Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930470P17Rik |
T |
C |
2: 170,443,225 (GRCm39) |
|
probably benign |
Het |
4932414N04Rik |
G |
A |
2: 68,561,548 (GRCm39) |
V292M |
possibly damaging |
Het |
Actn1 |
A |
T |
12: 80,221,328 (GRCm39) |
V575E |
possibly damaging |
Het |
Arhgef1 |
T |
C |
7: 24,612,003 (GRCm39) |
S129P |
probably benign |
Het |
Aup1 |
T |
C |
6: 83,032,908 (GRCm39) |
V214A |
probably benign |
Het |
Bbs10 |
A |
G |
10: 111,135,874 (GRCm39) |
E329G |
probably damaging |
Het |
Brinp2 |
A |
G |
1: 158,094,030 (GRCm39) |
|
probably null |
Het |
Ccdc3 |
A |
G |
2: 5,142,868 (GRCm39) |
T42A |
possibly damaging |
Het |
Cd276 |
T |
C |
9: 58,442,810 (GRCm39) |
N215S |
probably benign |
Het |
Col6a4 |
A |
C |
9: 105,960,087 (GRCm39) |
F19V |
probably benign |
Het |
Crybg1 |
G |
T |
10: 43,865,139 (GRCm39) |
A1446E |
probably benign |
Het |
Dach1 |
C |
T |
14: 98,140,670 (GRCm39) |
R496K |
probably damaging |
Het |
Dchs2 |
A |
G |
3: 83,253,513 (GRCm39) |
T2308A |
possibly damaging |
Het |
Duxf1 |
A |
G |
10: 58,058,885 (GRCm39) |
V623A |
possibly damaging |
Het |
Dync1h1 |
G |
A |
12: 110,585,080 (GRCm39) |
D828N |
probably damaging |
Het |
Eif2a |
A |
T |
3: 58,459,991 (GRCm39) |
H462L |
possibly damaging |
Het |
Flot2 |
A |
G |
11: 77,928,942 (GRCm39) |
|
probably null |
Het |
Gas2 |
T |
G |
7: 51,643,101 (GRCm39) |
Y263* |
probably null |
Het |
Gm5111 |
A |
G |
6: 48,567,027 (GRCm39) |
I81V |
unknown |
Het |
Iqcm |
A |
G |
8: 76,281,539 (GRCm39) |
I7M |
probably benign |
Het |
Kank1 |
G |
A |
19: 25,389,129 (GRCm39) |
|
probably null |
Het |
Lnx2 |
A |
T |
5: 146,961,333 (GRCm39) |
V533E |
probably damaging |
Het |
Mapk8ip3 |
G |
T |
17: 25,120,378 (GRCm39) |
P904T |
possibly damaging |
Het |
Mcm5 |
C |
A |
8: 75,850,551 (GRCm39) |
H596N |
probably benign |
Het |
Miip |
A |
T |
4: 147,947,371 (GRCm39) |
V237E |
probably null |
Het |
Mob3a |
G |
A |
10: 80,525,768 (GRCm39) |
A181V |
probably damaging |
Het |
Mrpl38 |
G |
A |
11: 116,026,104 (GRCm39) |
R99W |
probably benign |
Het |
Naa25 |
A |
G |
5: 121,564,042 (GRCm39) |
T486A |
probably benign |
Het |
Or2z9 |
T |
A |
8: 72,854,030 (GRCm39) |
L142Q |
probably damaging |
Het |
Or5b102 |
A |
G |
19: 13,041,445 (GRCm39) |
I223M |
probably damaging |
Het |
Or8g4 |
A |
G |
9: 39,662,597 (GRCm39) |
Y305C |
probably benign |
Het |
Pcdha8 |
A |
T |
18: 37,126,864 (GRCm39) |
N449Y |
probably damaging |
Het |
Pcdhb6 |
A |
T |
18: 37,467,562 (GRCm39) |
D161V |
probably damaging |
Het |
Pdlim3 |
A |
G |
8: 46,361,576 (GRCm39) |
D134G |
probably benign |
Het |
Phpt1 |
A |
G |
2: 25,464,799 (GRCm39) |
V18A |
probably benign |
Het |
Prg4 |
T |
C |
1: 150,333,293 (GRCm39) |
K177E |
possibly damaging |
Het |
Psmb1 |
A |
G |
17: 15,697,509 (GRCm39) |
F202S |
probably benign |
Het |
Rab14 |
A |
G |
2: 35,073,427 (GRCm39) |
F150L |
|
Het |
Rgs14 |
A |
G |
13: 55,527,138 (GRCm39) |
D169G |
probably damaging |
Het |
Rreb1 |
C |
T |
13: 38,114,092 (GRCm39) |
L484F |
possibly damaging |
Het |
Rsph14 |
A |
T |
10: 74,793,608 (GRCm39) |
Y264* |
probably null |
Het |
Scly |
T |
C |
1: 91,236,030 (GRCm39) |
I152T |
|
Het |
Ska1 |
A |
T |
18: 74,335,714 (GRCm39) |
H85Q |
probably damaging |
Het |
Slc35b3 |
T |
C |
13: 39,128,611 (GRCm39) |
M159V |
probably benign |
Het |
Smok2b |
A |
G |
17: 13,453,767 (GRCm39) |
|
probably benign |
Het |
Spock1 |
G |
A |
13: 57,735,472 (GRCm39) |
Q103* |
probably null |
Het |
Topbp1 |
T |
C |
9: 103,210,184 (GRCm39) |
V914A |
probably damaging |
Het |
Tspan3 |
A |
T |
9: 56,054,803 (GRCm39) |
Y41* |
probably null |
Het |
Ttll3 |
CAAAGTAA |
CAAAGTAAAGTAA |
6: 113,376,118 (GRCm39) |
|
probably null |
Het |
Ttn |
T |
G |
2: 76,560,028 (GRCm39) |
I29458L |
possibly damaging |
Het |
Tubgcp3 |
A |
G |
8: 12,705,974 (GRCm39) |
S183P |
probably benign |
Het |
Zfat |
C |
A |
15: 68,052,757 (GRCm39) |
E346* |
probably null |
Het |
Zfp341 |
T |
A |
2: 154,476,000 (GRCm39) |
|
probably null |
Het |
Zfp54 |
A |
G |
17: 21,654,357 (GRCm39) |
T284A |
probably benign |
Het |
|
Other mutations in Col24a1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00841:Col24a1
|
APN |
3 |
145,068,064 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00931:Col24a1
|
APN |
3 |
145,167,225 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01160:Col24a1
|
APN |
3 |
145,213,468 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01355:Col24a1
|
APN |
3 |
145,020,637 (GRCm39) |
missense |
probably benign |
0.07 |
IGL01409:Col24a1
|
APN |
3 |
145,244,319 (GRCm39) |
missense |
probably benign |
0.19 |
IGL01587:Col24a1
|
APN |
3 |
145,139,110 (GRCm39) |
splice site |
probably null |
|
IGL01666:Col24a1
|
APN |
3 |
145,050,447 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01717:Col24a1
|
APN |
3 |
145,230,018 (GRCm39) |
splice site |
probably benign |
|
IGL01721:Col24a1
|
APN |
3 |
145,244,322 (GRCm39) |
missense |
probably benign |
0.26 |
IGL01939:Col24a1
|
APN |
3 |
145,021,005 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01988:Col24a1
|
APN |
3 |
145,229,922 (GRCm39) |
splice site |
probably null |
|
IGL02002:Col24a1
|
APN |
3 |
145,062,699 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL02172:Col24a1
|
APN |
3 |
145,020,723 (GRCm39) |
missense |
probably benign |
0.34 |
IGL02552:Col24a1
|
APN |
3 |
145,179,962 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02559:Col24a1
|
APN |
3 |
145,019,934 (GRCm39) |
missense |
probably benign |
|
IGL02582:Col24a1
|
APN |
3 |
145,020,247 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02652:Col24a1
|
APN |
3 |
145,198,056 (GRCm39) |
nonsense |
probably null |
|
IGL02942:Col24a1
|
APN |
3 |
145,247,420 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03032:Col24a1
|
APN |
3 |
145,244,458 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03108:Col24a1
|
APN |
3 |
145,029,162 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03310:Col24a1
|
APN |
3 |
145,019,744 (GRCm39) |
splice site |
probably benign |
|
IGL03405:Col24a1
|
APN |
3 |
145,020,918 (GRCm39) |
missense |
possibly damaging |
0.73 |
R0066:Col24a1
|
UTSW |
3 |
145,250,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R0066:Col24a1
|
UTSW |
3 |
145,250,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R0379:Col24a1
|
UTSW |
3 |
145,229,897 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0502:Col24a1
|
UTSW |
3 |
145,251,071 (GRCm39) |
splice site |
probably benign |
|
R0556:Col24a1
|
UTSW |
3 |
145,020,489 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0587:Col24a1
|
UTSW |
3 |
144,998,906 (GRCm39) |
missense |
possibly damaging |
0.50 |
R0617:Col24a1
|
UTSW |
3 |
145,019,881 (GRCm39) |
missense |
probably damaging |
1.00 |
R0831:Col24a1
|
UTSW |
3 |
145,034,520 (GRCm39) |
missense |
probably damaging |
1.00 |
R1455:Col24a1
|
UTSW |
3 |
145,166,593 (GRCm39) |
missense |
probably damaging |
1.00 |
R1664:Col24a1
|
UTSW |
3 |
145,095,355 (GRCm39) |
critical splice donor site |
probably null |
|
R1713:Col24a1
|
UTSW |
3 |
145,072,624 (GRCm39) |
nonsense |
probably null |
|
R1854:Col24a1
|
UTSW |
3 |
145,164,895 (GRCm39) |
missense |
probably damaging |
1.00 |
R1855:Col24a1
|
UTSW |
3 |
145,164,895 (GRCm39) |
missense |
probably damaging |
1.00 |
R1861:Col24a1
|
UTSW |
3 |
145,243,022 (GRCm39) |
critical splice donor site |
probably null |
|
R1969:Col24a1
|
UTSW |
3 |
145,020,691 (GRCm39) |
missense |
probably benign |
0.03 |
R2216:Col24a1
|
UTSW |
3 |
145,020,742 (GRCm39) |
missense |
probably benign |
0.34 |
R2290:Col24a1
|
UTSW |
3 |
145,218,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R3702:Col24a1
|
UTSW |
3 |
145,043,621 (GRCm39) |
missense |
probably benign |
0.01 |
R3772:Col24a1
|
UTSW |
3 |
145,251,041 (GRCm39) |
missense |
probably damaging |
1.00 |
R4086:Col24a1
|
UTSW |
3 |
145,167,192 (GRCm39) |
missense |
probably damaging |
1.00 |
R4236:Col24a1
|
UTSW |
3 |
145,230,037 (GRCm39) |
nonsense |
probably null |
|
R4433:Col24a1
|
UTSW |
3 |
145,020,144 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4688:Col24a1
|
UTSW |
3 |
145,020,144 (GRCm39) |
missense |
probably benign |
0.00 |
R4972:Col24a1
|
UTSW |
3 |
145,215,439 (GRCm39) |
missense |
probably benign |
0.42 |
R5157:Col24a1
|
UTSW |
3 |
145,051,712 (GRCm39) |
nonsense |
probably null |
|
R5216:Col24a1
|
UTSW |
3 |
145,021,071 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5274:Col24a1
|
UTSW |
3 |
145,190,433 (GRCm39) |
missense |
probably benign |
0.03 |
R5334:Col24a1
|
UTSW |
3 |
145,167,280 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5416:Col24a1
|
UTSW |
3 |
145,020,786 (GRCm39) |
nonsense |
probably null |
|
R5473:Col24a1
|
UTSW |
3 |
145,243,016 (GRCm39) |
missense |
probably benign |
0.41 |
R5538:Col24a1
|
UTSW |
3 |
144,998,882 (GRCm39) |
missense |
probably damaging |
0.99 |
R5561:Col24a1
|
UTSW |
3 |
145,004,588 (GRCm39) |
missense |
probably benign |
0.26 |
R5648:Col24a1
|
UTSW |
3 |
145,064,321 (GRCm39) |
missense |
probably benign |
0.00 |
R5920:Col24a1
|
UTSW |
3 |
145,133,985 (GRCm39) |
missense |
probably damaging |
1.00 |
R6111:Col24a1
|
UTSW |
3 |
145,019,815 (GRCm39) |
missense |
probably damaging |
0.99 |
R6151:Col24a1
|
UTSW |
3 |
145,019,815 (GRCm39) |
missense |
probably damaging |
0.99 |
R6701:Col24a1
|
UTSW |
3 |
145,020,141 (GRCm39) |
missense |
probably benign |
0.00 |
R6728:Col24a1
|
UTSW |
3 |
145,020,957 (GRCm39) |
missense |
probably benign |
|
R6734:Col24a1
|
UTSW |
3 |
145,214,429 (GRCm39) |
missense |
probably benign |
0.06 |
R6861:Col24a1
|
UTSW |
3 |
145,166,589 (GRCm39) |
missense |
probably damaging |
1.00 |
R6982:Col24a1
|
UTSW |
3 |
145,020,807 (GRCm39) |
nonsense |
probably null |
|
R7001:Col24a1
|
UTSW |
3 |
145,004,627 (GRCm39) |
missense |
probably benign |
0.28 |
R7148:Col24a1
|
UTSW |
3 |
145,021,060 (GRCm39) |
missense |
probably damaging |
1.00 |
R7293:Col24a1
|
UTSW |
3 |
145,192,059 (GRCm39) |
nonsense |
probably null |
|
R7315:Col24a1
|
UTSW |
3 |
145,137,625 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7358:Col24a1
|
UTSW |
3 |
144,998,926 (GRCm39) |
critical splice donor site |
probably null |
|
R7371:Col24a1
|
UTSW |
3 |
145,049,459 (GRCm39) |
missense |
probably benign |
0.06 |
R7383:Col24a1
|
UTSW |
3 |
145,004,599 (GRCm39) |
missense |
probably benign |
|
R7605:Col24a1
|
UTSW |
3 |
145,244,442 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7650:Col24a1
|
UTSW |
3 |
145,020,214 (GRCm39) |
missense |
probably benign |
0.00 |
R7679:Col24a1
|
UTSW |
3 |
145,105,110 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7701:Col24a1
|
UTSW |
3 |
145,020,772 (GRCm39) |
missense |
probably benign |
|
R7805:Col24a1
|
UTSW |
3 |
145,019,901 (GRCm39) |
missense |
probably benign |
0.02 |
R7913:Col24a1
|
UTSW |
3 |
145,137,621 (GRCm39) |
nonsense |
probably null |
|
R7921:Col24a1
|
UTSW |
3 |
145,179,993 (GRCm39) |
missense |
probably damaging |
1.00 |
R8056:Col24a1
|
UTSW |
3 |
145,019,925 (GRCm39) |
missense |
possibly damaging |
0.73 |
R8240:Col24a1
|
UTSW |
3 |
145,213,457 (GRCm39) |
missense |
probably benign |
0.31 |
R8294:Col24a1
|
UTSW |
3 |
145,186,844 (GRCm39) |
missense |
probably null |
1.00 |
R8305:Col24a1
|
UTSW |
3 |
145,179,937 (GRCm39) |
missense |
probably benign |
0.00 |
R8430:Col24a1
|
UTSW |
3 |
145,021,060 (GRCm39) |
missense |
probably damaging |
1.00 |
R8708:Col24a1
|
UTSW |
3 |
145,251,020 (GRCm39) |
missense |
probably damaging |
0.99 |
R8880:Col24a1
|
UTSW |
3 |
145,019,798 (GRCm39) |
missense |
probably null |
|
R9056:Col24a1
|
UTSW |
3 |
145,021,009 (GRCm39) |
missense |
probably damaging |
0.96 |
R9461:Col24a1
|
UTSW |
3 |
145,186,879 (GRCm39) |
nonsense |
probably null |
|
R9612:Col24a1
|
UTSW |
3 |
145,250,960 (GRCm39) |
missense |
probably benign |
0.32 |
R9777:Col24a1
|
UTSW |
3 |
145,021,103 (GRCm39) |
nonsense |
probably null |
|
Z1176:Col24a1
|
UTSW |
3 |
145,048,259 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Col24a1
|
UTSW |
3 |
145,048,260 (GRCm39) |
missense |
probably damaging |
1.00 |
|