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SKINT1L Skint1 like (pseudogene) [ Homo sapiens (human) ]

Gene ID: 391037, updated on 23-Nov-2021

Summary

Official Symbol
SKINT1Lprovided by HGNC
Official Full Name
Skint1 like (pseudogene)provided by HGNC
Primary source
HGNC:HGNC:33993
See related
MIM:616392
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
BTN12; SKINT1; SKINTL; SKINTP
Expression
Low expression observed in reference dataset See more
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Genomic context

See SKINT1L in Genome Data Viewer
Location:
1p33
Exon count:
10
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 1 NC_000001.11 (48101715..48182428, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (48567387..48648100, complement)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene TraB domain containing 2B Neighboring gene Sharpr-MPRA regulatory region 2886 Neighboring gene long intergenic non-protein coding RNA 2794 Neighboring gene cytochrome P450 family 46 subfamily A member 4, pseudogene Neighboring gene solute carrier family 5 member 9 Neighboring gene spermatogenesis associated 6 Neighboring gene protein phosphatase 1 regulatory subunit 8 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

General gene information

Markers

Other Names

  • Skint-like, pseudogene

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_026749.2 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL109659, AL356289, BX118767, DN994130

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_000001.11 Reference GRCh38.p13 Primary Assembly

    Range
    48101715..48182428 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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