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H-InvDB_8.3 released on March 26, 2013.
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H-Invitational ID: HIT000297980 Accession number: CR618785 Created date: 26-Mar-2013 Last modified: 20-Apr-2012
Definition: WAS/WASL-interacting protein family member 1.
 
 

Transcript original information
Accession number CR618785.1
CAGE tag ID NA
EST ID NA
Clone Number CS0DD006YD05
Experimental resources NBRC: NITE Biological Resource Center  NBRC ; HGPD: Human Gene and Protein Database HGPD ; Antibody: searching human antibodies at "BIO-kaimono.com" Antibody (WIPF1) ; Catalog: searching experimental product catalogs at "BIO-kaimono.com" Catalog (WIPF1);
Sequence data provider NA
Annotation project NA
Length of cDNA 1987[bp] (No. of exon:8)[A:430 T:385 G:502 C:670]
Devision HTC
Molecular type mRNA
Library origin Cell type NA
Tissue type Neuroblastoma Cot 50-normalized
Develpmental stage NA
Mini-G
Sequence quality information
CDS feature Complete CDS
Kozak sequence NA
PolyA NA
Vector/adapter sequence NA
Frame shift NA
Remaining intron NA
Splice site acceptor (NAGNAG) NA
Transcript quality feature NA
Notes NA

Gene structure information  G-integra H-DBAS cDNA-genome alignment
H-Inv cluster ID HIX0002607
Genomic location  G-integra Help Chromosome 2
Location 2q31.1
Position 175426932- 175547595
Strand -
Possible duplicated location(s) NA
Gene structure 8 exon(s)
Database links RefSeq NM_003387NM_001077269
Ensembl ENST00000272746ENST00000359761ENST00000392546ENST00000392547ENST00000392548ENST00000409415ENST00000409891ENST00000410117ENST00000436221ENST00000455428ENST00000467149ENST00000469002ENST00000470752ENST00000474332ENST00000480400ENST00000487291ENST00000488830ENST00000490887
Entrez Gene Entrez Gene ID:7456
KEGG GENES KEGG GENES(7456)
GeneCard GeneCardWIPF1*GeneCards is provided free to academic non-profit institutions.
Related H-InvDB links H-DBASH-DBAS G-integraG-integra cDNA-genome alignmentcDNA-genome alignment

Predicted CDS information
HIP ID HIP000087464
Predicted CDS 133..1644;  503[aa];  Orientation:+1; 
Codon Adaptation Index (CAI). 0.761
Database links RefSeq NP_001070737NP_003378
UniProt O43516
CCDS CCDS2260

Motif information
ORF

length(503),orf(133:1644)
MPVPPPPAPPPPPTFALANTEKPTLNKTEQAGRNALLSDISKGKKLKKTV
TNDRSAPILDKPKGAGAGGGGGGFGGGGGFGGGGGGGGGGSFGGGGPPGL
GGLFQAGMPKLRSTANRDNDSGGSRPPLLPPGGRSTSAKPFSPPSGPGRF
PVPSPGHRSGPPEPQRNRMPPPRPDVGSKPDSIPPPVPSTPRPIQSSPHN
RGSPPVPGGPRQPSPGPTPPPFPGNRGTALGGGSIRQSPLSSSSPFSNRP
PLPPTPSRALDDKPPPPPPPVGNRPSIHREAVPPPPPQNNKPPVPSTPRP
SASSQAPPPPPPPSRPGPPPLPPSSSGNDETPRLPQRNLSLSSSTPPLPS
PGRSGPLPPPPSERPPPPVRDPPGRSGPLPPPPPVSRNGSTSRALPATPQ
LPSRSGVDSPRSGPRPPLPPDRPSAGAPPPPPPSTSIRNGFQDSPCEDEW
ESRFYFHPISDLPPPEPYVQTTKSYPSKLARNESRSGSNRRERGAPPLPP
IPR*
a.a.
length
InterPro Name
length(18), motif(32:49) 18 IPR003124 Actin-binding WH2 [Domain]

Gene function information  Gene family PPI viewer Similarity Search Tool TACT
H-Inv ID HIT000297980
H-Inv cluster ID Locus viewHIX0002607
Accession number CR618785.1
CAGE tag ID NA
EST ID NA
Transcript feature  Help NO;  Splicing isoformSplicing isoform
Coding potential  Help Protein coding; 
Definition WAS/WASL-interacting protein family member 1.
Similarity category  Help Category: Identical to known human protein(Category I).
Identical to known human protein (NP_003378)  [Identity/coverage = 100.0%/100.0%] to Homo sapiens protein.
Experimental evidence Protein evidence
PubMed ID NA
Gene family/group Gene family H-Inv gene family/group ID HIF0000034
Gene family/group name Putative Interferon-induced transmembrane protein (IPR007593).
Evidence motif (InterPro) ID IPR007593
Gene symbol/name HGNC symbol WIPF1
HGNC aliases "Wiskott-Aldrich syndrome protein interacting protein"
HGNC name WAS/WASL interacting protein family, member 1
DDBJ NA
UniProt NA
EC number NA
GGDB
(GlycoGene Database)
Gene symbol NA
Familly NA
Designation NA
Expression NA
KEGG metabolic pathway NA
Protein-protein interaction (PPI) PPI viewer H-Inv protein ID HIP000087464
No. of interaction 6
Interaction partner(s) HIP000039089HIP000082022HIP000082374HIP000099536HIP000100279HIP000109033
BIND NA
DIP 87916E; 
MINT NA
HPRD 01242;  04077;  07171;  09272;  17031; 
IntAct EBI-1184672;  EBI-2483335;  EBI-776423; 
Database links RefSeq NM_003387NM_001077269
Ensembl ENST00000272746ENST00000359761ENST00000392546ENST00000392547ENST00000392548ENST00000409415ENST00000409891ENST00000410117ENST00000436221ENST00000455428ENST00000467149ENST00000469002ENST00000470752ENST00000474332ENST00000480400ENST00000487291ENST00000488830ENST00000490887
Entrez Gene Entrez Gene ID:7456
KEGG GENES KEGG GENES(7456)
GeneCard GeneCardWIPF1*GeneCards is provided free to academic non-profit institutions.
etc H-GOLDHuman-Gene diversity Of Life-style related Diseases
Curation status Auto-annotated
Notes NA
Related H-InvDB links Putative Interferon-induced transmembrane protein (IPR007593). Similarity Search ToolSimilarity Search Tool;  TACTTACT
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 nuclear;  cytosol; 
Target P Other
SOSUI soluble protein
TMHMM soluble protein
PTS1 Not targeted
Related H-InvDB links LIFEdb LIFEdb; 
JRE-1.4.0 or later is required. Download JRE at Sun's web site.

Gene expression information  H-ANGEL DNAProbeLocator Last modified:20-Apr-2012
Tissue-specific expression  H-ANGEL NA
Probe
information DNAProbeLocator
AceGene AGhsA240212; 
Affymetrix
GeneChip
HG-Focus NA
HG-U133 202665_s_at; 
HG-U133A 202665_s_at; 
HG-U133A_2 202665_s_at; 
HG-U133B NA
HG-U133_Plus_2 202665_s_at; 
HG-U95 47755_at;  62743_at; 
HG-U95A NA
HG-U95B 47755_at; 
HG-U95C 62743_at; 
HG-U95D NA
HG-U95E NA
HG-U95Av2 NA
HuEx-1_0 2587851;  2587852;  2587853;  2587854;  2587858;  2587860;  2587866;  2587867;  2587868;  2587869;  2587871;  2587872;  2587873;  2587878;  2587879;  2587880;  2587924; 
HuGeneFL NA
Agilent Human 1A Oligo Microarray:PGID215 A_23_P251436;  A_23_P330612; 
Whole Human Genome Oligo Microarray:PGID247 A_23_P330611;  A_23_P330616; 
Related H-InvDB links H-ANGELH-ANGEL DNAProbeLocatorDNAProbeLocator

Disease/pathology information  DiseaseInfo Viewer LEGENDA 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:  600666607329609402
Disease related mutation NA
Literature-Extracted GENe-Disease Associations (LEGENDA) LEGENDA Gene name Entrez Gene ID:(7456)
Disease Entrez Gene ID:(7456)
Substance Entrez Gene ID:(7456)
Related H-InvDB links DiseaseInfo ViewerDiseaseInfo ViewerLEGENDALEGENDA

Polymorphism (SNP, indel), microsatellite (Short Tandem Repeat, STR) and repeat information  VaryGene Repeat mask viewer
 Single Nucleotide Polymorphism (SNP) and indel  VaryGene
Location Variation dbSNP ID Strand CDS/UTR Translation
66 .. 66 G/C rs113563347 - 5'UTR
174 .. 174 G/A rs111761533 - CDS Synonymous[Thr14Thr]
210 .. 210 T/C rs35923393 + CDS Synonymous[Asn26Asn]
402 .. 402 A/G rs114862098 - CDS Synonymous[Gly90Gly]
471 .. 471 C/G rs76308107 - CDS Synonymous[Ser113Ser]
725 .. 725 C/T rs4972450 - CDS Nonsynonymous[Pro198Leu]
782 .. 782 C/T rs11551322 + CDS Nonsynonymous[Pro217Leu]
1089 .. 1089 T/G rs112447307 - CDS Synonymous[Pro319Pro]
1279 .. 1279 C/T rs71417494 - CDS Nonsynonymous[Pro383Ser]
1282 .. 1282 C/T rs71417493 - CDS Nonsynonymous[Pro384Ser]
1296 .. 1296 C/T rs41270199 - CDS Synonymous[Asn388Asn]
1415 ^ 1416 -/T rs34236584 - CDS
1428 .. 1428 A/G rs76731102 - CDS Synonymous[Pro432Pro]
1445 .. 1445 G/A rs12052997 - CDS Nonsynonymous[Arg438Lys]
1546 .. 1546 A/G rs113179543 - CDS Nonsynonymous[Thr472Ala]
1578 .. 1578 C/T rs116757787 - CDS Synonymous[Asn482Asn]
1712 .. 1712 T/A rs113462357 - 3'UTR
1905 .. 1905 C/T rs115476647 - 3'UTR
1919 .. 1919 A/T rs41270197 - 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  Repeat mask viewer
No data available
Database links H-GOLDHuman-Gene diversity Of Life-style related Diseases(H-GOLD)
Related H-InvDB links VaryGeneVaryGene Repeat mask viewerRepeat Mask Viewer