Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Alg3 |
T |
C |
16: 20,424,736 (GRCm39) |
T270A |
possibly damaging |
Het |
Ambp |
G |
C |
4: 63,068,596 (GRCm39) |
H140Q |
probably benign |
Het |
Arhgef10 |
T |
C |
8: 14,978,786 (GRCm39) |
C18R |
probably benign |
Het |
Arhgef10l |
A |
G |
4: 140,271,730 (GRCm39) |
F548S |
probably damaging |
Het |
Armh3 |
A |
G |
19: 45,948,796 (GRCm39) |
Y228H |
probably damaging |
Het |
Cdhr1 |
T |
C |
14: 36,807,602 (GRCm39) |
D346G |
probably damaging |
Het |
Col1a2 |
T |
A |
6: 4,539,587 (GRCm39) |
L1285Q |
unknown |
Het |
Cspg5 |
T |
C |
9: 110,075,852 (GRCm39) |
L196P |
probably damaging |
Het |
Dusp10 |
T |
G |
1: 183,801,393 (GRCm39) |
Y387D |
probably damaging |
Het |
Epb41 |
A |
T |
4: 131,663,140 (GRCm39) |
D681E |
probably damaging |
Het |
Eps8 |
A |
G |
6: 137,489,255 (GRCm39) |
V381A |
probably damaging |
Het |
Fbxw16 |
A |
T |
9: 109,265,810 (GRCm39) |
S336R |
probably benign |
Het |
Gm49368 |
A |
G |
7: 127,680,901 (GRCm39) |
R277G |
probably benign |
Het |
Gsg1 |
C |
T |
6: 135,214,418 (GRCm39) |
V320I |
probably benign |
Het |
Iglc3 |
T |
A |
16: 18,884,258 (GRCm39) |
|
probably benign |
Het |
Klc4 |
A |
T |
17: 46,942,769 (GRCm39) |
N598K |
probably benign |
Het |
Malsu1 |
A |
G |
6: 49,052,185 (GRCm39) |
Y135C |
probably damaging |
Het |
Mapkbp1 |
T |
C |
2: 119,846,283 (GRCm39) |
I477T |
probably damaging |
Het |
Mtss1 |
G |
T |
15: 58,823,508 (GRCm39) |
S286R |
probably damaging |
Het |
Naip2 |
A |
C |
13: 100,298,549 (GRCm39) |
S496A |
probably benign |
Het |
Niban3 |
T |
A |
8: 72,058,315 (GRCm39) |
V540D |
probably damaging |
Het |
Npepps |
A |
T |
11: 97,158,470 (GRCm39) |
C98* |
probably null |
Het |
Nphp3 |
A |
C |
9: 103,919,153 (GRCm39) |
Y1267S |
probably damaging |
Het |
Npr3 |
A |
G |
15: 11,883,478 (GRCm39) |
V317A |
possibly damaging |
Het |
Nsun6 |
A |
G |
2: 15,053,788 (GRCm39) |
I7T |
probably damaging |
Het |
Or13p4 |
A |
G |
4: 118,546,728 (GRCm39) |
V307A |
possibly damaging |
Het |
Or51ai2 |
A |
T |
7: 103,587,066 (GRCm39) |
T160S |
possibly damaging |
Het |
Or5b121 |
C |
T |
19: 13,507,445 (GRCm39) |
T180I |
probably damaging |
Het |
Pcnx1 |
A |
G |
12: 82,018,150 (GRCm39) |
H1330R |
probably benign |
Het |
Rad17 |
T |
C |
13: 100,773,592 (GRCm39) |
I201V |
probably benign |
Het |
Slc26a4 |
G |
A |
12: 31,599,950 (GRCm39) |
T126M |
possibly damaging |
Het |
Slitrk6 |
A |
T |
14: 110,988,528 (GRCm39) |
L393* |
probably null |
Het |
Snx2 |
A |
G |
18: 53,345,951 (GRCm39) |
H378R |
probably damaging |
Het |
Tex21 |
A |
G |
12: 76,286,229 (GRCm39) |
|
probably null |
Het |
Trio |
A |
T |
15: 27,919,374 (GRCm39) |
|
probably benign |
Het |
Vpreb1b |
T |
C |
16: 17,798,820 (GRCm39) |
I102T |
probably damaging |
Het |
Zfp617 |
T |
G |
8: 72,686,010 (GRCm39) |
H113Q |
probably benign |
Het |
Zgpat |
T |
A |
2: 181,020,304 (GRCm39) |
I237N |
probably damaging |
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 |
|
R6309:Col18a1
|
UTSW |
10 |
76,948,576 (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 |
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 |
|
|