Incidental Mutation 'R1184:Dapk1'
ID |
101966 |
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 |
039256-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R1184 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
13 |
Chromosomal Location |
60749761-60911005 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 60844112 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Isoleucine to Phenylalanine
at position 44
(I44F)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000153607
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000044083]
[ENSMUST00000077453]
[ENSMUST00000226059]
|
AlphaFold |
Q80YE7 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000044083
AA Change: I44F
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000040825 Gene: ENSMUSG00000021559 AA Change: I44F
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 |
probably damaging
Transcript: ENSMUST00000077453
AA Change: I44F
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000076666 Gene: ENSMUSG00000021559 AA Change: I44F
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 |
probably benign
Transcript: ENSMUST00000224789
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000225632
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000226059
AA Change: I44F
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
Meta Mutation Damage Score |
0.7352 |
Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.2%
- 10x: 95.9%
- 20x: 91.5%
|
Validation Efficiency |
100% (83/83) |
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: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700003E16Rik |
A |
G |
6: 83,137,894 (GRCm39) |
R7G |
probably damaging |
Het |
Ahdc1 |
T |
A |
4: 132,792,707 (GRCm39) |
M1316K |
probably benign |
Het |
Alkal1 |
A |
G |
1: 6,459,712 (GRCm39) |
Y96C |
probably damaging |
Het |
Anxa2r1 |
A |
T |
13: 120,496,667 (GRCm39) |
N67K |
probably benign |
Het |
Arhgap17 |
T |
C |
7: 122,913,913 (GRCm39) |
Y199C |
probably damaging |
Het |
Bmp2 |
T |
C |
2: 133,403,388 (GRCm39) |
V313A |
probably damaging |
Het |
Cacna1b |
C |
T |
2: 24,577,757 (GRCm39) |
|
probably null |
Het |
Cars1 |
T |
C |
7: 143,140,876 (GRCm39) |
T141A |
probably damaging |
Het |
Ccdc57 |
A |
G |
11: 120,764,637 (GRCm39) |
|
probably benign |
Het |
Cenpe |
T |
C |
3: 134,970,183 (GRCm39) |
|
probably null |
Het |
Chadl |
T |
C |
15: 81,577,258 (GRCm39) |
S198G |
probably benign |
Het |
Chd6 |
G |
C |
2: 160,872,722 (GRCm39) |
P286R |
probably damaging |
Het |
Clec4a4 |
G |
T |
6: 122,989,671 (GRCm39) |
W104L |
probably benign |
Het |
Coq4 |
G |
A |
2: 29,678,346 (GRCm39) |
|
probably benign |
Het |
Cplane1 |
G |
T |
15: 8,245,971 (GRCm39) |
V1448L |
probably benign |
Het |
Crtc2 |
T |
A |
3: 90,169,940 (GRCm39) |
Y445* |
probably null |
Het |
Dcbld2 |
T |
A |
16: 58,270,204 (GRCm39) |
|
probably null |
Het |
Dcun1d4 |
T |
C |
5: 73,668,455 (GRCm39) |
|
probably benign |
Het |
Depdc7 |
A |
T |
2: 104,560,523 (GRCm39) |
|
probably benign |
Het |
Dna2 |
A |
G |
10: 62,794,977 (GRCm39) |
D416G |
probably benign |
Het |
Dnah2 |
A |
T |
11: 69,390,016 (GRCm39) |
I743N |
probably damaging |
Het |
Dnah9 |
A |
G |
11: 65,975,438 (GRCm39) |
|
probably null |
Het |
Dock3 |
A |
G |
9: 106,846,999 (GRCm39) |
S877P |
probably damaging |
Het |
Eif3l |
T |
A |
15: 78,959,966 (GRCm39) |
|
probably null |
Het |
Epha5 |
A |
T |
5: 84,219,134 (GRCm39) |
|
probably null |
Het |
Ffar3 |
T |
A |
7: 30,554,529 (GRCm39) |
N264Y |
probably damaging |
Het |
Fyb1 |
A |
T |
15: 6,668,381 (GRCm39) |
I525F |
probably damaging |
Het |
Fyco1 |
A |
G |
9: 123,648,218 (GRCm39) |
F1239L |
probably damaging |
Het |
Gcdh |
T |
C |
8: 85,620,071 (GRCm39) |
|
probably benign |
Het |
Gk5 |
T |
C |
9: 96,032,473 (GRCm39) |
|
probably benign |
Het |
Grm1 |
A |
G |
10: 10,595,778 (GRCm39) |
Y617H |
probably benign |
Het |
Gvin-ps3 |
A |
G |
7: 105,683,159 (GRCm39) |
V32A |
probably benign |
Het |
Hhipl2 |
A |
T |
1: 183,206,042 (GRCm39) |
I131L |
probably damaging |
Het |
Larp4b |
T |
C |
13: 9,216,345 (GRCm39) |
|
probably benign |
Het |
Lrig2 |
T |
A |
3: 104,398,227 (GRCm39) |
I301F |
possibly damaging |
Het |
Man2a2 |
A |
T |
7: 80,012,713 (GRCm39) |
I600N |
possibly damaging |
Het |
Mylk2 |
G |
C |
2: 152,755,661 (GRCm39) |
|
probably null |
Het |
Myo6 |
C |
T |
9: 80,193,664 (GRCm39) |
Q870* |
probably null |
Het |
Napg |
T |
G |
18: 63,127,409 (GRCm39) |
H204Q |
probably benign |
Het |
Neb |
G |
A |
2: 52,153,959 (GRCm39) |
T2384M |
probably damaging |
Het |
Nek10 |
A |
G |
14: 14,931,325 (GRCm38) |
|
probably benign |
Het |
Or11h23 |
A |
C |
14: 50,948,071 (GRCm39) |
T95P |
probably benign |
Het |
Or4c111 |
A |
G |
2: 88,844,057 (GRCm39) |
M117T |
probably damaging |
Het |
Or5an6 |
T |
C |
19: 12,372,221 (GRCm39) |
V198A |
probably benign |
Het |
Or5b108 |
T |
G |
19: 13,168,739 (GRCm39) |
L236R |
probably damaging |
Het |
Pclo |
A |
G |
5: 14,572,276 (GRCm39) |
T554A |
unknown |
Het |
Perm1 |
C |
A |
4: 156,301,771 (GRCm39) |
T105K |
probably damaging |
Het |
Pik3r1 |
T |
C |
13: 101,822,866 (GRCm39) |
|
probably null |
Het |
Pld5 |
A |
G |
1: 175,872,462 (GRCm39) |
I225T |
probably damaging |
Het |
Plxnc1 |
T |
C |
10: 94,667,195 (GRCm39) |
|
probably benign |
Het |
Ptpn12 |
A |
C |
5: 21,203,354 (GRCm39) |
S475A |
possibly damaging |
Het |
Ptprt |
A |
G |
2: 161,769,692 (GRCm39) |
V391A |
possibly damaging |
Het |
Rac2 |
T |
G |
15: 78,450,145 (GRCm39) |
D65A |
possibly damaging |
Het |
Rgl3 |
A |
G |
9: 21,888,676 (GRCm39) |
|
probably null |
Het |
Rif1 |
GCCACCA |
GCCA |
2: 52,000,336 (GRCm39) |
|
probably benign |
Het |
Sebox |
A |
T |
11: 78,394,675 (GRCm39) |
T47S |
probably damaging |
Het |
Sema4b |
A |
G |
7: 79,874,388 (GRCm39) |
T593A |
probably benign |
Het |
Serpina3a |
C |
T |
12: 104,082,787 (GRCm39) |
Q187* |
probably null |
Het |
Serpinb1a |
T |
C |
13: 33,027,199 (GRCm39) |
K248E |
probably benign |
Het |
Serpinb9e |
A |
C |
13: 33,443,757 (GRCm39) |
E259A |
probably benign |
Het |
Slc30a3 |
T |
A |
5: 31,247,510 (GRCm39) |
H44L |
probably damaging |
Het |
Smarca2 |
T |
C |
19: 26,748,333 (GRCm39) |
|
probably benign |
Het |
Snrnp200 |
T |
A |
2: 127,078,737 (GRCm39) |
C1801S |
probably damaging |
Het |
Soat1 |
G |
A |
1: 156,269,944 (GRCm39) |
|
probably null |
Het |
Spink6 |
T |
C |
18: 44,204,605 (GRCm39) |
|
probably benign |
Het |
Spta1 |
G |
A |
1: 174,012,256 (GRCm39) |
R354H |
probably damaging |
Het |
Tbck |
T |
A |
3: 132,543,733 (GRCm39) |
H861Q |
probably benign |
Het |
Tgfbrap1 |
G |
A |
1: 43,088,856 (GRCm39) |
T849M |
possibly damaging |
Het |
Tnrc6a |
A |
G |
7: 122,769,563 (GRCm39) |
N451S |
possibly damaging |
Het |
Trim36 |
T |
C |
18: 46,329,318 (GRCm39) |
T41A |
probably damaging |
Het |
Trmt112 |
C |
A |
19: 6,887,721 (GRCm39) |
|
probably benign |
Het |
Trpc4ap |
A |
G |
2: 155,486,990 (GRCm39) |
|
probably benign |
Het |
Ttll7 |
C |
T |
3: 146,645,746 (GRCm39) |
P535S |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,691,776 (GRCm39) |
|
probably benign |
Het |
Txndc11 |
C |
T |
16: 10,946,364 (GRCm39) |
R149Q |
probably benign |
Het |
Ubr4 |
C |
T |
4: 139,164,509 (GRCm39) |
|
probably benign |
Het |
Usp30 |
G |
A |
5: 114,241,888 (GRCm39) |
|
probably null |
Het |
Vmn1r195 |
A |
G |
13: 22,463,181 (GRCm39) |
Y217C |
probably damaging |
Het |
Vps33b |
T |
A |
7: 79,932,234 (GRCm39) |
D135E |
probably benign |
Het |
Vrk2 |
A |
G |
11: 26,433,331 (GRCm39) |
|
probably benign |
Het |
Wdr81 |
G |
T |
11: 75,343,809 (GRCm39) |
P486Q |
probably damaging |
Het |
Zfp788 |
T |
C |
7: 41,297,750 (GRCm39) |
Y129H |
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 |
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 |
R2131:Dapk1
|
UTSW |
13 |
60,877,345 (GRCm39) |
missense |
possibly damaging |
0.91 |
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'- CAGTCCGTGTGTCCCCATGTTATG -3'
(R):5'- ATCTTTCAGGCAGCTCAGGCTCAG -3'
Sequencing Primer
(F):5'- GTGTCCCCATGTTATGTCCTTG -3'
(R):5'- TTGGGATAACGATAGCCCATGC -3'
|
Posted On |
2014-01-15 |