C17orf100 chromosome 17 open reading frame 100 [Homo sapiens (human)] - Gene

Summary

Official Symbol: C17orf100provided by HGNC
Official Full Name: chromosome 17 open reading frame 100provided by HGNC
Primary source: HGNC:HGNC:34494
See related: Ensembl:ENSG00000256806 AllianceGenome:HGNC:34494
Gene type: protein coding
RefSeq status: VALIDATED
Organism: Homo sapiens
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Orthologs: mouse all
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Genomic context

Location:: 17p13.1

Exon count:: 1

Annotation release	Status	Assembly	Chr	Location
RS_2024_08	current	GRCh38.p14 (GCF_000001405.40)	17	NC_000017.11 (6651762..6653476)
RS_2024_08	current	T2T-CHM13v2.0 (GCF_009914755.1)	17	NC_060941.1 (6552391..6554105)
RS_2024_09	previous assembly	GRCh37.p13 (GCF_000001405.25)	17	NC_000017.10 (6555082..6556795)

Chromosome 17 - NC_000017.11 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Genomic Sequence:

Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

What's a GeneRIF?

Submit: New GeneRIF Correction

Phenotypes

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Find tests for this gene in the NIH Genetic Testing Registry (GTR)

Review eQTL and phenotype association data in this region using PheGenI

Variation

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See Variation Viewer (GRCh37.p13)

General gene information

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Markers

G73120 (e-PCR)
- UniSTS:231387

MARC_7243-7244:996687682:1 (e-PCR)
- UniSTS:231387

ALOX15-A611G (e-PCR)
- UniSTS:240885

ALOX15-F4-R4 (e-PCR)
- UniSTS:240886

General protein information

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Preferred Names: uncharacterized protein C17orf100

Names: hCG1985469

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.