Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933402J07Rik |
G |
A |
8: 88,315,585 (GRCm39) |
R225H |
possibly damaging |
Het |
9330159F19Rik |
A |
T |
10: 29,098,290 (GRCm39) |
H199L |
possibly damaging |
Het |
Acaca |
AC |
A |
11: 84,167,390 (GRCm39) |
|
probably null |
Het |
Adam23 |
G |
A |
1: 63,582,329 (GRCm39) |
V326M |
probably damaging |
Het |
Aldh1a2 |
T |
A |
9: 71,169,023 (GRCm39) |
Y168* |
probably null |
Het |
Ano6 |
A |
G |
15: 95,870,451 (GRCm39) |
K869E |
possibly damaging |
Het |
Aplp2 |
G |
A |
9: 31,088,400 (GRCm39) |
A106V |
probably damaging |
Het |
Arhgdib |
T |
A |
6: 136,906,612 (GRCm39) |
K30* |
probably null |
Het |
Arl11 |
A |
G |
14: 61,548,393 (GRCm39) |
T68A |
probably benign |
Het |
Atg7 |
A |
G |
6: 114,650,638 (GRCm39) |
T83A |
possibly damaging |
Het |
Card9 |
T |
C |
2: 26,249,546 (GRCm39) |
E5G |
probably damaging |
Het |
Cars1 |
A |
G |
7: 143,123,194 (GRCm39) |
V474A |
probably damaging |
Het |
Cd300ld2 |
A |
G |
11: 114,904,601 (GRCm39) |
F89L |
probably benign |
Het |
Celf2 |
T |
A |
2: 6,889,769 (GRCm39) |
M1L |
probably benign |
Het |
Cnot1 |
T |
C |
8: 96,451,205 (GRCm39) |
D2174G |
probably damaging |
Het |
Cox6b2 |
A |
G |
7: 4,754,937 (GRCm39) |
F74S |
probably damaging |
Het |
Cyp11b1 |
T |
A |
15: 74,710,383 (GRCm39) |
Q306L |
probably benign |
Het |
Ddx3y |
A |
G |
Y: 1,279,543 (GRCm39) |
I107T |
probably benign |
Het |
Dnah5 |
A |
T |
15: 28,326,782 (GRCm39) |
Y1997F |
probably damaging |
Het |
Dync2i1 |
A |
G |
12: 116,189,649 (GRCm39) |
L620P |
probably damaging |
Het |
Epha4 |
A |
T |
1: 77,364,460 (GRCm39) |
I683N |
probably damaging |
Het |
Fam120a |
G |
T |
13: 49,039,219 (GRCm39) |
A979E |
possibly damaging |
Het |
Gmip |
A |
G |
8: 70,266,774 (GRCm39) |
I296M |
probably damaging |
Het |
Gpr37l1 |
A |
G |
1: 135,094,639 (GRCm39) |
S202P |
probably damaging |
Het |
Ifi208 |
C |
A |
1: 173,505,476 (GRCm39) |
D75E |
possibly damaging |
Het |
Il24 |
T |
C |
1: 130,811,680 (GRCm39) |
N132S |
possibly damaging |
Het |
Katnal2 |
A |
G |
18: 77,099,763 (GRCm39) |
C124R |
probably benign |
Het |
Kcnq3 |
A |
T |
15: 65,867,270 (GRCm39) |
L791Q |
probably damaging |
Het |
Kcns3 |
T |
A |
12: 11,141,445 (GRCm39) |
D418V |
probably benign |
Het |
Kif13a |
A |
G |
13: 46,906,089 (GRCm39) |
V618A |
possibly damaging |
Het |
Kif13a |
A |
T |
13: 46,927,154 (GRCm39) |
V1179E |
possibly damaging |
Het |
Lpp |
A |
G |
16: 24,663,874 (GRCm39) |
I259V |
probably benign |
Het |
Mapkapk2 |
A |
G |
1: 130,986,087 (GRCm39) |
|
probably null |
Het |
Marchf7 |
T |
C |
2: 60,065,265 (GRCm39) |
S514P |
probably benign |
Het |
Nr4a2 |
T |
A |
2: 56,999,104 (GRCm39) |
L381F |
probably damaging |
Het |
Nt5dc3 |
A |
G |
10: 86,660,115 (GRCm39) |
D328G |
probably damaging |
Het |
Obox6 |
T |
C |
7: 15,568,445 (GRCm39) |
K144E |
probably damaging |
Het |
Oga |
A |
T |
19: 45,746,845 (GRCm39) |
M735K |
possibly damaging |
Het |
Olfml2b |
G |
A |
1: 170,509,346 (GRCm39) |
V565M |
probably damaging |
Het |
Or1d2 |
T |
C |
11: 74,255,819 (GRCm39) |
V108A |
probably damaging |
Het |
Orc3 |
G |
A |
4: 34,575,114 (GRCm39) |
A590V |
possibly damaging |
Het |
Picalm |
T |
C |
7: 89,809,757 (GRCm39) |
S78P |
possibly damaging |
Het |
Por |
T |
A |
5: 135,758,339 (GRCm39) |
Y105* |
probably null |
Het |
Ppara |
A |
G |
15: 85,682,180 (GRCm39) |
K292R |
probably benign |
Het |
Pramel27 |
T |
C |
4: 143,577,380 (GRCm39) |
F3S |
probably damaging |
Het |
Prss59 |
T |
G |
6: 40,903,096 (GRCm39) |
Y92S |
probably damaging |
Het |
Ralgds |
T |
A |
2: 28,440,558 (GRCm39) |
I844N |
probably damaging |
Het |
Rttn |
T |
C |
18: 89,027,441 (GRCm39) |
Y519H |
probably damaging |
Het |
Scn9a |
A |
G |
2: 66,332,060 (GRCm39) |
V1261A |
probably benign |
Het |
Slc2a2 |
T |
A |
3: 28,767,811 (GRCm39) |
|
probably null |
Het |
Slc5a7 |
T |
C |
17: 54,600,006 (GRCm39) |
M136V |
probably benign |
Het |
Smc4 |
C |
A |
3: 68,941,441 (GRCm39) |
A1232E |
probably damaging |
Het |
Smg1 |
A |
T |
7: 117,802,287 (GRCm39) |
C270* |
probably null |
Het |
Sparcl1 |
C |
T |
5: 104,240,690 (GRCm39) |
E245K |
probably benign |
Het |
Taf2 |
T |
C |
15: 54,879,850 (GRCm39) |
H1162R |
probably damaging |
Het |
Tlr3 |
T |
C |
8: 45,851,010 (GRCm39) |
D105G |
probably benign |
Het |
Tmem62 |
T |
C |
2: 120,814,958 (GRCm39) |
|
probably null |
Het |
Triobp |
G |
A |
15: 78,850,679 (GRCm39) |
A278T |
probably benign |
Het |
Ufd1 |
T |
G |
16: 18,642,003 (GRCm39) |
C151W |
probably damaging |
Het |
Upk1b |
T |
G |
16: 38,600,402 (GRCm39) |
M193L |
probably benign |
Het |
Usp15 |
A |
G |
10: 122,968,949 (GRCm39) |
M334T |
probably damaging |
Het |
Utp20 |
A |
G |
10: 88,645,631 (GRCm39) |
S541P |
probably benign |
Het |
Vmn1r61 |
A |
T |
7: 5,614,302 (GRCm39) |
L4* |
probably null |
Het |
Vmn2r96 |
G |
A |
17: 18,802,915 (GRCm39) |
G83D |
possibly damaging |
Het |
Zbtb8a |
T |
C |
4: 129,248,110 (GRCm39) |
D387G |
possibly damaging |
Het |
Zfp106 |
A |
T |
2: 120,365,656 (GRCm39) |
N250K |
probably damaging |
Het |
Zfp292 |
A |
G |
4: 34,811,043 (GRCm39) |
V667A |
probably benign |
Het |
|
Other mutations in Col1a2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00839:Col1a2
|
APN |
6 |
4,531,095 (GRCm39) |
splice site |
probably benign |
|
IGL01126:Col1a2
|
APN |
6 |
4,535,846 (GRCm39) |
missense |
unknown |
|
IGL01129:Col1a2
|
APN |
6 |
4,535,846 (GRCm39) |
missense |
unknown |
|
IGL01286:Col1a2
|
APN |
6 |
4,533,891 (GRCm39) |
missense |
unknown |
|
IGL01687:Col1a2
|
APN |
6 |
4,520,258 (GRCm39) |
nonsense |
probably null |
|
IGL01866:Col1a2
|
APN |
6 |
4,524,132 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02010:Col1a2
|
APN |
6 |
4,512,416 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02100:Col1a2
|
APN |
6 |
4,524,177 (GRCm39) |
splice site |
probably benign |
|
IGL02140:Col1a2
|
APN |
6 |
4,515,639 (GRCm39) |
missense |
unknown |
|
IGL02474:Col1a2
|
APN |
6 |
4,516,398 (GRCm39) |
missense |
unknown |
|
IGL02510:Col1a2
|
APN |
6 |
4,516,398 (GRCm39) |
missense |
unknown |
|
IGL02525:Col1a2
|
APN |
6 |
4,531,355 (GRCm39) |
splice site |
probably benign |
|
IGL02839:Col1a2
|
APN |
6 |
4,538,748 (GRCm39) |
missense |
unknown |
|
IGL03134:Col1a2
|
APN |
6 |
4,521,387 (GRCm39) |
unclassified |
probably benign |
|
IGL03385:Col1a2
|
APN |
6 |
4,539,612 (GRCm39) |
missense |
unknown |
|
hollow
|
UTSW |
6 |
4,538,680 (GRCm39) |
missense |
unknown |
|
marrow
|
UTSW |
6 |
4,531,316 (GRCm39) |
missense |
unknown |
|
myelo
|
UTSW |
6 |
4,515,682 (GRCm39) |
missense |
unknown |
|
P4717OSA:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
PIT4453001:Col1a2
|
UTSW |
6 |
4,527,079 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0021:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R0022:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R0025:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R0027:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R0028:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R0031:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R0038:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R0064:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R0102:Col1a2
|
UTSW |
6 |
4,520,775 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0147:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R0323:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R0326:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R0326:Col1a2
|
UTSW |
6 |
4,537,838 (GRCm39) |
missense |
unknown |
|
R0335:Col1a2
|
UTSW |
6 |
4,531,956 (GRCm39) |
splice site |
probably benign |
|
R0359:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R0363:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R0612:Col1a2
|
UTSW |
6 |
4,516,003 (GRCm39) |
missense |
unknown |
|
R0729:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R0746:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R0760:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R0761:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R0801:Col1a2
|
UTSW |
6 |
4,531,316 (GRCm39) |
missense |
unknown |
|
R0845:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R0846:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R0969:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R0970:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R1105:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R1106:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R1107:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R1134:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R1135:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R1152:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R1333:Col1a2
|
UTSW |
6 |
4,515,684 (GRCm39) |
critical splice donor site |
probably null |
|
R1341:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R1470:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R1470:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R1477:Col1a2
|
UTSW |
6 |
4,539,673 (GRCm39) |
missense |
unknown |
|
R1566:Col1a2
|
UTSW |
6 |
4,523,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R1691:Col1a2
|
UTSW |
6 |
4,536,038 (GRCm39) |
missense |
unknown |
|
R1713:Col1a2
|
UTSW |
6 |
4,538,691 (GRCm39) |
missense |
unknown |
|
R1754:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R2050:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R2178:Col1a2
|
UTSW |
6 |
4,531,143 (GRCm39) |
missense |
unknown |
|
R2194:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R2195:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R2235:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R2261:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R2262:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R2263:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R2289:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R2310:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R2312:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R2330:Col1a2
|
UTSW |
6 |
4,528,300 (GRCm39) |
splice site |
probably benign |
|
R2333:Col1a2
|
UTSW |
6 |
4,532,747 (GRCm39) |
missense |
unknown |
|
R2401:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R2403:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R2448:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R2513:Col1a2
|
UTSW |
6 |
4,531,223 (GRCm39) |
splice site |
probably null |
|
R2862:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R2884:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R2885:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R2913:Col1a2
|
UTSW |
6 |
4,519,923 (GRCm39) |
unclassified |
probably benign |
|
R2937:Col1a2
|
UTSW |
6 |
4,520,788 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2937:Col1a2
|
UTSW |
6 |
4,519,882 (GRCm39) |
unclassified |
probably benign |
|
R2938:Col1a2
|
UTSW |
6 |
4,520,788 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3608:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R3692:Col1a2
|
UTSW |
6 |
4,510,710 (GRCm39) |
missense |
possibly damaging |
0.84 |
R3805:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R3806:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R3826:Col1a2
|
UTSW |
6 |
4,516,960 (GRCm39) |
unclassified |
probably benign |
|
R3903:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R3904:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R3922:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R3926:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R4106:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R4107:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R4108:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R4109:Col1a2
|
UTSW |
6 |
4,510,705 (GRCm39) |
nonsense |
probably null |
|
R4509:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
R4667:Col1a2
|
UTSW |
6 |
4,512,412 (GRCm39) |
missense |
unknown |
|
R4909:Col1a2
|
UTSW |
6 |
4,529,058 (GRCm39) |
splice site |
probably benign |
|
R5418:Col1a2
|
UTSW |
6 |
4,516,931 (GRCm39) |
unclassified |
probably benign |
|
R5587:Col1a2
|
UTSW |
6 |
4,540,531 (GRCm39) |
missense |
unknown |
|
R5598:Col1a2
|
UTSW |
6 |
4,516,916 (GRCm39) |
unclassified |
probably benign |
|
R5673:Col1a2
|
UTSW |
6 |
4,539,622 (GRCm39) |
missense |
unknown |
|
R5678:Col1a2
|
UTSW |
6 |
4,536,239 (GRCm39) |
missense |
unknown |
|
R5763:Col1a2
|
UTSW |
6 |
4,515,682 (GRCm39) |
missense |
unknown |
|
R5786:Col1a2
|
UTSW |
6 |
4,530,223 (GRCm39) |
missense |
unknown |
|
R5872:Col1a2
|
UTSW |
6 |
4,531,926 (GRCm39) |
missense |
unknown |
|
R6084:Col1a2
|
UTSW |
6 |
4,505,840 (GRCm39) |
start codon destroyed |
probably benign |
0.01 |
R6134:Col1a2
|
UTSW |
6 |
4,538,035 (GRCm39) |
missense |
unknown |
|
R6221:Col1a2
|
UTSW |
6 |
4,539,490 (GRCm39) |
missense |
unknown |
|
R6481:Col1a2
|
UTSW |
6 |
4,538,680 (GRCm39) |
missense |
unknown |
|
R6500:Col1a2
|
UTSW |
6 |
4,515,517 (GRCm39) |
missense |
unknown |
|
R6890:Col1a2
|
UTSW |
6 |
4,539,587 (GRCm39) |
missense |
unknown |
|
R7022:Col1a2
|
UTSW |
6 |
4,534,639 (GRCm39) |
missense |
unknown |
|
R7033:Col1a2
|
UTSW |
6 |
4,516,904 (GRCm39) |
unclassified |
probably benign |
|
R7195:Col1a2
|
UTSW |
6 |
4,510,753 (GRCm39) |
missense |
unknown |
|
R7657:Col1a2
|
UTSW |
6 |
4,527,152 (GRCm39) |
missense |
probably null |
0.99 |
R7686:Col1a2
|
UTSW |
6 |
4,518,964 (GRCm39) |
missense |
unknown |
|
R7875:Col1a2
|
UTSW |
6 |
4,518,500 (GRCm39) |
missense |
unknown |
|
R8023:Col1a2
|
UTSW |
6 |
4,533,847 (GRCm39) |
missense |
unknown |
|
R8208:Col1a2
|
UTSW |
6 |
4,515,260 (GRCm39) |
splice site |
probably null |
|
R8277:Col1a2
|
UTSW |
6 |
4,516,410 (GRCm39) |
missense |
probably null |
|
R8438:Col1a2
|
UTSW |
6 |
4,515,518 (GRCm39) |
missense |
unknown |
|
R8438:Col1a2
|
UTSW |
6 |
4,515,517 (GRCm39) |
missense |
unknown |
|
R8993:Col1a2
|
UTSW |
6 |
4,535,451 (GRCm39) |
missense |
unknown |
|
R9109:Col1a2
|
UTSW |
6 |
4,515,260 (GRCm39) |
splice site |
probably null |
|
R9298:Col1a2
|
UTSW |
6 |
4,515,260 (GRCm39) |
splice site |
probably null |
|
R9315:Col1a2
|
UTSW |
6 |
4,540,544 (GRCm39) |
missense |
unknown |
|
R9490:Col1a2
|
UTSW |
6 |
4,505,901 (GRCm39) |
missense |
unknown |
|
V5622:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
V5622:Col1a2
|
UTSW |
6 |
4,518,822 (GRCm39) |
unclassified |
probably benign |
|
X0017:Col1a2
|
UTSW |
6 |
4,515,675 (GRCm39) |
missense |
unknown |
|
Z1176:Col1a2
|
UTSW |
6 |
4,532,750 (GRCm39) |
missense |
unknown |
|
|