90 results for lrrc73

LRRC73

(Homo sapiens)
Gene
Name: leucine rich repeat containing 73
Synonyms: FLJ44836, MGC131686, hypothetical protein LOC221424, leucine-rich repeat-containing protein 73, uncharacterized protein C6orf154, dJ337H4.2, C6orf154
Source: HGNC:21375
Biotype: protein coding gene
Symbol: LRRC73 (Hsa)
Symbol: LRRC73
Strict Orthology Symbols: lrrc73

lrrc73

(Danio rerio)
Gene
Name: leucine rich repeat containing 73
Synonyms: gb:eb985873
Source: ZFIN:ZDB-GENE-111118-2
Biotype: protein coding gene
Symbol: lrrc73 (Dre)
Symbol: lrrc73
Automated Gene Synopsis: Orthologous to human LRRC73 (leucine rich repeat containing 73).
Strict Orthology Symbols: LRRC73...Lrrc73

Lrrc73

(Mus musculus)
Gene
Name: leucine rich repeat containing 73
Synonyms: gene model 88, (NCBI), Gm88, LOC224813, predicted gene 88, nod3l
Source: MGI:2684934
Biotype: protein coding gene
Symbol: Lrrc73 (Mmu)
Symbol: Lrrc73
Automated Gene Synopsis: Orthologous to human LRRC73 (leucine rich repeat containing 73).
Strict Orthology Symbols: lrrc73

Lrrc73

(Rattus norvegicus)
Gene
Name: leucine rich repeat containing 73
Synonyms: hypothetical protein LOC501101, leucine-rich repeat-containing protein 73, NOD3-like protein, uncharacterized protein C6orf154 homolog, nod3l
Source: RGD:1561390
Biotype: protein coding gene
Symbol: Lrrc73 (Rno)
Symbol: Lrrc73
Gene Synopsis: Orthologous to human LRRC73 (leucine rich repeat containing 73); INTERACTS WITH 17beta-estradiol; 17beta-estradiol
Automated Gene Synopsis: Orthologous to human LRRC73 (leucine rich repeat containing 73).
Strict Orthology Symbols: lrrc73

lrrc73

(Xenopus tropicalis)
Gene
Name: leucine rich repeat containing 73
Synonyms: leucine rich repeat containing 73, lrrc73
Source: Xenbase:XB-GENE-6455532
Biotype: gene
Symbol: lrrc73 (Xtr)
Symbol: lrrc73
Synonyms: lrrc73...lrrc73...lrrc73
Strict Orthology Symbols: lrrc73.S...lrrc73.L

lrrc73.S

(Xenopus laevis)
Gene
Name: leucine rich repeat containing 73
Synonyms: lrrc73.S, leucine rich repeat containing 73
Source: Xenbase:XB-GENE-17341515
Biotype: gene
Symbol: lrrc73.S (Xla)
Automated Gene Synopsis: Orthologous to human LRRC73 (leucine rich repeat containing 73).
Strict Orthology Symbols: lrrc73
Symbol: lrrc73.S

lrrc73.L

(Xenopus laevis)
Gene
Name: leucine rich repeat containing 73
Synonyms: leucine rich repeat containing 73, lrrc73.L
Source: Xenbase:XB-GENE-17341514
Biotype: gene
Symbol: lrrc73.L (Xla)
Automated Gene Synopsis: Orthologous to human LRRC73 (leucine rich repeat containing 73).
Strict Orthology Symbols: lrrc73
Symbol: lrrc73.L

sa42124

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-160601-7957
Genes: lrrc73 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: lrrc73 (Dre)

Gene Ontology
Source: GO:0005575
Synonyms:
  • cell or subcellular entity
  • cellular component
Branch: cellular component
Genes: Lrrc73 (Mmu)

Gene Ontology
Source: GO:0008150
Synonyms:
  • biological process
  • physiological process
Branch: biological process
Genes: Lrrc73 (Mmu)

Gene Ontology
Source: GO:0003674
Synonyms:
  • molecular function
Branch: molecular function
Genes: Lrrc73 (Mmu)

Gene Ontology
Source: GO:0005515
Synonyms:
  • glycoprotein binding
  • protein amino acid binding
Branch: molecular function
Genes: LRRC73 (Hsa)

(GRCh38)6:43509628G>T

(Homo sapiens)
Allele/Variant
Source: rs755718839
Genes: LRRC73 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)6:43509628G>T

(GRCh38)6:43507639G>A

(Homo sapiens)
Allele/Variant
Source: rs761992197
Genes: LRRC73 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)6:43507639G>A

(GRCh38)6:43508816C>A

(Homo sapiens)
Allele/Variant
Source: NC_000006.12:g.43508816C>A
Genes: LRRC73 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)6:43508816C>A

(GRCh38)6:43508834A>C

(Homo sapiens)
Allele/Variant
Source: NC_000006.12:g.43508834A>C
Genes: LRRC73 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)6:43508834A>C

(GRCh38)6:43507468T>A

(Homo sapiens)
Allele/Variant
Source: rs576025527
Genes: LRRC73 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)6:43507468T>A

(GRCh38)6:43508906G>A

(Homo sapiens)
Allele/Variant
Source: NC_000006.12:g.43508906G>A
Genes: LRRC73 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)6:43508906G>A

(GRCh38)6:43507263C>T

(Homo sapiens)
Allele/Variant
Source: NC_000006.12:g.43507263C>T
Genes: LRRC73 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)6:43507263C>T

(GRCh38)6:43508810T>G

(Homo sapiens)
Allele/Variant
Source: rs199868414
Genes: LRRC73 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)6:43508810T>G

(GRCh38)6:43509620T>C

(Homo sapiens)
Allele/Variant
Source: NC_000006.12:g.43509620T>C
Genes: LRRC73 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)6:43509620T>C

(GRCh38)6:43507272A>G

(Homo sapiens)
Allele/Variant
Source: rs142261504
Genes: LRRC73 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)6:43507272A>G

(GRCh38)6:43507587A>G

(Homo sapiens)
Allele/Variant
Source: rs778487300
Genes: LRRC73 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)6:43507587A>G

(GRCh38)6:43507605G>A

(Homo sapiens)
Allele/Variant
Source: rs762857727
Genes: LRRC73 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)6:43507605G>A

(GRCh38)6:43508363C>A

(Homo sapiens)
Allele/Variant
Source: rs375969127
Genes: LRRC73 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)6:43508363C>A

(GRCh38)6:43509698C>G

(Homo sapiens)
Allele/Variant
Source: rs757129608
Genes: LRRC73 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)6:43509698C>G

(GRCh38)6:43509763A>G

(Homo sapiens)
Allele/Variant
Source: rs1263252182
Genes: LRRC73 (Hsa), POLR1C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)6:43509763A>G

(GRCh38)6:43509740C>T

(Homo sapiens)
Allele/Variant
Source: rs754424948
Genes: LRRC73 (Hsa), POLR1C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)6:43509740C>T

Allele/Variant
Source: rs260707422
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46566545C>T

Allele/Variant
Source: rs33064988
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46566722A>C

Allele/Variant
Source: rs241334609
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46566928A>G

Allele/Variant
Source: rs264912887
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46567053G>A

Allele/Variant
Source: rs242688556
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46567419G>A

Allele/Variant
Source: rs251702587
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46565957A>T

Allele/Variant
Source: rs108594605
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46567011T>C

Allele/Variant
Source: rs108836764
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46567666T>C

Allele/Variant
Source: rs262025152
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46567758C>T

Allele/Variant
Source: rs214393990
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46565812C>T

(mRatBN7.2)9:14726540C>T

(Rattus norvegicus)
Allele/Variant
Source: rs106505012
Genes: Lrrc73 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)9:14726540C>T

Allele/Variant
Source: rs108506596
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46567093T>C

Allele/Variant
Source: rs221369061
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46567562T>C

Allele/Variant
Source: rs216820724
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46564921C>T

Allele/Variant
Source: rs229425899
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46564937C>G

Allele/Variant
Source: rs250657332
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46565629C>T

Allele/Variant
Source: rs228550918
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46567078A>G

Allele/Variant
Source: rs221831711
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46564476A>G

Allele/Variant
Source: rs245966735
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46567291A>G

Allele/Variant
Source: rs252362412
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46567554C>T

(mRatBN7.2)9:14729553T>G

(Rattus norvegicus)
Allele/Variant
Source: rs199221109
Genes: Lrrc73 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)9:14729553T>G

Allele/Variant
Source: rs583874552
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46564523T>C