Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsm1 |
A |
T |
7: 119,257,538 (GRCm39) |
T435S |
probably damaging |
Het |
Agtpbp1 |
G |
A |
13: 59,648,014 (GRCm39) |
T602I |
probably benign |
Het |
Ahnak2 |
T |
A |
12: 112,749,154 (GRCm39) |
D231V |
probably damaging |
Het |
Ampd3 |
G |
A |
7: 110,392,876 (GRCm39) |
D215N |
probably benign |
Het |
Ate1 |
A |
G |
7: 130,105,523 (GRCm39) |
S332P |
probably damaging |
Het |
Ces1f |
T |
C |
8: 93,998,513 (GRCm39) |
E161G |
probably benign |
Het |
Ces2g |
A |
G |
8: 105,692,628 (GRCm39) |
|
probably benign |
Het |
Cntnap4 |
T |
G |
8: 113,529,796 (GRCm39) |
L668R |
probably damaging |
Het |
Csf1 |
A |
G |
3: 107,655,960 (GRCm39) |
V245A |
probably benign |
Het |
Ctss |
A |
G |
3: 95,457,448 (GRCm39) |
Y302C |
probably damaging |
Het |
Dbt |
C |
T |
3: 116,328,432 (GRCm39) |
H158Y |
probably benign |
Het |
Dennd6b |
T |
C |
15: 89,070,386 (GRCm39) |
I428V |
probably benign |
Het |
Dnah9 |
G |
A |
11: 65,860,781 (GRCm39) |
|
probably benign |
Het |
Dock3 |
G |
T |
9: 106,790,467 (GRCm39) |
Q1419K |
possibly damaging |
Het |
Enpp6 |
A |
G |
8: 47,519,035 (GRCm39) |
K268E |
probably damaging |
Het |
Eps15l1 |
T |
G |
8: 73,135,341 (GRCm39) |
|
probably benign |
Het |
Gm10800 |
C |
A |
2: 98,496,925 (GRCm39) |
M209I |
probably benign |
Het |
Herc3 |
C |
T |
6: 58,851,293 (GRCm39) |
P514L |
probably damaging |
Het |
Mark2 |
T |
C |
19: 7,263,287 (GRCm39) |
D160G |
probably damaging |
Het |
Mbd4 |
A |
G |
6: 115,821,529 (GRCm39) |
|
probably null |
Het |
Mink1 |
T |
C |
11: 70,503,868 (GRCm39) |
W1263R |
probably damaging |
Het |
Nlrp14 |
A |
T |
7: 106,780,465 (GRCm39) |
|
probably benign |
Het |
Osbp |
T |
C |
19: 11,961,322 (GRCm39) |
Y454H |
probably damaging |
Het |
Pak5 |
T |
C |
2: 135,942,704 (GRCm39) |
K479E |
possibly damaging |
Het |
Pard3 |
C |
A |
8: 127,888,058 (GRCm39) |
D73E |
probably damaging |
Het |
Pmp22 |
A |
T |
11: 63,049,076 (GRCm39) |
|
probably null |
Het |
Scn4a |
C |
T |
11: 106,215,386 (GRCm39) |
V1197I |
probably benign |
Het |
Slc36a2 |
A |
G |
11: 55,053,621 (GRCm39) |
L339P |
probably damaging |
Het |
Smg1 |
G |
A |
7: 117,811,666 (GRCm39) |
T104I |
possibly damaging |
Het |
Stx18 |
T |
A |
5: 38,249,908 (GRCm39) |
Y74N |
probably damaging |
Het |
Stxbp5 |
A |
T |
10: 9,638,492 (GRCm39) |
H1102Q |
probably damaging |
Het |
Tom1l2 |
T |
C |
11: 60,120,960 (GRCm39) |
K450E |
probably damaging |
Het |
Tpo |
T |
C |
12: 30,150,389 (GRCm39) |
Q497R |
probably benign |
Het |
Tsc2 |
A |
G |
17: 24,849,978 (GRCm39) |
|
probably benign |
Het |
Tut7 |
A |
T |
13: 59,953,142 (GRCm39) |
D99E |
probably benign |
Het |
Vit |
G |
A |
17: 78,907,264 (GRCm39) |
G229R |
probably benign |
Het |
Vwf |
T |
A |
6: 125,659,775 (GRCm39) |
I2658N |
probably benign |
Het |
Wdr36 |
T |
A |
18: 32,992,360 (GRCm39) |
D632E |
probably damaging |
Het |
Zfp654 |
A |
G |
16: 64,605,181 (GRCm39) |
V466A |
probably benign |
Het |
Zfp941 |
T |
C |
7: 140,393,185 (GRCm39) |
D58G |
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 |
|
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 |
|
R1755: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 |
|
|