Incidental Mutation 'R4820:Alpk1'
ID |
370111 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Alpk1
|
Ensembl Gene |
ENSMUSG00000028028 |
Gene Name |
alpha-kinase 1 |
Synonyms |
8430410J10Rik |
MMRRC Submission |
042436-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R4820 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
3 |
Chromosomal Location |
127463959-127574176 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to A
at 127464708 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Aspartic acid to Valine
at position 1190
(D1190V)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000143223
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000029662]
[ENSMUST00000198955]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably benign
Transcript: ENSMUST00000029662
AA Change: D1190V
PolyPhen 2
Score 0.057 (Sensitivity: 0.94; Specificity: 0.84)
|
SMART Domains |
Protein: ENSMUSP00000029662 Gene: ENSMUSG00000028028 AA Change: D1190V
Domain | Start | End | E-Value | Type |
low complexity region
|
85 |
97 |
N/A |
INTRINSIC |
low complexity region
|
618 |
628 |
N/A |
INTRINSIC |
low complexity region
|
700 |
714 |
N/A |
INTRINSIC |
low complexity region
|
902 |
914 |
N/A |
INTRINSIC |
low complexity region
|
924 |
947 |
N/A |
INTRINSIC |
Alpha_kinase
|
1008 |
1215 |
1.03e-81 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000160586
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000198955
AA Change: D1190V
PolyPhen 2
Score 0.057 (Sensitivity: 0.94; Specificity: 0.84)
|
SMART Domains |
Protein: ENSMUSP00000143223 Gene: ENSMUSG00000028028 AA Change: D1190V
Domain | Start | End | E-Value | Type |
low complexity region
|
85 |
97 |
N/A |
INTRINSIC |
low complexity region
|
618 |
628 |
N/A |
INTRINSIC |
low complexity region
|
700 |
714 |
N/A |
INTRINSIC |
low complexity region
|
902 |
914 |
N/A |
INTRINSIC |
low complexity region
|
924 |
947 |
N/A |
INTRINSIC |
Alpha_kinase
|
1008 |
1215 |
1.03e-81 |
SMART |
|
Meta Mutation Damage Score |
0.0898 |
Coding Region Coverage |
- 1x: 99.0%
- 3x: 98.3%
- 10x: 96.5%
- 20x: 92.9%
|
Validation Efficiency |
96% (104/108) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes an alpha kinase. Mice which were homozygous for disrupted copies of this gene exhibited coordination defects (PMID: 21208416). Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 95 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930488N24Rik |
T |
C |
17: 14,326,481 (GRCm39) |
|
noncoding transcript |
Het |
5730455P16Rik |
A |
T |
11: 80,266,346 (GRCm39) |
S132T |
possibly damaging |
Het |
Aadacl3 |
T |
A |
4: 144,184,527 (GRCm39) |
H77L |
probably damaging |
Het |
Actr5 |
T |
A |
2: 158,467,426 (GRCm39) |
V122D |
probably damaging |
Het |
Adamts7 |
A |
G |
9: 90,071,739 (GRCm39) |
D678G |
possibly damaging |
Het |
Apbb1ip |
A |
T |
2: 22,765,265 (GRCm39) |
N649Y |
unknown |
Het |
Atp6v0a1 |
A |
G |
11: 100,933,776 (GRCm39) |
I522V |
probably benign |
Het |
Brd10 |
T |
C |
19: 29,695,809 (GRCm39) |
N1228S |
possibly damaging |
Het |
Cars1 |
T |
C |
7: 143,124,301 (GRCm39) |
D375G |
probably damaging |
Het |
Catspere1 |
A |
T |
1: 177,687,441 (GRCm39) |
|
noncoding transcript |
Het |
Ccdc87 |
A |
G |
19: 4,890,579 (GRCm39) |
D357G |
probably damaging |
Het |
Cd101 |
A |
T |
3: 100,929,471 (GRCm39) |
S8T |
probably benign |
Het |
Cfap65 |
C |
T |
1: 74,966,791 (GRCm39) |
A299T |
probably benign |
Het |
Cic |
T |
C |
7: 24,971,157 (GRCm39) |
V296A |
possibly damaging |
Het |
Col7a1 |
T |
A |
9: 108,797,675 (GRCm39) |
S1686T |
possibly damaging |
Het |
Ctbp2 |
A |
C |
7: 132,615,423 (GRCm39) |
L504R |
probably damaging |
Het |
Cttnbp2nl |
T |
C |
3: 104,918,640 (GRCm39) |
K67E |
probably benign |
Het |
Cyp2c50 |
C |
T |
19: 40,102,024 (GRCm39) |
P480S |
probably damaging |
Het |
Dcdc5 |
A |
C |
2: 106,166,420 (GRCm39) |
|
noncoding transcript |
Het |
Defb2 |
G |
T |
8: 22,333,317 (GRCm39) |
E31* |
probably null |
Het |
Dhrs1 |
T |
A |
14: 55,977,083 (GRCm39) |
N244I |
possibly damaging |
Het |
Dop1b |
A |
G |
16: 93,589,978 (GRCm39) |
I134V |
probably benign |
Het |
Eif1ad11 |
A |
T |
12: 87,994,158 (GRCm39) |
I129F |
unknown |
Het |
Etl4 |
A |
G |
2: 20,811,496 (GRCm39) |
D1193G |
possibly damaging |
Het |
Ezh1 |
A |
C |
11: 101,094,594 (GRCm39) |
S399R |
probably damaging |
Het |
Fam161a |
T |
C |
11: 22,970,076 (GRCm39) |
S26P |
probably damaging |
Het |
Fcgbp |
C |
A |
7: 27,813,383 (GRCm39) |
S2306Y |
probably damaging |
Het |
Fras1 |
T |
C |
5: 96,876,512 (GRCm39) |
I2415T |
probably benign |
Het |
Gas2l3 |
A |
G |
10: 89,252,907 (GRCm39) |
L246P |
probably damaging |
Het |
Gdf15 |
C |
T |
8: 71,082,246 (GRCm39) |
V287M |
probably damaging |
Het |
Gm7742 |
T |
C |
17: 21,420,235 (GRCm39) |
|
noncoding transcript |
Het |
Grin2d |
T |
C |
7: 45,507,363 (GRCm39) |
D446G |
probably damaging |
Het |
Hemk1 |
A |
G |
9: 107,205,385 (GRCm39) |
F107L |
probably benign |
Het |
Hmgcr |
C |
T |
13: 96,796,700 (GRCm39) |
G197S |
probably damaging |
Het |
Ift52 |
G |
A |
2: 162,873,108 (GRCm39) |
G207D |
probably benign |
Het |
Il17re |
A |
G |
6: 113,442,816 (GRCm39) |
T275A |
probably benign |
Het |
Iqcf3 |
T |
C |
9: 106,430,788 (GRCm39) |
|
probably benign |
Het |
Kcna1 |
A |
G |
6: 126,619,099 (GRCm39) |
I407T |
probably damaging |
Het |
Kcnrg |
T |
A |
14: 61,845,386 (GRCm39) |
M142K |
probably benign |
Het |
Lhx9 |
C |
A |
1: 138,766,105 (GRCm39) |
V237L |
probably benign |
Het |
Lipo3 |
A |
C |
19: 33,560,497 (GRCm39) |
I56S |
probably damaging |
Het |
Loxhd1 |
C |
G |
18: 77,472,663 (GRCm39) |
P1060R |
probably damaging |
Het |
Map2k4 |
A |
C |
11: 65,587,201 (GRCm39) |
|
probably benign |
Het |
Methig1 |
A |
G |
15: 100,251,416 (GRCm39) |
K109R |
possibly damaging |
Het |
Mmrn1 |
G |
A |
6: 60,950,027 (GRCm39) |
V326I |
probably benign |
Het |
Myo15a |
G |
A |
11: 60,367,741 (GRCm39) |
R167H |
probably damaging |
Het |
Ncoa7 |
G |
A |
10: 30,524,472 (GRCm39) |
T142M |
probably damaging |
Het |
Nfkb2 |
C |
A |
19: 46,296,493 (GRCm39) |
Q254K |
probably damaging |
Het |
Nherf1 |
A |
G |
11: 115,070,918 (GRCm39) |
E290G |
probably benign |
Het |
Nol6 |
G |
T |
4: 41,121,508 (GRCm39) |
P278Q |
probably damaging |
Het |
Nptxr |
T |
A |
15: 79,677,027 (GRCm39) |
D285V |
probably damaging |
Het |
Oosp3 |
T |
C |
19: 11,688,997 (GRCm39) |
W82R |
probably damaging |
Het |
Or6b3 |
A |
T |
1: 92,438,812 (GRCm39) |
*313K |
probably null |
Het |
Or6n1 |
A |
G |
1: 173,916,742 (GRCm39) |
I45M |
possibly damaging |
Het |
Pa2g4 |
G |
T |
10: 128,395,199 (GRCm39) |
T322K |
probably damaging |
Het |
Parp16 |
C |
A |
9: 65,145,175 (GRCm39) |
F291L |
probably damaging |
Het |
Pdzd9 |
A |
T |
7: 120,267,619 (GRCm39) |
D65E |
probably damaging |
Het |
Pgap3 |
A |
G |
11: 98,281,300 (GRCm39) |
W238R |
probably damaging |
Het |
Pgf |
G |
A |
12: 85,218,538 (GRCm39) |
H67Y |
probably benign |
Het |
Pik3cb |
T |
C |
9: 98,955,679 (GRCm39) |
T413A |
probably benign |
Het |
Plcxd2 |
A |
T |
16: 45,800,700 (GRCm39) |
C175S |
probably benign |
Het |
Pou2f1 |
A |
T |
1: 165,719,517 (GRCm39) |
|
probably benign |
Het |
Ppfia1 |
T |
G |
7: 144,052,106 (GRCm39) |
N846T |
probably benign |
Het |
Ppid |
T |
A |
3: 79,502,504 (GRCm39) |
|
probably null |
Het |
Prkcq |
G |
A |
2: 11,231,797 (GRCm39) |
|
probably null |
Het |
Ptgds |
T |
C |
2: 25,359,058 (GRCm39) |
K66E |
probably benign |
Het |
Ptpmt1 |
A |
G |
2: 90,748,283 (GRCm39) |
|
noncoding transcript |
Het |
Rab3il1 |
G |
A |
19: 10,004,034 (GRCm39) |
G51D |
probably benign |
Het |
Rdx |
T |
C |
9: 51,974,891 (GRCm39) |
V9A |
probably damaging |
Het |
Rpl7l1 |
T |
C |
17: 47,089,014 (GRCm39) |
N239S |
probably benign |
Het |
Rrbp1 |
C |
A |
2: 143,806,685 (GRCm39) |
A978S |
possibly damaging |
Het |
Rsf1 |
GCGGCGGCG |
GCGGCGGCGCCGGCGGCG |
7: 97,229,126 (GRCm39) |
|
probably benign |
Het |
Scn3a |
A |
T |
2: 65,291,622 (GRCm39) |
I1708N |
probably damaging |
Het |
Serinc1 |
A |
G |
10: 57,401,466 (GRCm39) |
I109T |
possibly damaging |
Het |
Shroom1 |
G |
A |
11: 53,355,966 (GRCm39) |
V339I |
probably benign |
Het |
Slc30a8 |
T |
A |
15: 52,169,880 (GRCm39) |
C36S |
probably benign |
Het |
Slco1b2 |
A |
G |
6: 141,631,158 (GRCm39) |
I597M |
probably benign |
Het |
Snx27 |
A |
G |
3: 94,427,518 (GRCm39) |
F228S |
probably damaging |
Het |
Spata31f1a |
T |
A |
4: 42,851,815 (GRCm39) |
I114F |
probably damaging |
Het |
Speer4e2 |
G |
T |
5: 15,026,225 (GRCm39) |
T144K |
probably benign |
Het |
Stim1 |
T |
A |
7: 102,064,571 (GRCm39) |
F214I |
probably damaging |
Het |
Svep1 |
T |
C |
4: 58,082,664 (GRCm39) |
T1987A |
probably benign |
Het |
Tamm41 |
A |
G |
6: 115,002,378 (GRCm39) |
I18T |
possibly damaging |
Het |
Tmem150b |
T |
A |
7: 4,726,871 (GRCm39) |
D79V |
probably damaging |
Het |
Tmem167 |
T |
A |
13: 90,252,548 (GRCm39) |
I68N |
probably benign |
Het |
Traf3 |
A |
G |
12: 111,227,204 (GRCm39) |
E339G |
possibly damaging |
Het |
Tspan12 |
G |
A |
6: 21,795,660 (GRCm39) |
P177S |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,783,562 (GRCm39) |
I810T |
probably benign |
Het |
Ulk1 |
T |
C |
5: 110,939,996 (GRCm39) |
T407A |
probably benign |
Het |
Uroc1 |
G |
A |
6: 90,334,600 (GRCm39) |
|
probably null |
Het |
Vmn2r-ps69 |
T |
C |
7: 84,959,584 (GRCm39) |
|
noncoding transcript |
Het |
Wdr59 |
T |
C |
8: 112,207,446 (GRCm39) |
N476S |
probably benign |
Het |
Zfp472 |
A |
G |
17: 33,196,416 (GRCm39) |
M164V |
probably benign |
Het |
Zfp608 |
T |
C |
18: 55,120,756 (GRCm39) |
N277S |
probably benign |
Het |
Zfp831 |
T |
C |
2: 174,547,097 (GRCm39) |
C1427R |
possibly damaging |
Het |
|
Other mutations in Alpk1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00096:Alpk1
|
APN |
3 |
127,474,692 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00722:Alpk1
|
APN |
3 |
127,473,862 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01066:Alpk1
|
APN |
3 |
127,473,874 (GRCm39) |
missense |
probably benign |
0.22 |
IGL01351:Alpk1
|
APN |
3 |
127,466,011 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01412:Alpk1
|
APN |
3 |
127,473,621 (GRCm39) |
missense |
possibly damaging |
0.60 |
IGL01469:Alpk1
|
APN |
3 |
127,471,401 (GRCm39) |
splice site |
probably null |
|
IGL01585:Alpk1
|
APN |
3 |
127,473,462 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02308:Alpk1
|
APN |
3 |
127,522,931 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02325:Alpk1
|
APN |
3 |
127,473,552 (GRCm39) |
missense |
probably benign |
0.43 |
IGL02458:Alpk1
|
APN |
3 |
127,474,968 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02553:Alpk1
|
APN |
3 |
127,466,970 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02717:Alpk1
|
APN |
3 |
127,474,749 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL02729:Alpk1
|
APN |
3 |
127,474,721 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL02832:Alpk1
|
APN |
3 |
127,473,592 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL02892:Alpk1
|
APN |
3 |
127,473,771 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL03178:Alpk1
|
APN |
3 |
127,473,870 (GRCm39) |
nonsense |
probably null |
|
R0427:Alpk1
|
UTSW |
3 |
127,464,720 (GRCm39) |
missense |
probably damaging |
1.00 |
R0981:Alpk1
|
UTSW |
3 |
127,473,051 (GRCm39) |
missense |
possibly damaging |
0.62 |
R1174:Alpk1
|
UTSW |
3 |
127,474,459 (GRCm39) |
missense |
probably damaging |
0.99 |
R1793:Alpk1
|
UTSW |
3 |
127,471,447 (GRCm39) |
missense |
probably damaging |
1.00 |
R1859:Alpk1
|
UTSW |
3 |
127,474,749 (GRCm39) |
missense |
possibly damaging |
0.76 |
R2173:Alpk1
|
UTSW |
3 |
127,477,239 (GRCm39) |
missense |
probably damaging |
1.00 |
R2235:Alpk1
|
UTSW |
3 |
127,474,569 (GRCm39) |
missense |
probably benign |
0.01 |
R2373:Alpk1
|
UTSW |
3 |
127,473,457 (GRCm39) |
missense |
probably benign |
0.00 |
R3803:Alpk1
|
UTSW |
3 |
127,473,486 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3927:Alpk1
|
UTSW |
3 |
127,471,365 (GRCm39) |
missense |
probably damaging |
1.00 |
R4356:Alpk1
|
UTSW |
3 |
127,523,022 (GRCm39) |
missense |
probably damaging |
0.98 |
R4357:Alpk1
|
UTSW |
3 |
127,523,022 (GRCm39) |
missense |
probably damaging |
0.98 |
R4358:Alpk1
|
UTSW |
3 |
127,523,022 (GRCm39) |
missense |
probably damaging |
0.98 |
R4379:Alpk1
|
UTSW |
3 |
127,523,022 (GRCm39) |
missense |
probably damaging |
0.98 |
R4381:Alpk1
|
UTSW |
3 |
127,523,022 (GRCm39) |
missense |
probably damaging |
0.98 |
R4470:Alpk1
|
UTSW |
3 |
127,473,175 (GRCm39) |
missense |
probably damaging |
1.00 |
R4471:Alpk1
|
UTSW |
3 |
127,473,175 (GRCm39) |
missense |
probably damaging |
1.00 |
R4473:Alpk1
|
UTSW |
3 |
127,473,667 (GRCm39) |
missense |
probably damaging |
0.97 |
R4474:Alpk1
|
UTSW |
3 |
127,473,667 (GRCm39) |
missense |
probably damaging |
0.97 |
R4476:Alpk1
|
UTSW |
3 |
127,473,667 (GRCm39) |
missense |
probably damaging |
0.97 |
R4512:Alpk1
|
UTSW |
3 |
127,478,120 (GRCm39) |
intron |
probably benign |
|
R4594:Alpk1
|
UTSW |
3 |
127,477,203 (GRCm39) |
missense |
probably damaging |
1.00 |
R4678:Alpk1
|
UTSW |
3 |
127,473,507 (GRCm39) |
missense |
probably damaging |
0.99 |
R4707:Alpk1
|
UTSW |
3 |
127,481,241 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4784:Alpk1
|
UTSW |
3 |
127,481,241 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4785:Alpk1
|
UTSW |
3 |
127,481,241 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4887:Alpk1
|
UTSW |
3 |
127,467,124 (GRCm39) |
missense |
probably damaging |
1.00 |
R5088:Alpk1
|
UTSW |
3 |
127,478,969 (GRCm39) |
splice site |
probably benign |
|
R5169:Alpk1
|
UTSW |
3 |
127,464,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R5280:Alpk1
|
UTSW |
3 |
127,474,813 (GRCm39) |
missense |
probably benign |
0.00 |
R5351:Alpk1
|
UTSW |
3 |
127,522,941 (GRCm39) |
missense |
probably damaging |
0.96 |
R5478:Alpk1
|
UTSW |
3 |
127,471,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R5627:Alpk1
|
UTSW |
3 |
127,474,296 (GRCm39) |
missense |
probably damaging |
0.99 |
R5781:Alpk1
|
UTSW |
3 |
127,473,684 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5842:Alpk1
|
UTSW |
3 |
127,474,618 (GRCm39) |
missense |
probably damaging |
1.00 |
R5847:Alpk1
|
UTSW |
3 |
127,473,723 (GRCm39) |
missense |
probably benign |
0.06 |
R5940:Alpk1
|
UTSW |
3 |
127,464,595 (GRCm39) |
missense |
probably benign |
|
R6187:Alpk1
|
UTSW |
3 |
127,466,991 (GRCm39) |
missense |
probably damaging |
1.00 |
R6306:Alpk1
|
UTSW |
3 |
127,479,965 (GRCm39) |
missense |
probably damaging |
1.00 |
R6414:Alpk1
|
UTSW |
3 |
127,473,858 (GRCm39) |
missense |
probably benign |
|
R6701:Alpk1
|
UTSW |
3 |
127,522,985 (GRCm39) |
missense |
probably damaging |
1.00 |
R6735:Alpk1
|
UTSW |
3 |
127,518,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R6850:Alpk1
|
UTSW |
3 |
127,523,012 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7173:Alpk1
|
UTSW |
3 |
127,478,024 (GRCm39) |
nonsense |
probably null |
|
R7258:Alpk1
|
UTSW |
3 |
127,518,115 (GRCm39) |
missense |
probably damaging |
1.00 |
R7412:Alpk1
|
UTSW |
3 |
127,489,382 (GRCm39) |
missense |
probably damaging |
1.00 |
R7412:Alpk1
|
UTSW |
3 |
127,466,143 (GRCm39) |
missense |
probably damaging |
1.00 |
R7498:Alpk1
|
UTSW |
3 |
127,473,427 (GRCm39) |
missense |
probably benign |
0.22 |
R7635:Alpk1
|
UTSW |
3 |
127,489,310 (GRCm39) |
missense |
probably benign |
0.01 |
R7660:Alpk1
|
UTSW |
3 |
127,474,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R7682:Alpk1
|
UTSW |
3 |
127,466,195 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7732:Alpk1
|
UTSW |
3 |
127,478,041 (GRCm39) |
missense |
|
|
R7827:Alpk1
|
UTSW |
3 |
127,473,700 (GRCm39) |
missense |
probably benign |
0.00 |
R8029:Alpk1
|
UTSW |
3 |
127,522,934 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8383:Alpk1
|
UTSW |
3 |
127,518,085 (GRCm39) |
missense |
probably benign |
0.41 |
R8478:Alpk1
|
UTSW |
3 |
127,522,961 (GRCm39) |
missense |
probably damaging |
1.00 |
R8765:Alpk1
|
UTSW |
3 |
127,466,118 (GRCm39) |
missense |
probably damaging |
1.00 |
R8816:Alpk1
|
UTSW |
3 |
127,478,024 (GRCm39) |
nonsense |
probably null |
|
R8907:Alpk1
|
UTSW |
3 |
127,474,642 (GRCm39) |
nonsense |
probably null |
|
R8972:Alpk1
|
UTSW |
3 |
127,473,232 (GRCm39) |
missense |
probably damaging |
1.00 |
R8974:Alpk1
|
UTSW |
3 |
127,473,580 (GRCm39) |
missense |
probably benign |
0.03 |
R9039:Alpk1
|
UTSW |
3 |
127,473,192 (GRCm39) |
missense |
probably damaging |
1.00 |
R9202:Alpk1
|
UTSW |
3 |
127,479,938 (GRCm39) |
missense |
|
|
R9394:Alpk1
|
UTSW |
3 |
127,466,187 (GRCm39) |
missense |
probably damaging |
1.00 |
R9421:Alpk1
|
UTSW |
3 |
127,467,069 (GRCm39) |
missense |
probably damaging |
1.00 |
R9436:Alpk1
|
UTSW |
3 |
127,478,924 (GRCm39) |
missense |
|
|
R9785:Alpk1
|
UTSW |
3 |
127,473,594 (GRCm39) |
missense |
probably benign |
0.22 |
Z1176:Alpk1
|
UTSW |
3 |
127,467,087 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Alpk1
|
UTSW |
3 |
127,478,956 (GRCm39) |
missense |
|
|
|
Predicted Primers |
PCR Primer
(F):5'- AGACAGATCTGATGCTAGGCTC -3'
(R):5'- GCCTTGGCAGAAACGTACTAAG -3'
Sequencing Primer
(F):5'- ACAGATCTGATGCTAGGCTCTTGAAG -3'
(R):5'- CCTTGGCAGAAACGTACTAAGTCATG -3'
|
Posted On |
2016-02-04 |