Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4932414N04Rik |
T |
C |
2: 68,494,747 (GRCm39) |
|
probably null |
Het |
Ahnak2 |
A |
T |
12: 112,749,409 (GRCm39) |
I186N |
probably damaging |
Het |
Appbp2 |
A |
G |
11: 85,085,532 (GRCm39) |
I458T |
probably damaging |
Het |
Arhgef25 |
T |
C |
10: 127,021,013 (GRCm39) |
Y291C |
probably damaging |
Het |
Ate1 |
T |
C |
7: 130,069,022 (GRCm39) |
Y415C |
probably damaging |
Het |
B4galt4 |
G |
T |
16: 38,588,384 (GRCm39) |
A72S |
probably benign |
Het |
C3 |
T |
C |
17: 57,532,286 (GRCm39) |
R178G |
probably benign |
Het |
Cdh23 |
T |
C |
10: 60,493,105 (GRCm39) |
Y3C |
probably benign |
Het |
Col22a1 |
A |
G |
15: 71,849,207 (GRCm39) |
F294L |
possibly damaging |
Het |
Dera |
A |
G |
6: 137,814,118 (GRCm39) |
Y100C |
probably damaging |
Het |
Dync2h1 |
A |
T |
9: 7,112,061 (GRCm39) |
Y276* |
probably null |
Het |
Eea1 |
A |
T |
10: 95,877,996 (GRCm39) |
N1389I |
probably damaging |
Het |
Epha4 |
A |
T |
1: 77,376,353 (GRCm39) |
Y509N |
probably damaging |
Het |
Fat3 |
G |
A |
9: 15,909,567 (GRCm39) |
S2145F |
probably damaging |
Het |
Fezf1 |
T |
A |
6: 23,247,419 (GRCm39) |
K219* |
probably null |
Het |
Fsd1 |
G |
A |
17: 56,302,517 (GRCm39) |
|
probably null |
Het |
Haspin |
A |
G |
11: 73,027,221 (GRCm39) |
Y623H |
probably damaging |
Het |
Hsd3b1 |
C |
T |
3: 98,763,454 (GRCm39) |
V56M |
possibly damaging |
Het |
Hyou1 |
C |
T |
9: 44,296,524 (GRCm39) |
T483I |
probably damaging |
Het |
Kdm2a |
A |
G |
19: 4,393,260 (GRCm39) |
L365S |
possibly damaging |
Het |
Kdm6b |
G |
T |
11: 69,296,441 (GRCm39) |
P609T |
probably damaging |
Het |
Klhl18 |
T |
A |
9: 110,257,970 (GRCm39) |
Y490F |
probably damaging |
Het |
Ky |
C |
T |
9: 102,419,627 (GRCm39) |
Q545* |
probably null |
Het |
L1td1 |
T |
C |
4: 98,625,590 (GRCm39) |
L595P |
probably benign |
Het |
Map3k20 |
T |
G |
2: 72,268,644 (GRCm39) |
I550M |
probably damaging |
Het |
Mug1 |
T |
A |
6: 121,855,489 (GRCm39) |
V941E |
probably damaging |
Het |
Ndst1 |
T |
C |
18: 60,830,211 (GRCm39) |
N633S |
probably benign |
Het |
Ninl |
A |
T |
2: 150,794,408 (GRCm39) |
I740K |
possibly damaging |
Het |
Npepl1 |
A |
G |
2: 173,962,906 (GRCm39) |
N431D |
probably damaging |
Het |
Or5w10 |
T |
C |
2: 87,375,409 (GRCm39) |
T160A |
probably damaging |
Het |
Pacs2 |
T |
C |
12: 113,024,733 (GRCm39) |
S408P |
probably damaging |
Het |
Pard6b |
C |
T |
2: 167,941,114 (GRCm39) |
T367I |
probably damaging |
Het |
Pcdhga7 |
A |
G |
18: 37,849,568 (GRCm39) |
E525G |
probably damaging |
Het |
Pctp |
A |
G |
11: 89,878,144 (GRCm39) |
I130T |
probably benign |
Het |
Pcx |
C |
T |
19: 4,667,995 (GRCm39) |
H506Y |
probably benign |
Het |
Pdhx |
A |
G |
2: 102,865,586 (GRCm39) |
S199P |
probably damaging |
Het |
Pdia2 |
C |
A |
17: 26,416,590 (GRCm39) |
|
probably null |
Het |
Pif1 |
C |
A |
9: 65,499,116 (GRCm39) |
N445K |
probably damaging |
Het |
Prickle4 |
T |
C |
17: 47,999,507 (GRCm39) |
K349E |
probably benign |
Het |
Ptch1 |
T |
G |
13: 63,672,773 (GRCm39) |
E944A |
probably benign |
Het |
Ptpdc1 |
A |
T |
13: 48,742,670 (GRCm39) |
M173K |
probably damaging |
Het |
Rb1 |
A |
G |
14: 73,500,102 (GRCm39) |
L515P |
probably damaging |
Het |
Rcvrn |
A |
G |
11: 67,590,877 (GRCm39) |
K154E |
probably damaging |
Het |
Ros1 |
C |
T |
10: 51,942,484 (GRCm39) |
V2059I |
probably damaging |
Het |
Rtn4ip1 |
T |
A |
10: 43,785,893 (GRCm39) |
|
probably null |
Het |
Sema5a |
T |
C |
15: 32,689,484 (GRCm39) |
Y1050H |
probably damaging |
Het |
Slc25a28 |
C |
T |
19: 43,652,708 (GRCm39) |
V318I |
probably benign |
Het |
Srek1 |
G |
A |
13: 103,881,403 (GRCm39) |
R408W |
unknown |
Het |
Synrg |
C |
T |
11: 83,880,641 (GRCm39) |
T444I |
probably damaging |
Het |
Ticrr |
T |
C |
7: 79,331,817 (GRCm39) |
L776S |
probably damaging |
Het |
Tmem127 |
T |
C |
2: 127,090,577 (GRCm39) |
L31P |
probably damaging |
Het |
Tmprss15 |
T |
A |
16: 78,870,074 (GRCm39) |
T190S |
probably benign |
Het |
Trip10 |
T |
A |
17: 57,560,411 (GRCm39) |
|
probably null |
Het |
Ttc6 |
A |
G |
12: 57,696,292 (GRCm39) |
Y31C |
probably damaging |
Het |
Unc80 |
A |
T |
1: 66,661,729 (GRCm39) |
H1718L |
possibly damaging |
Het |
Zbtb38 |
A |
G |
9: 96,569,599 (GRCm39) |
F495S |
probably damaging |
Het |
Zfp280d |
G |
T |
9: 72,203,301 (GRCm39) |
Q16H |
possibly damaging |
Het |
Zfp521 |
A |
G |
18: 13,979,403 (GRCm39) |
S337P |
probably damaging |
Het |
Zswim9 |
T |
A |
7: 12,995,503 (GRCm39) |
T218S |
possibly damaging |
Het |
|
Other mutations in Col11a1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00474:Col11a1
|
APN |
3 |
113,860,182 (GRCm39) |
missense |
unknown |
|
IGL00578:Col11a1
|
APN |
3 |
113,987,755 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL00742:Col11a1
|
APN |
3 |
113,917,964 (GRCm39) |
missense |
unknown |
|
IGL01014:Col11a1
|
APN |
3 |
113,917,458 (GRCm39) |
splice site |
probably benign |
|
IGL01099:Col11a1
|
APN |
3 |
113,905,690 (GRCm39) |
nonsense |
probably null |
|
IGL01129:Col11a1
|
APN |
3 |
113,979,522 (GRCm39) |
splice site |
probably benign |
|
IGL01474:Col11a1
|
APN |
3 |
114,010,783 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL01884:Col11a1
|
APN |
3 |
113,860,191 (GRCm39) |
missense |
unknown |
|
IGL02104:Col11a1
|
APN |
3 |
113,975,046 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02715:Col11a1
|
APN |
3 |
113,923,058 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02978:Col11a1
|
APN |
3 |
113,855,211 (GRCm39) |
missense |
unknown |
|
IGL03203:Col11a1
|
APN |
3 |
114,005,733 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL03240:Col11a1
|
APN |
3 |
114,010,859 (GRCm39) |
splice site |
probably null |
|
IGL03357:Col11a1
|
APN |
3 |
113,987,740 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03390:Col11a1
|
APN |
3 |
113,883,902 (GRCm39) |
missense |
unknown |
|
gluon
|
UTSW |
3 |
114,010,819 (GRCm39) |
utr 3 prime |
probably benign |
|
uncovered
|
UTSW |
3 |
113,906,116 (GRCm39) |
unclassified |
probably benign |
|
weakforce
|
UTSW |
3 |
113,907,249 (GRCm39) |
missense |
unknown |
|
R0110:Col11a1
|
UTSW |
3 |
113,899,105 (GRCm39) |
splice site |
probably benign |
|
R0144:Col11a1
|
UTSW |
3 |
113,907,243 (GRCm39) |
missense |
unknown |
|
R0432:Col11a1
|
UTSW |
3 |
113,999,550 (GRCm39) |
splice site |
probably benign |
|
R0468:Col11a1
|
UTSW |
3 |
114,010,707 (GRCm39) |
utr 3 prime |
probably benign |
|
R0510:Col11a1
|
UTSW |
3 |
113,899,105 (GRCm39) |
splice site |
probably benign |
|
R0535:Col11a1
|
UTSW |
3 |
113,855,184 (GRCm39) |
missense |
unknown |
|
R0608:Col11a1
|
UTSW |
3 |
114,012,364 (GRCm39) |
utr 3 prime |
probably benign |
|
R0826:Col11a1
|
UTSW |
3 |
113,932,414 (GRCm39) |
missense |
unknown |
|
R0827:Col11a1
|
UTSW |
3 |
113,932,414 (GRCm39) |
missense |
unknown |
|
R0862:Col11a1
|
UTSW |
3 |
113,932,414 (GRCm39) |
missense |
unknown |
|
R0863:Col11a1
|
UTSW |
3 |
113,932,414 (GRCm39) |
missense |
unknown |
|
R0926:Col11a1
|
UTSW |
3 |
113,883,829 (GRCm39) |
missense |
unknown |
|
R0980:Col11a1
|
UTSW |
3 |
113,932,414 (GRCm39) |
missense |
unknown |
|
R0981:Col11a1
|
UTSW |
3 |
113,932,414 (GRCm39) |
missense |
unknown |
|
R1004:Col11a1
|
UTSW |
3 |
113,888,671 (GRCm39) |
splice site |
probably benign |
|
R1037:Col11a1
|
UTSW |
3 |
113,987,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R1171:Col11a1
|
UTSW |
3 |
113,860,213 (GRCm39) |
missense |
unknown |
|
R1316:Col11a1
|
UTSW |
3 |
113,932,619 (GRCm39) |
splice site |
probably null |
|
R1324:Col11a1
|
UTSW |
3 |
113,824,565 (GRCm39) |
missense |
unknown |
|
R1338:Col11a1
|
UTSW |
3 |
114,010,644 (GRCm39) |
utr 3 prime |
probably benign |
|
R1513:Col11a1
|
UTSW |
3 |
113,890,803 (GRCm39) |
missense |
unknown |
|
R1528:Col11a1
|
UTSW |
3 |
114,010,644 (GRCm39) |
utr 3 prime |
probably benign |
|
R1567:Col11a1
|
UTSW |
3 |
113,932,261 (GRCm39) |
missense |
unknown |
|
R1596:Col11a1
|
UTSW |
3 |
113,946,262 (GRCm39) |
utr 3 prime |
probably benign |
|
R1605:Col11a1
|
UTSW |
3 |
113,925,290 (GRCm39) |
missense |
probably damaging |
1.00 |
R1624:Col11a1
|
UTSW |
3 |
113,951,804 (GRCm39) |
missense |
probably damaging |
0.97 |
R1626:Col11a1
|
UTSW |
3 |
113,925,218 (GRCm39) |
missense |
probably damaging |
1.00 |
R1666:Col11a1
|
UTSW |
3 |
113,855,184 (GRCm39) |
missense |
unknown |
|
R1806:Col11a1
|
UTSW |
3 |
113,951,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R2001:Col11a1
|
UTSW |
3 |
113,958,942 (GRCm39) |
splice site |
probably null |
|
R2084:Col11a1
|
UTSW |
3 |
113,951,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R2085:Col11a1
|
UTSW |
3 |
113,951,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R3926:Col11a1
|
UTSW |
3 |
113,883,773 (GRCm39) |
splice site |
probably benign |
|
R3970:Col11a1
|
UTSW |
3 |
113,890,838 (GRCm39) |
missense |
unknown |
|
R4171:Col11a1
|
UTSW |
3 |
114,001,863 (GRCm39) |
missense |
probably damaging |
0.99 |
R4175:Col11a1
|
UTSW |
3 |
114,001,872 (GRCm39) |
missense |
possibly damaging |
0.83 |
R4176:Col11a1
|
UTSW |
3 |
114,001,872 (GRCm39) |
missense |
possibly damaging |
0.83 |
R4413:Col11a1
|
UTSW |
3 |
113,901,965 (GRCm39) |
missense |
unknown |
|
R4540:Col11a1
|
UTSW |
3 |
113,890,815 (GRCm39) |
missense |
unknown |
|
R5210:Col11a1
|
UTSW |
3 |
113,946,806 (GRCm39) |
missense |
probably damaging |
1.00 |
R5250:Col11a1
|
UTSW |
3 |
114,010,819 (GRCm39) |
utr 3 prime |
probably benign |
|
R5335:Col11a1
|
UTSW |
3 |
113,888,889 (GRCm39) |
missense |
unknown |
|
R5344:Col11a1
|
UTSW |
3 |
114,002,011 (GRCm39) |
critical splice donor site |
probably null |
|
R5394:Col11a1
|
UTSW |
3 |
113,987,833 (GRCm39) |
splice site |
probably null |
|
R5687:Col11a1
|
UTSW |
3 |
114,010,752 (GRCm39) |
utr 3 prime |
probably benign |
|
R5708:Col11a1
|
UTSW |
3 |
113,890,743 (GRCm39) |
missense |
unknown |
|
R5763:Col11a1
|
UTSW |
3 |
113,888,245 (GRCm39) |
intron |
probably benign |
|
R5792:Col11a1
|
UTSW |
3 |
113,925,242 (GRCm39) |
missense |
probably damaging |
1.00 |
R6259:Col11a1
|
UTSW |
3 |
113,932,096 (GRCm39) |
missense |
probably benign |
|
R6679:Col11a1
|
UTSW |
3 |
113,946,368 (GRCm39) |
splice site |
probably null |
|
R6738:Col11a1
|
UTSW |
3 |
113,906,116 (GRCm39) |
unclassified |
probably benign |
|
R6747:Col11a1
|
UTSW |
3 |
114,006,099 (GRCm39) |
nonsense |
probably null |
|
R6808:Col11a1
|
UTSW |
3 |
113,888,593 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6861:Col11a1
|
UTSW |
3 |
113,961,141 (GRCm39) |
missense |
probably damaging |
1.00 |
R7201:Col11a1
|
UTSW |
3 |
113,883,806 (GRCm39) |
missense |
unknown |
|
R7264:Col11a1
|
UTSW |
3 |
113,979,248 (GRCm39) |
missense |
unknown |
|
R7393:Col11a1
|
UTSW |
3 |
113,890,755 (GRCm39) |
missense |
unknown |
|
R7445:Col11a1
|
UTSW |
3 |
113,987,578 (GRCm39) |
missense |
unknown |
|
R7479:Col11a1
|
UTSW |
3 |
113,896,218 (GRCm39) |
missense |
unknown |
|
R7548:Col11a1
|
UTSW |
3 |
113,917,409 (GRCm39) |
missense |
unknown |
|
R7683:Col11a1
|
UTSW |
3 |
113,907,385 (GRCm39) |
missense |
unknown |
|
R7747:Col11a1
|
UTSW |
3 |
113,896,221 (GRCm39) |
missense |
unknown |
|
R7809:Col11a1
|
UTSW |
3 |
113,890,835 (GRCm39) |
missense |
unknown |
|
R7951:Col11a1
|
UTSW |
3 |
113,888,864 (GRCm39) |
missense |
unknown |
|
R8057:Col11a1
|
UTSW |
3 |
113,925,263 (GRCm39) |
missense |
unknown |
|
R8134:Col11a1
|
UTSW |
3 |
114,012,435 (GRCm39) |
missense |
unknown |
|
R8139:Col11a1
|
UTSW |
3 |
113,890,698 (GRCm39) |
missense |
unknown |
|
R8243:Col11a1
|
UTSW |
3 |
113,855,141 (GRCm39) |
missense |
unknown |
|
R8324:Col11a1
|
UTSW |
3 |
113,958,059 (GRCm39) |
missense |
probably damaging |
1.00 |
R8346:Col11a1
|
UTSW |
3 |
114,005,818 (GRCm39) |
missense |
unknown |
|
R8480:Col11a1
|
UTSW |
3 |
113,975,043 (GRCm39) |
missense |
probably benign |
0.04 |
R9113:Col11a1
|
UTSW |
3 |
113,888,192 (GRCm39) |
nonsense |
probably null |
|
R9122:Col11a1
|
UTSW |
3 |
113,907,249 (GRCm39) |
missense |
unknown |
|
R9137:Col11a1
|
UTSW |
3 |
113,855,172 (GRCm39) |
missense |
unknown |
|
R9224:Col11a1
|
UTSW |
3 |
114,001,929 (GRCm39) |
missense |
unknown |
|
R9264:Col11a1
|
UTSW |
3 |
114,005,809 (GRCm39) |
missense |
unknown |
|
R9272:Col11a1
|
UTSW |
3 |
113,901,948 (GRCm39) |
nonsense |
probably null |
|
R9382:Col11a1
|
UTSW |
3 |
113,899,046 (GRCm39) |
missense |
unknown |
|
R9492:Col11a1
|
UTSW |
3 |
114,005,752 (GRCm39) |
missense |
probably benign |
0.39 |
RF002:Col11a1
|
UTSW |
3 |
114,010,650 (GRCm39) |
missense |
unknown |
|
X0018:Col11a1
|
UTSW |
3 |
113,905,882 (GRCm39) |
unclassified |
probably benign |
|
Z1177:Col11a1
|
UTSW |
3 |
113,958,884 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1177:Col11a1
|
UTSW |
3 |
113,932,570 (GRCm39) |
missense |
unknown |
|
|