Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930486L24Rik |
T |
A |
13: 61,001,647 (GRCm39) |
M58L |
probably benign |
Het |
Abca8b |
A |
G |
11: 109,840,939 (GRCm39) |
V1078A |
probably benign |
Het |
Acvr2b |
A |
G |
9: 119,257,492 (GRCm39) |
D175G |
probably damaging |
Het |
Adad2 |
A |
G |
8: 120,339,769 (GRCm39) |
M84V |
probably benign |
Het |
Ahnak |
A |
T |
19: 8,994,411 (GRCm39) |
M5232L |
probably benign |
Het |
Ahsa1 |
T |
C |
12: 87,315,053 (GRCm39) |
S69P |
probably damaging |
Het |
Aipl1 |
C |
T |
11: 71,928,253 (GRCm39) |
G11D |
probably damaging |
Het |
Antxr2 |
G |
T |
5: 98,086,306 (GRCm39) |
P434T |
probably damaging |
Het |
Arap1 |
T |
C |
7: 101,037,382 (GRCm39) |
Y470H |
probably damaging |
Het |
Baz1a |
A |
G |
12: 54,963,372 (GRCm39) |
I907T |
probably damaging |
Het |
Baz1b |
A |
T |
5: 135,246,729 (GRCm39) |
Q726L |
probably benign |
Het |
Bean1 |
C |
T |
8: 104,908,739 (GRCm39) |
R39C |
probably damaging |
Het |
Cass4 |
A |
T |
2: 172,268,686 (GRCm39) |
N256I |
possibly damaging |
Het |
Cnot10 |
T |
C |
9: 114,460,897 (GRCm39) |
K91R |
probably benign |
Het |
Col6a6 |
C |
T |
9: 105,651,757 (GRCm39) |
V1085M |
probably damaging |
Het |
Dpf3 |
A |
G |
12: 83,534,449 (GRCm39) |
|
probably null |
Het |
Dync1i2 |
T |
A |
2: 71,093,019 (GRCm39) |
W605R |
probably damaging |
Het |
Exoc5 |
A |
T |
14: 49,286,297 (GRCm39) |
V110E |
probably damaging |
Het |
Fgfr2 |
T |
A |
7: 129,782,136 (GRCm39) |
H563L |
probably damaging |
Het |
Fosl2 |
A |
G |
5: 32,304,379 (GRCm39) |
T105A |
probably benign |
Het |
Fsip2 |
A |
G |
2: 82,818,604 (GRCm39) |
H4779R |
possibly damaging |
Het |
Fuca2 |
A |
G |
10: 13,382,518 (GRCm39) |
Y268C |
probably damaging |
Het |
Galnt13 |
G |
A |
2: 54,770,161 (GRCm39) |
E318K |
probably damaging |
Het |
Hc |
G |
A |
2: 34,876,294 (GRCm39) |
T1584I |
probably damaging |
Het |
Helb |
T |
C |
10: 119,928,556 (GRCm39) |
K762E |
probably damaging |
Het |
Hspg2 |
T |
G |
4: 137,296,827 (GRCm39) |
L4335R |
probably damaging |
Het |
Ift88 |
A |
C |
14: 57,718,920 (GRCm39) |
Q635P |
probably damaging |
Het |
Inpp5a |
C |
A |
7: 138,969,380 (GRCm39) |
D25E |
probably benign |
Het |
Kcnu1 |
A |
G |
8: 26,376,786 (GRCm39) |
T387A |
possibly damaging |
Het |
Lamb1 |
G |
A |
12: 31,374,223 (GRCm39) |
D1529N |
probably benign |
Het |
Lamb1 |
A |
T |
12: 31,374,224 (GRCm39) |
D1529V |
probably benign |
Het |
Lnx1 |
T |
C |
5: 74,758,584 (GRCm39) |
N476S |
probably benign |
Het |
Mup17 |
T |
C |
4: 61,512,633 (GRCm39) |
M87V |
probably benign |
Het |
Naip6 |
G |
A |
13: 100,452,494 (GRCm39) |
T189I |
probably damaging |
Het |
Nf1 |
T |
A |
11: 79,447,629 (GRCm39) |
Y462N |
possibly damaging |
Het |
Nup133 |
T |
C |
8: 124,664,881 (GRCm39) |
D270G |
probably benign |
Het |
Obox2 |
T |
C |
7: 15,130,789 (GRCm39) |
L7S |
probably damaging |
Het |
Obox6 |
A |
T |
7: 15,567,722 (GRCm39) |
S242T |
possibly damaging |
Het |
Ogfr |
AGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCAAAAGGCCAGGTGGAGCCAGAGGACCCAAAAGGCCAGGTGGGGCCAGAAGACCCAAAAGGCCAGGTGGGGCCAGAGGACCCAAAAGGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCCAAAGCCAGGTGGGGCCAGAG |
AGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCAAAAGGCCAGGTGGAGCCAGAGGACCCAAAAGGCCAGGTGGGGCCAGAAGACCCAAAAGGCCAGGTGGGGCCAGAGGACCCAAAAGGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCCAAAGCCAGGTGGGGCCAGAG |
2: 180,236,850 (GRCm39) |
|
probably benign |
Het |
Pigyl |
C |
T |
9: 22,069,130 (GRCm39) |
|
probably benign |
Het |
Rasa1 |
A |
G |
13: 85,369,649 (GRCm39) |
V891A |
probably damaging |
Het |
Rxrg |
A |
G |
1: 167,458,890 (GRCm39) |
D292G |
possibly damaging |
Het |
Saal1 |
A |
G |
7: 46,351,248 (GRCm39) |
F243L |
probably benign |
Het |
Sec24c |
G |
A |
14: 20,729,598 (GRCm39) |
V59M |
probably benign |
Het |
Sema4f |
C |
A |
6: 82,890,890 (GRCm39) |
G639V |
probably damaging |
Het |
Serpinb1c |
A |
T |
13: 33,066,172 (GRCm39) |
C258S |
probably benign |
Het |
Snx21 |
CACCTGCAGGCAGTGCCAGAGCTACGCCAAGCTCCGGACCTGCAGG |
CACCTGCAGG |
2: 164,633,849 (GRCm39) |
|
probably benign |
Het |
Syndig1 |
T |
C |
2: 149,845,175 (GRCm39) |
S233P |
probably damaging |
Het |
Taf6l |
A |
T |
19: 8,752,636 (GRCm39) |
L377M |
probably damaging |
Het |
Tcl1 |
T |
C |
12: 105,184,979 (GRCm39) |
Y77C |
probably damaging |
Het |
Tekt2 |
C |
A |
4: 126,216,952 (GRCm39) |
M272I |
probably benign |
Het |
Trp53bp1 |
T |
C |
2: 121,100,460 (GRCm39) |
E98G |
probably benign |
Het |
Ubr4 |
T |
A |
4: 139,182,763 (GRCm39) |
I383N |
unknown |
Het |
Wdr89 |
G |
T |
12: 75,679,937 (GRCm39) |
P106T |
probably benign |
Het |
Zfp534 |
T |
C |
4: 147,758,698 (GRCm39) |
E657G |
possibly damaging |
Het |
Zfp69 |
T |
C |
4: 120,788,013 (GRCm39) |
K434R |
probably damaging |
Het |
Zfyve26 |
T |
A |
12: 79,321,680 (GRCm39) |
K980* |
probably null |
Het |
|
Other mutations in Bcar3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00662:Bcar3
|
APN |
3 |
122,306,585 (GRCm39) |
missense |
probably benign |
0.36 |
IGL01372:Bcar3
|
APN |
3 |
122,316,943 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02681:Bcar3
|
APN |
3 |
122,306,417 (GRCm39) |
splice site |
probably null |
|
IGL03403:Bcar3
|
APN |
3 |
122,306,618 (GRCm39) |
missense |
probably benign |
0.01 |
R0408:Bcar3
|
UTSW |
3 |
122,302,033 (GRCm39) |
missense |
probably damaging |
0.98 |
R0531:Bcar3
|
UTSW |
3 |
122,220,148 (GRCm39) |
missense |
probably benign |
0.00 |
R0798:Bcar3
|
UTSW |
3 |
122,318,948 (GRCm39) |
missense |
probably benign |
0.01 |
R1445:Bcar3
|
UTSW |
3 |
122,316,840 (GRCm39) |
missense |
probably damaging |
0.98 |
R1892:Bcar3
|
UTSW |
3 |
122,301,785 (GRCm39) |
missense |
probably benign |
0.00 |
R2138:Bcar3
|
UTSW |
3 |
122,306,645 (GRCm39) |
missense |
probably damaging |
1.00 |
R3236:Bcar3
|
UTSW |
3 |
122,318,645 (GRCm39) |
missense |
probably benign |
0.02 |
R3237:Bcar3
|
UTSW |
3 |
122,318,645 (GRCm39) |
missense |
probably benign |
0.02 |
R3832:Bcar3
|
UTSW |
3 |
122,220,298 (GRCm39) |
missense |
probably damaging |
1.00 |
R4801:Bcar3
|
UTSW |
3 |
122,323,243 (GRCm39) |
missense |
probably benign |
0.22 |
R4802:Bcar3
|
UTSW |
3 |
122,323,243 (GRCm39) |
missense |
probably benign |
0.22 |
R5342:Bcar3
|
UTSW |
3 |
122,220,298 (GRCm39) |
missense |
probably damaging |
1.00 |
R5364:Bcar3
|
UTSW |
3 |
122,323,281 (GRCm39) |
missense |
probably benign |
0.41 |
R5560:Bcar3
|
UTSW |
3 |
122,220,224 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5714:Bcar3
|
UTSW |
3 |
122,248,736 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5716:Bcar3
|
UTSW |
3 |
122,306,564 (GRCm39) |
missense |
probably damaging |
1.00 |
R5944:Bcar3
|
UTSW |
3 |
122,316,932 (GRCm39) |
missense |
probably benign |
|
R6478:Bcar3
|
UTSW |
3 |
122,220,225 (GRCm39) |
missense |
probably benign |
0.04 |
R6615:Bcar3
|
UTSW |
3 |
122,220,282 (GRCm39) |
missense |
probably benign |
0.00 |
R6996:Bcar3
|
UTSW |
3 |
122,302,033 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7272:Bcar3
|
UTSW |
3 |
122,302,045 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7308:Bcar3
|
UTSW |
3 |
122,302,142 (GRCm39) |
missense |
probably benign |
0.00 |
R7353:Bcar3
|
UTSW |
3 |
122,306,341 (GRCm39) |
missense |
probably benign |
0.00 |
R7465:Bcar3
|
UTSW |
3 |
122,316,879 (GRCm39) |
missense |
probably benign |
0.13 |
R7816:Bcar3
|
UTSW |
3 |
122,220,343 (GRCm39) |
missense |
probably benign |
0.00 |
R7899:Bcar3
|
UTSW |
3 |
122,301,902 (GRCm39) |
missense |
probably damaging |
0.97 |
R8066:Bcar3
|
UTSW |
3 |
122,318,573 (GRCm39) |
missense |
probably damaging |
1.00 |
R8165:Bcar3
|
UTSW |
3 |
122,304,805 (GRCm39) |
unclassified |
probably benign |
|
R8285:Bcar3
|
UTSW |
3 |
122,306,383 (GRCm39) |
missense |
probably benign |
0.00 |
R9224:Bcar3
|
UTSW |
3 |
122,319,091 (GRCm39) |
missense |
probably damaging |
1.00 |
R9480:Bcar3
|
UTSW |
3 |
122,277,618 (GRCm39) |
nonsense |
probably null |
|
R9631:Bcar3
|
UTSW |
3 |
122,301,801 (GRCm39) |
missense |
possibly damaging |
0.91 |
Z1177:Bcar3
|
UTSW |
3 |
122,298,667 (GRCm39) |
missense |
probably damaging |
1.00 |
|