Other mutations in this stock |
Total: 99 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700030K09Rik |
T |
C |
8: 73,209,267 (GRCm39) |
S466P |
possibly damaging |
Het |
Ablim1 |
T |
C |
19: 57,068,298 (GRCm39) |
T267A |
probably damaging |
Het |
Acap2 |
A |
T |
16: 30,922,317 (GRCm39) |
L724Q |
possibly damaging |
Het |
Adcy4 |
T |
C |
14: 56,019,384 (GRCm39) |
T89A |
possibly damaging |
Het |
Agrp |
T |
C |
8: 106,294,000 (GRCm39) |
E41G |
probably benign |
Het |
Ajm1 |
T |
C |
2: 25,468,765 (GRCm39) |
Y382C |
probably damaging |
Het |
Akap9 |
G |
A |
5: 4,084,916 (GRCm39) |
|
probably benign |
Het |
Akr1d1 |
G |
A |
6: 37,541,426 (GRCm39) |
V308M |
probably damaging |
Het |
Ap1m2 |
C |
T |
9: 21,220,970 (GRCm39) |
R54Q |
probably benign |
Het |
Arhgap45 |
T |
A |
10: 79,862,900 (GRCm39) |
V692E |
probably damaging |
Het |
Arid5b |
G |
T |
10: 68,078,925 (GRCm39) |
N137K |
probably damaging |
Het |
Arsi |
G |
A |
18: 61,049,723 (GRCm39) |
G202E |
probably benign |
Het |
BC048679 |
T |
C |
7: 81,145,468 (GRCm39) |
N27D |
probably benign |
Het |
Ccdc78 |
A |
G |
17: 26,007,674 (GRCm39) |
N237S |
probably benign |
Het |
Cd46 |
G |
A |
1: 194,744,704 (GRCm39) |
L345F |
possibly damaging |
Het |
Cngb3 |
A |
T |
4: 19,425,569 (GRCm39) |
N459I |
possibly damaging |
Het |
Ctnnd2 |
A |
G |
15: 30,881,313 (GRCm39) |
E731G |
probably damaging |
Het |
Cul1 |
G |
T |
6: 47,494,080 (GRCm39) |
K464N |
probably benign |
Het |
Cul1 |
T |
A |
6: 47,494,125 (GRCm39) |
S479R |
probably damaging |
Het |
Dcaf5 |
A |
T |
12: 80,387,006 (GRCm39) |
D373E |
probably benign |
Het |
Dhcr7 |
A |
G |
7: 143,394,237 (GRCm39) |
Q126R |
probably benign |
Het |
Dnd1 |
C |
T |
18: 36,899,016 (GRCm39) |
|
probably benign |
Het |
Dok2 |
T |
C |
14: 71,014,956 (GRCm39) |
F228L |
probably damaging |
Het |
Dpep3 |
T |
G |
8: 106,702,821 (GRCm39) |
I314L |
probably benign |
Het |
Eps8 |
A |
G |
6: 137,491,293 (GRCm39) |
F362L |
probably damaging |
Het |
Espn |
G |
T |
4: 152,223,303 (GRCm39) |
R250S |
probably damaging |
Het |
Faf1 |
A |
C |
4: 109,600,093 (GRCm39) |
N163H |
probably damaging |
Het |
Fcho1 |
C |
T |
8: 72,163,125 (GRCm39) |
V635I |
probably benign |
Het |
Garin5b |
C |
T |
7: 4,760,468 (GRCm39) |
|
probably null |
Het |
Gask1b |
C |
A |
3: 79,843,981 (GRCm39) |
S36* |
probably null |
Het |
Gm7579 |
G |
A |
7: 141,765,645 (GRCm39) |
C17Y |
unknown |
Het |
Gpx8 |
G |
T |
13: 113,182,042 (GRCm39) |
Y130* |
probably null |
Het |
Grm6 |
C |
T |
11: 50,755,439 (GRCm39) |
T857M |
probably benign |
Het |
Gvin1 |
A |
T |
7: 105,762,643 (GRCm39) |
Y609N |
possibly damaging |
Het |
Hectd4 |
T |
A |
5: 121,443,881 (GRCm39) |
M30K |
probably benign |
Het |
Ilkap |
A |
G |
1: 91,315,105 (GRCm39) |
|
probably benign |
Het |
Iqub |
T |
C |
6: 24,450,841 (GRCm39) |
D586G |
probably damaging |
Het |
Klhl22 |
G |
A |
16: 17,594,880 (GRCm39) |
|
silent |
Het |
Klhl25 |
T |
C |
7: 75,516,798 (GRCm39) |
I568T |
probably benign |
Het |
Krr1 |
C |
T |
10: 111,821,596 (GRCm39) |
|
probably benign |
Het |
Larp6 |
A |
G |
9: 60,645,093 (GRCm39) |
E411G |
probably damaging |
Het |
Lepr |
A |
C |
4: 101,646,534 (GRCm39) |
I822L |
probably benign |
Het |
Lrig3 |
C |
A |
10: 125,846,921 (GRCm39) |
D896E |
probably benign |
Het |
Lrp1 |
C |
T |
10: 127,389,693 (GRCm39) |
G3114D |
probably damaging |
Het |
Lyset |
A |
T |
12: 102,710,314 (GRCm39) |
|
probably benign |
Het |
Macf1 |
A |
T |
4: 123,380,543 (GRCm39) |
Y1263N |
probably damaging |
Het |
Mapk10 |
T |
C |
5: 103,138,485 (GRCm39) |
D180G |
probably damaging |
Het |
Matr3 |
T |
A |
18: 35,714,693 (GRCm39) |
V113E |
probably damaging |
Het |
Mbd4 |
A |
T |
6: 115,825,887 (GRCm39) |
F368Y |
possibly damaging |
Het |
Mcpt8 |
G |
A |
14: 56,319,737 (GRCm39) |
R238W |
probably benign |
Het |
Mcrip2 |
G |
T |
17: 26,083,621 (GRCm39) |
T86N |
possibly damaging |
Het |
Mink1 |
A |
G |
11: 70,502,418 (GRCm39) |
N1043S |
probably damaging |
Het |
Nbeal2 |
G |
A |
9: 110,464,262 (GRCm39) |
T1128I |
probably benign |
Het |
Nrg2 |
T |
A |
18: 36,329,600 (GRCm39) |
Y205F |
probably damaging |
Het |
Nsmce4a |
A |
T |
7: 130,135,321 (GRCm39) |
|
probably benign |
Het |
Nubp2 |
A |
G |
17: 25,103,430 (GRCm39) |
M149T |
probably benign |
Het |
Or4d2b |
T |
A |
11: 87,780,051 (GRCm39) |
M224L |
probably damaging |
Het |
Or8d6 |
G |
T |
9: 39,853,800 (GRCm39) |
M81I |
probably benign |
Het |
Or8j3c |
T |
C |
2: 86,253,301 (GRCm39) |
T240A |
probably damaging |
Het |
Pax3 |
A |
G |
1: 78,169,093 (GRCm39) |
I191T |
possibly damaging |
Het |
Pdcd5 |
T |
C |
7: 35,343,135 (GRCm39) |
N137D |
possibly damaging |
Het |
Pik3c2a |
G |
A |
7: 115,939,391 (GRCm39) |
A1649V |
probably damaging |
Het |
Pik3r6 |
T |
A |
11: 68,434,879 (GRCm39) |
|
probably benign |
Het |
Pkhd1l1 |
T |
C |
15: 44,400,774 (GRCm39) |
S2183P |
possibly damaging |
Het |
Plekho1 |
T |
A |
3: 95,896,305 (GRCm39) |
Q388L |
possibly damaging |
Het |
Ppfibp1 |
A |
G |
6: 146,892,012 (GRCm39) |
T91A |
probably benign |
Het |
Ptger4 |
G |
T |
15: 5,272,087 (GRCm39) |
N177K |
probably benign |
Het |
Reln |
A |
G |
5: 22,106,749 (GRCm39) |
F3207S |
probably benign |
Het |
Rigi |
G |
T |
4: 40,210,000 (GRCm39) |
S644R |
probably damaging |
Het |
Ripk4 |
C |
T |
16: 97,552,736 (GRCm39) |
R194H |
probably damaging |
Het |
Rnf112 |
A |
T |
11: 61,343,570 (GRCm39) |
C112S |
possibly damaging |
Het |
Rprd1b |
T |
G |
2: 157,916,855 (GRCm39) |
Y278* |
probably null |
Het |
Sel1l |
A |
G |
12: 91,798,376 (GRCm39) |
L140P |
probably damaging |
Het |
Shroom3 |
G |
T |
5: 93,090,945 (GRCm39) |
V1151F |
probably damaging |
Het |
Slc38a3 |
A |
G |
9: 107,532,263 (GRCm39) |
V423A |
probably damaging |
Het |
Slitrk6 |
T |
C |
14: 110,989,315 (GRCm39) |
T131A |
probably damaging |
Het |
Slmap |
A |
T |
14: 26,181,364 (GRCm39) |
V323E |
probably benign |
Het |
Smim6 |
T |
C |
11: 115,804,330 (GRCm39) |
V39A |
probably benign |
Het |
Snapc3 |
C |
T |
4: 83,383,134 (GRCm39) |
|
probably benign |
Het |
Sorbs1 |
T |
C |
19: 40,325,449 (GRCm39) |
T382A |
probably benign |
Het |
Sparc |
G |
A |
11: 55,290,037 (GRCm39) |
T218I |
possibly damaging |
Het |
Steap1 |
A |
T |
5: 5,786,589 (GRCm39) |
F283I |
probably damaging |
Het |
Stil |
A |
G |
4: 114,895,671 (GRCm39) |
T586A |
probably benign |
Het |
Tango2 |
A |
G |
16: 18,128,765 (GRCm39) |
|
silent |
Het |
Tbce |
T |
A |
13: 14,194,380 (GRCm39) |
D93V |
probably damaging |
Het |
Tcf12 |
C |
T |
9: 71,766,122 (GRCm39) |
G504S |
probably null |
Het |
Tex55 |
A |
G |
16: 38,648,507 (GRCm39) |
S201P |
probably damaging |
Het |
Tle4 |
A |
T |
19: 14,441,709 (GRCm39) |
I435K |
probably benign |
Het |
Tmem245 |
A |
G |
4: 56,899,164 (GRCm39) |
F254S |
probably damaging |
Het |
Tubgcp3 |
T |
C |
8: 12,699,722 (GRCm39) |
K377R |
probably benign |
Het |
Ulk4 |
G |
A |
9: 121,079,968 (GRCm39) |
T497M |
possibly damaging |
Het |
Ush2a |
A |
T |
1: 188,285,472 (GRCm39) |
T2003S |
probably benign |
Het |
Usp53 |
A |
G |
3: 122,755,012 (GRCm39) |
S32P |
possibly damaging |
Het |
Vmn1r78 |
T |
A |
7: 11,886,683 (GRCm39) |
L98Q |
probably damaging |
Het |
Vmn2r84 |
T |
A |
10: 130,221,712 (GRCm39) |
D836V |
probably damaging |
Het |
Vps13d |
A |
G |
4: 144,813,731 (GRCm39) |
F165L |
probably benign |
Het |
Vstm4 |
A |
G |
14: 32,585,742 (GRCm39) |
E103G |
possibly damaging |
Het |
Zfp384 |
G |
A |
6: 125,007,893 (GRCm39) |
|
silent |
Het |
Zfp870 |
A |
T |
17: 33,102,314 (GRCm39) |
C339* |
probably null |
Het |
|
Other mutations in Acsbg3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01287:Acsbg3
|
APN |
17 |
57,189,203 (GRCm39) |
nonsense |
probably null |
|
IGL01833:Acsbg3
|
APN |
17 |
57,188,062 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02420:Acsbg3
|
APN |
17 |
57,187,494 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02969:Acsbg3
|
APN |
17 |
57,190,751 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03054:Acsbg3
|
UTSW |
17 |
57,193,528 (GRCm39) |
missense |
possibly damaging |
0.67 |
R0197:Acsbg3
|
UTSW |
17 |
57,190,835 (GRCm39) |
missense |
probably benign |
0.01 |
R0257:Acsbg3
|
UTSW |
17 |
57,192,169 (GRCm39) |
nonsense |
probably null |
|
R0279:Acsbg3
|
UTSW |
17 |
57,192,169 (GRCm39) |
nonsense |
probably null |
|
R0280:Acsbg3
|
UTSW |
17 |
57,192,169 (GRCm39) |
nonsense |
probably null |
|
R0281:Acsbg3
|
UTSW |
17 |
57,192,169 (GRCm39) |
nonsense |
probably null |
|
R0282:Acsbg3
|
UTSW |
17 |
57,192,169 (GRCm39) |
nonsense |
probably null |
|
R0329:Acsbg3
|
UTSW |
17 |
57,190,631 (GRCm39) |
missense |
probably benign |
0.02 |
R0330:Acsbg3
|
UTSW |
17 |
57,190,631 (GRCm39) |
missense |
probably benign |
0.02 |
R0349:Acsbg3
|
UTSW |
17 |
57,192,169 (GRCm39) |
nonsense |
probably null |
|
R0518:Acsbg3
|
UTSW |
17 |
57,192,169 (GRCm39) |
nonsense |
probably null |
|
R0519:Acsbg3
|
UTSW |
17 |
57,192,169 (GRCm39) |
nonsense |
probably null |
|
R0521:Acsbg3
|
UTSW |
17 |
57,192,169 (GRCm39) |
nonsense |
probably null |
|
R0604:Acsbg3
|
UTSW |
17 |
57,192,169 (GRCm39) |
nonsense |
probably null |
|
R0883:Acsbg3
|
UTSW |
17 |
57,190,835 (GRCm39) |
missense |
probably benign |
0.01 |
R1561:Acsbg3
|
UTSW |
17 |
57,184,431 (GRCm39) |
missense |
probably benign |
|
R1779:Acsbg3
|
UTSW |
17 |
57,192,169 (GRCm39) |
nonsense |
probably null |
|
R2008:Acsbg3
|
UTSW |
17 |
57,193,478 (GRCm39) |
missense |
probably benign |
0.04 |
R2102:Acsbg3
|
UTSW |
17 |
57,191,949 (GRCm39) |
nonsense |
probably null |
|
R2247:Acsbg3
|
UTSW |
17 |
57,184,435 (GRCm39) |
missense |
possibly damaging |
0.83 |
R2484:Acsbg3
|
UTSW |
17 |
57,189,641 (GRCm39) |
missense |
probably benign |
0.00 |
R2917:Acsbg3
|
UTSW |
17 |
57,192,141 (GRCm39) |
missense |
probably damaging |
1.00 |
R3149:Acsbg3
|
UTSW |
17 |
57,183,348 (GRCm39) |
missense |
probably benign |
|
R3773:Acsbg3
|
UTSW |
17 |
57,183,262 (GRCm39) |
start codon destroyed |
probably null |
0.00 |
R4829:Acsbg3
|
UTSW |
17 |
57,190,500 (GRCm39) |
splice site |
probably null |
|
R4860:Acsbg3
|
UTSW |
17 |
57,195,655 (GRCm39) |
missense |
probably benign |
0.09 |
R4887:Acsbg3
|
UTSW |
17 |
57,183,324 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5043:Acsbg3
|
UTSW |
17 |
57,192,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R5112:Acsbg3
|
UTSW |
17 |
57,184,465 (GRCm39) |
missense |
probably benign |
0.03 |
R5161:Acsbg3
|
UTSW |
17 |
57,189,888 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5214:Acsbg3
|
UTSW |
17 |
57,193,493 (GRCm39) |
missense |
probably benign |
|
R5287:Acsbg3
|
UTSW |
17 |
57,183,221 (GRCm39) |
unclassified |
probably benign |
|
R5403:Acsbg3
|
UTSW |
17 |
57,183,221 (GRCm39) |
unclassified |
probably benign |
|
R5779:Acsbg3
|
UTSW |
17 |
57,188,061 (GRCm39) |
missense |
probably benign |
0.02 |
R5997:Acsbg3
|
UTSW |
17 |
57,183,373 (GRCm39) |
missense |
probably benign |
0.02 |
R6198:Acsbg3
|
UTSW |
17 |
57,189,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R6259:Acsbg3
|
UTSW |
17 |
57,184,513 (GRCm39) |
missense |
probably benign |
0.04 |
R6357:Acsbg3
|
UTSW |
17 |
57,184,591 (GRCm39) |
critical splice donor site |
probably null |
|
R6754:Acsbg3
|
UTSW |
17 |
57,190,358 (GRCm39) |
missense |
probably damaging |
0.99 |
R6842:Acsbg3
|
UTSW |
17 |
57,184,432 (GRCm39) |
missense |
probably benign |
0.00 |
R7042:Acsbg3
|
UTSW |
17 |
57,192,098 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7181:Acsbg3
|
UTSW |
17 |
57,188,037 (GRCm39) |
missense |
probably benign |
0.03 |
R7445:Acsbg3
|
UTSW |
17 |
57,189,973 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7511:Acsbg3
|
UTSW |
17 |
57,189,954 (GRCm39) |
missense |
probably damaging |
0.98 |
R8122:Acsbg3
|
UTSW |
17 |
57,193,670 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8553:Acsbg3
|
UTSW |
17 |
57,188,021 (GRCm39) |
missense |
probably benign |
0.02 |
R8919:Acsbg3
|
UTSW |
17 |
57,189,218 (GRCm39) |
missense |
probably benign |
0.00 |
R9460:Acsbg3
|
UTSW |
17 |
57,183,316 (GRCm39) |
missense |
probably damaging |
0.99 |
R9469:Acsbg3
|
UTSW |
17 |
57,183,283 (GRCm39) |
missense |
probably benign |
0.00 |
R9766:Acsbg3
|
UTSW |
17 |
57,189,177 (GRCm39) |
missense |
probably benign |
0.02 |
Z1177:Acsbg3
|
UTSW |
17 |
57,190,463 (GRCm39) |
frame shift |
probably null |
|
|