Incidental Mutation 'R4793:Sphkap'
ID |
368729 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Sphkap
|
Ensembl Gene |
ENSMUSG00000026163 |
Gene Name |
SPHK1 interactor, AKAP domain containing |
Synonyms |
SKIP, A930009L15Rik, 4930544G21Rik |
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.079)
|
Stock # |
R4793 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
1 |
Chromosomal Location |
83233163-83385853 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 83255805 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Isoleucine to Lysine
at position 648
(I648K)
|
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 |
possibly damaging
Transcript: ENSMUST00000159078
AA Change: I361K
PolyPhen 2
Score 0.514 (Sensitivity: 0.88; Specificity: 0.90)
|
SMART Domains |
Protein: ENSMUSP00000124384 Gene: ENSMUSG00000026163 AA Change: I361K
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 |
possibly damaging
Transcript: ENSMUST00000160953
AA Change: I648K
PolyPhen 2
Score 0.775 (Sensitivity: 0.85; Specificity: 0.92)
|
SMART Domains |
Protein: ENSMUSP00000124872 Gene: ENSMUSG00000026163 AA Change: I648K
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 |
0.1795 |
Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.5%
- 10x: 96.8%
- 20x: 93.9%
|
Validation Efficiency |
100% (91/91) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 86 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca6 |
T |
A |
11: 110,082,544 (GRCm39) |
E1143V |
probably benign |
Het |
Abi2 |
T |
A |
1: 60,448,963 (GRCm39) |
M1K |
probably null |
Het |
Acp2 |
T |
C |
2: 91,037,134 (GRCm39) |
F205L |
probably benign |
Het |
Adam17 |
T |
C |
12: 21,397,396 (GRCm39) |
N219D |
probably benign |
Het |
Aldh2 |
T |
C |
5: 121,707,042 (GRCm39) |
S168G |
probably damaging |
Het |
Arhgap15 |
A |
T |
2: 44,032,353 (GRCm39) |
E312D |
probably damaging |
Het |
Calm5 |
T |
C |
13: 3,904,401 (GRCm39) |
S32P |
probably benign |
Het |
Capn12 |
G |
A |
7: 28,592,094 (GRCm39) |
D671N |
probably benign |
Het |
Ccdc73 |
A |
G |
2: 104,848,127 (GRCm39) |
|
probably null |
Het |
Cdc20 |
T |
A |
4: 118,294,261 (GRCm39) |
I20F |
probably benign |
Het |
Cdh23 |
A |
T |
10: 60,167,129 (GRCm39) |
I1841N |
probably damaging |
Het |
Cftr |
T |
C |
6: 18,226,087 (GRCm39) |
V345A |
probably damaging |
Het |
Col15a1 |
T |
C |
4: 47,262,997 (GRCm39) |
S550P |
possibly damaging |
Het |
Col4a4 |
A |
G |
1: 82,516,820 (GRCm39) |
Y133H |
unknown |
Het |
Csmd1 |
A |
G |
8: 16,138,277 (GRCm39) |
S1592P |
probably damaging |
Het |
Cts6 |
T |
A |
13: 61,349,626 (GRCm39) |
M56L |
probably benign |
Het |
Cybb |
C |
G |
X: 9,316,989 (GRCm39) |
D246H |
probably benign |
Het |
Dock5 |
A |
G |
14: 68,037,803 (GRCm39) |
S947P |
probably benign |
Het |
Dpysl2 |
G |
T |
14: 67,052,498 (GRCm39) |
A339D |
possibly damaging |
Het |
Ebf2 |
A |
G |
14: 67,647,531 (GRCm39) |
D360G |
probably damaging |
Het |
Ensa |
T |
C |
3: 95,532,489 (GRCm39) |
|
probably null |
Het |
Fap |
C |
A |
2: 62,374,713 (GRCm39) |
V229F |
probably damaging |
Het |
Fbn1 |
C |
A |
2: 125,163,155 (GRCm39) |
G2116* |
probably null |
Het |
Frmd4b |
A |
T |
6: 97,272,822 (GRCm39) |
S857T |
probably damaging |
Het |
Fsip2 |
T |
A |
2: 82,818,044 (GRCm39) |
Y4592* |
probably null |
Het |
Fubp1 |
T |
A |
3: 151,928,966 (GRCm39) |
Y135N |
possibly damaging |
Het |
Gdap2 |
T |
C |
3: 100,078,234 (GRCm39) |
L66P |
probably damaging |
Het |
Gm10257 |
T |
C |
13: 101,083,305 (GRCm39) |
|
noncoding transcript |
Het |
Gm1758 |
A |
T |
16: 14,325,036 (GRCm39) |
|
noncoding transcript |
Het |
Gna13 |
T |
C |
11: 109,254,455 (GRCm39) |
|
probably benign |
Het |
H2bc13 |
T |
C |
13: 21,900,088 (GRCm39) |
S76G |
probably benign |
Het |
Heatr1 |
T |
C |
13: 12,446,718 (GRCm39) |
I1689T |
probably benign |
Het |
Hephl1 |
A |
G |
9: 15,009,286 (GRCm39) |
I102T |
probably benign |
Het |
Hltf |
T |
G |
3: 20,118,114 (GRCm39) |
Y121D |
possibly damaging |
Het |
Hspg2 |
T |
C |
4: 137,256,784 (GRCm39) |
V1509A |
possibly damaging |
Het |
Ifitm5 |
G |
T |
7: 140,530,077 (GRCm39) |
R16S |
probably benign |
Het |
Il1rap |
A |
C |
16: 26,513,984 (GRCm39) |
D239A |
probably benign |
Het |
Kalrn |
C |
T |
16: 33,810,180 (GRCm39) |
D2525N |
possibly damaging |
Het |
Kcna6 |
T |
C |
6: 126,715,519 (GRCm39) |
I457V |
probably damaging |
Het |
Kctd17 |
T |
A |
15: 78,317,224 (GRCm39) |
L47Q |
probably damaging |
Het |
Kdm1b |
C |
T |
13: 47,216,553 (GRCm39) |
R308W |
probably damaging |
Het |
Klk14 |
G |
A |
7: 43,341,501 (GRCm39) |
C51Y |
probably damaging |
Het |
Lrrc63 |
A |
G |
14: 75,363,601 (GRCm39) |
S177P |
possibly damaging |
Het |
Lrriq1 |
T |
C |
10: 103,006,327 (GRCm39) |
D1266G |
probably benign |
Het |
Map3k2 |
G |
T |
18: 32,361,203 (GRCm39) |
M554I |
probably damaging |
Het |
Mst1r |
T |
A |
9: 107,797,124 (GRCm39) |
V1331E |
probably damaging |
Het |
Musk |
T |
C |
4: 58,373,400 (GRCm39) |
I775T |
probably damaging |
Het |
Mybl2 |
A |
G |
2: 162,916,683 (GRCm39) |
K7E |
probably damaging |
Het |
Nf1 |
T |
C |
11: 79,338,398 (GRCm39) |
S1137P |
probably damaging |
Het |
Nlrp5 |
A |
G |
7: 23,117,055 (GRCm39) |
I260V |
probably damaging |
Het |
Or13c7 |
A |
T |
4: 43,854,323 (GRCm39) |
N5Y |
probably benign |
Het |
Or9g4 |
A |
C |
2: 85,504,842 (GRCm39) |
Y218D |
probably damaging |
Het |
Or9s23 |
G |
T |
1: 92,501,207 (GRCm39) |
A105S |
possibly damaging |
Het |
Pabpc1l |
C |
T |
2: 163,869,542 (GRCm39) |
A114V |
possibly damaging |
Het |
Plac8l1 |
T |
A |
18: 42,311,973 (GRCm39) |
I149F |
possibly damaging |
Het |
Pou6f1 |
T |
A |
15: 100,476,293 (GRCm39) |
N531I |
probably damaging |
Het |
Prdm10 |
A |
G |
9: 31,264,701 (GRCm39) |
Y712C |
probably damaging |
Het |
Ptbp3 |
T |
C |
4: 59,514,297 (GRCm39) |
T43A |
possibly damaging |
Het |
Ptpn13 |
T |
C |
5: 103,730,644 (GRCm39) |
|
probably null |
Het |
Rnf135 |
T |
C |
11: 80,087,775 (GRCm39) |
|
probably null |
Het |
Rusf1 |
A |
T |
7: 127,887,374 (GRCm39) |
|
probably benign |
Het |
Serpinb3d |
A |
G |
1: 107,005,951 (GRCm39) |
L379P |
probably damaging |
Het |
Sh2d6 |
T |
A |
6: 72,494,581 (GRCm39) |
T124S |
probably benign |
Het |
Slc26a5 |
G |
A |
5: 22,042,992 (GRCm39) |
P153S |
probably damaging |
Het |
Slc5a7 |
A |
G |
17: 54,588,822 (GRCm39) |
F275S |
possibly damaging |
Het |
Snx14 |
A |
G |
9: 88,276,495 (GRCm39) |
S606P |
probably damaging |
Het |
Spon2 |
T |
C |
5: 33,371,904 (GRCm39) |
T301A |
probably damaging |
Het |
Srpra |
C |
T |
9: 35,124,447 (GRCm39) |
T48I |
probably benign |
Het |
Taar9 |
G |
A |
10: 23,985,408 (GRCm39) |
P9S |
probably benign |
Het |
Tacc1 |
A |
T |
8: 25,672,405 (GRCm39) |
S274R |
possibly damaging |
Het |
Tc2n |
A |
G |
12: 101,617,376 (GRCm39) |
S348P |
possibly damaging |
Het |
Timd2 |
G |
T |
11: 46,578,008 (GRCm39) |
T41K |
probably damaging |
Het |
Tmem132a |
T |
A |
19: 10,842,857 (GRCm39) |
E206V |
probably damaging |
Het |
Tmt1a3 |
A |
G |
15: 100,232,889 (GRCm39) |
M27V |
probably benign |
Het |
Tpi1 |
A |
T |
6: 124,789,544 (GRCm39) |
|
probably benign |
Het |
Traf5 |
T |
G |
1: 191,729,765 (GRCm39) |
T429P |
probably benign |
Het |
Trav4-3 |
A |
G |
14: 53,836,615 (GRCm39) |
S27G |
possibly damaging |
Het |
Tubd1 |
T |
C |
11: 86,457,895 (GRCm39) |
M462T |
probably benign |
Het |
Ube4a |
T |
C |
9: 44,860,120 (GRCm39) |
D314G |
probably damaging |
Het |
Utp25 |
T |
A |
1: 192,796,116 (GRCm39) |
Q50L |
probably null |
Het |
Vmn2r58 |
G |
T |
7: 41,514,495 (GRCm39) |
T158K |
probably damaging |
Het |
Vmn2r68 |
C |
A |
7: 84,883,648 (GRCm39) |
M152I |
probably benign |
Het |
Vmn2r91 |
A |
G |
17: 18,325,658 (GRCm39) |
E92G |
probably damaging |
Het |
Wdr20rt |
T |
C |
12: 65,273,395 (GRCm39) |
V113A |
probably damaging |
Het |
Zfp729a |
T |
C |
13: 67,768,546 (GRCm39) |
H561R |
probably damaging |
Het |
Zfp804a |
T |
A |
2: 82,066,186 (GRCm39) |
D52E |
probably 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 |
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 |
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'- ACTTTCCATCAAGGTGTCCAGAG -3'
(R):5'- AGAGGCGACATGTCCTGTAG -3'
Sequencing Primer
(F):5'- TCAAGGTGTCCAGAGTTCCACAG -3'
(R):5'- CCTACATCTGGGGCTTCTGAAG -3'
|
Posted On |
2016-02-04 |