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Q9BR10 (SPT25_HUMAN) Reviewed, UniProtKB/Swiss-Prot

Last modified January 25, 2012. Version 71. 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:
Spermatogenesis-associated protein 25
Alternative name(s):
Testis-specific gene 23 protein
Gene names
Name:SPATA25
Synonyms:C20orf165, TSG23
OrganismHomo sapiens (Human)
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length227 AA.
Sequence statusComplete.
Protein existenceEvidence at protein level

General annotation (Comments)

Function

May play a role in spermatogenesis.

Subcellular location

Membrane; Single-pass membrane protein Potential.

Tissue specificity

Expressed predominantly in testis (at protein level). Expression is lower in patients with obstructive azoospermia than in fertile controls and is not detected in patients with non-obstructive azoospermia.

Developmental stage

60-fold stronger expression found in adult than fetal testis. Detected in spermatocytes and round spermatids of the seminiferous tubule.

Sequence similarities

Belongs to the SPATA25 family.

Ontologies

Keywords
   Biological processDifferentiation
Spermatogenesis
   Cellular componentMembrane
   Coding sequence diversityPolymorphism
   DomainTransmembrane
Transmembrane helix
   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

Chain1 – 227227Spermatogenesis-associated protein 25
PRO_0000079478

Regions

Transmembrane152 – 17221Helical; Potential

Natural variations

Natural variant941P → L.
Corresponds to variant rs3827040 [ dbSNP | Ensembl ].
VAR_015146

Sequences

Sequence LengthMass (Da)Tools
Q9BR10 [UniParc].

Last modified June 1, 2001. Version 1.
Checksum: 938556AB1005C218

FASTA22723,834
        10         20         30         40         50         60 
MSYFRTPQTH PGPLPSGQGG AASPGLSLGL CSPVEPVVVA SGGTGPLSQK AEQVAPAAQA 

        70         80         90        100        110        120 
WGPALAMPQA RGCPGGTSWE TLRKEYSRNC HKFPHVRQLE SLGWDNGYSR SRAPDLGGPS 

       130        140        150        160        170        180 
RPRPLMLCGL SPRVLPVPSE AVGKEASSQP DICILTLAMM IAGIPTVPVP GVREEDLIWA 

       190        200        210        220 
AQAFMMAHPE PEGAVEGARW EQAHAHTASG KMPLVRSKRG QPPGSCL 

« Hide

References

« Hide 'large scale' references
[1]"The DNA sequence and comparative analysis of human chromosome 20."
Deloukas P., Matthews L.H., Ashurst J.L., Burton J., Gilbert J.G.R., Jones M., Stavrides G., Almeida J.P., Babbage A.K., Bagguley C.L., Bailey J., Barlow K.F., Bates K.N., Beard L.M., Beare D.M., Beasley O.P., Bird C.P., Blakey S.E. expand/collapse author list , Bridgeman A.M., Brown A.J., Buck D., Burrill W.D., Butler A.P., Carder C., Carter N.P., Chapman J.C., Clamp M., Clark G., Clark L.N., Clark S.Y., Clee C.M., Clegg S., Cobley V.E., Collier R.E., Connor R.E., Corby N.R., Coulson A., Coville G.J., Deadman R., Dhami P.D., Dunn M., Ellington A.G., Frankland J.A., Fraser A., French L., Garner P., Grafham D.V., Griffiths C., Griffiths M.N.D., Gwilliam R., Hall R.E., Hammond S., Harley J.L., Heath P.D., Ho S., Holden J.L., Howden P.J., Huckle E., Hunt A.R., Hunt S.E., Jekosch K., Johnson C.M., Johnson D., Kay M.P., Kimberley A.M., King A., Knights A., Laird G.K., Lawlor S., Lehvaeslaiho M.H., Leversha M.A., Lloyd C., Lloyd D.M., Lovell J.D., Marsh V.L., Martin S.L., McConnachie L.J., McLay K., McMurray A.A., Milne S.A., Mistry D., Moore M.J.F., Mullikin J.C., Nickerson T., Oliver K., Parker A., Patel R., Pearce T.A.V., Peck A.I., Phillimore B.J.C.T., Prathalingam S.R., Plumb R.W., Ramsay H., Rice C.M., Ross M.T., Scott C.E., Sehra H.K., Shownkeen R., Sims S., Skuce C.D., Smith M.L., Soderlund C., Steward C.A., Sulston J.E., Swann R.M., Sycamore N., Taylor R., Tee L., Thomas D.W., Thorpe A., Tracey A., Tromans A.C., Vaudin M., Wall M., Wallis J.M., Whitehead S.L., Whittaker P., Willey D.L., Williams L., Williams S.A., Wilming L., Wray P.W., Hubbard T., Durbin R.M., Bentley D.R., Beck S., Rogers J.
Nature 414:865-871(2001) [PubMed: 11780052] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
[2]"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].
Tissue: Brain.
[3]"Developmental expression pattern of a novel gene, TSG23/Tsg23, suggests a role in spermatogenesis."
Zhou Y., Qin D., Tang A., Zhou D., Qin J., Yan B., Diao R., Jiang Z., Cai Z., Gui Y.
Mol. Hum. Reprod. 15:223-230(2009) [PubMed: 19240080] [Abstract]
Cited for: FUNCTION, TISSUE SPECIFICITY, DEVELOPMENTAL STAGE.
+Additional computationally mapped references.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
AL008726 Genomic DNA. Translation: CAC36017.1.
BC039607 mRNA. Translation: AAH39607.1.
IPIIPI00028648.
RefSeqNP_542175.1. NM_080608.3.
UniGeneHs.128235.

3D structure databases

ProteinModelPortalQ9BR10.
ModBaseSearch...

Polymorphism databases

DMDM27805437.

Proteomic databases

PRIDEQ9BR10.

Protocols and materials databases

StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

EnsemblENST00000372519; ENSP00000361597; ENSG00000149634.
GeneID128497.
KEGGhsa:128497.
UCSCuc002xqf.1. human.

Organism-specific databases

CTD128497.
GeneCardsGC20M044515.
HGNCHGNC:16158. SPATA25.
HPACAB034457.
neXtProtNX_Q9BR10.
PharmGKBPA25707.
GenAtlasSearch...

Phylogenomic databases

eggNOGprNOG06376.
GeneTreeENSGT00390000018626.
HOGENOMHBG126076.
HOVERGENHBG051206.
InParanoidQ9BR10.
OMAQPPGSCL.
OrthoDBEOG4X97JB.
PhylomeDBQ9BR10.

Gene expression databases

ArrayExpressQ9BR10.
BgeeQ9BR10.
CleanExHS_C20orf165.
GenevestigatorQ9BR10.
GermOnlineENSG00000149634. Homo sapiens.

Family and domain databases

ProtoNetSearch...

Other

NextBio82372.

Entry information

Entry nameSPT25_HUMAN
AccessionPrimary (citable) accession number: Q9BR10
Entry history
Integrated into UniProtKB/Swiss-Prot: January 17, 2003
Last sequence update: June 1, 2001
Last modified: January 25, 2012
This is version 71 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 20

Human chromosome 20: 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