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Q8IVM7 (CM029_HUMAN) Reviewed, UniProtKB/Swiss-Prot

Last modified January 25, 2012. Version 38. Feed History...

Clusters with 100%, 90%, 50% identity | Documents (3) | 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:
Putative uncharacterized protein encoded by LINC00346
Gene names
Name:LINC00346
Synonyms:C13orf29
OrganismHomo sapiens (Human)
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length164 AA.
Sequence statusComplete.
Protein existenceUncertain

General annotation (Comments)

Caution

Product of a dubious CDS prediction. May be a non-coding RNA.

Ontologies

Keywords
   Coding sequence diversityPolymorphism
   Technical termComplete proteome
Reference proteome
Gene Ontology (GO)
None. [Check GOA]

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Chain1 – 164164Putative uncharacterized protein encoded by LINC00346
PRO_0000263715

Natural variations

Natural variant1541R → Q.
Corresponds to variant rs9588286 [ dbSNP | Ensembl ].
VAR_029613

Sequences

Sequence LengthMass (Da)Tools
Q8IVM7 [UniParc].

Last modified March 1, 2003. Version 1.
Checksum: 57C77BFB80F4E60B

FASTA16418,094
        10         20         30         40         50         60 
MRPQPRGGSG RKENTGEERE GRAERYHAIS ADGERRLQPG TAVLTRHVSF LFGGREAEEH 

        70         80         90        100        110        120 
VMETDRVEGA RDGDKRKEVC FVPIQGSFCF MRLTCARLVA ALDIHGLSFS LRFCGSRDTK 

       130        140        150        160 
HEDITGREGQ VTPLPRGTPQ LCTARVGLSS PRTRGQGVPI SCKT 

« Hide

References

[1]"Full length sequencing of some human and murine muscular transcripts (Telethon Italy project B41)."
Ievolella C., Zara I., Millino C., Faulkner G., Lanfranchi G.
Submitted (JAN-2003) to the EMBL/GenBank/DDBJ databases
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA].
Tissue: Skeletal muscle.
[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.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
AJ295981 mRNA. Translation: CAC82494.1.
BC093904 mRNA. Translation: AAH93904.1.
BC104998 mRNA. Translation: AAI04999.1.
IPIIPI00217066.
UniGeneHs.245390.

3D structure databases

ModBaseSearch...

Proteomic databases

PRIDEQ8IVM7.

Protocols and materials databases

StructuralBiologyKnowledgebaseSearch...

Organism-specific databases

GeneCardsGC13M111516.
HGNCHGNC:27492. LINC00346.
neXtProtNX_Q8IVM7.
GenAtlasSearch...

Phylogenomic databases

OMAEEHVMET.

Gene expression databases

BgeeQ8IVM7.
CleanExHS_C13orf29.
GenevestigatorQ8IVM7.

Family and domain databases

ProtoNetSearch...

Entry information

Entry nameCM029_HUMAN
AccessionPrimary (citable) accession number: Q8IVM7
Entry history
Integrated into UniProtKB/Swiss-Prot: December 12, 2006
Last sequence update: March 1, 2003
Last modified: January 25, 2012
This is version 38 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 13

Human chromosome 13: 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