Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9630041A04Rik |
A |
T |
9: 101,819,887 (GRCm39) |
R102S |
probably benign |
Het |
Abitram |
A |
T |
4: 56,806,141 (GRCm39) |
K184N |
probably benign |
Het |
Acvr2b |
C |
T |
9: 119,231,616 (GRCm39) |
T2M |
probably benign |
Het |
Adamtsl3 |
A |
G |
7: 82,206,710 (GRCm39) |
|
probably benign |
Het |
Adcy7 |
A |
G |
8: 89,052,014 (GRCm39) |
Y894C |
probably damaging |
Het |
Afdn |
T |
A |
17: 14,024,270 (GRCm39) |
C59S |
probably damaging |
Het |
Amt |
C |
A |
9: 108,178,410 (GRCm39) |
T339K |
probably benign |
Het |
Anxa10 |
G |
T |
8: 62,549,753 (GRCm39) |
Q31K |
probably damaging |
Het |
Ap1g2 |
T |
C |
14: 55,339,818 (GRCm39) |
T454A |
probably benign |
Het |
Boll |
A |
T |
1: 55,399,812 (GRCm39) |
I43N |
possibly damaging |
Het |
Cacna1c |
T |
C |
6: 118,601,394 (GRCm39) |
D1472G |
|
Het |
Calcrl |
T |
C |
2: 84,205,643 (GRCm39) |
N16S |
probably benign |
Het |
Ccdc191 |
C |
T |
16: 43,764,041 (GRCm39) |
Q501* |
probably null |
Het |
Cchcr1 |
T |
C |
17: 35,841,105 (GRCm39) |
L658P |
probably damaging |
Het |
Cfap46 |
A |
T |
7: 139,201,207 (GRCm39) |
C1919S |
unknown |
Het |
Col6a3 |
G |
A |
1: 90,735,403 (GRCm39) |
L1356F |
possibly damaging |
Het |
Dlc1 |
A |
G |
8: 37,046,558 (GRCm39) |
S680P |
possibly damaging |
Het |
Dock4 |
T |
G |
12: 40,699,404 (GRCm39) |
M206R |
possibly damaging |
Het |
Eml5 |
T |
C |
12: 98,765,060 (GRCm39) |
K1630E |
probably damaging |
Het |
Fat1 |
A |
G |
8: 45,488,514 (GRCm39) |
T3432A |
probably damaging |
Het |
Fcrl5 |
G |
T |
3: 87,343,138 (GRCm39) |
|
probably benign |
Het |
Fcrla |
A |
G |
1: 170,755,135 (GRCm39) |
|
probably benign |
Het |
Fut4 |
C |
A |
9: 14,662,572 (GRCm39) |
D241Y |
probably benign |
Het |
Fzd6 |
A |
G |
15: 38,870,962 (GRCm39) |
|
probably benign |
Het |
Gjc2 |
T |
C |
11: 59,068,453 (GRCm39) |
T10A |
probably damaging |
Het |
Gle1 |
C |
T |
2: 29,829,514 (GRCm39) |
H203Y |
possibly damaging |
Het |
Gm5565 |
A |
T |
5: 146,096,917 (GRCm39) |
I74N |
probably damaging |
Het |
Gnl2 |
T |
A |
4: 124,947,250 (GRCm39) |
I624K |
possibly damaging |
Het |
Gnpat |
C |
A |
8: 125,614,524 (GRCm39) |
N653K |
probably benign |
Het |
Gstcd |
A |
G |
3: 132,777,665 (GRCm39) |
L382S |
probably damaging |
Het |
Ipcef1 |
A |
G |
10: 6,857,936 (GRCm39) |
|
probably benign |
Het |
Jmjd7 |
T |
C |
2: 119,860,895 (GRCm39) |
V115A |
possibly damaging |
Het |
Ltbp2 |
G |
A |
12: 84,837,864 (GRCm39) |
P1192L |
probably benign |
Het |
Ltbp2 |
T |
G |
12: 84,876,885 (GRCm39) |
D440A |
possibly damaging |
Het |
Macf1 |
T |
G |
4: 123,328,501 (GRCm39) |
D4744A |
probably damaging |
Het |
Mapk11 |
T |
C |
15: 89,029,372 (GRCm39) |
D230G |
probably damaging |
Het |
Mfsd6 |
A |
C |
1: 52,747,514 (GRCm39) |
Y450* |
probably null |
Het |
Mtmr9 |
A |
G |
14: 63,781,001 (GRCm39) |
C30R |
probably damaging |
Het |
Ncf1 |
G |
A |
5: 134,250,693 (GRCm39) |
Q376* |
probably null |
Het |
Ncor2 |
C |
A |
5: 125,113,150 (GRCm39) |
R296M |
|
Het |
Or51ah3 |
A |
T |
7: 103,210,004 (GRCm39) |
T107S |
probably damaging |
Het |
Or5d37 |
A |
G |
2: 87,923,806 (GRCm39) |
V158A |
probably benign |
Het |
Or5k8 |
A |
G |
16: 58,644,734 (GRCm39) |
F113L |
probably benign |
Het |
Or8b57 |
A |
T |
9: 40,003,632 (GRCm39) |
I210K |
possibly damaging |
Het |
Or8b8 |
C |
A |
9: 37,809,415 (GRCm39) |
S238R |
probably benign |
Het |
Or8k31-ps1 |
A |
T |
2: 86,356,392 (GRCm39) |
L43* |
probably null |
Het |
Pate9 |
A |
T |
9: 36,445,727 (GRCm39) |
C75S |
probably damaging |
Het |
Pcsk6 |
A |
T |
7: 65,559,950 (GRCm39) |
I92F |
probably damaging |
Het |
Plec |
A |
G |
15: 76,060,445 (GRCm39) |
V3164A |
probably benign |
Het |
Prss16 |
A |
G |
13: 22,190,175 (GRCm39) |
|
probably benign |
Het |
Ptch2 |
T |
A |
4: 116,967,505 (GRCm39) |
H724Q |
probably damaging |
Het |
Pzp |
A |
T |
6: 128,499,077 (GRCm39) |
F190Y |
probably damaging |
Het |
Rab6a |
A |
G |
7: 100,275,809 (GRCm39) |
T41A |
probably benign |
Het |
Rbm6 |
A |
G |
9: 107,660,926 (GRCm39) |
L879P |
probably damaging |
Het |
Rem1 |
T |
A |
2: 152,469,969 (GRCm39) |
|
probably benign |
Het |
Rnf17 |
T |
C |
14: 56,719,554 (GRCm39) |
S935P |
probably damaging |
Het |
Ryr1 |
C |
A |
7: 28,802,254 (GRCm39) |
V789L |
probably damaging |
Het |
Scgb2b3 |
A |
T |
7: 31,059,528 (GRCm39) |
M82K |
possibly damaging |
Het |
Sgce |
T |
A |
6: 4,674,585 (GRCm39) |
L451F |
probably damaging |
Het |
Slc25a17 |
A |
C |
15: 81,207,814 (GRCm39) |
V258G |
probably benign |
Het |
Spidr |
G |
A |
16: 15,784,712 (GRCm39) |
T452I |
probably benign |
Het |
Tas2r129 |
A |
G |
6: 132,928,576 (GRCm39) |
N171S |
probably benign |
Het |
Tbc1d24 |
A |
T |
17: 24,405,114 (GRCm39) |
V10E |
probably damaging |
Het |
Tdo2 |
T |
G |
3: 81,876,885 (GRCm39) |
M115L |
probably benign |
Het |
Tdrd9 |
T |
C |
12: 111,980,935 (GRCm39) |
|
probably null |
Het |
Tead1 |
T |
A |
7: 112,493,601 (GRCm39) |
I376N |
probably damaging |
Het |
Tmem26 |
A |
G |
10: 68,614,488 (GRCm39) |
H301R |
possibly damaging |
Het |
Tnxb |
A |
G |
17: 34,929,134 (GRCm39) |
T2726A |
possibly damaging |
Het |
Trim43c |
T |
C |
9: 88,723,966 (GRCm39) |
M164T |
probably benign |
Het |
Trpc1 |
G |
A |
9: 95,590,288 (GRCm39) |
S723L |
probably benign |
Het |
Txndc15 |
A |
G |
13: 55,865,914 (GRCm39) |
D126G |
probably benign |
Het |
Urb1 |
C |
T |
16: 90,569,463 (GRCm39) |
|
probably benign |
Het |
Usp25 |
C |
T |
16: 76,910,721 (GRCm39) |
H926Y |
probably benign |
Het |
Uvssa |
T |
A |
5: 33,572,180 (GRCm39) |
M700K |
possibly damaging |
Het |
Vdac1 |
T |
A |
11: 52,274,789 (GRCm39) |
Y146N |
probably damaging |
Het |
Vmn1r231 |
A |
T |
17: 21,110,560 (GRCm39) |
S118R |
probably benign |
Het |
Vmn1r41 |
A |
G |
6: 89,724,080 (GRCm39) |
Y207C |
probably damaging |
Het |
Vmn2r79 |
A |
G |
7: 86,687,045 (GRCm39) |
I809V |
probably damaging |
Het |
Vnn1 |
G |
A |
10: 23,776,794 (GRCm39) |
G382R |
probably damaging |
Het |
Xcr1 |
A |
T |
9: 123,685,680 (GRCm39) |
H27Q |
probably benign |
Het |
Yeats2 |
T |
A |
16: 19,975,786 (GRCm39) |
N94K |
probably benign |
Het |
Zfp28 |
C |
T |
7: 6,397,440 (GRCm39) |
T625M |
probably damaging |
Het |
Zfp521 |
T |
C |
18: 13,977,698 (GRCm39) |
Q905R |
probably benign |
Het |
Zfp804b |
T |
C |
5: 6,821,398 (GRCm39) |
D555G |
probably damaging |
Het |
|
Other mutations in Ankrd27 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02021:Ankrd27
|
APN |
7 |
35,313,881 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02205:Ankrd27
|
APN |
7 |
35,316,364 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02372:Ankrd27
|
APN |
7 |
35,332,461 (GRCm39) |
splice site |
probably null |
|
IGL02629:Ankrd27
|
APN |
7 |
35,325,121 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03394:Ankrd27
|
APN |
7 |
35,306,523 (GRCm39) |
splice site |
probably null |
|
deep_blue
|
UTSW |
7 |
35,307,880 (GRCm39) |
missense |
probably benign |
0.01 |
Rapture
|
UTSW |
7 |
35,302,009 (GRCm39) |
critical splice donor site |
probably null |
|
R0008:Ankrd27
|
UTSW |
7 |
35,303,125 (GRCm39) |
missense |
probably benign |
0.11 |
R0008:Ankrd27
|
UTSW |
7 |
35,303,125 (GRCm39) |
missense |
probably benign |
0.11 |
R0233:Ankrd27
|
UTSW |
7 |
35,300,985 (GRCm39) |
missense |
probably damaging |
1.00 |
R0233:Ankrd27
|
UTSW |
7 |
35,300,985 (GRCm39) |
missense |
probably damaging |
1.00 |
R0240:Ankrd27
|
UTSW |
7 |
35,318,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0240:Ankrd27
|
UTSW |
7 |
35,318,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0281:Ankrd27
|
UTSW |
7 |
35,318,796 (GRCm39) |
missense |
probably damaging |
0.98 |
R0373:Ankrd27
|
UTSW |
7 |
35,337,478 (GRCm39) |
missense |
probably benign |
0.00 |
R0833:Ankrd27
|
UTSW |
7 |
35,307,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R0836:Ankrd27
|
UTSW |
7 |
35,307,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R1191:Ankrd27
|
UTSW |
7 |
35,301,912 (GRCm39) |
missense |
probably damaging |
0.96 |
R1394:Ankrd27
|
UTSW |
7 |
35,315,294 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1395:Ankrd27
|
UTSW |
7 |
35,315,294 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1493:Ankrd27
|
UTSW |
7 |
35,307,790 (GRCm39) |
missense |
probably benign |
0.11 |
R1648:Ankrd27
|
UTSW |
7 |
35,303,278 (GRCm39) |
missense |
probably benign |
0.00 |
R1664:Ankrd27
|
UTSW |
7 |
35,306,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R1698:Ankrd27
|
UTSW |
7 |
35,313,946 (GRCm39) |
missense |
probably benign |
0.01 |
R1717:Ankrd27
|
UTSW |
7 |
35,327,871 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1919:Ankrd27
|
UTSW |
7 |
35,332,410 (GRCm39) |
missense |
probably benign |
|
R1956:Ankrd27
|
UTSW |
7 |
35,303,264 (GRCm39) |
missense |
probably damaging |
1.00 |
R2276:Ankrd27
|
UTSW |
7 |
35,315,265 (GRCm39) |
unclassified |
probably benign |
|
R3000:Ankrd27
|
UTSW |
7 |
35,307,755 (GRCm39) |
missense |
probably damaging |
1.00 |
R4604:Ankrd27
|
UTSW |
7 |
35,327,915 (GRCm39) |
missense |
probably damaging |
1.00 |
R4647:Ankrd27
|
UTSW |
7 |
35,337,659 (GRCm39) |
missense |
probably benign |
|
R4838:Ankrd27
|
UTSW |
7 |
35,291,231 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4896:Ankrd27
|
UTSW |
7 |
35,307,800 (GRCm39) |
missense |
probably damaging |
1.00 |
R4973:Ankrd27
|
UTSW |
7 |
35,332,417 (GRCm39) |
missense |
probably benign |
|
R5004:Ankrd27
|
UTSW |
7 |
35,307,800 (GRCm39) |
missense |
probably damaging |
1.00 |
R5069:Ankrd27
|
UTSW |
7 |
35,327,860 (GRCm39) |
missense |
probably damaging |
0.98 |
R5182:Ankrd27
|
UTSW |
7 |
35,327,912 (GRCm39) |
missense |
probably damaging |
1.00 |
R5330:Ankrd27
|
UTSW |
7 |
35,315,351 (GRCm39) |
nonsense |
probably null |
|
R5458:Ankrd27
|
UTSW |
7 |
35,291,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R6293:Ankrd27
|
UTSW |
7 |
35,307,885 (GRCm39) |
missense |
possibly damaging |
0.65 |
R6341:Ankrd27
|
UTSW |
7 |
35,326,828 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6721:Ankrd27
|
UTSW |
7 |
35,311,976 (GRCm39) |
missense |
probably damaging |
1.00 |
R6860:Ankrd27
|
UTSW |
7 |
35,327,952 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7027:Ankrd27
|
UTSW |
7 |
35,311,951 (GRCm39) |
missense |
probably benign |
0.00 |
R7177:Ankrd27
|
UTSW |
7 |
35,318,822 (GRCm39) |
missense |
probably damaging |
1.00 |
R7231:Ankrd27
|
UTSW |
7 |
35,327,871 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7289:Ankrd27
|
UTSW |
7 |
35,330,674 (GRCm39) |
missense |
probably damaging |
1.00 |
R7933:Ankrd27
|
UTSW |
7 |
35,301,074 (GRCm39) |
splice site |
probably benign |
|
R8011:Ankrd27
|
UTSW |
7 |
35,316,306 (GRCm39) |
missense |
probably benign |
0.01 |
R8198:Ankrd27
|
UTSW |
7 |
35,307,880 (GRCm39) |
missense |
probably benign |
0.01 |
R8214:Ankrd27
|
UTSW |
7 |
35,313,944 (GRCm39) |
missense |
probably damaging |
1.00 |
R8327:Ankrd27
|
UTSW |
7 |
35,300,985 (GRCm39) |
missense |
probably damaging |
1.00 |
R8461:Ankrd27
|
UTSW |
7 |
35,326,911 (GRCm39) |
missense |
probably damaging |
1.00 |
R8508:Ankrd27
|
UTSW |
7 |
35,301,051 (GRCm39) |
nonsense |
probably null |
|
R8676:Ankrd27
|
UTSW |
7 |
35,302,009 (GRCm39) |
critical splice donor site |
probably null |
|
R8901:Ankrd27
|
UTSW |
7 |
35,332,243 (GRCm39) |
intron |
probably benign |
|
R9286:Ankrd27
|
UTSW |
7 |
35,326,869 (GRCm39) |
missense |
probably benign |
0.05 |
R9400:Ankrd27
|
UTSW |
7 |
35,316,282 (GRCm39) |
missense |
probably damaging |
1.00 |
R9624:Ankrd27
|
UTSW |
7 |
35,301,891 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9786:Ankrd27
|
UTSW |
7 |
35,291,294 (GRCm39) |
missense |
possibly damaging |
0.79 |
Z1177:Ankrd27
|
UTSW |
7 |
35,303,303 (GRCm39) |
missense |
possibly damaging |
0.84 |
|