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Gene

TNFRSF13C

TNF receptor superfamily member 13C

Summary

Cytogenetic location
22q13.2
Coordinates
Chromosome 22: 41,922,032–41,926,806 (GRCh38)
Exons
3 exons across 4.8 kb
Protein
184 amino acids
Also known as
BAFFR, CD268
MANE Select transcript
ENST00000291232.5NM_052945.4
Locus type
gene with protein product
  • Very high
  • Confident
  • Low
  • Very low

Reference genomeGRCh38

Positions on gene and variant pages follow this choice, in this browser.

Curated reports relevant to this gene

No Genome Test report reads TNFRSF13C yet. The test sequences your whole genome, so your data includes it all the same.

How TNFRSF13C is laid out

  • Coding sequence
  • Untranslated region
  • Intron
  • Direction of transcription
  • Known disease-causing sites
  • Stretches short reads find hard
Chromosome 22, with a bracket where TNFRSF13C sits. TNFRSF13C and 25 genes near it on chromosome 22, from 41,424,419 to 42,424,418.Chromosome 2222q13.2p13p12p11.2p11.1q11.1q11.21q11.22q11.23q12.1q12.2q12.3q13.1q13.2q13.31q13.32q13.3341.6 Mb41.8 Mb42 Mb42.2 Mb42.4 MbTOB2: 41,433,489–41,447,602, reverse strandTOB2ACO2: 41,447,830–41,529,273, forward strandACO2PHF5A: 41,448,895–41,468,713, reverse strandPHF5APOLR3H: 41,525,799–41,544,606, reverse strandPOLR3HCSDC2: 41,560,758–41,577,741, forward strandCSDC2PMM1: 41,576,886–41,595,275, reverse strandPMM1DESI1: 41,598,028–41,621,089, reverse strandDESI1XRCC6: 41,620,786–41,664,087, forward strandXRCC6SNU13: 41,666,627–41,690,504, reverse strandSNU13MEI1: 41,699,494–41,799,456, forward strandMEI1CCDC134: 41,800,321–41,832,178, forward strandCCDC134SREBF2: 41,833,029–41,907,308, forward strandSREBF2SHISA8: 41,906,316–41,915,129, reverse strandSHISA8TNFRSF13C: 41,922,032–41,926,806, reverse strandTNFRSF13CCENPM: 41,927,514–41,947,183, reverse strandCENPMSMIM45: 41,947,178–41,958,942, forward strandSMIM45SEPTIN3: 41,969,443–41,998,221, forward strandSEPTIN3WBP2NL: 41,998,725–42,058,456, forward strandWBP2NLNAGA: 42,032,595–42,071,198, reverse strandNAGAPHETA2: 42,073,789–42,079,439, forward strandPHETA2SMDT1: 42,079,564–42,090,033, forward strandSMDT1NDUFA6: 42,080,336–42,090,884, reverse strandCYP2D6: 42,120,962–42,131,727, reverse strandCYP2D6CYP2D7: 42,140,203–42,149,500, reverse strandCYP2D7TCF20: 42,160,013–42,343,616, reverse strandTCF20NFAM1: 42,380,407–42,432,425, reverse strandNFAM1Diagram of TNFRSF13C: 3 exons on the reverse strand of chromosome 22Exon 2: 1 known disease-causing siteExon 3: 41,922,032–41,925,554, 3,523 basesExon 2: 41,926,101–41,926,331, 231 basesExon 1: 41,926,638–41,926,806, 169 bases3215′3′

Exons of the gene's MANE Select transcript (release v1.5), from NCBI and EMBL-EBI, on the GRCh38 reference genome.

Chromosome bands from UCSC's GRCh38 ideogram (2022-10-29).

Nearby genes from Ensembl release 116, on GRCh38.

Exons make up 3.9 kb of the gene's 4.8 kb; 555 of those bases code for the protein.

How a genome test reads TNFRSF13C

1

position in TNFRSF13C where ClinVar classes a change as pathogenic or likely pathogenic

None of them falls in a region short reads find hard.

A whole genome covers all 4.8 kb of TNFRSF13C, introns included, not only the 3.9 kb of exons.

Where this comes from

  • HGNC: the gene's symbol, name, other symbols and location.
  • MANE Select v1.5, from NCBI and EMBL-EBI: the transcript, its exons and coding sequence.
  • ClinVar and the GIAB stratifications: known disease-causing sites, and the regions short reads find hard.
  • The Human Phenotype Ontology, release 2026-09-01: the traits linked to the gene. Find out more at hpo.jax.org.
  • Data release 2026.10.16-c6eea6bf.

Cite this page

APA

Dante Labs. (n.d.). TNFRSF13C gene: TNF receptor superfamily member 13C. Retrieved 16 October 2026, from https://dantelabs.com/genes/tnfrsf13c

Vancouver

Dante Labs. TNFRSF13C gene: TNF receptor superfamily member 13C [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/tnfrsf13c

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