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FAM95B1 family with sequence similarity 95 member B1 [ Homo sapiens (human) ]

Gene ID: 100133036, updated on 25-Oct-2022

Summary

Official Symbol
FAM95B1provided by HGNC
Official Full Name
family with sequence similarity 95 member B1provided by HGNC
Primary source
HGNC:HGNC:32318
See related
Ensembl:ENSG00000290718 AllianceGenome:HGNC:32318
Gene type
ncRNA
RefSeq status
PREDICTED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Expression
Biased expression in testis (RPKM 17.6), spleen (RPKM 1.7) and 3 other tissues See more
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Genomic context

See FAM95B1 in Genome Data Viewer
Location:
9p11.2
Exon count:
5
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 9 NC_000009.12 (40323571..40329220)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 9 NC_060933.1 (40338481..40344130)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (42468589..42474238)

Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene ankyrin repeat domain 20 family member A2, pseudogene Neighboring gene RNA, U6 small nuclear 1269, pseudogene Neighboring gene sorting nexin 18 pseudogene 8 Neighboring gene zinc finger protein 114 pseudogene Neighboring gene calponin 2 pseudogene 2

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

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_026759.1 RNA Sequence

    Status: PREDICTED

    Source sequence(s)
    BX664727
    Related
    ENST00000592053.5

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000009.12 Reference GRCh38.p14 Primary Assembly

    Range
    40323571..40329220
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060933.1 Alternate T2T-CHM13v2.0

    Range
    40338481..40344130
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)