FAM49A

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Family with sequence similarity 49, member A, also known as FAM49A, is a protein which in humans is encoded by the FAM49A gene.[5]

AliasesFAM49A, family with sequence similarity 49 member A
End16,666,331 bp[1]
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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
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Gene

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

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.[7]

References

Further reading

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