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FAM49A

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Protein-coding gene in the species Homo sapiens
FAM49A
Identifiers
AliasesFAM49A, family with sequence similarity 49 member A
External IDsMGI: 1261783; HomoloGene: 12657; GeneCards: FAM49A; OMA:FAM49A - orthologs
Gene location (Human)
Chromosome 2 (human)
Chr.Chromosome 2 (human)
Chromosome 2 (human)Genomic location for FAM49AGenomic location for FAM49A
Band2p24.2Start16,549,459 bp
End16,666,331 bp
Gene location (Mouse)
Chromosome 12 (mouse)
Chr.Chromosome 12 (mouse)
Chromosome 12 (mouse)Genomic location for FAM49AGenomic location for FAM49A
Band12 A1.1|12 5.63 cMStart12,312,140 bp
End12,430,966 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • Brodmann area 23

  • monocyte

  • middle temporal gyrus

  • superior frontal gyrus

  • prefrontal cortex

  • entorhinal cortex

  • dorsolateral prefrontal cortex

  • orbitofrontal cortex

  • primary visual cortex

  • lateral nuclear group of thalamus
Top expressed in
  • olfactory tubercle

  • piriform cortex

  • cingulate gyrus

  • primary motor cortex

  • subiculum

  • anterior amygdaloid area

  • visual cortex

  • subdivision of hippocampus

  • Region I of hippocampus proper

  • nucleus accumbens
More reference expression data
BioGPS


More reference expression data
Orthologs
SpeciesHumanMouse
Entrez

81553

76820

Ensembl

ENSG00000197872

ENSMUSG00000020589

UniProt

Q9H0Q0

Q8BHZ0

RefSeq (mRNA)

NM_030797

NM_001146119
NM_029758
NM_001364432

RefSeq (protein)

NP_110424

NP_001139591
NP_084034
NP_001351361

Location (UCSC)Chr 2: 16.55 – 16.67 MbChr 12: 12.31 – 12.43 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Family with sequence similarity 49, member A, also known as FAM49A, is a protein which in humans is encoded by the FAM49A gene.

Gene

Fam49A is located on human chromosome 2, at 2p24.3. It has 1512 base pairs in the reference sequence mRNA transcript.

Protein

The Fam49A gene product is a 323 amino acid protein. The protein contains two domains: Residues 15-319 comprise the "Domain of Unknown Function 1394" (DUF1394, Pfam PF07159). Residues 67->281 comprise the "Cytoplasmic Fragile X Interacting Superfamily" region.

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000197872Ensembl, May 2017
  2. ^ GRCm38: Ensembl release 89: ENSMUSG00000020589Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. "Entrez Gene: FAM49A family with sequence similarity 49, member A".
  6. "Nucleotide - family with sequence similarity 49, member A [Homo sapiens]". Nucleotide. National Center for Biotechnology Information, United States National Institutes of Health. Retrieved 2009-05-09.
  7. "Protein - family with sequence similarity 49, member A [Homo sapiens]". Protein. National Center for Biotechnology Information, United States National Institutes of Health. Retrieved 2009-05-09.

Further reading


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