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P59894 (DCDC1_HUMAN) Reviewed, UniProtKB/Swiss-Prot

Last modified December 14, 2011. Version 53. 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·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order

Names and origin

Protein namesRecommended name:
Doublecortin domain-containing protein 1
Gene names
Name:DCDC1
OrganismHomo sapiens (Human)
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length354 AA.
Sequence statusComplete.
Protein existenceEvidence at transcript level

General annotation (Comments)

Tissue specificity

Highly expressed in testis. Lower levels of expression in lung, kidney, and pancreas. Higher expression in fetal brain than in adult brain. Ref.1

Sequence similarities

Contains 1 doublecortin domain.

Ontologies

Keywords
   Coding sequence diversityPolymorphism
   Technical termComplete proteome
Reference proteome
Gene Ontology (GO)
   Biological processintracellular signal transduction

Inferred from electronic annotation. Source: InterPro

Complete GO annotation...

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Chain1 – 354354Doublecortin domain-containing protein 1
PRO_0000079803

Regions

Domain168 – 25285Doublecortin

Natural variations

Natural variant71E → G.
Corresponds to variant rs11031357 [ dbSNP | Ensembl ].
VAR_037284
Natural variant831V → M.
Corresponds to variant rs2761591 [ dbSNP | Ensembl ].
VAR_033767

Experimental info

Sequence conflict1921V → A in AAP75563. Ref.1

Sequences

Sequence LengthMass (Da)Tools
P59894 [UniParc].

Last modified November 13, 2007. Version 2.
Checksum: 4C30ED8D93F7FBEE

FASTA35439,859
        10         20         30         40         50         60 
MAKTGAEDHR EALSQSSLSL LTEAMEVLQQ SSPEGTLDGN TVNPIYKYIL NDLPREFMSS 

        70         80         90        100        110        120 
QAKAVIKTTD DYLQSQFGPN RLVHSAAVSE GSGLQDCSTH QTASDHSHDE ISDLDSYKSN 

       130        140        150        160        170        180 
SKNNSCSISA SKRNRPVSAP VGQLRVAEFS SLKFQSARNW QKLSQRHKLQ PRVIKVTAYK 

       190        200        210        220        230        240 
NGSRTVFARV TVPTITLLLE ECTEKLNLNM AARRVFLADG KEALEPEDIP HEADVYVSTG 

       250        260        270        280        290        300 
EPFLNPFKKI KDHLLLIKKV TWTMNGLMLP TDIKRRKTKP VLSIRMKKLT ERTSVRILFF 

       310        320        330        340        350 
KNGMGQDGHE ITVGKETMKK VLDTCTIRMN LNLPARYFYD LYGRKIEDIS KGKH 

« Hide

References

« Hide 'large scale' references
[1]"Identification of a novel human doublecortin-domain-containing gene (DCDC1) expressed mainly in testis."
Zeng L., Gu S., Li Y., Zhao E., Xu J., Ye X., Wu Q., Wang L., Xie Y., Mao Y.
J. Hum. Genet. 48:393-396(2003) [PubMed: 12820024] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [MRNA], TISSUE SPECIFICITY.
Tissue: Fetal brain.
[2]"Human chromosome 11 DNA sequence and analysis including novel gene identification."
Taylor T.D., Noguchi H., Totoki Y., Toyoda A., Kuroki Y., Dewar K., Lloyd C., Itoh T., Takeda T., Kim D.-W., She X., Barlow K.F., Bloom T., Bruford E., Chang J.L., Cuomo C.A., Eichler E., FitzGerald M.G. expand/collapse author list , Jaffe D.B., LaButti K., Nicol R., Park H.-S., Seaman C., Sougnez C., Yang X., Zimmer A.R., Zody M.C., Birren B.W., Nusbaum C., Fujiyama A., Hattori M., Rogers J., Lander E.S., Sakaki Y.
Nature 440:497-500(2006) [PubMed: 16554811] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
AY247970 mRNA. Translation: AAP75563.1.
AL162614, AL137804 Genomic DNA. Translation: CAO03494.1.
AL137804, AL162614 Genomic DNA. Translation: CAO03548.1.
IPIIPI00377096.
RefSeqNP_861523.2. NM_181807.3.
UniGeneHs.127405.
Hs.592000.

3D structure databases

ProteinModelPortalP59894.
SMRP59894. Positions 171-245.
ModBaseSearch...

Protein-protein interaction databases

STRINGP59894.

Polymorphism databases

DMDM160332323.

Proteomic databases

PRIDEP59894.

Protocols and materials databases

StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

EnsemblENST00000452803; ENSP00000389792; ENSG00000188682.
GeneID341019.
KEGGhsa:341019.
UCSCuc001msv.1. human.

Organism-specific databases

CTD341019.
GeneCardsGC11M030964.
H-InvDBHIX0009525.
HGNCHGNC:20625. DCDC1.
HPAHPA032083.
MIM608062. gene.
neXtProtNX_P59894.
PharmGKBPA134970075.
GenAtlasSearch...

Phylogenomic databases

eggNOGprNOG18133.
GeneTreeENSGT00390000016867.
HOVERGENHBG051318.
InParanoidP59894.
OMANGMGQDG.
PhylomeDBP59894.

Gene expression databases

ArrayExpressP59894.
BgeeP59894.
CleanExHS_DCDC1.
GenevestigatorP59894.

Family and domain databases

InterProIPR003533. Doublecortin_dom.
[Graphical view]
Gene3DG3DSA:3.10.20.230. Doublecortin_dom. 2 hits.
SUPFAMSSF89837. Doublecortin_dom. 2 hits.
PROSITEPS50309. DC. 1 hit.
[Graphical view]
ProtoNetSearch...

Other

NextBio98060.
SOURCESearch...

Entry information

Entry nameDCDC1_HUMAN
AccessionPrimary (citable) accession number: P59894
Secondary accession number(s): A6PVL6
Entry history
Integrated into UniProtKB/Swiss-Prot: October 3, 2003
Last sequence update: November 13, 2007
Last modified: December 14, 2011
This is version 53 of the entry and version 2 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 11

Human chromosome 11: 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