H-InvDB_9.0 released on May 27, 2015.
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H-Inv ID (HIT)
H-Inv cluster ID (HIX)
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Definition*
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---
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H-Invitational ID:
HIT000030459
Accession number:
BC001503
Created date:
26-Mar-2013
Last modified:
27-May-2015
Definition:
Proactivator polypeptide; Contains: Saposin-A; Protein A; Contains: Saposin-B-Val; Contains: Saposin-B; Cerebroside sulfate activator; CSAct; Dispersin; Sphingolipid activator protein 1; SAP-1; Sulfatide/GM1 activator; Contains: Saposin-C; A1 activator; Co-beta-glucosidase; Glucosylceramidase activator; Sphingolipid activator protein 2; SAP-2; Contains: Saposin-D; Component C; Protein C; Precursor;
Select format
Flat file
XML file
Nucleotide sequence fasta
Protein sequence fasta
Transcript original information
Accession number
BC001503.2
CAGE tag ID
NA
EST ID
NA
Clone Number
MGC:2254 IMAGE:3508263
Experimental resources
NBRC
;
HGPD
;
Antibody (PSAP)
;
Catalog (PSAP)
;
Sequence data provider
Provider:
MGC/NCI
;
Annotation project
H-Invitational FLcDNA
Length of cDNA
2762[bp] (No. of exon:14)[A:624 T:665 G:780 C:693]
Devision
HUM
Molecular type
mRNA
Library origin
Cell type
NA
Tissue type
Brain, neuroblastoma
Develpmental stage
NA
Sequence quality information
CDS feature
Complete CDS
Kozak sequence
NA
PolyA
Site: 2723(+) Signal: 2703-2707(+)
Vector/adapter sequence
NA
Frame shift
NA
Remaining intron
NA
Splice site acceptor (NAGNAG)
CAGAAG; TAGGAG;
Transcript quality feature
NA
Notes
NA
GCGCTATGTACGCCCTCTTCCTCCTGGCCAGCCTCCTGGGCGCGGCTCTA GCCGGCCCGGTCCTTGGACTGAAAGAATGCACCAGGGGCTCGGCAGTGTG GTGCCAGAATGTGAAGACGGCGTCCGACTGCGGGGCAGTGAAGCACTGCC TGCAGACCGTTTGGAACAAGCCAACAGTGAAATCCCTTCCCTGCGACATA TGCAAAGACGTTGTCACCGCAGCTGGTGATATGCTGAAGGACAATGCCAC TGAGGAGGAGATCCTTGTTTACTTGGAGAAGACCTGTGACTGGCTTCCGA AACCGAACATGTCTGCTTCATGCAAGGAGATAGTGGACTCCTACCTCCCT GTCATCCTGGACATCATTAAAGGAGAAATGAGCCGTCCTGGGGAGGTGTG CTCTGCTCTCAACCTCTGCGAGTCTCTCCAGAAGCACCTAGCAGAGCTGA ATCACCAGAAGCAGCTGGAGTCCAATAAGATCCCAGAGCTGGACATGACT GAGGTGGTGGCCCCCTTCATGGCCAACATCCCTCTCCTCCTCTACCCTCA GGACGGCCCCCGCAGCAAGCCCCAGCCAAAGGATAATGGGGACGTTTGCC AGGACTGCATTCAGATGGTGACTGACATCCAGACTGCTGTACGGACCAAC TCCACCTTTGTCCAGGCCTTGGTGGAACATGTCAAGGAGGAGTGTGACCG CCTGGGCCCTGGCATGGCCGACATATGCAAGAACTATATCAGCCAGTATT CTGAAATTGCTATCCAGATGATGATGCACATGCAACCCAAGGAGATCTGT GCGCTGGTTGGGTTCTGTGATGAGGTGAAAGAGATGCCCATGCAGACTCT GGTCCCCGCCAAAGTGGCCTCCAAGAATGTCATCCCTGCCCTGGAACTGG TGGAGCCCATTAAGAAGCACGAGGTCCCAGCAAAGTCTGATGTTTACTGT GAGGTGTGTGAATTCCTGGTGAAGGAGGTGACCAAGCTGATTGACAACAA CAAGACTGAGAAAGAAATACTCGACGCTTTTGACAAAATGTGCTCGAAGC TGCCGAAGTCCCTGTCGGAAGAGTGCCAGGAGGTGGTGGACACGTACGGC AGCTCCATCCTGTCCATCCTGCTGGAGGAGGTCAGCCCTGAGCTGGTGTG CAGCATGCTGCACCTCTGCTCTGGCACGCGGCTGCCTGCACTGACCGTTC ACGTGACTCAGCCAAAGGACGGTGGCTTCTGCGAAGTGTGCAAGAAGCTG GTGGGTTATTTGGATCGCAACCTGGAGAAAAACAGCACCAAGCAGGAGAT CCTGGCTGCTCTTGAGAAAGGCTGCAGCTTCCTGCCAGACCCTTACCAGA AGCAGTGTGATCAGTTTGTGGCAGAGTACGAGCCCGTGCTGATCGAGATC CTGGTGGAGGTGATGGATCCTTCCTTCGTGTGCTTGAAAATTGGAGCCTG CCCCTCGGCCCATAAGCCCTTGTTGGGAACTGAGAAGTGTATATGGGGCC CAAGCTACTGGTGCCAGAACACAGAGACAGCAGCCCAGTGCAATGCTGTC GAGCATTGCAAACGCCATGTGTGGAACTAGGAGGAGGAATATTCCATCTT GGCAGAAACCACAGCATTGGTTTTTTTCTACTTGTGTGTCTGGGGGAATG AACGCACAGATCTGTTTGACTTTGTTATAAAAATAGGGCTCCCCCACCTC CCCCATTTCTGTGTCCTTTATTGTAGCATTGCTGTCTGCAAGGGAGCCCC TAGCCCCTGGCAGACATAGCTGCTTCAGTGCCCCTTTTCTCTCTGCTAGA TGGATGTTGATGCACTGGAGGTCTTTTAGCCTGCCCTTGCATGGCGCCTG CTGGAGGAGGAGAGAGCTCTGCTGGCATGAGCCACAGTTTCTTGACTGGA GGCCATCAACCCTCTTGGTTGAGGCCTTGTTCTGAGCCCTGACATGTGCT TGGGCACTGGTGGGCCTGGGCTTCTGAGGTGGCCTCCTGCCCTGATCAGG GACCCTCCCCGCTTTCCTGGGCCTCTCAGTTGAACAAAGCAGCAAAACAA AGGCAGTTTTATATGAAAGATTAGAAGCCTGGAATAATCAGGCTTTTTAA ATGATGTAATTCCCACTGTAATAGCATAGGGATTTTGGAAGCAGCTGCTG GTGGCTTGGGACATCAGTGGGGCCAAGGGTTCTCTGTCCCTGGTTCAACT GTGATTTGGCTTTCCCGTGTCTTTCCTGGTGATGCCTTGTTTGGGGTTCT GTGGGTTTGGGTGGGAAGAGGGCCATCTGCCTGAATGTAACCTGCTAGCT CTCCGAAGGCCCTGCGGGCCTGGCTTGTGTGAGCGTGTGGACAGTGGTGG CCGCGCTGTGCCTGCTCGTGTTGCCTACATGTCCCTGGCTGTTGAGGCGC TGCTTCAGCCTGCACCCCTCCCTTGTCTCATAGATGCTCCTTTTGACCTT TTCAAATAAATATGGATGGCGAGCTCCTAGGCCTCTGGCTTCCTGGTAGA GGGCGGCATGCCGAAGGGTCTGCTGGGTGTGGATTGGATGCTGGGGTGTG GGGGTTGGAAGCTGTCTGTGGCCCACTTGGGCACCCACGCTTCTGTCCAC TTCTGGTTGCCAGGAGACAGCAAGCAAAGCCAGCAGGACATGAAGTTGCT ATTAAATGGACTTCGTGATTTTTGTTTTGCACTAAAGTTTCTGTGATTTA ACAATAAAATTCTGTTAGCCAGAAAAAAAAAAAAAAAAAAAAAAAAAAAA AAAAAAAAAAAA
Gene structure information
H-Inv cluster ID
HIX0008908
Genomic location
Chromosome
10
Location
10q22.1
Position
73576055- 73610983
Strand
-
Possible duplicated location(s)
NA
Gene structure
14 exon(s)
Database links
RefSeq
NA
Ensembl
NA
Entrez Gene
Entrez Gene ID:5660
;
KEGG GENES
KEGG GENES(5660)
;
GeneCard
PSAP
;
*GeneCards is provided free to academic non-profit institutions.
Related H-InvDB links
H-DBAS
;
G-integra
;
cDNA-genome alignment
;
Predicted CDS information
HIP ID
HIP000115885
Predicted CDS
6..1580; 524[aa]; Orientation:+3;
Codon Adaptation Index (CAI).
0.822
Database links
RefSeq
NP_002769
;
UniProt
P07602
;
CCDS
CCDS7311
;
MYALFLLASLLGAALAGPVLGLKECTRGSAVWCQNVKTASDCGAVKHCLQ TVWNKPTVKSLPCDICKDVVTAAGDMLKDNATEEEILVYLEKTCDWLPKP NMSASCKEIVDSYLPVILDIIKGEMSRPGEVCSALNLCESLQKHLAELNH QKQLESNKIPELDMTEVVAPFMANIPLLLYPQDGPRSKPQPKDNGDVCQD CIQMVTDIQTAVRTNSTFVQALVEHVKEECDRLGPGMADICKNYISQYSE IAIQMMMHMQPKEICALVGFCDEVKEMPMQTLVPAKVASKNVIPALELVE PIKKHEVPAKSDVYCEVCEFLVKEVTKLIDNNKTEKEILDAFDKMCSKLP KSLSEECQEVVDTYGSSILSILLEEVSPELVCSMLHLCSGTRLPALTVHV TQPKDGGFCEVCKKLVGYLDRNLEKNSTKQEILAALEKGCSFLPDPYQKQ CDQFVAEYEPVLIEILVEVMDPSFVCLKIGACPSAHKPLLGTEKCIWGPS YWCQNTETAAQCNAVEHCKRHVWN*
Motif information
a.a.
length
InterPro
Name
25
IPR008373
Saposin [Family]
41
IPR003119
Saposin type A [Domain]
34
IPR003119
Saposin type A [Domain]
21
IPR008373
Saposin [Family]
81
IPR011001
Saposin-like [Domain]
84
IPR008139
Saposin B [Domain]
82
IPR011001
Saposin-like [Domain]
78
IPR008139
Saposin B [Domain]
38
IPR007856
Saposin-like type B, 1 [Domain]
18
IPR008373
Saposin [Family]
34
IPR008138
Saposin-like type B, 2 [Domain]
19
IPR008373
Saposin [Family]
26
IPR008373
Saposin [Family]
79
IPR011001
Saposin-like [Domain]
82
IPR008139
Saposin B [Domain]
40
IPR007856
Saposin-like type B, 1 [Domain]
76
IPR008139
Saposin B [Domain]
22
IPR008373
Saposin [Family]
22
IPR008373
Saposin [Family]
114
IPR011001
Saposin-like [Domain]
34
IPR008138
Saposin-like type B, 2 [Domain]
80
IPR011001
Saposin-like [Domain]
82
IPR008139
Saposin B [Domain]
76
IPR008139
Saposin B [Domain]
38
IPR007856
Saposin-like type B, 1 [Domain]
21
IPR008373
Saposin [Family]
92
IPR011001
Saposin-like [Domain]
35
IPR008138
Saposin-like type B, 2 [Domain]
19
IPR008373
Saposin [Family]
80
IPR011001
Saposin-like [Domain]
82
IPR008139
Saposin B [Domain]
23
IPR008373
Saposin [Family]
76
IPR008139
Saposin B [Domain]
38
IPR007856
Saposin-like type B, 1 [Domain]
23
IPR008373
Saposin [Family]
78
IPR011001
Saposin-like [Domain]
34
IPR008138
Saposin-like type B, 2 [Domain]
24
IPR008373
Saposin [Family]
37
IPR003119
Saposin type A [Domain]
22
IPR008373
Saposin [Family]
34
IPR003119
Saposin type A [Domain]
Gene function information
H-Inv ID
HIT000030459
H-Inv cluster ID
HIX0008908
Accession number
BC001503.2
CAGE tag ID
NA
EST ID
NA
Transcript feature
NO;
Coding potential
Protein coding;
Definition
Proactivator polypeptide; Contains: Saposin-A; Protein A; Contains: Saposin-B-Val; Contains: Saposin-B; Cerebroside sulfate activator; CSAct; Dispersin; Sphingolipid activator protein 1; SAP-1; Sulfatide/GM1 activator; Contains: Saposin-C; A1 activator; Co-beta-glucosidase; Glucosylceramidase activator; Sphingolipid activator protein 2; SAP-2; Contains: Saposin-D; Component C; Protein C; Precursor;
Similarity category
Category: Identical to known human protein(Category I).
Identical to known human protein (
P07602
) [Identity/coverage = 100.0%/100.0%] to Homo sapiens (Human). protein.
Experimental evidence
Protein evidence
PubMed ID
1371116
;
1612590
;
1958198
;
2013321
;
2019586
;
2060627
;
2209618
;
2302219
;
2320574
;
2498298
;
2515150
;
2717620
;
2825202
;
2842863
;
2845979
;
2868718
;
3048308
;
3242555
;
3442600
;
7730378
;
7866401
;
8323276
;
8370464
;
10196694
;
10406958
;
10510427
;
10562467
;
10682309
;
11180632
;
11309366
;
12510003
;
12518053
;
15164054
;
15489334
;
15773042
;
17919309
;
19159218
;
19167329
;
21269460
;
ALL
;
Gene family/group
H-Inv gene family/group ID
NA
Gene family/group name
NA
Evidence motif (InterPro) ID
NA
Gene symbol/name
HGNC symbol
PSAP
HGNC aliases
"sphingolipid activator protein-1"
HGNC name
prosaposin
DDBJ
PSAP
UniProt
PSAP
EC number
NA
GGDB
(GlycoGene Database)
Gene symbol
NA
Familly
NA
Designation
NA
Expression
NA
KEGG metabolic pathway
NA
Protein-protein interaction (PPI)
H-Inv protein ID
HIP000115885
No. of interaction
42
Interaction partner(s)
HIP000021398
;
HIP000021398
;
HIP000021818
;
HIP000022671
;
HIP000023822
;
HIP000025218
;
HIP000027358
;
HIP000027358
;
HIP000027633
;
HIP000027819
;
HIP000027819
;
HIP000028809
;
HIP000036277
;
HIP000036277
;
HIP000043309
;
HIP000044974
;
HIP000045907
;
HIP000045907
;
HIP000046272
;
HIP000054389
;
HIP000060961
;
HIP000071861
;
HIP000076344
;
HIP000090978
;
HIP000090978
;
HIP000092457
;
HIP000094247
;
HIP000096658
;
HIP000100064
;
HIP000100064
;
HIP000100089
;
HIP000100824
;
HIP000105862
;
HIP000107528
;
HIP000112312
;
HIP000112312
;
HIP000128077
;
HIP000130959
;
HIP000137500
;
HIP000337035
;
HIP000347257
;
HIP000357639
;
BIND
149938; 150543; 262675;
DIP
103975E; 112158E;
MINT
MINT-2866200; MINT-60928; MINT-62098; MINT-63423; MINT-65660; MINT-65765; MINT-6797475; MINT-6797576; MINT-6797604; MINT-6797801;
HPRD
00291; 01775; 02170; 02971; 03013; 03883; 04484; 05160; 05343; 06973; 07255; 16735;
IntAct
NA
Database links
RefSeq
NA
Ensembl
NA
Entrez Gene
Entrez Gene ID:5660
;
KEGG GENES
KEGG GENES(5660)
;
GeneCard
PSAP
;
*GeneCards is provided free to academic non-profit institutions.
etc
Human-Gene diversity Of Life-style related Diseases
;
Curation status
Auto-annotated
Notes
NA
Related H-InvDB links
Gene family;
Similarity Search Tool;
TACT
;
fRNAdb (The functional RNA database) : overlapping fRNAdb entries with H-InvDB transcripts based on the location of the genome.
FR ID
FR006585
Accession
Description
Location
PMID
Gene ontology information
Biological process
sphingolipid metabolic process (
GO:0006665
); lipid metabolic process (
GO:0006629
);
Cellular component
lysosome (
GO:0005764
);
Subcellular localization information
Last modified:27-May-2015
WoLF PSORT
plasma membrane; endoplasmic; peroxisome; Other;
Target P
signal peptide
SOSUI
membrane protein
TMHMM
soluble protein
PTS1
Not targeted
Related H-InvDB links
LIFEdb;
JRE-1.4.0 or later is required.
Download JRE at
Sun's web site.
Protein structure information (GTOP)
Last modified:27-May-2015
Start
End
PDB_ID
E-value
Identity
Coverage
SCOP_ID
63
138
2gtgA1
4e-12
42.1
74/78
a.64.1.1
195
272
1n69A
2e-14
100.0
78/78
a.64.1.3
312
389
2gtgA1
1e-14
79.5
78/78
a.64.1.1
406
483
1nklA
9e-14
19.5
77/78
a.64.1.1
Related H-InvDB links
GTOP
Gene expression information
Last modified:27-May-2015
Tissue-specific expression
NA
Probe
information
AceGene
AGhsB130712;
Affymetrix
GeneChip
HG-Focus
NA
HG-U133
200871_s_at;
HG-U133A
200871_s_at;
HG-U133A_2
200871_s_at;
HG-U133B
NA
HG-U133_Plus_2
200871_s_at;
HG-U95
NA
HG-U95A
NA
HG-U95B
NA
HG-U95C
NA
HG-U95D
NA
HG-U95E
NA
HG-U95Av2
NA
HuEx-1_0
3251267; 3251274; 3293763; 3293775; 3293777; 3293779; 3293780; 3293781; 3293782; 3293787; 3293788; 3293789; 3293790; 3293793; 3293794; 3293795; 3293800;
HuGeneFL
NA
Agilent
Human 1A Oligo Microarray:PGID215
NA
Whole Human Genome Oligo Microarray:PGID247
A_24_P309317;
Related H-InvDB links
H-ANGEL
;
DNAProbeLocator
;
Disease/pathology information
Last modified:27-May-2015
Disease relation
Disease name: Combined SAP deficiency (
611721
); Disease name: Gaucher disease, atypical (
610539
); Disease name: Krabbe disease, atypical (
611722
); Disease name: Metachromatic leukodystrophy due to SAP-b deficiency (
249900
);
Related information in OMIM
OMIM ID:
176801
; Title: PROSAPOSIN
Co-localized orphan diseases
NA
Disease related mutation
MutationView:
176801
;
JRE-1.4.0 or later is required.Download JRE at
Sun's web site.
Literature-Extracted GENe-Disease Associations (LEGENDA)
Gene name
Entrez Gene ID:(5660)
Disease
Entrez Gene ID:(5660)
Substance
Entrez Gene ID:(5660)
Related H-InvDB links
DiseaseInfo Viewer
;
LEGENDA
;
Polymorphism (SNP, indel), microsatellite (Short Tandem Repeat, STR) and repeat information
Single Nucleotide Polymorphism (SNP) and indel
Location
Variation
dbSNP ID
Strand
CDS/UTR
Translation
2 .. 2
C/T
rs2070188
+
5'UTR
6 .. 6
A/T
rs121918106
+
CDS
Nonsynonymous[Met1Leu]
21 .. 21
C/T
rs148279196
-
CDS
Nonsynonymous[Leu6Phe]
41 .. 41
C/G
rs11555014
+
CDS
Synonymous[Gly12Gly]
53 .. 53
C/T
rs199808371
-
CDS
Synonymous[Ala16Ala]
65 .. 65
T/C
rs188252882
-
CDS
Synonymous[Leu20Leu]
72 .. 72
A/G
rs143016278
-
CDS
Nonsynonymous[Lys23Glu]
76 ^ 77
-/A
rs34228343
-
CDS
83 .. 83
C/T
rs74145688
-
CDS
Synonymous[Thr26Thr]
88 .. 88
G/T
rs185057837
-
CDS
Nonsynonymous[Gly28Val]
93 .. 93
G/T
rs144942998
-
CDS
Nonsynonymous[Ala30Ser]
99 .. 99
T/G
rs200008050
-
CDS
Nonsynonymous[Trp32Gly]
118 .. 118
C/T
rs145181011
-
CDS
Nonsynonymous[Thr38Met]
122 .. 122
G/A
rs200836594
-
CDS
Synonymous[Ala39Ala]
125 .. 125
C/T
rs141231601
-
CDS
Synonymous[Ser40Ser]
152 .. 152
G/A
rs112119208
-
CDS
Synonymous[Leu49Leu]
158 .. 158
C/T
rs11555016
+
CDS
Synonymous[Thr51Thr]
159 .. 159
G/A
rs147920923
-
CDS
Nonsynonymous[Val52Ile]
194 .. 194
C/T
rs111369573
-
CDS
Synonymous[Cys63Cys]
209 .. 209
C/T
rs143981174
-
CDS
Synonymous[Asp68Asp]
219 .. 219
G/A
rs150701404
-
CDS
Nonsynonymous[Ala72Thr]
222 .. 222
G/A
rs11555015
+
CDS
Nonsynonymous[Ala73Thr]
350 .. 350
T/G
rs11555017
+
CDS
Synonymous[Pro115Pro]
363 .. 363
A/G
rs142784765
-
CDS
Nonsynonymous[Ile120Val]
384 .. 384
C/T
rs148519599
-
CDS
Nonsynonymous[Arg127Cys]
493 .. 493
A/T
rs146301708
-
CDS
Nonsynonymous[Asp163Val]
545 .. 545
C/T
rs11555021
+
CDS
Synonymous[Tyr180Tyr]
554 .. 554
C/T
rs142002239
-
CDS
Synonymous[Asp183Asp]
561 .. 561
C/T
rs193088462
-
CDS
Nonsynonymous[Arg186Cys]
562 .. 562
G/A
rs138880818
-
CDS
Nonsynonymous[Arg186His]
570 .. 570
C/T
rs188854022
-
CDS
Nonsynonymous[Pro189Ser]
575 .. 575
G/T
rs142272618
-
CDS
Nonsynonymous[Gln190His]
582 .. 582
G/C
rs149305591
-
CDS
Nonsynonymous[Asp193His]
583 .. 583
A/G
rs138636858
-
CDS
Nonsynonymous[Asp193Gly]
587 .. 587
T/C
rs150177878
-
CDS
Synonymous[Asn194Asn]
594 .. 594
G/A
rs191952316
-
CDS
Nonsynonymous[Val197Ile]
621 .. 621
A/G
rs139503658
-
CDS
Nonsynonymous[Thr206Ala]
626 .. 626
C/T
rs140702696
-
CDS
Synonymous[Asp207Asp]
628 .. 628
T/G
rs200319381
-
CDS
Nonsynonymous[Ile208Ser]
642 .. 642
C/T
rs150521779
-
CDS
Nonsynonymous[Arg213Trp]
648 .. 648
A/C
rs121918107
+
CDS
Nonsynonymous[Asn215His]
655 .. 655
C/T
rs121918103
+
CDS
Nonsynonymous[Thr217Ile]
700 .. 700
G/T
rs147265566
-
CDS
Nonsynonymous[Arg232Leu]
702 .. 702
C/T/G
rs146934980
-
CDS
719 .. 719
C/G
rs141199649
-
CDS
Synonymous[Ala238Ala]
727 .. 727
G/C
rs121918104
+
CDS
Nonsynonymous[Cys241Ser]
728 .. 728
C/T
rs147805036
-
CDS
Synonymous[Cys241Cys]
737 .. 737
T/C
rs146732171
-
CDS
Synonymous[Tyr244Tyr]
746 .. 746
G/T
rs202069470
-
CDS
Nonsynonymous[Gln247His]
803 .. 803
G/A
rs199672678
-
CDS
Synonymous[Ala266Ala]
827 .. 827
G/A
rs149202005
-
CDS
Synonymous[Val274Val]
870 .. 870
T/C
rs145404688
-
CDS
Nonsynonymous[Ser289Pro]
899 .. 899
G/A
rs150048951
-
CDS
Synonymous[Leu298Leu]
919 .. 919
A/G
rs113554687
-
CDS
Nonsynonymous[His305Arg]
945 .. 945
T/C
rs202041927
-
CDS
Nonsynonymous[Tyr314His]
971 .. 971
G/A
rs139413990
-
CDS
Synonymous[Val322Val]
1022 .. 1022
C/T
rs146778046
-
CDS
Synonymous[Leu339Leu]
1025 .. 1025
C/T
rs113679008
-
CDS
Synonymous[Asp340Asp]
1034 .. 1034
C/A
rs199650747
-
CDS
Nonsynonymous[Asp343Glu]
1051 .. 1051
T/C
rs121918110
+
CDS
Nonsynonymous[Leu349Pro]
1054 .. 1054
C/T
rs201129306
-
CDS
Nonsynonymous[Pro350Leu]
1061 .. 1061
C/T
rs138328594
-
CDS
Synonymous[Ser352Ser]
1093 .. 1093
C/T
rs140066253
-
CDS
Nonsynonymous[Thr363Met]
1097 .. 1097
C/T
rs200226479
-
CDS
Synonymous[Tyr364Tyr]
1127 .. 1127
G/A
rs146102517
-
CDS
Synonymous[Glu374Glu]
1149 .. 1149
T/G
rs121918108
+
CDS
Nonsynonymous[Cys382Gly]
1150 .. 1150
G/T
rs121918105
+
CDS
Nonsynonymous[Cys382Phe]
1169 .. 1169
C/T
rs141254386
-
CDS
Synonymous[Cys388Cys]
1177 .. 1177
C/T
rs202125074
-
CDS
Nonsynonymous[Thr391Met]
1232 .. 1232
C/T
rs147030327
-
CDS
Synonymous[Cys409Cys]
1247 .. 1247
G/T
rs1803650
+
CDS
Nonsynonymous[Lys414Asn]
1284 .. 1284
A/G
rs148676984
-
CDS
Nonsynonymous[Ser427Gly]
1287 .. 1287
A/G
rs200379457
-
CDS
Nonsynonymous[Thr428Ala]
1293 .. 1293
C/T
rs121918109
+
CDS
AA-STOP[Gln430*]
1301 .. 1301
C/T
rs144042454
-
CDS
Synonymous[Ile432Ile]
1316 .. 1316
G/A
rs149525964
-
CDS
Synonymous[Glu437Glu]
1343 .. 1343
T/C
rs138217875
-
CDS
Synonymous[Pro446Pro]
1379 .. 1379
C/T
rs146925179
-
CDS
Synonymous[Tyr458Tyr]
1385 .. 1385
C/T
rs1049882
+
CDS
Synonymous[Pro460Pro]
1386 .. 1386
G/A
rs138716613
-
CDS
Nonsynonymous[Val461Met]
1457 .. 1457
G/A
rs114389264
-
CDS
Synonymous[Ser484Ser]
1466 .. 1466
G/A
rs140777530
-
CDS
Synonymous[Lys487Lys]
1481 .. 1481
T/C
rs139178900
-
CDS
Synonymous[Thr492Thr]
1500 .. 1500
C/T
rs143773764
-
CDS
Nonsynonymous[Pro499Ser]
1524 .. 1524
G/C
rs149000433
-
CDS
Nonsynonymous[Glu507Gln]
1596 .. 1596
A/T
rs199602243
-
3'UTR
1666 .. 1666
T/C
rs187964417
-
3'UTR
1673 .. 1673
T/C
rs183945494
-
3'UTR
1694 ^ 1695
-/C
rs71480591
-
3'UTR
1697 ^ 1698
-/C
rs36076120
-
3'UTR
1700 .. 1700
C/G
rs191704547
-
3'UTR
1702 .. 1702
C/G
rs113284884
-
3'UTR
1833 .. 1833
G/C
rs113209259
-
3'UTR
1845 .. 1845
C/T
rs150766866
-
3'UTR
1900 .. 1900
A/T
rs14595
-
3'UTR
1956 .. 1956
A/G
rs141906397
-
3'UTR
2009 .. 2009
C/G
rs11555018
+
3'UTR
2167 .. 2167
G/A
rs11555020
+
3'UTR
2179 .. 2179
G/T
rs1803651
+
3'UTR
2216 .. 2216
C/T
rs138390739
-
3'UTR
2234 .. 2234
G/T
rs41282246
-
3'UTR
2317 .. 2317
G/A
rs147046509
-
3'UTR
2354 .. 2354
C/T
rs200907537
-
3'UTR
2355 .. 2355
G/A
rs79662404
-
3'UTR
2376 .. 2376
T/C
rs12844
+
3'UTR
2377 .. 2377
A/G
rs141553639
-
3'UTR
2427 .. 2427
C/T
rs1053333
+
3'UTR
2446 .. 2446
A/C
rs1056711
+
3'UTR
2471 .. 2471
G/A/C
rs7869
+
3'UTR
2499 .. 2499
G/A
rs1054293
+
3'UTR
2514 .. 2514
A/C
rs188600883
-
3'UTR
2561 .. 2561
G/A
rs1054851
+
3'UTR
2603 .. 2603
C/T
rs1055754
+
3'UTR
2665 .. 2665
G/A
rs41282244
-
3'UTR
2674 .. 2674
G/T
rs10390
+
3'UTR
Microsatellite (Short Tandem Repeat, STR)
No data available
Microsatellite: Human-Gene diversity Of Life-style related Diseases (H-GOLD)
No data available
Repeat
No data available
Database links
Human-Gene diversity Of Life-style related Diseases(H-GOLD)
;
Related H-InvDB links
VaryGene;
Repeat Mask Viewer
;