Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcg3 |
A |
G |
5: 105,117,259 (GRCm39) |
|
probably null |
Het |
Ak4 |
T |
C |
4: 101,320,859 (GRCm39) |
Y223H |
probably benign |
Het |
Cerk |
T |
C |
15: 86,040,869 (GRCm39) |
|
probably null |
Het |
Chd1l |
G |
A |
3: 97,494,483 (GRCm39) |
A399V |
probably damaging |
Het |
Cpeb3 |
T |
G |
19: 37,022,089 (GRCm39) |
I569L |
possibly damaging |
Het |
Dis3 |
A |
T |
14: 99,323,358 (GRCm39) |
N569K |
probably benign |
Het |
Erich5 |
T |
C |
15: 34,471,602 (GRCm39) |
L277P |
probably benign |
Het |
Fam171b |
T |
C |
2: 83,690,804 (GRCm39) |
S256P |
probably damaging |
Het |
Glis3 |
A |
G |
19: 28,294,761 (GRCm39) |
V679A |
probably benign |
Het |
Gm10549 |
C |
A |
18: 33,597,358 (GRCm39) |
|
probably benign |
Het |
Gm8212 |
A |
G |
14: 44,438,636 (GRCm39) |
|
probably benign |
Het |
Grin2b |
T |
A |
6: 135,710,025 (GRCm39) |
T1174S |
probably benign |
Het |
Hipk2 |
T |
C |
6: 38,675,446 (GRCm39) |
Y1045C |
probably damaging |
Het |
Hsf2 |
C |
T |
10: 57,362,676 (GRCm39) |
|
probably benign |
Het |
Ighv1-4 |
G |
T |
12: 114,451,015 (GRCm39) |
A31E |
probably benign |
Het |
Il11ra1 |
A |
G |
4: 41,765,279 (GRCm39) |
K151E |
possibly damaging |
Het |
Inpp4b |
T |
A |
8: 82,768,546 (GRCm39) |
M685K |
probably damaging |
Het |
Itga4 |
T |
A |
2: 79,109,429 (GRCm39) |
D209E |
probably damaging |
Het |
L1td1 |
T |
C |
4: 98,625,328 (GRCm39) |
S508P |
probably damaging |
Het |
Lrrn3 |
G |
A |
12: 41,503,205 (GRCm39) |
R371C |
probably damaging |
Het |
Nbeal1 |
A |
G |
1: 60,277,878 (GRCm39) |
T755A |
probably benign |
Het |
Odad2 |
A |
G |
18: 7,214,617 (GRCm39) |
V728A |
probably benign |
Het |
Or10al7 |
T |
A |
17: 38,366,043 (GRCm39) |
Y138F |
probably damaging |
Het |
Or2n1 |
T |
C |
17: 38,486,410 (GRCm39) |
V145A |
probably benign |
Het |
Phf24 |
A |
G |
4: 42,933,960 (GRCm39) |
D14G |
probably damaging |
Het |
Prkd1 |
A |
T |
12: 50,441,443 (GRCm39) |
C314* |
probably null |
Het |
Rnf187 |
A |
T |
11: 58,827,986 (GRCm39) |
S155T |
possibly damaging |
Het |
Rsf1 |
G |
GACGGCGGCA |
7: 97,229,116 (GRCm39) |
|
probably benign |
Homo |
Scn10a |
A |
G |
9: 119,453,181 (GRCm39) |
I1237T |
possibly damaging |
Het |
Sec16a |
T |
C |
2: 26,328,583 (GRCm39) |
N1144S |
probably benign |
Het |
Sh3tc2 |
T |
C |
18: 62,101,081 (GRCm39) |
V58A |
probably damaging |
Het |
Slc37a3 |
T |
C |
6: 39,334,394 (GRCm39) |
*84W |
probably null |
Het |
Trpm2 |
T |
A |
10: 77,774,202 (GRCm39) |
I466F |
probably damaging |
Het |
Vmn2r108 |
T |
A |
17: 20,691,660 (GRCm39) |
I288F |
probably damaging |
Het |
Vmn2r67 |
T |
C |
7: 84,801,124 (GRCm39) |
T271A |
probably benign |
Het |
Vsig10l |
A |
G |
7: 43,120,397 (GRCm39) |
|
probably null |
Het |
Wdr95 |
A |
G |
5: 149,504,268 (GRCm39) |
|
probably null |
Het |
Zfp960 |
T |
C |
17: 17,308,639 (GRCm39) |
I451T |
probably benign |
Het |
|
Other mutations in Col18a1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00952:Col18a1
|
APN |
10 |
76,905,813 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01023:Col18a1
|
APN |
10 |
76,906,809 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01304:Col18a1
|
APN |
10 |
76,911,975 (GRCm39) |
unclassified |
probably benign |
|
IGL01519:Col18a1
|
APN |
10 |
76,895,157 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02217:Col18a1
|
APN |
10 |
76,889,132 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02275:Col18a1
|
APN |
10 |
76,895,217 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02283:Col18a1
|
APN |
10 |
76,948,943 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL02492:Col18a1
|
APN |
10 |
76,907,855 (GRCm39) |
splice site |
probably benign |
|
IGL02673:Col18a1
|
APN |
10 |
76,894,997 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02710:Col18a1
|
APN |
10 |
76,949,146 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02850:Col18a1
|
APN |
10 |
76,932,300 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03085:Col18a1
|
APN |
10 |
76,895,015 (GRCm39) |
splice site |
probably benign |
|
IGL03102:Col18a1
|
APN |
10 |
76,903,457 (GRCm39) |
splice site |
probably benign |
|
IGL03139:Col18a1
|
APN |
10 |
76,949,177 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL03181:Col18a1
|
APN |
10 |
76,891,532 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03183:Col18a1
|
APN |
10 |
76,909,588 (GRCm39) |
missense |
probably damaging |
1.00 |
R0039:Col18a1
|
UTSW |
10 |
76,913,002 (GRCm39) |
missense |
probably damaging |
1.00 |
R0180:Col18a1
|
UTSW |
10 |
76,932,351 (GRCm39) |
missense |
probably benign |
0.33 |
R0225:Col18a1
|
UTSW |
10 |
76,924,748 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0335:Col18a1
|
UTSW |
10 |
76,895,197 (GRCm39) |
missense |
probably damaging |
0.99 |
R0336:Col18a1
|
UTSW |
10 |
76,894,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R1471:Col18a1
|
UTSW |
10 |
76,932,040 (GRCm39) |
missense |
unknown |
|
R1538:Col18a1
|
UTSW |
10 |
76,907,170 (GRCm39) |
missense |
probably damaging |
1.00 |
R1594:Col18a1
|
UTSW |
10 |
76,948,870 (GRCm39) |
missense |
possibly damaging |
0.51 |
R1631:Col18a1
|
UTSW |
10 |
76,895,131 (GRCm39) |
missense |
probably damaging |
0.99 |
R1774:Col18a1
|
UTSW |
10 |
76,895,815 (GRCm39) |
missense |
probably damaging |
0.96 |
R1934:Col18a1
|
UTSW |
10 |
76,948,578 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1990:Col18a1
|
UTSW |
10 |
76,916,988 (GRCm39) |
missense |
unknown |
|
R1991:Col18a1
|
UTSW |
10 |
76,916,988 (GRCm39) |
missense |
unknown |
|
R1992:Col18a1
|
UTSW |
10 |
76,916,988 (GRCm39) |
missense |
unknown |
|
R2081:Col18a1
|
UTSW |
10 |
76,890,019 (GRCm39) |
missense |
probably damaging |
1.00 |
R2082:Col18a1
|
UTSW |
10 |
76,895,127 (GRCm39) |
missense |
probably damaging |
1.00 |
R2351:Col18a1
|
UTSW |
10 |
76,948,538 (GRCm39) |
missense |
probably benign |
0.00 |
R2510:Col18a1
|
UTSW |
10 |
76,932,102 (GRCm39) |
missense |
unknown |
|
R3076:Col18a1
|
UTSW |
10 |
76,924,762 (GRCm39) |
missense |
possibly damaging |
0.57 |
R3433:Col18a1
|
UTSW |
10 |
76,932,102 (GRCm39) |
missense |
unknown |
|
R3800:Col18a1
|
UTSW |
10 |
76,903,221 (GRCm39) |
nonsense |
probably null |
|
R3918:Col18a1
|
UTSW |
10 |
76,889,192 (GRCm39) |
missense |
probably benign |
0.05 |
R3981:Col18a1
|
UTSW |
10 |
76,924,721 (GRCm39) |
missense |
probably damaging |
0.99 |
R3983:Col18a1
|
UTSW |
10 |
76,924,721 (GRCm39) |
missense |
probably damaging |
0.99 |
R4182:Col18a1
|
UTSW |
10 |
76,894,675 (GRCm39) |
splice site |
probably null |
|
R4239:Col18a1
|
UTSW |
10 |
76,932,001 (GRCm39) |
missense |
unknown |
|
R5014:Col18a1
|
UTSW |
10 |
76,906,794 (GRCm39) |
critical splice donor site |
probably null |
|
R5107:Col18a1
|
UTSW |
10 |
76,913,057 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5413:Col18a1
|
UTSW |
10 |
76,905,310 (GRCm39) |
missense |
probably damaging |
1.00 |
R5503:Col18a1
|
UTSW |
10 |
76,907,454 (GRCm39) |
missense |
probably damaging |
1.00 |
R5524:Col18a1
|
UTSW |
10 |
76,894,558 (GRCm39) |
missense |
probably damaging |
1.00 |
R5772:Col18a1
|
UTSW |
10 |
77,002,177 (GRCm39) |
missense |
unknown |
|
R5958:Col18a1
|
UTSW |
10 |
76,932,231 (GRCm39) |
missense |
probably benign |
0.01 |
R6280:Col18a1
|
UTSW |
10 |
76,948,323 (GRCm39) |
intron |
probably benign |
|
R6603:Col18a1
|
UTSW |
10 |
76,899,811 (GRCm39) |
critical splice donor site |
probably null |
|
R6608:Col18a1
|
UTSW |
10 |
76,948,628 (GRCm39) |
intron |
probably benign |
|
R6805:Col18a1
|
UTSW |
10 |
76,890,073 (GRCm39) |
missense |
probably damaging |
1.00 |
R6890:Col18a1
|
UTSW |
10 |
76,949,318 (GRCm39) |
intron |
probably benign |
|
R6938:Col18a1
|
UTSW |
10 |
76,948,333 (GRCm39) |
intron |
probably benign |
|
R7002:Col18a1
|
UTSW |
10 |
77,002,177 (GRCm39) |
missense |
unknown |
|
R7154:Col18a1
|
UTSW |
10 |
76,908,799 (GRCm39) |
missense |
probably benign |
0.25 |
R7204:Col18a1
|
UTSW |
10 |
76,921,110 (GRCm39) |
missense |
unknown |
|
R7278:Col18a1
|
UTSW |
10 |
76,932,118 (GRCm39) |
missense |
unknown |
|
R7442:Col18a1
|
UTSW |
10 |
76,932,072 (GRCm39) |
missense |
unknown |
|
R7453:Col18a1
|
UTSW |
10 |
76,921,044 (GRCm39) |
splice site |
probably null |
|
R7597:Col18a1
|
UTSW |
10 |
76,949,137 (GRCm39) |
missense |
unknown |
|
R7615:Col18a1
|
UTSW |
10 |
76,902,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R7671:Col18a1
|
UTSW |
10 |
76,921,217 (GRCm39) |
missense |
unknown |
|
R7696:Col18a1
|
UTSW |
10 |
76,921,106 (GRCm39) |
missense |
unknown |
|
R7719:Col18a1
|
UTSW |
10 |
76,913,846 (GRCm39) |
missense |
probably benign |
0.13 |
R7772:Col18a1
|
UTSW |
10 |
76,904,220 (GRCm39) |
splice site |
probably null |
|
R8077:Col18a1
|
UTSW |
10 |
76,916,685 (GRCm39) |
missense |
unknown |
|
R8085:Col18a1
|
UTSW |
10 |
76,924,741 (GRCm39) |
missense |
unknown |
|
R8097:Col18a1
|
UTSW |
10 |
76,948,342 (GRCm39) |
missense |
unknown |
|
R8117:Col18a1
|
UTSW |
10 |
76,895,808 (GRCm39) |
missense |
probably benign |
0.41 |
R8130:Col18a1
|
UTSW |
10 |
76,910,284 (GRCm39) |
missense |
probably benign |
0.03 |
R8151:Col18a1
|
UTSW |
10 |
76,948,418 (GRCm39) |
missense |
unknown |
|
R8379:Col18a1
|
UTSW |
10 |
76,889,072 (GRCm39) |
missense |
probably benign |
0.08 |
R8479:Col18a1
|
UTSW |
10 |
76,916,988 (GRCm39) |
missense |
unknown |
|
R8523:Col18a1
|
UTSW |
10 |
76,890,068 (GRCm39) |
missense |
probably damaging |
0.99 |
R8862:Col18a1
|
UTSW |
10 |
76,949,044 (GRCm39) |
nonsense |
probably null |
|
R9109:Col18a1
|
UTSW |
10 |
76,893,204 (GRCm39) |
missense |
probably damaging |
1.00 |
R9298:Col18a1
|
UTSW |
10 |
76,893,204 (GRCm39) |
missense |
probably damaging |
1.00 |
R9312:Col18a1
|
UTSW |
10 |
76,894,606 (GRCm39) |
missense |
probably damaging |
0.98 |
R9366:Col18a1
|
UTSW |
10 |
76,932,258 (GRCm39) |
missense |
unknown |
|
R9399:Col18a1
|
UTSW |
10 |
76,916,584 (GRCm39) |
missense |
unknown |
|
R9559:Col18a1
|
UTSW |
10 |
76,913,630 (GRCm39) |
missense |
probably damaging |
1.00 |
R9649:Col18a1
|
UTSW |
10 |
76,916,673 (GRCm39) |
missense |
unknown |
|
R9689:Col18a1
|
UTSW |
10 |
76,916,578 (GRCm39) |
nonsense |
probably null |
|
R9719:Col18a1
|
UTSW |
10 |
76,949,432 (GRCm39) |
missense |
unknown |
|
Z1176:Col18a1
|
UTSW |
10 |
76,948,685 (GRCm39) |
missense |
unknown |
|
Z1176:Col18a1
|
UTSW |
10 |
76,891,543 (GRCm39) |
missense |
possibly damaging |
0.81 |
Z1177:Col18a1
|
UTSW |
10 |
76,948,672 (GRCm39) |
missense |
unknown |
|
|