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MXRA7 matrix remodeling associated 7 [ Homo sapiens (human) ]

Gene ID: 439921, updated on 1-Aug-2020

Summary

Official Symbol
MXRA7provided by HGNC
Official Full Name
matrix remodeling associated 7provided by HGNC
Primary source
HGNC:HGNC:7541
See related
Ensembl:ENSG00000182534
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
Expression
Broad expression in heart (RPKM 51.6), thyroid (RPKM 40.4) and 22 other tissues See more
Orthologs

Genomic context

See MXRA7 in Genome Data Viewer
Location:
17q25.1
Exon count:
9
Annotation release Status Assembly Chr Location
109.20200522 current GRCh38.p13 (GCF_000001405.39) 17 NC_000017.11 (76672551..76710965, complement)
105 previous assembly GRCh37.p13 (GCF_000001405.25) 17 NC_000017.10 (74669748..74707056, complement)

Chromosome 17 - NC_000017.11Genomic Context describing neighboring genes Neighboring gene prothymosin alpha pseudogene 13 Neighboring gene RNA, U6 small nuclear 227, pseudogene Neighboring gene uncharacterized LOC105274304 Neighboring gene RNY4 pseudogene 36 Neighboring gene jumonji domain containing 6, arginine demethylase and lysine hydroxylase Neighboring gene methyltransferase like 23 Neighboring gene serine and arginine rich splicing factor 2 Neighboring gene microRNA 636

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

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Markers

Homology

Clone Names

  • FLJ41492, FLJ46603

General protein information

Preferred Names
matrix-remodeling-associated protein 7
Names
matrix-remodelling associated 7

NCBI Reference Sequences (RefSeq)

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_001008528.3NP_001008528.1  matrix-remodeling-associated protein 7 isoform 1 precursor

    See identical proteins and their annotated locations for NP_001008528.1

    Status: VALIDATED

    Description
    Transcript Variant: This variant (1) represents the longest transcript and encodes the longest isoform (1).
    Source sequence(s)
    AC005837, AW297080, BC053983, CK300836
    Consensus CDS
    CCDS32745.1
    UniProtKB/Swiss-Prot
    P84157
    Related
    ENSP00000348050.2, ENST00000355797.7
    Conserved Domains (1) summary
    PHA03247
    Location:5298
    PHA03247; large tegument protein UL36; Provisional
  2. NM_001008529.3NP_001008529.1  matrix-remodeling-associated protein 7 isoform 2 precursor

    See identical proteins and their annotated locations for NP_001008529.1

    Status: VALIDATED

    Description
    Transcript Variant: This variant (2) contains alternate 3' exon structure, and it thus differs in the 3' coding region and 3' UTR, compared to variant 1. The encoded isoform (2) has a distinct C-terminus and is shorter than isoform 1.
    Source sequence(s)
    AC005837, AK128460, AL046940, AW166143, BC053983
    Consensus CDS
    CCDS32746.1
    UniProtKB/Swiss-Prot
    P84157
    UniProtKB/TrEMBL
    Q6ZR64
    Related
    ENSP00000364176.1, ENST00000375036.6
    Conserved Domains (1) summary
    PHA03247
    Location:5298
    PHA03247; large tegument protein UL36; Provisional
  3. NM_001363769.1NP_001350698.1  matrix-remodeling-associated protein 7 isoform 4

    Status: VALIDATED

    Source sequence(s)
    AC005837, AK128460
    Consensus CDS
    CCDS86640.1
    Related
    ENSP00000465103.1, ENST00000592148.1
  4. NM_198530.4NP_940932.2  matrix-remodeling-associated protein 7 isoform 3 precursor

    See identical proteins and their annotated locations for NP_940932.2

    Status: VALIDATED

    Description
    Transcript Variant: This variant (3) contains an alternate 3' terminal exon, and it thus differs in the 3' coding region and 3' UTR, compared to variant 1. The encoded isoform (3) has a distinct C-terminus and is shorter than isoform 1.
    Source sequence(s)
    AC005837, AL046940, BC053983
    Consensus CDS
    CCDS45786.1
    UniProtKB/Swiss-Prot
    P84157
    Related
    ENSP00000391466.1, ENST00000449428.6

RNA

  1. NR_130926.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (4) contains alternate 5' and 3' terminal exons, compared to variant 1. This variant is represented as non-coding because the predicted protein does not meet RefSeq quality criteria.
    Source sequence(s)
    AL046940, BC053983, DA362466
  2. NR_130927.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (5) contains alternate 5' and 3' terminal exons, and also includes an additional internal exon, compared to variant 1. This variant is represented as non-coding because the predicted protein does not meet RefSeq quality criteria.
    Source sequence(s)
    AL046940, BC053983, DA065905
  3. NR_130928.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (6) contains alternate 5' and 3' terminal exons, compared to variant 1. This variant is represented as non-coding because the predicted protein does not meet RefSeq quality criteria.
    Source sequence(s)
    AL046940, BC053983, BQ109532, DA065905

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109.20200522

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000017.11 Reference GRCh38.p13 Primary Assembly

    Range
    76672551..76710965 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. XM_011524830.1XP_011523132.1  matrix-remodeling-associated protein 7 isoform X4

  2. XM_005257382.2XP_005257439.1  matrix-remodeling-associated protein 7 isoform X1

  3. XM_005257383.2XP_005257440.1  matrix-remodeling-associated protein 7 isoform X2

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