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MFSD14C major facilitator superfamily domain containing 14C [ Homo sapiens (human) ]

Gene ID: 84278, updated on 5-Jan-2022

Summary

Official Symbol
MFSD14Cprovided by HGNC
Official Full Name
major facilitator superfamily domain containing 14Cprovided by HGNC
Primary source
HGNC:HGNC:23672
See related
Ensembl:ENSG00000196312
Gene type
pseudo
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
HIATL2
Summary
Predicted to enable transmembrane transporter activity. Predicted to be involved in transmembrane transport. Predicted to be integral component of membrane. [provided by Alliance of Genome Resources, Nov 2021]
Expression
Ubiquitous expression in brain (RPKM 4.9), testis (RPKM 4.7) and 25 other tissues See more
Orthologs
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Genomic context

See MFSD14C in Genome Data Viewer
Location:
9q22.33
Exon count:
6
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 9 NC_000009.12 (96942913..97013605, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (99705195..99775887, complement)

Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene proline-rich nuclear receptor coactivator 2-like Neighboring gene prothymosin alpha pseudogene 11 Neighboring gene NUT family member 2G Neighboring gene yrdC N(6)-threonylcarbamoyltransferase domain containing pseudogene 2 Neighboring gene cathepsin V Neighboring gene transcription elongation factor A1 pseudogene 1

Genomic regions, transcripts, and products

Expression

  • Project title: HPA RNA-seq normal tissues
  • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
  • BioProject: PRJEB4337
  • Publication: PMID 24309898
  • Analysis date: Wed Apr 4 07:08:55 2018

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Markers

Homology

Other Names

  • hippocampus abundant gene transcript-like 2
  • hippocampus abundant transcript-like protein 2

Clone Names

  • FLJ45467, MGC12945

Gene Ontology Provided by GOA

Function Evidence Code Pubs
enables protein binding IPI
Inferred from Physical Interaction
more info
PubMed 
enables transmembrane transporter activity IEA
Inferred from Electronic Annotation
more info
 
Process Evidence Code Pubs
involved_in transmembrane transport IEA
Inferred from Electronic Annotation
more info
 
Component Evidence Code Pubs
located_in integral component of membrane IEA
Inferred from Electronic Annotation
more info
 

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.

RNA

  1. NR_172874.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL158827, AL445670
    Related
    ENST00000652726.1
  2. NR_172875.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL158827, AL445670
  3. NR_172876.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL158827, AL445670
    Related
    ENST00000637864.1

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000009.12 Reference GRCh38.p13 Primary Assembly

    Range
    96942913..97013605 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_001355228.2: Suppressed sequence

    Description
    NM_001355228.2: This RefSeq was removed because it is now thought that this gene is a pseudogene.
  2. NM_001355229.2: Suppressed sequence

    Description
    NM_001355229.2: This RefSeq was removed because it is now thought that this gene is a pseudogene.
  3. NM_001355230.2: Suppressed sequence

    Description
    NM_001355230.2: This RefSeq was removed because it is now thought that this gene is a pseudogene.
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