Version: 8.0.0
Date: Tue Jan 28 2025
2,751 results for mrps27

mrps27

(Danio rerio)
Gene
Name: mitochondrial ribosomal protein S27
Synonyms: zgc:100970
Source: ZFIN:ZDB-GENE-040808-39
Biotype: protein coding gene
Symbol: mrps27 (Dre)
Symbol: mrps27
Automated Gene Synopsis: Orthologous to human MRPS27 (mitochondrial ribosomal protein S27).
Strict Orthology Symbols: MRPS27...Mrps27

MRPS27

(Homo sapiens)
Gene
Name: mitochondrial ribosomal protein S27
Synonyms: mitochondrial small ribosomal subunit protein mS27, mitochondrial 28S ribosomal protein S27, FLJ38645, S27mt, FLJ21764, FLJ23348, mS27, 28S ribosomal protein S27, mitochondrial, KIAA0264, MRP-S27, small ribosomal subunit protein mS27
Source: HGNC:14512
Biotype: protein coding gene
Symbol: MRPS27 (Hsa)
Symbol: MRPS27
Strict Orthology Symbols: mrps27

Mrps27

(Rattus norvegicus)
Gene
Name: mitochondrial ribosomal protein S27
Synonyms: LOC361883, 28S ribosomal protein S27, mitochondrial, small ribosomal subunit protein mS27
Source: RGD:1311829
Biotype: protein coding gene
Symbol: Mrps27 (Rno)
Symbol: Mrps27
Gene Synopsis: Orthologous to human MRPS27 (mitochondrial ribosomal protein S27); INTERACTS WITH 2,3,7,8-tetrachlorodibenzodioxine
Automated Gene Synopsis: Orthologous to human MRPS27 (mitochondrial ribosomal protein S27).
Strict Orthology Symbols: mrps27

Mrps27

(Mus musculus)
Gene
Name: mitochondrial ribosomal protein S27
Synonyms: 2610028H14Rik, RIKEN cDNA 2610028H14 gene
Source: MGI:1919064
Biotype: protein coding gene
Symbol: Mrps27 (Mmu)
Symbol: Mrps27
Automated Gene Synopsis: Orthologous to human MRPS27 (mitochondrial ribosomal protein S27).
Strict Orthology Symbols: mrps27

mrps27.L

(Xenopus laevis)
Gene
Name: mitochondrial ribosomal protein S27
Synonyms: mitochondrial ribosomal protein S27, mrps27.L
Source: Xenbase:XB-GENE-943406
Biotype: gene
Symbol: mrps27.L (Xla)
Automated Gene Synopsis: Orthologous to human MRPS27 (mitochondrial ribosomal protein S27).
Strict Orthology Symbols: mrps27
Symbol: mrps27.L

mrps27

(Xenopus tropicalis)
Gene
Name: mitochondrial ribosomal protein S27
Synonyms: mrps27, mitochondrial ribosomal protein S27
Source: Xenbase:XB-GENE-943403
Biotype: gene
Symbol: mrps27 (Xtr)
Symbol: mrps27
Synonyms: mrps27...mrps27...mrps27
Strict Orthology Symbols: mrps27.L

CG4882

(Drosophila melanogaster)
Gene
Name: Not Available
Synonyms: anon-60Aa, UD1, GM14313, LD24471, undefined 1
Source: FB:FBgn0025336
Biotype: protein coding gene
Automated Gene Synopsis: Orthologous to human MRPS27 (mitochondrial ribosomal protein S27).
Strict Orthology Symbols: mrps27

mrps-27

(Caenorhabditis elegans)
Gene
Name: Mitochondrial Ribosomal Protein, Small 27
Synonyms: K11B4.1, CELE_K11B4.1
Source: WB:WBGene00010766
Biotype: protein coding gene
Gene Synopsis: Is an ortholog of human MRPS27 (mitochondrial ribosomal protein S27).
Automated Gene Synopsis: Orthologous to human MRPS27 (mitochondrial ribosomal protein S27).
Strict Orthology Symbols: mrps27

mitochondrial ribosome binding

Gene Ontology
Source: GO:0097177
Synonyms: Not Available
Branch: molecular function
Genes: Mrps27 (Rno)...Mrps27 (Mmu)...MRPS27 (Hsa)

positive regulation of mitochondrial translation

Gene Ontology
Source: GO:0070131
Synonyms:
  • positive regulation of mitochondrial protein anabolism
  • positive regulation of mitochondrial protein biosynthesis
Branch: biological process
Genes: Mrps27 (Rno)...Mrps27 (Mmu)...MRPS27 (Hsa)

Hsap\MRPS27UAS.Tag:HA

(Drosophila melanogaster)
Allele/Variant
Source: FB:FBal0402444
Genes: Not Available
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Hsap\MRPS27
Construct Expressed Component: MRPS27 (Hsa)

mitochondrial small ribosomal subunit

Gene Ontology
Source: GO:0005763
Synonyms:
  • 28S ribosomal subunit, mitochondrial
  • mitochondrial ribosomal SSU complex
Branch: cellular component
Genes: MRPS27 (Hsa)...Mrps27 (Mmu)...Mrps27 (Rno)

rRNA binding

Gene Ontology
Source: GO:0019843
Synonyms:
  • base pairing with rRNA
Branch: molecular function
Genes: MRPS27 (Hsa)...Mrps27 (Mmu)...Mrps27 (Rno)

tRNA binding

Gene Ontology
Source: GO:0000049
Synonyms:
  • base pairing with tRNA
Branch: molecular function
Genes: MRPS27 (Hsa)...Mrps27 (Mmu)...Mrps27 (Rno)

mitochondrial translation

Gene Ontology
Source: GO:0032543
Synonyms:
  • mitochondrial protein anabolism
  • mitochondrial protein biosynthesis
Branch: biological process
Genes: MRPS27 (Hsa)...Mrps27 (Mmu)

cell population proliferation

Gene Ontology
Source: GO:0008283
Synonyms:
  • cell proliferation
Branch: biological process
Genes: MRPS27 (Hsa)...Mrps27 (Mmu)...Mrps27 (Rno)

regulation of translation

Gene Ontology
Source: GO:0006417
Synonyms:
  • regulation of protein anabolism
  • regulation of protein biosynthesis
Branch: biological process
Genes: MRPS27 (Hsa)

ribosome

Gene Ontology
Source: GO:0005840
Synonyms:
  • free ribosome
  • membrane bound ribosome
Branch: cellular component
Genes: MRPS27 (Hsa)...mrps27 (Dre)

ribonucleoprotein complex

Gene Ontology
Source: GO:1990904
Synonyms:
  • RNA-protein complex
  • RNP
Branch: cellular component
Genes: MRPS27 (Hsa)...mrps27 (Dre)

mitochondrial inner membrane

Gene Ontology
Source: GO:0005743
Synonyms:
  • inner mitochondrial membrane
  • inner mitochondrion membrane
Branch: cellular component
Genes: MRPS27 (Hsa)...Mrps27 (Mmu)

nucleolus

Gene Ontology
Source: GO:0005730
Synonyms: Not Available
Branch: cellular component
Genes: MRPS27 (Hsa)...Mrps27 (Mmu)...Mrps27 (Rno)

sa12506

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-130411-2229
Genes: mrps27 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: splice_region_variant, stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: mrps27 (Dre)

mitochondrion

Gene Ontology
Source: GO:0005739
Synonyms:
  • mitochondria
Branch: cellular component
Genes: MRPS27 (Hsa)...mrps27 (Dre)...Mrps27 (Rno)...Mrps27 (Mmu)

sa535

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-161003-17656
Genes: mrps27 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: splice_donor_variant
Diseases: Not Available
Variant Name: Not Available
Genes: mrps27 (Dre)

cytoplasm

Gene Ontology
Source: GO:0005737
Synonyms: Not Available
Branch: cellular component
Genes: Mrps27 (Rno)...MRPS27 (Hsa)...Mrps27 (Mmu)

protein binding

Gene Ontology
Source: GO:0005515
Synonyms:
  • glycoprotein binding
  • protein amino acid binding
Branch: molecular function
Genes: MRPS27 (Hsa)...Mrps27 (Mmu)

biological_process

Gene Ontology
Source: GO:0008150
Synonyms:
  • biological process
  • physiological process
Branch: biological process
Genes: mrps27 (Dre)

molecular_function

Gene Ontology
Source: GO:0003674
Synonyms:
  • molecular function
Branch: molecular function
Genes: mrps27 (Dre)

(GRCh38)5:72228277T>C

(Homo sapiens)
Allele/Variant
Source: rs377723468
Genes: MRPS27 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:72228277T>C

(GRCh38)5:72221015T>C

(Homo sapiens)
Allele/Variant
Source: rs943134978
Genes: MRPS27 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:72221015T>C

(GRCh38)5:72223767G>T

(Homo sapiens)
Allele/Variant
Source: NC_000005.10:g.72223767G>T
Genes: MRPS27 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:72223767G>T

(GRCh38)5:72238066T>C

(Homo sapiens)
Allele/Variant
Source: rs140284675
Genes: MRPS27 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:72238066T>C

(GRCh38)5:72226110C>T

(Homo sapiens)
Allele/Variant
Source: rs200844970
Genes: MRPS27 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:72226110C>T

(GRCh38)5:72226172C>T

(Homo sapiens)
Allele/Variant
Source: NC_000005.10:g.72226172C>T
Genes: MRPS27 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:72226172C>T

(GRCh38)5:72297676T>C

(Homo sapiens)
Allele/Variant
Source: NC_000005.10:g.72297676T>C
Genes: MRPS27 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:72297676T>C

(GRCh38)5:72221038G>C

(Homo sapiens)
Allele/Variant
Source: rs369816290
Genes: MRPS27 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:72221038G>C

(GRCh38)5:72223848G>A

(Homo sapiens)
Allele/Variant
Source: rs11557156
Genes: MRPS27 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:72223848G>A

(GRCh38)5:72223705G>A

(Homo sapiens)
Allele/Variant
Source: rs188517497
Genes: MRPS27 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:72223705G>A

(GRCh38)5:72320192C>A

(Homo sapiens)
Allele/Variant
Source: rs147211361
Genes: MRPS27 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:72320192C>A

(GRCh38)5:72221024T>C

(Homo sapiens)
Allele/Variant
Source: rs753727556
Genes: MRPS27 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:72221024T>C

(GRCh38)5:72221085T>C

(Homo sapiens)
Allele/Variant
Source: rs141373207
Genes: MRPS27 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:72221085T>C

(GRCh38)5:72223817T>C

(Homo sapiens)
Allele/Variant
Source: rs146439858
Genes: MRPS27 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:72223817T>C

(GRCh38)5:72226137G>A

(Homo sapiens)
Allele/Variant
Source: rs114360965
Genes: MRPS27 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:72226137G>A

(GRCh38)5:72297679T>C

(Homo sapiens)
Allele/Variant
Source: rs564459077
Genes: MRPS27 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:72297679T>C

(GRCh38)5:72221042T>G

(Homo sapiens)
Allele/Variant
Source: rs1161898674
Genes: MRPS27 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:72221042T>G

(GRCh38)5:72223847C>A

(Homo sapiens)
Allele/Variant
Source: rs749889500
Genes: MRPS27 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:72223847C>A

(GRCh38)5:72223690C>T

(Homo sapiens)
Allele/Variant
Source: rs745503396
Genes: MRPS27 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:72223690C>T

(GRCh38)5:72238111T>C

(Homo sapiens)
Allele/Variant
Source: rs754401193
Genes: MRPS27 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:72238111T>C

(GRCh38)5:72320203G>A

(Homo sapiens)
Allele/Variant
Source: rs1346394739
Genes: MRPS27 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:72320203G>A

(GRCh38)5:72221054C>T

(Homo sapiens)
Allele/Variant
Source: rs1053009588
Genes: MRPS27 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:72221054C>T