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)
H-Inv gene family/group (HIF)
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Definition*
Data source ID
---
CCDS ID
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H-Invitational ID:
HIT000046076
Accession number:
AK126203
Created date:
26-Mar-2013
Last modified:
20-Apr-2012
Definition:
Similar to RELT-like protein 2;
Select format
Flat file
XML file
Nucleotide sequence fasta
Protein sequence fasta
Transcript original information
Accession number
AK126203.1
CAGE tag ID
NA
EST ID
NA
Clone Number
THYMU3003565
Experimental resources
NBRC
;
HGPD
;
Antibody (FCHSD1)
;
Catalog (FCHSD1)
;
Sequence data provider
Project:FLJ; Provider:FLJ/HRI;
Annotation project
H-Invitational FLcDNA
Length of cDNA
3181[bp] (No. of exon:2)[A:656 T:832 G:827 C:866]
Devision
HUM
Molecular type
mRNA
Library origin
Cell type
NA
Tissue type
thymus
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
NMD predicted;
Notes
NA
ATATGCACCTTTTGCTCCTAGTGTCCAGATACCTAGCTTTGTATCATTAT TTTTTCTGATGCCCACTTTTTTTCTTTTTTAAATGTCTATAGCAGTTTTA TTTTATTATTTATTTTAGATTCAGGAGGTACATGTGCTTGTTTGTCATAT GGATATATTGCATACTGGTGGAGATTGGGCTTCTAGTGTACCTGTAACTC AAATAGTGAACATTGTACCTGATAGGTAATTTTTCAACCCTCGCCCCTGC CTCTACTCCTACCTTTGCCCCCTTTGGAGTCCTGGGAGTCTGTTATTTCC ATCTCTATGTCCATGTGTACCCGTTGTTTAGCTCCCACTTATAAGTGAGA ACATGCAATATTTGGTTTTCTGTTTCTGAGTTAGTTCACTTAGGATAATG GCATCCAACTCCATTCATGTTGCTGCAGAGGACATGATTTCATTCTTTTT TATGGCTGTGGAATGCCTGCCTTTTCTAAAACTTTCTGGTACTTCCACCT TGTCCACAAGGAGTCTCCCTCCCTGGAGTTACCACCATCTCCACCACCCC AAGTTCACTTTGCATGACTTAGCACTTAGTCATTTATTGTGTTTGTTGAG GTTTCATTATTGGTTTCTTGACAGCCATTGGGGGTGGGAGCACTATGCAT CCTATCTCCCTTAGTTTTGTACCTTGAGCAGAGCTGATTATACAGCAGTT GCCCAATAAATGTTGAGGACAGTGGATAGAGTGATGGATTTTATGGTCTA GGATGGTGACCATTAATTTAACAAATATTTATAGAATGCCACTGTCCTAA GTGCTGGAGATACAGCATTGAACAAAACAAAGTCTGAAGACTGACTTGTG GTTCTTATTTCCAGACAAAGCCCTGGACTTCCCTGGGTTCCTGGACATGA TGGCACCTCGACTCAGGCCGATGCGTCCACCACCTCCCCCGCCGGCTAAA GCCCCGGATCCTGGCCACCCAGATCCCCTCACCTGAAGGCCAGGGAAGCC TTGACCCCCAGTGATGCTGCTGTCCCTATCTTCAAGCTGTCAGACCACAC CATCAATGATCCAGAGCAACACAGCCAAAAGCTGGAATCGCCCTTATTTC CACCCTCACCTCCAAGGGTGGAAACTTGCCCCTTCCCATTTCTAGAGCTG GAACCCACTCCTTTTTTTCCCATTGTTCTATCATCTCTAGGACCGGAACT ACCTTCTCTTCTGTCATGACCCTATCTAGGGTGGTGAAATGCCTGAAATC TCTGGGGCTGGAAACCATCCATCAAGGTCTCTAGTAGTTCTGGCCCACCT CTTTCCCCACCCTGGCTCCATGACCCACCCCACTCTGGATGCCAGGGTCA CTGGGGTTGGGCTGGGGAGAGGAACAGGCCTTGGGAATCAGGAGCTGGAG CCAGGATGCGAAGCAGCTGTAATGGTCTGAGCGGATTTATTGACAATGAA TAAAGGGCACGAAGGCCAGGCCAGGGCCTGGGCCTCTTGTGCTAAGAGGG CAGGGGGCCTACGGTGCTATTGCTTTAGGGGCCCACCACGGGCAGGGGCC TGCTCCCAGCTGCCACGCTCTATCATATGGAGCGAGGTGTTGGGGAAGGC GGGGCAGGCAGCCTGTTGCAGGCAGGGGAAGGAGAAGAGACTGAGGGGCT GTGACCTCTCCTGAGGCCCCCAGCCTGAGACTGTGCAACTCCAGGTGGAA GTAGAGCTGGTCCCTCAGCTGGGGGGCAGTGCTGTCCAGTGGAGGGGAGG GCTTTCACGCCCACCCACCCCCTGGCCCTGCCAGCTGGTAGTCCATCAGC ACAATGAAGGAGACTTGGAGAAGAGGAAGAATAACACTGTTGCTTCCTGT TCAAGCTGTGTCCAGCTTTTCCCCTGGGGCTCTAGGACCTTCCCTACCTC CACCACCAAACCAAGGGATTTATAGCAAAGGCTAAGCCTGCAGTTTACTC GGGGGGTTCAGGGAGCCGAAAGGCTTAAATAGTTTAAGTAGGTGATGGGA AGATGAGATTACCTCATTTAGGGCTCAGGCAGACTCACCTCACATACTCC CTGCTCCCTGTGGTAGAGACACCTGAGAGAAAGGGGAGGGGTCAACAATG AGAGACCAGGAGTAGGTCCTATCAGTGCCCCCCAGAGTAGAGAGCAATAA GAGCCCAGCCCAGTGCAGTCCCGGCTGTGTTTTCCTACCTGGTGATCAGA AGTGTCTGGTTTGCTTGGCTGCCCATTTGCCTCTTGAGTGGGCAGCCCTG GGCTTGGGCCCCTCCCTCCGGCCCTCAGTGTTGGCTCTGCAGAAGCTCTG GGGTTCCCTTCAAGTGCACGAGGGGTTAGGCTGCTGTCCCTGAGTCCTCC ATTCTGTACTGGGGGGCTGGCTAGGACCTGGGGCTGTGGCCTCTCAGGGG GCAGCCTCTCCATGGCAGGCATCCCTGCCTTGGGCTGCCCTCCCCCAGAC CCCTGACCACCCCCTGGGTCCTGTCCCCCACCAGAGCCCCAGCTCCTGTC TGTGGGGGAGCCATCACGGTGTTCGTGCAGTCCATAGCGCTTCTCAATGT GTGTCACCCGGAACCTGGGAGGGGAGGGAACACTGGGGTTTAGGACCACA ACTCAGAGGCTGCTTGGCCCTCCCCTCTGACCAGGGACATCCTGAGTTTG GTGGCTACTTCCCTCTGGCCTAAGGTAGGGGAGGCCTTCTCAGATTGTGG GGCACATTGTGTAGCCTGACTTCTGCCGGAGCTCCCAGTCCAGGAGGAAA GAGCCAAGGCCCACTTTTGGGATCAGGTGCCTGATCACTGGGCCCCCTAC CTCAGCCCCCCTTTCCCTGGAGCACCTGCCCCACCTGCCCACAGAGAACA CAGTGGTCTCCCCTGTCCGGGGGCGGCTTTTTCCTTCCTTGGAGCGTCCC TGACGGACAAGTGGAGGCCTCTTGCTGCGGCTGCAATGGAGGCAAGGGGC TGCAGAGCCCAGGTGCACTGTGTGATGATGGGAGGGGGCTCCGTCCTGCA GGCTGGAGGTGGCATCCACACTGGACAGCAGGGAGGAGGGGAGTGAGGGT AACATTTCCATTTCCCTTCATGTTTTGTTTCTTACGTTCTTTCAGCATGC TCCTTAAAACCCCAGAAGCCCCAATTTCCCCAAGCCCCATTTTTTCTTGT CTTTATCTAATAAACTCAATATTAAGATGTT
Gene structure information
H-Inv cluster ID
HIX0200720
Genomic location
Chromosome
5
Location
NA
Position
141018870- 141022188
Strand
-
Possible duplicated location(s)
NA
Gene structure
2 exon(s)
Database links
RefSeq
NM_033449
;
Ensembl
ENST00000435817
;
ENST00000518160
;
ENST00000518499
;
ENST00000519800
;
ENST00000520747
;
ENST00000522126
;
ENST00000522386
;
ENST00000522763
;
ENST00000522783
;
ENST00000523856
;
Entrez Gene
Entrez Gene ID:89848
;
KEGG GENES
KEGG GENES(89848)
;
GeneCard
FCHSD1
;
*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
HIP000034232
Predicted CDS
398..664; 88[aa]; Orientation:+2;
Codon Adaptation Index (CAI).
0.761
MASNSIHVAAEDMISFFFMAVECLPFLKLSGTSTLSTRSLPPWSYHHLHH PKFTLHDLALSHLLCLLRFHYWFLDSHWGWEHYASYLP*
Gene function information
H-Inv ID
HIT000046076
H-Inv cluster ID
HIX0200720
Accession number
AK126203.1
CAGE tag ID
NA
EST ID
NA
Transcript feature
NO;
Splicing isoform
Coding potential
Protein coding;
Definition
Similar to RELT-like protein 2;
Similarity category
Category: Similar to known protein(Category II).
Similar to known protein (
Q8NC24
) [Identity/coverage = 100.0%/63.04%] to Homo sapiens (Human). protein.
Experimental evidence
Protein evidence
PubMed ID
12975309
;
15489334
;
16303743
;
16389068
;
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
FCHSD1
HGNC aliases
NA
HGNC name
FCH and double SH3 domains 1
DDBJ
NA
UniProt
RELL2
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
HIP000034232
No. of interaction
NA
Interaction partner(s)
NA
BIND
NA
DIP
NA
MINT
NA
HPRD
NA
IntAct
NA
Database links
RefSeq
NM_033449
;
Ensembl
ENST00000435817
;
ENST00000518160
;
ENST00000518499
;
ENST00000519800
;
ENST00000520747
;
ENST00000522126
;
ENST00000522386
;
ENST00000522763
;
ENST00000522783
;
ENST00000523856
;
Entrez Gene
Entrez Gene ID:89848
;
KEGG GENES
KEGG GENES(89848)
;
GeneCard
FCHSD1
;
*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; nuclear; cytosol;
Target P
Not predicted
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
NA
Affymetrix
GeneChip
HG-Focus
NA
HG-U133
NA
HG-U133A
NA
HG-U133A_2
NA
HG-U133B
NA
HG-U133_Plus_2
NA
HG-U95
NA
HG-U95A
NA
HG-U95B
NA
HG-U95C
NA
HG-U95D
NA
HG-U95E
NA
HG-U95Av2
NA
HuEx-1_0
2832874; 2878783; 2878785;
HuGeneFL
NA
Agilent
Human 1A Oligo Microarray:PGID215
NA
Whole Human Genome Oligo Microarray:PGID247
NA
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:
601888
;
608850
;
611091
;
612554
;
612571
;
Disease related mutation
NA
Literature-Extracted GENe-Disease Associations (LEGENDA)
Gene name
Entrez Gene ID:(89848)
Disease
Entrez Gene ID:(89848)
Substance
Entrez Gene ID:(89848)
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
67 .. 67
T/-
rs35094060
-
5'UTR
74 .. 74
C/T
rs77048297
-
5'UTR
74 .. 75
CT/-
rs111256073
-
5'UTR
103 .. 103
T/A
rs75212457
-
5'UTR
254 .. 254
T/C
rs251180
-
5'UTR
473 .. 473
T/A
rs6580193
-
CDS
Nonsynonymous[Phe26Ile]
883 .. 883
C/A
rs75142511
-
3'UTR
895 .. 895
A/C
rs116772138
-
3'UTR
955 .. 955
C/T
rs32957
-
3'UTR
1041 .. 1041
C/G
rs114773384
-
3'UTR
1197 ^ 1198
-/ACT
rs1160948
-
3'UTR
1198 ^ 1199
-/CTA
rs35590706
-
3'UTR
1199 ^ 1200
-/TAC
rs4042097
-
3'UTR
1202 ^ 1203
-/TAC
rs3833652
+
3'UTR
1286 .. 1286
A/G
rs187515
-
3'UTR
1290 .. 1290
C/T
rs1048452
+
3'UTR
1309 .. 1309
A/C
rs1048453
+
3'UTR
1327 .. 1327
A/C
rs1048455
+
3'UTR
1332 .. 1332
A/C
rs1048456
+
3'UTR
1494 .. 1494
A/G
rs116046686
-
3'UTR
1629 .. 1629
A/G
rs79685025
-
3'UTR
1758 .. 1758
C/T
rs78047479
-
3'UTR
1766 .. 1766
C/T
rs112543254
-
3'UTR
1799 .. 1799
G/A
rs117127684
-
3'UTR
1951 .. 1951
G/T
rs41098
-
3'UTR
2170 .. 2170
C/G
rs32956
-
3'UTR
2221 .. 2221
G/C
rs11742646
-
3'UTR
2308 ^ 2309
-/T
rs35340436
-
3'UTR
2482 .. 2482
C/G
rs17855844
-
3'UTR
2498 .. 2498
G/A
rs79900076
-
3'UTR
2727 .. 2727
C/T/G/A
rs73285814
-
3'UTR
2738 .. 2738
G/A
rs32955
-
3'UTR
2777 .. 2777
G/A
rs78820103
-
3'UTR
2801 .. 2801
C/T
rs56017834
-
3'UTR
2941 .. 2941
G/T
rs14251
-
3'UTR
2956 .. 2956
A/G
rs17855845
-
3'UTR
2992 .. 2992
C/T
rs113111824
-
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
Type
Start
End
Strand
L1PA17
96
464
-
L2a
761
831
-
Database links
Human-Gene diversity Of Life-style related Diseases(H-GOLD)
;
Related H-InvDB links
VaryGene
;
Repeat Mask Viewer
;