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Q5VUB5 (F1711_HUMAN) Reviewed, UniProtKB/Swiss-Prot

Last modified January 25, 2012. Version 61. Feed History...

Clusters with 100%, 90%, 50% identity | Documents (4) | 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:
Protein FAM171A1
Alternative name(s):
Astroprincin
Gene names
Name:FAM171A1
Synonyms:C10orf38
OrganismHomo sapiens (Human)
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length890 AA.
Sequence statusComplete.
Sequence processingThe displayed sequence is further processed into a mature form.
Protein existenceEvidence at protein level

General annotation (Comments)

Subcellular location

Membrane; Single-pass type I membrane protein Potential.

Sequence similarities

Belongs to the FAM171 family.

Ontologies

Keywords
   Cellular componentMembrane
   Coding sequence diversityPolymorphism
   DomainSignal
Transmembrane
Transmembrane helix
   PTMGlycoprotein
Phosphoprotein
   Technical termComplete proteome
Reference proteome
Gene Ontology (GO)
   Cellular componentintegral to membrane

Inferred from electronic annotation. Source: UniProtKB-KW

Complete GO annotation...

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Signal peptide1 – 2121 Potential
Chain22 – 890869Protein FAM171A1
PRO_0000274263

Regions

Topological domain22 – 303282Extracellular Potential
Transmembrane304 – 32421Helical; Potential
Topological domain325 – 890566Cytoplasmic Potential

Amino acid modifications

Modified residue8551Phosphoserine Ref.5
Glycosylation1591N-linked (GlcNAc...) Ref.6
Glycosylation1901N-linked (GlcNAc...) Potential
Glycosylation1941N-linked (GlcNAc...) Potential

Natural variations

Natural variant4651P → S. Ref.4
Corresponds to variant rs3814165 [ dbSNP | Ensembl ].
VAR_030220

Experimental info

Sequence conflict1181L → P in AAI09304. Ref.4
Sequence conflict5921G → R in AAH34232. Ref.4
Sequence conflict6701P → Q in AAH34232. Ref.4

Sequences

Sequence LengthMass (Da)Tools
Q5VUB5 [UniParc].

Last modified December 7, 2004. Version 1.
Checksum: A0718E29A639FB72

FASTA89097,854
        10         20         30         40         50         60 
MSRSATLLLC LLGCHVWKAV TKTLREPGAG AQEVTLKVHI SDASTHQPVA DALIEIFTNQ 

        70         80         90        100        110        120 
ASIASGTSGT DGVAFIKFQY KLGSQLIVTA SKHAYVPNSA PWKPIRLPVF SSLSLGLLPE 

       130        140        150        160        170        180 
RSATLMVYED VVQIVSGFQG ARPQPRVHFQ RRALRLPENT SYSDLTAFLT AASSPSEVDS 

       190        200        210        220        230        240 
FPYLRGLDGN GTGNSTRHDL TPVTAVSVHL LSSNGTPVLV DGPIYVTVPL ATQSSLRHNA 

       250        260        270        280        290        300 
YVAAWRFDQK LGTWLKSGLG LVHQEGSQLT WTYIAPQLGY WVAAMSPPIP GPVVTQDITT 

       310        320        330        340        350        360 
YHTVFLLAIL GGMAFILLVL LCLLLYYCRR KCLKPRQHHR KLQLPAGLES SKRDQSTSMS 

       370        380        390        400        410        420 
HINLLFSRRA SEFPGPLSVT SHGRPEAPGT KELMSGVHLE MMSPGGEGDL HTPMLKLSYS 

       430        440        450        460        470        480 
TSQEFSSREE LLSCKEEDKS QISFDNLTPS GTLGKDYHKS VEVFPLKARK SMEREGYESS 

       490        500        510        520        530        540 
GNDDYRGSYN TVLSQPLFEK QDREGPASTG SKLTIQEHLY PAPSSPEKEQ LLDRRPTECM 

       550        560        570        580        590        600 
MSRSVDHLER PTSFPRPGQL ICCSSVDQVN DSVYRKVLPA LVIPAHYMKL PGDHSYVSQP 

       610        620        630        640        650        660 
LVVPADQQLE IERLQAELSN PHAGIFPHPS SQIQPQPLSS QAISQQHLQD AGTREWSPQN 

       670        680        690        700        710        720 
ASMSESLSIP ASLNDAALAQ MNSEVQLLTE KALMELGGGK PLPHPRAWFV SLDGRSNAHV 

       730        740        750        760        770        780 
RHSYIDLQRA GRNGSNDASL DSGVDMNEPK SARKGRGDAL SLQQNYPPVQ EHQQKEPRAP 

       790        800        810        820        830        840 
DSTAYTQLVY LDDVEQSGSE CGTTVCTPED SALRCLLEGS SRRSGGQLPS LQEETTRRTA 

       850        860        870        880        890 
DAPSEPAASP HQRRSAHEEE EDDDDDDQGE DKKSPWQKRE ERPLMAFNIK 

« Hide

References

« Hide 'large scale' references
[1]"Cloning and expression profile of a novel gene isolated from DiGeorge syndrome critical region on chromosome 10."
Attalla H., Karlsson L., Paetau A., Andersson L.C.
Submitted (JUL-2004) to the EMBL/GenBank/DDBJ databases
Cited for: NUCLEOTIDE SEQUENCE [MRNA].
Tissue: Kidney.
[2]"The DNA sequence and comparative analysis of human chromosome 10."
Deloukas P., Earthrowl M.E., Grafham D.V., Rubenfield M., French L., Steward C.A., Sims S.K., Jones M.C., Searle S., Scott C., Howe K., Hunt S.E., Andrews T.D., Gilbert J.G.R., Swarbreck D., Ashurst J.L., Taylor A., Battles J. expand/collapse author list , Bird C.P., Ainscough R., Almeida J.P., Ashwell R.I.S., Ambrose K.D., Babbage A.K., Bagguley C.L., Bailey J., Banerjee R., Bates K., Beasley H., Bray-Allen S., Brown A.J., Brown J.Y., Burford D.C., Burrill W., Burton J., Cahill P., Camire D., Carter N.P., Chapman J.C., Clark S.Y., Clarke G., Clee C.M., Clegg S., Corby N., Coulson A., Dhami P., Dutta I., Dunn M., Faulkner L., Frankish A., Frankland J.A., Garner P., Garnett J., Gribble S., Griffiths C., Grocock R., Gustafson E., Hammond S., Harley J.L., Hart E., Heath P.D., Ho T.P., Hopkins B., Horne J., Howden P.J., Huckle E., Hynds C., Johnson C., Johnson D., Kana A., Kay M., Kimberley A.M., Kershaw J.K., Kokkinaki M., Laird G.K., Lawlor S., Lee H.M., Leongamornlert D.A., Laird G., Lloyd C., Lloyd D.M., Loveland J., Lovell J., McLaren S., McLay K.E., McMurray A., Mashreghi-Mohammadi M., Matthews L., Milne S., Nickerson T., Nguyen M., Overton-Larty E., Palmer S.A., Pearce A.V., Peck A.I., Pelan S., Phillimore B., Porter K., Rice C.M., Rogosin A., Ross M.T., Sarafidou T., Sehra H.K., Shownkeen R., Skuce C.D., Smith M., Standring L., Sycamore N., Tester J., Thorpe A., Torcasso W., Tracey A., Tromans A., Tsolas J., Wall M., Walsh J., Wang H., Weinstock K., West A.P., Willey D.L., Whitehead S.L., Wilming L., Wray P.W., Young L., Chen Y., Lovering R.C., Moschonas N.K., Siebert R., Fechtel K., Bentley D., Durbin R.M., Hubbard T., Doucette-Stamm L., Beck S., Smith D.R., Rogers J.
Nature 429:375-381(2004) [PubMed: 15164054] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
[3]Mural R.J., Istrail S., Sutton G.G., Florea L., Halpern A.L., Mobarry C.M., Lippert R., Walenz B., Shatkay H., Dew I., Miller J.R., Flanigan M.J., Edwards N.J., Bolanos R., Fasulo D., Halldorsson B.V., Hannenhalli S., Turner R. expand/collapse author list , Yooseph S., Lu F., Nusskern D.R., Shue B.C., Zheng X.H., Zhong F., Delcher A.L., Huson D.H., Kravitz S.A., Mouchard L., Reinert K., Remington K.A., Clark A.G., Waterman M.S., Eichler E.E., Adams M.D., Hunkapiller M.W., Myers E.W., Venter J.C.
Submitted (SEP-2005) to the EMBL/GenBank/DDBJ databases
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: 15489334] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA], VARIANT SER-465.
Tissue: Brain.
[5]"Large-scale phosphoproteome analysis of human liver tissue by enrichment and fractionation of phosphopeptides with strong anion exchange chromatography."
Han G., Ye M., Zhou H., Jiang X., Feng S., Jiang X., Tian R., Wan D., Zou H., Gu J.
Proteomics 8:1346-1361(2008) [PubMed: 18318008] [Abstract]
Cited for: PHOSPHORYLATION [LARGE SCALE ANALYSIS] AT SER-855, MASS SPECTROMETRY.
Tissue: Liver.
[6]"Glycoproteomics analysis of human liver tissue by combination of multiple enzyme digestion and hydrazide chemistry."
Chen R., Jiang X., Sun D., Han G., Wang F., Ye M., Wang L., Zou H.
J. Proteome Res. 8:651-661(2009) [PubMed: 19159218] [Abstract]
Cited for: GLYCOSYLATION [LARGE SCALE ANALYSIS] AT ASN-159, MASS SPECTROMETRY.
Tissue: Liver.
+Additional computationally mapped references.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
AY683003 mRNA. Translation: AAV85904.1.
AL590365, AL139338, AL607028 Genomic DNA. Translation: CAH73963.1.
AL139338, AL590365, AL607028 Genomic DNA. Translation: CAI12244.1.
AL607028, AL139338, AL590365 Genomic DNA. Translation: CAI12941.1.
CH471072 Genomic DNA. Translation: EAW86237.1.
BC034232 mRNA. Translation: AAH34232.1.
BC109302 mRNA. Translation: AAI09303.1.
BC109303 mRNA. Translation: AAI09304.1.
IPIIPI00000265.
RefSeqNP_001010924.1. NM_001010924.1.
UniGeneHs.66762.

3D structure databases

ProteinModelPortalQ5VUB5.
ModBaseSearch...

Protein-protein interaction databases

IntActQ5VUB5. 2 interactions.
STRINGQ5VUB5.

PTM databases

PhosphoSiteQ5VUB5.

Polymorphism databases

DMDM74747078.

Proteomic databases

PRIDEQ5VUB5.

Protocols and materials databases

StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

EnsemblENST00000378116; ENSP00000367356; ENSG00000148468.
GeneID221061.
KEGGhsa:221061.
UCSCuc001iob.1. human.

Organism-specific databases

CTD221061.
GeneCardsGC10M015254.
HGNCHGNC:23522. FAM171A1.
neXtProtNX_Q5VUB5.
GenAtlasSearch...

Phylogenomic databases

GeneTreeENSGT00530000063318.
HOGENOMHBG715100.
HOVERGENHBG057508.
InParanoidQ5VUB5.
OMAVDHLERP.
OrthoDBEOG4VDPZ3.

Gene expression databases

ArrayExpressQ5VUB5.
BgeeQ5VUB5.
CleanExHS_FAM171A1.
GenevestigatorQ5VUB5.

Family and domain databases

InterProIPR018890. Uncharacterised_FAM171.
[Graphical view]
PfamPF10577. UPF0560. 1 hit.
[Graphical view]
ProtoNetSearch...

Other

NextBio91175.

Entry information

Entry nameF1711_HUMAN
AccessionPrimary (citable) accession number: Q5VUB5
Secondary accession number(s): D3DRT9, Q32M49, Q8N4I0
Entry history
Integrated into UniProtKB/Swiss-Prot: February 6, 2007
Last sequence update: December 7, 2004
Last modified: January 25, 2012
This is version 61 of the entry and version 1 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 10

Human chromosome 10: 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

SIMILARITY comments

Index of protein domains and families