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RHBDD2 rhomboid domain containing 2 [ Homo sapiens (human) ]

Gene ID: 57414, updated on 22-Sep-2022

Summary

Official Symbol
RHBDD2provided by HGNC
Official Full Name
rhomboid domain containing 2provided by HGNC
Primary source
HGNC:HGNC:23082
See related
Ensembl:ENSG00000005486 MIM:615203; AllianceGenome:HGNC:23082
Gene type
protein coding
RefSeq status
REVIEWED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
NPD007; RHBDL7
Summary
The protein encoded by this gene is a member of the rhomboid family of membrane-bound proteases and is overexpressed in some breast cancers. Members of this family are involved in intramembrane proteolysis. In mouse, the orthologous protein associates with the Golgi body. [provided by RefSeq, Sep 2016]
Expression
Ubiquitous expression in brain (RPKM 72.8), adrenal (RPKM 57.9) and 25 other tissues See more
Orthologs
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Genomic context

See RHBDD2 in Genome Data Viewer
Location:
7q11.23
Exon count:
6
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 7 NC_000007.14 (75879034..75888926)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 7 NC_060931.1 (77166165..77176057)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 7 NC_000007.13 (75508352..75518244)

Chromosome 7 - NC_000007.14Genomic Context describing neighboring genes Neighboring gene THO complex 4 pseudogene Neighboring gene Sharpr-MPRA regulatory region 1050 Neighboring gene uncharacterized LOC124901680 Neighboring gene microRNA 4651 Neighboring gene cytochrome p450 oxidoreductase

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

Bibliography

GeneRIFs: Gene References Into Functions

What's a GeneRIF?

Pathways from PubChem

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Markers

Homology

Gene Ontology Provided by GOA

Function Evidence Code Pubs
enables misfolded protein binding IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
enables serine-type endopeptidase activity IEA
Inferred from Electronic Annotation
more info
 
enables ubiquitin-specific protease binding IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
Process Evidence Code Pubs
involved_in endoplasmic reticulum unfolded protein response IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
involved_in ubiquitin-dependent ERAD pathway IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
Component Evidence Code Pubs
located_in Golgi apparatus IDA
Inferred from Direct Assay
more info
 
located_in Golgi membrane IEA
Inferred from Electronic Annotation
more info
 
part_of Hrd1p ubiquitin ligase ERAD-L complex IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
is_active_in endoplasmic reticulum membrane IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
located_in nucleoplasm IDA
Inferred from Direct Assay
more info
 
located_in perinuclear region of cytoplasm IEA
Inferred from Electronic Annotation
more info
 

General protein information

Preferred Names
rhomboid domain-containing protein 2
Names
rhomboid, veinlet-like 7

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_051655.2 RefSeqGene

    Range
    5002..14894
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. NM_001040456.3NP_001035546.1  rhomboid domain-containing protein 2 isoform a

    See identical proteins and their annotated locations for NP_001035546.1

    Status: REVIEWED

    Description
    Transcript Variant: This variant (1) encodes the longest isoform (a).
    Source sequence(s)
    AC005067
    Consensus CDS
    CCDS43602.1
    UniProtKB/Swiss-Prot
    Q6NTF9, Q9UDT2
    Related
    ENSP00000006777.6, ENST00000006777.11
    Conserved Domains (2) summary
    pfam01694
    Location:54205
    Rhomboid; Rhomboid family
    pfam06583
    Location:242341
    Neogenin_C; Neogenin C-terminus
  2. NM_001040457.3NP_001035547.1  rhomboid domain-containing protein 2 isoform b

    See identical proteins and their annotated locations for NP_001035547.1

    Status: REVIEWED

    Description
    Transcript Variant: This variant (2) has an alternate exon in the 5' end compared to variant 1. This difference causes translation initiation at a downstream AUG and results in an isoform (b) with a shorter N-terminus, compared to isoform a. Variants 2-4 all encode the same isoform (b).
    Source sequence(s)
    AC005067
    Consensus CDS
    CCDS43603.1
    UniProtKB/Swiss-Prot
    Q6NTF9
    Related
    ENSP00000314144.4, ENST00000318622.8
    Conserved Domains (1) summary
    cl21536
    Location:164
    Rhomboid; Rhomboid family
  3. NM_001346186.2NP_001333115.1  rhomboid domain-containing protein 2 isoform b

    Status: REVIEWED

    Description
    Transcript Variant: This variant (3) has two alternate exons in the 5' end compared to variant 1. This difference causes translation initiation at a downstream AUG and results in an isoform (b) with a shorter N-terminus, compared to isoform a. Variants 2-4 all encode the same isoform (b).
    Source sequence(s)
    AC005067
    Consensus CDS
    CCDS43603.1
    UniProtKB/Swiss-Prot
    Q6NTF9
    Conserved Domains (1) summary
    cl21536
    Location:164
    Rhomboid; Rhomboid family
  4. NM_001346187.2NP_001333116.1  rhomboid domain-containing protein 2 isoform b

    Status: REVIEWED

    Description
    Transcript Variant: This variant (4) uses an alternate splice junction in the 5' end compared to variant 1. This difference causes translation initiation at a downstream AUG and results in an isoform (b) with a shorter N-terminus, compared to isoform a. Variants 2-4 all encode the same isoform (b).
    Source sequence(s)
    AC005067
    Consensus CDS
    CCDS43603.1
    UniProtKB/Swiss-Prot
    Q6NTF9
    Related
    ENSP00000391232.1, ENST00000428119.1
    Conserved Domains (1) summary
    cl21536
    Location:164
    Rhomboid; Rhomboid family
  5. NM_001346188.2NP_001333117.1  rhomboid domain-containing protein 2 isoform c

    Status: REVIEWED

    Description
    Transcript Variant: This variant (5) lacks an alternate in-frame exon compared to variant 1. The resulting isoform (c) has the same N- and C-termini but is shorter compare to isoform a.
    Source sequence(s)
    AC005067
    UniProtKB/Swiss-Prot
    Q6NTF9
  6. NM_001346189.2NP_001333118.1  rhomboid domain-containing protein 2 isoform d

    Status: REVIEWED

    Description
    Transcript Variant: This variant (6) lacks an alternate in-frame exon and uses an alternate in-frame splice junction compared to variant 1. The resulting isoform (d) has the same N- and C-termini but is shorter compared to isoform a.
    Source sequence(s)
    AC005067

RNA

  1. NR_144390.2 RNA Sequence

    Status: REVIEWED

    Description
    Transcript Variant: This variant (7) contains an alternate exon, lacks another alternate exon, and uses an alternate splice junction compared to variant 1. This variant is represented as non-coding because the predicted protein does not meet RefSeq quality criteria.
    Source sequence(s)
    AC005067
  2. NR_144391.2 RNA Sequence

    Status: REVIEWED

    Description
    Transcript Variant: This variant (8) contains an alternate exon and lacks two other alternate exons compared to variant 1. This variant is represented as non-coding because the use of the 5'-most expected translational start codon renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
    Source sequence(s)
    AC005067, CF128386

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_000007.14 Reference GRCh38.p14 Primary Assembly

    Range
    75879034..75888926
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. XM_047420655.1XP_047276611.1  rhomboid domain-containing protein 2 isoform X1

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060931.1 Alternate T2T-CHM13v2.0

    Range
    77166165..77176057
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_020684.2: Suppressed sequence

    Description
    NM_020684.2: This RefSeq was permanently suppressed because it is a nonsense-mediated mRNA decay (NMD) candidate.