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O76027 (ANXA9_HUMAN) Reviewed, UniProtKB/Swiss-Prot

Last modified May 1, 2013. Version 116. 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:
Annexin A9
Alternative name(s):
Annexin XXXI
Annexin-31
Annexin-9
Pemphaxin
Gene names
Name:ANXA9
Synonyms:ANX31
OrganismHomo sapiens (Human) [Reference proteome]
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length345 AA.
Sequence statusComplete.
Protein existenceEvidence at protein level

General annotation (Comments)

Function

Low affinity receptor for acetylcholine known to be targeted by disease-causing pemphigus vulgaris antibodies in keratinocytes. Ref.2

Subunit structure

Homodimer. Ref.2

Tissue specificity

Expressed in the stratified squamous skin epithelium, but not in epithelia of other types (at protein level). Ref.2

Sequence similarities

Belongs to the annexin family.

Contains 4 annexin repeats.

Sequence caution

The sequence AAH05830.2 differs from that shown. Reason: Erroneous initiation.

The sequence CAA08933.1 differs from that shown. Reason: Frameshift at position 7.

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Chain1 – 345345Annexin A9
PRO_0000067505

Regions

Repeat43 – 11068Annexin 1
Repeat115 – 18268Annexin 2
Repeat199 – 26466Annexin 3
Repeat272 – 33968Annexin 4

Natural variations

Natural variant281A → T.
Corresponds to variant rs16832595 [ dbSNP | Ensembl ].
VAR_048255
Natural variant1141T → A.
Corresponds to variant rs7536645 [ dbSNP | Ensembl ].
VAR_048256
Natural variant1191A → T.
Corresponds to variant rs16832602 [ dbSNP | Ensembl ].
VAR_048257
Natural variant1661D → G. Ref.1 Ref.2 Ref.5
Corresponds to variant rs267733 [ dbSNP | Ensembl ].
VAR_022814
Natural variant2251R → Q.
Corresponds to variant rs7542365 [ dbSNP | Ensembl ].
VAR_031212
Natural variant2321R → Q.
Corresponds to variant rs7542365 [ dbSNP | Ensembl ].
VAR_048258

Sequences

Sequence LengthMass (Da)Tools
O76027 [UniParc].

Last modified March 20, 2007. Version 3.
Checksum: DF0FE611CA6D56B9

FASTA34538,364
        10         20         30         40         50         60 
MSVTGGKMAP SLTQEILSHL GLASKTAAWG TLGTLRTFLN FSVDKDAQRL LRAITGQGVD 

        70         80         90        100        110        120 
RSAIVDVLTN RSREQRQLIS RNFQERTQQD LMKSLQAALS GNLERIVMAL LQPTAQFDAQ 

       130        140        150        160        170        180 
ELRTALKASD SAVDVAIEIL ATRTPPQLQE CLAVYKHNFQ VEAVDDITSE TSGILQDLLL 

       190        200        210        220        230        240 
ALAKGGRDSY SGIIDYNLAE QDVQALQRAE GPSREETWVP VFTQRNPEHL IRVFDQYQRS 

       250        260        270        280        290        300 
TGQELEEAVQ NRFHGDAQVA LLGLASVIKN TPLYFADKLH QALQETEPNY QVLIRILISR 

       310        320        330        340 
CETDLLSIRA EFRKKFGKSL YSSLQDAVKG DCQSALLALC RAEDM 

« Hide

References

« Hide 'large scale' references
[1]"Expression profile and structural divergence of novel human annexin 31."
Morgan R.O., Fernandez M.-P.
FEBS Lett. 434:300-304(1998) [PubMed] [Europe PMC] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [MRNA], VARIANT GLY-166.
Tissue: Liver and Spleen.
[2]"Pemphigus vulgaris antibody identifies pemphaxin. A novel keratinocyte annexin-like molecule binding acetylcholine."
Nguyen V.T., Ndoye A., Grando S.A.
J. Biol. Chem. 275:29466-29476(2000) [PubMed] [Europe PMC] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [MRNA], VARIANT GLY-166, TISSUE SPECIFICITY, FUNCTION, SUBUNIT, IDENTIFICATION AS AN AUTOANTIGEN IN PV.
[3]"The DNA sequence and biological annotation of human chromosome 1."
Gregory S.G., Barlow K.F., McLay K.E., Kaul R., Swarbreck D., Dunham A., Scott C.E., Howe K.L., Woodfine K., Spencer C.C.A., Jones M.C., Gillson C., Searle S., Zhou Y., Kokocinski F., McDonald L., Evans R., Phillips K. expand/collapse author list , Atkinson A., Cooper R., Jones C., Hall R.E., Andrews T.D., Lloyd C., Ainscough R., Almeida J.P., Ambrose K.D., Anderson F., Andrew R.W., Ashwell R.I.S., Aubin K., Babbage A.K., Bagguley C.L., Bailey J., Beasley H., Bethel G., Bird C.P., Bray-Allen S., Brown J.Y., Brown A.J., Buckley D., Burton J., Bye J., Carder C., Chapman J.C., Clark S.Y., Clarke G., Clee C., Cobley V., Collier R.E., Corby N., Coville G.J., Davies J., Deadman R., Dunn M., Earthrowl M., Ellington A.G., Errington H., Frankish A., Frankland J., French L., Garner P., Garnett J., Gay L., Ghori M.R.J., Gibson R., Gilby L.M., Gillett W., Glithero R.J., Grafham D.V., Griffiths C., Griffiths-Jones S., Grocock R., Hammond S., Harrison E.S.I., Hart E., Haugen E., Heath P.D., Holmes S., Holt K., Howden P.J., Hunt A.R., Hunt S.E., Hunter G., Isherwood J., James R., Johnson C., Johnson D., Joy A., Kay M., Kershaw J.K., Kibukawa M., Kimberley A.M., King A., Knights A.J., Lad H., Laird G., Lawlor S., Leongamornlert D.A., Lloyd D.M., Loveland J., Lovell J., Lush M.J., Lyne R., Martin S., Mashreghi-Mohammadi M., Matthews L., Matthews N.S.W., McLaren S., Milne S., Mistry S., Moore M.J.F., Nickerson T., O'Dell C.N., Oliver K., Palmeiri A., Palmer S.A., Parker A., Patel D., Pearce A.V., Peck A.I., Pelan S., Phelps K., Phillimore B.J., Plumb R., Rajan J., Raymond C., Rouse G., Saenphimmachak C., Sehra H.K., Sheridan E., Shownkeen R., Sims S., Skuce C.D., Smith M., Steward C., Subramanian S., Sycamore N., Tracey A., Tromans A., Van Helmond Z., Wall M., Wallis J.M., White S., Whitehead S.L., Wilkinson J.E., Willey D.L., Williams H., Wilming L., Wray P.W., Wu Z., Coulson A., Vaudin M., Sulston J.E., Durbin R.M., Hubbard T., Wooster R., Dunham I., Carter N.P., McVean G., Ross M.T., Harrow J., Olson M.V., Beck S., Rogers J., Bentley D.R.
Nature 441:315-321(2006) [PubMed] [Europe PMC] [Abstract]
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].
Tissue: Colon.
[5]"Cloning of human full open reading frames in Gateway(TM) system entry vector (pDONR201)."
Halleck A., Ebert L., Mkoundinya M., Schick M., Eisenstein S., Neubert P., Kstrang K., Schatten R., Shen B., Henze S., Mar W., Korn B., Zuo D., Hu Y., LaBaer J.
Submitted (JUN-2004) to the EMBL/GenBank/DDBJ databases
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] OF 8-345, VARIANT GLY-166.
+Additional computationally mapped references.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
AJ009985 mRNA. Translation: CAA08933.1. Frameshift.
AF230929 mRNA. Translation: AAG16780.1.
AL590133 Genomic DNA. Translation: CAI13335.1.
BC005830 mRNA. Translation: AAH05830.2. Different initiation.
CR536481 mRNA. Translation: CAG38720.1.
IPIIPI00008714.
RefSeqNP_003559.2. NM_003568.2.
UniGeneHs.3346.

3D structure databases

ProteinModelPortalO76027.
ModBaseSearch...

Protein-protein interaction databases

IntActO76027. 2 interactions.
MINTMINT-1415446.
STRING9606.ENSP00000357943.

PTM databases

PhosphoSiteO76027.

Proteomic databases

PaxDbO76027.
PRIDEO76027.

Protocols and materials databases

DNASU8416.
StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

EnsemblENST00000368947; ENSP00000357943; ENSG00000143412.
GeneID8416.
KEGGhsa:8416.
UCSCuc001ewa.2. human.

Organism-specific databases

CTD8416.
GeneCardsGC01P150954.
HGNCHGNC:547. ANXA9.
HPAHPA028404.
HPA028698.
MIM603319. gene.
neXtProtNX_O76027.
PharmGKBPA24837.
GenAtlasSearch...

Phylogenomic databases

eggNOGNOG303047.
HOGENOMHOG000158803.
HOVERGENHBG061815.
InParanoidO76027.
OMALQETEPN.
OrthoDBEOG490799.

Gene expression databases

BgeeO76027.
CleanExHS_ANXA9.
GenevestigatorO76027.
GermOnlineENSG00000143412. Homo sapiens.

Family and domain databases

Gene3D1.10.220.10. 4 hits.
InterProIPR001464. Annexin.
IPR018502. Annexin_repeat.
IPR018252. Annexin_repeat_CS.
IPR009116. AnnexinXXXI.
[Graphical view]
PANTHERPTHR10502. PTHR10502. 1 hit.
PfamPF00191. Annexin. 4 hits.
[Graphical view]
PRINTSPR00196. ANNEXIN.
PR01812. ANNEXINXXXI.
SMARTSM00335. ANX. 4 hits.
[Graphical view]
SUPFAMSSF47874. Annexin. 1 hit.
PROSITEPS00223. ANNEXIN. 1 hit.
[Graphical view]
ProtoNetSearch...

Other

GenomeRNAi8416.
NextBio31500.
SOURCESearch...

Entry information

Entry nameANXA9_HUMAN
AccessionPrimary (citable) accession number: O76027
Secondary accession number(s): Q5SZF1 expand/collapse secondary AC list , Q6FI55, Q9BS00, Q9HBJ6
Entry history
Integrated into UniProtKB/Swiss-Prot: February 21, 2001
Last sequence update: March 20, 2007
Last modified: May 1, 2013
This is version 116 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 1

Human chromosome 1: 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