Protein Eif4h

URN urn:agi-llid:7458
Total Entities 0
Connectivity 34
Name Eif4h
Description eukaryotic translation initiation factor 4H
Notes This gene encodes one of the translation initiation factors, which functions to stimulate the initiation of protein synthesis at the level of mRNA utilization. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternative splicing of this gene generates 2 transcript variants. [provided by RefSeq, Jul 2008]

GO Molecular Function translation initiation factor activity
translation factor activity, nucleic acid binding
nucleotide binding
nucleic acid binding
RNA binding

GO Cellular Component eukaryotic translation initiation factor 4F complex
cytoplasm
cytosol
perinuclear region of cytoplasm

GO Biological Process sexual reproduction
developmental growth
regulation of translational initiation
translational initiation
cellular protein metabolic process
translation
gene expression
modulation by virus of host morphology or physiology

Pathway translation pathway

Group Translation
sexual reproduction
developmental growth
regulation of translational initiation
translational initiation
translation initiation factor activity
cellular protein metabolic process
translation
translation factor activity, nucleic acid binding
gene expression
modulation by virus of host morphology or physiology
nucleotide binding
nucleic acid binding
RNA binding
eukaryotic translation initiation factor 4F complex
cytoplasm
cytosol
perinuclear region of cytoplasm

LocusLink ID 7458
22384
288599

Cell Localization Cytoplasm
Perinuclear region

GO ID 0003723
0000166
0008135
0003743
0044267
0048589
0010467
0019048
0006446
0019953
0006412
0006413
0005829
0016281
0048471
0003676
0005737

Alias WSCR1
WBSCR1
eIF-4H
eukaryotic translation initiation factor 4H
Williams-Beuren syndrome chromosome region 1
Ef4h
AU018978
mKIAA0038
D5Ertd355e
E430026L18Rik
Williams-Beuren syndrome chromosome region 1 homolog
williams-Beuren syndrome chromosomal region 1 protein homolog
Wbscr I
LOC367990
LOC91811
WSCR I
LOC93527
LOC221889
LOC94573
MGC94887
OTTHUMP00000024643
Wbscr1 alternative spliced product
williams-Beuren syndrome chromosomal region 1 protein
Williams-Beuren syndrome chromosome region I
LOC155284
DNA segment, Chr 5, ERATO Doi 355, expressed
E430026L18
KIAA0038
EIF4H
eIF-4Hs
eukaryotic initiation factor 4H
Eukaryotic translation initiating factor 4H
eukaryotic translation initiation factor 4H isoform II
eukaryotic translation initiating factor 4H isoform 2
eukaryotic translation initiating factor 4H isoform I
eukaryotic translation initiating factor 4H isoform II
eukaryotic translation initiation factor 4H isoform 1
eukaryotic translation initiation factor 4H isoform 2
eukaryotic translation initiation factor 4H isoform I
eukaryotic translation initiating factor 4H isoform 1

Mouse chromosome position 5 74.71 cM

OMIM ID 603431

Rat chromosome position 12q12

Hugo ID 12741

Human chromosome position 7q11.23

Swiss-Prot Accession Q15056
Q564E5
Q9WUK2
Q5XI72
Q9WUK3
A8K3R1
D3DXF6
D3DXF8

GenBank ID NC_000007
NM_022170
NP_071496
NM_031992
NP_114381
NW_003871064
NG_008869
NC_018918
AC_000068
AC_000139
ABBA01063907
ABBA01063908
AC005057
AAS07439
AAS07440
AC005081
AAS07403
AF045555
AAC04859
AAF75557
AMYH02016039
CH471200
EAW69615
EAW69616
EAW69617
EAW69618
EAW69619
AK290676
BAF83365
AK297651
BAG60018
AK314749
BC010021
AAH10021
BC021214
AAH21214
BC066928
AAH66928
D26068
BAA05063
Q15056
DQ891924
ABM82850
DQ895111
ABM86037
DQ895112
ABM86038
NC_000071
XM_006504419
XP_006504482
NM_033561
NP_291039
AC_000027
AAHY01049932
AC166938
AF139987
AAD34859
AAD34860
AF289664
AAF99330
AF289665
AAF99335
CH466529
EDL19418
EDL19419
AK045004
BAC32180
AK088818
BAC40593
AK132034
BAE20955
AK135390
BAE22517
AK136999
BAE23201
AK149841
BAE29116
AK150088
BAE29297
AK166567
BAE38858
AK168872
BAE40690
AK169312
BAE41067
AK169353
BAE41102
AK169407
BAE41153
AK177188
AK182256
AK184202
AK184510
AK185835
AK188319
AK188850
AK189467
AK191093
AK191422
AK191530
AK191915
AK192082
AK192982
AK193051
AK194320
AK194751
AK195162
AK195570
AK195976
AK196800
AK197136
AK197414
AK197761
AK197946
AK200162
AK200533
AK201461
AK202850
AK202900
AK203547
AK204156
AK208946
AK210675
AK211404
AK213570
AK214521
AK215628
AK219562
BC014796
AAH14796
BC023227
BC023337
Q9WUK2
AK122194
BAC65476
NC_005111
XM_006249134
XP_006249196
NM_001006957
NP_001006958
AC_000080
AABR06071186
AAHX01071817
AC091000
CH473973
EDM13418
EDM13419
BC083818
AAH83818
CB718613
Q5XI72

Unigene ID Hs.520943
Mm.27955
Rn.79423

KEGG ID hsa:7458
mmu:22384
rno:288599

Swiss-Prot ID IF4H_RAT
IF4H_MOUSE
IF4H_HUMAN

Ensembl ID ENSG00000106682
ENSP00000265753
ENST00000265753
ENSP00000265754
ENST00000353999
ENSMUSG00000040731
ENSMUSP00000048833
ENSMUST00000036125
ENSRNOG00000001454
ENSRNOP00000043254
ENSRNOT00000050059

Homologene ID 32536

Organism Homo sapiens
Mus musculus
Rattus norvegicus

MGI ID 1341822

RGD ID 1359222

MedScan ID 7458