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FAM181B family with sequence similarity 181 member B [ Homo sapiens (human) ]

Gene ID: 220382, updated on 23-Nov-2021

Summary

Official Symbol
FAM181Bprovided by HGNC
Official Full Name
family with sequence similarity 181 member Bprovided by HGNC
Primary source
HGNC:HGNC:28512
See related
Ensembl:ENSG00000182103
Gene type
protein coding
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Orthologs
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Genomic context

See FAM181B in Genome Data Viewer
Location:
11q14.1
Exon count:
1
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 11 NC_000011.10 (82729940..82733864, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 11 NC_000011.9 (82440982..82444906, complement)

Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene Sharpr-MPRA regulatory region 11396 Neighboring gene ribosomal protein S28 pseudogene 7 Neighboring gene long intergenic non-protein coding RNA 2734 Neighboring gene RBMX pseudogene 3 Neighboring gene prolylcarboxypeptidase Neighboring gene eukaryotic translation initiation factor 2 subunit 2 beta pseudogene 6

Genomic regions, transcripts, and products

General gene information

Markers

Homology

Clone Names

  • MGC33846

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.

mRNA and Protein(s)

  1. NM_175885.4NP_787081.2  protein FAM181B

    See identical proteins and their annotated locations for NP_787081.2

    Status: VALIDATED

    Source sequence(s)
    AP002796, BC039262, BE857184, BE858471
    Consensus CDS
    CCDS31648.1
    UniProtKB/Swiss-Prot
    A6NEQ2
    Related
    ENSP00000365295.2, ENST00000329203.5
    Conserved Domains (1) summary
    pfam15238
    Location:63235
    FAM181; FAM181

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_000011.10 Reference GRCh38.p13 Primary Assembly

    Range
    82729940..82733864 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_175891.2: Suppressed sequence

    Description
    NM_175891.2: This RefSeq record was removed by NCBI staff. Contact info@ncbi.nlm.nih.gov for further information.
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