FAM135B

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

FAM135B

FAM135B is a human gene coding for a protein of unknown function.[5] It is well conserved in primates, rodents, zebra fish. It has one paralog, FAM135A.

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FAM135B
Identifiers
AliasesFAM135B, C8ORFK32, family with sequence similarity 135 member B
External IDsMGI: 1917613; HomoloGene: 66605; GeneCards: FAM135B; OMA:FAM135B - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_015912
NM_001362965

NM_177819

RefSeq (protein)

NP_056996
NP_001349894

NP_808487

Location (UCSC)Chr 8: 138.13 – 138.5 MbChr 15: 71.3 – 71.6 Mb
PubMed search[3][4]
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Gene

FAM135B is located on the long arm of Chromosome 8 in humans on the anti-sense located at 24.23.[5] The following genes are near FAM135B on the chromosome:

  • COL22A1: Collagen producing gene that is a cell adhesion ligand for skin epithelial cells and fibroblast
  • FLJ45972: Gene function is unknown
  • KCNK9: Gene that encodes for a two pore potassium channel

Expression

FAM135B is expressed in the brain, ear, eye, pancreas and testis.[6] Within the brain, expression is apparent within the motor nucleus of trigeminal[7] In addition, it is mainly expressed in normal health states, although it has shown moderate expression in glioma, non-neoplasima as well as expression in germ cell tumors.[6]

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Interactions

FAM135B has shown to interact with KAT5, a gene that encodes for a histone acetyltransferase[8] through yeast two-hybrid experimentation.

Protein

The protein encoded on FAM135 is 1406 amino acids long. The protein contains a region called DUF676, believed to be a putative serine esterase as well as two protein regions called DUF3657.[5]

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Graphical representation of protein FAM135B

Clinical significance

FAM135B has shown to be expressed in individuals with extrapulmonary tuberculosis.[9]

References

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