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Reviewed, UniProtKB/Swiss-Prot Q24JQ0 (CR045_HUMAN)

Last modified December 15, 2009. Version 28. Feed History...

Clusters with 100%, 90%, 50% identity | Documents (3) | Third-party data | Customize display text xml rdf/xml gff fasta
Names and origin · Protein attributes · General annotation (Comments) · Ontologies · Alternative products · Sequence annotation (Features) · Sequences · References · Cross-references · Entry information · Relevant documents

Names and origin

Protein namesRecommended name:
    Transmembrane protein C18orf45
Gene names
Name: C18orf45
OrganismHomo sapiens (Human) [Complete proteome]
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length296 AA.
Sequence statusComplete.
Sequence processingThe displayed sequence is not processed.
Protein existenceEvidence at transcript level.

General annotation (Comments)

Subcellular location

Membrane; Multi-pass membrane protein Potential.

Ontologies

Keywords
   Cellular componentMembrane
   Coding sequence diversityAlternative splicing
Polymorphism
   DomainTransmembrane
   Technical termComplete proteome
Gene Ontology (GO)
   Cellular componentintegral to membrane

Inferred from electronic annotation. Source: UniProtKB-SubCell

Complete GO annotation...

Alternative products

This entry describes 3 isoforms produced by alternative splicing. [Align] [Select]
Isoform 1 (identifier: Q24JQ0-1)

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: Q24JQ0-2)

The sequence of this isoform differs from the canonical sequence as follows:
     146-159: FNPDGYFWAIIHLL → GLIKFYRSPRNPVH
     160-296: Missing.
Isoform 3 (identifier: Q24JQ0-3)

The sequence of this isoform differs from the canonical sequence as follows:
     41-66: Missing.
     128-149: SALLLLAAAGCLPFNDSQFNPD → RLHLERTRQNQTSRLSSCLKGD
     150-296: Missing.
Note: No experimental confirmation available.

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Chain1 – 296296Transmembrane protein C18orf45
PRO_0000307316

Regions

Transmembrane7 – 2923 Potential
Transmembrane32 – 5221 Potential
Transmembrane67 – 8721 Potential
Transmembrane93 – 11321 Potential
Transmembrane121 – 14121 Potential
Transmembrane146 – 16621 Potential
Transmembrane187 – 20721 Potential
Transmembrane211 – 23121 Potential
Transmembrane250 – 27021 Potential
Transmembrane271 – 29121 Potential

Natural variations

Alternative sequence41 – 6626Missing in isoform 3.
VSP_028704
Alternative sequence128 – 14922SALLL…QFNPD → RLHLERTRQNQTSRLSSCLK GD in isoform 3.
VSP_028705
Alternative sequence146 – 15914FNPDG…IIHLL → GLIKFYRSPRNPVH in isoform 2.
VSP_028706
Alternative sequence150 – 296147Missing in isoform 3.
VSP_028707
Alternative sequence160 – 296137Missing in isoform 2.
VSP_028708
Natural variant1311L → F: dbSNP rs8099409. Ref.1
VAR_035406

Sequences

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

Last modified April 18, 2006. Version 1.
Checksum: E84189255BCA2A96

FASTA29632,647
        10         20         30         40         50         60 
MCVRRSLVGL TFCTCYLASY LTNKYVLSVL KFTYPTLFQG WQTLIGGLLL HVSWKLGWVE 

        70         80         90        100        110        120 
INSSSRSHVL VWLPASVLFV GIIYAGSRAL SRLAIPVFLT LHNVAEVIIC GYQKCFQKEK 

       130        140        150        160        170        180 
TSPAKICSAL LLLAAAGCLP FNDSQFNPDG YFWAIIHLLC VGAYKILQKS QKPSALSDID 

       190        200        210        220        230        240 
QQYLNYIFSV VLLAFASHPT GDLFSVLDFP FLYFYRFHGS CCASGFLGFF LMFSTVKLKN 

       250        260        270        280        290 
LLAPGQCAAW IFFAKIITAG LSILLFDAIL TSATTGCLLL GALGEALLVF SERKSS 

« Hide

Isoform 2.

Checksum: AE3B9A24FBDDF9E8
Show »

FASTA15917,699
Isoform 3.

Checksum: 16F4EAACC00EFF80
Show »

FASTA12313,865

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] (ISOFORMS 2 AND 3), VARIANT PHE-131.
Tissue: Fibroblast and Liver.
[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] (ISOFORMS 1 AND 2).

Cross-references

Sequence databases

AK123623 mRNA. Translation: BAC85665.1.
AK126247 mRNA. Translation: BAC86502.1.
BC114510 mRNA. Translation: AAI14511.1.
BC114561 mRNA. Translation: AAI14562.1.
IPIIPI00446436.
IPI00798293.
IPI00868802.
RefSeqNP_116322.3.
UniGeneHs.137562

3D structure databases

ModBaseSearch...

Genome annotation databases

EnsemblENST00000383233; ENSP00000372720; ENSG00000134490; Homo sapiens. [Genome view]
GeneID85019.
KEGGhsa:85019.
UCSCuc002kuf.1. human.

Organism-specific databases

CTD85019.
GeneCardsGC18M019130.
HGNCHGNC:31723. C18orf45.
PharmGKBPA134952915.
GenAtlasSearch...

Phylogenomic databases

HOGENOMHBG717763.
HOVERGENQ24JQ0.
InParanoidQ24JQ0.
OMACVGAYKI.
OrthoDBEOG9QVFXQ.

Gene expression databases

ArrayExpressQ24JQ0.
BgeeQ24JQ0.
CleanExHS_C18orf45.
GenevestigatorQ24JQ0.

Family and domain databases

ProtoNetSearch...

Other Resources

NextBio75655.

Entry information

Entry nameCR045_HUMAN
AccessionPrimary (citable) accession number: Q24JQ0
Secondary accession number(s): Q6ZTS7, Q6ZW41
Entry history
Integrated into UniProtKB/Swiss-Prot: October 23, 2007
Last sequence update: April 18, 2006
Last modified: December 15, 2009
This is version 28 of the entry and version 1 of the sequence. [Complete history]
Entry statusReviewed (UniProtKB/Swiss-Prot)
Annotation projectHPI (Human Proteome Initiative)
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 18

Human chromosome 18: 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

Names and origin · Protein attributes · General annotation (Comments) · Ontologies · Alternative products · Sequence annotation (Features) · Sequences · References · Cross-references · Entry information · Relevant documents