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Q5T953 (IER5L_HUMAN) Reviewed, UniProtKB/Swiss-Prot

Last modified January 25, 2012. Version 52. Feed History...

Clusters with 100%, 90%, 50% identity | Documents (4) | Third-party data text xml rdf/xml gff fasta
to top of pageNames·Attributes·General annotation·Ontologies·Alt products·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order

Names and origin

Protein namesRecommended name:
Immediate early response gene 5-like protein
Gene names
Name:IER5L
OrganismHomo sapiens (Human)
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length404 AA.
Sequence statusComplete.
Protein existenceEvidence at transcript level

General annotation (Comments)

Sequence similarities

Belongs to the IER family.

Ontologies

Keywords
   Coding sequence diversityAlternative splicing
Polymorphism
   Technical termComplete proteome
Reference proteome
Gene Ontology (GO)
None. [Check GOA]

Alternative products

This entry describes 2 isoforms produced by alternative splicing. [Align] [Select]
Isoform 1 (identifier: Q5T953-1)

This isoform has been chosen as the 'canonical' sequence. All positional information in this entry refers to it. This is also the sequence that appears in the downloadable versions of the entry.
Isoform 2 (identifier: Q5T953-2)

The sequence of this isoform differs from the canonical sequence as follows:
     212-237: PGAAPPAAAASPPASPAPASSPGFYR → RSPPASAPASRTSARTRPRTRPTSQT
     238-404: Missing.
Note: No experimental confirmation available.

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Chain1 – 404404Immediate early response gene 5-like protein
PRO_0000334656

Regions

Compositional bias59 – 13072Gln-rich
Compositional bias138 – 23093Ala-rich

Natural variations

Alternative sequence212 – 23726PGAAP…PGFYR → RSPPASAPASRTSARTRPRT RPTSQT in isoform 2.
VSP_033726
Alternative sequence238 – 404167Missing in isoform 2.
VSP_033727
Natural variant1051P → S. Ref.3
Corresponds to variant rs184457 [ dbSNP | Ensembl ].
VAR_043450

Sequences

Sequence LengthMass (Da)Tools
Isoform 1 [UniParc].

Last modified December 21, 2004. Version 1.
Checksum: 72EF41BE313DEFB0

FASTA40442,109
        10         20         30         40         50         60 
MECALDAQSL ISISLRKIHS SRTQRGGIKL HKNLLVSYVL RNARQLYLSE RYAELYRRQQ 

        70         80         90        100        110        120 
QQQQQQPPHH QHQHLAYAAP GMPASAADFG PLQLGGGGDA EAREPAARHQ LHQLHQLHQL 

       130        140        150        160        170        180 
HLQQQLHQHQ HPAPRGCAAA AAAGAPAGGA GALSELPGCA ALQPPHGAPH RGQPLEPLQP 

       190        200        210        220        230        240 
GPAPLPLPLP PPAPAALCPR DPRAPAACSA PPGAAPPAAA ASPPASPAPA SSPGFYRGAY 

       250        260        270        280        290        300 
PTPSDFGLHC SSQTTVLDLD THVVTTVENG YLHQDCCASA HCPCCGQGAP GPGLASAAGC 

       310        320        330        340        350        360 
KRKYYPGQEE EEDDEEDAGG LGAEPPGGAP FAPCKRARFE DFCPDSSPDA SNISNLISIF 

       370        380        390        400 
GSGFSGLVSR QPDSSEQPPP LNGQLCAKQA LASLGAWTRA IVAF 

« Hide

Isoform 2 [UniParc].

Checksum: 36FF5C8F219B141B
Show »

FASTA23725,264

References

[1]"DNA sequence and analysis of human chromosome 9."
Humphray S.J., Oliver K., Hunt A.R., Plumb R.W., Loveland J.E., Howe K.L., Andrews T.D., Searle S., Hunt S.E., Scott C.E., Jones M.C., Ainscough R., Almeida J.P., Ambrose K.D., Ashwell R.I.S., Babbage A.K., Babbage S., Bagguley C.L. expand/collapse author list , Bailey J., Banerjee R., Barker D.J., Barlow K.F., Bates K., Beasley H., Beasley O., Bird C.P., Bray-Allen S., Brown A.J., Brown J.Y., Burford D., Burrill W., Burton J., Carder C., Carter N.P., Chapman J.C., Chen Y., Clarke G., Clark S.Y., Clee C.M., Clegg S., Collier R.E., Corby N., Crosier M., Cummings A.T., Davies J., Dhami P., Dunn M., Dutta I., Dyer L.W., Earthrowl M.E., Faulkner L., Fleming C.J., Frankish A., Frankland J.A., French L., Fricker D.G., Garner P., Garnett J., Ghori J., Gilbert J.G.R., Glison C., Grafham D.V., Gribble S., Griffiths C., Griffiths-Jones S., Grocock R., Guy J., Hall R.E., Hammond S., Harley J.L., Harrison E.S.I., Hart E.A., Heath P.D., Henderson C.D., Hopkins B.L., Howard P.J., Howden P.J., Huckle E., Johnson C., Johnson D., Joy A.A., Kay M., Keenan S., Kershaw J.K., Kimberley A.M., King A., Knights A., Laird G.K., Langford C., Lawlor S., Leongamornlert D.A., Leversha M., Lloyd C., Lloyd D.M., Lovell J., Martin S., Mashreghi-Mohammadi M., Matthews L., McLaren S., McLay K.E., McMurray A., Milne S., Nickerson T., Nisbett J., Nordsiek G., Pearce A.V., Peck A.I., Porter K.M., Pandian R., Pelan S., Phillimore B., Povey S., Ramsey Y., Rand V., Scharfe M., Sehra H.K., Shownkeen R., Sims S.K., Skuce C.D., Smith M., Steward C.A., Swarbreck D., Sycamore N., Tester J., Thorpe A., Tracey A., Tromans A., Thomas D.W., Wall M., Wallis J.M., West A.P., Whitehead S.L., Willey D.L., Williams S.A., Wilming L., Wray P.W., Young L., Ashurst J.L., Coulson A., Blocker H., Durbin R.M., Sulston J.E., Hubbard T., Jackson M.J., Bentley D.R., Beck S., Rogers J., Dunham I.
Nature 429:369-374(2004) [PubMed: 15164053] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
[2]Mural R.J., Istrail S., Sutton G.G., Florea L., Halpern A.L., Mobarry C.M., Lippert R., Walenz B., Shatkay H., Dew I., Miller J.R., Flanigan M.J., Edwards N.J., Bolanos R., Fasulo D., Halldorsson B.V., Hannenhalli S., Turner R. expand/collapse author list , Yooseph S., Lu F., Nusskern D.R., Shue B.C., Zheng X.H., Zhong F., Delcher A.L., Huson D.H., Kravitz S.A., Mouchard L., Reinert K., Remington K.A., Clark A.G., Waterman M.S., Eichler E.E., Adams M.D., Hunkapiller M.W., Myers E.W., Venter J.C.
Submitted (JUL-2005) to the EMBL/GenBank/DDBJ databases
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
[3]"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."
The MGC Project Team
Genome Res. 14:2121-2127(2004) [PubMed: 15489334] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA], VARIANT SER-105.
Tissue: Uterus.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
AL158151 Genomic DNA. Translation: CAI12875.1.
CH471090 Genomic DNA. Translation: EAW87886.1.
BC064028 mRNA. Translation: AAH64028.1.
IPIIPI00401073.
IPI00892732.
RefSeqNP_982258.2. NM_203434.2.
UniGeneHs.529857.

3D structure databases

ProteinModelPortalQ5T953.
ModBaseSearch...

Polymorphism databases

DMDM74745628.

Proteomic databases

PRIDEQ5T953.

Protocols and materials databases

StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

EnsemblENST00000372491; ENSP00000361569; ENSG00000188483.
GeneID389792.
KEGGhsa:389792.
UCSCuc010myt.1. human.

Organism-specific databases

CTD389792.
GeneCardsGC09M131937.
HGNCHGNC:23679. IER5L.
HPAHPA021327.
neXtProtNX_Q5T953.
PharmGKBPA134879111.
GenAtlasSearch...

Phylogenomic databases

eggNOGmaNOG18947.
GeneTreeENSGT00530000064009.
HOGENOMHBG716493.
HOVERGENHBG107988.
InParanoidQ5T953.
OMARNARQVY.
OrthoDBEOG40P47J.

Gene expression databases

ArrayExpressQ5T953.
BgeeQ5T953.
CleanExHS_IER5L.
GenevestigatorQ5T953.

Family and domain databases

InterProIPR008653. IER.
[Graphical view]
PANTHERPTHR15895. IER. 1 hit.
PfamPF05760. IER. 1 hit.
[Graphical view]
ProtoNetSearch...

Other

NextBio103095.

Entry information

Entry nameIER5L_HUMAN
AccessionPrimary (citable) accession number: Q5T953
Secondary accession number(s): Q6P3E2
Entry history
Integrated into UniProtKB/Swiss-Prot: May 20, 2008
Last sequence update: December 21, 2004
Last modified: January 25, 2012
This is version 52 of the entry and version 1 of the sequence. [Complete history]
Entry statusReviewed (UniProtKB/Swiss-Prot)
Annotation programChordata Protein Annotation Program
DisclaimerAny medical or genetic information present in this entry is provided for research, educational and informational purposes only. It is not in any way intended to be used as a substitute for professional medical advice, diagnosis, treatment or care.

Relevant documents

Human chromosome 9

Human chromosome 9: entries, gene names and cross-references to MIM

Human entries with polymorphisms or disease mutations

List of human entries with polymorphisms or disease mutations

Human polymorphisms and disease mutations

Index of human polymorphisms and disease mutations

SIMILARITY comments

Index of protein domains and families