Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrv1 |
C |
A |
13: 81,707,648 (GRCm39) |
V1253F |
probably damaging |
Het |
Apbb2 |
A |
G |
5: 66,557,574 (GRCm39) |
W296R |
probably damaging |
Het |
Armh3 |
G |
A |
19: 45,808,792 (GRCm39) |
T633I |
probably damaging |
Het |
Btbd3 |
T |
C |
2: 138,126,043 (GRCm39) |
V409A |
possibly damaging |
Het |
C130050O18Rik |
A |
T |
5: 139,400,820 (GRCm39) |
D291V |
probably damaging |
Het |
Catsper3 |
A |
G |
13: 55,955,848 (GRCm39) |
N318D |
probably benign |
Het |
Chd1 |
T |
A |
17: 15,945,543 (GRCm39) |
D22E |
possibly damaging |
Het |
Chrnb2 |
G |
A |
3: 89,670,681 (GRCm39) |
|
probably benign |
Het |
Cryl1 |
T |
C |
14: 57,550,534 (GRCm39) |
D110G |
probably damaging |
Het |
Deaf1 |
A |
G |
7: 140,902,874 (GRCm39) |
I150T |
probably damaging |
Het |
Eif3a |
A |
T |
19: 60,770,747 (GRCm39) |
D33E |
possibly damaging |
Het |
Fabp12 |
C |
A |
3: 10,315,114 (GRCm39) |
G78C |
probably benign |
Het |
Fat1 |
A |
G |
8: 45,476,651 (GRCm39) |
D1899G |
probably damaging |
Het |
Galnt13 |
G |
A |
2: 54,744,660 (GRCm39) |
V120I |
probably benign |
Het |
Ganab |
G |
A |
19: 8,889,840 (GRCm39) |
A635T |
probably damaging |
Het |
Gm17509 |
G |
A |
13: 117,357,380 (GRCm39) |
|
probably benign |
Het |
Gstm3 |
A |
T |
3: 107,875,080 (GRCm39) |
|
probably null |
Het |
Hfm1 |
T |
A |
5: 107,043,800 (GRCm39) |
|
probably benign |
Het |
Hoxd13 |
A |
C |
2: 74,500,440 (GRCm39) |
D327A |
probably damaging |
Het |
Ints4 |
G |
T |
7: 97,140,137 (GRCm39) |
|
probably null |
Het |
Kcna10 |
A |
T |
3: 107,102,259 (GRCm39) |
T297S |
probably benign |
Het |
Ldb2 |
G |
A |
5: 44,699,057 (GRCm39) |
T127I |
probably damaging |
Het |
Mapk7 |
T |
C |
11: 61,382,498 (GRCm39) |
D68G |
probably damaging |
Het |
Msh3 |
A |
T |
13: 92,357,596 (GRCm39) |
|
probably benign |
Het |
Muc6 |
A |
G |
7: 141,217,402 (GRCm39) |
S2359P |
possibly damaging |
Het |
Mup6 |
A |
T |
4: 60,005,990 (GRCm39) |
I161F |
possibly damaging |
Het |
Nup160 |
G |
A |
2: 90,534,169 (GRCm39) |
V665I |
probably benign |
Het |
Or13a22 |
A |
G |
7: 140,073,034 (GRCm39) |
N161S |
possibly damaging |
Het |
Or14a258 |
T |
C |
7: 86,034,929 (GRCm39) |
Y313C |
possibly damaging |
Het |
Or4e5 |
T |
A |
14: 52,727,533 (GRCm39) |
D296V |
probably damaging |
Het |
Otog |
G |
A |
7: 45,900,762 (GRCm39) |
V352I |
probably damaging |
Het |
Oxct1 |
T |
A |
15: 4,064,764 (GRCm39) |
V34D |
probably benign |
Het |
Pcdhb21 |
T |
A |
18: 37,648,944 (GRCm39) |
|
probably null |
Het |
Pcdhb8 |
T |
G |
18: 37,490,299 (GRCm39) |
V659G |
probably damaging |
Het |
Plxnb2 |
T |
C |
15: 89,042,234 (GRCm39) |
N1590S |
probably benign |
Het |
Rnf168 |
G |
T |
16: 32,097,099 (GRCm39) |
R56L |
possibly damaging |
Het |
Scn8a |
C |
T |
15: 100,872,496 (GRCm39) |
P362S |
probably benign |
Het |
Slc1a3 |
T |
A |
15: 8,668,562 (GRCm39) |
I468F |
probably damaging |
Het |
Slc39a14 |
G |
A |
14: 70,556,368 (GRCm39) |
R3W |
probably damaging |
Het |
Slc7a6 |
T |
A |
8: 106,921,149 (GRCm39) |
N373K |
probably damaging |
Het |
Snrnp200 |
T |
C |
2: 127,080,087 (GRCm39) |
S1955P |
possibly damaging |
Het |
Stat5a |
T |
A |
11: 100,753,965 (GRCm39) |
Y98* |
probably null |
Het |
Thsd7b |
G |
T |
1: 130,138,013 (GRCm39) |
G1564C |
probably damaging |
Het |
Zc3h13 |
T |
C |
14: 75,569,206 (GRCm39) |
V1351A |
possibly damaging |
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 |
|
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 |
145,072,656 (GRCm39) |
splice site |
probably null |
|
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 |
|