Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310003L06Rik |
A |
T |
5: 88,119,774 (GRCm39) |
Y177F |
possibly damaging |
Het |
Als2 |
C |
A |
1: 59,255,189 (GRCm39) |
|
probably benign |
Het |
Arhgap44 |
A |
G |
11: 64,915,038 (GRCm39) |
L410P |
probably damaging |
Het |
Atp13a2 |
C |
T |
4: 140,727,666 (GRCm39) |
A481V |
possibly damaging |
Het |
Bod1l |
C |
A |
5: 41,988,927 (GRCm39) |
L393F |
probably benign |
Het |
Cflar |
T |
A |
1: 58,780,179 (GRCm39) |
I258N |
probably damaging |
Het |
Csmd2 |
A |
T |
4: 128,412,834 (GRCm39) |
N2542I |
probably benign |
Het |
Cyp2b9 |
T |
C |
7: 25,898,025 (GRCm39) |
|
probably benign |
Het |
Dip2c |
A |
T |
13: 9,601,814 (GRCm39) |
I258F |
probably damaging |
Het |
Dock7 |
A |
G |
4: 98,854,585 (GRCm39) |
S1560P |
probably benign |
Het |
Drc7 |
C |
T |
8: 95,802,875 (GRCm39) |
|
probably benign |
Het |
Gm3667 |
T |
A |
14: 18,269,522 (GRCm39) |
S203C |
probably null |
Het |
Gramd2a |
A |
G |
9: 59,619,410 (GRCm39) |
E190G |
probably benign |
Het |
Gstm4 |
T |
C |
3: 107,951,263 (GRCm39) |
D8G |
probably damaging |
Het |
Heatr5b |
A |
T |
17: 79,067,928 (GRCm39) |
M1820K |
probably benign |
Het |
Irs4 |
A |
G |
X: 140,505,794 (GRCm39) |
Y801H |
unknown |
Het |
Loxhd1 |
C |
T |
18: 77,374,169 (GRCm39) |
T80I |
possibly damaging |
Het |
Lrrc40 |
G |
A |
3: 157,747,302 (GRCm39) |
|
probably benign |
Het |
Mapk8ip1 |
T |
G |
2: 92,216,958 (GRCm39) |
K446Q |
probably damaging |
Het |
Mettl21e |
C |
A |
1: 44,249,319 (GRCm39) |
|
probably null |
Het |
Mmp8 |
T |
A |
9: 7,558,530 (GRCm39) |
|
probably benign |
Het |
Muc19 |
A |
T |
15: 91,808,424 (GRCm39) |
|
noncoding transcript |
Het |
Nipsnap3b |
T |
A |
4: 53,015,016 (GRCm39) |
V21E |
possibly damaging |
Het |
Or1j15 |
C |
A |
2: 36,458,716 (GRCm39) |
Y35* |
probably null |
Het |
Or5al6 |
A |
G |
2: 85,977,043 (GRCm39) |
F12L |
probably damaging |
Het |
Or7a38 |
A |
T |
10: 78,753,471 (GRCm39) |
I266F |
probably benign |
Het |
Parp12 |
G |
A |
6: 39,064,520 (GRCm39) |
|
probably null |
Het |
Pramel14 |
C |
A |
4: 143,719,815 (GRCm39) |
L183F |
probably damaging |
Het |
Rgsl1 |
T |
A |
1: 153,701,948 (GRCm39) |
T169S |
possibly damaging |
Het |
Rnf38 |
T |
C |
4: 44,152,529 (GRCm39) |
R12G |
probably damaging |
Het |
Slc9c1 |
T |
C |
16: 45,363,624 (GRCm39) |
|
probably benign |
Het |
Slpi |
T |
C |
2: 164,197,367 (GRCm39) |
|
probably benign |
Het |
Snx17 |
G |
A |
5: 31,353,355 (GRCm39) |
V165I |
probably benign |
Het |
Tnfaip3 |
A |
G |
10: 18,880,357 (GRCm39) |
V570A |
probably benign |
Het |
Vmn1r63 |
A |
G |
7: 5,806,350 (GRCm39) |
M94T |
probably benign |
Het |
Vmn2r95 |
A |
G |
17: 18,672,575 (GRCm39) |
I771V |
probably benign |
Het |
Wiz |
A |
G |
17: 32,575,532 (GRCm39) |
V868A |
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 |
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 |
145,072,656 (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 |
|