Other mutations in this stock |
Total: 33 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Atm |
A |
G |
9: 53,367,159 (GRCm39) |
L2482P |
probably damaging |
Het |
Bcl11b |
T |
C |
12: 107,881,945 (GRCm39) |
Y718C |
probably damaging |
Het |
Bltp1 |
A |
G |
3: 37,102,262 (GRCm39) |
E1320G |
probably benign |
Het |
Ccrl2 |
A |
G |
9: 110,884,871 (GRCm39) |
I209T |
probably benign |
Het |
Cd200r2 |
A |
G |
16: 44,729,903 (GRCm39) |
K149R |
probably damaging |
Het |
Cdc45 |
C |
T |
16: 18,617,479 (GRCm39) |
M200I |
probably benign |
Het |
Cops5 |
T |
A |
1: 10,097,377 (GRCm39) |
T291S |
probably benign |
Het |
Csmd1 |
C |
A |
8: 16,052,597 (GRCm39) |
V2176F |
probably benign |
Het |
Ctse |
C |
A |
1: 131,595,972 (GRCm39) |
S221R |
probably damaging |
Het |
Cxcl3 |
A |
G |
5: 90,934,199 (GRCm39) |
|
probably null |
Het |
Cyp51 |
C |
T |
5: 4,154,304 (GRCm39) |
V2I |
probably benign |
Het |
Dennd5a |
A |
G |
7: 109,532,844 (GRCm39) |
F285L |
probably benign |
Het |
Dst |
T |
G |
1: 34,191,274 (GRCm39) |
|
probably benign |
Het |
Frzb |
A |
T |
2: 80,254,935 (GRCm39) |
|
probably benign |
Het |
Gm5070 |
A |
T |
3: 95,318,354 (GRCm39) |
|
noncoding transcript |
Het |
Gm9637 |
A |
G |
14: 19,402,182 (GRCm38) |
|
noncoding transcript |
Het |
Grip1 |
A |
G |
10: 119,765,945 (GRCm39) |
|
probably benign |
Het |
Itga4 |
C |
T |
2: 79,086,001 (GRCm39) |
|
probably benign |
Het |
Ltbp2 |
A |
T |
12: 84,856,439 (GRCm39) |
I675N |
probably damaging |
Het |
Or4n4b |
T |
G |
14: 50,536,060 (GRCm39) |
K235N |
probably damaging |
Het |
Pcdhb20 |
G |
T |
18: 37,639,453 (GRCm39) |
V660L |
probably benign |
Het |
Prex2 |
T |
G |
1: 11,194,069 (GRCm39) |
L484R |
possibly damaging |
Het |
Prkg1 |
A |
T |
19: 30,701,602 (GRCm39) |
V305D |
probably damaging |
Het |
Rab44 |
A |
G |
17: 29,365,023 (GRCm39) |
|
probably benign |
Het |
Smpd4 |
C |
T |
16: 17,457,215 (GRCm39) |
A391V |
probably damaging |
Het |
Smyd4 |
T |
C |
11: 75,294,252 (GRCm39) |
L711P |
probably benign |
Het |
Spag16 |
T |
G |
1: 69,926,688 (GRCm39) |
M261R |
probably benign |
Het |
Steap1 |
A |
G |
5: 5,790,561 (GRCm39) |
V129A |
possibly damaging |
Het |
Tbcd |
A |
T |
11: 121,387,960 (GRCm39) |
I364L |
probably benign |
Het |
Trmt13 |
C |
T |
3: 116,376,192 (GRCm39) |
D400N |
possibly damaging |
Het |
Vps13a |
A |
G |
19: 16,625,001 (GRCm39) |
S2753P |
probably damaging |
Het |
Xirp2 |
T |
G |
2: 67,346,511 (GRCm39) |
S2917R |
probably damaging |
Het |
Zfp983 |
G |
A |
17: 21,876,528 (GRCm39) |
|
probably null |
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 |
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 |
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 |
|
|