Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ankrd34c |
T |
C |
9: 89,611,058 (GRCm39) |
T428A |
possibly damaging |
Het |
Arfgef1 |
G |
C |
1: 10,275,115 (GRCm39) |
I312M |
probably benign |
Het |
Atr |
T |
C |
9: 95,833,610 (GRCm39) |
L2620P |
probably damaging |
Het |
Ccdc110 |
A |
G |
8: 46,391,955 (GRCm39) |
Y54C |
probably benign |
Het |
Cecr2 |
T |
C |
6: 120,732,548 (GRCm39) |
V480A |
possibly damaging |
Het |
Chfr |
A |
G |
5: 110,299,531 (GRCm39) |
D308G |
probably benign |
Het |
Cit |
T |
A |
5: 116,135,789 (GRCm39) |
I1919N |
probably damaging |
Het |
Ctsc |
T |
A |
7: 87,927,512 (GRCm39) |
D34E |
possibly damaging |
Het |
Diaph3 |
T |
A |
14: 87,328,594 (GRCm39) |
|
probably benign |
Het |
Dnah6 |
T |
A |
6: 73,044,452 (GRCm39) |
I3220F |
probably damaging |
Het |
Eif1ad16 |
C |
A |
12: 87,985,134 (GRCm39) |
E136D |
probably benign |
Het |
Eif4a3l1 |
G |
A |
6: 136,305,778 (GRCm39) |
A80T |
probably damaging |
Het |
Elmod3 |
A |
G |
6: 72,546,242 (GRCm39) |
|
probably null |
Het |
Fgd5 |
T |
C |
6: 92,043,165 (GRCm39) |
V1215A |
possibly damaging |
Het |
Filip1 |
T |
C |
9: 79,727,873 (GRCm39) |
M249V |
probably damaging |
Het |
Fmn1 |
C |
T |
2: 113,355,968 (GRCm39) |
P803L |
unknown |
Het |
Gcfc2 |
A |
G |
6: 81,921,401 (GRCm39) |
K469R |
probably damaging |
Het |
Itgad |
A |
G |
7: 127,790,111 (GRCm39) |
T637A |
probably damaging |
Het |
Kank2 |
T |
C |
9: 21,681,133 (GRCm39) |
S799G |
probably damaging |
Het |
Kcnc4 |
A |
T |
3: 107,355,520 (GRCm39) |
D309E |
possibly damaging |
Het |
Lamc2 |
G |
A |
1: 153,002,774 (GRCm39) |
T1069M |
probably benign |
Het |
Lepr |
T |
A |
4: 101,602,842 (GRCm39) |
M210K |
possibly damaging |
Het |
Lig3 |
T |
C |
11: 82,683,020 (GRCm39) |
|
probably null |
Het |
Oat |
G |
T |
7: 132,171,736 (GRCm39) |
T33K |
probably benign |
Het |
Or2ad1 |
T |
C |
13: 21,326,820 (GRCm39) |
M136V |
probably damaging |
Het |
Or4b1d |
A |
G |
2: 89,969,399 (GRCm39) |
F28S |
probably damaging |
Het |
Or7c70 |
T |
A |
10: 78,682,802 (GRCm39) |
M316L |
probably benign |
Het |
Pcnx3 |
G |
T |
19: 5,722,543 (GRCm39) |
A1383E |
probably damaging |
Het |
Pctp |
T |
C |
11: 89,879,561 (GRCm39) |
Y100C |
probably damaging |
Het |
Pex6 |
G |
T |
17: 47,023,063 (GRCm39) |
R213L |
probably benign |
Het |
Phlpp2 |
T |
C |
8: 110,660,655 (GRCm39) |
L770S |
possibly damaging |
Het |
Pkn2 |
A |
T |
3: 142,559,299 (GRCm39) |
D75E |
possibly damaging |
Het |
Pla2g12b |
T |
C |
10: 59,257,375 (GRCm39) |
|
probably null |
Het |
Plch2 |
C |
T |
4: 155,068,907 (GRCm39) |
V1135I |
probably damaging |
Het |
Pskh1 |
T |
A |
8: 106,639,453 (GRCm39) |
S44R |
probably benign |
Het |
Ptpra |
G |
T |
2: 30,327,602 (GRCm39) |
A119S |
probably benign |
Het |
Shld2 |
A |
G |
14: 33,989,607 (GRCm39) |
I433T |
probably damaging |
Het |
Slfn3 |
A |
G |
11: 83,103,541 (GRCm39) |
I137M |
probably damaging |
Het |
St6galnac1 |
A |
T |
11: 116,660,113 (GRCm39) |
S67T |
probably benign |
Het |
Timd5 |
T |
C |
11: 46,426,415 (GRCm39) |
I174T |
probably benign |
Het |
Treml1 |
A |
G |
17: 48,671,917 (GRCm39) |
E137G |
probably damaging |
Het |
Ubr2 |
A |
C |
17: 47,251,987 (GRCm39) |
C1518G |
probably benign |
Het |
Vmn2r55 |
A |
T |
7: 12,386,571 (GRCm39) |
C470S |
probably damaging |
Het |
|
Other mutations in Ankrd12 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00272:Ankrd12
|
APN |
17 |
66,293,169 (GRCm39) |
missense |
probably benign |
|
IGL00555:Ankrd12
|
APN |
17 |
66,291,971 (GRCm39) |
missense |
probably benign |
0.09 |
IGL00790:Ankrd12
|
APN |
17 |
66,291,175 (GRCm39) |
missense |
probably benign |
|
IGL00808:Ankrd12
|
APN |
17 |
66,290,960 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01355:Ankrd12
|
APN |
17 |
66,277,335 (GRCm39) |
splice site |
probably benign |
|
IGL01707:Ankrd12
|
APN |
17 |
66,291,273 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02045:Ankrd12
|
APN |
17 |
66,293,244 (GRCm39) |
missense |
probably benign |
0.17 |
IGL02125:Ankrd12
|
APN |
17 |
66,277,139 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02292:Ankrd12
|
APN |
17 |
66,349,582 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02376:Ankrd12
|
APN |
17 |
66,349,524 (GRCm39) |
intron |
probably benign |
|
IGL02435:Ankrd12
|
APN |
17 |
66,294,151 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02530:Ankrd12
|
APN |
17 |
66,291,398 (GRCm39) |
missense |
probably benign |
0.20 |
R0048:Ankrd12
|
UTSW |
17 |
66,291,798 (GRCm39) |
missense |
probably damaging |
1.00 |
R0048:Ankrd12
|
UTSW |
17 |
66,291,798 (GRCm39) |
missense |
probably damaging |
1.00 |
R0094:Ankrd12
|
UTSW |
17 |
66,277,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R0195:Ankrd12
|
UTSW |
17 |
66,356,943 (GRCm39) |
splice site |
probably null |
|
R0227:Ankrd12
|
UTSW |
17 |
66,294,222 (GRCm39) |
missense |
probably benign |
0.00 |
R0363:Ankrd12
|
UTSW |
17 |
66,292,676 (GRCm39) |
missense |
probably damaging |
1.00 |
R0366:Ankrd12
|
UTSW |
17 |
66,291,501 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0376:Ankrd12
|
UTSW |
17 |
66,360,004 (GRCm39) |
missense |
probably damaging |
0.98 |
R0470:Ankrd12
|
UTSW |
17 |
66,293,129 (GRCm39) |
missense |
probably benign |
0.00 |
R0480:Ankrd12
|
UTSW |
17 |
66,356,823 (GRCm39) |
missense |
possibly damaging |
0.47 |
R0538:Ankrd12
|
UTSW |
17 |
66,356,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R0883:Ankrd12
|
UTSW |
17 |
66,292,127 (GRCm39) |
missense |
probably benign |
0.19 |
R1181:Ankrd12
|
UTSW |
17 |
66,349,569 (GRCm39) |
missense |
probably benign |
0.36 |
R1386:Ankrd12
|
UTSW |
17 |
66,290,375 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1476:Ankrd12
|
UTSW |
17 |
66,293,300 (GRCm39) |
missense |
probably damaging |
0.99 |
R1574:Ankrd12
|
UTSW |
17 |
66,293,269 (GRCm39) |
missense |
probably benign |
0.08 |
R1574:Ankrd12
|
UTSW |
17 |
66,293,269 (GRCm39) |
missense |
probably benign |
0.08 |
R1728:Ankrd12
|
UTSW |
17 |
66,291,071 (GRCm39) |
missense |
probably benign |
0.01 |
R1729:Ankrd12
|
UTSW |
17 |
66,291,071 (GRCm39) |
missense |
probably benign |
0.01 |
R1784:Ankrd12
|
UTSW |
17 |
66,291,071 (GRCm39) |
missense |
probably benign |
0.01 |
R1795:Ankrd12
|
UTSW |
17 |
66,293,222 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1901:Ankrd12
|
UTSW |
17 |
66,293,698 (GRCm39) |
missense |
possibly damaging |
0.58 |
R1929:Ankrd12
|
UTSW |
17 |
66,293,681 (GRCm39) |
missense |
possibly damaging |
0.55 |
R1952:Ankrd12
|
UTSW |
17 |
66,338,566 (GRCm39) |
missense |
probably damaging |
0.98 |
R1997:Ankrd12
|
UTSW |
17 |
66,291,879 (GRCm39) |
missense |
probably damaging |
1.00 |
R2207:Ankrd12
|
UTSW |
17 |
66,338,569 (GRCm39) |
splice site |
probably null |
|
R3612:Ankrd12
|
UTSW |
17 |
66,290,542 (GRCm39) |
missense |
probably benign |
0.01 |
R3768:Ankrd12
|
UTSW |
17 |
66,292,715 (GRCm39) |
missense |
probably benign |
|
R3909:Ankrd12
|
UTSW |
17 |
66,291,000 (GRCm39) |
missense |
probably benign |
0.05 |
R3945:Ankrd12
|
UTSW |
17 |
66,283,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R4176:Ankrd12
|
UTSW |
17 |
66,334,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R4461:Ankrd12
|
UTSW |
17 |
66,292,932 (GRCm39) |
splice site |
probably null |
|
R4628:Ankrd12
|
UTSW |
17 |
66,292,989 (GRCm39) |
missense |
probably benign |
|
R4726:Ankrd12
|
UTSW |
17 |
66,277,319 (GRCm39) |
missense |
probably damaging |
1.00 |
R4785:Ankrd12
|
UTSW |
17 |
66,289,994 (GRCm39) |
missense |
probably damaging |
1.00 |
R4828:Ankrd12
|
UTSW |
17 |
66,291,632 (GRCm39) |
missense |
probably damaging |
0.99 |
R4847:Ankrd12
|
UTSW |
17 |
66,331,087 (GRCm39) |
missense |
probably benign |
0.14 |
R4858:Ankrd12
|
UTSW |
17 |
66,338,428 (GRCm39) |
missense |
probably damaging |
1.00 |
R5344:Ankrd12
|
UTSW |
17 |
66,356,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R5749:Ankrd12
|
UTSW |
17 |
66,293,091 (GRCm39) |
missense |
probably benign |
0.02 |
R7132:Ankrd12
|
UTSW |
17 |
66,290,242 (GRCm39) |
missense |
probably benign |
|
R7205:Ankrd12
|
UTSW |
17 |
66,292,160 (GRCm39) |
missense |
probably damaging |
1.00 |
R7379:Ankrd12
|
UTSW |
17 |
66,292,242 (GRCm39) |
nonsense |
probably null |
|
R7569:Ankrd12
|
UTSW |
17 |
66,289,900 (GRCm39) |
missense |
probably damaging |
1.00 |
R7570:Ankrd12
|
UTSW |
17 |
66,292,355 (GRCm39) |
missense |
probably benign |
|
R7783:Ankrd12
|
UTSW |
17 |
66,334,245 (GRCm39) |
critical splice donor site |
probably null |
|
R7790:Ankrd12
|
UTSW |
17 |
66,291,225 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7808:Ankrd12
|
UTSW |
17 |
66,292,648 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7834:Ankrd12
|
UTSW |
17 |
66,294,347 (GRCm39) |
missense |
probably damaging |
1.00 |
R7896:Ankrd12
|
UTSW |
17 |
66,292,680 (GRCm39) |
nonsense |
probably null |
|
R7985:Ankrd12
|
UTSW |
17 |
66,291,191 (GRCm39) |
missense |
probably benign |
0.00 |
R8251:Ankrd12
|
UTSW |
17 |
66,291,554 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8304:Ankrd12
|
UTSW |
17 |
66,291,542 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8379:Ankrd12
|
UTSW |
17 |
66,290,939 (GRCm39) |
missense |
probably benign |
0.01 |
R8441:Ankrd12
|
UTSW |
17 |
66,349,546 (GRCm39) |
missense |
probably benign |
0.21 |
R8485:Ankrd12
|
UTSW |
17 |
66,290,711 (GRCm39) |
missense |
probably benign |
0.00 |
R8507:Ankrd12
|
UTSW |
17 |
66,293,904 (GRCm39) |
nonsense |
probably null |
|
R8677:Ankrd12
|
UTSW |
17 |
66,331,209 (GRCm39) |
missense |
probably damaging |
1.00 |
R8790:Ankrd12
|
UTSW |
17 |
66,290,153 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8888:Ankrd12
|
UTSW |
17 |
66,338,568 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8944:Ankrd12
|
UTSW |
17 |
66,277,195 (GRCm39) |
nonsense |
probably null |
|
R8957:Ankrd12
|
UTSW |
17 |
66,291,491 (GRCm39) |
missense |
probably benign |
|
R9069:Ankrd12
|
UTSW |
17 |
66,356,874 (GRCm39) |
missense |
probably benign |
|
R9226:Ankrd12
|
UTSW |
17 |
66,292,754 (GRCm39) |
missense |
probably damaging |
0.99 |
R9275:Ankrd12
|
UTSW |
17 |
66,344,599 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9278:Ankrd12
|
UTSW |
17 |
66,344,599 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9339:Ankrd12
|
UTSW |
17 |
66,291,408 (GRCm39) |
missense |
probably benign |
0.00 |
R9400:Ankrd12
|
UTSW |
17 |
66,291,875 (GRCm39) |
missense |
probably damaging |
1.00 |
R9581:Ankrd12
|
UTSW |
17 |
66,290,415 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:Ankrd12
|
UTSW |
17 |
66,277,333 (GRCm39) |
critical splice acceptor site |
probably null |
|
|