Incidental Mutation 'R7412:Alpk1'
| ID |
575130 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Alpk1
|
| Ensembl Gene |
ENSMUSG00000028028 |
| Gene Name |
alpha-kinase 1 |
| Synonyms |
8430410J10Rik |
| MMRRC Submission |
045493-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R7412 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
3 |
| Chromosomal Location |
127463959-127574176 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 127466143 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Leucine to Glutamine
at position 1121
(L1121Q)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000029662
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000029662]
[ENSMUST00000198955]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000029662
AA Change: L1121Q
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000029662
Gene: ENSMUSG00000028028
AA Change: L1121Q
| 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 |
probably damaging
Transcript: ENSMUST00000198955
AA Change: L1121Q
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000143223
Gene: ENSMUSG00000028028
AA Change: L1121Q
| 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 |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.7%
- 20x: 99.1%
|
| Validation Efficiency |
97% (71/73) |
| 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: 74 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1700017N19Rik |
T |
A |
10: 100,448,691 (GRCm39) |
Y335* |
probably null |
Het |
| Ap2a2 |
T |
A |
7: 141,206,049 (GRCm39) |
F717I |
probably damaging |
Het |
| Arhgap33 |
C |
T |
7: 30,222,477 (GRCm39) |
D1152N |
probably benign |
Het |
| Arvcf |
A |
G |
16: 18,220,350 (GRCm39) |
D642G |
probably benign |
Het |
| Astn1 |
T |
G |
1: 158,329,919 (GRCm39) |
M258R |
probably damaging |
Het |
| Brinp3 |
C |
G |
1: 146,777,748 (GRCm39) |
L732V |
possibly damaging |
Het |
| Carmil1 |
T |
C |
13: 24,282,793 (GRCm39) |
D547G |
possibly damaging |
Het |
| Ccdc177 |
A |
G |
12: 80,805,792 (GRCm39) |
F161L |
possibly damaging |
Het |
| Cfap57 |
C |
T |
4: 118,472,128 (GRCm39) |
V84I |
probably benign |
Het |
| Cnot10 |
A |
G |
9: 114,454,971 (GRCm39) |
Y221H |
probably damaging |
Het |
| Col6a3 |
T |
A |
1: 90,755,855 (GRCm39) |
I145F |
probably damaging |
Het |
| Crybg2 |
A |
G |
4: 133,801,434 (GRCm39) |
T865A |
probably benign |
Het |
| Cyp4f37 |
A |
G |
17: 32,848,818 (GRCm39) |
S229G |
possibly damaging |
Het |
| Ddx56 |
G |
A |
11: 6,211,720 (GRCm39) |
T462I |
probably damaging |
Het |
| Dhx30 |
T |
C |
9: 109,921,966 (GRCm39) |
M239V |
probably benign |
Het |
| Dusp9 |
TAAAGCGGAGGCCAAAGCGGAGGCCAAAGCGGAGGCTAAAGCGGAGGCCAAAGCGGAGGCCAAAGCGGAGGCCAAAGCGGAGGCTAAAGCGGAGGCCAAAGCGGAGGCCAAAG |
TAAAGCGGAGGCCAAAGCGGAGGCCAAAGCGGAGGCTAAAGCGGAGGCCAAAGCGGAGGCCAAAG |
X: 72,684,217 (GRCm39) |
|
probably benign |
Het |
| Enpp5 |
G |
A |
17: 44,396,155 (GRCm39) |
G356S |
probably damaging |
Het |
| Ephb6 |
A |
G |
6: 41,597,173 (GRCm39) |
K994E |
probably damaging |
Het |
| Fam83a |
A |
C |
15: 57,849,821 (GRCm39) |
T122P |
probably benign |
Het |
| Fbxo24 |
C |
A |
5: 137,617,885 (GRCm39) |
C293F |
possibly damaging |
Het |
| Fech |
A |
T |
18: 64,591,255 (GRCm39) |
S390T |
probably benign |
Het |
| Fras1 |
A |
G |
5: 96,762,748 (GRCm39) |
H750R |
probably benign |
Het |
| Frmpd2 |
A |
G |
14: 33,293,926 (GRCm39) |
D1364G |
probably benign |
Het |
| Ganab |
T |
C |
19: 8,889,892 (GRCm39) |
I652T |
probably benign |
Het |
| Gm21103 |
T |
A |
14: 17,482,943 (GRCm39) |
T153S |
probably benign |
Het |
| Gm21886 |
GGGCCTGCAGACAGTAGGTGCTCACTGAGGCCTGCAGTTAGTAGGTGCTCACTGAGGCCTGCAGACAGTAGGTACTCACTGAGGCCTGCAGACAGTAGGTGCTCACTGAGGCCTGCAGACAGTAGGTGCTCACTGAGGCCTGCAGACAGTAGGTGCTCACTGAGACCTGCAGACAGTAGGTGCTCACTGAG |
GGGCCTGCAGACAGTAGGTACTCACTGAGGCCTGCAGACAGTAGGTGCTCACTGAGGCCTGCAGACAGTAGGTGCTCACTGAGGCCTGCAGACAGTAGGTGCTCACTGAGACCTGCAGACAGTAGGTGCTCACTGAG |
18: 80,132,967 (GRCm39) |
|
probably benign |
Het |
| Gm5799 |
A |
G |
14: 43,781,995 (GRCm39) |
I56V |
possibly damaging |
Het |
| Gm7276 |
T |
C |
18: 77,273,183 (GRCm39) |
R184G |
unknown |
Het |
| Gmip |
T |
G |
8: 70,273,149 (GRCm39) |
D845E |
probably benign |
Het |
| Hspa9 |
T |
C |
18: 35,082,082 (GRCm39) |
K175E |
probably damaging |
Het |
| Ipo13 |
A |
G |
4: 117,752,068 (GRCm39) |
F890L |
probably benign |
Het |
| Irag1 |
A |
T |
7: 110,522,963 (GRCm39) |
V160D |
probably benign |
Het |
| Klrb1f |
C |
T |
6: 129,033,308 (GRCm39) |
R179* |
probably null |
Het |
| Nasp |
A |
G |
4: 116,467,785 (GRCm39) |
V400A |
possibly damaging |
Het |
| Ncoa7 |
T |
A |
10: 30,598,847 (GRCm39) |
K25N |
possibly damaging |
Het |
| Ndrg1 |
A |
C |
15: 66,832,382 (GRCm39) |
M1R |
probably null |
Het |
| Nf1 |
G |
A |
11: 79,364,240 (GRCm39) |
A1557T |
probably damaging |
Het |
| Nrde2 |
G |
A |
12: 100,108,509 (GRCm39) |
Q361* |
probably null |
Het |
| Opn1sw |
A |
T |
6: 29,379,856 (GRCm39) |
L126Q |
probably damaging |
Het |
| Or10ak16 |
A |
T |
4: 118,750,327 (GRCm39) |
I16F |
possibly damaging |
Het |
| Or1af1 |
C |
T |
2: 37,109,774 (GRCm39) |
T91I |
possibly damaging |
Het |
| Or1j4 |
T |
C |
2: 36,740,478 (GRCm39) |
L140P |
probably benign |
Het |
| Or5au1 |
A |
T |
14: 52,273,310 (GRCm39) |
L86* |
probably null |
Het |
| Or7g17 |
A |
T |
9: 18,768,085 (GRCm39) |
I46F |
possibly damaging |
Het |
| Or8g50 |
T |
C |
9: 39,648,422 (GRCm39) |
F104L |
probably benign |
Het |
| Osmr |
A |
G |
15: 6,853,048 (GRCm39) |
Y616H |
probably damaging |
Het |
| Pagr1a |
T |
C |
7: 126,615,736 (GRCm39) |
T120A |
probably benign |
Het |
| Patj |
A |
G |
4: 98,299,376 (GRCm39) |
E166G |
probably damaging |
Het |
| Plk4 |
G |
A |
3: 40,766,613 (GRCm39) |
V764I |
probably benign |
Het |
| Polr3h |
G |
A |
15: 81,800,602 (GRCm39) |
|
probably null |
Het |
| Ptprb |
T |
A |
10: 116,177,043 (GRCm39) |
D989E |
probably benign |
Het |
| Sdk2 |
A |
T |
11: 113,758,909 (GRCm39) |
|
probably null |
Het |
| Setd1b |
C |
A |
5: 123,290,639 (GRCm39) |
R869S |
unknown |
Het |
| Sgcz |
T |
C |
8: 37,990,565 (GRCm39) |
I263V |
probably benign |
Het |
| Skint8 |
G |
A |
4: 111,785,758 (GRCm39) |
G68D |
probably benign |
Het |
| Slc22a7 |
A |
T |
17: 46,745,553 (GRCm39) |
V326E |
probably benign |
Het |
| Slc39a1 |
T |
G |
3: 90,156,396 (GRCm39) |
L38R |
probably damaging |
Het |
| Slc4a4 |
A |
G |
5: 89,362,506 (GRCm39) |
|
probably null |
Het |
| Sptlc3 |
A |
G |
2: 139,431,537 (GRCm39) |
E353G |
possibly damaging |
Het |
| Ssh2 |
G |
T |
11: 77,340,934 (GRCm39) |
L695F |
probably damaging |
Het |
| Tacr2 |
C |
A |
10: 62,097,427 (GRCm39) |
Y302* |
probably null |
Het |
| Tas2r117 |
T |
C |
6: 132,780,192 (GRCm39) |
L110P |
probably damaging |
Het |
| Tex9 |
A |
T |
9: 72,394,060 (GRCm39) |
|
probably null |
Het |
| Tmem17 |
A |
T |
11: 22,468,645 (GRCm39) |
T195S |
probably benign |
Het |
| Trcg1 |
T |
A |
9: 57,148,766 (GRCm39) |
S113T |
probably benign |
Het |
| Trpa1 |
A |
T |
1: 14,954,422 (GRCm39) |
F826I |
probably benign |
Het |
| Usp17lc |
A |
G |
7: 103,067,575 (GRCm39) |
Y290C |
probably damaging |
Het |
| Vmn2r32 |
T |
A |
7: 7,477,212 (GRCm39) |
D393V |
possibly damaging |
Het |
| Wdfy4 |
A |
G |
14: 32,871,541 (GRCm39) |
L290P |
|
Het |
| Xpnpep1 |
G |
C |
19: 52,994,722 (GRCm39) |
A302G |
probably benign |
Het |
| Xrn2 |
T |
C |
2: 146,891,266 (GRCm39) |
L692P |
probably damaging |
Het |
| Zgrf1 |
A |
G |
3: 127,356,720 (GRCm39) |
S649G |
probably benign |
Het |
| Zscan4b |
C |
T |
7: 10,634,791 (GRCm39) |
C484Y |
probably damaging |
Het |
| Zscan4b |
T |
C |
7: 10,635,820 (GRCm39) |
D169G |
probably benign |
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 |
|
R4820:Alpk1
|
UTSW |
3 |
127,464,708 (GRCm39) |
missense |
probably benign |
0.06 |
|
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 |
|
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'- ACCCTGCACATAGAATGGTC -3'
(R):5'- TAGCTCTGAGGACACTGAAGTC -3'
Sequencing Primer
(F):5'- CCACCACATCTCTATGGTTAG -3'
(R):5'- CTGAAGTCTAGAATAAGTCCCCATGG -3'
|
| Posted On |
2019-10-07 |
Incidental Mutation