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Q6ZN30

- BNC2_HUMAN

UniProt

Q6ZN30 - BNC2_HUMAN

Protein

Zinc finger protein basonuclin-2

Gene

BNC2

Organism
Homo sapiens (Human)
Status
Reviewed - Annotation score: 5 out of 5- Experimental evidence at protein leveli
    • BLAST
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    • History
      Entry version 98 (01 Oct 2014)
      Sequence version 1 (05 Jul 2004)
      Previous versions | rss
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    Functioni

    Probable transcription factor specific for skin keratinocytes. May play a role in the differentiation of spermatozoa and oocytes.

    Regions

    Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifierActions
    Zinc fingeri441 – 46424C2H2-type 1PROSITE-ProRule annotationAdd
    BLAST
    Zinc fingeri833 – 85624C2H2-type 2PROSITE-ProRule annotationAdd
    BLAST
    Zinc fingeri1035 – 105824C2H2-type 3PROSITE-ProRule annotationAdd
    BLAST
    Zinc fingeri1063 – 109028C2H2-type 4PROSITE-ProRule annotationAdd
    BLAST

    GO - Molecular functioni

    1. DNA binding Source: Ensembl
    2. metal ion binding Source: UniProtKB-KW

    GO - Biological processi

    1. endochondral bone growth Source: Ensembl
    2. mesenchyme development Source: Ensembl
    3. palate development Source: Ensembl
    4. regulation of transcription, DNA-templated Source: UniProtKB-KW
    5. tongue development Source: Ensembl
    6. transcription, DNA-templated Source: UniProtKB-KW

    Keywords - Biological processi

    Transcription, Transcription regulation

    Keywords - Ligandi

    Metal-binding, Zinc

    Names & Taxonomyi

    Protein namesi
    Recommended name:
    Zinc finger protein basonuclin-2
    Gene namesi
    Name:BNC2Imported
    OrganismiHomo sapiens (Human)
    Taxonomic identifieri9606 [NCBI]
    Taxonomic lineageiEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo
    ProteomesiUP000005640: Chromosome 9

    Organism-specific databases

    HGNCiHGNC:30988. BNC2.

    Subcellular locationi

    Nucleus 1 Publication

    GO - Cellular componenti

    1. cytoplasm Source: HPA
    2. nucleus Source: HPA
    3. plasma membrane Source: HPA

    Keywords - Cellular componenti

    Nucleus

    Pathology & Biotechi

    Organism-specific databases

    PharmGKBiPA134953132.

    PTM / Processingi

    Molecule processing

    Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifierActions
    Chaini1 – 10991099Zinc finger protein basonuclin-2PRO_0000046934Add
    BLAST

    Amino acid modifications

    Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifierActions
    Modified residuei561 – 5611Phosphoserine1 Publication

    Keywords - PTMi

    Phosphoprotein

    Proteomic databases

    PaxDbiQ6ZN30.
    PRIDEiQ6ZN30.

    PTM databases

    PhosphoSiteiQ6ZN30.

    Expressioni

    Tissue specificityi

    Highly expressed in testis, uterus and small intestine, and weakly expressed in colon and prostate. Also expressed in skin, primary keratinocytes, immortalized keratinocytes, and HeLa and HEK293 cells. Not detected in blood, thymus, spleen or Hep-G2 cells.2 Publications

    Gene expression databases

    ArrayExpressiQ6ZN30.
    BgeeiQ6ZN30.
    CleanExiHS_BNC2.
    GenevestigatoriQ6ZN30.

    Organism-specific databases

    HPAiHPA018525.

    Interactioni

    Protein-protein interaction databases

    BioGridi120155. 2 interactions.
    IntActiQ6ZN30. 1 interaction.
    STRINGi9606.ENSP00000370047.

    Structurei

    3D structure databases

    ProteinModelPortaliQ6ZN30.
    SMRiQ6ZN30. Positions 437-490, 822-895, 1029-1066.
    ModBaseiSearch...
    MobiDBiSearch...

    Family & Domainsi

    Compositional bias

    Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifierActions
    Compositional biasi534 – 61481Pro-richSequence AnalysisAdd
    BLAST

    Sequence similaritiesi

    Contains 4 C2H2-type zinc fingers.PROSITE-ProRule annotation

    Zinc finger

    Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifierActions
    Zinc fingeri441 – 46424C2H2-type 1PROSITE-ProRule annotationAdd
    BLAST
    Zinc fingeri833 – 85624C2H2-type 2PROSITE-ProRule annotationAdd
    BLAST
    Zinc fingeri1035 – 105824C2H2-type 3PROSITE-ProRule annotationAdd
    BLAST
    Zinc fingeri1063 – 109028C2H2-type 4PROSITE-ProRule annotationAdd
    BLAST

    Keywords - Domaini

    Repeat, Zinc-finger

    Phylogenomic databases

    eggNOGiNOG82846.
    HOGENOMiHOG000049098.
    HOVERGENiHBG050706.
    InParanoidiQ6ZN30.
    OMAiKVPGCNM.
    OrthoDBiEOG7SV0TM.
    PhylomeDBiQ6ZN30.
    TreeFamiTF350399.

    Family and domain databases

    InterProiIPR007087. Znf_C2H2.
    IPR015880. Znf_C2H2-like.
    [Graphical view]
    PfamiPF00096. zf-C2H2. 1 hit.
    [Graphical view]
    SMARTiSM00355. ZnF_C2H2. 6 hits.
    [Graphical view]
    PROSITEiPS00028. ZINC_FINGER_C2H2_1. 3 hits.
    PS50157. ZINC_FINGER_C2H2_2. 3 hits.
    [Graphical view]

    Sequences (2)i

    Sequence statusi: Complete.

    This entry describes 2 isoformsi produced by alternative splicing. Align

    Isoform 11 Publication (identifier: Q6ZN30-1) [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

    MAHLGPTPPP HSLNYKSEDR LSEQDWPAYF KVPCCGVDTS QIESEEAEVD     50
    VRERETQRDR EPKRARDLTL RDSCTDNSMQ FGTRTTTAEP GFMGTWQNAD 100
    TNLLFRMSQQ AIRCTLVNCT CECFQPGKIN LRTCDQCKHG WVAHALDKLS 150
    TQHLYHPTQV EIVQSNVVFD ISSLMLYGTQ AVPVRLKILL DRLFSVLKQE 200
    EVLHILHGLG WTLRDYVRGY ILQDAAGKVL DRWAIMSREE EIITLQQFLR 250
    FGETKSIVEL MAIQEKEGQA VAVPSSKTDS DIRTFIESNN RTRSPSLLAH 300
    LENSNPSSIH HFENIPNSLA FLLPFQYINP VSAPLLGLPP NGLLLEQPGL 350
    RLREPSLSTQ NEYNESSESE VSPTPYKNDQ TPNRNALTSI TNVEPKTEPA 400
    CVSPIQNSAP VSDLTKTEHP KSSFRIHRMR RMGSASRKGR VFCNACGKTF 450
    YDKGTLKIHY NAVHLKIKHR CTIEGCNMVF SSLRSRNRHS ANPNPRLHMP 500
    MLRNNRDKDL IRATSGAATP VIASTKSNLA LTSPGRPPMG FTTPPLDPVL 550
    QNPLPSQLVF SGLKTVQPVP PFYRSLLTPG EMVSPPTSLP TSPIIPTSGT 600
    IEQHPPPPSE PVVPAVMMAT HEPSADLAPK KKPRKSSMPV KIEKEIIDTA 650
    DEFDDEDDDP NDGGAVVNDM SHDNHCHSQE EMSPGMSVKD FSKHNRTRCI 700
    SRTEIRRADS MTSEDQEPER DYENESESSE PKLGEESMEG DEHIHSEVSE 750
    KVLMNSERPD ENHSEPSHQD VIKVKEEFTD PTYDMFYMSQ YGLYNGGGAS 800
    MAALHESFTS SLNYGSPQKF SPEGDLCSSP DPKICYVCKK SFKSSYSVKL 850
    HYRNVHLKEM HVCTVAGCNA AFPSRRSRDR HSANINLHRK LLTKELDDMG 900
    LDSSQPSLSK DLRDEFLVKI YGAQHPMGLD VREDASSPAG TEDSHLNGYG 950
    RGMAEDYMVL DLSTTSSLQS SSSIHSSRES DAGSDEGILL DDIDGASDSG 1000
    ESAHKAEAPA LPGSLGAEVS GSLMFSSLSG SNGGIMCNIC HKMYSNKGTL 1050
    RVHYKTVHLR EMHKCKVPGC NMMFSSVRSR NRHSQNPNLH KNIPFTSVD 1099
    Length:1,099
    Mass (Da):122,330
    Last modified:July 5, 2004 - v1
    Checksum:iB1601EACD158D3D3
    GO
    Isoform 2Curated (identifier: Q6ZN30-2) [UniParc]FASTAAdd to Basket

    The sequence of this isoform differs from the canonical sequence as follows:
         881-903: HSANINLHRKLLTKELDDMGLDS → YWEKSNEQNGLLVSWGETLSSLK
         904-1099: Missing.

    Note: No experimental confirmation available.Curated

    Show »
    Length:903
    Mass (Da):101,333
    Checksum:iCDE800F776B4644F
    GO

    Sequence cautioni

    The sequence AAR99389.1 differs from that shown. Reason: Erroneous initiation.
    The sequence BAA90908.1 differs from that shown. Reason: Erroneous initiation.
    The sequence BAB15269.1 differs from that shown. Reason: Erroneous initiation.
    The sequence BAC03837.1 differs from that shown. Reason: Erroneous initiation.

    Experimental Info

    Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifierActions
    Sequence conflicti560 – 5601F → L in BAC03837. (PubMed:14702039)Curated
    Sequence conflicti630 – 6301K → T in BAC03837. (PubMed:14702039)Curated
    Sequence conflicti797 – 7971G → E in BAB15269. (PubMed:14702039)Curated

    Natural variant

    Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifierActions
    Natural varianti550 – 5501L → V.
    Corresponds to variant rs4961490 [ dbSNP | Ensembl ].
    VAR_052707
    Natural varianti782 – 7821T → A.
    Corresponds to variant rs3739714 [ dbSNP | Ensembl ].
    VAR_033543

    Alternative sequence

    Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifierActions
    Alternative sequencei881 – 90323HSANI…MGLDS → YWEKSNEQNGLLVSWGETLS SLK in isoform 2. 1 PublicationVSP_051873Add
    BLAST
    Alternative sequencei904 – 1099196Missing in isoform 2. 1 PublicationVSP_051874Add
    BLAST

    Sequence databases

    Select the link destinations:
    EMBL
    GenBank
    DDBJ
    Links Updated
    AK000050 mRNA. Translation: BAA90908.1. Different initiation.
    AK025882 mRNA. Translation: BAB15269.1. Different initiation.
    AK092247 mRNA. Translation: BAC03837.1. Different initiation.
    AK131398 mRNA. Translation: BAD18545.1.
    AL450105, AL449983, AL450003 Genomic DNA. Translation: CAM21221.1.
    AY438376 mRNA. Translation: AAR99389.1. Different initiation.
    CCDSiCCDS6482.2. [Q6ZN30-1]
    RefSeqiNP_060107.3. NM_017637.5. [Q6ZN30-1]
    UniGeneiHs.656581.
    Hs.693436.
    Hs.740070.

    Genome annotation databases

    EnsembliENST00000380666; ENSP00000370041; ENSG00000173068. [Q6ZN30-2]
    ENST00000380672; ENSP00000370047; ENSG00000173068. [Q6ZN30-1]
    ENST00000484726; ENSP00000431516; ENSG00000173068. [Q6ZN30-2]
    GeneIDi54796.
    KEGGihsa:54796.
    UCSCiuc003zmi.3. human. [Q6ZN30-1]

    Polymorphism databases

    DMDMi74762393.

    Keywords - Coding sequence diversityi

    Alternative splicing, Polymorphism

    Cross-referencesi

    Sequence databases

    Select the link destinations:
    EMBL
    GenBank
    DDBJ
    Links Updated
    AK000050 mRNA. Translation: BAA90908.1 . Different initiation.
    AK025882 mRNA. Translation: BAB15269.1 . Different initiation.
    AK092247 mRNA. Translation: BAC03837.1 . Different initiation.
    AK131398 mRNA. Translation: BAD18545.1 .
    AL450105 , AL449983 , AL450003 Genomic DNA. Translation: CAM21221.1 .
    AY438376 mRNA. Translation: AAR99389.1 . Different initiation.
    CCDSi CCDS6482.2. [Q6ZN30-1 ]
    RefSeqi NP_060107.3. NM_017637.5. [Q6ZN30-1 ]
    UniGenei Hs.656581.
    Hs.693436.
    Hs.740070.

    3D structure databases

    ProteinModelPortali Q6ZN30.
    SMRi Q6ZN30. Positions 437-490, 822-895, 1029-1066.
    ModBasei Search...
    MobiDBi Search...

    Protein-protein interaction databases

    BioGridi 120155. 2 interactions.
    IntActi Q6ZN30. 1 interaction.
    STRINGi 9606.ENSP00000370047.

    PTM databases

    PhosphoSitei Q6ZN30.

    Polymorphism databases

    DMDMi 74762393.

    Proteomic databases

    PaxDbi Q6ZN30.
    PRIDEi Q6ZN30.

    Protocols and materials databases

    DNASUi 54796.
    Structural Biology Knowledgebase Search...

    Genome annotation databases

    Ensembli ENST00000380666 ; ENSP00000370041 ; ENSG00000173068 . [Q6ZN30-2 ]
    ENST00000380672 ; ENSP00000370047 ; ENSG00000173068 . [Q6ZN30-1 ]
    ENST00000484726 ; ENSP00000431516 ; ENSG00000173068 . [Q6ZN30-2 ]
    GeneIDi 54796.
    KEGGi hsa:54796.
    UCSCi uc003zmi.3. human. [Q6ZN30-1 ]

    Organism-specific databases

    CTDi 54796.
    GeneCardsi GC09M016410.
    HGNCi HGNC:30988. BNC2.
    HPAi HPA018525.
    MIMi 608669. gene.
    neXtProti NX_Q6ZN30.
    PharmGKBi PA134953132.
    GenAtlasi Search...

    Phylogenomic databases

    eggNOGi NOG82846.
    HOGENOMi HOG000049098.
    HOVERGENi HBG050706.
    InParanoidi Q6ZN30.
    OMAi KVPGCNM.
    OrthoDBi EOG7SV0TM.
    PhylomeDBi Q6ZN30.
    TreeFami TF350399.

    Miscellaneous databases

    ChiTaRSi BNC2. human.
    GeneWikii BNC2.
    GenomeRNAii 54796.
    NextBioi 57475.
    PROi Q6ZN30.
    SOURCEi Search...

    Gene expression databases

    ArrayExpressi Q6ZN30.
    Bgeei Q6ZN30.
    CleanExi HS_BNC2.
    Genevestigatori Q6ZN30.

    Family and domain databases

    InterProi IPR007087. Znf_C2H2.
    IPR015880. Znf_C2H2-like.
    [Graphical view ]
    Pfami PF00096. zf-C2H2. 1 hit.
    [Graphical view ]
    SMARTi SM00355. ZnF_C2H2. 6 hits.
    [Graphical view ]
    PROSITEi PS00028. ZINC_FINGER_C2H2_1. 3 hits.
    PS50157. ZINC_FINGER_C2H2_2. 3 hits.
    [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 AND 2).
      Tissue: ColonImported, Kidney epitheliumImported, TeratocarcinomaImported and TongueImported.
    2. "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.
      , 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] [Europe PMC] [Abstract]
      Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
    3. "Identification of Basonuclin2, a DNA-binding zinc-finger protein expressed in germ tissues and skin keratinocytes."
      Romano R.-A., Li H., Tummala R., Maul R., Sinha S.
      Genomics 83:821-833(2004) [PubMed] [Europe PMC] [Abstract]
      Cited for: NUCLEOTIDE SEQUENCE [MRNA] OF 73-1099 (ISOFORM 1), SUBCELLULAR LOCATION, TISSUE SPECIFICITY.
    4. "Basonuclin 2: an extremely conserved homolog of the zinc finger protein basonuclin."
      Vanhoutteghem A., Djian P.
      Proc. Natl. Acad. Sci. U.S.A. 101:3468-3473(2004) [PubMed] [Europe PMC] [Abstract]
      Cited for: PROBABLE FUNCTION, TISSUE SPECIFICITY.
    5. "Quantitative phosphoproteomics reveals widespread full phosphorylation site occupancy during mitosis."
      Olsen J.V., Vermeulen M., Santamaria A., Kumar C., Miller M.L., Jensen L.J., Gnad F., Cox J., Jensen T.S., Nigg E.A., Brunak S., Mann M.
      Sci. Signal. 3:RA3-RA3(2010) [PubMed] [Europe PMC] [Abstract]
      Cited for: PHOSPHORYLATION [LARGE SCALE ANALYSIS] AT SER-561, IDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS].
      Tissue: Cervix carcinoma.

    Entry informationi

    Entry nameiBNC2_HUMAN
    AccessioniPrimary (citable) accession number: Q6ZN30
    Secondary accession number(s): B1APG9
    , Q6T3A3, Q8NAR2, Q9H6J0, Q9NXV0
    Entry historyi
    Integrated into UniProtKB/Swiss-Prot: November 8, 2005
    Last sequence update: July 5, 2004
    Last modified: October 1, 2014
    This is version 98 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 9
      Human chromosome 9: 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