Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
C |
T |
3: 137,776,109 (GRCm39) |
P1766L |
probably damaging |
Het |
Abca13 |
A |
G |
11: 9,199,658 (GRCm39) |
Q119R |
possibly damaging |
Het |
Acot11 |
C |
T |
4: 106,617,327 (GRCm39) |
G240R |
probably damaging |
Het |
Aipl1 |
A |
C |
11: 71,921,108 (GRCm39) |
C237G |
probably benign |
Het |
Ankdd1a |
C |
T |
9: 65,416,978 (GRCm39) |
A154T |
probably benign |
Het |
Arglu1 |
T |
C |
8: 8,740,047 (GRCm39) |
S91G |
probably benign |
Het |
Arhgef33 |
C |
A |
17: 80,644,709 (GRCm39) |
H13N |
probably benign |
Het |
Atp1a4 |
A |
G |
1: 172,059,841 (GRCm39) |
I796T |
possibly damaging |
Het |
Birc6 |
C |
G |
17: 74,906,232 (GRCm39) |
S1374R |
probably damaging |
Het |
Birc6 |
T |
A |
17: 74,906,233 (GRCm39) |
S72T |
probably damaging |
Het |
Bmpr1b |
T |
C |
3: 141,577,128 (GRCm39) |
*59W |
probably null |
Het |
Btbd16 |
A |
T |
7: 130,386,011 (GRCm39) |
Q63L |
probably damaging |
Het |
Cacna1c |
C |
T |
6: 118,589,541 (GRCm39) |
R1592H |
probably damaging |
Het |
Caps2 |
G |
A |
10: 112,051,351 (GRCm39) |
E541K |
probably benign |
Het |
Card9 |
T |
C |
2: 26,242,509 (GRCm39) |
E500G |
probably damaging |
Het |
Carnmt1 |
T |
C |
19: 18,681,469 (GRCm39) |
V396A |
probably benign |
Het |
Cdh20 |
A |
C |
1: 104,912,396 (GRCm39) |
D550A |
probably damaging |
Het |
Cdhr1 |
T |
A |
14: 36,811,419 (GRCm39) |
T231S |
probably benign |
Het |
Cenpe |
T |
C |
3: 134,967,389 (GRCm39) |
V2177A |
probably benign |
Het |
Cfap69 |
A |
G |
5: 5,690,183 (GRCm39) |
C161R |
probably damaging |
Het |
Ctsd |
C |
T |
7: 141,930,316 (GRCm39) |
V403I |
probably benign |
Het |
Cyth1 |
C |
T |
11: 118,076,585 (GRCm39) |
|
probably null |
Het |
Dazl |
A |
T |
17: 50,594,781 (GRCm39) |
|
probably null |
Het |
Disp3 |
A |
T |
4: 148,325,770 (GRCm39) |
C1329* |
probably null |
Het |
Dld |
C |
T |
12: 31,383,982 (GRCm39) |
V374I |
probably benign |
Het |
Dnah7c |
T |
C |
1: 46,558,375 (GRCm39) |
Y494H |
probably damaging |
Het |
Dnttip2 |
T |
A |
3: 122,069,217 (GRCm39) |
M144K |
probably benign |
Het |
Drc1 |
A |
T |
5: 30,502,873 (GRCm39) |
D132V |
probably damaging |
Het |
Enpp6 |
A |
G |
8: 47,519,039 (GRCm39) |
D269G |
probably benign |
Het |
Ephx4 |
T |
A |
5: 107,551,631 (GRCm39) |
|
probably null |
Het |
Evl |
T |
C |
12: 108,649,516 (GRCm39) |
S345P |
possibly damaging |
Het |
Fam193a |
A |
T |
5: 34,623,024 (GRCm39) |
D1204V |
probably damaging |
Het |
Fat2 |
A |
T |
11: 55,174,877 (GRCm39) |
D1945E |
probably damaging |
Het |
Fat4 |
T |
C |
3: 39,005,524 (GRCm39) |
|
probably null |
Het |
Fbln7 |
A |
T |
2: 128,719,418 (GRCm39) |
M72L |
probably benign |
Het |
Flnc |
T |
C |
6: 29,441,105 (GRCm39) |
V353A |
probably damaging |
Het |
Fry |
T |
C |
5: 150,314,265 (GRCm39) |
|
probably benign |
Het |
Galnt14 |
A |
T |
17: 73,833,300 (GRCm39) |
C225S |
probably benign |
Het |
Gapvd1 |
T |
C |
2: 34,574,303 (GRCm39) |
S1265G |
probably benign |
Het |
Gm13030 |
A |
G |
4: 138,598,515 (GRCm39) |
F136S |
unknown |
Het |
Gucy1a1 |
T |
C |
3: 82,002,114 (GRCm39) |
H655R |
probably damaging |
Het |
Hk1 |
A |
G |
10: 62,105,773 (GRCm39) |
L890P |
probably damaging |
Het |
Igfn1 |
T |
A |
1: 135,898,341 (GRCm39) |
R742* |
probably null |
Het |
Igkv12-49 |
T |
C |
6: 69,693,553 (GRCm39) |
|
noncoding transcript |
Het |
Igkv2-109 |
T |
A |
6: 68,279,965 (GRCm39) |
L62Q |
possibly damaging |
Het |
Itgb3 |
A |
G |
11: 104,528,805 (GRCm39) |
T311A |
possibly damaging |
Het |
Kl |
A |
G |
5: 150,912,948 (GRCm39) |
E899G |
probably damaging |
Het |
Kyat3 |
A |
T |
3: 142,429,021 (GRCm39) |
D151V |
probably damaging |
Het |
Morc2b |
A |
T |
17: 33,357,583 (GRCm39) |
M63K |
possibly damaging |
Het |
Mtbp |
T |
A |
15: 55,434,723 (GRCm39) |
F298L |
possibly damaging |
Het |
Mtmr3 |
C |
T |
11: 4,448,951 (GRCm39) |
V272I |
probably benign |
Het |
Muc4 |
A |
G |
16: 32,574,480 (GRCm39) |
T977A |
probably benign |
Het |
Nebl |
G |
A |
2: 17,408,998 (GRCm39) |
H367Y |
probably benign |
Het |
Nop58 |
T |
A |
1: 59,743,824 (GRCm39) |
Y274* |
probably null |
Het |
Nuak1 |
T |
A |
10: 84,210,666 (GRCm39) |
Q474L |
probably damaging |
Het |
Obscn |
A |
G |
11: 58,889,331 (GRCm39) |
S7523P |
unknown |
Het |
Oosp3 |
T |
A |
19: 11,682,753 (GRCm39) |
D140E |
probably benign |
Het |
Or52z15 |
T |
A |
7: 103,332,680 (GRCm39) |
C242S |
probably damaging |
Het |
Padi2 |
G |
A |
4: 140,644,952 (GRCm39) |
R62H |
probably benign |
Het |
Patl1 |
A |
G |
19: 11,917,136 (GRCm39) |
N661S |
probably benign |
Het |
Pcyox1l |
G |
T |
18: 61,831,544 (GRCm39) |
N238K |
probably benign |
Het |
Pmch |
A |
G |
10: 87,927,011 (GRCm39) |
T5A |
probably benign |
Het |
Polr3h |
A |
G |
15: 81,800,835 (GRCm39) |
L169P |
probably damaging |
Het |
Ptpn4 |
A |
G |
1: 119,615,453 (GRCm39) |
V567A |
probably damaging |
Het |
Rasgrp2 |
T |
G |
19: 6,452,543 (GRCm39) |
F39V |
probably damaging |
Het |
Setd1b |
G |
A |
5: 123,296,815 (GRCm39) |
|
probably benign |
Het |
Sh3glb2 |
A |
T |
2: 30,240,401 (GRCm39) |
|
probably null |
Het |
Slc46a3 |
A |
T |
5: 147,830,700 (GRCm39) |
N44K |
probably benign |
Het |
Slc9b1 |
T |
A |
3: 135,099,756 (GRCm39) |
N425K |
probably benign |
Het |
Slfn14 |
A |
T |
11: 83,170,288 (GRCm39) |
V452E |
probably damaging |
Het |
Slfn8 |
A |
T |
11: 82,894,161 (GRCm39) |
M826K |
probably benign |
Het |
Slit3 |
G |
A |
11: 35,520,578 (GRCm39) |
V572M |
probably benign |
Het |
Smr3a |
C |
A |
5: 88,155,873 (GRCm39) |
|
probably null |
Het |
Snap29 |
T |
C |
16: 17,224,194 (GRCm39) |
S70P |
probably damaging |
Het |
Svopl |
T |
A |
6: 37,993,949 (GRCm39) |
|
probably benign |
Het |
Tbc1d17 |
A |
T |
7: 44,494,761 (GRCm39) |
F186I |
probably damaging |
Het |
Tgm6 |
T |
C |
2: 129,983,176 (GRCm39) |
V255A |
probably damaging |
Het |
Tjp1 |
G |
T |
7: 64,952,600 (GRCm39) |
T1498K |
probably benign |
Het |
Tkfc |
C |
A |
19: 10,574,711 (GRCm39) |
E176D |
probably benign |
Het |
Tmem102 |
C |
T |
11: 69,694,506 (GRCm39) |
V489I |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,551,781 (GRCm39) |
V22930A |
probably damaging |
Het |
Tyms |
A |
T |
5: 30,278,357 (GRCm39) |
|
probably null |
Het |
Uaca |
T |
A |
9: 60,748,238 (GRCm39) |
D67E |
probably damaging |
Het |
Unc119b |
G |
A |
5: 115,265,508 (GRCm39) |
|
probably benign |
Het |
Usp29 |
A |
T |
7: 6,964,744 (GRCm39) |
T196S |
probably benign |
Het |
Usp37 |
A |
G |
1: 74,525,141 (GRCm39) |
S228P |
probably damaging |
Het |
Usp42 |
C |
A |
5: 143,701,270 (GRCm39) |
A918S |
probably benign |
Het |
Vmn2r72 |
T |
A |
7: 85,387,058 (GRCm39) |
L835F |
probably benign |
Het |
Vps13a |
T |
C |
19: 16,637,894 (GRCm39) |
T2396A |
probably benign |
Het |
Whrn |
A |
T |
4: 63,412,945 (GRCm39) |
S176T |
probably damaging |
Het |
Zbtb42 |
T |
C |
12: 112,647,055 (GRCm39) |
F410S |
probably damaging |
Het |
Zfp616 |
T |
C |
11: 73,973,952 (GRCm39) |
S74P |
probably damaging |
Het |
Zswim6 |
A |
G |
13: 107,880,642 (GRCm39) |
|
noncoding transcript |
Het |
|
Other mutations in Ccnl1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01969:Ccnl1
|
APN |
3 |
65,855,908 (GRCm39) |
splice site |
probably benign |
|
IGL02353:Ccnl1
|
APN |
3 |
65,856,141 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02360:Ccnl1
|
APN |
3 |
65,856,141 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02454:Ccnl1
|
APN |
3 |
65,864,318 (GRCm39) |
missense |
probably damaging |
0.99 |
R1598:Ccnl1
|
UTSW |
3 |
65,854,191 (GRCm39) |
missense |
probably damaging |
0.97 |
R1903:Ccnl1
|
UTSW |
3 |
65,854,332 (GRCm39) |
missense |
possibly damaging |
0.73 |
R2392:Ccnl1
|
UTSW |
3 |
65,856,173 (GRCm39) |
missense |
probably damaging |
1.00 |
R3879:Ccnl1
|
UTSW |
3 |
65,856,179 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4607:Ccnl1
|
UTSW |
3 |
65,854,131 (GRCm39) |
utr 3 prime |
probably benign |
|
R4608:Ccnl1
|
UTSW |
3 |
65,854,131 (GRCm39) |
utr 3 prime |
probably benign |
|
R4739:Ccnl1
|
UTSW |
3 |
65,854,092 (GRCm39) |
utr 3 prime |
probably benign |
|
R4885:Ccnl1
|
UTSW |
3 |
65,864,320 (GRCm39) |
missense |
probably damaging |
1.00 |
R5833:Ccnl1
|
UTSW |
3 |
65,855,922 (GRCm39) |
missense |
probably benign |
0.23 |
R6933:Ccnl1
|
UTSW |
3 |
65,855,373 (GRCm39) |
missense |
probably benign |
0.00 |
R7425:Ccnl1
|
UTSW |
3 |
65,856,179 (GRCm39) |
missense |
probably damaging |
1.00 |
R7943:Ccnl1
|
UTSW |
3 |
65,864,326 (GRCm39) |
missense |
probably benign |
0.30 |
R7988:Ccnl1
|
UTSW |
3 |
65,865,282 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7990:Ccnl1
|
UTSW |
3 |
65,854,314 (GRCm39) |
missense |
possibly damaging |
0.73 |
R8137:Ccnl1
|
UTSW |
3 |
65,865,291 (GRCm39) |
missense |
possibly damaging |
0.96 |
R8690:Ccnl1
|
UTSW |
3 |
65,855,165 (GRCm39) |
missense |
possibly damaging |
0.73 |
R8736:Ccnl1
|
UTSW |
3 |
65,865,447 (GRCm39) |
missense |
unknown |
|
R8865:Ccnl1
|
UTSW |
3 |
65,854,269 (GRCm39) |
missense |
probably benign |
0.18 |
R8914:Ccnl1
|
UTSW |
3 |
65,854,080 (GRCm39) |
missense |
unknown |
|
R9186:Ccnl1
|
UTSW |
3 |
65,865,426 (GRCm39) |
missense |
unknown |
|
R9612:Ccnl1
|
UTSW |
3 |
65,865,404 (GRCm39) |
missense |
probably damaging |
1.00 |
|