Other mutations in this stock |
Total: 104 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aar2 |
T |
G |
2: 156,392,893 (GRCm39) |
V94G |
probably benign |
Het |
Acp5 |
A |
T |
9: 22,041,218 (GRCm39) |
S70T |
possibly damaging |
Het |
Adcy1 |
C |
G |
11: 7,089,162 (GRCm39) |
N525K |
possibly damaging |
Het |
Adra1d |
C |
A |
2: 131,388,134 (GRCm39) |
V474F |
probably benign |
Het |
Aknad1 |
A |
G |
3: 108,688,555 (GRCm39) |
M628V |
probably benign |
Het |
Alg8 |
A |
T |
7: 97,032,891 (GRCm39) |
|
probably null |
Het |
Cacna1d |
A |
G |
14: 29,845,453 (GRCm39) |
V572A |
probably benign |
Het |
Ccdc158 |
A |
C |
5: 92,809,977 (GRCm39) |
M177R |
probably benign |
Het |
Ccdc191 |
A |
T |
16: 43,767,859 (GRCm39) |
R678* |
probably null |
Het |
Cdkn2d |
C |
A |
9: 21,202,288 (GRCm39) |
|
probably benign |
Het |
Cdx2 |
G |
T |
5: 147,240,097 (GRCm39) |
T193K |
probably damaging |
Het |
Cfap44 |
T |
A |
16: 44,242,681 (GRCm39) |
M695K |
probably benign |
Het |
Cfap70 |
A |
C |
14: 20,498,673 (GRCm39) |
S5A |
probably benign |
Het |
Chd9 |
T |
C |
8: 91,659,456 (GRCm39) |
S139P |
probably damaging |
Het |
Chmp7 |
A |
G |
14: 69,958,446 (GRCm39) |
V241A |
probably damaging |
Het |
Cnga1 |
A |
G |
5: 72,762,374 (GRCm39) |
I380T |
probably damaging |
Het |
Cts6 |
T |
A |
13: 61,349,633 (GRCm39) |
E53D |
probably damaging |
Het |
Cul2 |
A |
G |
18: 3,414,115 (GRCm39) |
|
probably benign |
Het |
Dclk3 |
A |
T |
9: 111,311,696 (GRCm39) |
N646I |
probably damaging |
Het |
Dnhd1 |
A |
G |
7: 105,370,738 (GRCm39) |
S4673G |
probably benign |
Het |
Dock4 |
G |
T |
12: 40,787,539 (GRCm39) |
S818I |
probably damaging |
Het |
Dysf |
C |
T |
6: 84,041,461 (GRCm39) |
Q156* |
probably null |
Het |
Espnl |
T |
C |
1: 91,250,009 (GRCm39) |
V52A |
probably damaging |
Het |
Fam163b |
T |
C |
2: 27,002,646 (GRCm39) |
N117S |
probably damaging |
Het |
Fam89a |
A |
G |
8: 125,467,971 (GRCm39) |
Y114H |
probably damaging |
Het |
Flcn |
T |
C |
11: 59,691,902 (GRCm39) |
N249S |
probably benign |
Het |
Gnai1 |
A |
G |
5: 18,478,548 (GRCm39) |
S206P |
probably damaging |
Het |
H1f6 |
G |
T |
13: 23,880,307 (GRCm39) |
K153N |
possibly damaging |
Het |
Hal |
T |
C |
10: 93,339,344 (GRCm39) |
S478P |
possibly damaging |
Het |
Haus3 |
G |
A |
5: 34,323,600 (GRCm39) |
P337S |
possibly damaging |
Het |
Hectd1 |
T |
A |
12: 51,816,101 (GRCm39) |
M1324L |
possibly damaging |
Het |
Hpn |
G |
T |
7: 30,798,815 (GRCm39) |
|
probably benign |
Het |
Hspa9 |
A |
T |
18: 35,079,699 (GRCm39) |
Y243* |
probably null |
Het |
Htr3a |
T |
C |
9: 48,817,686 (GRCm39) |
T96A |
probably benign |
Het |
Ift140 |
C |
A |
17: 25,264,497 (GRCm39) |
C557* |
probably null |
Het |
Il4ra |
T |
C |
7: 125,174,371 (GRCm39) |
|
probably benign |
Het |
Ipo9 |
A |
G |
1: 135,332,074 (GRCm39) |
|
probably benign |
Het |
Irag2 |
G |
A |
6: 145,117,704 (GRCm39) |
|
probably benign |
Het |
Jph3 |
A |
G |
8: 122,480,459 (GRCm39) |
Q379R |
possibly damaging |
Het |
Kcnb1 |
A |
G |
2: 166,946,889 (GRCm39) |
V653A |
probably benign |
Het |
Kif14 |
A |
G |
1: 136,455,131 (GRCm39) |
E1551G |
probably damaging |
Het |
Krt17 |
G |
A |
11: 100,151,704 (GRCm39) |
R30* |
probably null |
Het |
Lamb3 |
A |
T |
1: 193,003,361 (GRCm39) |
D100V |
probably damaging |
Het |
Map2 |
A |
G |
1: 66,455,265 (GRCm39) |
D1385G |
probably damaging |
Het |
Map3k21 |
A |
G |
8: 126,671,709 (GRCm39) |
D999G |
possibly damaging |
Het |
Marf1 |
T |
C |
16: 13,969,147 (GRCm39) |
I109V |
probably benign |
Het |
Mcam |
T |
G |
9: 44,051,502 (GRCm39) |
|
probably null |
Het |
Med18 |
T |
C |
4: 132,187,337 (GRCm39) |
H99R |
probably damaging |
Het |
Mettl25 |
C |
T |
10: 105,662,386 (GRCm39) |
V195I |
probably damaging |
Het |
Micu2 |
G |
A |
14: 58,154,835 (GRCm39) |
|
probably benign |
Het |
Mpl |
A |
G |
4: 118,314,060 (GRCm39) |
|
probably benign |
Het |
Myh8 |
A |
G |
11: 67,192,518 (GRCm39) |
T1466A |
probably benign |
Het |
Myo1e |
A |
T |
9: 70,249,408 (GRCm39) |
I503F |
possibly damaging |
Het |
Myo3b |
T |
A |
2: 69,935,769 (GRCm39) |
C61S |
probably benign |
Het |
Myorg |
A |
T |
4: 41,498,912 (GRCm39) |
N239K |
probably benign |
Het |
Nbn |
T |
C |
4: 15,986,672 (GRCm39) |
|
probably benign |
Het |
Ndufa4 |
C |
T |
6: 11,906,023 (GRCm39) |
V10I |
probably benign |
Het |
Nf1 |
A |
T |
11: 79,309,400 (GRCm39) |
K438M |
possibly damaging |
Het |
Nlrp9c |
A |
G |
7: 26,077,437 (GRCm39) |
S727P |
possibly damaging |
Het |
Nmbr |
C |
T |
10: 14,646,139 (GRCm39) |
Q338* |
probably null |
Het |
Nt5e |
A |
G |
9: 88,249,385 (GRCm39) |
S440G |
possibly damaging |
Het |
Nubp2 |
T |
C |
17: 25,103,445 (GRCm39) |
E144G |
probably damaging |
Het |
Or12e7 |
T |
C |
2: 87,288,381 (GRCm39) |
F291L |
probably benign |
Het |
Or2ag1b |
A |
G |
7: 106,288,462 (GRCm39) |
Y159H |
probably benign |
Het |
Or52s1 |
G |
A |
7: 102,861,933 (GRCm39) |
V289M |
possibly damaging |
Het |
Otogl |
T |
A |
10: 107,642,557 (GRCm39) |
N1291I |
probably damaging |
Het |
Pa2g4 |
T |
C |
10: 128,399,511 (GRCm39) |
K51R |
probably benign |
Het |
Pah |
C |
T |
10: 87,403,143 (GRCm39) |
P173S |
possibly damaging |
Het |
Pcdhb12 |
A |
G |
18: 37,569,780 (GRCm39) |
I309V |
probably benign |
Het |
Pck1 |
T |
G |
2: 172,998,861 (GRCm39) |
I373S |
possibly damaging |
Het |
Pga5 |
A |
G |
19: 10,646,817 (GRCm39) |
Y305H |
probably damaging |
Het |
Plxnd1 |
G |
T |
6: 115,945,754 (GRCm39) |
D906E |
probably benign |
Het |
Ppfia4 |
T |
C |
1: 134,256,927 (GRCm39) |
E98G |
possibly damaging |
Het |
Pzp |
C |
T |
6: 128,466,119 (GRCm39) |
|
probably benign |
Het |
Rab39 |
G |
A |
9: 53,617,330 (GRCm39) |
T29I |
probably damaging |
Het |
Raet1e |
C |
A |
10: 22,056,761 (GRCm39) |
H112Q |
possibly damaging |
Het |
Rars2 |
T |
C |
4: 34,645,838 (GRCm39) |
Y252H |
probably damaging |
Het |
Rars2 |
A |
C |
4: 34,656,030 (GRCm39) |
Q421P |
probably benign |
Het |
Rasa2 |
A |
T |
9: 96,450,460 (GRCm39) |
D479E |
probably damaging |
Het |
Rbl2 |
A |
T |
8: 91,833,135 (GRCm39) |
T689S |
probably damaging |
Het |
Rims4 |
C |
T |
2: 163,705,945 (GRCm39) |
V230M |
probably benign |
Het |
Scgb1b27 |
G |
A |
7: 33,721,377 (GRCm39) |
|
probably benign |
Het |
Sec31b |
G |
A |
19: 44,513,908 (GRCm39) |
|
probably benign |
Het |
Six3 |
G |
A |
17: 85,928,818 (GRCm39) |
G51R |
probably damaging |
Het |
Skp2 |
A |
C |
15: 9,127,971 (GRCm39) |
|
probably null |
Het |
Slc35f4 |
A |
T |
14: 49,541,713 (GRCm39) |
I347N |
possibly damaging |
Het |
Slc4a2 |
A |
T |
5: 24,641,272 (GRCm39) |
|
probably null |
Het |
Slc52a3 |
T |
C |
2: 151,850,076 (GRCm39) |
*461Q |
probably null |
Het |
Slc6a1 |
G |
A |
6: 114,279,761 (GRCm39) |
V142I |
probably benign |
Het |
Susd5 |
A |
G |
9: 113,925,977 (GRCm39) |
*620W |
probably null |
Het |
Timm21 |
T |
C |
18: 84,965,791 (GRCm39) |
N239S |
probably damaging |
Het |
Tmem131 |
T |
C |
1: 36,867,131 (GRCm39) |
|
probably benign |
Het |
Tmem63c |
T |
C |
12: 87,122,413 (GRCm39) |
W404R |
probably damaging |
Het |
Tnrc6b |
A |
G |
15: 80,772,065 (GRCm39) |
D1118G |
probably damaging |
Het |
Traf2 |
G |
C |
2: 25,427,138 (GRCm39) |
A71G |
possibly damaging |
Het |
Trim54 |
A |
G |
5: 31,291,463 (GRCm39) |
M195V |
probably benign |
Het |
Trip11 |
C |
T |
12: 101,850,987 (GRCm39) |
E741K |
probably damaging |
Het |
Trp73 |
AGCTGCTGCTGCTGCTGCTG |
AGCTGCTGCTGCTGCTG |
4: 154,146,981 (GRCm39) |
|
probably benign |
Het |
Trpm5 |
G |
T |
7: 142,636,695 (GRCm39) |
T414N |
probably damaging |
Het |
Vps51 |
G |
T |
19: 6,121,467 (GRCm39) |
S185* |
probably null |
Het |
Zfp329 |
G |
T |
7: 12,544,756 (GRCm39) |
T256K |
probably damaging |
Het |
Zfp729b |
A |
G |
13: 67,740,022 (GRCm39) |
Y748H |
probably damaging |
Het |
Zfp777 |
T |
C |
6: 48,001,903 (GRCm39) |
E773G |
probably damaging |
Het |
Zfp866 |
T |
C |
8: 70,219,365 (GRCm39) |
Y53C |
probably damaging |
Het |
|
Other mutations in Col4a1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00336:Col4a1
|
APN |
8 |
11,290,077 (GRCm39) |
splice site |
probably benign |
|
IGL00503:Col4a1
|
APN |
8 |
11,290,076 (GRCm39) |
splice site |
probably benign |
|
IGL00938:Col4a1
|
APN |
8 |
11,286,456 (GRCm39) |
intron |
probably benign |
|
IGL01295:Col4a1
|
APN |
8 |
11,286,075 (GRCm39) |
intron |
probably benign |
|
IGL01406:Col4a1
|
APN |
8 |
11,268,898 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01807:Col4a1
|
APN |
8 |
11,297,056 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL01865:Col4a1
|
APN |
8 |
11,251,790 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02166:Col4a1
|
APN |
8 |
11,294,509 (GRCm39) |
unclassified |
probably benign |
|
IGL02234:Col4a1
|
APN |
8 |
11,266,713 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02445:Col4a1
|
APN |
8 |
11,283,911 (GRCm39) |
intron |
probably benign |
|
IGL02719:Col4a1
|
APN |
8 |
11,281,950 (GRCm39) |
intron |
probably benign |
|
IGL02817:Col4a1
|
APN |
8 |
11,270,259 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02821:Col4a1
|
APN |
8 |
11,271,375 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02870:Col4a1
|
APN |
8 |
11,271,375 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02935:Col4a1
|
APN |
8 |
11,269,166 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03085:Col4a1
|
APN |
8 |
11,272,198 (GRCm39) |
nonsense |
probably null |
|
Wayne
|
UTSW |
8 |
11,259,650 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03134:Col4a1
|
UTSW |
8 |
11,290,069 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0076:Col4a1
|
UTSW |
8 |
11,268,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R0076:Col4a1
|
UTSW |
8 |
11,268,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R0239:Col4a1
|
UTSW |
8 |
11,268,780 (GRCm39) |
splice site |
probably benign |
|
R0268:Col4a1
|
UTSW |
8 |
11,317,588 (GRCm39) |
splice site |
probably benign |
|
R0320:Col4a1
|
UTSW |
8 |
11,292,782 (GRCm39) |
splice site |
probably null |
|
R0402:Col4a1
|
UTSW |
8 |
11,249,838 (GRCm39) |
utr 3 prime |
probably benign |
|
R0483:Col4a1
|
UTSW |
8 |
11,286,423 (GRCm39) |
splice site |
probably benign |
|
R0511:Col4a1
|
UTSW |
8 |
11,258,333 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0544:Col4a1
|
UTSW |
8 |
11,276,487 (GRCm39) |
intron |
probably benign |
|
R0630:Col4a1
|
UTSW |
8 |
11,249,889 (GRCm39) |
splice site |
probably benign |
|
R0648:Col4a1
|
UTSW |
8 |
11,296,892 (GRCm39) |
missense |
unknown |
|
R0733:Col4a1
|
UTSW |
8 |
11,268,934 (GRCm39) |
missense |
possibly damaging |
0.46 |
R0839:Col4a1
|
UTSW |
8 |
11,271,015 (GRCm39) |
missense |
probably damaging |
0.96 |
R0900:Col4a1
|
UTSW |
8 |
11,268,014 (GRCm39) |
small deletion |
probably benign |
|
R0941:Col4a1
|
UTSW |
8 |
11,258,296 (GRCm39) |
missense |
unknown |
|
R1456:Col4a1
|
UTSW |
8 |
11,292,829 (GRCm39) |
splice site |
probably benign |
|
R1728:Col4a1
|
UTSW |
8 |
11,262,712 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1832:Col4a1
|
UTSW |
8 |
11,264,644 (GRCm39) |
splice site |
probably benign |
|
R1862:Col4a1
|
UTSW |
8 |
11,276,439 (GRCm39) |
intron |
probably benign |
|
R1955:Col4a1
|
UTSW |
8 |
11,258,228 (GRCm39) |
splice site |
probably null |
|
R2058:Col4a1
|
UTSW |
8 |
11,260,792 (GRCm39) |
missense |
probably damaging |
0.96 |
R2263:Col4a1
|
UTSW |
8 |
11,362,586 (GRCm39) |
unclassified |
probably benign |
|
R2696:Col4a1
|
UTSW |
8 |
11,285,092 (GRCm39) |
splice site |
probably null |
|
R3826:Col4a1
|
UTSW |
8 |
11,259,650 (GRCm39) |
missense |
probably damaging |
1.00 |
R3828:Col4a1
|
UTSW |
8 |
11,259,650 (GRCm39) |
missense |
probably damaging |
1.00 |
R3829:Col4a1
|
UTSW |
8 |
11,259,650 (GRCm39) |
missense |
probably damaging |
1.00 |
R3830:Col4a1
|
UTSW |
8 |
11,259,650 (GRCm39) |
missense |
probably damaging |
1.00 |
R3923:Col4a1
|
UTSW |
8 |
11,251,665 (GRCm39) |
utr 3 prime |
probably benign |
|
R3980:Col4a1
|
UTSW |
8 |
11,289,155 (GRCm39) |
intron |
probably benign |
|
R4120:Col4a1
|
UTSW |
8 |
11,256,263 (GRCm39) |
missense |
unknown |
|
R4152:Col4a1
|
UTSW |
8 |
11,267,227 (GRCm39) |
splice site |
probably null |
|
R4437:Col4a1
|
UTSW |
8 |
11,256,387 (GRCm39) |
nonsense |
probably null |
|
R5237:Col4a1
|
UTSW |
8 |
11,295,068 (GRCm39) |
unclassified |
probably benign |
|
R5362:Col4a1
|
UTSW |
8 |
11,295,760 (GRCm39) |
unclassified |
probably benign |
|
R5488:Col4a1
|
UTSW |
8 |
11,362,550 (GRCm39) |
unclassified |
probably benign |
|
R5489:Col4a1
|
UTSW |
8 |
11,362,550 (GRCm39) |
unclassified |
probably benign |
|
R5864:Col4a1
|
UTSW |
8 |
11,252,973 (GRCm39) |
utr 3 prime |
probably benign |
|
R5929:Col4a1
|
UTSW |
8 |
11,266,788 (GRCm39) |
missense |
probably benign |
0.17 |
R6159:Col4a1
|
UTSW |
8 |
11,270,007 (GRCm39) |
missense |
probably damaging |
1.00 |
R6261:Col4a1
|
UTSW |
8 |
11,257,409 (GRCm39) |
splice site |
probably null |
|
R6404:Col4a1
|
UTSW |
8 |
11,257,409 (GRCm39) |
splice site |
probably null |
|
R6520:Col4a1
|
UTSW |
8 |
11,269,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R6862:Col4a1
|
UTSW |
8 |
11,252,926 (GRCm39) |
utr 3 prime |
probably benign |
|
R6974:Col4a1
|
UTSW |
8 |
11,362,538 (GRCm39) |
unclassified |
probably benign |
|
R7329:Col4a1
|
UTSW |
8 |
11,276,494 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7893:Col4a1
|
UTSW |
8 |
11,270,243 (GRCm39) |
missense |
unknown |
|
R8392:Col4a1
|
UTSW |
8 |
11,258,333 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8809:Col4a1
|
UTSW |
8 |
11,295,916 (GRCm39) |
missense |
unknown |
|
R8957:Col4a1
|
UTSW |
8 |
11,295,906 (GRCm39) |
unclassified |
probably benign |
|
R9013:Col4a1
|
UTSW |
8 |
11,272,270 (GRCm39) |
missense |
probably benign |
0.02 |
R9048:Col4a1
|
UTSW |
8 |
11,281,944 (GRCm39) |
splice site |
probably benign |
|
R9102:Col4a1
|
UTSW |
8 |
11,253,007 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9154:Col4a1
|
UTSW |
8 |
11,267,446 (GRCm39) |
missense |
probably damaging |
0.99 |
R9379:Col4a1
|
UTSW |
8 |
11,249,838 (GRCm39) |
missense |
unknown |
|
Z1088:Col4a1
|
UTSW |
8 |
11,296,859 (GRCm39) |
splice site |
probably benign |
|
Z1177:Col4a1
|
UTSW |
8 |
11,289,024 (GRCm39) |
missense |
unknown |
|
Z1177:Col4a1
|
UTSW |
8 |
11,285,218 (GRCm39) |
missense |
unknown |
|
|