Other mutations in this stock |
Total: 34 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Accs |
A |
G |
2: 93,669,587 (GRCm39) |
|
probably benign |
Het |
Actl7b |
T |
C |
4: 56,740,677 (GRCm39) |
Y227C |
probably damaging |
Het |
Adam26a |
A |
T |
8: 44,021,485 (GRCm39) |
H668Q |
probably benign |
Het |
Alcam |
A |
T |
16: 52,094,653 (GRCm39) |
|
probably benign |
Het |
Aldh3a2 |
C |
T |
11: 61,144,624 (GRCm39) |
|
probably benign |
Het |
Atp11b |
G |
T |
3: 35,891,130 (GRCm39) |
G801V |
probably damaging |
Het |
C3 |
G |
A |
17: 57,522,866 (GRCm39) |
T1006I |
probably benign |
Het |
Cacna2d4 |
T |
C |
6: 119,259,134 (GRCm39) |
|
probably benign |
Het |
Cldn34b3 |
A |
T |
X: 75,310,680 (GRCm39) |
I83F |
probably damaging |
Het |
Clec2g |
G |
A |
6: 128,925,736 (GRCm39) |
M48I |
probably benign |
Het |
Coch |
A |
G |
12: 51,650,136 (GRCm39) |
D375G |
probably damaging |
Het |
Erbb2 |
C |
T |
11: 98,323,745 (GRCm39) |
T653I |
possibly damaging |
Het |
Etv3 |
A |
G |
3: 87,443,025 (GRCm39) |
H203R |
possibly damaging |
Het |
Fat4 |
A |
G |
3: 39,003,683 (GRCm39) |
R1801G |
possibly damaging |
Het |
Gars1 |
T |
A |
6: 55,042,505 (GRCm39) |
S413T |
probably benign |
Het |
Gnat1 |
G |
A |
9: 107,553,500 (GRCm39) |
R253C |
possibly damaging |
Het |
Hook3 |
A |
T |
8: 26,578,217 (GRCm39) |
L91I |
possibly damaging |
Het |
Lrp8 |
T |
C |
4: 107,712,881 (GRCm39) |
Y377H |
probably damaging |
Het |
Lztr1 |
G |
A |
16: 17,340,255 (GRCm39) |
|
probably null |
Het |
Malt1 |
A |
G |
18: 65,609,471 (GRCm39) |
D825G |
possibly damaging |
Het |
Nlrp9b |
T |
C |
7: 19,779,859 (GRCm39) |
|
probably null |
Het |
Or1x2 |
C |
T |
11: 50,918,416 (GRCm39) |
R196* |
probably null |
Het |
Or2v2 |
A |
T |
11: 49,004,403 (GRCm39) |
I50N |
probably damaging |
Het |
Orc1 |
A |
G |
4: 108,459,249 (GRCm39) |
R473G |
probably damaging |
Het |
Pard6g |
G |
A |
18: 80,160,661 (GRCm39) |
R258H |
probably damaging |
Het |
Pkdrej |
T |
C |
15: 85,702,264 (GRCm39) |
D1224G |
possibly damaging |
Het |
Polr1e |
A |
G |
4: 45,018,723 (GRCm39) |
T18A |
probably benign |
Het |
Pycr3 |
T |
C |
15: 75,788,853 (GRCm39) |
T240A |
probably damaging |
Het |
Ralgapa1 |
C |
A |
12: 55,766,442 (GRCm39) |
G1284V |
probably damaging |
Het |
Sec24c |
C |
T |
14: 20,732,839 (GRCm39) |
T134I |
possibly damaging |
Het |
Sis |
A |
G |
3: 72,843,253 (GRCm39) |
|
probably benign |
Het |
Susd5 |
A |
C |
9: 113,897,947 (GRCm39) |
|
probably benign |
Het |
Tlk1 |
T |
C |
2: 70,582,610 (GRCm39) |
N173S |
probably benign |
Het |
Uroc1 |
T |
C |
6: 90,340,082 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Rcl1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01325:Rcl1
|
APN |
19 |
29,098,662 (GRCm39) |
splice site |
probably null |
|
IGL02625:Rcl1
|
APN |
19 |
29,095,741 (GRCm39) |
missense |
probably benign |
0.04 |
R0512:Rcl1
|
UTSW |
19 |
29,105,497 (GRCm39) |
missense |
probably damaging |
1.00 |
R2249:Rcl1
|
UTSW |
19 |
29,099,268 (GRCm39) |
missense |
possibly damaging |
0.46 |
R3610:Rcl1
|
UTSW |
19 |
29,095,630 (GRCm39) |
missense |
probably benign |
0.00 |
R4415:Rcl1
|
UTSW |
19 |
29,095,762 (GRCm39) |
missense |
probably benign |
0.01 |
R5324:Rcl1
|
UTSW |
19 |
29,105,401 (GRCm39) |
missense |
probably benign |
0.23 |
R5679:Rcl1
|
UTSW |
19 |
29,098,658 (GRCm39) |
splice site |
probably null |
|
R5988:Rcl1
|
UTSW |
19 |
29,099,167 (GRCm39) |
missense |
probably damaging |
1.00 |
R7332:Rcl1
|
UTSW |
19 |
29,108,096 (GRCm39) |
missense |
probably benign |
0.03 |
R7936:Rcl1
|
UTSW |
19 |
29,095,805 (GRCm39) |
splice site |
probably null |
|
R8353:Rcl1
|
UTSW |
19 |
29,093,159 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8453:Rcl1
|
UTSW |
19 |
29,093,159 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9282:Rcl1
|
UTSW |
19 |
29,093,170 (GRCm39) |
missense |
probably damaging |
0.99 |
R9747:Rcl1
|
UTSW |
19 |
29,105,482 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1176:Rcl1
|
UTSW |
19 |
29,079,017 (GRCm39) |
missense |
probably benign |
|
|