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Q8IYF3

- TEX11_HUMAN

UniProt

Q8IYF3 - TEX11_HUMAN

Protein

Testis-expressed sequence 11 protein

Gene

TEX11

Organism
Homo sapiens (Human)
Status
Reviewed - Annotation score: 4 out of 5- Experimental evidence at protein leveli
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    • History
      Entry version 99 (01 Oct 2014)
      Sequence version 3 (24 Jul 2007)
      Previous versions | rss
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    Functioni

    Regulator of crossing-over during meiosis. Involved in initiation and/or maintenance of chromosome synapsis and formation of crossovers By similarity.By similarity

    GO - Molecular functioni

    1. protein binding Source: IntAct

    GO - Biological processi

    1. chiasma assembly Source: Ensembl
    2. fertilization Source: Ensembl
    3. male gonad development Source: Ensembl
    4. male meiosis chromosome segregation Source: Ensembl
    5. meiotic gene conversion Source: UniProtKB
    6. negative regulation of apoptotic process Source: Ensembl
    7. reciprocal meiotic recombination Source: UniProtKB
    8. resolution of meiotic recombination intermediates Source: Ensembl
    9. synaptonemal complex assembly Source: Ensembl

    Keywords - Biological processi

    Meiosis

    Names & Taxonomyi

    Protein namesi
    Recommended name:
    Testis-expressed sequence 11 protein
    Gene namesi
    Name:TEX11
    OrganismiHomo sapiens (Human)
    Taxonomic identifieri9606 [NCBI]
    Taxonomic lineageiEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo
    ProteomesiUP000005640: Chromosome X

    Organism-specific databases

    HGNCiHGNC:11733. TEX11.

    Subcellular locationi

    Chromosome By similarity
    Note: Forms arrays of discrete foci along synaptonemal complexes in spermatocytes and fetal oocytes.By similarity

    GO - Cellular componenti

    1. central element Source: Ensembl

    Keywords - Cellular componenti

    Chromosome

    Pathology & Biotechi

    Organism-specific databases

    PharmGKBiPA36450.

    PTM / Processingi

    Molecule processing

    Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifierActions
    Chaini1 – 940940Testis-expressed sequence 11 proteinPRO_0000296955Add
    BLAST

    Proteomic databases

    PaxDbiQ8IYF3.
    PRIDEiQ8IYF3.

    PTM databases

    PhosphoSiteiQ8IYF3.

    Expressioni

    Tissue specificityi

    Testis-specific. Not expressed in adult ovaries.1 Publication

    Gene expression databases

    BgeeiQ8IYF3.
    CleanExiHS_TEX11.
    GenevestigatoriQ8IYF3.

    Organism-specific databases

    HPAiHPA002950.

    Interactioni

    Subunit structurei

    Interacts with SYCP2. Interacts with PBXIP1; may prevent interaction between PBXIP1 and ESR2 By similarity.By similarity

    Binary interactionsi

    WithEntry#Exp.IntActNotes
    LIN37Q96GY32EBI-742397,EBI-748884
    MEF2BNBQ96FH02EBI-742397,EBI-744076
    STMN2Q930452EBI-742397,EBI-714194

    Protein-protein interaction databases

    BioGridi121093. 24 interactions.
    IntActiQ8IYF3. 22 interactions.
    MINTiMINT-1443835.
    STRINGi9606.ENSP00000340995.

    Structurei

    3D structure databases

    ProteinModelPortaliQ8IYF3.
    SMRiQ8IYF3. Positions 455-517.
    ModBaseiSearch...
    MobiDBiSearch...

    Family & Domainsi

    Sequence similaritiesi

    Belongs to the SPO22 family.Curated

    Phylogenomic databases

    eggNOGiNOG314839.
    HOGENOMiHOG000154551.
    HOVERGENiHBG069003.
    InParanoidiQ8IYF3.
    OMAiFRKIAWN.
    OrthoDBiEOG79PJNG.
    PhylomeDBiQ8IYF3.
    TreeFamiTF333356.

    Family and domain databases

    Gene3Di1.25.40.10. 1 hit.
    InterProiIPR013940. Meiosis_specific_SPO22.
    IPR011990. TPR-like_helical.
    [Graphical view]
    PfamiPF08631. SPO22. 1 hit.
    [Graphical view]

    Sequences (3)i

    Sequence statusi: Complete.

    This entry describes 3 isoformsi produced by alternative splicing. Align

    Isoform 1 (identifier: Q8IYF3-1) [UniParc]FASTAAdd to Basket

    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.

    « Hide

    MISAHCNLRL LCSSDSSASA SQVAGTTEVV ENLVTNDNSP NIPEAIDRLF    50
    SDIANINRES MAEITDIQIE EMAVNLWNWA LTIGGGWLVN EEQKIRLHYV 100
    ACKLLSMCEA SFASEQSIQR LIMMNMRIGK EWLDAGNFLI ADECFQAAVA 150
    SLEQLYVKLI QRSSPEADLT MEKITVESDH FRVLSYQAES AVAQGDFQRA 200
    SMCVLQCKDM LMRLPQMTSS LHHLCYNFGV ETQKNNKYEE SSFWLSQSYD 250
    IGKMDKKSTG PEMLAKVLRL LATNYLDWDD TKYYDKALNA VNLANKEHLS 300
    SPGLFLKMKI LLKGETSNEE LLEAVMEILH LDMPLDFCLN IAKLLMDHER 350
    ESVGFHFLTI IHERFKSSEN IGKVLILHTD MLLQRKEELL AKEKIEEIFL 400
    AHQTGRQLTA ESMNWLHNIL WRQAASSFEV QNYTDALQWY YYSLRFYSTD 450
    EMDLDFTKLQ RNMACCYLNL QQLDKAKEAV AEAERHDPRN VFTQFYIFKI 500
    AVIEGNSERA LQAIITLENI LTDEESEDND LVAERGSPTM LLSLAAQFAL 550
    ENGQQIVAEK ALEYLAQHSE DQEQVLTAVK CLLRFLLPKI AEMPESEDKK 600
    KEMDRLLTCL NRAFVKLSQP FGEEALSLES RANEAQWFRK TAWNLAVQCD 650
    KDPVMMREFF ILSYKMSQFC PSDQVILIAR KTCLLMAVAV DLEQGRKAST 700
    AFEQTMFLSR ALEEIQTCND IHNFLKQTGT FSNDSCEKLL LLYEFEVRAK 750
    LNDPLLESFL ESVWELPHLE TKTFETIAII AMEKPAHYPL IALKALKKAL 800
    LLYKKEEPID ISQYSKCMHN LVNLSVPDGA SNVELCPLEE VWGYFEDALS 850
    HISRTKDYPE MEILWLMVKS WNTGVLMFSR SKYASAEKWC GLALRFLNHL 900
    TSFKESYETQ MNMLYSQLVE ALSNNKGPVF HEHGYWSKSD 940
    Length:940
    Mass (Da):107,889
    Last modified:July 24, 2007 - v3
    Checksum:i20A3B0BF58B82EF9
    GO
    Isoform 2 (identifier: Q8IYF3-2) [UniParc]FASTAAdd to Basket

    The sequence of this isoform differs from the canonical sequence as follows:
         1-325: Missing.

    Note: No experimental confirmation available.

    Show »
    Length:615
    Mass (Da):71,284
    Checksum:i004C5FCD1B5BA3C4
    GO
    Isoform 3 (identifier: Q8IYF3-3) [UniParc]FASTAAdd to Basket

    The sequence of this isoform differs from the canonical sequence as follows:
         1-27: MISAHCNLRLLCSSDSSASASQVAGTT → MDNDDFFSMDFK

    Show »
    Length:925
    Mass (Da):106,689
    Checksum:i94CD50F30C857FD1
    GO

    Sequence cautioni

    The sequence AAK31973.1 differs from that shown. Reason: Erroneous initiation.
    The sequence CAI39958.1 differs from that shown. Reason: Erroneous initiation.
    The sequence CAI40155.1 differs from that shown. Reason: Erroneous initiation.
    The sequence CAI41496.1 differs from that shown. Reason: Erroneous initiation.

    Experimental Info

    Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifierActions
    Sequence conflicti65 – 651T → A in BAB71520. (PubMed:14702039)Curated
    Sequence conflicti600 – 6001K → E in BAB71465. (PubMed:14702039)Curated

    Natural variant

    Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifierActions
    Natural varianti130 – 1301K → R.
    Corresponds to variant rs6525433 [ dbSNP | Ensembl ].
    VAR_034635
    Natural varianti451 – 4511E → K.1 Publication
    Corresponds to variant rs4844247 [ dbSNP | Ensembl ].
    VAR_034636

    Alternative sequence

    Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifierActions
    Alternative sequencei1 – 325325Missing in isoform 2. 1 PublicationVSP_027260Add
    BLAST
    Alternative sequencei1 – 2727MISAH…VAGTT → MDNDDFFSMDFK in isoform 3. 3 PublicationsVSP_027261Add
    BLAST

    Sequence databases

    Select the link destinations:
    EMBL
    GenBank
    DDBJ
    Links Updated
    AK057391 mRNA. Translation: BAB71465.1.
    AK057523 mRNA. Translation: BAB71520.1.
    AK292471 mRNA. Translation: BAF85160.1.
    AL627390, AL139109 Genomic DNA. Translation: CAI41495.1.
    AL139109, AL627390 Genomic DNA. Translation: CAI39957.1.
    AL627390, AL139109, AL627071 Genomic DNA. Translation: CAI41496.1. Different initiation.
    AL627071, AL139109, AL627390 Genomic DNA. Translation: CAI40155.1. Different initiation.
    AL139109, AL627071, AL627390 Genomic DNA. Translation: CAI39958.1. Different initiation.
    CH471132 Genomic DNA. Translation: EAX05331.1.
    BC036016 mRNA. Translation: AAH36016.2.
    AF285594 mRNA. Translation: AAK31973.1. Different initiation.
    CCDSiCCDS35323.1. [Q8IYF3-1]
    CCDS43968.1. [Q8IYF3-3]
    RefSeqiNP_001003811.1. NM_001003811.1. [Q8IYF3-1]
    NP_112566.2. NM_031276.2. [Q8IYF3-3]
    UniGeneiHs.121776.

    Genome annotation databases

    EnsembliENST00000344304; ENSP00000340995; ENSG00000120498. [Q8IYF3-1]
    ENST00000374320; ENSP00000363440; ENSG00000120498. [Q8IYF3-2]
    ENST00000374333; ENSP00000363453; ENSG00000120498. [Q8IYF3-3]
    ENST00000395889; ENSP00000379226; ENSG00000120498. [Q8IYF3-1]
    GeneIDi56159.
    KEGGihsa:56159.
    UCSCiuc004dyk.3. human. [Q8IYF3-1]
    uc004dym.3. human. [Q8IYF3-3]

    Polymorphism databases

    DMDMi156637425.

    Keywords - Coding sequence diversityi

    Alternative splicing, Polymorphism

    Cross-referencesi

    Sequence databases

    Select the link destinations:
    EMBL
    GenBank
    DDBJ
    Links Updated
    AK057391 mRNA. Translation: BAB71465.1 .
    AK057523 mRNA. Translation: BAB71520.1 .
    AK292471 mRNA. Translation: BAF85160.1 .
    AL627390 , AL139109 Genomic DNA. Translation: CAI41495.1 .
    AL139109 , AL627390 Genomic DNA. Translation: CAI39957.1 .
    AL627390 , AL139109 , AL627071 Genomic DNA. Translation: CAI41496.1 . Different initiation.
    AL627071 , AL139109 , AL627390 Genomic DNA. Translation: CAI40155.1 . Different initiation.
    AL139109 , AL627071 , AL627390 Genomic DNA. Translation: CAI39958.1 . Different initiation.
    CH471132 Genomic DNA. Translation: EAX05331.1 .
    BC036016 mRNA. Translation: AAH36016.2 .
    AF285594 mRNA. Translation: AAK31973.1 . Different initiation.
    CCDSi CCDS35323.1. [Q8IYF3-1 ]
    CCDS43968.1. [Q8IYF3-3 ]
    RefSeqi NP_001003811.1. NM_001003811.1. [Q8IYF3-1 ]
    NP_112566.2. NM_031276.2. [Q8IYF3-3 ]
    UniGenei Hs.121776.

    3D structure databases

    ProteinModelPortali Q8IYF3.
    SMRi Q8IYF3. Positions 455-517.
    ModBasei Search...
    MobiDBi Search...

    Protein-protein interaction databases

    BioGridi 121093. 24 interactions.
    IntActi Q8IYF3. 22 interactions.
    MINTi MINT-1443835.
    STRINGi 9606.ENSP00000340995.

    PTM databases

    PhosphoSitei Q8IYF3.

    Polymorphism databases

    DMDMi 156637425.

    Proteomic databases

    PaxDbi Q8IYF3.
    PRIDEi Q8IYF3.

    Protocols and materials databases

    DNASUi 56159.
    Structural Biology Knowledgebase Search...

    Genome annotation databases

    Ensembli ENST00000344304 ; ENSP00000340995 ; ENSG00000120498 . [Q8IYF3-1 ]
    ENST00000374320 ; ENSP00000363440 ; ENSG00000120498 . [Q8IYF3-2 ]
    ENST00000374333 ; ENSP00000363453 ; ENSG00000120498 . [Q8IYF3-3 ]
    ENST00000395889 ; ENSP00000379226 ; ENSG00000120498 . [Q8IYF3-1 ]
    GeneIDi 56159.
    KEGGi hsa:56159.
    UCSCi uc004dyk.3. human. [Q8IYF3-1 ]
    uc004dym.3. human. [Q8IYF3-3 ]

    Organism-specific databases

    CTDi 56159.
    GeneCardsi GC0XM069748.
    H-InvDB HIX0022351.
    HGNCi HGNC:11733. TEX11.
    HPAi HPA002950.
    MIMi 300311. gene.
    neXtProti NX_Q8IYF3.
    PharmGKBi PA36450.
    GenAtlasi Search...

    Phylogenomic databases

    eggNOGi NOG314839.
    HOGENOMi HOG000154551.
    HOVERGENi HBG069003.
    InParanoidi Q8IYF3.
    OMAi FRKIAWN.
    OrthoDBi EOG79PJNG.
    PhylomeDBi Q8IYF3.
    TreeFami TF333356.

    Miscellaneous databases

    GenomeRNAii 56159.
    NextBioi 61780.
    PROi Q8IYF3.
    SOURCEi Search...

    Gene expression databases

    Bgeei Q8IYF3.
    CleanExi HS_TEX11.
    Genevestigatori Q8IYF3.

    Family and domain databases

    Gene3Di 1.25.40.10. 1 hit.
    InterProi IPR013940. Meiosis_specific_SPO22.
    IPR011990. TPR-like_helical.
    [Graphical view ]
    Pfami PF08631. SPO22. 1 hit.
    [Graphical view ]
    ProtoNeti Search...

    Publicationsi

    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.
      , 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] [Europe PMC] [Abstract]
      Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORMS 1; 2 AND 3).
      Tissue: Testis.
    2. "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].
    3. Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
    4. "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] [Europe PMC] [Abstract]
      Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 3), VARIANT LYS-451.
      Tissue: Testis.
    5. "An abundance of X-linked genes expressed in spermatogonia."
      Wang P.J., McCarrey J.R., Yang F., Page D.C.
      Nat. Genet. 27:422-426(2001) [PubMed] [Europe PMC] [Abstract]
      Cited for: NUCLEOTIDE SEQUENCE [MRNA] OF 20-940 (ISOFORM 3).
      Tissue: Testis.
    6. "ZIP4H (TEX11) deficiency in the mouse impairs meiotic double strand break repair and the regulation of crossing over."
      Adelman C.A., Petrini J.H.
      PLoS Genet. 4:E1000042-E1000042(2008) [PubMed] [Europe PMC] [Abstract]
      Cited for: TISSUE SPECIFICITY.

    Entry informationi

    Entry nameiTEX11_HUMAN
    AccessioniPrimary (citable) accession number: Q8IYF3
    Secondary accession number(s): A8K8V6
    , Q5JQQ8, Q96LZ4, Q96M47, Q9BXU6
    Entry historyi
    Integrated into UniProtKB/Swiss-Prot: July 24, 2007
    Last sequence update: July 24, 2007
    Last modified: October 1, 2014
    This is version 99 of the entry and version 3 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
    4. MIM cross-references
      Online Mendelian Inheritance in Man (MIM) cross-references in UniProtKB/Swiss-Prot
    5. SIMILARITY comments
      Index of protein domains and families

    External Data

    Dasty 3