Version: 8.0.0Date: Tue Jan 28 2025
Category
MYL6B
(Homo sapiens)Gene
Name: myosin light chain 6B
Synonyms: myosin light chain 1 slow-twitch muscle A isoform, myosin, light chain 6B, alkali, smooth muscle and non-muscle, smooth muscle and non-muscle myosin alkali light chain 6B, myosin alkali light chain 1 slow a, MLC1SA, myosin light chain 1 slow a, myosin light chain 1, slow-twitch muscle A isoform, myosin, light polypeptide 6B, alkali, smooth muscle and non-muscle, smooth muscle and nonmuscle myosin light chain alkali 6B
Source: HGNC:29823
Biotype: protein coding gene
Symbol: MYL6B (Hsa)
Symbol: MYL6B
Strict Orthology Symbols: Myl6bl1...Myl6b
Myl6b
(Mus musculus)Gene
Name: myosin, light polypeptide 6B
Synonyms: RIKEN cDNA 5730437E04 gene, 5730437E04Rik, cDNA sequence BC037527, BC037527, MGC:41229
Source: MGI:1917789
Biotype: protein coding gene
Symbol: Myl6b (Mmu)
Symbol: Myl6b
Automated Gene Synopsis: Orthologous to human MYL6B (myosin light chain 6B).
Strict Orthology Symbols: Myl6bl1...MYL6B
Alleles: Myl6b
Myl6bl1
(Rattus norvegicus)Gene
Name: myosin light chain 6B like 1
Synonyms: AC128207.1, myosin light chain 6B, LOC120093525
Source: RGD:41207417
Biotype: protein coding gene
Symbol: Myl6bl1 (Rno)
Gene Synopsis: Orthologous to human MYL6B (myosin light chain 6B).
Automated Gene Synopsis: Orthologous to human MYL6B (myosin light chain 6B).
Strict Orthology Symbols: Myl6b...MYL6B
Symbol: Myl6bl1
MYL6B-AS1
(Homo sapiens)Gene
Name: MYL6B antisense RNA 1
Synonyms: Not Available
Source: HGNC:55472
Biotype: ncRNA gene
Symbol: MYL6B-AS1 (Hsa)
Symbol: MYL6B-AS1
Myl6b
(Rattus norvegicus)Gene
Name: myosin light chain 6B
Synonyms: myosin, light chain 6B, alkali, smooth muscle and non-muscle, RGD1560334, LOC317454, similar to Myosin light chain 1 slow a
Source: RGD:1560334
Biotype: pseudogene
Symbol: Myl6b (Rno)
Symbol: Myl6b
Gene Synopsis: Orthologous to human MYL6B (myosin light chain 6B); INTERACTS WITH 17beta-estradiol; 3H-1,2-dithiole-
Automated Gene Synopsis: Orthologous to human MYL6B (myosin light chain 6B).
Strict Orthology Symbols: MYL6B
Myl6bem1(IMPC)J
(Mus musculus)Allele/Variant
Source: MGI:7666147
Genes: Myl6b (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Myl6b
Genes: Myl6b (Mmu)
Symbol: Myl6bem1(IMPC)J
MYL6BP1
(Homo sapiens)Gene
Name: MYL6B pseudogene 1
Synonyms: myosin light chain 6B pseudogene 1
Source: HGNC:51647
Biotype: pseudogene
Symbol: MYL6BP1 (Hsa)
Symbol: MYL6BP1
Myl6b-ps1
(Rattus norvegicus)Gene
Name: myosin light chain 6B, pseudogene 1
Synonyms: similar to myosin light chain 1 slow a, LOC689693
Source: RGD:1589885
Biotype: pseudogene
Symbol: Myl6b-ps1 (Rno)
Symbol: Myl6b-ps1
mlc-3
(Caenorhabditis elegans)Gene
Name: Myosin Light Chain 3
Synonyms: CELE_F09F7.2, F09F7.2
Source: WB:WBGene00003371
Biotype: protein coding gene
Automated Gene Synopsis: Orthologous to human MYL3 (myosin light chain 3) and MYL6B (myosin light chain 6B).
Strict Orthology Symbols: MYL6B...Myl6bl1...Myl6b
mlc-6
(Caenorhabditis elegans)Gene
Name: Myosin Light Chain 6
Synonyms: K04C1.4, CELE_K04C1.4
Source: WB:WBGene00010554
Biotype: protein coding gene
Gene Synopsis: Is an ortholog of human MYL4 (myosin light chain 4); MYL6 (myosin light chain 6); and MYL6B (myosin light
Automated Gene Synopsis: Orthologous to human MYL4 (myosin light chain 4); MYL6 (myosin light chain 6); and MYL6B (myosin light
Strict Orthology Symbols: MYL6B...Myl6bl1...Myl6b
Mlc-c
(Drosophila melanogaster)Gene
Name: Myosin light chain cytoplasmic
Synonyms: non-muscle myosin II, essential light chain-cytoplasmic, Myosin II, essential light chain, mlc-c, Myosin light chain-cytoplasmic, CG3201, alkali light chain of non-muscle myosin-II, essential myosin light chain-cytoplasmic, non-muscle Myosin II, non-muscle myosin-II, ELC1, MyoII, Myosin-II, myosin II, DmMLC_C, Myosin, ELC, nmELC
Source: FB:FBgn0004687
Biotype: protein coding gene
Automated Gene Synopsis: Orthologous to several human genes including MYL4 (myosin light chain 4); MYL6 (myosin light chain 6); and MYL6B
Strict Orthology Symbols: MYL6B...Myl6bl1...Myl6b
mlc-5
(Caenorhabditis elegans)Gene
Name: Myosin Light Chain 5
Synonyms: CELE_T12D8.6, T12D8.6
Source: WB:WBGene00011734
Biotype: protein coding gene
Automated Gene Synopsis: Orthologous to several human genes including MYL4 (myosin light chain 4); MYL6 (myosin light chain 6); and MYL6B
Strict Orthology Symbols: MYL6B...Myl6bl1...Myl6b
MLC1
(Saccharomyces cerevisiae)Gene
Name: Myosin Light Chain
Synonyms: YGL106W
Source: SGD:S000003074
Biotype: protein coding gene
Automated Gene Synopsis: Orthologous to several human genes including MYL4 (myosin light chain 4); MYL6 (myosin light chain 6); and MYL6B
Strict Orthology Symbols: MYL6B...Myl6bl1...Myl6b
Mlc1
(Drosophila melanogaster)Gene
Name: Myosin alkali light chain 1
Synonyms: Mlci, MLC-ALK, MLC, Mlc-1, MLC1, myosin light chain, ELC2, Myosin, p-MLC, LC1, ELC_3, MlcI, mlc, Myosin alkali light chain l, mlc-alk, Myosin Light Chain-1, Myosin 3R alkali light chain l, Myosin light chain 1, CG5596, mlcl, DmMLC1, Myosin light chain alkali, ELC, chr3R:23484557..23484663, mlc1
Source: FB:FBgn0002772
Biotype: protein coding gene
Automated Gene Synopsis: Orthologous to human MYL3 (myosin light chain 3) and MYL6B (myosin light chain 6B).
Strict Orthology Symbols: MYL6B
mlc-7
(Caenorhabditis elegans)Gene
Name: Myosin Light Chain 7
Synonyms: CELE_K08E3.10, K08E3.10
Source: WB:WBGene00023451
Biotype: protein coding gene
Strict Orthology Symbols: MYL6B...Myl6bl1...Myl6b
myl6
(Xenopus tropicalis)Gene
Name: myosin light chain 6
Synonyms: myosin light chain 6, MGC76324, myl6
Source: Xenbase:XB-GENE-5931386
Biotype: gene
Strict Orthology Symbols: Myl6b...MYL6B
Gene Ontology
Source: GO:0016461
Synonyms:
- non-muscle myosin
Branch: cellular component
Genes: MYL6B (Hsa)...Myl6b (Mmu)
Gene Ontology
Source: GO:0030049
Synonyms: Not Available
Branch: biological process
Genes: Myl6b (Mmu)...MYL6B (Hsa)
Gene Ontology
Source: GO:0005859
Synonyms: Not Available
Branch: cellular component
Genes: MYL6B (Hsa)
Gene Ontology
Source: GO:0008307
Synonyms: Not Available
Branch: molecular function
Genes: MYL6B (Hsa)...Myl6b (Mmu)
Gene Ontology
Source: GO:0016460
Synonyms:
- conventional myosin
Branch: cellular component
Genes: MYL6B (Hsa)...Myl6b (Mmu)
Gene Ontology
Source: GO:0016459
Synonyms: Not Available
Branch: cellular component
Genes: MYL6B (Hsa)...Myl6b (Mmu)
Gene Ontology
Source: GO:0006936
Synonyms: Not Available
Branch: biological process
Genes: MYL6B (Hsa)...Myl6b (Mmu)
Gene Ontology
Source: GO:0003774
Synonyms:
- motor activity
Branch: molecular function
Genes: MYL6B (Hsa)...Myl6b (Mmu)
Gene Ontology
Source: GO:0007519
Synonyms:
- myogenesis
Branch: biological process
Genes: MYL6B (Hsa)...Myl6b (Mmu)
Gene Ontology
Source: GO:0005509
Synonyms:
- calcium ion storage activity
Branch: molecular function
Genes: MYL6B (Hsa)...Myl6b (Mmu)...Myl6bl1 (Rno)
Gene Ontology
Source: GO:0070062
Synonyms:
- exosome
- extracellular vesicular exosome
Branch: cellular component
Genes: MYL6B (Hsa)
Gene Ontology
Source: GO:0005829
Synonyms: Not Available
Branch: cellular component
Genes: MYL6B (Hsa)
Gene Ontology
Source: GO:0005515
Synonyms:
- glycoprotein binding
- protein amino acid binding
Branch: molecular function
Genes: MYL6B (Hsa)
(GRCh38)12:56158687G>A
(Homo sapiens)Allele/Variant
Source: NC_000012.12:g.56158687G>A
Genes: MYL6B (Hsa), MYL6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:56158687G>A
(GRCh38)12:56155061A>G
(Homo sapiens)Allele/Variant
Source: rs1186790119
Genes: MYL6B-AS1 (Hsa), MYL6B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:56155061A>G
(GRCh38)12:56155119T>G
(Homo sapiens)Allele/Variant
Source: rs202164722
Genes: MYL6B-AS1 (Hsa), MYL6B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:56155119T>G
(GRCh38)12:56155186C>T
(Homo sapiens)Allele/Variant
Source: rs77682403
Genes: MYL6B-AS1 (Hsa), MYL6B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:56155186C>T
(GRCh38)12:56157480C>G
(Homo sapiens)Allele/Variant
Source: rs139194953
Genes: MYL6B-AS1 (Hsa), MYL6B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:56157480C>G
(GRCh38)12:56155091G>A
(Homo sapiens)Allele/Variant
Source: rs1871255245
Genes: MYL6B-AS1 (Hsa), MYL6B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:56155091G>A
(GRCh38)12:56155159G>A
(Homo sapiens)Allele/Variant
Source: rs777515431
Genes: MYL6B-AS1 (Hsa), MYL6B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:56155159G>A
(GRCh38)12:56155547G>A
(Homo sapiens)Allele/Variant
Source: rs141538526
Genes: MYL6B-AS1 (Hsa), MYL6B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:56155547G>A
(GRCh38)12:56155547G>C
(Homo sapiens)Allele/Variant
Source: rs141538526
Genes: MYL6B-AS1 (Hsa), MYL6B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:56155547G>C
(GRCh38)12:56155169T>C
(Homo sapiens)Allele/Variant
Source: rs776464405
Genes: MYL6B-AS1 (Hsa), MYL6B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:56155169T>C
(GRCh38)12:56155117T>C
(Homo sapiens)Allele/Variant
Source: rs774948098
Genes: MYL6B-AS1 (Hsa), MYL6B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:56155117T>C
(GRCh38)12:56155523C>T
(Homo sapiens)Allele/Variant
Source: rs768327872
Genes: MYL6B-AS1 (Hsa), MYL6B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:56155523C>T
(GRCh38)12:56155129A>G
(Homo sapiens)Allele/Variant
Source: rs200968245
Genes: MYL6B-AS1 (Hsa), MYL6B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:56155129A>G
(GRCh38)12:56155460A>T
(Homo sapiens)Allele/Variant
Source: rs529967791
Genes: MYL6B-AS1 (Hsa), MYL6B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:56155460A>T
(GRCh38)12:56158684T>C
(Homo sapiens)Allele/Variant
Source: rs757154921
Genes: MYL6B (Hsa), MYL6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:56158684T>C
(GRCm39)10:128331551C>T
(Mus musculus)Allele/Variant
Source: rs221804796
Genes: Myl6b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:128331551C>T
(GRCm39)10:128333259A>G
(Mus musculus)Allele/Variant
Source: rs212714984
Genes: Myl6b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:128333259A>G
(GRCm39)10:128330493G>T
(Mus musculus)Allele/Variant
Source: rs241137044
Genes: Myl6b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)10:128330493G>T
(GRCm39)10:128333432C>T
(Mus musculus)Allele/Variant
Source: rs223709888
Genes: Myl6b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:128333432C>T
(GRCm39)10:128331864C>T
(Mus musculus)Allele/Variant
Source: rs260403808
Genes: Myl6b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:128331864C>T
(GRCm39)10:128332368G>A
(Mus musculus)Allele/Variant
Source: rs237331892
Genes: Myl6b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:128332368G>A