Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aipl1 |
G |
T |
11: 71,922,272 (GRCm39) |
P146T |
probably damaging |
Het |
Arnt2 |
T |
A |
7: 83,924,559 (GRCm39) |
T423S |
probably damaging |
Het |
Bend5 |
A |
G |
4: 111,305,787 (GRCm39) |
N277S |
probably null |
Het |
Cd22 |
G |
T |
7: 30,566,471 (GRCm39) |
T816N |
probably damaging |
Het |
Cep126 |
G |
A |
9: 8,120,679 (GRCm39) |
R115C |
probably damaging |
Het |
Cep85 |
T |
C |
4: 133,858,741 (GRCm39) |
H710R |
possibly damaging |
Het |
Cmya5 |
A |
T |
13: 93,230,003 (GRCm39) |
L1695H |
probably damaging |
Het |
Csmd1 |
T |
A |
8: 17,077,355 (GRCm39) |
|
probably null |
Het |
Cyp1a1 |
T |
A |
9: 57,609,352 (GRCm39) |
|
probably null |
Het |
Dennd1c |
C |
T |
17: 57,381,492 (GRCm39) |
|
probably null |
Het |
Dmxl1 |
G |
A |
18: 50,026,990 (GRCm39) |
V2033I |
probably benign |
Het |
Dtna |
A |
G |
18: 23,702,622 (GRCm39) |
H51R |
probably damaging |
Het |
Dysf |
G |
A |
6: 84,184,227 (GRCm39) |
|
probably null |
Het |
Gcn1 |
T |
A |
5: 115,731,720 (GRCm39) |
V945E |
probably benign |
Het |
Gpbar1 |
C |
G |
1: 74,318,053 (GRCm39) |
L99V |
probably damaging |
Het |
Hdac9 |
A |
T |
12: 34,479,516 (GRCm39) |
D212E |
probably damaging |
Het |
Itga1 |
A |
T |
13: 115,133,565 (GRCm39) |
D448E |
probably benign |
Het |
Itga2b |
T |
A |
11: 102,358,692 (GRCm39) |
N75I |
probably benign |
Het |
Klra7 |
T |
C |
6: 130,205,549 (GRCm39) |
E117G |
probably benign |
Het |
Kmt2b |
G |
A |
7: 30,273,490 (GRCm39) |
R2349C |
probably benign |
Het |
Masp1 |
T |
C |
16: 23,310,805 (GRCm39) |
N209S |
probably benign |
Het |
Mybpc2 |
C |
T |
7: 44,161,924 (GRCm39) |
|
probably null |
Het |
Myh15 |
C |
G |
16: 48,986,201 (GRCm39) |
S1557* |
probably null |
Het |
Myo3a |
A |
C |
2: 22,467,783 (GRCm39) |
T346P |
probably benign |
Het |
Nim1k |
A |
G |
13: 120,175,751 (GRCm39) |
Y152H |
probably damaging |
Het |
Nrp2 |
C |
T |
1: 62,802,077 (GRCm39) |
R507* |
probably null |
Het |
Or13n4 |
T |
A |
7: 106,423,205 (GRCm39) |
H176L |
probably damaging |
Het |
Or5e1 |
C |
T |
7: 108,354,819 (GRCm39) |
T252M |
probably damaging |
Het |
Parp14 |
T |
C |
16: 35,677,575 (GRCm39) |
I798V |
probably benign |
Het |
Pcnx2 |
C |
T |
8: 126,614,816 (GRCm39) |
A212T |
probably benign |
Het |
Pkhd1l1 |
A |
T |
15: 44,437,291 (GRCm39) |
H3522L |
probably damaging |
Het |
Pram1 |
C |
T |
17: 33,860,258 (GRCm39) |
A275V |
probably benign |
Het |
Pramel18 |
T |
A |
4: 101,767,257 (GRCm39) |
W169R |
probably damaging |
Het |
Prkag1 |
A |
T |
15: 98,713,827 (GRCm39) |
M1K |
probably null |
Het |
Prss52 |
T |
C |
14: 64,351,042 (GRCm39) |
S276P |
probably damaging |
Het |
Ranbp17 |
A |
T |
11: 33,431,125 (GRCm39) |
V284D |
probably damaging |
Het |
Reln |
T |
C |
5: 22,253,003 (GRCm39) |
D648G |
probably benign |
Het |
Rnf112 |
A |
G |
11: 61,343,105 (GRCm39) |
L190P |
probably damaging |
Het |
Scn5a |
G |
T |
9: 119,314,678 (GRCm39) |
P2010Q |
probably benign |
Het |
Scn5a |
T |
C |
9: 119,342,151 (GRCm39) |
Y1138C |
probably benign |
Het |
Slc4a9 |
A |
G |
18: 36,663,798 (GRCm39) |
H274R |
probably benign |
Het |
Slc5a6 |
T |
G |
5: 31,196,679 (GRCm39) |
E391D |
possibly damaging |
Het |
Speer2 |
T |
C |
16: 69,655,730 (GRCm39) |
Q32R |
possibly damaging |
Het |
Tars1 |
A |
G |
15: 11,389,794 (GRCm39) |
V372A |
probably benign |
Het |
Thsd7a |
A |
T |
6: 12,337,267 (GRCm39) |
L1250Q |
possibly damaging |
Het |
Tnnt3 |
A |
G |
7: 142,066,301 (GRCm39) |
Y222C |
probably benign |
Het |
Trim40 |
T |
C |
17: 37,199,875 (GRCm39) |
I68V |
probably benign |
Het |
Trp53tg5 |
T |
C |
2: 164,313,226 (GRCm39) |
I150V |
probably benign |
Het |
Ube2u |
T |
C |
4: 100,389,365 (GRCm39) |
V109A |
probably benign |
Het |
Usp54 |
A |
T |
14: 20,611,908 (GRCm39) |
D969E |
probably benign |
Het |
Vil1 |
G |
T |
1: 74,464,838 (GRCm39) |
R495L |
probably benign |
Het |
Wfs1 |
T |
A |
5: 37,124,564 (GRCm39) |
K700* |
probably null |
Het |
Zcchc8 |
A |
G |
5: 123,845,466 (GRCm39) |
L298P |
probably damaging |
Het |
Zfp946 |
A |
T |
17: 22,673,697 (GRCm39) |
Q150H |
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 |
|
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 |
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 |
|