H-InvDB_8.3 released on March 26, 2013. Search by Keyword H-Inv ID (HIT) H-Inv cluster ID (HIX) H-Inv protein ID (HIP) H-Inv gene family/group (HIF) Accession number Chromosome number Chromosome band Definition* Data source ID --- CCDS ID dbSNP ID (rs number) EC number Ensembl ID EntrezGene ID FR ID FR Accession number GO ID GO name* HGNC gene symbol HGNC gene name* InterPro ID InterPro name* OMIM ID OMIM title* Pathway ID Pathway name* RefSeq (gene) ID RefSeq (protein) ID SCOP ID UniProt for Advanced Search

Home Quick guide Navi BLAST Site map Download Contact us Help

Locus view Protein view G-integra DiseaseInfo Viewer H-ANGEL Evola PPI view Gene Family/Group Hyperlink MS

H-Invitational ID: HIT000260838 Accession number: BC063317 Created date: 26-Mar-2013 Last modified: 20-Apr-2012 Definition: Prostaglandin F2 receptor negative regulator; CD9 partner 1; CD9P-1; Glu-Trp-Ile EWI motif-containing protein F; EWI-F; Prostaglandin F2-alpha receptor regulatory protein; Prostaglandin F2-alpha receptor-associated protein; AltName: CD_antigen=CD315; Precursor;

		Select format Flat file XML file Nucleotide sequence fasta Protein sequence fasta

Transcript original information Accession number BC063317.1 CAGE tag ID NA EST ID NA Clone Number IMAGE:30347731 Experimental resources   NBRC ; HGPD ; Antibody (PTGFRN) ; Catalog (PTGFRN); Sequence data provider NA Annotation project NA Length of cDNA 6139[bp] (No. of exon:9)[A:1447 T:1538 G:1642 C:1512] Devision HTC Molecular type mRNA Library origin Cell type NA Tissue type Placenta, normal Develpmental stage NA

Sequence quality information CDS feature Complete CDS Kozak sequence NA PolyA Site: 6124(+) Signal: 6105-6109(+) Vector/adapter sequence NA Frame shift NA Remaining intron NA Splice site acceptor (NAGNAG) NA Transcript quality feature NA Notes NA

GAGGAGCGCCGACTCTGGAGCAGCCGGAGCTGGAAGAGGAGGAGGAGGAG AGGCGGCGGGGAAGGAGGAGGAGGGGGAGAGTCGCTCCCGCCGGGCGAGC ATGGGGCGCCTGGCCTCGAGGCCGCTGCTGCTGGCGCTCCTGTCGTTGGC TCTTTGCCGAGGGCGTGTGGTGAGAGTCCCCACAGCGACCCTGGTTCGAG TGGTGGGCACTGAGCTGGTCATCCCCTGCAACGTCAGTGACTATGATGGC CCCAGCGAGCAAAACTTTGACTGGAGCTTCTCATCTTTGGGGAGCAGCTT TGTGGAGCTTGCAAGCACCTGGGAGGTGGGGTTCCCAGCCCAGCTGTACC AGGAGCGGCTGCAGAGGGGCGAGATCCTGTTAAGGCGGACTGCCAACGAC GCCGTGGAGCTCCACATAAAGAACGTCCAGCCTTCAGACCAAGGCCACTA CAAATGTTCAACCCCCAGCACAGATGCCACTGTCCAGGGAAACTATGAGG ACACAGTGCAGGTTAAAGTGCTGGCCGACTCCCTGCACGTGGGCCCCAGC GCGCGGCCCCCGCCGAGCCTGAGCCTGCGGGAGGGGGAGCCCTTCGAGCT GCGCTGCACCGCCGCCTCCGCCTCGCCGCTGCACACGCACCTGGCGCTGC TGTGGGAGGTGCACCGCGGCCCGGCCAGGCGGAGCGTCCTCGCCCTGACC CACGAGGGCAGGTTCCACCCGGGCCTGGGGTACGAGCAGCGCTACCACAG TGGGGACGTGCGCCTCGACACCGTGGGCAGCGACGCCTACCGCCTCTCAG TGTCCCGGGCTCTGTCTGCCGACCAGGGCTCCTACAGGTGTATCGTCAGC GAGTGGATCGCCGAGCAGGGCAACTGGCAGGAAATCCAAGAAAAGGCCGT GGAAGTTGCCACCGTGGTGATCCAGCCGACAGTTCTGCGAGCAGCTGTGC CCAAGAATGTGTCTGTGGCTGAAGGAAAGGAACTGGACCTGACCTGTAAC ATCACAACAGACCGAGCCGATGACGTCCGGCCCGAGGTGACGTGGTCCTT CAGCAGGATGCCTGACAGCACCCTACCTGGCTCCCGCGTGTTGGCGCGGC TTGACCGTGATTCCCTGGTGCACAGCTCGCCTCATGTTGCTTTGAGTCAT GTGGATGCACGCTCCTACCATTTACTGGTTCGGGATGTTAGCAAAGAAAA CTCTGGCTACTATTACTGCCACGTGTCCCTGTGGGCACCCGGACACAACA GGAGCTGGCACAAAGTGGCAGAGGCCGTGTCTTCCCCAGCTGGTGTGGGG TGACCTGGCTAGAACCAGACTACCAGGTGTACCTGAATGCTTCCAAGGTC CCCGGGTTTGCGGATGACCCCACAGAGCTGGCATGCCGGGTGGTGGACAC GAAGAGTGGGGAGGCGAATGTCCGATTCACGGTTTCGTGGTACTACAGGA TGAACCGGCGCAGCGACAATGTGGTGACCAGCGAGCTGCTTGCAGTCATG GACGGGGACTGGACGCTAAAATATGGAGAGAGGAGCAAGCAGCGGGCCCA GGATGGAGACTTTATTTTTTCTAAGGAACATACAGACACGTTCAATTTCC GGATCCAAAGGACTACAGAGGAAGACAGAGGCAATTATTACTGTGTTGTG TCTGCCTAGACCAAACAGCGGAACAACAGCTGGGTGAAAAGCAAGGATGT CTTCTCCAAGCCTGTTAACATATTTTGGGCATTAGAAGATTCCGTGCTTG TGGTGAAGGCGAGGCAGCCAAAGCCTTTCTTTGCTGCCGGAAATACATTT GAGATGACTTGCAAAGTATCTTCCAAGAATATTAAGTCGCCACGCTACTC TGTTCTCATCATGGCTGAGAAGCCTGTCGGCGACCTCTCCAGTCCCAATG AAACGAAGTACATCATCTCTCTGGACCAGGATTCTGTGGTGAAGCTGGAG AATTGGACAGATGCATCACGGGTGGATGGCGTTGTTTTAGAAAAAGTGCA GGAGGATGAGTTCCGCTATCGAATGTACCAGACTCAGGTCTCAGACGCAG GGCTGTACCGCTGCATGGTGACAGCCTGGTCTCCTGTCAGGGGCAGCCTT TGGCGAGAAGCAGCAACCAGTCTCTCCAATCCTATTGAGATAGACTTCCA AACCTCAGGTCCTATATTTAATGCTTCTGTGCATTCAGACACACCATCAG TAATTCGGGGAGATCTGATCAAATTGTTCTGTATCATCACTGTCGAGGGA GCAGCACTGGATCCAGATGACATGGCCTTTGATGTGTCCTGGTTTGCGGT GCACTCTTTTGGCCTGGACAAGGCTCCTGTGCTCCTGTCTTCCCTGGATC GGAAGGGCATCGTGACCACCTCCCGGAGGGACTGGAAGAGCGACCTCAGC CTGGAGCGCGTGAGTGTGCTGGAATTCTTGCTGCAAGTGCATGGCTCCGA GGACCAGGACTTTGGCAACTACTACTGTTCCGTGACTCCATGGGTGAAGT CACCAACAGGTTCCTGGCAGAAGGAGGCAGAGATCCACTCCAAGCCCGTT TTTATAACTGTGAAGATGGATGTGCTGAACGCCTTCAAGTATCCCTTGCT GATCGGCGTCGGTCTGTCCACGGTCATCGGGCTCCTGTCCTGTCTCATCG GGTACTGCAGCTCCCACTGGTGTTGTAAGAAGGAGGTTCAGGAGACACGG CGCGAGCGCCGCAGGCTCATGTCGATGGAGATGGACTAGGCTGGCCCGGG AGGGGAGTGACAGAGGGACGTTCTAGGAGCAATTGGGGCAAGAAGAGGAC AGTGATATTTTAAAACAAAGTGTGTTACACTAAAAACCAGTCCTCTCTAA TCTCAGGTGGGACTTGGCGCTCTCTCTTTTCTGCATGTCAAGTTCTGAGC GCGGACATGTTTACCAGCACACGGCTCTTCTTCCCACGGCACTTTCTGAT GTAACAATCGAGTGTGTGTTTTCCCAACTGCAGCTTTTTAATGGTTAACC TTCATCTAATTTTTTTTCTCCCACTGGTTTATAGATCCTCTGACTTGTGT GTGTTTATAGCTTTTGTTTCGCGGGGTTGTGGTGAGGAAGGGGTGATGGC ATGCGGAGTTCTTTATCTTCAGTGAGAATGTGCCTGCCCGCCTGAGAGCC AGCTTCCGCGTTGGAGGCACGTGTTCAGAGAGCTGCTGAGCGCCACCCTC TACCCGGCTGACAGACAACACAGACCTGTGCCGAAGGCTAATTTGTGGCT TTTACGACCCTACCCCACCCCCTGTTTTCAGGGGTTTAGACTACATTTGA AATCCAAACTTGGAGTATATAACTTCTTATTGAGCCCAACTGCTTTTTTT TTTTTTTTTTTTTTGCTTCTCTGCCCCTTTTCCATTTCTTTTGTATTTGT TTTCTGTGAGAGCACTGAAATGGCAGCCCTGGAATCTACAATTTGGCTCT CCACTGAGCACCTTATCTTGCCACCTTAGCCTTAAGAATGAATATGAAGA AAAATACACAGCCACCTCTGTCCAGGGCAGTAAGAAGGGCTGCAAGGAAG GGGAGGATGGGGACAAGGAAAGGATCAGATACCTGCTCCAGTAGTTGTGA GGCCACTGTGTCTCAGGGGACTCCAGGAGGAGCAGAAGAGGGATCCCACG AAGTTATTCTTACGCAGCTGGGGCCAGGAGGGTCAGAGTGGTGCCAGGTG CAAGTTAGGCTAAAGAAGCCACCACTATTCCTCTCTCTTGCCCATTGTGG GGGGCAAAGGCATTGGTCACCAAGAGTCTTGCAGGGGGACCCACAGATAT GCCATGTCCTTCACACGTGCTTGGGCTCCTTAACCTGAAGGCAAATTGCT ACTTGCAAGACTGACTGACTTCAAGGAATCAGAAATTACCTAGAAGCACC ATGTTTTTTCTATGACCTTTTCAGTCCTTCAGGTCATTTTAAGGTCCACT GCAGGGGGTTAGTGAGAAAGGGTATACTTTGTGGTATGTTTTGCTTTCCT AATAGGGACATGAAGGAAACCCAGCAATTTGCTGTTATGTGAATGGCCTG TAGAGCAGAGTCAAGAGCGGTGTGCTTTGCCCGACTGCTCCCATCAGGAA TAGGAGAGTAGACAGAGATCTTCCACATCCCAGGCTTCTGCTGCTGCTTT AAAAGCTCTGTCCTTGGAGCCTCCCGCTCCCTGAAGTGTCTCGCCCCCTG CACAGCACTGGCCTTTCGGAAGCATCCCAGTAGGGTTTTCTGAGGCTCGC TGGTGACTCATGCCCTAATTGCAATCCTCTGCTTTTATCTTGACTTTGAA GGATCTAACACTGCTCTCTCTTCCAAAGGGGAAAAAAAGATTCATTTGTT TTGAGCAATAAACTAATACAAAATGATGGCCATTCATGTGCAGCTCTTTG TCACCATGGGCCGGATGAGTTGTGCTCCTCCTGGCTCACCATTTCCCCCT GCTCCCCCACAGCCGGTTCTGCACTTATCACCGAGTCGCCCCTGGAAGCA GATTCCCATTGAGTTTTCCCCACCAAGGGGACCATGCACATGGTAGAAAC ATTAGATTCTGCATTGACAGTAGCCTTTCCTTGGCCCGGGCCTGTGGTGG GAAGACGGGCAACAAGTATACCCCACCAGGGCCTGAGTGACTAGAGGAAG AGGACGAGGCCTTGTTGGCACTAGATTTGGGTATTTTCTGCATGTCATAA CATATCCTAACTGCTATTTCAGAAGAGGCAGCTTGTAGGTGATTGTACAA GTGAGAATTAAAGAGAGAACAGATATTTAAACAGGTGCTGTATTAGTAAC AGCCAGTGCCCTTTCAGCCCTTGCATCTATTAAAAGGAGATTCAGGATTT TATTGGCACAGGCCCTTCTTAGTAGGAAGAAAGGGTGCTTAGCTTTGGAC CTGACCGGGTGTGTGTAAAACCATGGACTGAGTCACAGCAGACACTCGAT GGTGGTAAATGTGATGGGTGCTTACACACTGTACCTTTTCCTTTCATACT GATGCTGCAGTTCAGGGCTGGAGTTGTTAAGGCATTGACCTCCACCCACC TGCCCCATGTCCACTGGGCTGCCCAAGCTGCATGTCACCTGAGGGCTGGC AGGAAGGGGCGAGAAATCCCAGGGCATTGTACCAAGGACCTAGTTCCTTC TAGGGATATAAATTTCCGGAATGTGTATTTTTAATGTGGTGAGATGCACT CTTTTGTTGTACCAAATAGGGCTCCCCACCCCACCCCTGCGACAAGTGCT CTTCTAGAACAGGTTCCTACCAGCAGCACTGGTGTGAATGAAAGAGAGAC CCAGCCGCGTCTCACACAGGTGGAATTGCACTTCTTAACAAAAAGGAACT TTATAAAAGTTTGGGATTTTTTTTCCTAATCATAAAAATAGCCCCAGAAA GAGCCTAAGCTATGTTCAGATAGAAGCCTCGAAATTCCTGTAAATTGTTT ACTTTATGATGTTTACATACACGTTTCACTTTGAAAAAAAATGCAAATCG ACTTTTTAACAACTGTTGAGATGTTTCATGGGACAGTAGAACTCTGACTC ACCAACTGGGCTAAATTTTAATTTAAAAATGTATTTATTTGAGTGTCTTT CCCCCCCTCACCCTCACCATCTGAGGGGCTCCCTGAGATCTTGGTAGAGG AGGCCCCTCCTGCCCAGACCTTCGTTTGTTTCCCCGGTGGCCCTTGCTTC TTGCTTTGCAGACTGCCTGCAGCCATGATTTTGTCACTGACATCTGTGAG CCAAAGACTGAGCCTTTTTGGCAGGAATAATAAGCAATACTACACAACTT GCTACTTTCAGAAAACTTTTTTTTAGCTTCACCGATGACAACAGAGGAAG AAGGGAACTGGGATTTGGGTAAGTTCTCCTCCACTGTTTGACCAAATTCT CAGTGATAAATATGTGTGCAGATCCCTAGAAGAGAAAACGCTGACTTTCT TTTTAAGTGTGGCACATAAGGATCTGCAGAATTTTCCGTAGACAAAGAAA GGATCTTGTGTATTTTTGTCCATATCCAATGTTATATGAACTAATTGTAT TGTTTTATACTGTGACCACAAATATTATGCAATGCACCATTTGTTTTTTA TTTCATTAAAGGAAGTTTAATTTAAAAAAAAAAAAAAAA

Gene structure information

H-Inv cluster ID		HIX0000932
Genomic location	Chromosome	1
	Location	1p13.1
	Position	117452726- 117532973
	Strand	+
Possible duplicated location(s)		NA
Gene structure		9 exon(s)
Database links	RefSeq	NM_020440;
	Ensembl	ENST00000393203;  ENST00000496699;  ENST00000497385;  ENST00000544471;
	Entrez Gene	Entrez Gene ID:5738;
	KEGG GENES	KEGG GENES(5738);
	GeneCard	PTGFRN;  *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 HIP000346952 Predicted CDS 101..1303;  400[aa];  Orientation:+2;  Codon Adaptation Index (CAI). 0.8

MGRLASRPLLLALLSLALCRGRVVRVPTATLVRVVGTELVIPCNVSDYDG PSEQNFDWSFSSLGSSFVELASTWEVGFPAQLYQERLQRGEILLRRTAND AVELHIKNVQPSDQGHYKCSTPSTDATVQGNYEDTVQVKVLADSLHVGPS ARPPPSLSLREGEPFELRCTAASASPLHTHLALLWEVHRGPARRSVLALT HEGRFHPGLGYEQRYHSGDVRLDTVGSDAYRLSVSRALSADQGSYRCIVS EWIAEQGNWQEIQEKAVEVATVVIQPTVLRAAVPKNVSVAEGKELDLTCN ITTDRADDVRPEVTWSFSRMPDSTLPGSRVLARLDRDSLVHSSPHVALSH VDARSYHLLVRDVSKENSGYYYCHVSLWAPGHNRSWHKVAEAVSSPAGVG *

Motif information

	a.a. length	InterPro	Name
	122	IPR007110	Immunoglobulin-like [Domain]
	119	IPR013783	Immunoglobulin-like fold [Domain]
	114	IPR003599	Immunoglobulin subtype [Domain]
	102	IPR013106	Immunoglobulin V-set [Domain]
	84	IPR003596	Immunoglobulin V-set, subgroup [Domain]
	120	IPR007110	Immunoglobulin-like [Domain]
	108	IPR013783	Immunoglobulin-like fold [Domain]
	117	IPR003599	Immunoglobulin subtype [Domain]
	119	IPR007110	Immunoglobulin-like [Domain]
	94	IPR013106	Immunoglobulin V-set [Domain]
	101	IPR013783	Immunoglobulin-like fold [Domain]
	107	IPR003599	Immunoglobulin subtype [Domain]
	82	IPR003596	Immunoglobulin V-set, subgroup [Domain]

Gene function information

H-Inv ID		HIT000260838
H-Inv cluster ID		HIX0000932
Accession number		BC063317.1
CAGE tag ID		NA
EST ID		NA
Transcript feature		NO;
Coding potential		Protein coding;
Definition		Prostaglandin F2 receptor negative regulator; CD9 partner 1; CD9P-1; Glu-Trp-Ile EWI motif-containing protein F; EWI-F; Prostaglandin F2-alpha receptor regulatory protein; Prostaglandin F2-alpha receptor-associated protein; AltName: CD_antigen=CD315; Precursor;
Similarity category		Category: Identical to known human protein(Category I).
		Identical to known human protein (Q9P2B2)  [Identity/coverage = 99.772%/100.0%] to Homo sapiens (Human). protein.
Experimental evidence		Protein evidence
PubMed ID		10718198;  11278880;  14702039;  15489334;  16710414;  17924679;  19159218;  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	PTGFRN
	HGNC aliases	NA
	HGNC name	prostaglandin F2 receptor negative regulator
	DDBJ	NA
	UniProt	PTGFRN
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	HIP000346952
	No. of interaction	NA
	Interaction partner(s)	NA
	BIND	NA
	DIP	NA
	MINT	NA
	HPRD	NA
	IntAct	NA
Database links	RefSeq	NM_020440;
	Ensembl	ENST00000393203;  ENST00000496699;  ENST00000497385;  ENST00000544471;
	Entrez Gene	Entrez Gene ID:5738;
	KEGG GENES	KEGG GENES(5738);
	GeneCard	PTGFRN;  *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.

NA

Subcellular localization information

Last modified:20-Apr-2012

WoLF PSORT	extracellular;  lysosome;  cytosol;  mitochondria;  Other;
Target P	signal peptide
SOSUI	soluble 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:20-Apr-2012

Start End PDB_ID E-value Identity Coverage SCOP_ID 23 141 1neuA 4e-08 15.9 113/115 b.1.1.1 161 264 1neuA 5e-04 12.5 103/115 b.1.1.1 284 395 1od7A 1e-07 16.1 112/118 b.1.1.1

Related H-InvDB links GTOP

Gene expression information

Last modified:20-Apr-2012

Tissue-specific expression			NA
Probe information	AceGene		NA
	Affymetrix GeneChip	HG-Focus	NA
		HG-U133	224937_at;  224950_at;
		HG-U133A	NA
		HG-U133A_2	NA
		HG-U133B	224937_at;  224950_at;
		HG-U133_Plus_2	224937_at;  224950_at;
		HG-U95	55585_at;  55637_at;  65900_at;
		HG-U95A	NA
		HG-U95B	55585_at;
		HG-U95C	55637_at;  65900_at;
		HG-U95D	NA
		HG-U95E	NA
		HG-U95Av2	NA
		HuEx-1_0	2353718;  2353719;  2353724;  2353725;  2353726;  2353727;  2353728;  2353733;  2353734;  2353737;  2353738;  2353740;  2353741;  2353742;  2353743;  2353744;  2353745;  2353746;  2430087;  2430088;  2430089;  2430090;  2430091;  2430093;  2430094;  2430096;  2430097;  2430098;
		HuGeneFL	NA
	Agilent	Human 1A Oligo Microarray:PGID215	A_23_P114968;
		Whole Human Genome Oligo Microarray:PGID247	A_23_P114968;  A_32_P190334;
Related H-InvDB links			H-ANGEL;  DNAProbeLocator;

Disease/pathology information

Last modified:20-Apr-2012

Disease relation		Disease name:NA
Related information in OMIM		OMIM ID:NA Title:NA
Co-localized orphan diseases		OMIM ID:  115665;  116600;  155600;  600975;  605225;  605606;  606788;  606852;  606928;  607317;  607671;  608543;  608553;  608995;  610320;  612367;  612596;
Disease related mutation		NA
Literature-Extracted GENe-Disease Associations (LEGENDA)	Gene name	Entrez Gene ID:(5738)
	Disease	Entrez Gene ID:(5738)
	Substance	Entrez Gene ID:(5738)
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 144 .. 144 C/G rs77292583 + CDS Nonsynonymous[Ser15Trp] 244 .. 244 T/C rs34531926 + CDS Synonymous[Tyr48Tyr] 378 .. 378 T/C rs111346071 + CDS Nonsynonymous[Leu93Pro] 394 .. 394 C/T rs77895792 + CDS Synonymous[Ala98Ala] 562 .. 562 G/A rs80123219 + CDS Synonymous[Pro154Pro] 928 .. 928 G/A rs10159095 + CDS Synonymous[Pro276Pro] 928 .. 929 GA/AT rs71483896 + CDS 929 .. 929 A/T rs4546904 + CDS Nonsynonymous[Thr277Ser] 1243 .. 1243 A/G rs57119360 + CDS Synonymous[Gly381Gly] 1388 .. 1388 G/A rs34625170 + 3'UTR 1641 .. 1641 C/T rs6658749 + 3'UTR 1827 .. 1827 G/C rs4381168 + 3'UTR 2244 .. 2244 C/T rs61789097 + 3'UTR 2305 .. 2305 T/A rs78836817 + 3'UTR 2409 .. 2409 C/T rs17036676 + 3'UTR 2559 .. 2559 T/C rs111289655 + 3'UTR 2608 .. 2608 G/A rs10801922 + 3'UTR 2698 ^ 2699 -/G rs34483540 + 3'UTR 2713 ^ 2714 -/G rs35699551 + 3'UTR 3009 ^ 3010 -/T rs3841437 - 3'UTR 3017 ^ 3018 -/T rs71096894 + 3'UTR 3018 ^ 3019 -/T rs67986355 + 3'UTR 3060 .. 3060 G/C rs112158356 + 3'UTR 3115 .. 3115 A/G rs55948695 + 3'UTR 3232 .. 3232 C/T rs74873663 + 3'UTR 3357 ^ 3358 -/T rs72159230 + 3'UTR 3362 .. 3364 TTT/- rs79031036 + 3'UTR 3363 .. 3364 TT/- rs60366817 + 3'UTR 3365 .. 3365 G/T rs115664330 + 3'UTR 3366 .. 3366 C/T rs117934778 + 3'UTR 3374 .. 3374 C/T rs77794467 + 3'UTR 3425 .. 3425 A/C/G rs3885 + 3'UTR 3629 .. 3629 G/A rs10801923 + 3'UTR 3659 .. 3659 C/T rs1127655 + 3'UTR 3663 .. 3663 C/T rs1127656 + 3'UTR 3739 .. 3739 T/C rs78586059 + 3'UTR 3773 .. 3773 A/G rs4620527 + 3'UTR 3879 .. 3879 T/C rs41275576 + 3'UTR 3923 .. 3923 A/G rs41275578 + 3'UTR 4019 ^ 4020 -/C rs34107612 + 3'UTR 4274 .. 4274 A/G rs80348030 + 3'UTR 4332 .. 4332 A/- rs35107839 + 3'UTR 4385 .. 4385 C/T rs79753626 + 3'UTR 4479 .. 4479 C/T rs114176432 + 3'UTR 4772 .. 4772 G/A rs13951 + 3'UTR 4773 .. 4773 A/G rs74984838 + 3'UTR 4779 .. 4779 A/G rs77598758 + 3'UTR 4799 .. 4799 A/C rs79934283 + 3'UTR 4846 ^ 4847 -/C rs34965021 + 3'UTR 4929 .. 4929 T/A rs57573398 + 3'UTR 4965 .. 4965 T/C rs3829881 - 3'UTR 5063 .. 5063 A/G rs10923191 + 3'UTR 5306 .. 5306 C/T rs59226759 + 3'UTR 5442 .. 5442 A/G rs8254 + 3'UTR 5523 .. 5523 G/T rs11836 - 3'UTR 5660 .. 5660 C/A rs78683029 + 3'UTR 5941 .. 5941 C/T rs1127215 + 3'UTR 5949 .. 5949 C/G rs944 + 3'UTR 6042 .. 6042 T/C rs6589 + 3'UTR  Microsatellite (Short Tandem Repeat, STR) Location Variation Strand 36..50 (gag)5 +  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;