Incidental Mutation 'R1993:Sphkap'
ID |
223805 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Sphkap
|
Ensembl Gene |
ENSMUSG00000026163 |
Gene Name |
SPHK1 interactor, AKAP domain containing |
Synonyms |
SKIP, A930009L15Rik, 4930544G21Rik |
MMRRC Submission |
040004-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.079)
|
Stock # |
R1993 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
1 |
Chromosomal Location |
83233163-83385853 bp(-) (GRCm39) |
Type of Mutation |
nonsense |
DNA Base Change (assembly) |
G to A
at 83255236 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Arginine to Stop codon
at position 838
(R838*)
|
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 null
Transcript: ENSMUST00000159078
AA Change: R551*
|
SMART Domains |
Protein: ENSMUSP00000124384 Gene: ENSMUSG00000026163 AA Change: R551*
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 null
Transcript: ENSMUST00000160953
AA Change: R838*
|
SMART Domains |
Protein: ENSMUSP00000124872 Gene: ENSMUSG00000026163 AA Change: R838*
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 |
0.9755 |
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.5%
- 10x: 97.0%
- 20x: 94.3%
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 104 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb1b |
T |
G |
5: 8,871,322 (GRCm39) |
I292S |
possibly damaging |
Het |
Abcc4 |
T |
C |
14: 118,763,694 (GRCm39) |
N1047S |
probably benign |
Het |
Abcc8 |
G |
T |
7: 45,766,847 (GRCm39) |
|
probably null |
Het |
Akap9 |
T |
A |
5: 4,088,520 (GRCm39) |
|
probably null |
Het |
Alox5 |
T |
A |
6: 116,392,424 (GRCm39) |
I366F |
probably damaging |
Het |
Amn |
A |
G |
12: 111,242,526 (GRCm39) |
N447S |
probably damaging |
Het |
Ankrd22 |
A |
T |
19: 34,143,174 (GRCm39) |
M1K |
probably null |
Het |
Asic1 |
G |
T |
15: 99,569,765 (GRCm39) |
G29C |
probably damaging |
Het |
Atxn7l1 |
A |
G |
12: 33,395,976 (GRCm39) |
N235S |
probably benign |
Het |
AY358078 |
T |
A |
14: 52,063,519 (GRCm39) |
D388E |
probably damaging |
Het |
Bod1l |
A |
G |
5: 41,974,679 (GRCm39) |
S2212P |
probably damaging |
Het |
Cacna1e |
T |
A |
1: 154,353,563 (GRCm39) |
Q423L |
probably damaging |
Het |
Calu |
T |
C |
6: 29,366,974 (GRCm39) |
I62T |
possibly damaging |
Het |
Cars2 |
A |
G |
8: 11,564,515 (GRCm39) |
V75A |
probably benign |
Het |
Catsperb |
T |
A |
12: 101,569,026 (GRCm39) |
N899K |
possibly damaging |
Het |
Ccdc50 |
T |
A |
16: 27,228,089 (GRCm39) |
C86* |
probably null |
Het |
Cdh5 |
G |
T |
8: 104,864,447 (GRCm39) |
L469F |
probably damaging |
Het |
Clrn3 |
A |
T |
7: 135,115,848 (GRCm39) |
D167E |
probably benign |
Het |
Csmd1 |
A |
T |
8: 16,396,698 (GRCm39) |
C411S |
probably damaging |
Het |
Dchs1 |
A |
T |
7: 105,411,755 (GRCm39) |
S1454T |
probably benign |
Het |
Ddx20 |
G |
A |
3: 105,586,660 (GRCm39) |
Q562* |
probably null |
Het |
Dgkg |
T |
G |
16: 22,419,344 (GRCm39) |
Y52S |
probably damaging |
Het |
Dhx58 |
T |
C |
11: 100,594,316 (GRCm39) |
|
probably null |
Het |
Dpp6 |
A |
T |
5: 27,604,004 (GRCm39) |
I145L |
probably benign |
Het |
Efna2 |
A |
T |
10: 80,022,711 (GRCm39) |
Y85F |
possibly damaging |
Het |
Eif3a |
C |
T |
19: 60,769,954 (GRCm39) |
V127I |
probably benign |
Het |
Exph5 |
A |
T |
9: 53,284,935 (GRCm39) |
H672L |
possibly damaging |
Het |
Fam131b |
T |
C |
6: 42,297,818 (GRCm39) |
T112A |
possibly damaging |
Het |
Fcgr1 |
A |
T |
3: 96,193,184 (GRCm39) |
V271E |
probably damaging |
Het |
Fgfr4 |
A |
G |
13: 55,313,715 (GRCm39) |
D508G |
probably damaging |
Het |
Fndc3b |
A |
G |
3: 27,473,549 (GRCm39) |
M1172T |
probably benign |
Het |
Fryl |
G |
T |
5: 73,265,836 (GRCm39) |
T495K |
probably damaging |
Het |
Garin5b |
A |
T |
7: 4,761,017 (GRCm39) |
V565E |
probably damaging |
Het |
Gm5134 |
A |
T |
10: 75,802,227 (GRCm39) |
I93F |
probably damaging |
Het |
Gpbar1 |
G |
A |
1: 74,318,603 (GRCm39) |
G282D |
possibly damaging |
Het |
Gria2 |
G |
A |
3: 80,709,664 (GRCm39) |
L10F |
probably benign |
Het |
Grm7 |
T |
C |
6: 111,184,769 (GRCm39) |
Y367H |
probably benign |
Het |
H1f9 |
T |
A |
11: 94,858,858 (GRCm39) |
V51E |
probably damaging |
Het |
Hivep1 |
G |
A |
13: 42,310,969 (GRCm39) |
A1070T |
probably benign |
Het |
Il33 |
A |
G |
19: 29,934,304 (GRCm39) |
D155G |
possibly damaging |
Het |
Kdm6b |
T |
C |
11: 69,297,129 (GRCm39) |
S408G |
probably null |
Het |
Kntc1 |
A |
G |
5: 123,948,874 (GRCm39) |
|
probably null |
Het |
Kntc1 |
G |
A |
5: 123,897,162 (GRCm39) |
|
probably null |
Het |
Ltbp2 |
T |
G |
12: 84,855,220 (GRCm39) |
|
probably null |
Het |
Mapk8ip3 |
G |
T |
17: 25,133,562 (GRCm39) |
L83I |
probably damaging |
Het |
Meltf |
C |
A |
16: 31,711,440 (GRCm39) |
Y554* |
probably null |
Het |
Mov10 |
A |
C |
3: 104,706,735 (GRCm39) |
F725C |
probably damaging |
Het |
Ms4a6d |
A |
C |
19: 11,567,523 (GRCm39) |
L18R |
probably damaging |
Het |
Naip2 |
T |
C |
13: 100,298,515 (GRCm39) |
N507S |
probably benign |
Het |
Nodal |
A |
G |
10: 61,254,113 (GRCm39) |
Q12R |
probably benign |
Het |
Npy6r |
T |
C |
18: 44,409,575 (GRCm39) |
L332P |
probably damaging |
Het |
Nrxn3 |
A |
G |
12: 89,227,181 (GRCm39) |
K272R |
possibly damaging |
Het |
Obox2 |
G |
T |
7: 15,131,174 (GRCm39) |
K93N |
probably benign |
Het |
Or10j27 |
C |
T |
1: 172,958,418 (GRCm39) |
R122H |
possibly damaging |
Het |
Or51a6 |
G |
T |
7: 102,603,953 (GRCm39) |
P285Q |
probably damaging |
Het |
Or5b112 |
A |
G |
19: 13,319,178 (GRCm39) |
T19A |
possibly damaging |
Het |
Or5w13 |
C |
T |
2: 87,523,777 (GRCm39) |
V150M |
probably benign |
Het |
Pcdh12 |
T |
A |
18: 38,415,196 (GRCm39) |
D643V |
possibly damaging |
Het |
Pcsk2 |
A |
G |
2: 143,529,539 (GRCm39) |
D112G |
probably benign |
Het |
Pms1 |
A |
G |
1: 53,234,174 (GRCm39) |
S781P |
probably benign |
Het |
Prtg |
A |
G |
9: 72,752,178 (GRCm39) |
D188G |
probably benign |
Het |
Psg21 |
A |
T |
7: 18,388,695 (GRCm39) |
N132K |
probably benign |
Het |
Psip1 |
A |
G |
4: 83,400,769 (GRCm39) |
V25A |
probably damaging |
Het |
Psmd13 |
T |
A |
7: 140,478,107 (GRCm39) |
I319N |
probably damaging |
Het |
Ptges2 |
A |
G |
2: 32,290,104 (GRCm39) |
T173A |
probably benign |
Het |
Ptprm |
G |
A |
17: 67,054,155 (GRCm39) |
R975W |
probably damaging |
Het |
Rdh1 |
A |
G |
10: 127,601,214 (GRCm39) |
D254G |
probably benign |
Het |
Rnf138 |
T |
G |
18: 21,157,540 (GRCm39) |
N212K |
probably damaging |
Het |
Serpine2 |
A |
G |
1: 79,799,159 (GRCm39) |
S32P |
probably damaging |
Het |
Serpini1 |
G |
T |
3: 75,521,971 (GRCm39) |
W154L |
probably damaging |
Het |
Sf3a1 |
C |
A |
11: 4,129,177 (GRCm39) |
Q713K |
possibly damaging |
Het |
Sgo2b |
A |
T |
8: 64,379,867 (GRCm39) |
H988Q |
probably benign |
Het |
Sin3a |
T |
C |
9: 57,008,483 (GRCm39) |
F468L |
probably damaging |
Het |
Slamf6 |
A |
T |
1: 171,761,776 (GRCm39) |
I66F |
possibly damaging |
Het |
Slc22a28 |
A |
T |
19: 8,094,488 (GRCm39) |
C178S |
possibly damaging |
Het |
Slc35a1 |
A |
C |
4: 34,675,181 (GRCm39) |
V119G |
probably damaging |
Het |
Slc39a12 |
A |
T |
2: 14,439,030 (GRCm39) |
H428L |
probably damaging |
Het |
Speer2 |
A |
G |
16: 69,654,965 (GRCm39) |
S167P |
probably benign |
Het |
Spsb2 |
T |
C |
6: 124,786,329 (GRCm39) |
|
probably null |
Het |
Stam2 |
A |
T |
2: 52,593,168 (GRCm39) |
Y341* |
probably null |
Het |
Sv2b |
G |
A |
7: 74,856,089 (GRCm39) |
A67V |
probably benign |
Het |
Svep1 |
A |
G |
4: 58,064,170 (GRCm39) |
|
probably null |
Het |
Syt15 |
A |
T |
14: 33,944,969 (GRCm39) |
Q172L |
probably benign |
Het |
T |
G |
A |
17: 8,660,634 (GRCm39) |
S415N |
probably benign |
Het |
Tep1 |
A |
G |
14: 51,061,641 (GRCm39) |
F2625S |
possibly damaging |
Het |
Tex14 |
T |
C |
11: 87,427,581 (GRCm39) |
V11A |
possibly damaging |
Het |
Tiam2 |
A |
T |
17: 3,465,401 (GRCm39) |
R377* |
probably null |
Het |
Tirap |
A |
G |
9: 35,102,312 (GRCm39) |
|
probably null |
Het |
Tm4sf20 |
T |
C |
1: 82,737,938 (GRCm39) |
T118A |
probably benign |
Het |
Trank1 |
A |
T |
9: 111,207,900 (GRCm39) |
Q1715L |
probably benign |
Het |
Trpm2 |
C |
T |
10: 77,783,823 (GRCm39) |
V217M |
probably damaging |
Het |
Ubap1l |
G |
A |
9: 65,279,078 (GRCm39) |
E126K |
possibly damaging |
Het |
Urgcp |
G |
T |
11: 5,666,526 (GRCm39) |
P604Q |
probably damaging |
Het |
Vmn1r63 |
A |
G |
7: 5,806,254 (GRCm39) |
V126A |
probably benign |
Het |
Vmn2r90 |
T |
C |
17: 17,933,525 (GRCm39) |
C362R |
probably damaging |
Het |
Vmn2r96 |
A |
G |
17: 18,804,138 (GRCm39) |
I271V |
probably damaging |
Het |
Vps13a |
A |
T |
19: 16,699,822 (GRCm39) |
I740K |
probably benign |
Het |
Vps13c |
A |
G |
9: 67,883,138 (GRCm39) |
T3562A |
probably damaging |
Het |
Wdr91 |
T |
A |
6: 34,869,297 (GRCm39) |
H409L |
probably damaging |
Het |
Wnt7a |
T |
A |
6: 91,342,938 (GRCm39) |
T315S |
possibly damaging |
Het |
Zfp616 |
A |
G |
11: 73,975,795 (GRCm39) |
H688R |
probably benign |
Het |
Zfp763 |
A |
T |
17: 33,237,413 (GRCm39) |
H577Q |
probably damaging |
Het |
Zfp808 |
G |
A |
13: 62,320,721 (GRCm39) |
S650N |
probably benign |
Het |
Zfp977 |
A |
T |
7: 42,229,409 (GRCm39) |
M372K |
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 |
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 |
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'- TCGGACTGCTTTGCCTCTAG -3'
(R):5'- CTCCTAAGTCAAACAAGGGCGG -3'
Sequencing Primer
(F):5'- TGCCTCTAGAGTAGACTGAGC -3'
(R):5'- CGGAGCAAGGCCAGAACTG -3'
|
Posted On |
2014-08-25 |