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Protein

Uncharacterized protein CXorf65

Gene

CXorf65

Organism
Homo sapiens (Human)
Status
Reviewed-Annotation score: Annotation score: 1 out of 5-Protein predictedi

Names & Taxonomyi

Protein namesi
Recommended name:
Uncharacterized protein CXorf65
Gene namesi
Name:CXorf65
OrganismiHomo sapiens (Human)
Taxonomic identifieri9606 [NCBI]
Taxonomic lineageiEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo
ProteomesiUP000005640 Componenti: Chromosome X

Organism-specific databases

HGNCiHGNC:33713. CXorf65.

Pathology & Biotechi

Organism-specific databases

PharmGKBiPA164718500.

Polymorphism and mutation databases

BioMutaiCXorf65.

PTM / Processingi

Molecule processing

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifierActions
Chaini1 – 183183Uncharacterized protein CXorf65PRO_0000346434Add
BLAST

Proteomic databases

PaxDbiA6NEN9.
PRIDEiA6NEN9.

PTM databases

PhosphoSiteiA6NEN9.

Expressioni

Gene expression databases

BgeeiA6NEN9.
ExpressionAtlasiA6NEN9. baseline and differential.
GenevisibleiA6NEN9. HS.

Organism-specific databases

HPAiHPA047396.

Structurei

3D structure databases

ProteinModelPortaliA6NEN9.
ModBaseiSearch...
MobiDBiSearch...

Family & Domainsi

Phylogenomic databases

eggNOGiNOG120989.
GeneTreeiENSGT00510000049291.
HOGENOMiHOG000112109.
InParanoidiA6NEN9.
OMAiYIRSKVK.
OrthoDBiEOG73RBDP.
PhylomeDBiA6NEN9.
TreeFamiTF328811.

Sequencei

Sequence statusi: Complete.

A6NEN9-1 [UniParc]FASTAAdd to basket

« Hide

        10         20         30         40         50
MFIFIKHGDN QQFLVNTNCA VVVLLYYIRS KVKLPKTNTI DLCEQTGKMK
60 70 80 90 100
MLFLMKPNHA EYASKYLTAR STYYVCKVER GPPGTRLENA YRAFVPLLKN
110 120 130 140 150
PEPWLLVALR IQCDALERRR IQMLKMKEAK KVVIIEPPAS VPSKQSGRSD
160 170 180
KKKSTRKSPT FRNRPDFRKN KGRQLNKTTK QKK
Length:183
Mass (Da):21,305
Last modified:July 24, 2007 - v1
Checksum:iCCC8209694661532
GO

Natural variant

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifierActions
Natural varianti156 – 1561R → H.
Corresponds to variant rs12009522 [ dbSNP | Ensembl ].
VAR_045896

Sequence databases

Select the link destinations:
EMBLi
GenBanki
DDBJi
Links Updated
AL590764 Genomic DNA. No translation available.
CH471132 Genomic DNA. Translation: EAX05320.1.
CCDSiCCDS35324.1.
RefSeqiNP_001020436.1. NM_001025265.2.
UniGeneiHs.443936.

Genome annotation databases

EnsembliENST00000374251; ENSP00000363369; ENSG00000204165.
GeneIDi158830.
KEGGihsa:158830.
UCSCiuc011mpo.2. human.

Keywords - Coding sequence diversityi

Polymorphism

Cross-referencesi

Sequence databases

Select the link destinations:
EMBLi
GenBanki
DDBJi
Links Updated
AL590764 Genomic DNA. No translation available.
CH471132 Genomic DNA. Translation: EAX05320.1.
CCDSiCCDS35324.1.
RefSeqiNP_001020436.1. NM_001025265.2.
UniGeneiHs.443936.

3D structure databases

ProteinModelPortaliA6NEN9.
ModBaseiSearch...
MobiDBiSearch...

PTM databases

PhosphoSiteiA6NEN9.

Polymorphism and mutation databases

BioMutaiCXorf65.

Proteomic databases

PaxDbiA6NEN9.
PRIDEiA6NEN9.

Protocols and materials databases

Structural Biology KnowledgebaseSearch...

Genome annotation databases

EnsembliENST00000374251; ENSP00000363369; ENSG00000204165.
GeneIDi158830.
KEGGihsa:158830.
UCSCiuc011mpo.2. human.

Organism-specific databases

CTDi158830.
GeneCardsiGC0XM070323.
HGNCiHGNC:33713. CXorf65.
HPAiHPA047396.
neXtProtiNX_A6NEN9.
PharmGKBiPA164718500.
GenAtlasiSearch...

Phylogenomic databases

eggNOGiNOG120989.
GeneTreeiENSGT00510000049291.
HOGENOMiHOG000112109.
InParanoidiA6NEN9.
OMAiYIRSKVK.
OrthoDBiEOG73RBDP.
PhylomeDBiA6NEN9.
TreeFamiTF328811.

Miscellaneous databases

GenomeRNAii158830.
NextBioi87823.
PROiA6NEN9.

Gene expression databases

BgeeiA6NEN9.
ExpressionAtlasiA6NEN9. baseline and differential.
GenevisibleiA6NEN9. HS.

Family and domain databases

ProtoNetiSearch...

Publicationsi

  1. "The DNA sequence of the human X chromosome."
    Ross M.T., Grafham D.V., Coffey A.J., Scherer S., McLay K., Muzny D., Platzer M., Howell G.R., Burrows C., Bird C.P., Frankish A., Lovell F.L., Howe K.L., Ashurst J.L., Fulton R.S., Sudbrak R., Wen G., Jones M.C.
    , Hurles M.E., Andrews T.D., Scott C.E., Searle S., Ramser J., Whittaker A., Deadman R., Carter N.P., Hunt S.E., Chen R., Cree A., Gunaratne P., Havlak P., Hodgson A., Metzker M.L., Richards S., Scott G., Steffen D., Sodergren E., Wheeler D.A., Worley K.C., Ainscough R., Ambrose K.D., Ansari-Lari M.A., Aradhya S., Ashwell R.I., Babbage A.K., Bagguley C.L., Ballabio A., Banerjee R., Barker G.E., Barlow K.F., Barrett I.P., Bates K.N., Beare D.M., Beasley H., Beasley O., Beck A., Bethel G., Blechschmidt K., Brady N., Bray-Allen S., Bridgeman A.M., Brown A.J., Brown M.J., Bonnin D., Bruford E.A., Buhay C., Burch P., Burford D., Burgess J., Burrill W., Burton J., Bye J.M., Carder C., Carrel L., Chako J., Chapman J.C., Chavez D., Chen E., Chen G., Chen Y., Chen Z., Chinault C., Ciccodicola A., Clark S.Y., Clarke G., Clee C.M., Clegg S., Clerc-Blankenburg K., Clifford K., Cobley V., Cole C.G., Conquer J.S., Corby N., Connor R.E., David R., Davies J., Davis C., Davis J., Delgado O., Deshazo D., Dhami P., Ding Y., Dinh H., Dodsworth S., Draper H., Dugan-Rocha S., Dunham A., Dunn M., Durbin K.J., Dutta I., Eades T., Ellwood M., Emery-Cohen A., Errington H., Evans K.L., Faulkner L., Francis F., Frankland J., Fraser A.E., Galgoczy P., Gilbert J., Gill R., Gloeckner G., Gregory S.G., Gribble S., Griffiths C., Grocock R., Gu Y., Gwilliam R., Hamilton C., Hart E.A., Hawes A., Heath P.D., Heitmann K., Hennig S., Hernandez J., Hinzmann B., Ho S., Hoffs M., Howden P.J., Huckle E.J., Hume J., Hunt P.J., Hunt A.R., Isherwood J., Jacob L., Johnson D., Jones S., de Jong P.J., Joseph S.S., Keenan S., Kelly S., Kershaw J.K., Khan Z., Kioschis P., Klages S., Knights A.J., Kosiura A., Kovar-Smith C., Laird G.K., Langford C., Lawlor S., Leversha M., Lewis L., Liu W., Lloyd C., Lloyd D.M., Loulseged H., Loveland J.E., Lovell J.D., Lozado R., Lu J., Lyne R., Ma J., Maheshwari M., Matthews L.H., McDowall J., McLaren S., McMurray A., Meidl P., Meitinger T., Milne S., Miner G., Mistry S.L., Morgan M., Morris S., Mueller I., Mullikin J.C., Nguyen N., Nordsiek G., Nyakatura G., O'dell C.N., Okwuonu G., Palmer S., Pandian R., Parker D., Parrish J., Pasternak S., Patel D., Pearce A.V., Pearson D.M., Pelan S.E., Perez L., Porter K.M., Ramsey Y., Reichwald K., Rhodes S., Ridler K.A., Schlessinger D., Schueler M.G., Sehra H.K., Shaw-Smith C., Shen H., Sheridan E.M., Shownkeen R., Skuce C.D., Smith M.L., Sotheran E.C., Steingruber H.E., Steward C.A., Storey R., Swann R.M., Swarbreck D., Tabor P.E., Taudien S., Taylor T., Teague B., Thomas K., Thorpe A., Timms K., Tracey A., Trevanion S., Tromans A.C., d'Urso M., Verduzco D., Villasana D., Waldron L., Wall M., Wang Q., Warren J., Warry G.L., Wei X., West A., Whitehead S.L., Whiteley M.N., Wilkinson J.E., Willey D.L., Williams G., Williams L., Williamson A., Williamson H., Wilming L., Woodmansey R.L., Wray P.W., Yen J., Zhang J., Zhou J., Zoghbi H., Zorilla S., Buck D., Reinhardt R., Poustka A., Rosenthal A., Lehrach H., Meindl A., Minx P.J., Hillier L.W., Willard H.F., Wilson R.K., Waterston R.H., Rice C.M., Vaudin M., Coulson A., Nelson D.L., Weinstock G., Sulston J.E., Durbin R.M., Hubbard T., Gibbs R.A., Beck S., Rogers J., Bentley D.R.
    Nature 434:325-337(2005) [PubMed] [Europe PMC] [Abstract]
    Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
  2. Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].

Entry informationi

Entry nameiCX065_HUMAN
AccessioniPrimary (citable) accession number: A6NEN9
Entry historyi
Integrated into UniProtKB/Swiss-Prot: September 2, 2008
Last sequence update: July 24, 2007
Last modified: July 22, 2015
This is version 53 of the entry and version 1 of the sequence. [Complete history]
Entry statusiReviewed (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.

Miscellaneousi

Keywords - Technical termi

Complete proteome, Reference proteome

Documents

  1. Human chromosome X
    Human chromosome X: entries, gene names and cross-references to MIM
  2. Human entries with polymorphisms or disease mutations
    List of human entries with polymorphisms or disease mutations
  3. Human polymorphisms and disease mutations
    Index of human polymorphisms and disease mutations

External Data

Dasty 3

Similar proteinsi

Links to similar proteins from the UniProt Reference Clusters (UniRef) at 100%, 90% and 50% sequence identity:
100%UniRef100 combines identical sequences and sub-fragments with 11 or more residues from any organism into Uniref entry.
90%UniRef90 is built by clustering UniRef100 sequences that have at least 90% sequence identity to, and 80% overlap with, the longest sequence (a.k.a seed sequence).
50%UniRef50 is built by clustering UniRef90 seed sequences that have at least 50% sequence identity to, and 80% overlap with, the longest sequence in the cluster.