRCm39) |
D257Y |
probably damaging |
Het |
Tcfl5 |
G |
T |
2: 180,277,055 (GRCm39) |
L447I |
probably damaging |
Het |
Tlr11 |
T |
C |
14: 50,600,311 (GRCm39) |
W766R |
probably benign |
Het |
Usp33 |
T |
A |
3: 152,074,124 (GRCm39) |
D19E |
possibly damaging |
Het |
Vmn1r123 |
T |
A |
7: 20,896,868 (GRCm39) |
Y253* |
probably null |
Het |
Wdr55 |
G |
A |
18: 36,896,177 (GRCm39) |
G289D |
probably damaging |
Het |
Zfp523 |
C |
T |
17: 28,421,194 (GRCm39) |
T235M |
probably damaging |
Het |
|
Other mutations in Col5a3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00834:Col5a3
|
APN |
9 |
20,697,685 (GRCm39) |
nonsense |
probably null |
|
IGL01548:Col5a3
|
APN |
9 |
20,714,296 (GRCm39) |
splice site |
probably benign |
|
IGL02164:Col5a3
|
APN |
9 |
20,703,939 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02297:Col5a3
|
APN |
9 |
20,683,450 (GRCm39) |
missense |
unknown |
|
IGL02333:Col5a3
|
APN |
9 |
20,710,602 (GRCm39) |
missense |
unknown |
|
IGL02349:Col5a3
|
APN |
9 |
20,683,657 (GRCm39) |
missense |
unknown |
|
IGL02390:Col5a3
|
APN |
9 |
20,688,292 (GRCm39) |
missense |
unknown |
|
IGL02685:Col5a3
|
APN |
9 |
20,683,501 (GRCm39) |
missense |
unknown |
|
IGL02941:Col5a3
|
APN |
9 |
20,715,962 (GRCm39) |
missense |
unknown |
|
IGL03001:Col5a3
|
APN |
9 |
20,719,040 (GRCm39) |
missense |
unknown |
|
IGL03061:Col5a3
|
APN |
9 |
20,708,868 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03102:Col5a3
|
APN |
9 |
20,715,931 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03308:Col5a3
|
APN |
9 |
20,719,675 (GRCm39) |
missense |
unknown |
|
IGL03372:Col5a3
|
APN |
9 |
20,686,624 (GRCm39) |
missense |
unknown |
|
Guppy
|
UTSW |
9 |
20,690,329 (GRCm39) |
missense |
probably damaging |
1.00 |
minifish
|
UTSW |
9 |
20,696,882 (GRCm39) |
missense |
probably damaging |
0.99 |
R0002:Col5a3
|
UTSW |
9 |
20,721,152 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0012:Col5a3
|
UTSW |
9 |
20,688,404 (GRCm39) |
splice site |
probably benign |
|
R0316:Col5a3
|
UTSW |
9 |
20,686,621 (GRCm39) |
missense |
unknown |
|
R0357:Col5a3
|
UTSW |
9 |
20,719,064 (GRCm39) |
splice site |
probably benign |
|
R0360:Col5a3
|
UTSW |
9 |
20,683,762 (GRCm39) |
missense |
unknown |
|
R0483:Col5a3
|
UTSW |
9 |
20,693,777 (GRCm39) |
splice site |
probably null |
|
R0485:Col5a3
|
UTSW |
9 |
20,694,004 (GRCm39) |
missense |
probably damaging |
0.99 |
R0627:Col5a3
|
UTSW |
9 |
20,686,781 (GRCm39) |
missense |
unknown |
|
R1035:Col5a3
|
UTSW |
9 |
20,704,795 (GRCm39) |
splice site |
probably benign |
|
R1051:Col5a3
|
UTSW |
9 |
20,686,531 (GRCm39) |
missense |
unknown |
|
R1295:Col5a3
|
UTSW |
9 |
20,719,714 (GRCm39) |
missense |
unknown |
|
R1438:Col5a3
|
UTSW |
9 |
20,691,253 (GRCm39) |
missense |
probably damaging |
0.99 |
R1622:Col5a3
|
UTSW |
9 |
20,683,516 (GRCm39) |
missense |
unknown |
|
R1668:Col5a3
|
UTSW |
9 |
20,682,392 (GRCm39) |
missense |
unknown |
|
R1680:Col5a3
|
UTSW |
9 |
20,695,964 (GRCm39) |
critical splice donor site |
probably null |
|
R2112:Col5a3
|
UTSW |
9 |
20,721,073 (GRCm39) |
missense |
unknown |
|
R2149:Col5a3
|
UTSW |
9 |
20,682,566 (GRCm39) |
missense |
unknown |
|
R2159:Col5a3
|
UTSW |
9 |
20,682,606 (GRCm39) |
missense |
unknown |
|
R2939:Col5a3
|
UTSW |
9 |
20,706,954 (GRCm39) |
missense |
unknown |
|
R3236:Col5a3
|
UTSW |
9 |
20,718,949 (GRCm39) |
missense |
unknown |
|
R3845:Col5a3
|
UTSW |
9 |
20,719,673 (GRCm39) |
missense |
unknown |
|
R4598:Col5a3
|
UTSW |
9 |
20,685,855 (GRCm39) |
critical splice donor site |
probably null |
|
R4599:Col5a3
|
UTSW |
9 |
20,685,855 (GRCm39) |
critical splice donor site |
probably null |
|
R4611:Col5a3
|
UTSW |
9 |
20,726,192 (GRCm39) |
unclassified |
probably benign |
|
R4713:Col5a3
|
UTSW |
9 |
20,704,870 (GRCm39) |
missense |
unknown |
|
R4723:Col5a3
|
UTSW |
9 |
20,720,887 (GRCm39) |
missense |
unknown |
|
R5209:Col5a3
|
UTSW |
9 |
20,689,939 (GRCm39) |
intron |
probably benign |
|
R5336:Col5a3
|
UTSW |
9 |
20,710,597 (GRCm39) |
missense |
unknown |
|
R5378:Col5a3
|
UTSW |
9 |
20,708,872 (GRCm39) |
missense |
unknown |
|
R5614:Col5a3
|
UTSW |
9 |
20,694,772 (GRCm39) |
splice site |
probably benign |
|
R5775:Col5a3
|
UTSW |
9 |
20,712,368 (GRCm39) |
missense |
unknown |
|
R5895:Col5a3
|
UTSW |
9 |
20,683,738 (GRCm39) |
missense |
unknown |
|
R6048:Col5a3
|
UTSW |
9 |
20,718,915 (GRCm39) |
missense |
unknown |
|
R6265:Col5a3
|
UTSW |
9 |
20,705,060 (GRCm39) |
missense |
unknown |
|
R6372:Col5a3
|
UTSW |
9 |
20,696,882 (GRCm39) |
missense |
probably damaging |
0.99 |
R6520:Col5a3
|
UTSW |
9 |
20,685,348 (GRCm39) |
missense |
unknown |
|
R6558:Col5a3
|
UTSW |
9 |
20,690,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R6608:Col5a3
|
UTSW |
9 |
20,685,315 (GRCm39) |
missense |
unknown |
|
R6680:Col5a3
|
UTSW |
9 |
20,690,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R6696:Col5a3
|
UTSW |
9 |
20,690,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R6698:Col5a3
|
UTSW |
9 |
20,690,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R6700:Col5a3
|
UTSW |
9 |
20,690,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R6708:Col5a3
|
UTSW |
9 |
20,686,331 (GRCm39) |
missense |
unknown |
|
R6712:Col5a3
|
UTSW |
9 |
20,690,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R6714:Col5a3
|
UTSW |
9 |
20,690,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R6828:Col5a3
|
UTSW |
9 |
20,709,748 (GRCm39) |
missense |
unknown |
|
R7343:Col5a3
|
UTSW |
9 |
20,705,242 (GRCm39) |
critical splice donor site |
probably null |
|
R7431:Col5a3
|
UTSW |
9 |
20,682,131 (GRCm39) |
makesense |
probably null |
|
R7500:Col5a3
|
UTSW |
9 |
20,711,585 (GRCm39) |
missense |
unknown |
|
R7592:Col5a3
|
UTSW |
9 |
20,708,689 (GRCm39) |
missense |
unknown |
|
R7671:Col5a3
|
UTSW |
9 |
20,686,382 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7957:Col5a3
|
UTSW |
9 |
20,685,347 (GRCm39) |
missense |
unknown |
|
R8510:Col5a3
|
UTSW |
9 |
20,705,028 (GRCm39) |
missense |
unknown |
|
R8979:Col5a3
|
UTSW |
9 |
20,686,597 (GRCm39) |
missense |
unknown |
|
R9050:Col5a3
|
UTSW |
9 |
20,697,691 (GRCm39) |
missense |
probably damaging |
1.00 |
R9052:Col5a3
|
UTSW |
9 |
20,710,733 (GRCm39) |
missense |
unknown |
|
R9072:Col5a3
|
UTSW |
9 |
20,682,453 (GRCm39) |
missense |
unknown |
|
R9341:Col5a3
|
UTSW |
9 |
20,704,909 (GRCm39) |
missense |
unknown |
|
R9343:Col5a3
|
UTSW |
9 |
20,704,909 (GRCm39) |
missense |
unknown |
|
R9529:Col5a3
|
UTSW |
9 |
20,685,308 (GRCm39) |
critical splice donor site |
probably null |
|
R9562:Col5a3
|
UTSW |
9 |
20,714,429 (GRCm39) |
missense |
unknown |
|
R9781:Col5a3
|
UTSW |
9 |
20,721,272 (GRCm39) |
missense |
unknown |
|
Z1177:Col5a3
|
UTSW |
9 |
20,686,630 (GRCm39) |
missense |
unknown |
|
|