Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgra3 |
A |
G |
5: 50,118,096 (GRCm39) |
F1151L |
probably benign |
Het |
Afg3l2 |
G |
T |
18: 67,554,329 (GRCm39) |
L458M |
probably damaging |
Het |
Aldh4a1 |
A |
C |
4: 139,375,612 (GRCm39) |
|
probably benign |
Het |
Anln |
A |
T |
9: 22,264,077 (GRCm39) |
|
probably null |
Het |
Aste1 |
T |
C |
9: 105,282,253 (GRCm39) |
S74P |
probably damaging |
Het |
Atp6v0e2 |
G |
A |
6: 48,517,051 (GRCm39) |
R77H |
probably benign |
Het |
Brpf1 |
A |
G |
6: 113,296,902 (GRCm39) |
D962G |
possibly damaging |
Het |
Btbd2 |
T |
C |
10: 80,482,253 (GRCm39) |
D249G |
probably damaging |
Het |
Catsper3 |
T |
C |
13: 55,955,989 (GRCm39) |
|
probably null |
Het |
Cfap43 |
A |
G |
19: 47,885,811 (GRCm39) |
L268P |
probably damaging |
Het |
Cftr |
T |
C |
6: 18,255,413 (GRCm39) |
V540A |
probably benign |
Het |
Col22a1 |
C |
T |
15: 71,881,255 (GRCm39) |
G32D |
probably damaging |
Het |
Col5a2 |
G |
T |
1: 45,432,241 (GRCm39) |
P804Q |
probably benign |
Het |
Cyp2d41-ps |
A |
G |
15: 82,662,981 (GRCm39) |
|
noncoding transcript |
Het |
Cyp39a1 |
T |
G |
17: 44,057,429 (GRCm39) |
L423V |
possibly damaging |
Het |
Elmo1 |
T |
G |
13: 20,748,607 (GRCm39) |
V484G |
probably benign |
Het |
Eps8 |
C |
A |
6: 137,467,288 (GRCm39) |
Q656H |
probably damaging |
Het |
Eps8 |
T |
C |
6: 137,467,289 (GRCm39) |
Q656R |
possibly damaging |
Het |
Fshb |
T |
C |
2: 106,887,854 (GRCm39) |
D55G |
possibly damaging |
Het |
Garin1a |
G |
T |
6: 29,281,221 (GRCm39) |
|
probably benign |
Het |
H3c4 |
T |
A |
13: 23,760,304 (GRCm39) |
L110Q |
probably damaging |
Het |
Herc1 |
C |
A |
9: 66,355,786 (GRCm39) |
Q2346K |
probably damaging |
Het |
Htr3b |
T |
C |
9: 48,856,815 (GRCm39) |
D221G |
probably benign |
Het |
Ift74 |
T |
A |
4: 94,550,833 (GRCm39) |
D328E |
probably benign |
Het |
Kif21b |
A |
T |
1: 136,072,363 (GRCm39) |
K23M |
probably damaging |
Het |
Lgr6 |
C |
T |
1: 134,921,748 (GRCm39) |
A199T |
probably damaging |
Het |
Lipc |
T |
A |
9: 70,705,673 (GRCm39) |
E470V |
probably benign |
Het |
Lrrc4 |
G |
T |
6: 28,830,142 (GRCm39) |
T68K |
probably damaging |
Het |
Lrrc63 |
T |
A |
14: 75,322,322 (GRCm39) |
H594L |
possibly damaging |
Het |
Mfsd14a |
A |
T |
3: 116,442,150 (GRCm39) |
|
probably benign |
Het |
Mob2 |
T |
C |
7: 141,563,274 (GRCm39) |
|
probably null |
Het |
Nckap5 |
T |
A |
1: 126,150,410 (GRCm39) |
H105L |
possibly damaging |
Het |
Ngef |
C |
A |
1: 87,437,090 (GRCm39) |
G133* |
probably null |
Het |
Or14j2 |
T |
G |
17: 37,886,111 (GRCm39) |
I68L |
probably benign |
Het |
Or1e16 |
AGCGGTCGTAGGC |
AGC |
11: 73,286,480 (GRCm39) |
|
probably null |
Het |
Or2t1 |
T |
A |
14: 14,328,462 (GRCm38) |
M117K |
probably damaging |
Het |
Or52s1 |
G |
A |
7: 102,861,207 (GRCm39) |
V47I |
probably benign |
Het |
Or5b120 |
G |
T |
19: 13,479,748 (GRCm39) |
V14F |
possibly damaging |
Het |
Or5g23 |
T |
C |
2: 85,438,791 (GRCm39) |
I154M |
probably benign |
Het |
Pard3 |
A |
G |
8: 127,800,040 (GRCm39) |
|
probably null |
Het |
Pgm2 |
C |
T |
5: 64,263,175 (GRCm39) |
A274V |
possibly damaging |
Het |
Ppp1r9a |
T |
A |
6: 5,156,177 (GRCm39) |
S1144R |
probably damaging |
Het |
Pramel23 |
A |
C |
4: 143,424,632 (GRCm39) |
C270W |
possibly damaging |
Het |
Prkcq |
C |
T |
2: 11,304,227 (GRCm39) |
P590L |
probably damaging |
Het |
Psmd13 |
T |
A |
7: 140,474,374 (GRCm39) |
|
probably null |
Het |
Rab3gap1 |
T |
A |
1: 127,816,931 (GRCm39) |
D63E |
probably benign |
Het |
Rag2 |
C |
A |
2: 101,461,085 (GRCm39) |
T465K |
probably damaging |
Het |
Rnase6 |
A |
G |
14: 51,367,670 (GRCm39) |
M21V |
unknown |
Het |
Rufy4 |
T |
C |
1: 74,186,822 (GRCm39) |
C537R |
probably damaging |
Het |
Ryr2 |
A |
T |
13: 11,653,316 (GRCm39) |
|
probably null |
Het |
Sash1 |
T |
G |
10: 8,615,989 (GRCm39) |
R624S |
probably damaging |
Het |
Slc1a2 |
A |
G |
2: 102,586,460 (GRCm39) |
I355V |
probably benign |
Het |
Srrm2 |
T |
C |
17: 24,036,358 (GRCm39) |
S1097P |
probably benign |
Het |
Sugct |
C |
T |
13: 17,497,861 (GRCm39) |
A271T |
probably damaging |
Het |
Tdrd7 |
T |
C |
4: 46,034,350 (GRCm39) |
V1065A |
probably damaging |
Het |
Tmprss6 |
T |
A |
15: 78,338,389 (GRCm39) |
Y307F |
probably damaging |
Het |
Tram1 |
T |
C |
1: 13,642,126 (GRCm39) |
N216S |
probably benign |
Het |
Ttk |
T |
C |
9: 83,721,394 (GRCm39) |
V93A |
probably benign |
Het |
Ubr4 |
A |
G |
4: 139,195,408 (GRCm39) |
Y1210C |
probably damaging |
Het |
Wdr7 |
A |
G |
18: 63,871,937 (GRCm39) |
K364E |
probably benign |
Het |
Xrcc2 |
G |
T |
5: 25,897,656 (GRCm39) |
H98N |
probably benign |
Het |
Zdhhc11 |
A |
G |
13: 74,113,688 (GRCm39) |
I77V |
probably benign |
Het |
Zfp54 |
C |
T |
17: 21,654,442 (GRCm39) |
S312L |
probably benign |
Het |
Zfp647 |
G |
A |
15: 76,796,285 (GRCm39) |
P125L |
probably damaging |
Het |
|
Other mutations in Acsbg1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00507:Acsbg1
|
APN |
9 |
54,529,712 (GRCm39) |
splice site |
probably benign |
|
IGL00757:Acsbg1
|
APN |
9 |
54,530,003 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL01665:Acsbg1
|
APN |
9 |
54,530,004 (GRCm39) |
missense |
probably benign |
|
IGL02213:Acsbg1
|
APN |
9 |
54,523,254 (GRCm39) |
missense |
probably damaging |
0.98 |
R0388:Acsbg1
|
UTSW |
9 |
54,516,347 (GRCm39) |
missense |
probably damaging |
1.00 |
R0426:Acsbg1
|
UTSW |
9 |
54,530,030 (GRCm39) |
missense |
probably benign |
|
R0445:Acsbg1
|
UTSW |
9 |
54,523,179 (GRCm39) |
missense |
probably damaging |
1.00 |
R0644:Acsbg1
|
UTSW |
9 |
54,517,110 (GRCm39) |
missense |
probably damaging |
1.00 |
R1779:Acsbg1
|
UTSW |
9 |
54,523,346 (GRCm39) |
missense |
probably damaging |
1.00 |
R1826:Acsbg1
|
UTSW |
9 |
54,529,840 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4224:Acsbg1
|
UTSW |
9 |
54,523,325 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5435:Acsbg1
|
UTSW |
9 |
54,523,153 (GRCm39) |
nonsense |
probably null |
|
R6241:Acsbg1
|
UTSW |
9 |
54,549,946 (GRCm39) |
missense |
probably damaging |
0.99 |
R6260:Acsbg1
|
UTSW |
9 |
54,535,751 (GRCm39) |
splice site |
probably null |
|
R6275:Acsbg1
|
UTSW |
9 |
54,517,056 (GRCm39) |
missense |
probably benign |
0.00 |
R6940:Acsbg1
|
UTSW |
9 |
54,516,381 (GRCm39) |
missense |
probably benign |
0.00 |
R7178:Acsbg1
|
UTSW |
9 |
54,535,745 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7685:Acsbg1
|
UTSW |
9 |
54,535,843 (GRCm39) |
missense |
unknown |
|
R7943:Acsbg1
|
UTSW |
9 |
54,530,021 (GRCm39) |
missense |
probably damaging |
0.98 |
R8210:Acsbg1
|
UTSW |
9 |
54,517,083 (GRCm39) |
missense |
probably damaging |
1.00 |
R8256:Acsbg1
|
UTSW |
9 |
54,525,345 (GRCm39) |
missense |
probably damaging |
1.00 |
R8322:Acsbg1
|
UTSW |
9 |
54,523,268 (GRCm39) |
missense |
probably benign |
0.15 |
R8377:Acsbg1
|
UTSW |
9 |
54,529,789 (GRCm39) |
missense |
probably damaging |
1.00 |
R8726:Acsbg1
|
UTSW |
9 |
54,525,462 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Acsbg1
|
UTSW |
9 |
54,529,250 (GRCm39) |
missense |
possibly damaging |
0.94 |
Z1177:Acsbg1
|
UTSW |
9 |
54,522,218 (GRCm39) |
missense |
probably damaging |
1.00 |
|