Incidental Mutation 'R0606:Sphkap'
ID |
216248 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Sphkap
|
Ensembl Gene |
ENSMUSG00000026163 |
Gene Name |
SPHK1 interactor, AKAP domain containing |
Synonyms |
SKIP, A930009L15Rik, 4930544G21Rik |
MMRRC Submission |
038795-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.079)
|
Stock # |
R0606 (G1)
|
Quality Score |
79 |
Status
|
Validated
|
Chromosome |
1 |
Chromosomal Location |
83233163-83385853 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 83258145 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Aspartic acid to Glutamic Acid
at position 199
(D199E)
|
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
|
SMART Domains |
Protein: ENSMUSP00000124384 Gene: ENSMUSG00000026163
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 damaging
Transcript: ENSMUST00000160953
AA Change: D199E
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000124872 Gene: ENSMUSG00000026163 AA Change: D199E
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 |
0.0663 |
Coding Region Coverage |
- 1x: 99.3%
- 3x: 98.8%
- 10x: 97.3%
- 20x: 94.2%
|
Validation Efficiency |
98% (99/101) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 95 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actl9 |
T |
C |
17: 33,652,572 (GRCm39) |
Y211H |
probably damaging |
Het |
Actn1 |
A |
T |
12: 80,221,421 (GRCm39) |
|
probably benign |
Het |
Adtrp |
A |
G |
13: 41,920,881 (GRCm39) |
F197L |
probably damaging |
Het |
Ankrd11 |
G |
A |
8: 123,619,571 (GRCm39) |
T1406I |
probably benign |
Het |
Arhgap24 |
A |
T |
5: 103,045,086 (GRCm39) |
R620W |
probably damaging |
Het |
Atg13 |
A |
G |
2: 91,512,418 (GRCm39) |
Y284H |
probably benign |
Het |
Atrn |
A |
G |
2: 130,748,776 (GRCm39) |
E99G |
possibly damaging |
Het |
Cage1 |
A |
T |
13: 38,200,470 (GRCm39) |
|
probably benign |
Het |
Cblif |
A |
T |
19: 11,729,658 (GRCm39) |
I206F |
possibly damaging |
Het |
Ccr3 |
T |
A |
9: 123,828,839 (GRCm39) |
M58K |
probably benign |
Het |
Cdk18 |
G |
T |
1: 132,045,355 (GRCm39) |
|
probably benign |
Het |
Chst5 |
A |
G |
8: 112,617,551 (GRCm39) |
V23A |
probably benign |
Het |
Col4a3 |
T |
C |
1: 82,650,307 (GRCm39) |
|
probably benign |
Het |
Col4a6 |
A |
G |
X: 139,975,219 (GRCm39) |
|
probably benign |
Het |
Csmd3 |
T |
C |
15: 48,321,058 (GRCm39) |
I251V |
probably benign |
Het |
Csnk1g3 |
G |
A |
18: 54,050,100 (GRCm39) |
V115M |
probably damaging |
Het |
Cst7 |
A |
T |
2: 150,412,439 (GRCm39) |
M1L |
probably benign |
Het |
Cyp4f17 |
A |
T |
17: 32,746,817 (GRCm39) |
D373V |
probably damaging |
Het |
Dclk2 |
G |
A |
3: 86,813,311 (GRCm39) |
R212W |
probably damaging |
Het |
Dhrs7b |
T |
G |
11: 60,721,572 (GRCm39) |
|
probably benign |
Het |
Dhx58 |
T |
A |
11: 100,593,077 (GRCm39) |
H210L |
probably benign |
Het |
Dnah9 |
T |
C |
11: 65,732,159 (GRCm39) |
Y4249C |
probably damaging |
Het |
Eif5b |
T |
A |
1: 38,087,974 (GRCm39) |
L990H |
probably damaging |
Het |
Faap24 |
T |
C |
7: 35,094,388 (GRCm39) |
|
probably benign |
Het |
Fryl |
T |
A |
5: 73,282,077 (GRCm39) |
H174L |
probably benign |
Het |
Gabrr1 |
T |
C |
4: 33,132,696 (GRCm39) |
W15R |
probably benign |
Het |
Gm15446 |
T |
C |
5: 110,091,347 (GRCm39) |
V533A |
probably benign |
Het |
Gm6760 |
T |
A |
X: 63,195,259 (GRCm39) |
K63* |
probably null |
Het |
Gne |
C |
T |
4: 44,042,244 (GRCm39) |
E444K |
possibly damaging |
Het |
Gpr173 |
T |
A |
X: 151,130,036 (GRCm39) |
M146L |
possibly damaging |
Het |
Hira |
C |
T |
16: 18,753,797 (GRCm39) |
S547L |
probably benign |
Het |
Hnf1b |
A |
G |
11: 83,754,810 (GRCm39) |
H161R |
probably benign |
Het |
Hnrnpm |
T |
A |
17: 33,877,364 (GRCm39) |
N53I |
probably damaging |
Het |
Hs3st5 |
A |
T |
10: 36,708,584 (GRCm39) |
I40F |
probably benign |
Het |
Hydin |
C |
T |
8: 111,276,430 (GRCm39) |
|
probably benign |
Het |
Ift172 |
A |
G |
5: 31,411,657 (GRCm39) |
I1607T |
probably damaging |
Het |
Igfn1 |
T |
C |
1: 135,887,639 (GRCm39) |
Q2475R |
probably damaging |
Het |
Il6st |
T |
C |
13: 112,640,806 (GRCm39) |
S800P |
possibly damaging |
Het |
Iqub |
G |
A |
6: 24,501,260 (GRCm39) |
|
probably benign |
Het |
Itgb1 |
A |
T |
8: 129,448,853 (GRCm39) |
|
probably benign |
Het |
Kctd21 |
G |
A |
7: 96,996,808 (GRCm39) |
E94K |
probably benign |
Het |
Kir3dl2 |
A |
G |
X: 135,354,260 (GRCm39) |
V233A |
possibly damaging |
Het |
Klra2 |
A |
T |
6: 131,197,187 (GRCm39) |
C271S |
probably damaging |
Het |
Lacc1 |
A |
T |
14: 77,267,061 (GRCm39) |
C401S |
probably damaging |
Het |
Lmna |
T |
C |
3: 88,389,885 (GRCm39) |
E580G |
probably damaging |
Het |
Matn2 |
A |
G |
15: 34,345,296 (GRCm39) |
Y101C |
probably damaging |
Het |
Mrps16 |
G |
A |
14: 20,441,457 (GRCm39) |
R116* |
probably null |
Het |
Ndrg2 |
G |
T |
14: 52,143,674 (GRCm39) |
R333S |
probably damaging |
Het |
Nf2 |
A |
G |
11: 4,732,194 (GRCm39) |
I507T |
possibly damaging |
Het |
Nktr |
A |
G |
9: 121,578,356 (GRCm39) |
|
probably benign |
Het |
Nkx3-1 |
G |
A |
14: 69,428,455 (GRCm39) |
|
probably benign |
Het |
Npat |
T |
C |
9: 53,467,781 (GRCm39) |
|
probably null |
Het |
Nrxn1 |
T |
C |
17: 90,872,801 (GRCm39) |
N1047S |
probably damaging |
Het |
Nup210 |
A |
T |
6: 91,003,911 (GRCm39) |
I1402N |
possibly damaging |
Het |
Or5d40 |
G |
T |
2: 88,015,624 (GRCm39) |
M134I |
possibly damaging |
Het |
Parp14 |
G |
A |
16: 35,677,130 (GRCm39) |
A946V |
probably benign |
Het |
Pdcl2 |
C |
T |
5: 76,460,328 (GRCm39) |
S182N |
probably benign |
Het |
Pdia3 |
G |
A |
2: 121,262,858 (GRCm39) |
G275S |
probably damaging |
Het |
Pla2g4a |
A |
G |
1: 149,716,455 (GRCm39) |
F669L |
probably benign |
Het |
Plekha8 |
A |
G |
6: 54,606,805 (GRCm39) |
K367E |
probably damaging |
Het |
Pola1 |
A |
G |
X: 92,531,693 (GRCm39) |
|
probably benign |
Het |
Ppm1d |
C |
T |
11: 85,236,703 (GRCm39) |
T494I |
probably benign |
Het |
Pramel16 |
T |
A |
4: 143,676,453 (GRCm39) |
Y217F |
probably benign |
Het |
Prl6a1 |
A |
T |
13: 27,498,177 (GRCm39) |
|
probably benign |
Het |
Ptprg |
T |
A |
14: 12,154,131 (GRCm38) |
S617R |
probably benign |
Het |
R3hdm2 |
G |
A |
10: 127,280,313 (GRCm39) |
G45D |
probably damaging |
Het |
Rev1 |
T |
A |
1: 38,098,204 (GRCm39) |
R780W |
probably null |
Het |
Rnf139 |
T |
A |
15: 58,771,676 (GRCm39) |
F567Y |
probably damaging |
Het |
Scarf1 |
T |
C |
11: 75,405,174 (GRCm39) |
V71A |
probably damaging |
Het |
Shtn1 |
A |
G |
19: 58,988,372 (GRCm39) |
S438P |
probably damaging |
Het |
Slc30a3 |
T |
A |
5: 31,246,067 (GRCm39) |
H221L |
probably benign |
Het |
Smo |
A |
C |
6: 29,753,603 (GRCm39) |
I160L |
possibly damaging |
Het |
Snapc5 |
A |
T |
9: 64,086,582 (GRCm39) |
|
probably benign |
Het |
Snf8 |
G |
T |
11: 95,925,799 (GRCm39) |
|
probably benign |
Het |
Spata31d1a |
T |
C |
13: 59,850,245 (GRCm39) |
S628G |
probably benign |
Het |
Spring1 |
T |
C |
5: 118,397,154 (GRCm39) |
Y128H |
probably damaging |
Het |
Stxbp5l |
T |
C |
16: 37,024,883 (GRCm39) |
T572A |
possibly damaging |
Het |
Thada |
C |
A |
17: 84,723,731 (GRCm39) |
V1108L |
possibly damaging |
Het |
Tln1 |
T |
C |
4: 43,547,756 (GRCm39) |
Q735R |
probably benign |
Het |
Trim24 |
G |
A |
6: 37,848,169 (GRCm39) |
E42K |
probably benign |
Het |
Trnt1 |
T |
A |
6: 106,754,869 (GRCm39) |
|
probably benign |
Het |
Ttbk2 |
A |
T |
2: 120,604,353 (GRCm39) |
M215K |
probably damaging |
Het |
Ttc8 |
C |
T |
12: 98,909,718 (GRCm39) |
|
probably benign |
Het |
Ube3c |
A |
G |
5: 29,795,926 (GRCm39) |
Y105C |
probably damaging |
Het |
Unc13c |
A |
G |
9: 73,438,265 (GRCm39) |
|
probably benign |
Het |
Usp36 |
A |
G |
11: 118,153,854 (GRCm39) |
|
probably benign |
Het |
Vcf2 |
C |
T |
X: 149,181,360 (GRCm39) |
A144T |
probably benign |
Het |
Vmn2r102 |
T |
C |
17: 19,899,106 (GRCm39) |
S483P |
possibly damaging |
Het |
Wdr95 |
A |
G |
5: 149,511,595 (GRCm39) |
T432A |
probably damaging |
Het |
Wnk1 |
G |
T |
6: 119,903,644 (GRCm39) |
P2523H |
probably damaging |
Het |
Xpo4 |
A |
G |
14: 57,875,665 (GRCm39) |
|
probably benign |
Het |
Zar1 |
G |
T |
5: 72,737,886 (GRCm39) |
P71Q |
probably damaging |
Het |
Zbtb41 |
T |
C |
1: 139,351,348 (GRCm39) |
Y154H |
probably benign |
Het |
Zer1 |
G |
T |
2: 29,994,809 (GRCm39) |
|
probably benign |
Het |
Zfp454 |
A |
G |
11: 50,765,012 (GRCm39) |
F140S |
probably benign |
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 |
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 |
R1893:Sphkap
|
UTSW |
1 |
83,256,687 (GRCm39) |
missense |
probably benign |
0.02 |
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'- AGCACATAGTTTTCCCTCAGCATCC -3'
(R):5'- GTGTGCCACATTCCGAAATGCC -3'
Sequencing Primer
(F):5'- GACATGGCTGGAAACCTTTCTC -3'
(R):5'- CCAGTCAATTTTGAGGAAGTGCC -3'
|
Posted On |
2014-07-31 |