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NTF6B neurotrophin 6 beta (pseudogene) [ Homo sapiens (human) ]

Gene ID: 4911, updated on 10-Oct-2023

Summary

Official Symbol
NTF6Bprovided by HGNC
Official Full Name
neurotrophin 6 beta (pseudogene)provided by HGNC
Primary source
HGNC:HGNC:8026
See related
AllianceGenome:HGNC:8026
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

Location:
19q13.33
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 19 NC_000019.10 (49038222..49039126, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 19 NC_060943.1 (52033007..52033911, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 19 NC_000019.9 (49541479..49542383, complement)

Chromosome 19 - NC_000019.10Genomic Context describing neighboring genes Neighboring gene chorionic gonadotropin subunit beta 1 Neighboring gene small NF90 (ILF3) associated RNA G1 Neighboring gene neurotrophin 4 pseudogene Neighboring gene H3K4me1 hESC enhancer GRCh37_chr19:49546442-49546951 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr19:49546952-49547460 Neighboring gene chorionic gonadotropin subunit beta 5

Genomic regions, transcripts, and products

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.

Genomic

  1. NG_029363.2 

    Range
    101..1005
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000019.10 Reference GRCh38.p14 Primary Assembly

    Range
    49038222..49039126 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060943.1 Alternate T2T-CHM13v2.0

    Range
    52033007..52033911 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_021085.1: Suppressed sequence

    Description
    NM_021085.1: This RefSeq record was removed by NCBI staff. Contact info@ncbi.nlm.nih.gov for further information.