Incidental Mutation 'R1893:Sphkap'
ID |
211663 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Sphkap
|
Ensembl Gene |
ENSMUSG00000026163 |
Gene Name |
SPHK1 interactor, AKAP domain containing |
Synonyms |
SKIP, A930009L15Rik, 4930544G21Rik |
MMRRC Submission |
039913-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.079)
|
Stock # |
R1893 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
1 |
Chromosomal Location |
83233163-83385853 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to A
at 83256687 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Proline to Leucine
at position 354
(P354L)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000124872
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000159078]
[ENSMUST00000160953]
|
AlphaFold |
no structure available at present |
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000053075
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000159078
AA Change: P67L
PolyPhen 2
Score 0.012 (Sensitivity: 0.96; Specificity: 0.78)
|
SMART Domains |
Protein: ENSMUSP00000124384 Gene: ENSMUSG00000026163 AA Change: P67L
Domain | Start | End | E-Value | Type |
low complexity region
|
303 |
314 |
N/A |
INTRINSIC |
SCOP:d1ash__
|
382 |
462 |
5e-3 |
SMART |
low complexity region
|
809 |
819 |
N/A |
INTRINSIC |
low complexity region
|
854 |
865 |
N/A |
INTRINSIC |
low complexity region
|
1202 |
1221 |
N/A |
INTRINSIC |
low complexity region
|
1243 |
1254 |
N/A |
INTRINSIC |
Pfam:AKAP_110
|
1281 |
1398 |
7.5e-13 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000160953
AA Change: P354L
PolyPhen 2
Score 0.019 (Sensitivity: 0.95; Specificity: 0.80)
|
SMART Domains |
Protein: ENSMUSP00000124872 Gene: ENSMUSG00000026163 AA Change: P354L
Domain | Start | End | E-Value | Type |
low complexity region
|
590 |
601 |
N/A |
INTRINSIC |
SCOP:d1ash__
|
669 |
749 |
6e-3 |
SMART |
low complexity region
|
1096 |
1106 |
N/A |
INTRINSIC |
low complexity region
|
1141 |
1152 |
N/A |
INTRINSIC |
low complexity region
|
1489 |
1508 |
N/A |
INTRINSIC |
Pfam:AKAP_110
|
1540 |
1655 |
6.4e-12 |
PFAM |
|
Meta Mutation Damage Score |
0.0898 |
Coding Region Coverage |
- 1x: 97.4%
- 3x: 96.8%
- 10x: 95.4%
- 20x: 93.0%
|
Validation Efficiency |
99% (99/100) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2210408I21Rik |
T |
C |
13: 77,415,928 (GRCm39) |
Y674H |
possibly damaging |
Het |
Aars2 |
G |
A |
17: 45,825,725 (GRCm39) |
R347Q |
probably benign |
Het |
Abca15 |
A |
T |
7: 119,939,776 (GRCm39) |
M293L |
possibly damaging |
Het |
Abcb7 |
A |
T |
X: 103,386,142 (GRCm39) |
H97Q |
probably damaging |
Het |
Aldh1l2 |
G |
T |
10: 83,328,400 (GRCm39) |
N772K |
probably damaging |
Het |
Ascc2 |
T |
A |
11: 4,622,305 (GRCm39) |
L457Q |
probably benign |
Het |
Aspm |
T |
A |
1: 139,407,605 (GRCm39) |
I2164N |
probably damaging |
Het |
Cabs1 |
A |
G |
5: 88,127,894 (GRCm39) |
T182A |
probably benign |
Het |
Carmil1 |
T |
C |
13: 24,208,446 (GRCm39) |
E833G |
possibly damaging |
Het |
Ccdc102a |
G |
A |
8: 95,640,171 (GRCm39) |
T41M |
probably damaging |
Het |
Cimap1c |
A |
G |
9: 56,756,498 (GRCm39) |
Y173H |
probably benign |
Het |
Clec2h |
T |
C |
6: 128,647,795 (GRCm39) |
V48A |
probably benign |
Het |
Cpb2 |
G |
A |
14: 75,493,403 (GRCm39) |
V27I |
probably benign |
Het |
Cr2 |
T |
C |
1: 194,837,495 (GRCm39) |
H1201R |
probably benign |
Het |
Cyp2d9 |
T |
C |
15: 82,336,807 (GRCm39) |
V52A |
probably damaging |
Het |
Cyp4a12a |
C |
A |
4: 115,183,864 (GRCm39) |
N223K |
probably benign |
Het |
Cyp7b1 |
G |
A |
3: 18,150,731 (GRCm39) |
S336L |
possibly damaging |
Het |
Dnah10 |
T |
C |
5: 124,831,381 (GRCm39) |
V803A |
probably benign |
Het |
Dnah17 |
T |
A |
11: 117,957,794 (GRCm39) |
T2745S |
probably benign |
Het |
Ep300 |
T |
A |
15: 81,515,847 (GRCm39) |
|
probably benign |
Het |
Epha3 |
A |
G |
16: 63,388,762 (GRCm39) |
S829P |
probably damaging |
Het |
Fads3 |
C |
A |
19: 10,033,868 (GRCm39) |
H418N |
probably benign |
Het |
Fat1 |
T |
C |
8: 45,476,893 (GRCm39) |
S1980P |
probably damaging |
Het |
Fgf20 |
T |
C |
8: 40,732,844 (GRCm39) |
E198G |
possibly damaging |
Het |
Fgl2 |
G |
A |
5: 21,580,669 (GRCm39) |
R337H |
probably benign |
Het |
Gbp2 |
G |
T |
3: 142,335,933 (GRCm39) |
|
probably benign |
Het |
Gja10 |
G |
A |
4: 32,601,541 (GRCm39) |
S281L |
probably benign |
Het |
Gm5422 |
G |
A |
10: 31,125,609 (GRCm39) |
|
noncoding transcript |
Het |
Gmpr |
T |
A |
13: 45,674,423 (GRCm39) |
D129E |
possibly damaging |
Het |
Gtf3c4 |
C |
T |
2: 28,724,374 (GRCm39) |
V453I |
possibly damaging |
Het |
Heatr6 |
T |
C |
11: 83,648,140 (GRCm39) |
V111A |
probably benign |
Het |
Hipk3 |
G |
A |
2: 104,263,601 (GRCm39) |
R905W |
probably damaging |
Het |
Hpn |
T |
A |
7: 30,798,773 (GRCm39) |
D103V |
probably damaging |
Het |
Ipcef1 |
G |
A |
10: 6,850,680 (GRCm39) |
R304W |
probably damaging |
Het |
Iqcb1 |
A |
G |
16: 36,652,245 (GRCm39) |
D52G |
probably damaging |
Het |
Klhdc7b |
C |
T |
15: 89,271,898 (GRCm39) |
|
probably null |
Het |
Klhl1 |
A |
T |
14: 96,477,642 (GRCm39) |
|
probably null |
Het |
Lrrn1 |
A |
T |
6: 107,545,083 (GRCm39) |
I294F |
possibly damaging |
Het |
Map3k1 |
A |
T |
13: 111,904,567 (GRCm39) |
F406I |
possibly damaging |
Het |
Map4k4 |
T |
A |
1: 40,040,717 (GRCm39) |
V579E |
probably benign |
Het |
Mapre2 |
A |
G |
18: 23,986,774 (GRCm39) |
K62R |
probably damaging |
Het |
Mdga1 |
A |
T |
17: 30,068,200 (GRCm39) |
Y305N |
probably damaging |
Het |
Mgl2 |
T |
A |
11: 70,024,993 (GRCm39) |
|
probably null |
Het |
Mnx1 |
C |
T |
5: 29,682,828 (GRCm39) |
G149D |
unknown |
Het |
Mtbp |
T |
A |
15: 55,421,064 (GRCm39) |
S17T |
probably benign |
Het |
Neu3 |
T |
C |
7: 99,472,627 (GRCm39) |
T37A |
possibly damaging |
Het |
Nr1i3 |
T |
C |
1: 171,044,792 (GRCm39) |
|
probably null |
Het |
Or10al2 |
A |
T |
17: 37,983,747 (GRCm39) |
K278* |
probably null |
Het |
Or10g6 |
A |
T |
9: 39,934,270 (GRCm39) |
I194F |
possibly damaging |
Het |
Or6ae1 |
T |
C |
7: 139,742,734 (GRCm39) |
N43S |
probably damaging |
Het |
Or9s18 |
T |
A |
13: 65,300,806 (GRCm39) |
M256K |
possibly damaging |
Het |
Osr2 |
A |
G |
15: 35,300,608 (GRCm39) |
T55A |
possibly damaging |
Het |
Palld |
A |
G |
8: 61,969,655 (GRCm39) |
V981A |
probably damaging |
Het |
Pbx1 |
A |
T |
1: 168,030,979 (GRCm39) |
M213K |
possibly damaging |
Het |
Pcdhb12 |
C |
A |
18: 37,570,136 (GRCm39) |
H427Q |
probably benign |
Het |
Perm1 |
C |
T |
4: 156,302,340 (GRCm39) |
R295C |
probably benign |
Het |
Phaf1 |
G |
T |
8: 105,973,133 (GRCm39) |
V248F |
probably damaging |
Het |
Polm |
T |
C |
11: 5,785,574 (GRCm39) |
T162A |
possibly damaging |
Het |
Prox1 |
A |
G |
1: 189,892,715 (GRCm39) |
|
probably benign |
Het |
Ptpn7 |
A |
T |
1: 135,062,641 (GRCm39) |
T127S |
probably benign |
Het |
Pxk |
C |
T |
14: 8,151,507 (GRCm38) |
R441* |
probably null |
Het |
Rab21 |
T |
C |
10: 115,126,805 (GRCm39) |
T181A |
probably benign |
Het |
Rab38 |
A |
T |
7: 88,139,924 (GRCm39) |
T198S |
probably benign |
Het |
Rnase4 |
C |
G |
14: 51,342,395 (GRCm39) |
Q40E |
possibly damaging |
Het |
Rnf213 |
T |
A |
11: 119,307,274 (GRCm39) |
W645R |
probably damaging |
Het |
Rnf8 |
A |
G |
17: 29,840,524 (GRCm39) |
I51M |
probably damaging |
Het |
Sbpl |
T |
A |
17: 24,172,241 (GRCm39) |
D226V |
unknown |
Het |
Sdf4 |
T |
G |
4: 156,085,205 (GRCm39) |
I180S |
probably benign |
Het |
Simc1 |
A |
G |
13: 54,687,528 (GRCm39) |
K99R |
probably damaging |
Het |
Slc2a4 |
T |
C |
11: 69,837,398 (GRCm39) |
Q49R |
probably damaging |
Het |
Slco1a4 |
T |
C |
6: 141,780,342 (GRCm39) |
|
probably null |
Het |
Slco5a1 |
C |
A |
1: 12,964,696 (GRCm39) |
C527F |
probably damaging |
Het |
Sox6 |
T |
A |
7: 115,143,803 (GRCm39) |
N405I |
probably benign |
Het |
Spi1 |
A |
G |
2: 90,944,702 (GRCm39) |
D149G |
probably benign |
Het |
Sptan1 |
T |
A |
2: 29,910,472 (GRCm39) |
D1812E |
probably damaging |
Het |
Sub1 |
A |
T |
15: 11,991,130 (GRCm39) |
V37E |
possibly damaging |
Het |
Sult2a6 |
T |
C |
7: 13,959,814 (GRCm39) |
T240A |
probably benign |
Het |
Tacc2 |
A |
G |
7: 130,227,055 (GRCm39) |
S1247G |
probably benign |
Het |
Taf4 |
T |
C |
2: 179,574,823 (GRCm39) |
D594G |
probably damaging |
Het |
Tap1 |
T |
G |
17: 34,413,915 (GRCm39) |
D643E |
probably damaging |
Het |
Ticam1 |
T |
C |
17: 56,578,894 (GRCm39) |
N67S |
probably benign |
Het |
Tlr6 |
A |
G |
5: 65,110,556 (GRCm39) |
F784L |
probably damaging |
Het |
Tmprss15 |
A |
G |
16: 78,868,306 (GRCm39) |
V202A |
probably benign |
Het |
Trp53bp2 |
T |
C |
1: 182,259,193 (GRCm39) |
V82A |
probably benign |
Het |
Ube2o |
C |
T |
11: 116,439,661 (GRCm39) |
V170I |
possibly damaging |
Het |
Ube2q2l |
A |
G |
6: 136,378,825 (GRCm39) |
S2P |
possibly damaging |
Het |
Vmn1r177 |
G |
A |
7: 23,565,573 (GRCm39) |
T101I |
probably benign |
Het |
Vmn2r68 |
A |
T |
7: 84,883,867 (GRCm39) |
Y79* |
probably null |
Het |
Wdr35 |
A |
C |
12: 9,035,994 (GRCm39) |
Y255S |
probably benign |
Het |
Zfp507 |
A |
T |
7: 35,502,052 (GRCm39) |
|
probably benign |
Het |
Zfp688 |
G |
A |
7: 127,018,409 (GRCm39) |
R239C |
probably damaging |
Het |
Zfp74 |
T |
A |
7: 29,635,470 (GRCm39) |
|
probably null |
Het |
Zfp932 |
A |
G |
5: 110,157,069 (GRCm39) |
N223D |
possibly damaging |
Het |
|
Other mutations in Sphkap |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00332:Sphkap
|
APN |
1 |
83,258,237 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00337:Sphkap
|
APN |
1 |
83,317,329 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00470:Sphkap
|
APN |
1 |
83,255,631 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL00577:Sphkap
|
APN |
1 |
83,256,565 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00657:Sphkap
|
APN |
1 |
83,254,096 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01868:Sphkap
|
APN |
1 |
83,258,120 (GRCm39) |
splice site |
probably null |
|
IGL02101:Sphkap
|
APN |
1 |
83,268,708 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02471:Sphkap
|
APN |
1 |
83,253,897 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02943:Sphkap
|
APN |
1 |
83,254,552 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02945:Sphkap
|
APN |
1 |
83,254,552 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03008:Sphkap
|
APN |
1 |
83,254,552 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03031:Sphkap
|
APN |
1 |
83,254,552 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03059:Sphkap
|
APN |
1 |
83,234,963 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03085:Sphkap
|
APN |
1 |
83,258,075 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL03355:Sphkap
|
APN |
1 |
83,258,224 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03356:Sphkap
|
APN |
1 |
83,254,552 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03368:Sphkap
|
APN |
1 |
83,253,397 (GRCm39) |
missense |
probably benign |
0.14 |
R0294:Sphkap
|
UTSW |
1 |
83,255,966 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0308:Sphkap
|
UTSW |
1 |
83,254,690 (GRCm39) |
missense |
probably damaging |
1.00 |
R0478:Sphkap
|
UTSW |
1 |
83,256,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R0606:Sphkap
|
UTSW |
1 |
83,258,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R0678:Sphkap
|
UTSW |
1 |
83,256,349 (GRCm39) |
missense |
probably benign |
0.03 |
R1216:Sphkap
|
UTSW |
1 |
83,268,698 (GRCm39) |
missense |
probably damaging |
1.00 |
R1253:Sphkap
|
UTSW |
1 |
83,256,619 (GRCm39) |
missense |
possibly damaging |
0.56 |
R1532:Sphkap
|
UTSW |
1 |
83,234,924 (GRCm39) |
missense |
probably damaging |
1.00 |
R1635:Sphkap
|
UTSW |
1 |
83,256,121 (GRCm39) |
missense |
probably benign |
0.03 |
R1655:Sphkap
|
UTSW |
1 |
83,255,236 (GRCm39) |
nonsense |
probably null |
|
R1657:Sphkap
|
UTSW |
1 |
83,255,236 (GRCm39) |
nonsense |
probably null |
|
R1700:Sphkap
|
UTSW |
1 |
83,255,236 (GRCm39) |
nonsense |
probably null |
|
R1701:Sphkap
|
UTSW |
1 |
83,255,236 (GRCm39) |
nonsense |
probably null |
|
R1734:Sphkap
|
UTSW |
1 |
83,255,236 (GRCm39) |
nonsense |
probably null |
|
R1736:Sphkap
|
UTSW |
1 |
83,255,236 (GRCm39) |
nonsense |
probably null |
|
R1743:Sphkap
|
UTSW |
1 |
83,255,236 (GRCm39) |
nonsense |
probably null |
|
R1744:Sphkap
|
UTSW |
1 |
83,255,236 (GRCm39) |
nonsense |
probably null |
|
R1760:Sphkap
|
UTSW |
1 |
83,255,265 (GRCm39) |
missense |
probably benign |
0.29 |
R1937:Sphkap
|
UTSW |
1 |
83,245,162 (GRCm39) |
nonsense |
probably null |
|
R1986:Sphkap
|
UTSW |
1 |
83,255,643 (GRCm39) |
missense |
probably damaging |
1.00 |
R1993:Sphkap
|
UTSW |
1 |
83,255,236 (GRCm39) |
nonsense |
probably null |
|
R1995:Sphkap
|
UTSW |
1 |
83,255,236 (GRCm39) |
nonsense |
probably null |
|
R2001:Sphkap
|
UTSW |
1 |
83,254,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R2004:Sphkap
|
UTSW |
1 |
83,255,632 (GRCm39) |
missense |
probably benign |
0.04 |
R2111:Sphkap
|
UTSW |
1 |
83,253,602 (GRCm39) |
missense |
probably benign |
0.00 |
R2112:Sphkap
|
UTSW |
1 |
83,253,602 (GRCm39) |
missense |
probably benign |
0.00 |
R2156:Sphkap
|
UTSW |
1 |
83,255,710 (GRCm39) |
missense |
probably benign |
0.03 |
R2182:Sphkap
|
UTSW |
1 |
83,254,405 (GRCm39) |
missense |
probably damaging |
1.00 |
R2271:Sphkap
|
UTSW |
1 |
83,234,942 (GRCm39) |
missense |
probably damaging |
1.00 |
R3712:Sphkap
|
UTSW |
1 |
83,254,833 (GRCm39) |
missense |
probably benign |
0.27 |
R3919:Sphkap
|
UTSW |
1 |
83,254,179 (GRCm39) |
missense |
probably damaging |
1.00 |
R3980:Sphkap
|
UTSW |
1 |
83,245,215 (GRCm39) |
splice site |
probably null |
|
R4130:Sphkap
|
UTSW |
1 |
83,255,619 (GRCm39) |
missense |
probably damaging |
0.96 |
R4539:Sphkap
|
UTSW |
1 |
83,255,514 (GRCm39) |
missense |
probably benign |
0.00 |
R4602:Sphkap
|
UTSW |
1 |
83,256,782 (GRCm39) |
nonsense |
probably null |
|
R4735:Sphkap
|
UTSW |
1 |
83,256,838 (GRCm39) |
missense |
probably benign |
0.01 |
R4793:Sphkap
|
UTSW |
1 |
83,255,805 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4849:Sphkap
|
UTSW |
1 |
83,255,105 (GRCm39) |
missense |
probably benign |
0.03 |
R4880:Sphkap
|
UTSW |
1 |
83,266,538 (GRCm39) |
missense |
probably damaging |
1.00 |
R5213:Sphkap
|
UTSW |
1 |
83,258,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R5277:Sphkap
|
UTSW |
1 |
83,253,885 (GRCm39) |
missense |
probably benign |
0.04 |
R5331:Sphkap
|
UTSW |
1 |
83,254,503 (GRCm39) |
missense |
probably benign |
0.08 |
R5632:Sphkap
|
UTSW |
1 |
83,256,006 (GRCm39) |
missense |
probably benign |
0.01 |
R5647:Sphkap
|
UTSW |
1 |
83,385,720 (GRCm39) |
missense |
probably damaging |
0.98 |
R5751:Sphkap
|
UTSW |
1 |
83,253,618 (GRCm39) |
missense |
probably benign |
0.27 |
R5935:Sphkap
|
UTSW |
1 |
83,317,320 (GRCm39) |
missense |
probably damaging |
1.00 |
R5999:Sphkap
|
UTSW |
1 |
83,245,126 (GRCm39) |
missense |
probably benign |
0.02 |
R6232:Sphkap
|
UTSW |
1 |
83,258,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R6318:Sphkap
|
UTSW |
1 |
83,256,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R6474:Sphkap
|
UTSW |
1 |
83,256,544 (GRCm39) |
missense |
probably damaging |
1.00 |
R6602:Sphkap
|
UTSW |
1 |
83,253,479 (GRCm39) |
missense |
possibly damaging |
0.75 |
R6674:Sphkap
|
UTSW |
1 |
83,255,555 (GRCm39) |
missense |
probably benign |
0.37 |
R6716:Sphkap
|
UTSW |
1 |
83,339,949 (GRCm39) |
critical splice donor site |
probably null |
|
R6803:Sphkap
|
UTSW |
1 |
83,258,231 (GRCm39) |
missense |
probably damaging |
1.00 |
R6880:Sphkap
|
UTSW |
1 |
83,234,978 (GRCm39) |
missense |
probably damaging |
1.00 |
R6941:Sphkap
|
UTSW |
1 |
83,385,811 (GRCm39) |
start gained |
probably benign |
|
R7170:Sphkap
|
UTSW |
1 |
83,243,706 (GRCm39) |
missense |
probably damaging |
0.99 |
R7263:Sphkap
|
UTSW |
1 |
83,254,399 (GRCm39) |
missense |
probably damaging |
1.00 |
R7422:Sphkap
|
UTSW |
1 |
83,241,547 (GRCm39) |
missense |
probably benign |
0.02 |
R7640:Sphkap
|
UTSW |
1 |
83,256,649 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7722:Sphkap
|
UTSW |
1 |
83,256,642 (GRCm39) |
missense |
probably benign |
0.00 |
R7810:Sphkap
|
UTSW |
1 |
83,254,021 (GRCm39) |
missense |
probably damaging |
1.00 |
R7887:Sphkap
|
UTSW |
1 |
83,255,133 (GRCm39) |
missense |
probably benign |
0.00 |
R7974:Sphkap
|
UTSW |
1 |
83,256,683 (GRCm39) |
missense |
probably damaging |
1.00 |
R7990:Sphkap
|
UTSW |
1 |
83,245,066 (GRCm39) |
missense |
probably damaging |
0.99 |
R8096:Sphkap
|
UTSW |
1 |
83,255,279 (GRCm39) |
missense |
probably damaging |
0.98 |
R8110:Sphkap
|
UTSW |
1 |
83,256,492 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8125:Sphkap
|
UTSW |
1 |
83,241,303 (GRCm39) |
missense |
probably damaging |
1.00 |
R8153:Sphkap
|
UTSW |
1 |
83,255,730 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8245:Sphkap
|
UTSW |
1 |
83,256,492 (GRCm39) |
missense |
probably benign |
0.14 |
R8394:Sphkap
|
UTSW |
1 |
83,253,797 (GRCm39) |
missense |
probably benign |
0.08 |
R8443:Sphkap
|
UTSW |
1 |
83,255,953 (GRCm39) |
missense |
probably benign |
0.00 |
R8508:Sphkap
|
UTSW |
1 |
83,254,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R8531:Sphkap
|
UTSW |
1 |
83,254,909 (GRCm39) |
missense |
probably damaging |
1.00 |
R8673:Sphkap
|
UTSW |
1 |
83,253,561 (GRCm39) |
missense |
probably benign |
0.01 |
R8674:Sphkap
|
UTSW |
1 |
83,255,565 (GRCm39) |
missense |
probably benign |
0.04 |
R8682:Sphkap
|
UTSW |
1 |
83,256,997 (GRCm39) |
missense |
probably benign |
0.21 |
R8837:Sphkap
|
UTSW |
1 |
83,253,384 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8857:Sphkap
|
UTSW |
1 |
83,258,288 (GRCm39) |
missense |
probably damaging |
1.00 |
R8902:Sphkap
|
UTSW |
1 |
83,256,685 (GRCm39) |
missense |
probably benign |
0.21 |
R8916:Sphkap
|
UTSW |
1 |
83,255,108 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8944:Sphkap
|
UTSW |
1 |
83,256,927 (GRCm39) |
missense |
probably benign |
0.39 |
R9154:Sphkap
|
UTSW |
1 |
83,234,982 (GRCm39) |
missense |
probably damaging |
1.00 |
R9579:Sphkap
|
UTSW |
1 |
83,255,295 (GRCm39) |
missense |
probably damaging |
0.99 |
R9616:Sphkap
|
UTSW |
1 |
83,254,989 (GRCm39) |
missense |
probably damaging |
1.00 |
R9781:Sphkap
|
UTSW |
1 |
83,255,772 (GRCm39) |
missense |
possibly damaging |
0.62 |
Z1088:Sphkap
|
UTSW |
1 |
83,256,325 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Sphkap
|
UTSW |
1 |
83,254,329 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Sphkap
|
UTSW |
1 |
83,258,163 (GRCm39) |
missense |
possibly damaging |
0.61 |
Z1176:Sphkap
|
UTSW |
1 |
83,253,754 (GRCm39) |
nonsense |
probably null |
|
Z1177:Sphkap
|
UTSW |
1 |
83,254,152 (GRCm39) |
missense |
probably damaging |
0.96 |
|
Predicted Primers |
PCR Primer
(F):5'- GGAGAGCACTTCGCATAGAG -3'
(R):5'- CACGTCCTTGAAAAGTCTCAATCG -3'
Sequencing Primer
(F):5'- AACTGACTGCAGATTCCTGG -3'
(R):5'- AAGTCTCAATCGTTTAGTCAGGCC -3'
|
Posted On |
2014-06-30 |