Skip Header

Contribute Send feedback
Read comments (?) or add your own

Q9H607 (OCEL1_HUMAN) Reviewed, UniProtKB/Swiss-Prot

Last modified January 25, 2012. Version 62. 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·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order

Names and origin

Protein namesRecommended name:
Occludin/ELL domain-containing protein 1
Gene names
Name:OCEL1
OrganismHomo sapiens (Human)
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length264 AA.
Sequence statusComplete.
Protein existenceEvidence at transcript level

General annotation (Comments)

Sequence similarities

Belongs to the ELL/occludin family.

Ontologies

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

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Chain1 – 264264Occludin/ELL domain-containing protein 1
PRO_0000271531

Regions

Compositional bias28 – 10679Pro-rich

Natural variations

Natural variant421R → L.
Corresponds to variant rs10425488 [ dbSNP | Ensembl ].
VAR_034356
Natural variant1091A → G.
Corresponds to variant rs891203 [ dbSNP | Ensembl ].
VAR_034357

Sequences

Sequence LengthMass (Da)Tools
Q9H607 [UniParc].

Last modified March 1, 2001. Version 1.
Checksum: 7B25A634A844B1E7

FASTA26429,404
        10         20         30         40         50         60 
MHNPDGSASP TADPGSELQT LGQAARRPPP PRAGHDAPRR TRPSARKPLS CFSRRPMPTR 

        70         80         90        100        110        120 
EPPKTRGSRG HLHTHPPGPG PPLQGLAPRG LKTSAPRPPC QPQPGPHKAK TKKIVFEDEL 

       130        140        150        160        170        180 
LSQALLGAKK PIGAIPKGHK PRPHPVPDYE LKYPPVSSER ERSRYVAVFQ DQYGEFLELQ 

       190        200        210        220        230        240 
HEVGCAQAKL RQLEALLSSL PPPQSQKEAQ VAARVWREFE MKRMDPGFLD KQARCHYLKG 

       250        260 
KLRHLKTQIQ KFDDQGDSEG SVYF 

« Hide

References

[1]"Complete sequencing and characterization of 21,243 full-length human cDNAs."
Ota T., Suzuki Y., Nishikawa T., Otsuki T., Sugiyama T., Irie R., Wakamatsu A., Hayashi K., Sato H., Nagai K., Kimura K., Makita H., Sekine M., Obayashi M., Nishi T., Shibahara T., Tanaka T., Ishii S. expand/collapse author list , Yamamoto J., Saito K., Kawai Y., Isono Y., Nakamura Y., Nagahari K., Murakami K., Yasuda T., Iwayanagi T., Wagatsuma M., Shiratori A., Sudo H., Hosoiri T., Kaku Y., Kodaira H., Kondo H., Sugawara M., Takahashi M., Kanda K., Yokoi T., Furuya T., Kikkawa E., Omura Y., Abe K., Kamihara K., Katsuta N., Sato K., Tanikawa M., Yamazaki M., Ninomiya K., Ishibashi T., Yamashita H., Murakawa K., Fujimori K., Tanai H., Kimata M., Watanabe M., Hiraoka S., Chiba Y., Ishida S., Ono Y., Takiguchi S., Watanabe S., Yosida M., Hotuta T., Kusano J., Kanehori K., Takahashi-Fujii A., Hara H., Tanase T.-O., Nomura Y., Togiya S., Komai F., Hara R., Takeuchi K., Arita M., Imose N., Musashino K., Yuuki H., Oshima A., Sasaki N., Aotsuka S., Yoshikawa Y., Matsunawa H., Ichihara T., Shiohata N., Sano S., Moriya S., Momiyama H., Satoh N., Takami S., Terashima Y., Suzuki O., Nakagawa S., Senoh A., Mizoguchi H., Goto Y., Shimizu F., Wakebe H., Hishigaki H., Watanabe T., Sugiyama A., Takemoto M., Kawakami B., Yamazaki M., Watanabe K., Kumagai A., Itakura S., Fukuzumi Y., Fujimori Y., Komiyama M., Tashiro H., Tanigami A., Fujiwara T., Ono T., Yamada K., Fujii Y., Ozaki K., Hirao M., Ohmori Y., Kawabata A., Hikiji T., Kobatake N., Inagaki H., Ikema Y., Okamoto S., Okitani R., Kawakami T., Noguchi S., Itoh T., Shigeta K., Senba T., Matsumura K., Nakajima Y., Mizuno T., Morinaga M., Sasaki M., Togashi T., Oyama M., Hata H., Watanabe M., Komatsu T., Mizushima-Sugano J., Satoh T., Shirai Y., Takahashi Y., Nakagawa K., Okumura K., Nagase T., Nomura N., Kikuchi H., Masuho Y., Yamashita R., Nakai K., Yada T., Nakamura Y., Ohara O., Isogai T., Sugano S.
Nat. Genet. 36:40-45(2004) [PubMed: 14702039] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA].
Tissue: Small intestine.
[2]"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].
Tissue: Bone marrow.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
AK026362 mRNA. Translation: BAB15460.1.
BC029361 mRNA. Translation: AAH29361.1.
IPIIPI00002305.
RefSeqNP_078854.1. NM_024578.1.
UniGeneHs.422676.

3D structure databases

ProteinModelPortalQ9H607.
SMRQ9H607. Positions 148-257.
ModBaseSearch...

Protein-protein interaction databases

STRINGQ9H607.

Polymorphism databases

DMDM74733590.

Proteomic databases

PRIDEQ9H607.

Protocols and materials databases

StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

EnsemblENST00000215061; ENSP00000215061; ENSG00000099330.
GeneID79629.
KEGGhsa:79629.
UCSCuc002nfp.1. human.

Organism-specific databases

CTD79629.
GeneCardsGC19P017337.
HGNCHGNC:26221. OCEL1.
neXtProtNX_Q9H607.
PharmGKBPA162398385.
GenAtlasSearch...

Phylogenomic databases

eggNOGprNOG06479.
GeneTreeENSGT00550000074378.
HOVERGENHBG082082.
InParanoidQ9H607.
OMAARCHYLK.
OrthoDBEOG4HHP3B.
PhylomeDBQ9H607.

Gene expression databases

ArrayExpressQ9H607.
BgeeQ9H607.
CleanExHS_OCEL1.
GenevestigatorQ9H607.

Family and domain databases

InterProIPR010844. Occludin_RNApol2_elong_fac_ELL.
[Graphical view]
PfamPF07303. Occludin_ELL. 1 hit.
[Graphical view]
ProtoNetSearch...

Other

NextBio68721.

Entry information

Entry nameOCEL1_HUMAN
AccessionPrimary (citable) accession number: Q9H607
Entry history
Integrated into UniProtKB/Swiss-Prot: January 9, 2007
Last sequence update: March 1, 2001
Last modified: January 25, 2012
This is version 62 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 19

Human chromosome 19: 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