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Gene

TIMCC

TIM double twin CX3C motif chaperone

Summary

Cytogenetic location
2p13.3
Coordinates
Chromosome 2: 70,295,976–70,302,067 (GRCh38)
Exons
3 exons across 6.1 kb
Protein
245 amino acids
Also known as
FLJ14668
Previous symbols
FAM136A
MANE Select transcript
ENST00000430566.6NM_001329752.2
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 TIMCC yet. The test sequences your whole genome, so your data includes it all the same.

How TIMCC is laid out

  • Coding sequence
  • Untranslated region
  • Intron
  • Direction of transcription
  • Known disease-causing sites
  • Stretches short reads find hard
Chromosome 2, with a bracket where TIMCC sits. TIMCC and 15 genes near it on chromosome 2, from 69,799,022 to 70,799,021.Chromosome 22p13.3p25.3p25.2p25.1p24.3p24.2p24.1p23.3p23.2p23.1p22.3p22.2p22.1p21p16.3p16.2p16.1p15p14p13.3p13.2p13.1p12p11.2p11.1q11.1q11.2q12.1q12.2q12.3q13q14.1q14.2q14.3q21.1q21.2q21.3q22.1q22.2q22.3q23.1q23.2q23.3q24.1q24.2q24.3q31.1q31.2q31.3q32.1q32.2q32.3q33.1q33.2q33.3q34q35q36.1q36.2q36.3q37.1q37.2q37.369.8 Mb70 Mb70.2 Mb70.4 Mb70.6 MbANXA4: 69,643,109–69,827,121, forward strandANXA4GMCL1: 69,829,612–69,881,393, forward strandGMCL1: 69,829,739–69,829,798, forward strandSNRNP27: 69,893,944–69,907,658, forward strandSNRNP27MXD1: 69,897,688–69,942,945, forward strandMXD1ASPRV1: 69,960,089–69,961,631, reverse strandASPRV1: 69,960,104–70,087,320, reverse strandPCBP1: 70,087,477–70,089,203, forward strandPCBP1C2orf42: 70,149,882–70,248,615, reverse strandC2orf42TIA1: 70,209,444–70,248,761, reverse strandTIA1PCYOX1: 70,257,386–70,281,185, forward strandPCYOX1SNRPG: 70,281,204–70,293,766, reverse strandSNRPGTIMCC: 70,295,976–70,302,067, reverse strandTIMCCTGFA: 70,447,284–70,554,193, reverse strandTGFAADD2: 70,607,618–70,768,499, reverse strandADD2FIGLA: 70,777,310–70,790,643, reverse strandFIGLADiagram of TIMCC: 3 exons on the reverse strand of chromosome 2Exon 2: 1 known disease-causing siteExon 3: 70,295,976–70,297,477, 1,502 basesExon 2: 70,300,840–70,300,980, 141 basesExon 1: 70,301,604–70,302,067, 464 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 2.1 kb of the gene's 6.1 kb; 738 of those bases code for the protein.

How a genome test reads TIMCC

1

position in TIMCC 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 6.1 kb of TIMCC, introns included, not only the 2.1 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.
  • Data release 2026.10.16-c6eea6bf.

Cite this page

APA

Dante Labs. (n.d.). TIMCC gene: TIM double twin CX3C motif chaperone. Retrieved 17 October 2026, from https://dantelabs.com/genes/timcc

Vancouver

Dante Labs. TIMCC gene: TIM double twin CX3C motif chaperone [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/timcc

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