Incidental Mutation 'R0268:Casp8ap2'
ID |
35051 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Casp8ap2
|
Ensembl Gene |
ENSMUSG00000028282 |
Gene Name |
caspase 8 associated protein 2 |
Synonyms |
FLASH, D4Ertd659e |
MMRRC Submission |
038494-MU
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R0268 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
4 |
Chromosomal Location |
32615462-32653271 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 32644079 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Isoleucine to Phenylalanine
at position 1051
(I1051F)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000136016
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000029950]
[ENSMUST00000108178]
[ENSMUST00000178925]
|
AlphaFold |
Q9WUF3 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000029950
AA Change: I1051F
PolyPhen 2
Score 0.993 (Sensitivity: 0.70; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000029950 Gene: ENSMUSG00000028282 AA Change: I1051F
Domain | Start | End | E-Value | Type |
coiled coil region
|
68 |
142 |
N/A |
INTRINSIC |
low complexity region
|
292 |
303 |
N/A |
INTRINSIC |
low complexity region
|
458 |
477 |
N/A |
INTRINSIC |
low complexity region
|
1124 |
1135 |
N/A |
INTRINSIC |
low complexity region
|
1250 |
1268 |
N/A |
INTRINSIC |
low complexity region
|
1360 |
1377 |
N/A |
INTRINSIC |
low complexity region
|
1458 |
1470 |
N/A |
INTRINSIC |
low complexity region
|
1477 |
1498 |
N/A |
INTRINSIC |
low complexity region
|
1882 |
1895 |
N/A |
INTRINSIC |
PDB:2LR8|A
|
1896 |
1962 |
1e-31 |
PDB |
Blast:SANT
|
1905 |
1955 |
2e-21 |
BLAST |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000108178
|
SMART Domains |
Protein: ENSMUSP00000103813 Gene: ENSMUSG00000028282
Domain | Start | End | E-Value | Type |
PDB:2LR8|A
|
126 |
190 |
4e-26 |
PDB |
Blast:SANT
|
139 |
183 |
4e-19 |
BLAST |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000127619
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000178925
AA Change: I1051F
PolyPhen 2
Score 0.993 (Sensitivity: 0.70; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000136016 Gene: ENSMUSG00000028282 AA Change: I1051F
Domain | Start | End | E-Value | Type |
coiled coil region
|
68 |
142 |
N/A |
INTRINSIC |
low complexity region
|
292 |
303 |
N/A |
INTRINSIC |
low complexity region
|
458 |
477 |
N/A |
INTRINSIC |
low complexity region
|
1124 |
1135 |
N/A |
INTRINSIC |
low complexity region
|
1250 |
1268 |
N/A |
INTRINSIC |
low complexity region
|
1360 |
1377 |
N/A |
INTRINSIC |
low complexity region
|
1458 |
1470 |
N/A |
INTRINSIC |
low complexity region
|
1477 |
1498 |
N/A |
INTRINSIC |
low complexity region
|
1882 |
1895 |
N/A |
INTRINSIC |
PDB:2LR8|A
|
1896 |
1962 |
1e-31 |
PDB |
Blast:SANT
|
1905 |
1955 |
2e-21 |
BLAST |
|
Meta Mutation Damage Score |
0.1091 |
Coding Region Coverage |
- 1x: 98.7%
- 3x: 97.7%
- 10x: 95.9%
- 20x: 93.0%
|
Validation Efficiency |
98% (93/95) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This protein is highly similar to FLASH, a mouse apoptotic protein identified by its interaction with the death-effector domain (DED) of caspase 8. Studies of FLASH protein suggested that this protein may be a component of the death-inducing signaling complex that includes Fas receptor, Fas-binding adapter FADD, and caspase 8, and plays a regulatory role in Fas-mediated apoptosis. Alternative splicing results in multiple transcript variants encoding the same protein.[provided by RefSeq, Nov 2008] PHENOTYPE: Mice homozygous for disruption of this gene die before implantation. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 87 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930432E11Rik |
T |
A |
7: 29,274,027 (GRCm39) |
|
noncoding transcript |
Het |
Aadacl4 |
A |
T |
4: 144,349,565 (GRCm39) |
H274L |
probably benign |
Het |
Aldh1a7 |
T |
A |
19: 20,686,866 (GRCm39) |
|
probably null |
Het |
Ap3m1 |
A |
C |
14: 21,087,170 (GRCm39) |
|
probably benign |
Het |
Atp5f1a |
C |
A |
18: 77,867,895 (GRCm39) |
N356K |
probably damaging |
Het |
AU021092 |
A |
T |
16: 5,040,031 (GRCm39) |
M31K |
possibly damaging |
Het |
Avpr1a |
T |
C |
10: 122,285,614 (GRCm39) |
V302A |
probably damaging |
Het |
Bicral |
A |
G |
17: 47,124,978 (GRCm39) |
|
probably benign |
Het |
Btbd9 |
C |
T |
17: 30,493,916 (GRCm39) |
D492N |
possibly damaging |
Het |
Cd209e |
T |
C |
8: 3,899,125 (GRCm39) |
I196V |
probably benign |
Het |
Cdc42bpa |
G |
T |
1: 179,983,347 (GRCm39) |
|
probably benign |
Het |
Cdcp3 |
A |
G |
7: 130,839,905 (GRCm39) |
D609G |
probably damaging |
Het |
Clec16a |
T |
A |
16: 10,462,692 (GRCm39) |
L670* |
probably null |
Het |
Cmtm2b |
A |
G |
8: 105,049,066 (GRCm39) |
E27G |
probably damaging |
Het |
Col4a1 |
T |
A |
8: 11,317,588 (GRCm39) |
|
probably benign |
Het |
Cyp26b1 |
A |
T |
6: 84,551,554 (GRCm39) |
F221I |
probably damaging |
Het |
D430041D05Rik |
G |
C |
2: 103,998,295 (GRCm39) |
P1836R |
probably damaging |
Het |
Dennd6b |
T |
C |
15: 89,080,432 (GRCm39) |
Q56R |
probably benign |
Het |
Dip2c |
G |
A |
13: 9,687,186 (GRCm39) |
R1270H |
probably damaging |
Het |
Dlg1 |
T |
C |
16: 31,503,011 (GRCm39) |
C73R |
probably benign |
Het |
Dnah8 |
A |
G |
17: 30,988,681 (GRCm39) |
D3217G |
probably damaging |
Het |
Dtx1 |
T |
C |
5: 120,819,356 (GRCm39) |
E614G |
probably damaging |
Het |
Dut |
C |
A |
2: 125,099,011 (GRCm39) |
A166E |
probably damaging |
Het |
Ebf1 |
C |
A |
11: 44,534,240 (GRCm39) |
D166E |
probably damaging |
Het |
Egln2 |
A |
T |
7: 26,864,672 (GRCm39) |
D84E |
possibly damaging |
Het |
Exosc7 |
T |
A |
9: 122,948,025 (GRCm39) |
S65T |
probably benign |
Het |
Fam83e |
G |
A |
7: 45,376,334 (GRCm39) |
R349Q |
probably benign |
Het |
Fbxl17 |
G |
A |
17: 63,692,062 (GRCm39) |
|
probably benign |
Het |
Fras1 |
A |
G |
5: 96,884,868 (GRCm39) |
N2582S |
probably damaging |
Het |
Fubp1 |
T |
C |
3: 151,925,350 (GRCm39) |
V164A |
probably damaging |
Het |
Gfral |
A |
T |
9: 76,104,383 (GRCm39) |
C210S |
probably damaging |
Het |
Gls |
GGCTGCTGCTGCTGCTGCTGCTGCTGCTG |
GGCTGCTGCTGCTGCTGCTGCTGCTG |
1: 52,271,853 (GRCm39) |
|
probably benign |
Het |
Hcn4 |
A |
C |
9: 58,767,445 (GRCm39) |
E1002A |
unknown |
Het |
Hcrtr2 |
A |
G |
9: 76,135,470 (GRCm39) |
V449A |
probably benign |
Het |
Hectd1 |
T |
C |
12: 51,815,891 (GRCm39) |
S1394G |
possibly damaging |
Het |
Hectd1 |
C |
A |
12: 51,815,890 (GRCm39) |
S1394I |
probably damaging |
Het |
Hecw2 |
A |
G |
1: 53,965,857 (GRCm39) |
|
probably benign |
Het |
Herc3 |
A |
G |
6: 58,845,613 (GRCm39) |
|
probably benign |
Het |
Ipo4 |
T |
C |
14: 55,863,399 (GRCm39) |
Q1073R |
possibly damaging |
Het |
Itsn2 |
G |
A |
12: 4,750,333 (GRCm39) |
R1199Q |
probably benign |
Het |
Kcnj3 |
C |
A |
2: 55,484,971 (GRCm39) |
Y356* |
probably null |
Het |
Klb |
T |
A |
5: 65,506,180 (GRCm39) |
D142E |
probably benign |
Het |
Klhl35 |
T |
A |
7: 99,120,958 (GRCm39) |
S409T |
probably benign |
Het |
Krt16 |
T |
A |
11: 100,137,351 (GRCm39) |
|
probably benign |
Het |
Krt82 |
C |
A |
15: 101,450,148 (GRCm39) |
R516L |
probably benign |
Het |
Lce3a |
A |
T |
3: 92,833,038 (GRCm39) |
C21S |
unknown |
Het |
Lims2 |
A |
G |
18: 32,077,573 (GRCm39) |
E103G |
probably benign |
Het |
Map2 |
A |
T |
1: 66,419,881 (GRCm39) |
K71* |
probably null |
Het |
Mthfr |
C |
G |
4: 148,139,885 (GRCm39) |
S618W |
probably damaging |
Het |
Mycbp2 |
T |
A |
14: 103,551,761 (GRCm39) |
R157* |
probably null |
Het |
Nat10 |
C |
A |
2: 103,558,262 (GRCm39) |
|
probably benign |
Het |
Obscn |
G |
A |
11: 58,958,098 (GRCm39) |
T3810M |
possibly damaging |
Het |
Or13a19 |
G |
A |
7: 139,903,068 (GRCm39) |
S152N |
possibly damaging |
Het |
Or1x6 |
T |
A |
11: 50,939,768 (GRCm39) |
M278K |
probably damaging |
Het |
Or5d35 |
A |
T |
2: 87,855,812 (GRCm39) |
I249F |
probably damaging |
Het |
Or5g29 |
A |
G |
2: 85,421,645 (GRCm39) |
T254A |
possibly damaging |
Het |
Or6c209 |
A |
T |
10: 129,483,045 (GRCm39) |
D16V |
possibly damaging |
Het |
Or7a38 |
C |
T |
10: 78,753,439 (GRCm39) |
T255I |
probably damaging |
Het |
Park7 |
A |
G |
4: 150,992,806 (GRCm39) |
V20A |
possibly damaging |
Het |
Pgm2 |
T |
A |
5: 64,263,151 (GRCm39) |
V266E |
probably damaging |
Het |
Phip |
G |
A |
9: 82,753,341 (GRCm39) |
T1801I |
probably damaging |
Het |
Pkhd1l1 |
C |
A |
15: 44,460,407 (GRCm39) |
H4205Q |
probably benign |
Het |
Ppp1r12a |
T |
A |
10: 108,109,242 (GRCm39) |
|
probably benign |
Het |
Pramel26 |
A |
T |
4: 143,537,338 (GRCm39) |
I331N |
probably damaging |
Het |
Ptprq |
A |
T |
10: 107,541,409 (GRCm39) |
D372E |
probably benign |
Het |
Ptprr |
G |
A |
10: 116,088,868 (GRCm39) |
V340I |
possibly damaging |
Het |
Qki |
A |
G |
17: 10,428,575 (GRCm39) |
|
probably benign |
Het |
Qpct |
T |
A |
17: 79,385,081 (GRCm39) |
D240E |
probably benign |
Het |
Ren1 |
A |
G |
1: 133,283,349 (GRCm39) |
T162A |
possibly damaging |
Het |
Rif1 |
T |
C |
2: 51,980,298 (GRCm39) |
|
probably null |
Het |
Sart3 |
A |
G |
5: 113,890,460 (GRCm39) |
V461A |
probably damaging |
Het |
Saxo4 |
A |
G |
19: 10,454,449 (GRCm39) |
V329A |
possibly damaging |
Het |
Scgb1b24 |
G |
A |
7: 33,443,278 (GRCm39) |
G19R |
probably null |
Het |
Spen |
A |
T |
4: 141,204,868 (GRCm39) |
I1253N |
unknown |
Het |
Sspo |
C |
A |
6: 48,442,489 (GRCm39) |
H1995N |
probably benign |
Het |
Tfap2c |
A |
G |
2: 172,393,423 (GRCm39) |
T113A |
probably benign |
Het |
Togaram2 |
T |
C |
17: 72,004,993 (GRCm39) |
|
probably null |
Het |
Trim65 |
T |
A |
11: 116,017,470 (GRCm39) |
|
probably benign |
Het |
Trpm3 |
T |
A |
19: 22,874,885 (GRCm39) |
|
probably null |
Het |
Ubxn7 |
T |
C |
16: 32,178,864 (GRCm39) |
I87T |
probably benign |
Het |
Vav1 |
T |
C |
17: 57,603,090 (GRCm39) |
F81L |
probably damaging |
Het |
Vmn2r102 |
A |
G |
17: 19,898,112 (GRCm39) |
T376A |
probably benign |
Het |
Vmn2r105 |
A |
T |
17: 20,428,938 (GRCm39) |
C713S |
probably benign |
Het |
Zbtb45 |
C |
T |
7: 12,742,254 (GRCm39) |
M1I |
probably null |
Het |
Zfp229 |
A |
T |
17: 21,964,822 (GRCm39) |
M351L |
probably benign |
Het |
Zfp932 |
T |
C |
5: 110,156,929 (GRCm39) |
I176T |
probably benign |
Het |
Zswim1 |
G |
A |
2: 164,668,046 (GRCm39) |
E433K |
probably damaging |
Het |
|
Other mutations in Casp8ap2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00686:Casp8ap2
|
APN |
4 |
32,641,433 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00714:Casp8ap2
|
APN |
4 |
32,649,192 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00754:Casp8ap2
|
APN |
4 |
32,641,036 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00954:Casp8ap2
|
APN |
4 |
32,645,403 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00970:Casp8ap2
|
APN |
4 |
32,646,182 (GRCm39) |
missense |
probably benign |
|
IGL01534:Casp8ap2
|
APN |
4 |
32,648,134 (GRCm39) |
splice site |
probably benign |
|
IGL01596:Casp8ap2
|
APN |
4 |
32,646,365 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01686:Casp8ap2
|
APN |
4 |
32,641,294 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02002:Casp8ap2
|
APN |
4 |
32,639,391 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02273:Casp8ap2
|
APN |
4 |
32,643,974 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02510:Casp8ap2
|
APN |
4 |
32,639,704 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02600:Casp8ap2
|
APN |
4 |
32,630,246 (GRCm39) |
missense |
probably null |
1.00 |
IGL02929:Casp8ap2
|
APN |
4 |
32,624,105 (GRCm39) |
utr 5 prime |
probably benign |
|
F5770:Casp8ap2
|
UTSW |
4 |
32,639,944 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02988:Casp8ap2
|
UTSW |
4 |
32,644,590 (GRCm39) |
missense |
probably benign |
0.14 |
R0023:Casp8ap2
|
UTSW |
4 |
32,640,185 (GRCm39) |
missense |
probably damaging |
0.99 |
R0027:Casp8ap2
|
UTSW |
4 |
32,643,810 (GRCm39) |
missense |
probably benign |
0.01 |
R0090:Casp8ap2
|
UTSW |
4 |
32,640,327 (GRCm39) |
missense |
probably damaging |
1.00 |
R0117:Casp8ap2
|
UTSW |
4 |
32,640,817 (GRCm39) |
missense |
probably benign |
0.00 |
R0144:Casp8ap2
|
UTSW |
4 |
32,643,797 (GRCm39) |
missense |
possibly damaging |
0.50 |
R0344:Casp8ap2
|
UTSW |
4 |
32,644,079 (GRCm39) |
missense |
probably damaging |
0.99 |
R0555:Casp8ap2
|
UTSW |
4 |
32,640,381 (GRCm39) |
missense |
probably damaging |
1.00 |
R1051:Casp8ap2
|
UTSW |
4 |
32,640,790 (GRCm39) |
missense |
probably benign |
0.28 |
R1165:Casp8ap2
|
UTSW |
4 |
32,640,563 (GRCm39) |
missense |
probably benign |
0.01 |
R1243:Casp8ap2
|
UTSW |
4 |
32,645,687 (GRCm39) |
missense |
probably benign |
0.03 |
R1311:Casp8ap2
|
UTSW |
4 |
32,648,111 (GRCm39) |
missense |
probably damaging |
0.98 |
R1337:Casp8ap2
|
UTSW |
4 |
32,645,721 (GRCm39) |
missense |
possibly damaging |
0.64 |
R1471:Casp8ap2
|
UTSW |
4 |
32,639,386 (GRCm39) |
nonsense |
probably null |
|
R1497:Casp8ap2
|
UTSW |
4 |
32,639,938 (GRCm39) |
missense |
probably benign |
0.00 |
R1521:Casp8ap2
|
UTSW |
4 |
32,631,867 (GRCm39) |
missense |
probably damaging |
1.00 |
R1588:Casp8ap2
|
UTSW |
4 |
32,640,541 (GRCm39) |
missense |
probably benign |
0.00 |
R1625:Casp8ap2
|
UTSW |
4 |
32,648,068 (GRCm39) |
missense |
probably benign |
0.04 |
R1731:Casp8ap2
|
UTSW |
4 |
32,641,442 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1899:Casp8ap2
|
UTSW |
4 |
32,643,647 (GRCm39) |
missense |
probably damaging |
0.98 |
R2000:Casp8ap2
|
UTSW |
4 |
32,634,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R2021:Casp8ap2
|
UTSW |
4 |
32,644,560 (GRCm39) |
missense |
probably benign |
0.05 |
R2022:Casp8ap2
|
UTSW |
4 |
32,644,560 (GRCm39) |
missense |
probably benign |
0.05 |
R2023:Casp8ap2
|
UTSW |
4 |
32,644,560 (GRCm39) |
missense |
probably benign |
0.05 |
R2088:Casp8ap2
|
UTSW |
4 |
32,631,126 (GRCm39) |
missense |
probably damaging |
1.00 |
R2104:Casp8ap2
|
UTSW |
4 |
32,644,727 (GRCm39) |
missense |
probably benign |
0.00 |
R2128:Casp8ap2
|
UTSW |
4 |
32,640,142 (GRCm39) |
missense |
probably benign |
0.06 |
R2129:Casp8ap2
|
UTSW |
4 |
32,640,142 (GRCm39) |
missense |
probably benign |
0.06 |
R2305:Casp8ap2
|
UTSW |
4 |
32,646,411 (GRCm39) |
missense |
probably damaging |
1.00 |
R2316:Casp8ap2
|
UTSW |
4 |
32,643,781 (GRCm39) |
missense |
probably benign |
0.31 |
R2919:Casp8ap2
|
UTSW |
4 |
32,645,343 (GRCm39) |
missense |
probably damaging |
1.00 |
R4091:Casp8ap2
|
UTSW |
4 |
32,643,611 (GRCm39) |
missense |
probably damaging |
1.00 |
R4357:Casp8ap2
|
UTSW |
4 |
32,646,150 (GRCm39) |
missense |
probably benign |
0.00 |
R4807:Casp8ap2
|
UTSW |
4 |
32,644,505 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4828:Casp8ap2
|
UTSW |
4 |
32,639,807 (GRCm39) |
missense |
probably benign |
|
R4908:Casp8ap2
|
UTSW |
4 |
32,639,905 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4945:Casp8ap2
|
UTSW |
4 |
32,631,163 (GRCm39) |
missense |
possibly damaging |
0.57 |
R4962:Casp8ap2
|
UTSW |
4 |
32,640,554 (GRCm39) |
missense |
probably damaging |
0.99 |
R6014:Casp8ap2
|
UTSW |
4 |
32,641,400 (GRCm39) |
missense |
probably damaging |
0.97 |
R6092:Casp8ap2
|
UTSW |
4 |
32,639,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R6257:Casp8ap2
|
UTSW |
4 |
32,641,364 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6289:Casp8ap2
|
UTSW |
4 |
32,639,590 (GRCm39) |
missense |
probably damaging |
1.00 |
R6482:Casp8ap2
|
UTSW |
4 |
32,634,813 (GRCm39) |
missense |
probably damaging |
1.00 |
R6496:Casp8ap2
|
UTSW |
4 |
32,641,553 (GRCm39) |
missense |
probably benign |
0.05 |
R6515:Casp8ap2
|
UTSW |
4 |
32,646,423 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7015:Casp8ap2
|
UTSW |
4 |
32,644,278 (GRCm39) |
missense |
probably damaging |
1.00 |
R7033:Casp8ap2
|
UTSW |
4 |
32,639,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R7072:Casp8ap2
|
UTSW |
4 |
32,644,766 (GRCm39) |
missense |
probably damaging |
1.00 |
R7448:Casp8ap2
|
UTSW |
4 |
32,643,974 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7944:Casp8ap2
|
UTSW |
4 |
32,645,909 (GRCm39) |
missense |
probably benign |
0.12 |
R7945:Casp8ap2
|
UTSW |
4 |
32,645,909 (GRCm39) |
missense |
probably benign |
0.12 |
R8170:Casp8ap2
|
UTSW |
4 |
32,615,490 (GRCm39) |
splice site |
probably benign |
|
R8179:Casp8ap2
|
UTSW |
4 |
32,643,939 (GRCm39) |
nonsense |
probably null |
|
R8207:Casp8ap2
|
UTSW |
4 |
32,646,446 (GRCm39) |
missense |
possibly damaging |
0.63 |
R8263:Casp8ap2
|
UTSW |
4 |
32,644,072 (GRCm39) |
missense |
probably damaging |
1.00 |
R8298:Casp8ap2
|
UTSW |
4 |
32,640,429 (GRCm39) |
missense |
probably benign |
0.30 |
R9441:Casp8ap2
|
UTSW |
4 |
32,645,873 (GRCm39) |
missense |
probably benign |
0.00 |
R9455:Casp8ap2
|
UTSW |
4 |
32,643,924 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9729:Casp8ap2
|
UTSW |
4 |
32,643,807 (GRCm39) |
missense |
possibly damaging |
0.71 |
V7580:Casp8ap2
|
UTSW |
4 |
32,639,944 (GRCm39) |
missense |
probably benign |
0.00 |
X0018:Casp8ap2
|
UTSW |
4 |
32,643,738 (GRCm39) |
missense |
probably benign |
0.03 |
|
Predicted Primers |
PCR Primer
(F):5'- AGGACTGCTGTAAAACTCCCTCGG -3'
(R):5'- AACGGTCAACTATGCCATTCTTCTTCA -3'
Sequencing Primer
(F):5'- TGTAAAACTCCCTCGGGACAG -3'
(R):5'- GCCATTCTTCTTCACTTGTTTAAGG -3'
|
Posted On |
2013-05-09 |