H-InvDB_8.3 released on March 26, 2013.
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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*
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InterPro name*
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OMIM title*
Pathway ID
Pathway name*
RefSeq (gene) ID
RefSeq (protein) ID
SCOP ID
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H-Invitational ID:
HIT000265621
Accession number:
BC075806
Created date:
26-Mar-2013
Last modified:
20-Apr-2012
Definition:
Histone H4.
Select format
Flat file
XML file
Nucleotide sequence fasta
Protein sequence fasta
Transcript original information
Accession number
BC075806.1
CAGE tag ID
NA
EST ID
NA
Clone Number
IMAGE:5225467
Experimental resources
NBRC
;
HGPD
;
Antibody (HIST1H4I)
;
Catalog (HIST1H4I)
;
Sequence data provider
NA
Annotation project
NA
Length of cDNA
1418[bp] (No. of exon:1)[A:422 T:379 G:314 C:303]
Devision
HTC
Molecular type
mRNA
Library origin
Cell type
NA
Tissue type
Pancreas, Spleen, adult pooled
Develpmental stage
NA
Sequence quality information
CDS feature
Complete CDS
Kozak sequence
NA
PolyA
Site: 1344(+) Signal: 1319-1323(+)
Vector/adapter sequence
NA
Frame shift
NA
Remaining intron
NA
Splice site acceptor (NAGNAG)
NA
Transcript quality feature
NA
Notes
NA
GACCACTTGATAATGTCAGGACGCGGCAAAGGAGGTAAGGGCCTGGGGAA AGGGGGTGCCAAGCGCCACCGCAAGGTGCTGCGCGACAACATCCAGGGTA TCACCAAGCCAGCCATTCGGCGCCTTGCTCGCCGCGGCGGCGTGAAGCGC ATTTCTGGCCTCATCTATGAGGAGACCCGCGGAGTGTTGAAGGTGTTCCT GGAGAACGTGATCCGGGACGCCGTGACCTACACGGAGCACGCCAAGCGCA AGACGGTCACCGCCATGGACGTGGTCTACGCGCTCAAGCGCCAGGGCCGC ACCCTCTATGGCTTCGGCGGCTAAATGGCATTTTGAAGCCCAGTCATTCT CTAAAAAGGCCCTTTTTAGGGCCCCTAAGCTTTCAACAAAAGAGTTGAAA TGACTGCAAACTGAGTCTCTTAATAGGGCCATTGTCAGTGAGTTCTGTCA TCCTATTTTACAAGATTAACTCGACGCCGAAAATGGGCTGATGACTACAG GTGACCTTGGGCCGAGATTTTTCCAAGGCCAGAAGAGCCTCTGCTGGCCA GTAACTTCTGGCGGCTGCCTGGAAATTGCCTGCAGCCGGTTTACCGCTCG GATTAGTTTAGAAAGCCAAGGGGTCTGCGGTCCAAATAGGGGCGGGCTAG ATAATTAACTTCCCTCTGGACCTTCAAATACGTCTCAGGAGATAATGAGT TTGATGGGCTCCACTAAATGCTAGAACCTCCAGGAAAACTTCGTGGTGGC TGGTTTAAGAGGACTTGGCGGGCACAGAGCTCTGCATGGGGGGGAGGGGG ACAGACCATGCTTTTACTACTGTAGAACAGTAGGGCAGTCTTAAGAGTCT TAGTAATAATATTCCTTTATATGTTTGCCTTTTAAATACTGGAATATATC AAGTATACAAAATGCGCTGGTGACCACACCACTTATTCAAGTGCATCTAA AATCCTTATGTCCCTTTCTCAGTAGCACAGCCCTCCCTTTTTCCTATCTA GAATTAACTAATATTCTAGGATAAACTGATATTCTAAATTTGTTTACTGT TCCCACGCGTTTTAACTTTAGATGCACATACCCCTAATCTATTTTAATCG TCATGAATTTTTACATTTGCTCTTGAAATATATCCGTGTTGAAATGTGCA GTTCTAGGTTATTTTTACCATTAATCTAGTTTTCTAATGTGTCAGTAAAT ACTTTATTCATTTCTCTGTTGATTTTTTTTCCTCATTACAAAACAGCACT GTATACAGCTGTGCATTTTCTGGTTACATGGAAGTGGAATTATTTGGTAA ATGTGCATATTCAACATGAATAAAAATGAACAATTTGCTTTCCAAAAAAA AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA AAAAAAAAAAAAAAAAAA
Gene structure information
H-Inv cluster ID
HIX0005658
Genomic location
Chromosome
6
Location
6p22.1
Position
27107076- 27108419
Strand
+
Possible duplicated location(s)
NA
Gene structure
1 exon(s)
Database links
RefSeq
NM_003495
;
Ensembl
ENST00000354348
;
Entrez Gene
Entrez Gene ID:8294
;
KEGG GENES
KEGG GENES(8294)
;
GeneCard
HIST1H4I
;
*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
HIP000098402
Predicted CDS
13..324; 103[aa]; Orientation:+1;
Codon Adaptation Index (CAI).
0.841
Database links
RefSeq
NP_001029249
;
NP_003486
;
NP_003529
;
NP_003530
;
NP_003531
;
NP_003532
;
NP_003533
;
NP_003534
;
NP_003535
;
NP_003536
;
NP_003537
;
NP_003539
;
NP_068803
;
NP_778224
;
UniProt
A2CI30
;
A3KPR4
;
A7VME9
;
B2R4R0
;
B2RTM0
;
B3FEB2
;
B3FEB7
;
B5DDY3
;
B5FXC8
;
C1C500
;
C3XQS8
;
C4QBN1
;
D2HZU2
;
D2N2J2
;
D5J6Z3
;
D9IA14
;
E7D161
;
F2Z4N2
;
P62794
;
P62795
;
P62796
;
P62797
;
P62798
;
P62799
;
P62800
;
P62801
;
P62802
;
P62803
;
P62804
;
P62805
;
P62806
;
Q28DR4
;
Q45RT4
;
Q4PM69
;
Q4R362
;
Q4SKJ2
;
Q5DET3
;
Q5RCS7
;
Q6WV72
;
Q6WV73
;
Q6WV90
;
Q7K8C0
;
Q7KQD1
;
CCDS
CCDS30847
;
CCDS30851
;
CCDS4571
;
CCDS4572
;
CCDS4583
;
CCDS4589
;
CCDS4593
;
CCDS4598
;
CCDS4604
;
CCDS4620
;
CCDS4630
;
CCDS4631
;
CCDS4637
;
CCDS8665
;
MSGRGKGGKGLGKGGAKRHRKVLRDNIQGITKPAIRRLARRGGVKRISGL IYEETRGVLKVFLENVIRDAVTYTEHAKRKTVTAMDVVYALKRQGRTLYG FGG*
Motif information
a.a.
length
InterPro
Name
102
IPR001951
Histone H4 [Family]
102
IPR009072
Histone-fold [Domain]
100
IPR009072
Histone-fold [Domain]
12
IPR001951
Histone H4 [Family]
5
IPR019809
Histone H4, conserved site [Conserved_site]
75
IPR001951
Histone H4 [Family]
20
IPR001951
Histone H4 [Family]
67
IPR007125
Histone core [Domain]
66
IPR004823
TATA box binding protein associated factor (TAF) [Domain]
21
IPR001951
Histone H4 [Family]
15
IPR001951
Histone H4 [Family]
13
IPR001951
Histone H4 [Family]
12
IPR001951
Histone H4 [Family]
Gene function information
H-Inv ID
HIT000265621
H-Inv cluster ID
HIX0005658
Accession number
BC075806.1
CAGE tag ID
NA
EST ID
NA
Transcript feature
Representative transcript;
Coding potential
Protein coding;
Definition
Histone H4.
Similarity category
Category: Identical to known human protein(Category I).
Identical to known human protein (
NP_778224
) [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
HIF0000790
Gene family/group name
Histone H4 (IPR001951).
Evidence motif (InterPro) ID
IPR001951
Gene symbol/name
HGNC symbol
HIST1H4I
HGNC aliases
"H4 histone family, member M", "histone 1, H4i"
HGNC name
histone cluster 1, H4i
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
HIP000098402
No. of interaction
129
Interaction partner(s)
HIP000000470
;
HIP000005979
;
HIP000021401
;
HIP000021427
;
HIP000022242
;
HIP000023266
;
HIP000023694
;
HIP000023789
;
HIP000024053
;
HIP000026502
;
HIP000026502
;
HIP000027917
;
HIP000028305
;
HIP000029551
;
HIP000029910
;
HIP000029985
;
HIP000030139
;
HIP000030994
;
HIP000031656
;
HIP000033190
;
HIP000033190
;
HIP000034291
;
HIP000034507
;
HIP000034622
;
HIP000035861
;
HIP000036396
;
HIP000036396
;
HIP000036549
;
HIP000039590
;
HIP000040678
;
HIP000040680
;
HIP000041828
;
HIP000044307
;
HIP000044667
;
HIP000046743
;
HIP000049801
;
HIP000049801
;
HIP000053167
;
HIP000054593
;
HIP000054593
;
HIP000054826
;
HIP000055870
;
HIP000057536
;
HIP000058916
;
HIP000059185
;
HIP000059982
;
HIP000059982
;
HIP000060692
;
HIP000061444
;
HIP000064438
;
HIP000064456
;
HIP000065414
;
HIP000065414
;
HIP000066578
;
HIP000066604
;
HIP000066936
;
HIP000068180
;
HIP000068180
;
HIP000068736
;
HIP000070217
;
HIP000070356
;
HIP000072983
;
HIP000073894
;
HIP000073894
;
HIP000076124
;
HIP000076357
;
HIP000077597
;
HIP000077597
;
HIP000078197
;
HIP000078197
;
HIP000079679
;
HIP000079679
;
HIP000080656
;
HIP000081421
;
HIP000083074
;
HIP000083279
;
HIP000083623
;
HIP000085006
;
HIP000088104
;
HIP000089945
;
HIP000089945
;
HIP000091250
;
HIP000091666
;
HIP000091666
;
HIP000092689
;
HIP000092689
;
HIP000095247
;
HIP000096037
;
HIP000096070
;
HIP000097214
;
HIP000098079
;
HIP000098409
;
HIP000099408
;
HIP000100997
;
HIP000101847
;
HIP000102204
;
HIP000102317
;
HIP000103109
;
HIP000103653
;
HIP000103706
;
HIP000104193
;
HIP000104340
;
HIP000104785
;
HIP000106438
;
HIP000107442
;
HIP000107442
;
HIP000107493
;
HIP000110770
;
HIP000114950
;
HIP000115324
;
HIP000115602
;
HIP000116212
;
HIP000116775
;
HIP000125020
;
HIP000125493
;
HIP000130328
;
HIP000136193
;
HIP000137998
;
HIP000139098
;
HIP000150678
;
HIP000183185
;
HIP000183185
;
HIP000194034
;
HIP000205251
;
HIP000253284
;
HIP000258392
;
HIP000338892
;
HIP000345899
;
HIP000346335
;
BIND
153992; 177961; 182216; 183262; 183265; 183266; 200016; 295234; 297476; 318897; 318900; 318903; 318904; 318905; 318908; 318910; 335969; 335973; 89741; 89745;
DIP
133139E; 135184E; 135188E; 135189E; 135190E; 137167E; 149E; 150E; 177021E; 177022E; 177023E; 177024E; 177025E; 177026E; 177027E; 177028E; 177029E; 177030E; 180094E; 180095E; 181755E; 45888E; 46794E; 59049E; 87759E; 87760E;
MINT
MINT-19344; MINT-2490745; MINT-2829358; MINT-2829504; MINT-2829542; MINT-2829576; MINT-2829624; MINT-2829876; MINT-2829895; MINT-2829913; MINT-2830323; MINT-2830357; MINT-2830381; MINT-2830405; MINT-2830429; MINT-2981755; MINT-2981779; MINT-3296655; MINT-48337; MINT-48494; MINT-49244; MINT-49356; MINT-4950280; MINT-4950315; MINT-56509; MINT-6543302; MINT-6543323; MINT-6543349; MINT-6665465; MINT-7220359; MINT-7899812; MINT-7900157; MINT-7914854; MINT-7989539; MINT-7989824; MINT-7989846; MINT-7989865; MINT-7989882; MINT-8010325;
HPRD
00102; 00428; 00590; 00906; 00950; 00996; 00998; 01287; 01464; 01542; 01613; 01706; 01733; 02114; 02135; 02251; 02336; 02476; 02665; 02890; 02931; 03254; 03290; 03491; 03494; 03518; 03997; 04152; 04153; 04155; 04389; 04392; 04440; 04621; 04666; 04713; 04746; 04768; 05219; 05227; 05373; 05400; 05448; 05866; 06014; 06015; 06735; 06736; 06928; 07535; 07536; 08366; 08447; 08851; 08864; 09096; 09102; 09103; 09104; 09105; 09107; 09798; 09949; 09951; 10293; 10536; 11425; 11516; 11822; 11897; 11899; 11901; 11906; 11907; 11909; 11912; 12397; 12601; 13588; 13626; 13657; 13660; 15326; 15979; 15991; 16184; 16309; 16759; 17158; 17493;
IntAct
EBI-2880211; EBI-2941238; EBI-4288874; EBI-1785756; EBI-2418377; EBI-1785741; EBI-297600; EBI-269146; EBI-1265536; EBI-1264642; EBI-1785771; EBI-2349206; EBI-1264624; EBI-1785708; EBI-1264601; EBI-1251862; EBI-1264651; EBI-1265385; EBI-1264710; EBI-1265363; EBI-1265150; EBI-1264717; EBI-1270446; EBI-1382486; EBI-1268966; EBI-2349158; EBI-1265624; EBI-1642362; EBI-1270468; EBI-1270487; EBI-2349080; EBI-2001855; EBI-1642094; EBI-1389994; EBI-1389981; EBI-2349066; EBI-299155; EBI-2477251; EBI-2477216; EBI-302174; EBI-2477193; EBI-2658272; EBI-2426765; EBI-2658174; EBI-364198; EBI-2477085; EBI-2477238; EBI-2477228; EBI-2477221; EBI-2657519; EBI-3043770; EBI-2477264; EBI-362394; EBI-3043800; EBI-2651586; EBI-2549359; EBI-2477278; EBI-2651040; EBI-2564373; EBI-361974; EBI-3048562; EBI-3046676; EBI-360207; EBI-3050465; EBI-350217; EBI-3946100; EBI-3951754; EBI-3892655; EBI-4288861; EBI-364504; EBI-3951861; EBI-4288898; EBI-4288896; EBI-4288900; EBI-4288943; EBI-4288945; EBI-4288996; EBI-4288947; EBI-4289175; EBI-4289129; EBI-4289111; EBI-4289000; EBI-4288998; EBI-4289145; EBI-4291492; EBI-4289455; EBI-4289511; EBI-4289462; EBI-4289485; EBI-4289466; EBI-4407543; EBI-4407371; EBI-923469; EBI-4488912; EBI-4407598; EBI-923503; EBI-996840; EBI-923564; EBI-923575;
Database links
RefSeq
NM_003495
;
Ensembl
ENST00000354348
;
Entrez Gene
Entrez Gene ID:8294
;
KEGG GENES
KEGG GENES(8294)
;
GeneCard
HIST1H4I
;
*GeneCards is provided free to academic non-profit institutions.
etc
Human-Gene diversity Of Life-style related Diseases
;
Curation status
Human curated
Notes
NA
Related H-InvDB links
Histone H4 (IPR001951).
Similarity Search Tool
;
TACT
;
fRNAdb (The functional RNA database) : overlapping fRNAdb entries with H-InvDB transcripts based on the location of the genome.
NA
Gene ontology information
Molecular function
DNA binding (
GO:0003677
); transcription initiation factor activity (
GO:0016986
);
Biological process
transcription initiation (
GO:0006352
); nucleosome assembly (
GO:0006334
);
Cellular component
nucleus (
GO:0005634
); nucleosome (
GO:0000786
);
Subcellular localization information
Last modified:20-Apr-2012
WoLF PSORT
nuclear;
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.
Protein structure information (GTOP)
Last modified:20-Apr-2012
Start
End
PDB_ID
E-value
Identity
Coverage
SCOP_ID
24
103
1aoiB
2e-14
100.0
80/83
a.22.1.1
Related H-InvDB links
GTOP
Gene expression information
Last modified:20-Apr-2012
Tissue-specific expression
NA
Probe
information
AceGene
AGhsB011101;
Affymetrix
GeneChip
HG-Focus
214634_at;
HG-U133
214634_at;
HG-U133A
214634_at;
HG-U133A_2
214634_at;
HG-U133B
NA
HG-U133_Plus_2
214634_at;
HG-U95
762_f_at;
HG-U95A
762_f_at;
HG-U95B
NA
HG-U95C
NA
HG-U95D
NA
HG-U95E
NA
HG-U95Av2
NA
HuEx-1_0
2899770; 2899771; 2946719;
HuGeneFL
AB000905_at;
Agilent
Human 1A Oligo Microarray:PGID215
A_23_P361347; A_23_P70458;
Whole Human Genome Oligo Microarray:PGID247
A_24_P20873;
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:
122550
;
143400
;
604519
;
608545
;
610294
;
611724
;
612558
;
Disease related mutation
NA
Literature-Extracted GENe-Disease Associations (LEGENDA)
Gene name
Entrez Gene ID:(8294)
Disease
Entrez Gene ID:(8294)
Substance
Entrez Gene ID:(8294)
Related H-InvDB links
DiseaseInfo Viewer
;
LEGENDA
;
Evolutionary information
Last modified:20-Apr-2012
Relationship
Species
Accession number
MGI
Links
Orthology
Rattus sp.
(Rat)
BC100619
G-integra
Orthology
Mus sp.
(Mouse)
BC152397
G-integra
Orthology
Tetraodon sp.
(Tetraodon)
CR719166
G-integra
Orthology
Bos sp.
(Cow)
ENSBTAT00000044998
G-integra
Orthology
Equus sp.
(Horse)
ENSECAT00000002444
G-integra
Orthology
Pongo sp.
(Orangutan)
ENSPPYT00000018996
G-integra
Orthology
Macaca sp.
(Macaque)
XM_001092924
G-integra
Orthology
Pan sp.
(Chimpanzee)
XM_001134995
G-integra
Orthology
Canis sp.
(Dog)
XM_849000
G-integra
Phylogenetic tree [View by
ATV]
Neighbor-joining (phb)
Related H-InvDB links
Evola
;
d
N
/
d
S
(under constraction);
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
248 .. 248
G/A
rs116193614
+
CDS
Nonsynonymous[Arg79His]
318 .. 318
C/T
rs61742445
+
CDS
Synonymous[Gly102Gly]
327 .. 327
G/A
rs112207956
+
3'UTR
445 .. 445
C/T
rs116675691
+
3'UTR
532 .. 532
G/A
rs76213641
+
3'UTR
535 .. 535
G/A
rs79400360
+
3'UTR
724 .. 724
G/A
rs75206923
+
3'UTR
790 .. 790
G/A
rs6456769
+
3'UTR
923 .. 923
A/G
rs73739600
+
3'UTR
1122 .. 1122
C/G
rs16894241
+
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
;