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P51522 (ZNF83_HUMAN) Reviewed, UniProtKB/Swiss-Prot

Last modified May 1, 2013. Version 115. Feed History...

Clusters with 100%, 90%, 50% identity | Documents (5) | Third-party data text xml rdf/xml gff fasta
to top of pageNames·Attributes·General annotation·Ontologies·Alt products·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order

Names and origin

Protein namesRecommended name:
Zinc finger protein 83
Alternative name(s):
Zinc finger protein 816B
Zinc finger protein HPF1
Gene names
Name:ZNF83
Synonyms:ZNF816B
OrganismHomo sapiens (Human) [Reference proteome]
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length516 AA.
Sequence statusComplete.
Protein existenceEvidence at transcript level

General annotation (Comments)

Function

May be involved in transcriptional regulation.

Subcellular location

Nucleus Probable.

Sequence similarities

Belongs to the krueppel C2H2-type zinc-finger protein family.

Contains 15 C2H2-type zinc fingers.

Ontologies

Keywords
   Biological processTranscription
Transcription regulation
   Cellular componentNucleus
   Coding sequence diversityAlternative splicing
Polymorphism
   DomainRepeat
Zinc-finger
   LigandDNA-binding
Metal-binding
Zinc
   Technical termComplete proteome
Reference proteome
Gene Ontology (GO)
   Biological_processtranscription, DNA-dependent

Inferred from electronic annotation. Source: UniProtKB-KW

   Cellular_componentnucleus

Non-traceable author statement. Source: UniProtKB

   Molecular_functionDNA binding

Inferred from electronic annotation. Source: UniProtKB-KW

sequence-specific DNA binding transcription factor activity

Non-traceable author statement. Source: UniProtKB

zinc ion binding

Inferred from electronic annotation. Source: InterPro

Complete GO annotation...

Alternative products

This entry describes 2 isoforms produced by alternative splicing. [Align] [Select]
Isoform 1 (identifier: P51522-1)

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: P51522-2)

The sequence of this isoform differs from the canonical sequence as follows:
     271-298: Missing.

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Chain1 – 516516Zinc finger protein 83
PRO_0000047396

Regions

Zinc finger93 – 11523C2H2-type 1; degenerate
Zinc finger121 – 14323C2H2-type 2
Zinc finger149 – 17123C2H2-type 3
Zinc finger177 – 19923C2H2-type 4
Zinc finger205 – 22723C2H2-type 5
Zinc finger233 – 25523C2H2-type 6
Zinc finger261 – 28323C2H2-type 7
Zinc finger289 – 31123C2H2-type 8
Zinc finger317 – 33923C2H2-type 9
Zinc finger345 – 36723C2H2-type 10
Zinc finger373 – 39523C2H2-type 11
Zinc finger401 – 42323C2H2-type 12
Zinc finger429 – 45123C2H2-type 13
Zinc finger457 – 47923C2H2-type 14
Zinc finger485 – 50723C2H2-type 15

Natural variations

Alternative sequence271 – 29828Missing in isoform 2.
VSP_037663
Natural variant701T → I.
Corresponds to variant rs3786490 [ dbSNP | Ensembl ].
VAR_058206
Natural variant961S → N. Ref.1 Ref.3 Ref.4
Corresponds to variant rs1056185 [ dbSNP | Ensembl ].
VAR_058207
Natural variant1191T → M.
Corresponds to variant rs329940 [ dbSNP | Ensembl ].
VAR_058208
Natural variant3921H → R. Ref.3
Corresponds to variant rs11545619 [ dbSNP | Ensembl ].
VAR_058209

Experimental info

Sequence conflict89 – 913GTE → MDR in AAG41760. Ref.4
Sequence conflict108 – 1092FT → LP in AAG41760. Ref.4

Sequences

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

Last modified July 13, 2010. Version 3.
Checksum: A6CA428CFAEA5D69

FASTA51659,710
        10         20         30         40         50         60 
MHGRKDDAQK QPVKNQLGLN PQSHLPELQL FQAEGKIYKY DHMEKSVNSS SLVSPPQRIS 

        70         80         90        100        110        120 
STVKTHISHT YECNFVDSLF TQKEKANIGT EHYKCSERGK AFHQGLHFTI HQIIHTKETQ 

       130        140        150        160        170        180 
FKCDICGKIF NKKSNLASHQ RIHTGEKPYK CNECGKVFHN MSHLAQHRRI HTGEKPYKCN 

       190        200        210        220        230        240 
ECGKVFNQIS HLAQHQRIHT GEKPYKCNEC GKVFHQISHL AQHRTIHTGE KPYECNKCGK 

       250        260        270        280        290        300 
VFSRNSYLVQ HLIIHTGEKP YRCNVCGKVF HHISHLAQHQ RIHTGEKPYK CNECGKVFSH 

       310        320        330        340        350        360 
KSSLVNHWRI HTGEKPYKCN ECGKVFSHKS SLVNHWRIHT GEKPYKCNEC GKVFSRNSYL 

       370        380        390        400        410        420 
AQHLIIHAGE KPYKCDECDK AFSQNSHLVQ HHRIHTGEKP YKCDECGKVF SQNSYLAYHW 

       430        440        450        460        470        480 
RIHTGEKAYK CNECGKVFGL NSSLAHHRKI HTGEKPFKCN ECGKAFSMRS SLTNHHAIHT 

       490        500        510 
GEKHFKCNEC GKLFRDNSYL VRHQRFHAGK KSNTCN 

« Hide

Isoform 2 [UniParc].

Checksum: 02D19C75A1677C48
Show »

FASTA48856,429

References

« Hide 'large scale' 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] [Europe PMC] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 2), VARIANT ASN-96.
[2]"The DNA sequence and biology of human chromosome 19."
Grimwood J., Gordon L.A., Olsen A.S., Terry A., Schmutz J., Lamerdin J.E., Hellsten U., Goodstein D., Couronne O., Tran-Gyamfi M., Aerts A., Altherr M., Ashworth L., Bajorek E., Black S., Branscomb E., Caenepeel S., Carrano A.V. expand/collapse author list , Caoile C., Chan Y.M., Christensen M., Cleland C.A., Copeland A., Dalin E., Dehal P., Denys M., Detter J.C., Escobar J., Flowers D., Fotopulos D., Garcia C., Georgescu A.M., Glavina T., Gomez M., Gonzales E., Groza M., Hammon N., Hawkins T., Haydu L., Ho I., Huang W., Israni S., Jett J., Kadner K., Kimball H., Kobayashi A., Larionov V., Leem S.-H., Lopez F., Lou Y., Lowry S., Malfatti S., Martinez D., McCready P.M., Medina C., Morgan J., Nelson K., Nolan M., Ovcharenko I., Pitluck S., Pollard M., Popkie A.P., Predki P., Quan G., Ramirez L., Rash S., Retterer J., Rodriguez A., Rogers S., Salamov A., Salazar A., She X., Smith D., Slezak T., Solovyev V., Thayer N., Tice H., Tsai M., Ustaszewska A., Vo N., Wagner M., Wheeler J., Wu K., Xie G., Yang J., Dubchak I., Furey T.S., DeJong P., Dickson M., Gordon D., Eichler E.E., Pennacchio L.A., Richardson P., Stubbs L., Rokhsar D.S., Myers R.M., Rubin E.M., Lucas S.M.
Nature 428:529-535(2004) [PubMed] [Europe PMC] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
[3]"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] (ISOFORMS 1 AND 2), VARIANTS ASN-96 AND ARG-392.
Tissue: PNS.
[4]"The human genome contains hundreds of genes coding for finger proteins of the Kruppel type."
Bellefroid E.J., Lecocq P.J., Benhida A., Poncelet D.A., Belayew A., Martial J.A.
DNA 8:377-387(1989) [PubMed] [Europe PMC] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [MRNA] OF 89-428 (ISOFORM 1), VARIANT ASN-96.
Tissue: Placenta.
+Additional computationally mapped references.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
AK289399 mRNA. Translation: BAF82088.1.
AC022150 Genomic DNA. No translation available.
BC050407 mRNA. Translation: AAH50407.1.
BC032867 mRNA. Translation: AAH32867.1.
M27877 mRNA. Translation: AAG41760.1.
IPIIPI00479920.
IPI00937015.
PIRA32891.
RefSeqNP_001099019.1. NM_001105549.1.
NP_001099020.1. NM_001105550.1.
NP_001099021.1. NM_001105551.1.
NP_001099022.1. NM_001105552.1.
NP_001099023.1. NM_001105553.1.
NP_001099024.1. NM_001105554.1.
NP_001229467.1. NM_001242538.1.
NP_060770.3. NM_018300.3.
UniGeneHs.467210.
Hs.659798.
Hs.665751.
Hs.710125.
Hs.742063.

3D structure databases

ProteinModelPortalP51522.
SMRP51522. Positions 27-69, 93-515.
ModBaseSearch...

Protein-protein interaction databases

IntActP51522. 1 interaction.
MINTMINT-1182660.
STRING9606.ENSP00000301096.

PTM databases

PhosphoSiteP51522.

Polymorphism databases

DMDM300669707.

Proteomic databases

PaxDbP51522.
PRIDEP51522.

Protocols and materials databases

StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

EnsemblENST00000301096; ENSP00000301096; ENSG00000167766.
ENST00000391789; ENSP00000375666; ENSG00000167766.
ENST00000434535; ENSP00000412334; ENSG00000167766.
ENST00000536937; ENSP00000445993; ENSG00000167766.
ENST00000541777; ENSP00000439681; ENSG00000167766.
ENST00000544146; ENSP00000445470; ENSG00000167766.
ENST00000545872; ENSP00000440713; ENSG00000167766.
ENST00000597597; ENSP00000472619; ENSG00000167766.
GeneID55769.
KEGGhsa:55769.
UCSCuc002pzu.4. human.
uc010eps.3. human.

Organism-specific databases

CTD55769.
GeneCardsGC19M053115.
HGNCHGNC:13158. ZNF83.
HPAHPA025970.
MIM194558. gene.
neXtProtNX_P51522.
PharmGKBPA37731.
GenAtlasSearch...

Phylogenomic databases

eggNOGCOG5048.
HOGENOMHOG000234617.
HOVERGENHBG018163.
InParanoidP51522.
KOK09228.
OMANSYLAYH.
OrthoDBEOG47WNND.
PhylomeDBP51522.

Gene expression databases

ArrayExpressP51522.
BgeeP51522.
CleanExHS_ZNF83.
GenevestigatorP51522.
GermOnlineENSG00000167766. Homo sapiens.

Family and domain databases

Gene3D3.30.160.60. 15 hits.
InterProIPR007087. Znf_C2H2.
IPR015880. Znf_C2H2-like.
IPR013087. Znf_C2H2/integrase_DNA-bd.
[Graphical view]
PfamPF00096. zf-C2H2. 1 hit.
[Graphical view]
SMARTSM00355. ZnF_C2H2. 15 hits.
[Graphical view]
PROSITEPS00028. ZINC_FINGER_C2H2_1. 14 hits.
PS50157. ZINC_FINGER_C2H2_2. 15 hits.
[Graphical view]
ProtoNetSearch...

Other

ChiTaRSZNF83. human.
GenomeRNAi55769.
NextBio60821.
SOURCESearch...

Entry information

Entry nameZNF83_HUMAN
AccessionPrimary (citable) accession number: P51522
Secondary accession number(s): A8MT75, Q3ZCX0, Q6PI08
Entry history
Integrated into UniProtKB/Swiss-Prot: October 1, 1996
Last sequence update: July 13, 2010
Last modified: May 1, 2013
This is version 115 of the entry and version 3 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

MIM cross-references

Online Mendelian Inheritance in Man (MIM) cross-references in UniProtKB/Swiss-Prot

SIMILARITY comments

Index of protein domains and families