Version: 8.0.0Date: Tue Jan 28 2025
Category
lrrc39
(Danio rerio)Gene
Name: leucine rich repeat containing 39
Synonyms: myomasp, zgc:112088
Source: ZFIN:ZDB-GENE-050417-279
Biotype: protein coding gene
Symbol: lrrc39 (Dre)
Symbol: lrrc39
Automated Gene Synopsis: Orthologous to human LRRC39 (leucine rich repeat containing 39).
Strict Orthology Symbols: lrrc39
Lrrc39
(Rattus norvegicus)Gene
Name: leucine rich repeat containing 39
Synonyms: LOC691307, myomasp, similar to leucine rich repeat containing 39 isoform 2, leucine-rich repeat-containing protein 39
Source: RGD:1585106
Biotype: protein coding gene
Symbol: Lrrc39 (Rno)
Symbol: Lrrc39
Gene Synopsis: Orthologous to human LRRC39 (leucine rich repeat containing 39); INTERACTS WITH 2,3,7,8-tetrachlorodibenzodioxine
Automated Gene Synopsis: Orthologous to human LRRC39 (leucine rich repeat containing 39).
Strict Orthology Symbols: lrrc39
LRRC39
(Homo sapiens)Gene
Name: leucine rich repeat containing 39
Synonyms: myomasp, MGC14816, densin hlg, DKFZp313O1122, leucine-rich repeat-containing protein 39
Source: HGNC:28228
Biotype: protein coding gene
Symbol: LRRC39 (Hsa)
Symbol: LRRC39
Strict Orthology Symbols: lrrc39
Lrrc39
(Mus musculus)Gene
Name: leucine rich repeat containing 39
Synonyms: 9430028I06Rik, 2010005E21Rik, RIKEN cDNA 2010005E21 gene, RIKEN cDNA 9430028I06 gene, Myomasp
Source: MGI:1924557
Biotype: protein coding gene
Symbol: Lrrc39 (Mmu)
Symbol: Lrrc39
Automated Gene Synopsis: Orthologous to human LRRC39 (leucine rich repeat containing 39).
Strict Orthology Symbols: lrrc39
Alleles: Lrrc39
lrrc39
(Xenopus tropicalis)Gene
Name: leucine rich repeat containing 39
Synonyms: leucine rich repeat containing 39, lrrc39
Source: Xenbase:XB-GENE-984701
Biotype: gene
Symbol: lrrc39
Symbol: lrrc39 (Xtr)
Automated Gene Synopsis: Orthologous to human LRRC39 (leucine rich repeat containing 39).
Synonyms: lrrc39...lrrc39...lrrc39
Strict Orthology Symbols: lrrc39
lrrc39.L
(Xenopus laevis)Gene
Name: leucine rich repeat containing 39
Synonyms: lrrc39.L, leucine rich repeat containing 39
Source: Xenbase:XB-GENE-6488665
Biotype: gene
Symbol: lrrc39.L (Xla)
Automated Gene Synopsis: Orthologous to human LRRC39 (leucine rich repeat containing 39).
Strict Orthology Symbols: lrrc39
Symbol: lrrc39.L
Lrrc39tm1a(KOMP)Wtsi
(Mus musculus)Allele/Variant
Source: MGI:4362191
Genes: Lrrc39 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Lrrc39
Genes: Lrrc39 (Mmu)
Symbol: Lrrc39tm1a(KOMP)Wtsi
CG10307
(Drosophila melanogaster)Gene
Name: Not Available
Synonyms: CT28947
Source: FB:FBgn0034655
Biotype: protein coding gene
Strict Orthology Symbols: Lrrc39
s883Tg + MO1-lrrc39
(Danio rerio)Model
Id: ZFIN:ZDB-FISH-150901-277
Synonyms: Not Available
Genes: lrrc39 (Dre)
Name: s883Tg + MO1-lrrc39
WT + MO2-lrrc39
(Danio rerio)Model
Id: ZFIN:ZDB-FISH-150901-20994
Synonyms: Not Available
Genes: lrrc39 (Dre)
Name: WT + MO2-lrrc39
Gene Ontology
Source: GO:0031430
Synonyms:
- M disc
- M line
Branch: cellular component
Genes: LRRC39 (Hsa)...Lrrc39 (Mmu)...lrrc39 (Dre)...Lrrc39 (Rno)
Gene Ontology
Source: GO:0055008
Synonyms:
- heart muscle morphogenesis
- myocardium morphogenesis
Branch: biological process
Genes: lrrc39 (Dre)
Gene Ontology
Source: GO:0060047
Synonyms:
- cardiac contraction
- heart beating
Branch: biological process
Genes: lrrc39 (Dre)
Gene Ontology
Source: GO:0045214
Synonyms:
- sarcomere alignment
- sarcomere organisation
Branch: biological process
Genes: lrrc39 (Dre)
Gene Ontology
Source: GO:0035556
Synonyms:
- intracellular signal transduction pathway
- intracellular signaling cascade
Branch: biological process
Genes: lrrc39 (Dre)...LRRC39 (Hsa)...Lrrc39 (Rno)...Lrrc39 (Mmu)
Gene Ontology
Source: GO:0005737
Synonyms: Not Available
Branch: cellular component
Genes: LRRC39 (Hsa)...lrrc39 (Dre)
Gene Ontology
Source: GO:0005515
Synonyms:
- glycoprotein binding
- protein amino acid binding
Branch: molecular function
Genes: LRRC39 (Hsa)
(GRCh38)1:100159405G>A
(Homo sapiens)Allele/Variant
Source: rs201723295
Genes: LRRC39 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:100159405G>A
(GRCh38)1:100156206T>G
(Homo sapiens)Allele/Variant
Source: rs145422779
Genes: LRRC39 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:100156206T>G
(GRCh38)1:100155157A>T
(Homo sapiens)Allele/Variant
Source: rs148005305
Genes: LRRC39 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:100155157A>T
(GRCh38)1:100159309A>G
(Homo sapiens)Allele/Variant
Source: rs780755554
Genes: LRRC39 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:100159309A>G
(GRCh38)1:100155074G>C
(Homo sapiens)Allele/Variant
Source: rs528764115
Genes: LRRC39 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:100155074G>C
(GRCh38)1:100168495T>G
(Homo sapiens)Allele/Variant
Source: NC_000001.11:g.100168495T>G
Genes: LRRC39 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:100168495T>G
(GRCh38)1:100152445G>A
(Homo sapiens)Allele/Variant
Source: rs765807301
Genes: LRRC39 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:100152445G>A
(GRCh38)1:100155081G>T
(Homo sapiens)Allele/Variant
Source: rs147649568
Genes: LRRC39 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:100155081G>T
(GRCh38)1:100152396C>T
(Homo sapiens)Allele/Variant
Source: rs372225768
Genes: LRRC39 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:100152396C>T
(GRCh38)1:100159287G>C
(Homo sapiens)Allele/Variant
Source: rs762111111
Genes: LRRC39 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:100159287G>C
(GRCh38)1:100159391G>A
(Homo sapiens)Allele/Variant
Source: rs80221535
Genes: LRRC39 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:100159391G>A
(GRCh38)1:100152498A>G
(Homo sapiens)Allele/Variant
Source: NC_000001.11:g.100152498A>G
Genes: LRRC39 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:100152498A>G
(GRCh38)1:100158232T>G
(Homo sapiens)Allele/Variant
Source: NC_000001.11:g.100158232T>G
Genes: LRRC39 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:100158232T>G
(GRCh38)1:100158234T>A
(Homo sapiens)Allele/Variant
Source: rs199927631
Genes: LRRC39 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:100158234T>A
(GRCh38)1:100168455C>T
(Homo sapiens)Allele/Variant
Source: rs140092228
Genes: LRRC39 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:100168455C>T
(GRCh38)1:100156278T>C
(Homo sapiens)Allele/Variant
Source: rs978856356
Genes: LRRC39 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:100156278T>C
(GRCh38)1:100158250A>G
(Homo sapiens)Allele/Variant
Source: rs144639407
Genes: LRRC39 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:100158250A>G
(GRCh38)1:100158325T>G
(Homo sapiens)Allele/Variant
Source: rs868076216
Genes: LRRC39 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:100158325T>G
(GRCh38)1:100160498C>T
(Homo sapiens)Allele/Variant
Source: rs763730162
Genes: LRRC39 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:100160498C>T
(GRCh38)1:100155168T>C
(Homo sapiens)Allele/Variant
Source: NC_000001.11:g.100155168T>C
Genes: LRRC39 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:100155168T>C
(GRCh38)1:100155186G>A
(Homo sapiens)Allele/Variant
Source: rs149823600
Genes: LRRC39 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:100155186G>A
(GRCh38)1:100160485A>G
(Homo sapiens)Allele/Variant
Source: rs752977918
Genes: LRRC39 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:100160485A>G
(GRCh38)1:100156229A>G
(Homo sapiens)Allele/Variant
Source: rs140341572
Genes: LRRC39 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:100156229A>G
(GRCh38)1:100148720G>T
(Homo sapiens)Allele/Variant
Source: rs201994806
Genes: LRRC39 (Hsa), TRMT13 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)1:100148720G>T
(GRCh38)1:100148662C>A
(Homo sapiens)Allele/Variant
Source: rs767533656
Genes: LRRC39 (Hsa), TRMT13 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)1:100148662C>A
(mRatBN7.2)2:204523960G>C
(Rattus norvegicus)Allele/Variant
Source: rs106771144
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204523960G>C
(mRatBN7.2)2:204524838G>T
(Rattus norvegicus)Allele/Variant
Source: rs3319657101
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204524838G>T
(mRatBN7.2)2:204529649T>C
(Rattus norvegicus)Allele/Variant
Source: rs3319692292
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204529649T>C
(mRatBN7.2)2:204528938G>A
(Rattus norvegicus)Allele/Variant
Source: rs3319683554
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204528938G>A
(mRatBN7.2)2:204529348G>A
(Rattus norvegicus)Allele/Variant
Source: rs3319657071
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204529348G>A
(mRatBN7.2)2:204530037T>C
(Rattus norvegicus)Allele/Variant
Source: rs3319657035
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204530037T>C
(mRatBN7.2)2:204522087C>T
(Rattus norvegicus)Allele/Variant
Source: rs197932558
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204522087C>T
(mRatBN7.2)2:204522107A>G
(Rattus norvegicus)Allele/Variant
Source: rs3319678996
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204522107A>G