Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abraxas1 |
C |
T |
5: 100,965,827 (GRCm39) |
|
probably null |
Het |
Acsl3 |
A |
G |
1: 78,679,004 (GRCm39) |
D520G |
probably damaging |
Het |
Adgrl3 |
T |
C |
5: 81,796,560 (GRCm39) |
V623A |
probably benign |
Het |
Ak9 |
G |
T |
10: 41,223,218 (GRCm39) |
V454L |
probably damaging |
Het |
Arhgef12 |
T |
C |
9: 42,893,281 (GRCm39) |
Y974C |
probably damaging |
Het |
Armc8 |
C |
T |
9: 99,418,211 (GRCm39) |
|
probably benign |
Het |
Atp2a2 |
C |
T |
5: 122,595,696 (GRCm39) |
|
probably benign |
Het |
Atrn |
T |
C |
2: 130,812,147 (GRCm39) |
|
probably null |
Het |
Caps2 |
T |
A |
10: 112,039,943 (GRCm39) |
|
probably benign |
Het |
Cep76 |
A |
G |
18: 67,756,374 (GRCm39) |
S486P |
probably damaging |
Het |
Cep97 |
C |
T |
16: 55,735,265 (GRCm39) |
R583H |
probably benign |
Het |
Cog7 |
A |
G |
7: 121,555,363 (GRCm39) |
|
probably benign |
Het |
Commd5 |
T |
A |
15: 76,784,768 (GRCm39) |
V55E |
probably damaging |
Het |
Csmd3 |
A |
T |
15: 47,874,543 (GRCm39) |
D684E |
possibly damaging |
Het |
Ctxn2 |
T |
C |
2: 124,989,376 (GRCm39) |
M1T |
probably null |
Het |
Exph5 |
A |
G |
9: 53,288,775 (GRCm39) |
D1952G |
unknown |
Het |
Fmo2 |
A |
T |
1: 162,704,343 (GRCm39) |
L521Q |
possibly damaging |
Het |
Fryl |
T |
A |
5: 73,222,702 (GRCm39) |
T1960S |
probably damaging |
Het |
G6pd2 |
T |
C |
5: 61,967,017 (GRCm39) |
L264P |
probably damaging |
Het |
Gne |
A |
T |
4: 44,039,033 (GRCm39) |
V647E |
possibly damaging |
Het |
Grb14 |
G |
A |
2: 64,745,071 (GRCm39) |
Q96* |
probably null |
Het |
Gtf3c1 |
A |
G |
7: 125,298,134 (GRCm39) |
F146L |
probably damaging |
Het |
Gvin3 |
C |
A |
7: 106,202,093 (GRCm39) |
V384L |
possibly damaging |
Het |
Irak2 |
A |
G |
6: 113,615,525 (GRCm39) |
Y6C |
probably damaging |
Het |
Kel |
T |
A |
6: 41,679,965 (GRCm39) |
N75I |
probably damaging |
Het |
Lgr4 |
T |
A |
2: 109,842,132 (GRCm39) |
F706I |
possibly damaging |
Het |
Lox |
A |
T |
18: 52,661,955 (GRCm39) |
S149R |
probably benign |
Het |
Lrrc66 |
T |
G |
5: 73,768,287 (GRCm39) |
D218A |
probably benign |
Het |
Luc7l |
C |
T |
17: 26,485,296 (GRCm39) |
R99W |
probably damaging |
Het |
Megf10 |
T |
C |
18: 57,385,968 (GRCm39) |
V327A |
probably benign |
Het |
Mthfd1l |
G |
T |
10: 3,997,976 (GRCm39) |
|
probably null |
Het |
Myh11 |
C |
A |
16: 14,041,883 (GRCm39) |
Q720H |
probably damaging |
Het |
Myh8 |
G |
T |
11: 67,175,358 (GRCm39) |
|
probably null |
Het |
Or5b109 |
A |
T |
19: 13,212,424 (GRCm39) |
D270V |
possibly damaging |
Het |
Pdia3 |
G |
A |
2: 121,262,858 (GRCm39) |
G275S |
probably damaging |
Het |
Pgf |
C |
T |
12: 85,216,159 (GRCm39) |
R153K |
probably benign |
Het |
Pramel12 |
A |
T |
4: 143,144,170 (GRCm39) |
Q172L |
probably damaging |
Het |
Prdm2 |
A |
G |
4: 142,861,835 (GRCm39) |
V485A |
probably damaging |
Het |
Rag1 |
T |
C |
2: 101,473,028 (GRCm39) |
T705A |
probably damaging |
Het |
Rflna |
A |
C |
5: 125,080,774 (GRCm39) |
D48A |
possibly damaging |
Het |
Rnf148 |
A |
T |
6: 23,654,456 (GRCm39) |
I180N |
probably damaging |
Het |
Rtn4 |
T |
A |
11: 29,656,475 (GRCm39) |
S94T |
probably damaging |
Het |
Scn11a |
G |
A |
9: 119,640,226 (GRCm39) |
T223I |
probably benign |
Het |
Scube2 |
T |
A |
7: 109,436,327 (GRCm39) |
|
probably benign |
Het |
Septin14 |
T |
C |
5: 129,774,972 (GRCm39) |
I68V |
probably benign |
Het |
Sil1 |
A |
T |
18: 35,399,910 (GRCm39) |
L365Q |
possibly damaging |
Het |
Sirt1 |
A |
G |
10: 63,157,515 (GRCm39) |
|
probably benign |
Het |
Slc9a1 |
T |
C |
4: 133,147,810 (GRCm39) |
|
probably benign |
Het |
Smpdl3a |
A |
G |
10: 57,687,336 (GRCm39) |
T355A |
probably damaging |
Het |
Syne2 |
T |
C |
12: 76,141,110 (GRCm39) |
I6074T |
probably damaging |
Het |
Thbs2 |
T |
A |
17: 14,900,587 (GRCm39) |
H540L |
probably benign |
Het |
Tsc22d4 |
T |
C |
5: 137,766,283 (GRCm39) |
S450P |
probably benign |
Het |
Tshr |
C |
A |
12: 91,505,000 (GRCm39) |
S54* |
probably null |
Het |
Ubxn4 |
G |
A |
1: 128,190,641 (GRCm39) |
E256K |
probably benign |
Het |
Uncx |
G |
T |
5: 139,529,942 (GRCm39) |
C65F |
probably damaging |
Het |
Vmn1r87 |
A |
T |
7: 12,865,756 (GRCm39) |
M177K |
probably damaging |
Het |
Vmn2r56 |
A |
T |
7: 12,444,235 (GRCm39) |
C466S |
probably benign |
Het |
Wnk1 |
G |
A |
6: 119,925,466 (GRCm39) |
P1831S |
probably damaging |
Het |
Zfp820 |
T |
C |
17: 22,037,901 (GRCm39) |
S476G |
probably benign |
Het |
|
Other mutations in Alpk2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00468:Alpk2
|
APN |
18 |
65,438,894 (GRCm39) |
missense |
probably benign |
0.27 |
IGL00478:Alpk2
|
APN |
18 |
65,440,297 (GRCm39) |
nonsense |
probably null |
|
IGL00898:Alpk2
|
APN |
18 |
65,483,644 (GRCm39) |
missense |
probably benign |
0.29 |
IGL00978:Alpk2
|
APN |
18 |
65,424,605 (GRCm39) |
splice site |
probably benign |
|
IGL01093:Alpk2
|
APN |
18 |
65,482,400 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01094:Alpk2
|
APN |
18 |
65,439,673 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01109:Alpk2
|
APN |
18 |
65,440,211 (GRCm39) |
missense |
probably benign |
0.09 |
IGL01370:Alpk2
|
APN |
18 |
65,483,662 (GRCm39) |
missense |
possibly damaging |
0.56 |
IGL01393:Alpk2
|
APN |
18 |
65,440,779 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL01629:Alpk2
|
APN |
18 |
65,433,113 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01872:Alpk2
|
APN |
18 |
65,437,824 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01983:Alpk2
|
APN |
18 |
65,483,753 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02294:Alpk2
|
APN |
18 |
65,439,146 (GRCm39) |
missense |
possibly damaging |
0.45 |
IGL02333:Alpk2
|
APN |
18 |
65,482,551 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02493:Alpk2
|
APN |
18 |
65,483,402 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02551:Alpk2
|
APN |
18 |
65,505,822 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02864:Alpk2
|
APN |
18 |
65,440,670 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02901:Alpk2
|
APN |
18 |
65,439,482 (GRCm39) |
missense |
probably benign |
|
IGL02954:Alpk2
|
APN |
18 |
65,439,207 (GRCm39) |
missense |
probably benign |
|
IGL03257:Alpk2
|
APN |
18 |
65,482,945 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03389:Alpk2
|
APN |
18 |
65,437,937 (GRCm39) |
missense |
possibly damaging |
0.92 |
3-1:Alpk2
|
UTSW |
18 |
65,437,959 (GRCm39) |
missense |
probably damaging |
0.99 |
PIT4131001:Alpk2
|
UTSW |
18 |
65,439,450 (GRCm39) |
missense |
possibly damaging |
0.84 |
R0098:Alpk2
|
UTSW |
18 |
65,482,982 (GRCm39) |
missense |
probably damaging |
1.00 |
R0098:Alpk2
|
UTSW |
18 |
65,482,982 (GRCm39) |
missense |
probably damaging |
1.00 |
R0414:Alpk2
|
UTSW |
18 |
65,439,230 (GRCm39) |
missense |
probably benign |
0.04 |
R0546:Alpk2
|
UTSW |
18 |
65,439,788 (GRCm39) |
missense |
probably benign |
0.05 |
R0628:Alpk2
|
UTSW |
18 |
65,440,367 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0731:Alpk2
|
UTSW |
18 |
65,438,461 (GRCm39) |
missense |
probably damaging |
0.98 |
R0919:Alpk2
|
UTSW |
18 |
65,440,544 (GRCm39) |
missense |
probably benign |
|
R1069:Alpk2
|
UTSW |
18 |
65,438,085 (GRCm39) |
missense |
probably benign |
0.25 |
R1186:Alpk2
|
UTSW |
18 |
65,427,412 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1508:Alpk2
|
UTSW |
18 |
65,482,376 (GRCm39) |
missense |
probably damaging |
1.00 |
R1535:Alpk2
|
UTSW |
18 |
65,483,275 (GRCm39) |
missense |
probably benign |
|
R1558:Alpk2
|
UTSW |
18 |
65,483,301 (GRCm39) |
missense |
probably benign |
|
R1600:Alpk2
|
UTSW |
18 |
65,511,108 (GRCm39) |
missense |
probably damaging |
0.96 |
R1664:Alpk2
|
UTSW |
18 |
65,482,944 (GRCm39) |
missense |
probably damaging |
0.96 |
R1672:Alpk2
|
UTSW |
18 |
65,414,030 (GRCm39) |
missense |
probably damaging |
1.00 |
R1829:Alpk2
|
UTSW |
18 |
65,427,165 (GRCm39) |
missense |
possibly damaging |
0.75 |
R2110:Alpk2
|
UTSW |
18 |
65,440,151 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2111:Alpk2
|
UTSW |
18 |
65,482,845 (GRCm39) |
missense |
probably benign |
|
R2113:Alpk2
|
UTSW |
18 |
65,438,754 (GRCm39) |
missense |
probably benign |
0.31 |
R2126:Alpk2
|
UTSW |
18 |
65,483,439 (GRCm39) |
nonsense |
probably null |
|
R2198:Alpk2
|
UTSW |
18 |
65,483,255 (GRCm39) |
missense |
probably benign |
0.42 |
R2227:Alpk2
|
UTSW |
18 |
65,511,147 (GRCm39) |
missense |
probably damaging |
1.00 |
R2245:Alpk2
|
UTSW |
18 |
65,438,234 (GRCm39) |
missense |
probably benign |
0.02 |
R2282:Alpk2
|
UTSW |
18 |
65,440,697 (GRCm39) |
missense |
probably benign |
|
R2421:Alpk2
|
UTSW |
18 |
65,439,687 (GRCm39) |
missense |
probably benign |
0.00 |
R2512:Alpk2
|
UTSW |
18 |
65,483,591 (GRCm39) |
missense |
probably damaging |
0.96 |
R3105:Alpk2
|
UTSW |
18 |
65,483,281 (GRCm39) |
missense |
possibly damaging |
0.57 |
R3700:Alpk2
|
UTSW |
18 |
65,438,222 (GRCm39) |
missense |
probably damaging |
0.99 |
R4205:Alpk2
|
UTSW |
18 |
65,438,282 (GRCm39) |
missense |
possibly damaging |
0.76 |
R4239:Alpk2
|
UTSW |
18 |
65,433,212 (GRCm39) |
missense |
probably damaging |
1.00 |
R4353:Alpk2
|
UTSW |
18 |
65,424,523 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4572:Alpk2
|
UTSW |
18 |
65,414,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R4584:Alpk2
|
UTSW |
18 |
65,440,035 (GRCm39) |
missense |
probably damaging |
0.99 |
R4591:Alpk2
|
UTSW |
18 |
65,438,894 (GRCm39) |
missense |
probably benign |
0.27 |
R4595:Alpk2
|
UTSW |
18 |
65,422,819 (GRCm39) |
missense |
probably damaging |
1.00 |
R4648:Alpk2
|
UTSW |
18 |
65,482,953 (GRCm39) |
missense |
probably damaging |
0.99 |
R4815:Alpk2
|
UTSW |
18 |
65,483,026 (GRCm39) |
missense |
probably damaging |
1.00 |
R4828:Alpk2
|
UTSW |
18 |
65,482,184 (GRCm39) |
missense |
probably benign |
|
R4910:Alpk2
|
UTSW |
18 |
65,399,357 (GRCm39) |
nonsense |
probably null |
|
R5042:Alpk2
|
UTSW |
18 |
65,483,579 (GRCm39) |
nonsense |
probably null |
|
R5295:Alpk2
|
UTSW |
18 |
65,438,109 (GRCm39) |
missense |
probably damaging |
0.98 |
R5375:Alpk2
|
UTSW |
18 |
65,505,809 (GRCm39) |
missense |
probably damaging |
1.00 |
R5475:Alpk2
|
UTSW |
18 |
65,440,083 (GRCm39) |
missense |
probably benign |
0.16 |
R5480:Alpk2
|
UTSW |
18 |
65,482,979 (GRCm39) |
missense |
probably damaging |
1.00 |
R5486:Alpk2
|
UTSW |
18 |
65,427,425 (GRCm39) |
splice site |
probably null |
|
R5503:Alpk2
|
UTSW |
18 |
65,439,312 (GRCm39) |
missense |
probably benign |
0.00 |
R5595:Alpk2
|
UTSW |
18 |
65,399,319 (GRCm39) |
missense |
probably damaging |
1.00 |
R5648:Alpk2
|
UTSW |
18 |
65,482,988 (GRCm39) |
missense |
probably damaging |
0.96 |
R5714:Alpk2
|
UTSW |
18 |
65,438,532 (GRCm39) |
missense |
possibly damaging |
0.55 |
R5862:Alpk2
|
UTSW |
18 |
65,440,360 (GRCm39) |
missense |
probably damaging |
1.00 |
R5894:Alpk2
|
UTSW |
18 |
65,414,143 (GRCm39) |
missense |
probably damaging |
0.99 |
R5898:Alpk2
|
UTSW |
18 |
65,440,694 (GRCm39) |
missense |
probably damaging |
0.99 |
R5936:Alpk2
|
UTSW |
18 |
65,483,591 (GRCm39) |
missense |
probably damaging |
0.96 |
R6142:Alpk2
|
UTSW |
18 |
65,438,456 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6291:Alpk2
|
UTSW |
18 |
65,438,972 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6339:Alpk2
|
UTSW |
18 |
65,482,877 (GRCm39) |
missense |
probably benign |
0.00 |
R6407:Alpk2
|
UTSW |
18 |
65,422,809 (GRCm39) |
missense |
probably benign |
0.22 |
R6487:Alpk2
|
UTSW |
18 |
65,399,254 (GRCm39) |
missense |
possibly damaging |
0.62 |
R6667:Alpk2
|
UTSW |
18 |
65,440,811 (GRCm39) |
missense |
probably damaging |
1.00 |
R6786:Alpk2
|
UTSW |
18 |
65,439,705 (GRCm39) |
missense |
probably benign |
|
R6833:Alpk2
|
UTSW |
18 |
65,439,480 (GRCm39) |
missense |
probably benign |
0.08 |
R6984:Alpk2
|
UTSW |
18 |
65,438,749 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6999:Alpk2
|
UTSW |
18 |
65,437,584 (GRCm39) |
missense |
probably damaging |
0.99 |
R7157:Alpk2
|
UTSW |
18 |
65,399,348 (GRCm39) |
nonsense |
probably null |
|
R7167:Alpk2
|
UTSW |
18 |
65,440,049 (GRCm39) |
missense |
probably benign |
0.40 |
R7225:Alpk2
|
UTSW |
18 |
65,438,270 (GRCm39) |
missense |
probably benign |
0.00 |
R7409:Alpk2
|
UTSW |
18 |
65,440,023 (GRCm39) |
missense |
probably benign |
0.01 |
R7533:Alpk2
|
UTSW |
18 |
65,437,674 (GRCm39) |
missense |
probably damaging |
1.00 |
R7576:Alpk2
|
UTSW |
18 |
65,439,887 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7589:Alpk2
|
UTSW |
18 |
65,433,144 (GRCm39) |
missense |
probably damaging |
1.00 |
R7598:Alpk2
|
UTSW |
18 |
65,437,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R7664:Alpk2
|
UTSW |
18 |
65,440,073 (GRCm39) |
missense |
probably benign |
0.03 |
R7711:Alpk2
|
UTSW |
18 |
65,439,555 (GRCm39) |
missense |
probably benign |
|
R7722:Alpk2
|
UTSW |
18 |
65,483,228 (GRCm39) |
missense |
probably damaging |
1.00 |
R7783:Alpk2
|
UTSW |
18 |
65,439,325 (GRCm39) |
nonsense |
probably null |
|
R7806:Alpk2
|
UTSW |
18 |
65,482,487 (GRCm39) |
missense |
probably benign |
|
R7953:Alpk2
|
UTSW |
18 |
65,482,901 (GRCm39) |
missense |
probably damaging |
1.00 |
R8024:Alpk2
|
UTSW |
18 |
65,438,106 (GRCm39) |
missense |
probably benign |
0.01 |
R8043:Alpk2
|
UTSW |
18 |
65,482,901 (GRCm39) |
missense |
probably damaging |
1.00 |
R8063:Alpk2
|
UTSW |
18 |
65,483,417 (GRCm39) |
missense |
probably benign |
0.15 |
R8171:Alpk2
|
UTSW |
18 |
65,439,054 (GRCm39) |
missense |
probably benign |
0.00 |
R8280:Alpk2
|
UTSW |
18 |
65,440,274 (GRCm39) |
missense |
probably benign |
|
R8383:Alpk2
|
UTSW |
18 |
65,438,469 (GRCm39) |
missense |
probably benign |
0.03 |
R8414:Alpk2
|
UTSW |
18 |
65,440,542 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8791:Alpk2
|
UTSW |
18 |
65,438,597 (GRCm39) |
missense |
probably benign |
0.00 |
R8872:Alpk2
|
UTSW |
18 |
65,413,977 (GRCm39) |
missense |
probably damaging |
1.00 |
R9352:Alpk2
|
UTSW |
18 |
65,439,783 (GRCm39) |
missense |
probably benign |
0.01 |
R9449:Alpk2
|
UTSW |
18 |
65,424,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R9525:Alpk2
|
UTSW |
18 |
65,399,288 (GRCm39) |
missense |
probably damaging |
1.00 |
R9564:Alpk2
|
UTSW |
18 |
65,439,014 (GRCm39) |
missense |
probably damaging |
1.00 |
R9710:Alpk2
|
UTSW |
18 |
65,482,646 (GRCm39) |
missense |
probably damaging |
1.00 |
X0023:Alpk2
|
UTSW |
18 |
65,424,471 (GRCm39) |
missense |
probably damaging |
1.00 |
X0027:Alpk2
|
UTSW |
18 |
65,440,542 (GRCm39) |
missense |
possibly damaging |
0.89 |
X0063:Alpk2
|
UTSW |
18 |
65,440,434 (GRCm39) |
missense |
probably benign |
|
X0064:Alpk2
|
UTSW |
18 |
65,482,755 (GRCm39) |
missense |
probably benign |
0.09 |
Z1176:Alpk2
|
UTSW |
18 |
65,438,682 (GRCm39) |
missense |
probably damaging |
0.98 |
|