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VTI1BP2 vesicle transport through interaction with t-SNAREs 1B pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 389246, updated on 17-Sep-2024

Summary

Official Symbol
VTI1BP2provided by HGNC
Official Full Name
vesicle transport through interaction with t-SNAREs 1B pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:43728
See related
AllianceGenome:HGNC:43728
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

See VTI1BP2 in Genome Data Viewer
Location:
4q35.1
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 4 NC_000004.12 (183483350..183484428)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 4 NC_060928.1 (186826146..186827224)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 4 NC_000004.11 (184404503..184405581)

Chromosome 4 - NC_000004.12Genomic Context describing neighboring genes Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 15827 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 22184 Neighboring gene CDKN2A interacting protein Neighboring gene uncharacterized LOC124900823 Neighboring gene H3K27ac hESC enhancer GRCh37_chr4:184403604-184404104 Neighboring gene H3K27ac hESC enhancer GRCh37_chr4:184404105-184404605 Neighboring gene ING2 divergent transcript Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 15828 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 15829 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 15830 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr4:184430298-184430798 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr4:184430799-184431299 Neighboring gene inhibitor of growth family member 2

Genomic regions, transcripts, and products

General gene information

Other Names

  • VTI1B pseudogene
  • vesicle transport through interaction with t-SNAREs homolog 1B pseudogene 2

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_005181.4 

    Range
    101..1179
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000004.12 Reference GRCh38.p14 Primary Assembly

    Range
    183483350..183484428
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    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060928.1 Alternate T2T-CHM13v2.0

    Range
    186826146..186827224
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    GenBank, FASTA, Sequence Viewer (Graphics)