Human Gene FAM71A (uc001hjk.3)
  Description: Homo sapiens family with sequence similarity 71, member A (FAM71A), mRNA.
RefSeq Summary (NM_153606): This gene encodes a protein that interacts with the Rab2B small GTPase and may be important for integrity of the Golgi body. A knockdown of this gene induces fragmentation of the Golgi, similar to the effect seen with a knockdown of the Rab2B small GTPase. The encoded protein has an N-terminal Rab-binding domain specific for Rab2B. [provided by RefSeq, Feb 2017].
Transcript (Including UTRs)
   Position: hg19 chr1:212,797,789-212,800,120 Size: 2,332 Total Exon Count: 1 Strand: +
Coding Region
   Position: hg19 chr1:212,798,220-212,800,004 Size: 1,785 Coding Exon Count: 1 

Page IndexSequence and LinksUniProtKB CommentsPrimersCTDGene Alleles
RNA-Seq ExpressionMicroarray ExpressionRNA StructureProtein StructureOther SpeciesGO Annotations
mRNA DescriptionsOther NamesModel InformationMethods
Data last updated at UCSC: 2013-06-14

-  Sequence and Links to Tools and Databases
 
Genomic Sequence (chr1:212,797,789-212,800,120)mRNA (may differ from genome)Protein (594 aa)
Gene SorterGenome BrowserOther Species FASTATable SchemaAlphaFoldBioGPS
EnsemblEntrez GeneExonPrimerGeneCardsGeneNetworkH-INV
HGNCHPRDLynxMGIneXtProtPubMed
TreefamUniProtKBBioGrid CRISPR DB

-  Comments and Description Text from UniProtKB
  ID: FA71A_HUMAN
DESCRIPTION: RecName: Full=Protein FAM71A;
SIMILARITY: Belongs to the FAM71 family.

-  Primer design for this transcript
 

Primer3Plus can design qPCR Primers that straddle exon-exon-junctions, which amplify only cDNA, not genomic DNA.
Click here to load the transcript sequence and exon structure into Primer3Plus

Exonprimer can design one pair of Sanger sequencing primers around every exon, located in non-genic sequence.
Click here to open Exonprimer with this transcript

To design primers for a non-coding sequence, zoom to a region of interest and select from the drop-down menu: View > In External Tools > Primer3


-  Comparative Toxicogenomics Database (CTD)
  The following chemicals interact with this gene

+  Common Gene Haplotype Alleles
  Press "+" in the title bar above to open this section.

-  RNA-Seq Expression Data from GTEx (53 Tissues, 570 Donors)
  Highest median expression: 91.90 RPKM in Testis
Total median expression: 93.38 RPKM



View in GTEx track of Genome Browser    View at GTEx portal     View GTEx Body Map

+  Microarray Expression Data
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-  mRNA Secondary Structure of 3' and 5' UTRs
 
RegionFold EnergyBasesEnergy/Base
Display As
5' UTR -193.50431-0.449 Picture PostScript Text
3' UTR -30.20116-0.260 Picture PostScript Text

The RNAfold program from the Vienna RNA Package is used to perform the secondary structure predictions and folding calculations. The estimated folding energy is in kcal/mol. The more negative the energy, the more secondary structure the RNA is likely to have.

-  Protein Domain and Structure Information
  InterPro Domains: Graphical view of domain structure
IPR022168 - DUF3699

Pfam Domains:
PF12480 - Protein of unknown function (DUF3699)

ModBase Predicted Comparative 3D Structure on Q8IYT1
FrontTopSide
The pictures above may be empty if there is no ModBase structure for the protein. The ModBase structure frequently covers just a fragment of the protein. You may be asked to log onto ModBase the first time you click on the pictures. It is simplest after logging in to just click on the picture again to get to the specific info on that model.

-  Orthologous Genes in Other Species
  Orthologies between human, mouse, and rat are computed by taking the best BLASTP hit, and filtering out non-syntenic hits. For more distant species reciprocal-best BLASTP hits are used. Note that the absence of an ortholog in the table below may reflect incomplete annotations in the other species rather than a true absence of the orthologous gene.
MouseRatZebrafishD. melanogasterC. elegansS. cerevisiae
No orthologNo orthologNo orthologNo orthologNo orthologNo ortholog
Gene Details     
Gene Sorter     
      
      
      

-  Gene Ontology (GO) Annotations with Structured Vocabulary
  Cellular Component:
GO:0005634 nucleus


-  Descriptions from all associated GenBank mRNAs
  AK301981 - Homo sapiens cDNA FLJ51372 complete cds.
BC035007 - Homo sapiens family with sequence similarity 71, member A, mRNA (cDNA clone MGC:33363 IMAGE:5267155), complete cds.
HM005622 - Homo sapiens clone HTL-S-209a testis secretory sperm-binding protein Li 209a mRNA, complete cds.
JD227905 - Sequence 208929 from Patent EP1572962.
JD051945 - Sequence 32969 from Patent EP1572962.
JD302757 - Sequence 283781 from Patent EP1572962.
JD084517 - Sequence 65541 from Patent EP1572962.
JD369888 - Sequence 350912 from Patent EP1572962.
JD142507 - Sequence 123531 from Patent EP1572962.
JD425108 - Sequence 406132 from Patent EP1572962.
JD185052 - Sequence 166076 from Patent EP1572962.
JD347205 - Sequence 328229 from Patent EP1572962.
JD328843 - Sequence 309867 from Patent EP1572962.
AK315021 - Homo sapiens cDNA, FLJ95956.
JD043198 - Sequence 24222 from Patent EP1572962.
AK057358 - Homo sapiens cDNA FLJ32796 fis, clone TESTI2002465, weakly similar to FIBROIN HEAVY CHAIN PRECURSOR.
JD173046 - Sequence 154070 from Patent EP1572962.
CU690020 - Synthetic construct Homo sapiens gateway clone IMAGE:100018370 5' read FAM71A mRNA.
KJ900270 - Synthetic construct Homo sapiens clone ccsbBroadEn_09664 FAM71A gene, encodes complete protein.
DQ596692 - Homo sapiens piRNA piR-34758, complete sequence.
JD065320 - Sequence 46344 from Patent EP1572962.

-  Other Names for This Gene
  Alternate Gene Symbols: FA71A_HUMAN, NM_153606, NP_705834, Q5VTZ1, Q8IYT1
UCSC ID: uc001hjk.3
RefSeq Accession: NM_153606
Protein: Q8IYT1 (aka FA71A_HUMAN)
CCDS: CCDS1507.1

-  Gene Model Information
 
category: coding nonsense-mediated-decay: no RNA accession: NM_153606.3
exon count: 1CDS single in 3' UTR: no RNA size: 2332
ORF size: 1785CDS single in intron: no Alignment % ID: 100.00
txCdsPredict score: 3749.00frame shift in genome: no % Coverage: 100.00
has start codon: yes stop codon in genome: no # of Alignments: 1
has end codon: yes retained intron: no # AT/AC introns 0
selenocysteine: no end bleed into intron: 0# strange splices: 0
Click here for a detailed description of the fields of the table above.

-  Methods, Credits, and Use Restrictions
  Click here for details on how this gene model was made and data restrictions if any.