Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Cand2 |
A |
G |
6: 115,764,197 (GRCm39) |
M324V |
probably damaging |
Het |
Cap1 |
C |
T |
4: 122,756,512 (GRCm39) |
V340M |
probably benign |
Het |
Ccdc110 |
T |
C |
8: 46,388,175 (GRCm39) |
V44A |
possibly damaging |
Het |
Cps1 |
A |
G |
1: 67,183,059 (GRCm39) |
D139G |
probably benign |
Het |
Cwc27 |
T |
A |
13: 104,768,124 (GRCm39) |
E457V |
unknown |
Het |
Cxxc1 |
C |
T |
18: 74,351,962 (GRCm39) |
P280S |
probably benign |
Het |
Dennd2b |
A |
T |
7: 109,140,635 (GRCm39) |
V197D |
probably damaging |
Het |
Dop1b |
T |
A |
16: 93,559,393 (GRCm39) |
L595Q |
probably benign |
Het |
Dscam |
G |
T |
16: 96,453,372 (GRCm39) |
S1292R |
possibly damaging |
Het |
E2f4 |
C |
A |
8: 106,030,851 (GRCm39) |
F353L |
probably damaging |
Het |
Ep300 |
A |
G |
15: 81,485,097 (GRCm39) |
|
probably benign |
Het |
Fads1 |
C |
T |
19: 10,160,429 (GRCm39) |
P5L |
probably benign |
Het |
Fign |
T |
A |
2: 63,811,135 (GRCm39) |
H45L |
probably damaging |
Het |
Flcn |
T |
A |
11: 59,685,025 (GRCm39) |
|
probably benign |
Het |
Gm5141 |
A |
T |
13: 62,922,408 (GRCm39) |
F254I |
probably damaging |
Het |
Gpr37 |
A |
T |
6: 25,669,823 (GRCm39) |
C340* |
probably null |
Het |
Gtf3c2 |
A |
T |
5: 31,315,476 (GRCm39) |
|
probably benign |
Het |
Hcfc2 |
T |
A |
10: 82,574,242 (GRCm39) |
F139I |
probably damaging |
Het |
Hectd4 |
T |
C |
5: 121,486,539 (GRCm39) |
L3178P |
possibly damaging |
Het |
Hrc |
AGAGGAGGAGGAAGAGGAGGAGGA |
AGAGGAGGAGGAGGAAGAGGAGGAGGA |
7: 44,986,659 (GRCm39) |
|
probably benign |
Het |
Igf2bp1 |
A |
G |
11: 95,857,622 (GRCm39) |
|
probably benign |
Het |
Igsf9b |
T |
G |
9: 27,244,358 (GRCm39) |
|
probably null |
Het |
Il23r |
G |
A |
6: 67,403,572 (GRCm39) |
A443V |
probably benign |
Het |
Kcnv1 |
A |
G |
15: 44,972,645 (GRCm39) |
F413L |
probably damaging |
Het |
Lipe |
C |
A |
7: 25,087,611 (GRCm39) |
A150S |
possibly damaging |
Het |
Lrrcc1 |
T |
C |
3: 14,622,333 (GRCm39) |
S557P |
probably damaging |
Het |
Mrpl54 |
C |
A |
10: 81,102,687 (GRCm39) |
W13L |
probably damaging |
Het |
Mtcl3 |
T |
A |
10: 29,056,952 (GRCm39) |
|
probably benign |
Het |
Myrf |
G |
C |
19: 10,195,526 (GRCm39) |
T428S |
probably benign |
Het |
Npy1r |
C |
A |
8: 67,157,670 (GRCm39) |
Q327K |
probably damaging |
Het |
Nt5el |
C |
A |
13: 105,218,762 (GRCm39) |
S32* |
probably null |
Het |
Or51b17 |
C |
T |
7: 103,542,438 (GRCm39) |
R168H |
probably benign |
Het |
Osbpl10 |
C |
T |
9: 114,996,246 (GRCm39) |
L139F |
probably damaging |
Het |
P2rx6 |
A |
C |
16: 17,385,768 (GRCm39) |
T199P |
probably damaging |
Het |
Phyhip |
A |
T |
14: 70,699,199 (GRCm39) |
M1L |
possibly damaging |
Het |
Pkd1l3 |
C |
G |
8: 110,350,281 (GRCm39) |
D375E |
possibly damaging |
Het |
Psmc1 |
T |
A |
12: 100,086,389 (GRCm39) |
I342N |
possibly damaging |
Het |
Reln |
A |
T |
5: 22,152,406 (GRCm39) |
D2353E |
probably damaging |
Het |
Rmdn3 |
T |
C |
2: 118,976,851 (GRCm39) |
E294G |
probably benign |
Het |
Scnn1g |
A |
G |
7: 121,366,647 (GRCm39) |
M615V |
probably benign |
Het |
Shcbp1l |
T |
A |
1: 153,304,314 (GRCm39) |
D124E |
possibly damaging |
Het |
Sipa1l1 |
T |
C |
12: 82,472,054 (GRCm39) |
S1345P |
possibly damaging |
Het |
Taf7l2 |
T |
C |
10: 115,948,707 (GRCm39) |
E273G |
possibly damaging |
Het |
Timp4 |
A |
G |
6: 115,226,802 (GRCm39) |
Y114H |
probably damaging |
Het |
Tlr9 |
T |
A |
9: 106,102,086 (GRCm39) |
L459Q |
probably benign |
Het |
Tmem104 |
C |
A |
11: 115,091,654 (GRCm39) |
T59K |
probably damaging |
Het |
Wdr59 |
GGGTGGTG |
GGGTG |
8: 112,207,172 (GRCm39) |
|
probably benign |
Het |
Zfp622 |
A |
T |
15: 25,984,654 (GRCm39) |
I7F |
possibly damaging |
Het |
|
Other mutations in Gpbp1l1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00926:Gpbp1l1
|
APN |
4 |
116,444,710 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03342:Gpbp1l1
|
APN |
4 |
116,431,740 (GRCm39) |
missense |
probably benign |
|
R0964:Gpbp1l1
|
UTSW |
4 |
116,438,436 (GRCm39) |
splice site |
probably benign |
|
R1136:Gpbp1l1
|
UTSW |
4 |
116,450,115 (GRCm39) |
missense |
probably damaging |
1.00 |
R1169:Gpbp1l1
|
UTSW |
4 |
116,431,563 (GRCm39) |
missense |
possibly damaging |
0.53 |
R3975:Gpbp1l1
|
UTSW |
4 |
116,428,182 (GRCm39) |
critical splice donor site |
probably null |
|
R4296:Gpbp1l1
|
UTSW |
4 |
116,444,656 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4676:Gpbp1l1
|
UTSW |
4 |
116,447,462 (GRCm39) |
missense |
probably damaging |
1.00 |
R4870:Gpbp1l1
|
UTSW |
4 |
116,430,714 (GRCm39) |
missense |
probably benign |
|
R5086:Gpbp1l1
|
UTSW |
4 |
116,445,789 (GRCm39) |
missense |
probably benign |
0.04 |
R5931:Gpbp1l1
|
UTSW |
4 |
116,447,457 (GRCm39) |
missense |
probably benign |
0.00 |
R6486:Gpbp1l1
|
UTSW |
4 |
116,438,572 (GRCm39) |
missense |
probably damaging |
0.99 |
R6604:Gpbp1l1
|
UTSW |
4 |
116,430,702 (GRCm39) |
missense |
probably benign |
0.09 |
R6973:Gpbp1l1
|
UTSW |
4 |
116,438,479 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7031:Gpbp1l1
|
UTSW |
4 |
116,450,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R7230:Gpbp1l1
|
UTSW |
4 |
116,445,807 (GRCm39) |
missense |
probably damaging |
0.99 |
R7286:Gpbp1l1
|
UTSW |
4 |
116,447,442 (GRCm39) |
missense |
probably benign |
0.02 |
R7368:Gpbp1l1
|
UTSW |
4 |
116,430,655 (GRCm39) |
missense |
probably benign |
0.04 |
R7791:Gpbp1l1
|
UTSW |
4 |
116,431,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R9475:Gpbp1l1
|
UTSW |
4 |
116,431,558 (GRCm39) |
missense |
possibly damaging |
0.87 |
|