Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8b |
G |
A |
11: 109,870,711 (GRCm39) |
S147L |
probably benign |
Het |
Abraxas1 |
A |
G |
5: 100,957,649 (GRCm39) |
V190A |
probably benign |
Het |
Aoc1l2 |
A |
T |
6: 48,907,298 (GRCm39) |
K99N |
probably benign |
Het |
Aox1 |
T |
A |
1: 58,104,501 (GRCm39) |
H559Q |
possibly damaging |
Het |
Arhgap31 |
C |
T |
16: 38,422,988 (GRCm39) |
G1026D |
probably benign |
Het |
C1ra |
T |
C |
6: 124,490,819 (GRCm39) |
F71L |
probably benign |
Het |
C530025M09Rik |
T |
C |
2: 149,672,640 (GRCm39) |
H165R |
unknown |
Het |
Celf2 |
A |
T |
2: 6,726,404 (GRCm39) |
M43K |
probably damaging |
Het |
Celsr3 |
T |
C |
9: 108,706,961 (GRCm39) |
V1148A |
possibly damaging |
Het |
Cmya5 |
T |
G |
13: 93,229,884 (GRCm39) |
K1735Q |
probably benign |
Het |
Cntln |
A |
C |
4: 84,968,318 (GRCm39) |
M846L |
probably benign |
Het |
Cntn5 |
T |
C |
9: 9,673,817 (GRCm39) |
T762A |
probably benign |
Het |
Col12a1 |
T |
C |
9: 79,589,364 (GRCm39) |
T1064A |
probably benign |
Het |
Cyc1 |
T |
C |
15: 76,229,273 (GRCm39) |
V211A |
possibly damaging |
Het |
Ddx56 |
A |
G |
11: 6,215,516 (GRCm39) |
S296P |
probably damaging |
Het |
Deptor |
A |
T |
15: 54,975,798 (GRCm39) |
|
probably benign |
Het |
Ezh1 |
C |
T |
11: 101,094,265 (GRCm39) |
R409H |
possibly damaging |
Het |
Fam228b |
T |
A |
12: 4,798,147 (GRCm39) |
E190V |
probably damaging |
Het |
Fkbp15 |
A |
T |
4: 62,237,210 (GRCm39) |
L635H |
probably damaging |
Het |
Frem1 |
G |
A |
4: 82,901,622 (GRCm39) |
L969F |
possibly damaging |
Het |
Gabrg2 |
T |
C |
11: 41,858,433 (GRCm39) |
R232G |
probably benign |
Het |
Gpr26 |
G |
A |
7: 131,568,963 (GRCm39) |
D103N |
probably damaging |
Het |
Grid2ip |
T |
G |
5: 143,361,103 (GRCm39) |
|
probably null |
Het |
Ints7 |
T |
C |
1: 191,351,793 (GRCm39) |
V834A |
probably damaging |
Het |
Kcnh7 |
T |
A |
2: 62,667,612 (GRCm39) |
H309L |
probably benign |
Het |
Mael |
T |
C |
1: 166,053,282 (GRCm39) |
E241G |
probably damaging |
Het |
Neb |
T |
A |
2: 52,122,277 (GRCm39) |
E584V |
|
Het |
Nexn |
C |
T |
3: 151,959,401 (GRCm39) |
V23M |
probably damaging |
Het |
Npas1 |
T |
C |
7: 16,190,231 (GRCm39) |
|
probably null |
Het |
Or51f1 |
T |
C |
7: 102,506,014 (GRCm39) |
I158M |
probably benign |
Het |
Pcdh17 |
T |
G |
14: 84,685,522 (GRCm39) |
V663G |
probably damaging |
Het |
Pga5 |
C |
T |
19: 10,646,897 (GRCm39) |
G303S |
probably damaging |
Het |
Poln |
T |
A |
5: 34,164,842 (GRCm39) |
K844N |
probably damaging |
Het |
Prkar1b |
C |
T |
5: 139,036,442 (GRCm39) |
D227N |
probably damaging |
Het |
Proc |
T |
A |
18: 32,256,336 (GRCm39) |
I444F |
probably damaging |
Het |
Ptprn |
G |
T |
1: 75,229,135 (GRCm39) |
H791N |
probably benign |
Het |
Ror1 |
T |
C |
4: 100,191,709 (GRCm39) |
S160P |
probably benign |
Het |
Satb2 |
T |
A |
1: 56,870,797 (GRCm39) |
|
probably null |
Het |
Slc43a3 |
C |
T |
2: 84,780,771 (GRCm39) |
A332V |
probably benign |
Het |
Sp100 |
G |
A |
1: 85,627,336 (GRCm39) |
V410M |
probably damaging |
Het |
Srgap2 |
T |
C |
1: 131,217,346 (GRCm39) |
T989A |
probably benign |
Het |
Ssc5d |
T |
C |
7: 4,930,283 (GRCm39) |
|
probably null |
Het |
Tll2 |
A |
G |
19: 41,116,997 (GRCm39) |
Y273H |
probably benign |
Het |
Tub |
T |
C |
7: 108,626,211 (GRCm39) |
V295A |
possibly damaging |
Het |
Unc13b |
T |
A |
4: 43,172,512 (GRCm39) |
D1113E |
unknown |
Het |
Usp9y |
C |
A |
Y: 1,364,776 (GRCm39) |
M1012I |
probably benign |
Het |
Vmn1r238 |
A |
G |
18: 3,122,676 (GRCm39) |
V246A |
probably damaging |
Het |
Vmn2r88 |
T |
G |
14: 51,656,197 (GRCm39) |
V802G |
|
Het |
Wnt7b |
T |
C |
15: 85,443,175 (GRCm39) |
Q76R |
probably damaging |
Het |
Zan |
T |
C |
5: 137,389,917 (GRCm39) |
R4852G |
unknown |
Het |
Zfp618 |
A |
T |
4: 63,051,258 (GRCm39) |
T680S |
probably damaging |
Het |
Zfp784 |
T |
A |
7: 5,041,338 (GRCm39) |
D25V |
unknown |
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 |
|
R3950:Col11a1
|
UTSW |
3 |
113,915,094 (GRCm39) |
critical splice donor site |
probably null |
|
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 |
|
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 |
|
|