H-InvDB_8.3 released on March 26, 2013.
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H-Inv ID (HIT)
H-Inv cluster ID (HIX)
H-Inv protein ID (HIP)
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Definition*
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---
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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.
Select format
Flat file
XML file
Nucleotide sequence fasta
Protein sequence fasta
Transcript original information
Accession number
CR618785.1
CAGE tag ID
NA
EST ID
NA
Clone Number
CS0DD006YD05
Experimental resources
NBRC
;
HGPD
;
Antibody (WIPF1)
;
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
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
CGCCCGGCTCAGCCCTGCGGACCCCGGGAGAAGTTTCCCAGAAAAAATGC CCAGCGCGGCGCGGGGCTGCGGAGTCGTCCGGAGCCGCTGCGCGATTTAT CAGCAAGACTGTTGAACGCATAACTGCCCAAGATGCCTGTCCCTCCCCCT CCAGCACCCCCGCCGCCCCCGACGTTTGCACTGGCCAATACAGAGAAGCC TACCTTGAATAAGACAGAGCAGGCTGGGAGAAATGCTCTCCTTTCTGATA TCAGCAAAGGGAAGAAACTAAAGAAGACGGTCACCAATGACAGAAGTGCA CCAATACTGGACAAACCTAAAGGAGCTGGTGCTGGAGGCGGTGGTGGTGG CTTTGGTGGAGGCGGCGGATTTGGCGGAGGAGGTGGTGGCGGAGGCGGTG GAAGTTTTGGAGGGGGCGGACCTCCAGGTCTGGGAGGATTGTTCCAGGCT GGAATGCCGAAGCTGAGATCCACGGCCAACAGGGATAATGATTCTGGAGG AAGCCGACCACCATTGTTGCCACCGGGAGGAAGATCCACATCTGCGAAAC CCTTTTCACCCCCAAGTGGCCCAGGGAGGTTTCCTGTGCCTTCTCCAGGC CACAGAAGTGGTCCCCCAGAGCCTCAGAGGAACCGAATGCCGCCCCCAAG GCCCGACGTGGGCTCAAAGCCTGATAGCATTCCTCCTCCAGTACCTAGTA CTCCAAGACCCATTCAATCAAGTCCGCACAACCGGGGGTCCCCACCAGTG CCCGGAGGCCCCAGGCAGCCCAGCCCCGGGCCCACTCCTCCCCCTTTCCC TGGAAACCGCGGCACTGCTTTGGGAGGAGGCTCAATACGTCAGTCCCCCT TGAGCTCCTCCTCGCCCTTCTCCAACCGGCCTCCCCTGCCGCCTACCCCC AGCAGGGCCTTGGATGACAAACCCCCTCCACCACCTCCTCCAGTGGGCAA CAGGCCCTCCATCCACAGGGAAGCGGTTCCCCCTCCTCCTCCTCAGAACA ACAAGCCTCCAGTGCCTTCCACTCCGCGGCCTTCGGCCTCCTCACAGGCC CCACCTCCGCCGCCACCTCCCAGCAGGCCCGGGCCGCCTCCTCTGCCTCC AAGTTCCAGCGGCAATGACGAAACCCCAAGACTCCCACAGCGGAATCTGT CCCTCAGTTCGTCCACGCCCCCGTTACCTTCGCCAGGACGTTCAGGTCCT CTTCCTCCCCCGCCCAGTGAGAGACCCCCACCTCCAGTGAGGGACCCGCC AGGCCGATCAGGCCCCCTCCCACCACCTCCTCCAGTAAGCAGAAACGGCA GCACATCTCGGGCCCTGCCTGCTACCCCTCAGTTGCCATCCAGGAGTGGA GTAGACAGTCCCAGGAGTGGACCCAGGCCTCCCCTTCCTCCTGATAGGCC CAGTGCTGGGGCACCTCCCCCACCTCCACCATCAACATCTATTAGAAATG GCTTCCAAGACTCTCCATGTGAAGATGAGTGGGAAAGCAGATTCTACTTC CATCCGATTTCCGATTTGCCACCTCCAGAGCCATATGTACAAACGACCAA AAGTTATCCCAGCAAACTGGCAAGAAACGAAAGCCGGAGTGGATCCAACC GAAGAGAAAGGGGTGCTCCACCACTCCCTCCCATCCCGAGGTGATCTTTG CCTGCTCTTCTCTACCCAAGCTCAAGAGCTGCTTCTGTTGCTATCTAAGA ACTGCATACCCTCCTCCCTGCTTCTTCCCTTGTGCCTCATGTATGGGCAG GAGGAAAGGTGGGAGGGGGAGTGGGAATATGCGTGTGTGGGTGGGAATCG GTAAGAAATGCACCTAGCTTTTCATATTGTGTTTATTCTCCAGGCTATTG CTTGCTTCAGCTGCAGCCTGCCTGTGCTGGCTGCTGGGGTCGATAGGCTT TTGTCGTAATAGGCAGAGATGACTTGCATCCCAGCTTTCCACCAACCAAA TTCAAACATTCACTGCTTATTTGTTACAGACTGTAAT
Gene structure information
H-Inv cluster ID
HIX0002607
Genomic location
Chromosome
2
Location
2q31.1
Position
175426932- 175547595
Strand
-
Possible duplicated location(s)
NA
Gene structure
8 exon(s)
Database links
RefSeq
NM_003387
;
NM_001077269
;
Ensembl
ENST00000272746
;
ENST00000359761
;
ENST00000392546
;
ENST00000392547
;
ENST00000392548
;
ENST00000409415
;
ENST00000409891
;
ENST00000410117
;
ENST00000436221
;
ENST00000455428
;
ENST00000467149
;
ENST00000469002
;
ENST00000470752
;
ENST00000474332
;
ENST00000480400
;
ENST00000487291
;
ENST00000488830
;
ENST00000490887
;
Entrez Gene
Entrez Gene ID:7456
;
KEGG GENES
KEGG GENES(7456)
;
GeneCard
WIPF1
;
*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
HIP000087464
Predicted CDS
133..1644; 503[aa]; Orientation:+1;
Codon Adaptation Index (CAI).
0.761
Database links
RefSeq
NP_001070737
;
NP_003378
;
UniProt
O43516
;
CCDS
CCDS2260
;
MPVPPPPAPPPPPTFALANTEKPTLNKTEQAGRNALLSDISKGKKLKKTV TNDRSAPILDKPKGAGAGGGGGGFGGGGGFGGGGGGGGGGSFGGGGPPGL GGLFQAGMPKLRSTANRDNDSGGSRPPLLPPGGRSTSAKPFSPPSGPGRF PVPSPGHRSGPPEPQRNRMPPPRPDVGSKPDSIPPPVPSTPRPIQSSPHN RGSPPVPGGPRQPSPGPTPPPFPGNRGTALGGGSIRQSPLSSSSPFSNRP PLPPTPSRALDDKPPPPPPPVGNRPSIHREAVPPPPPQNNKPPVPSTPRP SASSQAPPPPPPPSRPGPPPLPPSSSGNDETPRLPQRNLSLSSSTPPLPS PGRSGPLPPPPSERPPPPVRDPPGRSGPLPPPPPVSRNGSTSRALPATPQ LPSRSGVDSPRSGPRPPLPPDRPSAGAPPPPPPSTSIRNGFQDSPCEDEW ESRFYFHPISDLPPPEPYVQTTKSYPSKLARNESRSGSNRRERGAPPLPP IPR*
Motif information
a.a.
length
InterPro
Name
18
IPR003124
Actin-binding WH2 [Domain]
Gene function information
H-Inv ID
HIT000297980
H-Inv cluster ID
HIX0002607
Accession number
CR618785.1
CAGE tag ID
NA
EST ID
NA
Transcript feature
NO;
Splicing isoform
Coding potential
Protein coding;
Definition
WAS/WASL-interacting protein family member 1.
Similarity category
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
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)
H-Inv protein ID
HIP000087464
No. of interaction
6
Interaction partner(s)
HIP000039089
;
HIP000082022
;
HIP000082374
;
HIP000099536
;
HIP000100279
;
HIP000109033
;
BIND
NA
DIP
87916E;
MINT
NA
HPRD
01242; 04077; 07171; 09272; 17031;
IntAct
EBI-1184672; EBI-2483335; EBI-776423;
Database links
RefSeq
NM_003387
;
NM_001077269
;
Ensembl
ENST00000272746
;
ENST00000359761
;
ENST00000392546
;
ENST00000392547
;
ENST00000392548
;
ENST00000409415
;
ENST00000409891
;
ENST00000410117
;
ENST00000436221
;
ENST00000455428
;
ENST00000467149
;
ENST00000469002
;
ENST00000470752
;
ENST00000474332
;
ENST00000480400
;
ENST00000487291
;
ENST00000488830
;
ENST00000490887
;
Entrez Gene
Entrez Gene ID:7456
;
KEGG GENES
KEGG GENES(7456)
;
GeneCard
WIPF1
;
*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
Putative Interferon-induced transmembrane protein (IPR007593).
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
nuclear; cytosol;
Target P
Other
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.
Gene expression information
Last modified:20-Apr-2012
Tissue-specific expression
NA
Probe
information
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-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:
600666
;
607329
;
609402
;
Disease related mutation
NA
Literature-Extracted GENe-Disease Associations (LEGENDA)
Gene name
Entrez Gene ID:(7456)
Disease
Entrez Gene ID:(7456)
Substance
Entrez Gene ID:(7456)
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
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
No data available
Database links
Human-Gene diversity Of Life-style related Diseases(H-GOLD)
;
Related H-InvDB links
VaryGene
;
Repeat Mask Viewer
;