Jump to content

FAM49A

From Wikipedia, the free encyclopedia
(Redirected from FAM49A (gene))
FAM49A
Identifiers
AliasesFAM49A, family with sequence similarity 49 member A
External IDsMGI: 1261783; HomoloGene: 12657; GeneCards: FAM49A; OMA:FAM49A - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
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[3][4]
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.[5]

Gene

[edit]

Fam49A is located on human chromosome 2, at 2p24.3. It has 1512 base pairs in the reference sequence mRNA transcript.[6]

Protein

[edit]

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.[7]

References

[edit]
  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000197872Ensembl, May 2017
  2. ^ a b c 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

[edit]