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SNX29P2 sorting nexin 29 pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 440352, updated on 1-Jun-2020

Summary

Official Symbol
SNX29P2provided by HGNC
Official Full Name
sorting nexin 29 pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:31914
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
RUNDC2C
Expression
Biased expression in lymph node (RPKM 18.9), ovary (RPKM 5.9) and 8 other tissues See more

Genomic context

See SNX29P2 in Genome Data Viewer
Location:
16p11.2
Exon count:
9
Annotation release Status Assembly Chr Location
109.20200522 current GRCh38.p13 (GCF_000001405.39) 16 NC_000016.10 (29302287..29365059)
105 previous assembly GRCh37.p13 (GCF_000001405.25) 16 NC_000016.9 (29313608..29376380)

Chromosome 16 - NC_000016.10Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC102723708 Neighboring gene uncharacterized LOC105371159 Neighboring gene translation initiation factor IF-2-like Neighboring gene nuclear pore complex interacting protein family member B11 Neighboring gene BOLA2-SMG1P6 readthrough Neighboring gene SMG1 pseudogene 6

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

General gene information

Markers

Other Names

  • RUN domain containing 2C

Clone Names

  • MGC52410

NCBI Reference Sequences (RefSeq)

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_002939.3 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC025279, BC024293, BX648280

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000016.10 Reference GRCh38.p13 Primary Assembly

    Range
    29302287..29365059
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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