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Q9H9R9 (DBND1_HUMAN) Reviewed, UniProtKB/Swiss-Prot

Last modified January 25, 2012. Version 56. Feed History...

Clusters with 100%, 90%, 50% identity | Documents (2) | 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:
Dysbindin domain-containing protein 1
Gene names
Name:DBNDD1
OrganismHomo sapiens (Human)
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length158 AA.
Sequence statusComplete.
Protein existenceEvidence at transcript level

General annotation (Comments)

Sequence similarities

Belongs to the dysbindin family.

Ontologies

Keywords
   Coding sequence diversityAlternative splicing
   Technical termComplete proteome
Reference proteome
Gene Ontology (GO)
   Cellular componentcytoplasm

Inferred from electronic annotation. Source: InterPro

Complete GO annotation...

Alternative products

This entry describes 3 isoforms produced by alternative splicing. [Align] [Select]
Isoform 1 (identifier: Q9H9R9-1)

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: Q9H9R9-2)

The sequence of this isoform differs from the canonical sequence as follows:
     1-10: MEPPEGAGTG → MGETWKNICSTVRHGWWLRDHRMAGLPIPP
Isoform 3 (identifier: Q9H9R9-3)

The sequence of this isoform differs from the canonical sequence as follows:
     1-11: MEPPEGAGTGE → MTQQWREVNE...RGRQRARPPK

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Chain1 – 158158Dysbindin domain-containing protein 1
PRO_0000292438

Natural variations

Alternative sequence1 – 1111MEPPEGAGTGE → MTQQWREVNEDREAVAQARS WQSLNLGDRDMGVSFIETAL ALSAARARRPLLTSHPPSRP FQPPKHTPSPPPAPRVNSRH PGRSVSLSLPSASQAPPVPL ASPEGRPHTVGAPHASTWKR TRGRQRARPPK in isoform 3.
VSP_037541
Alternative sequence1 – 1010MEPPEGAGTG → MGETWKNICSTVRHGWWLRD HRMAGLPIPP in isoform 2.
VSP_026214

Experimental info

Sequence conflict261P → S in BAB14152. Ref.1

Sequences

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

Last modified June 16, 2009. Version 2.
Checksum: 498F80B5002A2C33

FASTA15817,042
        10         20         30         40         50         60 
MEPPEGAGTG EIVKEAEVPQ AALGVPAQGT GDNGHTPVEE EVGGIPVPAP GLLQVTERRQ 

        70         80         90        100        110        120 
PLSSVSSLEV HFDLLDLTEL TDMSDQELAE VFADSDDENL NTESPAGLHP LPRAGYLRSP 

       130        140        150 
SWTRTRAEQS HEKQPLGDPE RQATVLDTFL TVERPQED 

« Hide

Isoform 2 [UniParc].

Checksum: FB6433859E619A48
Show »

FASTA17819,643
Isoform 3 [UniParc].

Checksum: 8C506340A84A02D8
Show »

FASTA27830,344

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: 14702039] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORMS 1 AND 3).
[2]"The sequence and analysis of duplication-rich human chromosome 16."
Martin J., Han C., Gordon L.A., Terry A., Prabhakar S., She X., Xie G., Hellsten U., Chan Y.M., Altherr M., Couronne O., Aerts A., Bajorek E., Black S., Blumer H., Branscomb E., Brown N.C., Bruno W.J. expand/collapse author list , Buckingham J.M., Callen D.F., Campbell C.S., Campbell M.L., Campbell E.W., Caoile C., Challacombe J.F., Chasteen L.A., Chertkov O., Chi H.C., Christensen M., Clark L.M., Cohn J.D., Denys M., Detter J.C., Dickson M., Dimitrijevic-Bussod M., Escobar J., Fawcett J.J., Flowers D., Fotopulos D., Glavina T., Gomez M., Gonzales E., Goodstein D., Goodwin L.A., Grady D.L., Grigoriev I., Groza M., Hammon N., Hawkins T., Haydu L., Hildebrand C.E., Huang W., Israni S., Jett J., Jewett P.B., Kadner K., Kimball H., Kobayashi A., Krawczyk M.-C., Leyba T., Longmire J.L., Lopez F., Lou Y., Lowry S., Ludeman T., Manohar C.F., Mark G.A., McMurray K.L., Meincke L.J., Morgan J., Moyzis R.K., Mundt M.O., Munk A.C., Nandkeshwar R.D., Pitluck S., Pollard M., Predki P., Parson-Quintana B., Ramirez L., Rash S., Retterer J., Ricke D.O., Robinson D.L., Rodriguez A., Salamov A., Saunders E.H., Scott D., Shough T., Stallings R.L., Stalvey M., Sutherland R.D., Tapia R., Tesmer J.G., Thayer N., Thompson L.S., Tice H., Torney D.C., Tran-Gyamfi M., Tsai M., Ulanovsky L.E., Ustaszewska A., Vo N., White P.S., Williams A.L., Wills P.L., Wu J.-R., Wu K., Yang J., DeJong P., Bruce D., Doggett N.A., Deaven L., Schmutz J., Grimwood J., Richardson P., Rokhsar D.S., Eichler E.E., Gilna P., Lucas S.M., Myers R.M., Rubin E.M., Pennacchio L.A.
Nature 432:988-994(2004) [PubMed: 15616553] [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: 15489334] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 2).
Tissue: Eye.
[4]"The full-ORF clone resource of the German cDNA consortium."
Bechtel S., Rosenfelder H., Duda A., Schmidt C.P., Ernst U., Wellenreuther R., Mehrle A., Schuster C., Bahr A., Bloecker H., Heubner D., Hoerlein A., Michel G., Wedler H., Koehrer K., Ottenwaelder B., Poustka A., Wiemann S., Schupp I.
BMC Genomics 8:399-399(2007) [PubMed: 17974005] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] OF 122-158.
Tissue: Amygdala.
+Additional computationally mapped references.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
AK022644 mRNA. Translation: BAB14152.1.
AK298932 mRNA. Translation: BAG61035.1.
AC092143 Genomic DNA. No translation available.
BC000700 mRNA. Translation: AAH00700.2.
AL713678 mRNA. Translation: CAH10640.1.
IPIIPI00031533.
IPI00304285.
IPI00872543.
RefSeqNP_001036075.1. NM_001042610.1.
NP_076948.2. NM_024043.2.
UniGeneHs.301394.

3D structure databases

ProteinModelPortalQ9H9R9.
ModBaseSearch...

Protein-protein interaction databases

STRINGQ9H9R9.

Polymorphism databases

DMDM239938618.

Protocols and materials databases

StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

EnsemblENST00000002501; ENSP00000002501; ENSG00000003249.
GeneID79007.
KEGGhsa:79007.
UCSCuc002fqe.1. human.
uc002fqf.1. human.

Organism-specific databases

CTD79007.
GeneCardsGC16M090071.
HGNCHGNC:28455. DBNDD1.
HPAHPA043018.
neXtProtNX_Q9H9R9.
PharmGKBPA144596443.
GenAtlasSearch...

Phylogenomic databases

eggNOGprNOG18885.
GeneTreeENSGT00390000018903.
HOVERGENHBG056558.
OMAPAIVDTF.
OrthoDBEOG4GB77R.

Gene expression databases

ArrayExpressQ9H9R9.
BgeeQ9H9R9.
CleanExHS_DBNDD1.
GenevestigatorQ9H9R9.

Family and domain databases

InterProIPR007531. Dysbindin.
[Graphical view]
PANTHERPTHR16294. Dysbindin. 1 hit.
PfamPF04440. Dysbindin. 1 hit.
[Graphical view]
ProtoNetSearch...

Other

NextBio67641.

Entry information

Entry nameDBND1_HUMAN
AccessionPrimary (citable) accession number: Q9H9R9
Secondary accession number(s): B4DQS3, Q69YT2, Q9BW25
Entry history
Integrated into UniProtKB/Swiss-Prot: June 26, 2007
Last sequence update: June 16, 2009
Last modified: January 25, 2012
This is version 56 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 16

Human chromosome 16: entries, gene names and cross-references to MIM

SIMILARITY comments

Index of protein domains and families