Incidental Mutation 'R2131:Dapk1'
ID |
228115 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Dapk1
|
Ensembl Gene |
ENSMUSG00000021559 |
Gene Name |
death associated protein kinase 1 |
Synonyms |
DAP-Kinase, D13Ucla1, 2810425C21Rik, 2310039H24Rik |
MMRRC Submission |
040134-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R2131 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
13 |
Chromosomal Location |
60749761-60911005 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 60877345 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Glutamic Acid to Glycine
at position 528
(E528G)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000153607
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000044083]
[ENSMUST00000077453]
[ENSMUST00000226059]
|
AlphaFold |
Q80YE7 |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000044083
AA Change: E528G
PolyPhen 2
Score 0.908 (Sensitivity: 0.81; Specificity: 0.94)
|
SMART Domains |
Protein: ENSMUSP00000040825 Gene: ENSMUSG00000021559 AA Change: E528G
Domain | Start | End | E-Value | Type |
S_TKc
|
13 |
275 |
6.35e-99 |
SMART |
low complexity region
|
295 |
306 |
N/A |
INTRINSIC |
ANK
|
378 |
407 |
5.09e-2 |
SMART |
ANK
|
411 |
440 |
6.61e-1 |
SMART |
ANK
|
444 |
473 |
7.64e-6 |
SMART |
ANK
|
477 |
506 |
2.13e-4 |
SMART |
ANK
|
510 |
539 |
1.31e-4 |
SMART |
ANK
|
543 |
572 |
7.83e-3 |
SMART |
ANK
|
576 |
605 |
8.52e-4 |
SMART |
ANK
|
609 |
638 |
1.85e-4 |
SMART |
ANK
|
642 |
671 |
7.29e2 |
SMART |
low complexity region
|
711 |
725 |
N/A |
INTRINSIC |
DEATH
|
1299 |
1396 |
2.65e-18 |
SMART |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000077453
AA Change: E528G
PolyPhen 2
Score 0.908 (Sensitivity: 0.81; Specificity: 0.94)
|
SMART Domains |
Protein: ENSMUSP00000076666 Gene: ENSMUSG00000021559 AA Change: E528G
Domain | Start | End | E-Value | Type |
S_TKc
|
13 |
275 |
6.35e-99 |
SMART |
low complexity region
|
295 |
306 |
N/A |
INTRINSIC |
ANK
|
378 |
407 |
5.09e-2 |
SMART |
ANK
|
411 |
440 |
6.61e-1 |
SMART |
ANK
|
444 |
473 |
7.64e-6 |
SMART |
ANK
|
477 |
506 |
2.13e-4 |
SMART |
ANK
|
510 |
539 |
1.31e-4 |
SMART |
ANK
|
543 |
572 |
7.83e-3 |
SMART |
ANK
|
576 |
605 |
8.52e-4 |
SMART |
ANK
|
609 |
638 |
1.85e-4 |
SMART |
ANK
|
642 |
671 |
7.29e2 |
SMART |
low complexity region
|
711 |
725 |
N/A |
INTRINSIC |
Pfam:COR
|
984 |
1176 |
4.2e-10 |
PFAM |
DEATH
|
1299 |
1396 |
2.65e-18 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000224340
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000226059
AA Change: E528G
PolyPhen 2
Score 0.908 (Sensitivity: 0.81; Specificity: 0.94)
|
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.3%
- 20x: 95.0%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Death-associated protein kinase 1 is a positive mediator of gamma-interferon induced programmed cell death. DAPK1 encodes a structurally unique 160-kD calmodulin dependent serine-threonine kinase that carries 8 ankyrin repeats and 2 putative P-loop consensus sites. It is a tumor suppressor candidate. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2013] PHENOTYPE: Mice homozygous for a knock-out allele show decreased sensitivity to ER stress-induced cell death and reduced tunicamycin-induced kidney damage. Mice homozygous for a gene trapped allele show decreased infarct size and neuronal death with improved neurological scores after ischemic brain injury. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 122 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2ml1 |
T |
A |
6: 128,553,223 (GRCm39) |
N178I |
probably damaging |
Het |
Acvr2b |
A |
G |
9: 119,261,874 (GRCm39) |
R437G |
probably damaging |
Het |
Adamtsl3 |
C |
A |
7: 82,227,802 (GRCm39) |
A1329E |
probably damaging |
Het |
Adgrl2 |
T |
C |
3: 148,596,124 (GRCm39) |
I71V |
probably damaging |
Het |
Adra1a |
A |
T |
14: 66,964,981 (GRCm39) |
I324F |
possibly damaging |
Het |
Akap13 |
G |
T |
7: 75,261,182 (GRCm39) |
A1269S |
probably benign |
Het |
Ampd1 |
G |
T |
3: 103,002,194 (GRCm39) |
|
probably null |
Het |
Ankrd16 |
T |
A |
2: 11,788,506 (GRCm39) |
D211E |
probably damaging |
Het |
Aopep |
T |
A |
13: 63,357,963 (GRCm39) |
C656S |
probably benign |
Het |
Aox3 |
A |
G |
1: 58,209,002 (GRCm39) |
H845R |
probably damaging |
Het |
Apc |
C |
A |
18: 34,445,098 (GRCm39) |
Q665K |
possibly damaging |
Het |
Arap2 |
T |
C |
5: 62,835,301 (GRCm39) |
N747S |
probably damaging |
Het |
Arsk |
A |
T |
13: 76,239,931 (GRCm39) |
C47* |
probably null |
Het |
Atp8b5 |
T |
A |
4: 43,370,726 (GRCm39) |
F1001I |
probably benign |
Het |
Bap1 |
T |
A |
14: 30,980,288 (GRCm39) |
Y645* |
probably null |
Het |
Brca2 |
A |
G |
5: 150,480,594 (GRCm39) |
Y2760C |
probably damaging |
Het |
Cad |
T |
A |
5: 31,215,416 (GRCm39) |
F76I |
probably damaging |
Het |
Capn9 |
G |
A |
8: 125,332,450 (GRCm39) |
G430R |
possibly damaging |
Het |
Castor2 |
G |
A |
5: 134,164,992 (GRCm39) |
C187Y |
probably damaging |
Het |
Ccdc27 |
TTCCTCCTCCTCCTCCTCCTC |
TTCCTCCTCCTCCTCCTC |
4: 154,120,763 (GRCm39) |
|
probably benign |
Het |
Cdkn2c |
A |
C |
4: 109,522,260 (GRCm39) |
N28K |
probably null |
Het |
Celsr1 |
T |
A |
15: 85,847,424 (GRCm39) |
I1438F |
probably benign |
Het |
Cfhr2 |
T |
G |
1: 139,758,893 (GRCm39) |
R52S |
probably benign |
Het |
Cldn1 |
G |
C |
16: 26,190,300 (GRCm39) |
A26G |
probably damaging |
Het |
Col20a1 |
T |
A |
2: 180,634,366 (GRCm39) |
F110L |
probably damaging |
Het |
Creg2 |
T |
C |
1: 39,664,146 (GRCm39) |
N204S |
probably benign |
Het |
Cx3cl1 |
C |
A |
8: 95,506,201 (GRCm39) |
Q69K |
probably benign |
Het |
Cyfip2 |
T |
C |
11: 46,176,958 (GRCm39) |
E74G |
possibly damaging |
Het |
Cyp2g1 |
A |
T |
7: 26,520,135 (GRCm39) |
I456F |
probably damaging |
Het |
Dbt |
T |
A |
3: 116,332,773 (GRCm39) |
D16E |
probably damaging |
Het |
Depdc5 |
T |
A |
5: 33,148,125 (GRCm39) |
L1469* |
probably null |
Het |
Dnah3 |
T |
A |
7: 119,566,982 (GRCm39) |
T2415S |
possibly damaging |
Het |
Dnmbp |
A |
G |
19: 43,842,750 (GRCm39) |
L1210S |
probably damaging |
Het |
Dpyd |
T |
C |
3: 118,468,217 (GRCm39) |
V77A |
probably benign |
Het |
Eps15l1 |
A |
T |
8: 73,140,712 (GRCm39) |
V260D |
probably benign |
Het |
Eya1 |
A |
G |
1: 14,241,198 (GRCm39) |
V573A |
probably benign |
Het |
Fam171b |
T |
A |
2: 83,710,202 (GRCm39) |
S625T |
probably damaging |
Het |
Fam186a |
T |
C |
15: 99,831,557 (GRCm39) |
|
probably benign |
Het |
Gabra4 |
G |
T |
5: 71,798,567 (GRCm39) |
D137E |
probably benign |
Het |
Gemin4 |
G |
C |
11: 76,101,876 (GRCm39) |
P962A |
probably damaging |
Het |
Gm43302 |
T |
C |
5: 105,422,610 (GRCm39) |
D474G |
probably damaging |
Het |
Golim4 |
A |
T |
3: 75,815,456 (GRCm39) |
V116D |
probably damaging |
Het |
Gpr19 |
T |
C |
6: 134,847,405 (GRCm39) |
M1V |
probably null |
Het |
Hnf4a |
T |
A |
2: 163,389,338 (GRCm39) |
N29K |
probably benign |
Het |
Htt |
A |
G |
5: 35,034,453 (GRCm39) |
R1975G |
possibly damaging |
Het |
Ift20 |
G |
A |
11: 78,430,860 (GRCm39) |
E68K |
probably damaging |
Het |
Il4i1 |
G |
A |
7: 44,489,494 (GRCm39) |
V420M |
probably damaging |
Het |
Insrr |
G |
A |
3: 87,717,879 (GRCm39) |
|
probably null |
Het |
Ipo9 |
ATCCTCCTCCTCCTCCTC |
ATCCTCCTCCTCCTCCTCCTC |
1: 135,314,006 (GRCm39) |
|
probably benign |
Het |
Ipo9 |
A |
G |
1: 135,329,988 (GRCm39) |
V484A |
probably benign |
Het |
Jmjd4 |
A |
T |
11: 59,345,781 (GRCm39) |
H287L |
probably damaging |
Het |
Kcnj13 |
A |
G |
1: 87,314,256 (GRCm39) |
V322A |
probably benign |
Het |
Kdm5d |
T |
C |
Y: 941,483 (GRCm39) |
L1228P |
probably benign |
Het |
Klra3 |
A |
G |
6: 130,312,738 (GRCm39) |
S9P |
probably benign |
Het |
Ldhd |
C |
T |
8: 112,355,169 (GRCm39) |
|
probably null |
Het |
Lmo2 |
T |
C |
2: 103,811,407 (GRCm39) |
Y147H |
probably damaging |
Het |
Lmo7 |
A |
T |
14: 102,137,674 (GRCm39) |
D670V |
probably damaging |
Het |
Lmtk2 |
C |
T |
5: 144,111,806 (GRCm39) |
T842I |
possibly damaging |
Het |
Lrp5 |
T |
C |
19: 3,672,708 (GRCm39) |
T534A |
possibly damaging |
Het |
Lrrc24 |
A |
T |
15: 76,599,781 (GRCm39) |
F453I |
possibly damaging |
Het |
Magel2 |
A |
T |
7: 62,027,486 (GRCm39) |
H130L |
unknown |
Het |
Mcpt8 |
T |
C |
14: 56,319,740 (GRCm39) |
I237V |
probably damaging |
Het |
Med4 |
A |
G |
14: 73,755,436 (GRCm39) |
N248S |
possibly damaging |
Het |
Mest |
C |
T |
6: 30,745,884 (GRCm39) |
L269F |
probably damaging |
Het |
Mib2 |
C |
T |
4: 155,739,695 (GRCm39) |
|
probably null |
Het |
Mki67 |
T |
A |
7: 135,305,970 (GRCm39) |
|
probably null |
Het |
Mnx1 |
T |
A |
5: 29,679,187 (GRCm39) |
S299C |
unknown |
Het |
Nbr1 |
T |
A |
11: 101,457,017 (GRCm39) |
|
probably null |
Het |
Ncapd3 |
T |
G |
9: 26,994,642 (GRCm39) |
V1174G |
probably damaging |
Het |
Nyap1 |
A |
C |
5: 137,731,943 (GRCm39) |
|
probably null |
Het |
Olfml3 |
T |
A |
3: 103,643,185 (GRCm39) |
M399L |
probably benign |
Het |
Oosp1 |
T |
C |
19: 11,668,314 (GRCm39) |
D23G |
probably damaging |
Het |
Optc |
A |
T |
1: 133,831,534 (GRCm39) |
|
probably null |
Het |
Or1j13 |
A |
G |
2: 36,370,059 (GRCm39) |
S28P |
possibly damaging |
Het |
Or6c205 |
T |
C |
10: 129,086,943 (GRCm39) |
F180S |
probably benign |
Het |
Osbpl6 |
T |
A |
2: 76,416,558 (GRCm39) |
I546K |
probably damaging |
Het |
Otog |
A |
T |
7: 45,899,524 (GRCm39) |
N275I |
probably damaging |
Het |
Pcdhb14 |
C |
A |
18: 37,580,923 (GRCm39) |
Q10K |
probably benign |
Het |
Pcx |
T |
C |
19: 4,652,579 (GRCm39) |
F189L |
probably benign |
Het |
Pde6b |
A |
G |
5: 108,576,069 (GRCm39) |
D718G |
probably damaging |
Het |
Pklr |
C |
A |
3: 89,049,967 (GRCm39) |
P314Q |
probably damaging |
Het |
Plcb1 |
T |
A |
2: 135,167,587 (GRCm39) |
Y460* |
probably null |
Het |
Plekha6 |
C |
A |
1: 133,207,103 (GRCm39) |
|
probably null |
Het |
Plekho1 |
A |
G |
3: 95,896,429 (GRCm39) |
S347P |
probably damaging |
Het |
Plxna2 |
G |
A |
1: 194,327,058 (GRCm39) |
D331N |
probably benign |
Het |
Prelp |
C |
T |
1: 133,842,869 (GRCm39) |
R92K |
probably benign |
Het |
Prkra |
A |
T |
2: 76,477,480 (GRCm39) |
I75K |
probably damaging |
Het |
Ptpn11 |
G |
A |
5: 121,310,089 (GRCm39) |
A31V |
probably damaging |
Het |
Pzp |
T |
C |
6: 128,468,124 (GRCm39) |
|
probably null |
Het |
Rbm12 |
A |
T |
2: 155,937,430 (GRCm39) |
C947* |
probably null |
Het |
Ren1 |
C |
G |
1: 133,278,516 (GRCm39) |
|
probably null |
Het |
Ro60 |
T |
C |
1: 143,635,772 (GRCm39) |
D458G |
probably benign |
Het |
Sarm1 |
A |
T |
11: 78,366,133 (GRCm39) |
C649S |
probably benign |
Het |
Septin12 |
T |
A |
16: 4,809,643 (GRCm39) |
Q223L |
probably damaging |
Het |
Septin4 |
A |
T |
11: 87,474,262 (GRCm39) |
Q60L |
probably benign |
Het |
Slc22a21 |
A |
T |
11: 53,870,559 (GRCm39) |
L42Q |
probably damaging |
Het |
Slc44a1 |
GCCC |
GCCCCCCC |
4: 53,563,246 (GRCm39) |
|
probably null |
Het |
Slc9a4 |
T |
G |
1: 40,646,901 (GRCm39) |
|
probably null |
Het |
Sort1 |
T |
A |
3: 108,259,002 (GRCm39) |
F678Y |
probably benign |
Het |
Spag6 |
T |
A |
2: 18,737,908 (GRCm39) |
C259* |
probably null |
Het |
Spata31e2 |
T |
C |
1: 26,724,935 (GRCm39) |
R82G |
probably benign |
Het |
Stard13 |
T |
C |
5: 150,968,633 (GRCm39) |
Y879C |
probably damaging |
Het |
Stk24 |
A |
T |
14: 121,539,623 (GRCm39) |
I191N |
probably damaging |
Het |
Tacc1 |
A |
T |
8: 25,654,509 (GRCm39) |
N271K |
probably damaging |
Het |
Tacc2 |
T |
A |
7: 130,223,587 (GRCm39) |
S91T |
possibly damaging |
Het |
Tacr3 |
T |
C |
3: 134,637,941 (GRCm39) |
V366A |
probably benign |
Het |
Tasor |
A |
G |
14: 27,198,571 (GRCm39) |
N1301S |
possibly damaging |
Het |
Tbccd1 |
A |
G |
16: 22,660,739 (GRCm39) |
S26P |
probably benign |
Het |
Tecpr1 |
T |
A |
5: 144,145,463 (GRCm39) |
T595S |
probably benign |
Het |
Tjp3 |
T |
A |
10: 81,113,888 (GRCm39) |
M457L |
possibly damaging |
Het |
Tor1aip2 |
A |
G |
1: 155,941,095 (GRCm39) |
Y467C |
probably damaging |
Het |
Ttc9b |
T |
A |
7: 27,353,774 (GRCm39) |
|
probably null |
Het |
Tti1 |
T |
C |
2: 157,842,663 (GRCm39) |
R789G |
probably benign |
Het |
Ttn |
A |
T |
2: 76,662,561 (GRCm39) |
|
probably null |
Het |
Txk |
T |
A |
5: 72,853,922 (GRCm39) |
T472S |
probably damaging |
Het |
Ube3d |
A |
T |
9: 86,254,540 (GRCm39) |
|
probably null |
Het |
Vav2 |
C |
A |
2: 27,189,408 (GRCm39) |
R176L |
possibly damaging |
Het |
Vps35l |
T |
C |
7: 118,393,798 (GRCm39) |
Y516H |
probably damaging |
Het |
Wdr27 |
T |
A |
17: 15,148,594 (GRCm39) |
D133V |
probably damaging |
Het |
Zc3h7a |
A |
T |
16: 10,968,469 (GRCm39) |
Y503* |
probably null |
Het |
Zdhhc13 |
T |
A |
7: 48,474,392 (GRCm39) |
L548Q |
possibly damaging |
Het |
Zfp467 |
A |
C |
6: 48,419,595 (GRCm39) |
S38A |
probably damaging |
Het |
|
Other mutations in Dapk1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00089:Dapk1
|
APN |
13 |
60,908,854 (GRCm39) |
missense |
probably benign |
0.23 |
IGL00500:Dapk1
|
APN |
13 |
60,908,618 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL00801:Dapk1
|
APN |
13 |
60,909,062 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00903:Dapk1
|
APN |
13 |
60,909,211 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01468:Dapk1
|
APN |
13 |
60,908,612 (GRCm39) |
missense |
probably benign |
|
IGL01535:Dapk1
|
APN |
13 |
60,878,845 (GRCm39) |
splice site |
probably benign |
|
IGL01755:Dapk1
|
APN |
13 |
60,908,990 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL01755:Dapk1
|
APN |
13 |
60,908,989 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01862:Dapk1
|
APN |
13 |
60,874,424 (GRCm39) |
missense |
probably benign |
0.39 |
IGL01985:Dapk1
|
APN |
13 |
60,884,074 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02124:Dapk1
|
APN |
13 |
60,878,696 (GRCm39) |
missense |
probably benign |
|
IGL02376:Dapk1
|
APN |
13 |
60,844,208 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02449:Dapk1
|
APN |
13 |
60,867,584 (GRCm39) |
splice site |
probably benign |
|
IGL02490:Dapk1
|
APN |
13 |
60,897,148 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02503:Dapk1
|
APN |
13 |
60,909,621 (GRCm39) |
nonsense |
probably null |
|
IGL02516:Dapk1
|
APN |
13 |
60,844,161 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02544:Dapk1
|
APN |
13 |
60,899,031 (GRCm39) |
missense |
probably benign |
|
IGL02604:Dapk1
|
APN |
13 |
60,896,134 (GRCm39) |
missense |
probably benign |
|
IGL03035:Dapk1
|
APN |
13 |
60,864,587 (GRCm39) |
missense |
probably damaging |
0.99 |
H8562:Dapk1
|
UTSW |
13 |
60,909,126 (GRCm39) |
missense |
probably damaging |
0.98 |
P0026:Dapk1
|
UTSW |
13 |
60,865,963 (GRCm39) |
splice site |
probably benign |
|
R0116:Dapk1
|
UTSW |
13 |
60,908,914 (GRCm39) |
missense |
probably benign |
|
R0165:Dapk1
|
UTSW |
13 |
60,909,407 (GRCm39) |
missense |
probably benign |
0.39 |
R0357:Dapk1
|
UTSW |
13 |
60,877,372 (GRCm39) |
nonsense |
probably null |
|
R0446:Dapk1
|
UTSW |
13 |
60,873,101 (GRCm39) |
splice site |
probably null |
|
R0502:Dapk1
|
UTSW |
13 |
60,878,662 (GRCm39) |
splice site |
probably null |
|
R0503:Dapk1
|
UTSW |
13 |
60,878,662 (GRCm39) |
splice site |
probably null |
|
R0597:Dapk1
|
UTSW |
13 |
60,909,198 (GRCm39) |
missense |
probably benign |
0.40 |
R0614:Dapk1
|
UTSW |
13 |
60,865,946 (GRCm39) |
missense |
probably damaging |
1.00 |
R0751:Dapk1
|
UTSW |
13 |
60,844,112 (GRCm39) |
missense |
probably damaging |
1.00 |
R0930:Dapk1
|
UTSW |
13 |
60,905,262 (GRCm39) |
missense |
probably benign |
0.14 |
R1023:Dapk1
|
UTSW |
13 |
60,878,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R1033:Dapk1
|
UTSW |
13 |
60,869,679 (GRCm39) |
critical splice donor site |
probably null |
|
R1101:Dapk1
|
UTSW |
13 |
60,864,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R1184:Dapk1
|
UTSW |
13 |
60,844,112 (GRCm39) |
missense |
probably damaging |
1.00 |
R1430:Dapk1
|
UTSW |
13 |
60,901,957 (GRCm39) |
missense |
probably benign |
0.28 |
R1630:Dapk1
|
UTSW |
13 |
60,877,345 (GRCm39) |
missense |
probably damaging |
0.99 |
R1681:Dapk1
|
UTSW |
13 |
60,866,278 (GRCm39) |
critical splice donor site |
probably null |
|
R1799:Dapk1
|
UTSW |
13 |
60,867,468 (GRCm39) |
missense |
probably damaging |
1.00 |
R2012:Dapk1
|
UTSW |
13 |
60,869,671 (GRCm39) |
missense |
probably damaging |
1.00 |
R2068:Dapk1
|
UTSW |
13 |
60,899,022 (GRCm39) |
missense |
probably damaging |
1.00 |
R2131:Dapk1
|
UTSW |
13 |
60,909,481 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2154:Dapk1
|
UTSW |
13 |
60,877,317 (GRCm39) |
missense |
probably benign |
0.36 |
R2288:Dapk1
|
UTSW |
13 |
60,909,563 (GRCm39) |
missense |
probably damaging |
1.00 |
R2312:Dapk1
|
UTSW |
13 |
60,905,167 (GRCm39) |
missense |
probably damaging |
0.99 |
R2362:Dapk1
|
UTSW |
13 |
60,878,745 (GRCm39) |
missense |
probably damaging |
0.98 |
R2400:Dapk1
|
UTSW |
13 |
60,900,030 (GRCm39) |
missense |
probably benign |
0.34 |
R2909:Dapk1
|
UTSW |
13 |
60,864,631 (GRCm39) |
critical splice donor site |
probably null |
|
R2926:Dapk1
|
UTSW |
13 |
60,867,564 (GRCm39) |
missense |
possibly damaging |
0.58 |
R3741:Dapk1
|
UTSW |
13 |
60,896,014 (GRCm39) |
missense |
probably benign |
0.09 |
R3810:Dapk1
|
UTSW |
13 |
60,908,503 (GRCm39) |
missense |
probably damaging |
0.98 |
R4374:Dapk1
|
UTSW |
13 |
60,867,498 (GRCm39) |
missense |
probably benign |
0.01 |
R4375:Dapk1
|
UTSW |
13 |
60,909,403 (GRCm39) |
missense |
probably benign |
|
R4377:Dapk1
|
UTSW |
13 |
60,867,498 (GRCm39) |
missense |
probably benign |
0.01 |
R4490:Dapk1
|
UTSW |
13 |
60,865,942 (GRCm39) |
missense |
probably benign |
0.26 |
R4576:Dapk1
|
UTSW |
13 |
60,869,636 (GRCm39) |
missense |
probably benign |
0.13 |
R4599:Dapk1
|
UTSW |
13 |
60,865,861 (GRCm39) |
missense |
probably benign |
0.22 |
R4682:Dapk1
|
UTSW |
13 |
60,898,961 (GRCm39) |
missense |
probably benign |
0.41 |
R4717:Dapk1
|
UTSW |
13 |
60,874,476 (GRCm39) |
critical splice donor site |
probably null |
|
R4775:Dapk1
|
UTSW |
13 |
60,897,156 (GRCm39) |
missense |
probably benign |
0.02 |
R4790:Dapk1
|
UTSW |
13 |
60,870,919 (GRCm39) |
frame shift |
probably null |
|
R4897:Dapk1
|
UTSW |
13 |
60,909,600 (GRCm39) |
missense |
probably benign |
0.01 |
R4931:Dapk1
|
UTSW |
13 |
60,908,774 (GRCm39) |
missense |
probably benign |
0.04 |
R5113:Dapk1
|
UTSW |
13 |
60,869,592 (GRCm39) |
missense |
probably benign |
0.01 |
R5503:Dapk1
|
UTSW |
13 |
60,873,126 (GRCm39) |
missense |
probably benign |
0.15 |
R5948:Dapk1
|
UTSW |
13 |
60,877,209 (GRCm39) |
missense |
probably damaging |
0.97 |
R6012:Dapk1
|
UTSW |
13 |
60,909,476 (GRCm39) |
missense |
probably benign |
0.00 |
R6035:Dapk1
|
UTSW |
13 |
60,909,013 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6035:Dapk1
|
UTSW |
13 |
60,909,013 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6268:Dapk1
|
UTSW |
13 |
60,909,580 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6330:Dapk1
|
UTSW |
13 |
60,909,140 (GRCm39) |
missense |
probably benign |
0.01 |
R6331:Dapk1
|
UTSW |
13 |
60,877,256 (GRCm39) |
nonsense |
probably null |
|
R6553:Dapk1
|
UTSW |
13 |
60,908,975 (GRCm39) |
missense |
probably damaging |
0.99 |
R6598:Dapk1
|
UTSW |
13 |
60,909,161 (GRCm39) |
missense |
probably benign |
0.03 |
R6602:Dapk1
|
UTSW |
13 |
60,897,018 (GRCm39) |
missense |
probably benign |
0.20 |
R6640:Dapk1
|
UTSW |
13 |
60,864,628 (GRCm39) |
missense |
probably damaging |
0.99 |
R6684:Dapk1
|
UTSW |
13 |
60,908,708 (GRCm39) |
missense |
probably damaging |
1.00 |
R6747:Dapk1
|
UTSW |
13 |
60,873,154 (GRCm39) |
missense |
probably benign |
0.22 |
R6799:Dapk1
|
UTSW |
13 |
60,900,049 (GRCm39) |
missense |
probably benign |
|
R6809:Dapk1
|
UTSW |
13 |
60,899,103 (GRCm39) |
missense |
probably benign |
0.00 |
R6915:Dapk1
|
UTSW |
13 |
60,844,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R6949:Dapk1
|
UTSW |
13 |
60,884,138 (GRCm39) |
missense |
probably benign |
0.11 |
R6979:Dapk1
|
UTSW |
13 |
60,896,095 (GRCm39) |
missense |
probably damaging |
1.00 |
R7161:Dapk1
|
UTSW |
13 |
60,844,209 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7171:Dapk1
|
UTSW |
13 |
60,909,599 (GRCm39) |
missense |
probably damaging |
0.97 |
R7199:Dapk1
|
UTSW |
13 |
60,902,024 (GRCm39) |
missense |
probably benign |
0.02 |
R7203:Dapk1
|
UTSW |
13 |
60,844,149 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7404:Dapk1
|
UTSW |
13 |
60,867,455 (GRCm39) |
missense |
probably benign |
0.00 |
R7448:Dapk1
|
UTSW |
13 |
60,898,990 (GRCm39) |
missense |
probably damaging |
1.00 |
R7480:Dapk1
|
UTSW |
13 |
60,905,311 (GRCm39) |
missense |
probably benign |
0.18 |
R7532:Dapk1
|
UTSW |
13 |
60,878,700 (GRCm39) |
missense |
probably damaging |
1.00 |
R7574:Dapk1
|
UTSW |
13 |
60,908,987 (GRCm39) |
missense |
probably damaging |
1.00 |
R7711:Dapk1
|
UTSW |
13 |
60,909,365 (GRCm39) |
missense |
probably damaging |
1.00 |
R7753:Dapk1
|
UTSW |
13 |
60,899,007 (GRCm39) |
missense |
possibly damaging |
0.58 |
R7804:Dapk1
|
UTSW |
13 |
60,873,153 (GRCm39) |
missense |
probably benign |
0.41 |
R7822:Dapk1
|
UTSW |
13 |
60,873,715 (GRCm39) |
missense |
probably benign |
0.05 |
R7973:Dapk1
|
UTSW |
13 |
60,909,377 (GRCm39) |
missense |
probably damaging |
1.00 |
R8103:Dapk1
|
UTSW |
13 |
60,897,009 (GRCm39) |
missense |
probably damaging |
0.98 |
R8121:Dapk1
|
UTSW |
13 |
60,909,212 (GRCm39) |
missense |
probably damaging |
0.99 |
R8245:Dapk1
|
UTSW |
13 |
60,878,710 (GRCm39) |
missense |
probably benign |
|
R8401:Dapk1
|
UTSW |
13 |
60,870,904 (GRCm39) |
missense |
probably benign |
0.01 |
R8419:Dapk1
|
UTSW |
13 |
60,887,911 (GRCm39) |
missense |
probably benign |
0.00 |
R8926:Dapk1
|
UTSW |
13 |
60,908,734 (GRCm39) |
missense |
probably damaging |
0.98 |
R9063:Dapk1
|
UTSW |
13 |
60,866,264 (GRCm39) |
missense |
probably benign |
0.06 |
R9131:Dapk1
|
UTSW |
13 |
60,909,208 (GRCm39) |
missense |
probably damaging |
1.00 |
R9176:Dapk1
|
UTSW |
13 |
60,866,262 (GRCm39) |
missense |
probably damaging |
1.00 |
R9301:Dapk1
|
UTSW |
13 |
60,866,125 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9407:Dapk1
|
UTSW |
13 |
60,898,991 (GRCm39) |
nonsense |
probably null |
|
R9491:Dapk1
|
UTSW |
13 |
60,877,369 (GRCm39) |
missense |
probably benign |
0.44 |
R9510:Dapk1
|
UTSW |
13 |
60,910,203 (GRCm39) |
missense |
unknown |
|
R9624:Dapk1
|
UTSW |
13 |
60,895,937 (GRCm39) |
missense |
probably benign |
0.31 |
R9726:Dapk1
|
UTSW |
13 |
60,898,948 (GRCm39) |
missense |
probably benign |
0.25 |
R9794:Dapk1
|
UTSW |
13 |
60,909,082 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1176:Dapk1
|
UTSW |
13 |
60,908,618 (GRCm39) |
frame shift |
probably null |
|
|
Predicted Primers |
PCR Primer
(F):5'- CACACTGGCTGCAATCTCTG -3'
(R):5'- CCAAAGAGGCCTGTTCAATCAG -3'
Sequencing Primer
(F):5'- TGCTTCCATGGCCTTGAC -3'
(R):5'- GAGGCCTGTTCAATCAGAAACTTAG -3'
|
Posted On |
2014-09-17 |