Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actr10 |
G |
A |
12: 70,989,032 (GRCm39) |
|
probably null |
Het |
Adgrd1 |
A |
G |
5: 129,219,574 (GRCm39) |
K465E |
probably benign |
Het |
Aktip |
A |
T |
8: 91,853,402 (GRCm39) |
V105E |
probably benign |
Het |
Ankrd7 |
A |
G |
6: 18,870,006 (GRCm39) |
Y253C |
probably damaging |
Het |
Bag6 |
T |
C |
17: 35,361,041 (GRCm39) |
M440T |
unknown |
Het |
Camk2b |
T |
A |
11: 5,922,838 (GRCm39) |
N426Y |
probably damaging |
Het |
Ccdc82 |
T |
A |
9: 13,289,706 (GRCm39) |
Y500* |
probably null |
Het |
Cenpe |
T |
A |
3: 134,930,777 (GRCm39) |
D341E |
probably damaging |
Het |
Cyp2j13 |
A |
T |
4: 95,956,428 (GRCm39) |
M227K |
probably benign |
Het |
Dmbt1 |
G |
A |
7: 130,692,134 (GRCm39) |
V967I |
unknown |
Het |
Dnmt3b |
A |
T |
2: 153,515,933 (GRCm39) |
N447Y |
probably benign |
Het |
Dtymk |
A |
C |
1: 93,729,543 (GRCm39) |
S3A |
probably benign |
Het |
Eefsec |
G |
A |
6: 88,423,253 (GRCm39) |
T70M |
possibly damaging |
Het |
Fam171a1 |
C |
T |
2: 3,221,344 (GRCm39) |
T270M |
probably damaging |
Het |
Gm17728 |
T |
C |
17: 9,641,159 (GRCm39) |
S90P |
probably benign |
Het |
Hdlbp |
A |
G |
1: 93,359,053 (GRCm39) |
L213P |
probably damaging |
Het |
Heatr5b |
T |
C |
17: 79,109,188 (GRCm39) |
I1024V |
probably benign |
Het |
Hr |
C |
T |
14: 70,799,305 (GRCm39) |
R597* |
probably null |
Het |
Ifit3 |
T |
C |
19: 34,564,988 (GRCm39) |
I178T |
probably damaging |
Het |
Ifna6 |
A |
G |
4: 88,746,222 (GRCm39) |
*190W |
probably null |
Het |
Igkv4-55 |
A |
T |
6: 69,584,315 (GRCm39) |
M99K |
probably benign |
Het |
Klk1 |
T |
A |
7: 43,877,056 (GRCm39) |
I53N |
probably damaging |
Het |
Lpcat2b |
A |
G |
5: 107,580,692 (GRCm39) |
H7R |
probably benign |
Het |
Lrrc37a |
G |
A |
11: 103,393,481 (GRCm39) |
P648L |
|
Het |
Mast4 |
G |
T |
13: 102,895,174 (GRCm39) |
P975H |
probably damaging |
Het |
Mfrp |
C |
T |
9: 44,013,807 (GRCm39) |
L106F |
probably benign |
Het |
Mllt10 |
T |
A |
2: 18,201,469 (GRCm39) |
S652T |
probably benign |
Het |
Mroh8 |
C |
A |
2: 157,083,673 (GRCm39) |
G400W |
probably damaging |
Het |
Neurl4 |
A |
G |
11: 69,794,788 (GRCm39) |
|
probably benign |
Het |
Nop14 |
A |
C |
5: 34,817,352 (GRCm39) |
V13G |
probably benign |
Het |
Nup188 |
T |
A |
2: 30,217,576 (GRCm39) |
L837Q |
probably damaging |
Het |
Or2a54 |
T |
A |
6: 43,092,905 (GRCm39) |
N76K |
possibly damaging |
Het |
Or2ak5 |
T |
A |
11: 58,611,572 (GRCm39) |
T101S |
probably benign |
Het |
Or7g30 |
T |
C |
9: 19,352,817 (GRCm39) |
S203P |
probably damaging |
Het |
Or8k39 |
T |
C |
2: 86,563,302 (GRCm39) |
Y218C |
probably damaging |
Het |
Pate10 |
A |
G |
9: 35,652,391 (GRCm39) |
Y16C |
probably damaging |
Het |
Pde8b |
A |
T |
13: 95,226,793 (GRCm39) |
V185E |
probably benign |
Het |
Pink1 |
G |
T |
4: 138,047,333 (GRCm39) |
A247D |
probably damaging |
Het |
Pla2g10 |
A |
T |
16: 13,545,914 (GRCm39) |
V40D |
probably damaging |
Het |
Plce1 |
G |
A |
19: 38,512,811 (GRCm39) |
G37R |
probably benign |
Het |
Pld1 |
A |
G |
3: 28,166,439 (GRCm39) |
E826G |
possibly damaging |
Het |
Poc5 |
G |
T |
13: 96,535,228 (GRCm39) |
K164N |
possibly damaging |
Het |
Polr2b |
A |
T |
5: 77,463,761 (GRCm39) |
M53L |
probably benign |
Het |
Ppp1r10 |
C |
T |
17: 36,239,690 (GRCm39) |
P470S |
probably damaging |
Het |
Rasef |
A |
G |
4: 73,645,840 (GRCm39) |
S510P |
probably damaging |
Het |
Rnf17 |
T |
A |
14: 56,722,658 (GRCm39) |
L1073Q |
probably damaging |
Het |
Rpl13a-ps1 |
C |
T |
19: 50,018,739 (GRCm39) |
G146R |
probably damaging |
Het |
Scn2a |
A |
G |
2: 65,518,730 (GRCm39) |
D368G |
probably damaging |
Het |
Shc3 |
T |
A |
13: 51,634,248 (GRCm39) |
S86C |
probably benign |
Het |
Sos1 |
T |
C |
17: 80,741,405 (GRCm39) |
H460R |
probably damaging |
Het |
Steap1 |
T |
A |
5: 5,790,838 (GRCm39) |
M37L |
probably benign |
Het |
Themis |
G |
T |
10: 28,673,492 (GRCm39) |
C593F |
possibly damaging |
Het |
Tnn |
A |
G |
1: 159,937,814 (GRCm39) |
|
probably null |
Het |
Trabd |
G |
T |
15: 88,969,667 (GRCm39) |
|
probably benign |
Het |
Trim42 |
T |
A |
9: 97,248,047 (GRCm39) |
K216N |
probably damaging |
Het |
Trmt44 |
G |
A |
5: 35,721,673 (GRCm39) |
P497S |
probably benign |
Het |
Trp53bp2 |
A |
G |
1: 182,256,475 (GRCm39) |
Y15C |
probably damaging |
Het |
Trpm7 |
T |
A |
2: 126,652,100 (GRCm39) |
I1458L |
probably benign |
Het |
Ttc17 |
G |
T |
2: 94,237,003 (GRCm39) |
A3E |
possibly damaging |
Het |
Ttn |
C |
A |
2: 76,704,208 (GRCm39) |
V9274L |
unknown |
Het |
Tut7 |
T |
A |
13: 59,937,011 (GRCm39) |
Q1212L |
possibly damaging |
Het |
Vmn2r105 |
T |
A |
17: 20,428,872 (GRCm39) |
I735F |
probably damaging |
Het |
Vmn2r22 |
A |
G |
6: 123,614,454 (GRCm39) |
C379R |
probably damaging |
Het |
Vmn2r97 |
G |
A |
17: 19,149,607 (GRCm39) |
E332K |
probably benign |
Het |
Xrn1 |
A |
G |
9: 95,920,732 (GRCm39) |
T1331A |
probably benign |
Het |
|
Other mutations in Dtl |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00678:Dtl
|
APN |
1 |
191,278,738 (GRCm39) |
splice site |
probably null |
|
IGL01069:Dtl
|
APN |
1 |
191,293,651 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL01135:Dtl
|
APN |
1 |
191,280,442 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01307:Dtl
|
APN |
1 |
191,302,811 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL01461:Dtl
|
APN |
1 |
191,278,729 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL01809:Dtl
|
APN |
1 |
191,280,415 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01958:Dtl
|
APN |
1 |
191,300,489 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02217:Dtl
|
APN |
1 |
191,300,426 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02408:Dtl
|
APN |
1 |
191,273,352 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02445:Dtl
|
APN |
1 |
191,290,172 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02661:Dtl
|
APN |
1 |
191,273,483 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02864:Dtl
|
APN |
1 |
191,288,938 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02897:Dtl
|
APN |
1 |
191,273,656 (GRCm39) |
splice site |
probably benign |
|
IGL03069:Dtl
|
APN |
1 |
191,289,008 (GRCm39) |
splice site |
probably benign |
|
PIT4418001:Dtl
|
UTSW |
1 |
191,273,429 (GRCm39) |
missense |
possibly damaging |
0.46 |
R0370:Dtl
|
UTSW |
1 |
191,307,462 (GRCm39) |
missense |
probably benign |
0.05 |
R0513:Dtl
|
UTSW |
1 |
191,301,819 (GRCm39) |
nonsense |
probably null |
|
R1386:Dtl
|
UTSW |
1 |
191,301,829 (GRCm39) |
missense |
probably damaging |
1.00 |
R1424:Dtl
|
UTSW |
1 |
191,293,649 (GRCm39) |
missense |
probably benign |
0.13 |
R1575:Dtl
|
UTSW |
1 |
191,293,658 (GRCm39) |
splice site |
probably null |
|
R2128:Dtl
|
UTSW |
1 |
191,290,222 (GRCm39) |
missense |
probably damaging |
0.99 |
R2297:Dtl
|
UTSW |
1 |
191,273,207 (GRCm39) |
missense |
probably benign |
0.41 |
R2344:Dtl
|
UTSW |
1 |
191,280,490 (GRCm39) |
missense |
probably benign |
0.00 |
R3121:Dtl
|
UTSW |
1 |
191,285,175 (GRCm39) |
nonsense |
probably null |
|
R3808:Dtl
|
UTSW |
1 |
191,280,466 (GRCm39) |
missense |
probably damaging |
1.00 |
R4722:Dtl
|
UTSW |
1 |
191,288,953 (GRCm39) |
missense |
possibly damaging |
0.52 |
R4753:Dtl
|
UTSW |
1 |
191,301,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R4904:Dtl
|
UTSW |
1 |
191,300,457 (GRCm39) |
missense |
probably damaging |
0.99 |
R4965:Dtl
|
UTSW |
1 |
191,278,677 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5068:Dtl
|
UTSW |
1 |
191,300,485 (GRCm39) |
missense |
probably damaging |
1.00 |
R5119:Dtl
|
UTSW |
1 |
191,273,618 (GRCm39) |
missense |
probably damaging |
1.00 |
R5872:Dtl
|
UTSW |
1 |
191,278,680 (GRCm39) |
missense |
probably benign |
0.00 |
R5911:Dtl
|
UTSW |
1 |
191,300,519 (GRCm39) |
missense |
probably damaging |
1.00 |
R5992:Dtl
|
UTSW |
1 |
191,300,684 (GRCm39) |
splice site |
probably null |
|
R6425:Dtl
|
UTSW |
1 |
191,278,735 (GRCm39) |
missense |
probably benign |
0.02 |
R7403:Dtl
|
UTSW |
1 |
191,295,285 (GRCm39) |
missense |
probably damaging |
1.00 |
R8756:Dtl
|
UTSW |
1 |
191,271,371 (GRCm39) |
missense |
probably benign |
|
R8835:Dtl
|
UTSW |
1 |
191,293,609 (GRCm39) |
missense |
probably damaging |
1.00 |
R9091:Dtl
|
UTSW |
1 |
191,288,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R9270:Dtl
|
UTSW |
1 |
191,288,923 (GRCm39) |
missense |
probably damaging |
1.00 |
X0018:Dtl
|
UTSW |
1 |
191,300,522 (GRCm39) |
missense |
probably damaging |
1.00 |
|