Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700019A02Rik |
A |
C |
1: 53,221,025 (GRCm39) |
D68E |
possibly damaging |
Het |
Abca3 |
T |
C |
17: 24,618,954 (GRCm39) |
V870A |
possibly damaging |
Het |
Aldh3a2 |
A |
T |
11: 61,139,885 (GRCm39) |
F416I |
probably damaging |
Het |
Armc6 |
A |
T |
8: 70,678,098 (GRCm39) |
L77Q |
possibly damaging |
Het |
Asb17 |
A |
G |
3: 153,556,570 (GRCm39) |
I226V |
probably benign |
Het |
Aspm |
A |
G |
1: 139,396,406 (GRCm39) |
I862V |
probably benign |
Het |
Atr |
T |
A |
9: 95,753,502 (GRCm39) |
D701E |
probably damaging |
Het |
Baz1b |
C |
T |
5: 135,247,097 (GRCm39) |
L849F |
possibly damaging |
Het |
Cbr1 |
T |
C |
16: 93,405,677 (GRCm39) |
V97A |
probably benign |
Het |
Cep295 |
G |
A |
9: 15,243,306 (GRCm39) |
Q1669* |
probably null |
Het |
Cfap54 |
T |
C |
10: 92,820,089 (GRCm39) |
T1242A |
possibly damaging |
Het |
Chrm3 |
T |
A |
13: 9,928,350 (GRCm39) |
T229S |
possibly damaging |
Het |
Cimip4 |
C |
A |
15: 78,270,474 (GRCm39) |
R98M |
probably damaging |
Het |
Cnga3 |
A |
G |
1: 37,300,066 (GRCm39) |
Y300C |
probably damaging |
Het |
Crocc |
T |
C |
4: 140,752,776 (GRCm39) |
E1208G |
probably damaging |
Het |
Cyp2j8 |
A |
T |
4: 96,358,713 (GRCm39) |
|
probably benign |
Het |
Dcbld2 |
T |
C |
16: 58,285,713 (GRCm39) |
I624T |
possibly damaging |
Het |
Ddah1 |
A |
C |
3: 145,597,227 (GRCm39) |
I258L |
probably benign |
Het |
Dnah6 |
G |
A |
6: 73,026,114 (GRCm39) |
Q3460* |
probably null |
Het |
Dync2h1 |
T |
A |
9: 7,140,911 (GRCm39) |
D1372V |
probably damaging |
Het |
Egln1 |
G |
A |
8: 125,674,980 (GRCm39) |
R272* |
probably null |
Het |
Elf1 |
A |
G |
14: 79,804,620 (GRCm39) |
D95G |
possibly damaging |
Het |
Fkbp5 |
A |
G |
17: 28,621,729 (GRCm39) |
F374L |
probably damaging |
Het |
Fli1 |
T |
C |
9: 32,372,540 (GRCm39) |
|
probably benign |
Het |
Gabbr2 |
T |
C |
4: 46,846,436 (GRCm39) |
T158A |
probably damaging |
Het |
Gp2 |
A |
C |
7: 119,049,302 (GRCm39) |
Y412D |
probably damaging |
Het |
Hmcn1 |
A |
G |
1: 150,610,283 (GRCm39) |
V1462A |
possibly damaging |
Het |
Ide |
T |
C |
19: 37,258,160 (GRCm39) |
|
probably null |
Het |
Kalrn |
T |
C |
16: 34,134,648 (GRCm39) |
K372R |
possibly damaging |
Het |
Kcnj16 |
A |
G |
11: 110,916,067 (GRCm39) |
D243G |
possibly damaging |
Het |
Kif7 |
A |
G |
7: 79,363,905 (GRCm39) |
M1T |
probably null |
Het |
Klri2 |
A |
T |
6: 129,709,174 (GRCm39) |
L226Q |
probably damaging |
Het |
Kremen1 |
T |
C |
11: 5,165,373 (GRCm39) |
|
probably null |
Het |
Lama3 |
T |
C |
18: 12,646,788 (GRCm39) |
|
probably benign |
Het |
Lmln |
C |
A |
16: 32,908,581 (GRCm39) |
R336S |
probably benign |
Het |
Lrch4 |
T |
A |
5: 137,635,818 (GRCm39) |
D266E |
probably benign |
Het |
Lrrc28 |
C |
T |
7: 67,209,677 (GRCm39) |
R174H |
probably damaging |
Het |
Mib1 |
T |
A |
18: 10,798,474 (GRCm39) |
D778E |
probably damaging |
Het |
Msra |
T |
C |
14: 64,360,775 (GRCm39) |
I125V |
possibly damaging |
Het |
Or10c1 |
A |
G |
17: 37,522,244 (GRCm39) |
F167L |
probably damaging |
Het |
Or4k37 |
T |
A |
2: 111,158,964 (GRCm39) |
S67T |
probably damaging |
Het |
Or4p19 |
A |
T |
2: 88,242,555 (GRCm39) |
V149E |
possibly damaging |
Het |
Or52e18 |
A |
G |
7: 104,609,747 (GRCm39) |
F64S |
probably damaging |
Het |
Or6c75 |
C |
A |
10: 129,337,491 (GRCm39) |
T246N |
probably damaging |
Het |
Or8d23 |
A |
G |
9: 38,841,955 (GRCm39) |
M163V |
possibly damaging |
Het |
Pes1 |
T |
A |
11: 3,926,824 (GRCm39) |
Y369N |
probably damaging |
Het |
Pgam2 |
T |
C |
11: 5,751,773 (GRCm39) |
D221G |
possibly damaging |
Het |
Prl2c5 |
T |
C |
13: 13,365,265 (GRCm39) |
V137A |
possibly damaging |
Het |
Rasal1 |
T |
A |
5: 120,814,914 (GRCm39) |
D721E |
possibly damaging |
Het |
Sass6 |
G |
T |
3: 116,412,381 (GRCm39) |
E385D |
possibly damaging |
Het |
Sema5a |
A |
G |
15: 32,460,418 (GRCm39) |
R60G |
probably benign |
Het |
Sesn1 |
T |
C |
10: 41,779,762 (GRCm39) |
S399P |
probably damaging |
Het |
Skic2 |
G |
A |
17: 35,067,398 (GRCm39) |
L47F |
probably damaging |
Het |
Slc10a2 |
C |
T |
8: 5,141,755 (GRCm39) |
V210M |
probably damaging |
Het |
Slc8a3 |
C |
T |
12: 81,362,331 (GRCm39) |
G163S |
probably damaging |
Het |
Sorbs2 |
T |
C |
8: 46,212,234 (GRCm39) |
|
probably benign |
Het |
Speer4f1 |
T |
C |
5: 17,684,490 (GRCm39) |
W173R |
probably damaging |
Het |
Spon2 |
C |
A |
5: 33,374,108 (GRCm39) |
G92W |
probably damaging |
Het |
Sycp2 |
A |
T |
2: 178,037,009 (GRCm39) |
|
probably benign |
Het |
Tfb1m |
A |
G |
17: 3,605,241 (GRCm39) |
V84A |
probably damaging |
Het |
Tmem18 |
G |
T |
12: 30,637,198 (GRCm39) |
|
probably null |
Het |
Tom1l1 |
A |
G |
11: 90,547,210 (GRCm39) |
L290S |
possibly damaging |
Het |
Tube1 |
T |
G |
10: 39,021,711 (GRCm39) |
|
probably null |
Het |
Ugt2b35 |
T |
A |
5: 87,155,156 (GRCm39) |
|
probably null |
Het |
Unc93b1 |
T |
A |
19: 3,992,403 (GRCm39) |
Y269N |
probably benign |
Het |
Usp16 |
T |
C |
16: 87,259,030 (GRCm39) |
|
probably null |
Het |
Vmn1r38 |
A |
T |
6: 66,753,370 (GRCm39) |
S249T |
probably benign |
Het |
Vmn1r42 |
T |
A |
6: 89,821,733 (GRCm39) |
M279L |
possibly damaging |
Het |
Zdhhc23 |
T |
A |
16: 43,791,829 (GRCm39) |
T315S |
possibly damaging |
Het |
Zfp472 |
T |
C |
17: 33,194,900 (GRCm39) |
F12L |
probably benign |
Het |
Zfr2 |
T |
C |
10: 81,083,225 (GRCm39) |
S634P |
probably benign |
Het |
|
Other mutations in Col14a1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00663:Col14a1
|
APN |
15 |
55,274,981 (GRCm39) |
missense |
unknown |
|
IGL01290:Col14a1
|
APN |
15 |
55,286,903 (GRCm39) |
missense |
unknown |
|
IGL01300:Col14a1
|
APN |
15 |
55,331,372 (GRCm39) |
missense |
unknown |
|
IGL01505:Col14a1
|
APN |
15 |
55,318,619 (GRCm39) |
missense |
unknown |
|
IGL01533:Col14a1
|
APN |
15 |
55,284,236 (GRCm39) |
missense |
unknown |
|
IGL01563:Col14a1
|
APN |
15 |
55,351,337 (GRCm39) |
missense |
unknown |
|
IGL01650:Col14a1
|
APN |
15 |
55,270,089 (GRCm39) |
missense |
unknown |
|
IGL01659:Col14a1
|
APN |
15 |
55,309,568 (GRCm39) |
unclassified |
probably benign |
|
IGL01670:Col14a1
|
APN |
15 |
55,192,662 (GRCm39) |
missense |
unknown |
|
IGL01760:Col14a1
|
APN |
15 |
55,286,855 (GRCm39) |
missense |
unknown |
|
IGL01803:Col14a1
|
APN |
15 |
55,282,210 (GRCm39) |
missense |
unknown |
|
IGL01966:Col14a1
|
APN |
15 |
55,312,121 (GRCm39) |
unclassified |
probably benign |
|
IGL01990:Col14a1
|
APN |
15 |
55,226,859 (GRCm39) |
missense |
unknown |
|
IGL02124:Col14a1
|
APN |
15 |
55,327,099 (GRCm39) |
missense |
unknown |
|
IGL02138:Col14a1
|
APN |
15 |
55,284,231 (GRCm39) |
missense |
unknown |
|
IGL02192:Col14a1
|
APN |
15 |
55,225,798 (GRCm39) |
missense |
unknown |
|
IGL02326:Col14a1
|
APN |
15 |
55,282,193 (GRCm39) |
missense |
unknown |
|
IGL02335:Col14a1
|
APN |
15 |
55,327,165 (GRCm39) |
splice site |
probably benign |
|
IGL02407:Col14a1
|
APN |
15 |
55,312,272 (GRCm39) |
splice site |
probably benign |
|
IGL02486:Col14a1
|
APN |
15 |
55,252,092 (GRCm39) |
splice site |
probably benign |
|
IGL02537:Col14a1
|
APN |
15 |
55,208,310 (GRCm39) |
nonsense |
probably null |
|
IGL02567:Col14a1
|
APN |
15 |
55,208,357 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02643:Col14a1
|
APN |
15 |
55,284,258 (GRCm39) |
missense |
unknown |
|
IGL02669:Col14a1
|
APN |
15 |
55,282,178 (GRCm39) |
missense |
unknown |
|
IGL02673:Col14a1
|
APN |
15 |
55,282,178 (GRCm39) |
missense |
unknown |
|
IGL02674:Col14a1
|
APN |
15 |
55,282,178 (GRCm39) |
missense |
unknown |
|
IGL03201:Col14a1
|
APN |
15 |
55,272,300 (GRCm39) |
missense |
unknown |
|
IGL03334:Col14a1
|
APN |
15 |
55,312,217 (GRCm39) |
unclassified |
probably benign |
|
IGL03370:Col14a1
|
APN |
15 |
55,351,937 (GRCm39) |
splice site |
probably null |
|
IGL03385:Col14a1
|
APN |
15 |
55,273,600 (GRCm39) |
missense |
unknown |
|
IGL03385:Col14a1
|
APN |
15 |
55,335,104 (GRCm39) |
missense |
unknown |
|
PIT4131001:Col14a1
|
UTSW |
15 |
55,312,272 (GRCm39) |
splice site |
probably benign |
|
R0046:Col14a1
|
UTSW |
15 |
55,272,359 (GRCm39) |
splice site |
probably benign |
|
R0046:Col14a1
|
UTSW |
15 |
55,272,359 (GRCm39) |
splice site |
probably benign |
|
R0173:Col14a1
|
UTSW |
15 |
55,351,928 (GRCm39) |
missense |
probably damaging |
1.00 |
R0242:Col14a1
|
UTSW |
15 |
55,360,907 (GRCm39) |
missense |
probably damaging |
1.00 |
R0242:Col14a1
|
UTSW |
15 |
55,360,907 (GRCm39) |
missense |
probably damaging |
1.00 |
R0359:Col14a1
|
UTSW |
15 |
55,271,264 (GRCm39) |
splice site |
probably benign |
|
R0391:Col14a1
|
UTSW |
15 |
55,309,655 (GRCm39) |
unclassified |
probably benign |
|
R0468:Col14a1
|
UTSW |
15 |
55,252,042 (GRCm39) |
missense |
unknown |
|
R0652:Col14a1
|
UTSW |
15 |
55,208,278 (GRCm39) |
missense |
unknown |
|
R0692:Col14a1
|
UTSW |
15 |
55,205,134 (GRCm39) |
missense |
unknown |
|
R0745:Col14a1
|
UTSW |
15 |
55,201,813 (GRCm39) |
missense |
unknown |
|
R1006:Col14a1
|
UTSW |
15 |
55,383,331 (GRCm39) |
missense |
probably benign |
0.04 |
R1331:Col14a1
|
UTSW |
15 |
55,273,584 (GRCm39) |
missense |
unknown |
|
R1537:Col14a1
|
UTSW |
15 |
55,244,163 (GRCm39) |
missense |
unknown |
|
R1721:Col14a1
|
UTSW |
15 |
55,310,858 (GRCm39) |
unclassified |
probably benign |
|
R1737:Col14a1
|
UTSW |
15 |
55,208,357 (GRCm39) |
critical splice donor site |
probably benign |
|
R1837:Col14a1
|
UTSW |
15 |
55,245,891 (GRCm39) |
missense |
unknown |
|
R1867:Col14a1
|
UTSW |
15 |
55,310,858 (GRCm39) |
unclassified |
probably benign |
|
R1868:Col14a1
|
UTSW |
15 |
55,310,858 (GRCm39) |
unclassified |
probably benign |
|
R1991:Col14a1
|
UTSW |
15 |
55,313,336 (GRCm39) |
missense |
unknown |
|
R2020:Col14a1
|
UTSW |
15 |
55,309,577 (GRCm39) |
unclassified |
probably benign |
|
R2103:Col14a1
|
UTSW |
15 |
55,313,336 (GRCm39) |
missense |
unknown |
|
R2116:Col14a1
|
UTSW |
15 |
55,271,160 (GRCm39) |
missense |
unknown |
|
R2163:Col14a1
|
UTSW |
15 |
55,308,041 (GRCm39) |
unclassified |
probably benign |
|
R2207:Col14a1
|
UTSW |
15 |
55,327,082 (GRCm39) |
missense |
unknown |
|
R2215:Col14a1
|
UTSW |
15 |
55,244,238 (GRCm39) |
missense |
unknown |
|
R2264:Col14a1
|
UTSW |
15 |
55,330,086 (GRCm39) |
splice site |
probably null |
|
R2383:Col14a1
|
UTSW |
15 |
55,310,913 (GRCm39) |
unclassified |
probably benign |
|
R2397:Col14a1
|
UTSW |
15 |
55,201,835 (GRCm39) |
missense |
unknown |
|
R2422:Col14a1
|
UTSW |
15 |
55,313,318 (GRCm39) |
missense |
unknown |
|
R3793:Col14a1
|
UTSW |
15 |
55,226,909 (GRCm39) |
missense |
unknown |
|
R4082:Col14a1
|
UTSW |
15 |
55,300,429 (GRCm39) |
missense |
unknown |
|
R4112:Col14a1
|
UTSW |
15 |
55,226,955 (GRCm39) |
missense |
unknown |
|
R4519:Col14a1
|
UTSW |
15 |
55,251,975 (GRCm39) |
missense |
unknown |
|
R4628:Col14a1
|
UTSW |
15 |
55,313,229 (GRCm39) |
nonsense |
probably null |
|
R4692:Col14a1
|
UTSW |
15 |
55,286,864 (GRCm39) |
missense |
unknown |
|
R4696:Col14a1
|
UTSW |
15 |
55,235,998 (GRCm39) |
missense |
unknown |
|
R4749:Col14a1
|
UTSW |
15 |
55,315,732 (GRCm39) |
missense |
unknown |
|
R5324:Col14a1
|
UTSW |
15 |
55,201,841 (GRCm39) |
missense |
unknown |
|
R5382:Col14a1
|
UTSW |
15 |
55,225,832 (GRCm39) |
missense |
unknown |
|
R5634:Col14a1
|
UTSW |
15 |
55,381,694 (GRCm39) |
missense |
probably damaging |
1.00 |
R5781:Col14a1
|
UTSW |
15 |
55,286,908 (GRCm39) |
missense |
unknown |
|
R5828:Col14a1
|
UTSW |
15 |
55,300,372 (GRCm39) |
missense |
unknown |
|
R5873:Col14a1
|
UTSW |
15 |
55,309,182 (GRCm39) |
unclassified |
probably benign |
|
R5966:Col14a1
|
UTSW |
15 |
55,315,779 (GRCm39) |
critical splice donor site |
probably null |
|
R6106:Col14a1
|
UTSW |
15 |
55,383,404 (GRCm39) |
missense |
probably damaging |
1.00 |
R6135:Col14a1
|
UTSW |
15 |
55,244,246 (GRCm39) |
missense |
unknown |
|
R6319:Col14a1
|
UTSW |
15 |
55,379,565 (GRCm39) |
missense |
probably damaging |
0.99 |
R6475:Col14a1
|
UTSW |
15 |
55,309,218 (GRCm39) |
unclassified |
probably benign |
|
R6540:Col14a1
|
UTSW |
15 |
55,235,977 (GRCm39) |
missense |
unknown |
|
R6893:Col14a1
|
UTSW |
15 |
55,308,044 (GRCm39) |
unclassified |
probably benign |
|
R6992:Col14a1
|
UTSW |
15 |
55,274,958 (GRCm39) |
splice site |
probably null |
|
R7284:Col14a1
|
UTSW |
15 |
55,381,715 (GRCm39) |
missense |
probably damaging |
1.00 |
R7404:Col14a1
|
UTSW |
15 |
55,252,024 (GRCm39) |
nonsense |
probably null |
|
R7655:Col14a1
|
UTSW |
15 |
55,225,846 (GRCm39) |
missense |
unknown |
|
R7656:Col14a1
|
UTSW |
15 |
55,225,846 (GRCm39) |
missense |
unknown |
|
R7715:Col14a1
|
UTSW |
15 |
55,351,379 (GRCm39) |
missense |
unknown |
|
R7841:Col14a1
|
UTSW |
15 |
55,245,876 (GRCm39) |
missense |
unknown |
|
R7861:Col14a1
|
UTSW |
15 |
55,308,012 (GRCm39) |
missense |
unknown |
|
R7866:Col14a1
|
UTSW |
15 |
55,252,016 (GRCm39) |
missense |
unknown |
|
R7902:Col14a1
|
UTSW |
15 |
55,364,832 (GRCm39) |
missense |
probably benign |
0.16 |
R8041:Col14a1
|
UTSW |
15 |
55,318,626 (GRCm39) |
missense |
unknown |
|
R8159:Col14a1
|
UTSW |
15 |
55,291,324 (GRCm39) |
missense |
unknown |
|
R8224:Col14a1
|
UTSW |
15 |
55,271,137 (GRCm39) |
missense |
unknown |
|
R8282:Col14a1
|
UTSW |
15 |
55,284,276 (GRCm39) |
missense |
unknown |
|
R8729:Col14a1
|
UTSW |
15 |
55,310,893 (GRCm39) |
nonsense |
probably null |
|
R8737:Col14a1
|
UTSW |
15 |
55,318,706 (GRCm39) |
nonsense |
probably null |
|
R8871:Col14a1
|
UTSW |
15 |
55,245,958 (GRCm39) |
missense |
unknown |
|
R9069:Col14a1
|
UTSW |
15 |
55,251,990 (GRCm39) |
missense |
unknown |
|
R9081:Col14a1
|
UTSW |
15 |
55,291,387 (GRCm39) |
missense |
unknown |
|
R9088:Col14a1
|
UTSW |
15 |
55,226,923 (GRCm39) |
missense |
unknown |
|
R9113:Col14a1
|
UTSW |
15 |
55,201,825 (GRCm39) |
missense |
unknown |
|
R9193:Col14a1
|
UTSW |
15 |
55,242,964 (GRCm39) |
missense |
unknown |
|
R9274:Col14a1
|
UTSW |
15 |
55,381,671 (GRCm39) |
missense |
probably damaging |
0.99 |
R9288:Col14a1
|
UTSW |
15 |
55,286,918 (GRCm39) |
missense |
unknown |
|
R9320:Col14a1
|
UTSW |
15 |
55,364,780 (GRCm39) |
missense |
probably benign |
0.16 |
R9602:Col14a1
|
UTSW |
15 |
55,351,345 (GRCm39) |
missense |
unknown |
|
R9620:Col14a1
|
UTSW |
15 |
55,225,781 (GRCm39) |
missense |
unknown |
|
R9629:Col14a1
|
UTSW |
15 |
55,382,545 (GRCm39) |
missense |
|
|
X0023:Col14a1
|
UTSW |
15 |
55,286,843 (GRCm39) |
missense |
unknown |
|
X0063:Col14a1
|
UTSW |
15 |
55,273,611 (GRCm39) |
missense |
unknown |
|
Z1177:Col14a1
|
UTSW |
15 |
55,235,966 (GRCm39) |
critical splice acceptor site |
probably null |
|
|