Other mutations in this stock |
Total: 34 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrb3 |
G |
T |
1: 25,865,829 (GRCm39) |
R5S |
possibly damaging |
Het |
Ccdc168 |
G |
A |
1: 44,100,151 (GRCm39) |
L316F |
possibly damaging |
Het |
Ccdc187 |
T |
A |
2: 26,170,681 (GRCm39) |
K599I |
probably damaging |
Het |
Ccn5 |
G |
A |
2: 163,670,906 (GRCm39) |
V138M |
probably damaging |
Het |
Cd38 |
A |
C |
5: 44,026,431 (GRCm39) |
I72L |
probably benign |
Het |
Cep19 |
C |
T |
16: 31,925,883 (GRCm39) |
T97M |
probably damaging |
Het |
Ces2a |
T |
G |
8: 105,463,766 (GRCm39) |
D159E |
probably damaging |
Het |
Dcc |
G |
A |
18: 71,507,561 (GRCm39) |
A917V |
probably damaging |
Het |
Dennd6b |
G |
A |
15: 89,072,866 (GRCm39) |
A196V |
probably benign |
Het |
Dlgap3 |
T |
C |
4: 127,108,141 (GRCm39) |
S475P |
possibly damaging |
Het |
Doc2a |
C |
T |
7: 126,450,321 (GRCm39) |
P156S |
probably damaging |
Het |
Fbf1 |
A |
G |
11: 116,038,568 (GRCm39) |
V851A |
probably benign |
Het |
Fhdc1 |
C |
A |
3: 84,352,133 (GRCm39) |
V1031F |
probably benign |
Het |
Gm5878 |
G |
A |
6: 85,102,633 (GRCm39) |
R31* |
probably null |
Het |
Klk1b8 |
C |
A |
7: 43,595,186 (GRCm39) |
|
probably benign |
Het |
Lmcd1 |
T |
A |
6: 112,264,968 (GRCm39) |
|
probably benign |
Het |
Lyst |
T |
A |
13: 13,873,051 (GRCm39) |
I2750K |
probably benign |
Het |
Muc4 |
A |
G |
16: 32,590,666 (GRCm39) |
N2958S |
possibly damaging |
Het |
Plod3 |
G |
C |
5: 137,017,000 (GRCm39) |
A50P |
probably benign |
Het |
Ppp1r16b |
G |
A |
2: 158,591,106 (GRCm39) |
V163I |
probably damaging |
Het |
Prkdc |
T |
A |
16: 15,585,886 (GRCm39) |
W2475R |
probably damaging |
Het |
Rad54l |
C |
T |
4: 115,954,551 (GRCm39) |
C684Y |
probably damaging |
Het |
Ralgds |
T |
C |
2: 28,442,107 (GRCm39) |
L96P |
probably damaging |
Het |
Rasef |
T |
A |
4: 73,663,326 (GRCm39) |
H167L |
probably damaging |
Het |
Sh3bp2 |
T |
C |
5: 34,712,886 (GRCm39) |
F165L |
possibly damaging |
Het |
Slc38a9 |
T |
C |
13: 112,865,749 (GRCm39) |
I482T |
probably benign |
Het |
Tmprss6 |
T |
A |
15: 78,343,627 (GRCm39) |
|
probably null |
Het |
Trpm3 |
A |
T |
19: 22,875,061 (GRCm39) |
S568C |
probably damaging |
Het |
Ttc39c |
T |
A |
18: 12,861,667 (GRCm39) |
|
probably null |
Het |
Ttn |
A |
T |
2: 76,641,587 (GRCm39) |
L5176Q |
possibly damaging |
Het |
Ugt2b5 |
A |
T |
5: 87,287,582 (GRCm39) |
V195E |
probably damaging |
Het |
Vmn2r22 |
C |
T |
6: 123,614,756 (GRCm39) |
G278D |
probably damaging |
Het |
Yme1l1 |
G |
A |
2: 23,063,073 (GRCm39) |
A215T |
probably benign |
Het |
Zmynd15 |
C |
T |
11: 70,351,894 (GRCm39) |
R38* |
probably null |
Het |
|
Other mutations in Elmo1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00548:Elmo1
|
APN |
13 |
20,445,749 (GRCm39) |
missense |
probably benign |
|
IGL00814:Elmo1
|
APN |
13 |
20,470,894 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL00849:Elmo1
|
APN |
13 |
20,766,493 (GRCm39) |
nonsense |
probably null |
|
IGL01417:Elmo1
|
APN |
13 |
20,435,345 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01994:Elmo1
|
APN |
13 |
20,526,634 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02435:Elmo1
|
APN |
13 |
20,773,826 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02605:Elmo1
|
APN |
13 |
20,789,372 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02716:Elmo1
|
APN |
13 |
20,633,672 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03389:Elmo1
|
APN |
13 |
20,526,596 (GRCm39) |
missense |
probably damaging |
0.98 |
braveheart
|
UTSW |
13 |
20,458,791 (GRCm39) |
critical splice donor site |
probably benign |
|
Debil
|
UTSW |
13 |
20,557,331 (GRCm39) |
missense |
probably damaging |
1.00 |
Dollie
|
UTSW |
13 |
20,756,616 (GRCm39) |
missense |
possibly damaging |
0.91 |
Edinburg
|
UTSW |
13 |
20,474,553 (GRCm39) |
nonsense |
probably null |
|
glasgow
|
UTSW |
13 |
20,773,812 (GRCm39) |
critical splice acceptor site |
probably null |
|
Golly
|
UTSW |
13 |
20,557,286 (GRCm39) |
missense |
possibly damaging |
0.96 |
Lockerbie
|
UTSW |
13 |
20,784,371 (GRCm39) |
missense |
probably damaging |
1.00 |
sesame
|
UTSW |
13 |
20,784,382 (GRCm39) |
nonsense |
probably null |
|
Tickle
|
UTSW |
13 |
20,464,973 (GRCm39) |
splice site |
probably null |
|
Wilmut
|
UTSW |
13 |
20,766,438 (GRCm39) |
nonsense |
probably null |
|
Writhe
|
UTSW |
13 |
20,784,429 (GRCm39) |
critical splice donor site |
probably null |
|
H8562:Elmo1
|
UTSW |
13 |
20,465,033 (GRCm39) |
missense |
probably damaging |
1.00 |
R0360:Elmo1
|
UTSW |
13 |
20,748,663 (GRCm39) |
nonsense |
probably null |
|
R0364:Elmo1
|
UTSW |
13 |
20,748,663 (GRCm39) |
nonsense |
probably null |
|
R0372:Elmo1
|
UTSW |
13 |
20,756,629 (GRCm39) |
critical splice donor site |
probably null |
|
R0975:Elmo1
|
UTSW |
13 |
20,435,307 (GRCm39) |
missense |
probably damaging |
0.98 |
R1167:Elmo1
|
UTSW |
13 |
20,369,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R1511:Elmo1
|
UTSW |
13 |
20,474,647 (GRCm39) |
missense |
possibly damaging |
0.60 |
R1671:Elmo1
|
UTSW |
13 |
20,472,054 (GRCm39) |
splice site |
probably benign |
|
R1677:Elmo1
|
UTSW |
13 |
20,773,841 (GRCm39) |
missense |
probably benign |
0.22 |
R1868:Elmo1
|
UTSW |
13 |
20,773,823 (GRCm39) |
missense |
possibly damaging |
0.78 |
R2941:Elmo1
|
UTSW |
13 |
20,784,382 (GRCm39) |
nonsense |
probably null |
|
R3508:Elmo1
|
UTSW |
13 |
20,789,402 (GRCm39) |
missense |
probably damaging |
1.00 |
R4378:Elmo1
|
UTSW |
13 |
20,557,286 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4423:Elmo1
|
UTSW |
13 |
20,784,382 (GRCm39) |
nonsense |
probably null |
|
R4425:Elmo1
|
UTSW |
13 |
20,784,382 (GRCm39) |
nonsense |
probably null |
|
R4516:Elmo1
|
UTSW |
13 |
20,467,084 (GRCm39) |
missense |
probably benign |
0.11 |
R4862:Elmo1
|
UTSW |
13 |
20,633,682 (GRCm39) |
missense |
probably benign |
|
R4990:Elmo1
|
UTSW |
13 |
20,526,689 (GRCm39) |
missense |
probably damaging |
1.00 |
R4991:Elmo1
|
UTSW |
13 |
20,526,689 (GRCm39) |
missense |
probably damaging |
1.00 |
R4992:Elmo1
|
UTSW |
13 |
20,526,689 (GRCm39) |
missense |
probably damaging |
1.00 |
R5197:Elmo1
|
UTSW |
13 |
20,748,607 (GRCm39) |
missense |
probably benign |
0.20 |
R5269:Elmo1
|
UTSW |
13 |
20,633,656 (GRCm39) |
missense |
probably benign |
0.00 |
R5386:Elmo1
|
UTSW |
13 |
20,784,380 (GRCm39) |
missense |
probably benign |
0.01 |
R5471:Elmo1
|
UTSW |
13 |
20,756,555 (GRCm39) |
missense |
probably benign |
0.01 |
R5922:Elmo1
|
UTSW |
13 |
20,789,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R5947:Elmo1
|
UTSW |
13 |
20,474,553 (GRCm39) |
nonsense |
probably null |
|
R6512:Elmo1
|
UTSW |
13 |
20,557,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R6531:Elmo1
|
UTSW |
13 |
20,756,616 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7338:Elmo1
|
UTSW |
13 |
20,464,982 (GRCm39) |
missense |
probably benign |
0.37 |
R7378:Elmo1
|
UTSW |
13 |
20,465,105 (GRCm39) |
missense |
probably benign |
0.00 |
R7477:Elmo1
|
UTSW |
13 |
20,469,489 (GRCm39) |
missense |
|
|
R7593:Elmo1
|
UTSW |
13 |
20,474,610 (GRCm39) |
missense |
probably benign |
|
R7721:Elmo1
|
UTSW |
13 |
20,464,973 (GRCm39) |
splice site |
probably null |
|
R7778:Elmo1
|
UTSW |
13 |
20,773,812 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8001:Elmo1
|
UTSW |
13 |
20,470,902 (GRCm39) |
missense |
probably benign |
0.05 |
R8133:Elmo1
|
UTSW |
13 |
20,557,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R8248:Elmo1
|
UTSW |
13 |
20,784,371 (GRCm39) |
missense |
probably damaging |
1.00 |
R8685:Elmo1
|
UTSW |
13 |
20,474,594 (GRCm39) |
missense |
possibly damaging |
0.61 |
R8713:Elmo1
|
UTSW |
13 |
20,458,791 (GRCm39) |
critical splice donor site |
probably benign |
|
R8888:Elmo1
|
UTSW |
13 |
20,748,630 (GRCm39) |
missense |
probably damaging |
1.00 |
R8895:Elmo1
|
UTSW |
13 |
20,748,630 (GRCm39) |
missense |
probably damaging |
1.00 |
R8945:Elmo1
|
UTSW |
13 |
20,766,438 (GRCm39) |
nonsense |
probably null |
|
R9292:Elmo1
|
UTSW |
13 |
20,784,429 (GRCm39) |
critical splice donor site |
probably null |
|
R9389:Elmo1
|
UTSW |
13 |
20,369,661 (GRCm39) |
missense |
probably benign |
0.01 |
R9417:Elmo1
|
UTSW |
13 |
20,756,573 (GRCm39) |
missense |
possibly damaging |
0.57 |
R9472:Elmo1
|
UTSW |
13 |
20,470,897 (GRCm39) |
missense |
probably benign |
0.31 |
R9622:Elmo1
|
UTSW |
13 |
20,392,310 (GRCm39) |
missense |
probably benign |
0.01 |
R9661:Elmo1
|
UTSW |
13 |
20,469,531 (GRCm39) |
critical splice donor site |
probably null |
|
RF008:Elmo1
|
UTSW |
13 |
20,458,706 (GRCm39) |
missense |
probably benign |
0.32 |
|