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FAM22C family with sequence similarity 22, member C [ Homo sapiens (human) ]

Gene ID: 727807, discontinued on 25-Aug-2009
  • This record has been withdrawn by HGNC, and the sequence is not represented in the GRCh37.1 reference assembly.

Summary

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Official Symbol
FAM22Cprovided by HGNC
Official Full Name
family with sequence similarity 22, member Cprovided by HGNC
Primary source
HGNC:HGNC:23446
Gene type
protein coding
RefSeq status
WITHDRAWN
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Summary
DISCONTINUED: This record has been withdrawn by HGNC, and the sequence is not represented in the GRCh37.1 reference assembly.
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Genomic context

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Location:
10q22.3
Exon count:
7
Sequence:
Chromosome: 10; NC_000010.9 (81451610..81462705)

Genomic regions, transcripts, and products

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Genomic Sequence:
NC_000010.9 chromosome

Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

General protein information

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Names
family with sequence similarity 22, member C

NCBI Reference Sequences (RefSeq)

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RefSeqs of Annotated Genomes: Build 36.3 (NOTE: not current)

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference assembly

Genomic

  1. NC_000010.9 Reference assembly

    Range
    81451610..81462705
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. XM_001125950.1 → XP_001125950.2  

Nucleotide Protein
Heading Accession and Version