Incidental Mutation 'R2126:Alpk2'
ID |
229955 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Alpk2
|
Ensembl Gene |
ENSMUSG00000032845 |
Gene Name |
alpha-kinase 2 |
Synonyms |
Hak |
MMRRC Submission |
040129-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R2126 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
18 |
Chromosomal Location |
65398600-65526959 bp(-) (GRCm39) |
Type of Mutation |
nonsense |
DNA Base Change (assembly) |
G to A
at 65483439 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Glutamine to Stop codon
at position 190
(Q190*)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000048752
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000035548]
[ENSMUST00000141250]
|
AlphaFold |
Q91ZB0 |
Predicted Effect |
probably null
Transcript: ENSMUST00000035548
AA Change: Q190*
|
SMART Domains |
Protein: ENSMUSP00000048752 Gene: ENSMUSG00000032845 AA Change: Q190*
Domain | Start | End | E-Value | Type |
IGc2
|
24 |
94 |
9.34e-4 |
SMART |
low complexity region
|
196 |
209 |
N/A |
INTRINSIC |
low complexity region
|
722 |
734 |
N/A |
INTRINSIC |
low complexity region
|
1025 |
1037 |
N/A |
INTRINSIC |
low complexity region
|
1337 |
1353 |
N/A |
INTRINSIC |
IG
|
1766 |
1849 |
2.27e-2 |
SMART |
Alpha_kinase
|
1879 |
2098 |
3.72e-79 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000141250
|
SMART Domains |
Protein: ENSMUSP00000114658 Gene: ENSMUSG00000032845
Domain | Start | End | E-Value | Type |
low complexity region
|
255 |
267 |
N/A |
INTRINSIC |
low complexity region
|
558 |
570 |
N/A |
INTRINSIC |
low complexity region
|
870 |
886 |
N/A |
INTRINSIC |
IG
|
1299 |
1382 |
2.27e-2 |
SMART |
Alpha_kinase
|
1412 |
1603 |
2.45e-56 |
SMART |
|
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.2%
- 20x: 94.8%
|
Validation Efficiency |
|
Allele List at MGI |
All alleles(1) : Targeted, knock-out(1) |
Other mutations in this stock |
Total: 116 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadac |
A |
G |
3: 59,947,066 (GRCm39) |
T255A |
possibly damaging |
Het |
Acat3 |
C |
T |
17: 13,146,294 (GRCm39) |
A230T |
probably benign |
Het |
Acsl1 |
C |
A |
8: 46,986,663 (GRCm39) |
P650Q |
probably benign |
Het |
Adgrl3 |
T |
A |
5: 81,660,383 (GRCm39) |
I316N |
probably damaging |
Het |
Agrp |
G |
T |
8: 106,293,467 (GRCm39) |
T106K |
probably damaging |
Het |
AI429214 |
T |
A |
8: 37,461,362 (GRCm39) |
V170E |
probably benign |
Het |
Akap13 |
G |
A |
7: 75,375,052 (GRCm39) |
G1895S |
possibly damaging |
Het |
Aox3 |
C |
A |
1: 58,197,375 (GRCm39) |
Q574K |
probably benign |
Het |
Apeh |
A |
G |
9: 107,962,866 (GRCm39) |
Y702H |
probably damaging |
Het |
Aqp11 |
A |
G |
7: 97,386,692 (GRCm39) |
I151T |
probably benign |
Het |
Arhgap28 |
A |
G |
17: 68,176,010 (GRCm39) |
V363A |
possibly damaging |
Het |
Arhgef18 |
A |
G |
8: 3,501,939 (GRCm39) |
N699S |
probably damaging |
Het |
Asnsd1 |
A |
G |
1: 53,386,476 (GRCm39) |
S384P |
probably benign |
Het |
Atl1 |
G |
T |
12: 69,978,431 (GRCm39) |
|
probably null |
Het |
Atp13a2 |
A |
T |
4: 140,722,702 (GRCm39) |
D203V |
possibly damaging |
Het |
Axdnd1 |
A |
T |
1: 156,160,784 (GRCm39) |
N164K |
probably benign |
Het |
Bnipl |
T |
A |
3: 95,152,994 (GRCm39) |
I162F |
probably damaging |
Het |
Cacna1d |
A |
T |
14: 29,845,120 (GRCm39) |
L655I |
probably damaging |
Het |
Canx |
T |
C |
11: 50,195,185 (GRCm39) |
I294M |
probably damaging |
Het |
Casz1 |
T |
C |
4: 149,030,521 (GRCm39) |
F1180S |
probably damaging |
Het |
Cav3 |
T |
C |
6: 112,449,344 (GRCm39) |
Y121H |
probably benign |
Het |
Cd4 |
A |
C |
6: 124,847,499 (GRCm39) |
S222A |
probably benign |
Het |
Cds1 |
T |
C |
5: 101,960,416 (GRCm39) |
I289T |
probably benign |
Het |
Cep112 |
T |
C |
11: 108,399,084 (GRCm39) |
F328L |
probably damaging |
Het |
Ces4a |
G |
A |
8: 105,864,729 (GRCm39) |
G69S |
probably damaging |
Het |
Cfap44 |
A |
T |
16: 44,230,838 (GRCm39) |
D273V |
probably benign |
Het |
Cfap91 |
T |
C |
16: 38,162,124 (GRCm39) |
T6A |
probably benign |
Het |
Clec7a |
C |
T |
6: 129,447,918 (GRCm39) |
G49D |
probably benign |
Het |
Col22a1 |
G |
A |
15: 71,729,102 (GRCm39) |
Q599* |
probably null |
Het |
Col6a5 |
T |
A |
9: 105,822,799 (GRCm39) |
H186L |
unknown |
Het |
Dclk2 |
C |
T |
3: 86,712,946 (GRCm39) |
R503Q |
possibly damaging |
Het |
Dnah12 |
A |
T |
14: 26,445,613 (GRCm39) |
R725* |
probably null |
Het |
Dnajc10 |
G |
A |
2: 80,181,078 (GRCm39) |
|
probably null |
Het |
Edem3 |
A |
T |
1: 151,670,482 (GRCm39) |
H337L |
possibly damaging |
Het |
Eif2ak4 |
A |
T |
2: 118,252,604 (GRCm39) |
H392L |
probably benign |
Het |
Ercc6l2 |
G |
A |
13: 63,996,585 (GRCm39) |
V365I |
probably damaging |
Het |
Fan1 |
T |
C |
7: 63,996,636 (GRCm39) |
E978G |
probably damaging |
Het |
Fcrl6 |
C |
T |
1: 172,426,815 (GRCm39) |
V44M |
probably benign |
Het |
Gaa |
G |
A |
11: 119,161,108 (GRCm39) |
W50* |
probably null |
Het |
Gm10032 |
T |
C |
14: 67,030,227 (GRCm39) |
|
noncoding transcript |
Het |
Gm10985 |
CTCTAT |
CT |
3: 53,752,670 (GRCm39) |
|
probably null |
Het |
Gprc5b |
G |
T |
7: 118,583,398 (GRCm39) |
P157Q |
probably damaging |
Het |
Gsdmc3 |
G |
A |
15: 63,730,383 (GRCm39) |
Q394* |
probably null |
Het |
Gucd1 |
A |
G |
10: 75,347,922 (GRCm39) |
S38P |
probably damaging |
Het |
Higd1a |
A |
T |
9: 121,679,313 (GRCm39) |
I58N |
probably damaging |
Het |
Hmx3 |
G |
C |
7: 131,146,278 (GRCm39) |
V329L |
possibly damaging |
Het |
Hnrnpul2 |
A |
T |
19: 8,801,802 (GRCm39) |
R337* |
probably null |
Het |
Idua |
T |
A |
5: 108,829,304 (GRCm39) |
H368Q |
possibly damaging |
Het |
Ifih1 |
A |
G |
2: 62,453,811 (GRCm39) |
V218A |
probably benign |
Het |
Ip6k1 |
G |
A |
9: 107,918,195 (GRCm39) |
E77K |
possibly damaging |
Het |
Kif1b |
G |
A |
4: 149,272,097 (GRCm39) |
S1568L |
possibly damaging |
Het |
Klhl30 |
T |
A |
1: 91,286,499 (GRCm39) |
|
probably null |
Het |
Lasp1 |
T |
A |
11: 97,726,960 (GRCm39) |
D227E |
probably benign |
Het |
Lhx6 |
A |
G |
2: 35,981,336 (GRCm39) |
I85T |
possibly damaging |
Het |
Limch1 |
A |
G |
5: 67,187,103 (GRCm39) |
D840G |
probably damaging |
Het |
Loxl4 |
C |
G |
19: 42,592,402 (GRCm39) |
E385D |
probably damaging |
Het |
Lrrtm4 |
A |
T |
6: 79,998,722 (GRCm39) |
I44F |
probably damaging |
Het |
Ltbp2 |
T |
C |
12: 84,832,483 (GRCm39) |
|
probably null |
Het |
Lyg1 |
T |
C |
1: 37,989,755 (GRCm39) |
Y44C |
probably damaging |
Het |
Map1a |
A |
G |
2: 121,129,122 (GRCm39) |
I129V |
probably damaging |
Het |
Med27 |
C |
T |
2: 29,414,442 (GRCm39) |
Q150* |
probably null |
Het |
Ms4a5 |
A |
T |
19: 11,256,732 (GRCm39) |
I55N |
probably damaging |
Het |
Muc5ac |
T |
C |
7: 141,364,479 (GRCm39) |
S2597P |
possibly damaging |
Het |
Mxd1 |
A |
C |
6: 86,628,422 (GRCm39) |
|
probably null |
Het |
Myo3a |
A |
G |
2: 22,468,186 (GRCm39) |
D480G |
probably benign |
Het |
Neb |
T |
C |
2: 52,200,650 (GRCm39) |
Y343C |
probably damaging |
Het |
Niban1 |
A |
C |
1: 151,571,886 (GRCm39) |
E277A |
probably damaging |
Het |
Niban1 |
A |
G |
1: 151,584,884 (GRCm39) |
I494V |
possibly damaging |
Het |
Nrn1 |
A |
C |
13: 36,914,180 (GRCm39) |
V34G |
probably damaging |
Het |
Or4k52 |
A |
G |
2: 111,610,841 (GRCm39) |
M59V |
probably damaging |
Het |
Or4n5 |
A |
G |
14: 50,132,524 (GRCm39) |
I245T |
probably benign |
Het |
Or52b1 |
C |
T |
7: 104,978,459 (GRCm39) |
W313* |
probably null |
Het |
Or56a3 |
A |
G |
7: 104,735,822 (GRCm39) |
T300A |
probably damaging |
Het |
Or8b39 |
G |
T |
9: 37,996,572 (GRCm39) |
V147L |
probably benign |
Het |
Or8h9 |
T |
C |
2: 86,789,442 (GRCm39) |
Y120C |
possibly damaging |
Het |
Or8k40 |
A |
T |
2: 86,584,796 (GRCm39) |
N95K |
probably benign |
Het |
Pdia4 |
A |
T |
6: 47,773,771 (GRCm39) |
V526E |
probably damaging |
Het |
Pdia6 |
T |
C |
12: 17,328,546 (GRCm39) |
V167A |
probably damaging |
Het |
Pgk2 |
A |
G |
17: 40,518,400 (GRCm39) |
F343L |
probably damaging |
Het |
Piwil1 |
T |
C |
5: 128,831,160 (GRCm39) |
V827A |
probably damaging |
Het |
Plag1 |
A |
T |
4: 3,904,169 (GRCm39) |
Y341N |
possibly damaging |
Het |
Plch2 |
T |
C |
4: 155,083,456 (GRCm39) |
E393G |
probably damaging |
Het |
Ptprg |
T |
A |
14: 12,154,355 (GRCm38) |
M692K |
probably benign |
Het |
Rassf8 |
G |
A |
6: 145,760,908 (GRCm39) |
R78H |
probably benign |
Het |
Rif1 |
GCCACCA |
GCCA |
2: 52,000,336 (GRCm39) |
|
probably benign |
Het |
Rnf213 |
A |
G |
11: 119,341,027 (GRCm39) |
Q3556R |
probably damaging |
Het |
Rpa2 |
T |
C |
4: 132,496,099 (GRCm39) |
|
probably null |
Het |
Rpe |
T |
G |
1: 66,755,139 (GRCm39) |
F174V |
possibly damaging |
Het |
Sbf2 |
T |
C |
7: 110,159,502 (GRCm39) |
D36G |
probably damaging |
Het |
Scn2a |
T |
A |
2: 65,582,423 (GRCm39) |
Y1590* |
probably null |
Het |
Slc24a4 |
T |
C |
12: 102,189,018 (GRCm39) |
V151A |
probably damaging |
Het |
Slc30a8 |
A |
T |
15: 52,159,330 (GRCm39) |
M17L |
probably benign |
Het |
Slit3 |
T |
C |
11: 35,579,506 (GRCm39) |
Y1228H |
probably damaging |
Het |
Smad4 |
G |
A |
18: 73,795,815 (GRCm39) |
T193M |
probably benign |
Het |
Smtn |
T |
A |
11: 3,480,045 (GRCm39) |
H392L |
probably benign |
Het |
St8sia3 |
A |
G |
18: 64,402,745 (GRCm39) |
D128G |
probably damaging |
Het |
Sucla2 |
A |
T |
14: 73,830,108 (GRCm39) |
M382L |
possibly damaging |
Het |
Tbx5 |
A |
G |
5: 119,974,988 (GRCm39) |
T4A |
probably benign |
Het |
Tdrd5 |
T |
C |
1: 156,104,143 (GRCm39) |
R528G |
probably damaging |
Het |
Tex44 |
T |
C |
1: 86,354,811 (GRCm39) |
L240P |
probably benign |
Het |
Tns4 |
A |
T |
11: 98,970,904 (GRCm39) |
|
probably null |
Het |
Trappc10 |
A |
T |
10: 78,039,758 (GRCm39) |
V731E |
possibly damaging |
Het |
Ttf1 |
A |
G |
2: 28,961,357 (GRCm39) |
K582E |
probably damaging |
Het |
Ttf2 |
C |
A |
3: 100,855,509 (GRCm39) |
Q895H |
possibly damaging |
Het |
Ttll6 |
A |
G |
11: 96,038,358 (GRCm39) |
E402G |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,720,436 (GRCm39) |
|
probably null |
Het |
Ugt8a |
T |
C |
3: 125,669,195 (GRCm39) |
D303G |
probably damaging |
Het |
Ulk1 |
G |
T |
5: 110,940,302 (GRCm39) |
A373D |
probably benign |
Het |
Vmn2r13 |
A |
G |
5: 109,306,058 (GRCm39) |
S507P |
probably benign |
Het |
Vmn2r19 |
T |
A |
6: 123,293,033 (GRCm39) |
D358E |
possibly damaging |
Het |
Vmn2r88 |
T |
C |
14: 51,651,264 (GRCm39) |
S201P |
probably benign |
Het |
Zfp36l2 |
A |
G |
17: 84,494,403 (GRCm39) |
F78S |
probably damaging |
Het |
Zfp454 |
A |
C |
11: 50,764,822 (GRCm39) |
S203R |
probably benign |
Het |
Zfp616 |
C |
A |
11: 73,976,229 (GRCm39) |
Q833K |
probably benign |
Het |
Znhit2 |
A |
G |
19: 6,112,091 (GRCm39) |
T279A |
probably benign |
Het |
Zswim3 |
T |
A |
2: 164,661,913 (GRCm39) |
I131N |
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 |
R0658:Alpk2
|
UTSW |
18 |
65,482,558 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
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 |
|
Predicted Primers |
PCR Primer
(F):5'- TGATGACTAGGGCTGACACTC -3'
(R):5'- GATCTGCTGTTCAGCATCCC -3'
Sequencing Primer
(F):5'- GACTAGGGCTGACACTCTCATTAG -3'
(R):5'- AGGTCTCTCCTGATCCTGGAG -3'
|
Posted On |
2014-09-17 |