Version: 8.0.0
Date: Tue Jan 28 2025
6,445 results for lrriq1

lrriq1

(Danio rerio)
Gene
Name: leucine-rich repeats and IQ motif containing 1
Synonyms: si:ch211-154h20.2
Source: ZFIN:ZDB-GENE-050419-235
Biotype: protein coding gene
Symbol: lrriq1 (Dre)
Symbol: lrriq1
Automated Gene Synopsis: Orthologous to human LRRIQ1 (leucine rich repeats and IQ motif containing 1).
Strict Orthology Symbols: lrriq1

Lrriq1

(Rattus norvegicus)
Gene
Name: leucine-rich repeats and IQ motif containing 1
Synonyms: LOC299759, similar to leucine-rich repeats and IQ motif containing 1, leucine-rich repeat and IQ domain-containing protein 1, RGD1564903
Source: RGD:1564903
Biotype: protein coding gene
Symbol: Lrriq1 (Rno)
Symbol: Lrriq1
Gene Synopsis: Orthologous to human LRRIQ1 (leucine rich repeats and IQ motif containing 1); INTERACTS WITH bisphenol
Automated Gene Synopsis: Orthologous to human LRRIQ1 (leucine rich repeats and IQ motif containing 1).
Strict Orthology Symbols: lrriq1

Lrriq1

(Mus musculus)
Gene
Name: leucine-rich repeats and IQ motif containing 1
Synonyms: Gm1557, gene model 1557, (NCBI), predicted gene 1557, RIKEN cDNA 4930503E15 gene, 4930503E15Rik, LOC380658, RGD1564903
Source: MGI:1922228
Biotype: protein coding gene
Symbol: Lrriq1 (Mmu)
Symbol: Lrriq1
Automated Gene Synopsis: Orthologous to human LRRIQ1 (leucine rich repeats and IQ motif containing 1).
Strict Orthology Symbols: lrriq1
Alleles: Lrriq1 (Mmu)...Lrriq1 (Mmu)...Lrriq1 (Mmu)

LRRIQ1

(Homo sapiens)
Gene
Name: leucine rich repeats and IQ motif containing 1
Synonyms: testicular tissue protein Li 111, RP11-193M21.1, leucine-rich repeats and IQ motif containing 1, FLJ12303, leucine-rich repeat and IQ domain-containing protein 1
Source: HGNC:25708
Biotype: protein coding gene
Symbol: LRRIQ1 (Hsa)
Symbol: LRRIQ1
Strict Orthology Symbols: lrriq1

lrriq1

(Xenopus tropicalis)
Gene
Name: leucine-rich repeats and IQ motif containing 1
Synonyms: lrriq1, leucine-rich repeats and IQ motif containing 1
Source: Xenbase:XB-GENE-6468255
Biotype: gene
Symbol: lrriq1
Symbol: lrriq1 (Xtr)
Automated Gene Synopsis: Orthologous to human LRRIQ1 (leucine rich repeats and IQ motif containing 1).
Synonyms: lrriq1...lrriq1...lrriq1
Strict Orthology Symbols: lrriq1

lrriq1.L

(Xenopus laevis)
Gene
Name: leucine-rich repeats and IQ motif containing 1
Synonyms: lrriq1.L, leucine-rich repeats and IQ motif containing 1
Source: Xenbase:XB-GENE-17341937
Biotype: gene
Symbol: lrriq1.L (Xla)
Automated Gene Synopsis: Orthologous to human LRRIQ1 (leucine rich repeats and IQ motif containing 1).
Strict Orthology Symbols: lrriq1
Symbol: lrriq1.L

Lrriq1em1Cya

(Mus musculus)
Allele/Variant
Source: MGI:7584868
Genes: Lrriq1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Lrriq1 (Mmu)
Genes: Lrriq1 (Mmu)
Symbol: Lrriq1em1Cya

Lrriq1em3Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7301790
Genes: Lrriq1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Lrriq1 (Mmu)
Genes: Lrriq1 (Mmu)
Symbol: Lrriq1em3Gpt

Lrriq1em1Ysato

(Mus musculus)
Allele/Variant
Source: MGI:7711345
Genes: Lrriq1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Lrriq1 (Mmu)
Genes: Lrriq1 (Mmu)
Symbol: Lrriq1em1Ysato

Lrriq1em1Ysato/Lrriq1em1Ysato [background:] C57BL/6N-Lrriq1em1Ysato

(Mus musculus)
Model
Id: MGI:7711347
Synonyms: Not Available
Symbol: Lrriq1/Lrriq1 [background:] C57BL/6N-Lrriq1 (Mmu)
Genes: Lrriq1 (Mmu)
Alleles: Lrriq1 (Mmu)
Name: Lrriq1/Lrriq1 [background:] C57BL/6N-Lrriq1

sa1898

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-161003-10476
Genes: lrriq1 (Dre)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Genes: lrriq1 (Dre)

microtubule cytoskeleton

Gene Ontology
Source: GO:0015630
Synonyms: Not Available
Branch: cellular component
Genes: Lrriq1 (Rno)...lrriq1 (Dre)...Lrriq1 (Mmu)

regulation of signal transduction

Gene Ontology
Source: GO:0009966
Synonyms:
  • regulation of signaling pathway
  • regulation of signalling pathway
Branch: biological process
Genes: LRRIQ1 (Hsa)

biological_process

Gene Ontology
Source: GO:0008150
Synonyms:
  • biological process
  • physiological process
Branch: biological process
Genes: Lrriq1 (Mmu)

molecular_function

Gene Ontology
Source: GO:0003674
Synonyms:
  • molecular function
Branch: molecular function
Genes: Lrriq1 (Mmu)

(GRCh38)12:85047357C>G

(Homo sapiens)
Allele/Variant
Source: rs766173852
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85047357C>G

(GRCh38)12:85047439T>C

(Homo sapiens)
Allele/Variant
Source: rs142687579
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85047439T>C

(GRCh38)12:85055580G>A

(Homo sapiens)
Allele/Variant
Source: rs112921634
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85055580G>A

(GRCh38)12:85055751G>A

(Homo sapiens)
Allele/Variant
Source: rs772693447
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85055751G>A

(GRCh38)12:85056630T>A

(Homo sapiens)
Allele/Variant
Source: rs1303911195
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85056630T>A

(GRCh38)12:85056723G>A

(Homo sapiens)
Allele/Variant
Source: rs762250297
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85056723G>A

(GRCh38)12:85065379A>T

(Homo sapiens)
Allele/Variant
Source: NC_000012.12:g.85065379A>T
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85065379A>T

(GRCh38)12:85046065G>T

(Homo sapiens)
Allele/Variant
Source: rs781016761
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85046065G>T

(GRCh38)12:85056034A>G

(Homo sapiens)
Allele/Variant
Source: rs755969062
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85056034A>G

(GRCh38)12:85056513A>G

(Homo sapiens)
Allele/Variant
Source: rs200192265
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85056513A>G

(GRCh38)12:85046087T>C

(Homo sapiens)
Allele/Variant
Source: rs140252116
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85046087T>C

(GRCh38)12:85052240A>C

(Homo sapiens)
Allele/Variant
Source: rs61740062
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85052240A>C

(GRCh38)12:85055933C>A

(Homo sapiens)
Allele/Variant
Source: rs754722038
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85055933C>A

(GRCh38)12:85056796A>G

(Homo sapiens)
Allele/Variant
Source: rs1203544550
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85056796A>G

(GRCh38)12:85046065G>A

(Homo sapiens)
Allele/Variant
Source: rs781016761
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85046065G>A

(GRCh38)12:85066755A>G

(Homo sapiens)
Allele/Variant
Source: rs201707498
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85066755A>G

(GRCh38)12:85244910G>C

(Homo sapiens)
Allele/Variant
Source: rs759423232
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, splice_donor_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85244910G>C

(GRCh38)12:85055679G>A

(Homo sapiens)
Allele/Variant
Source: rs781405194
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85055679G>A

(GRCh38)12:85055779G>A

(Homo sapiens)
Allele/Variant
Source: rs200640188
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85055779G>A

(GRCh38)12:85056651A>G

(Homo sapiens)
Allele/Variant
Source: rs371965033
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85056651A>G

(GRCh38)12:85055800G>T

(Homo sapiens)
Allele/Variant
Source: rs756097902
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85055800G>T

(GRCh38)12:85056049A>C

(Homo sapiens)
Allele/Variant
Source: NC_000012.12:g.85056049A>C
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85056049A>C

(GRCh38)12:85055896A>G

(Homo sapiens)
Allele/Variant
Source: rs775801562
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85055896A>G

(GRCh38)12:85044802T>C

(Homo sapiens)
Allele/Variant
Source: rs374855317
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, stop_lost
Diseases: Not Available
Variant Name: (GRCh38)12:85044802T>C

(GRCh38)12:85056165A>G

(Homo sapiens)
Allele/Variant
Source: rs1239650105
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85056165A>G

(GRCh38)12:85056484G>A

(Homo sapiens)
Allele/Variant
Source: rs762937434
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85056484G>A

(GRCh38)12:85056636T>C

(Homo sapiens)
Allele/Variant
Source: rs1331226552
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85056636T>C

(GRCh38)12:85153737A>G

(Homo sapiens)
Allele/Variant
Source: rs746399504
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85153737A>G

(GRCh38)12:85153746T>C

(Homo sapiens)
Allele/Variant
Source: NC_000012.12:g.85153746T>C
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85153746T>C

(GRCh38)12:85229609G>A

(Homo sapiens)
Allele/Variant
Source: rs371519477
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85229609G>A

(GRCh38)12:85160647T>G

(Homo sapiens)
Allele/Variant
Source: rs761433062
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85160647T>G

(GRCh38)12:85244847G>A

(Homo sapiens)
Allele/Variant
Source: rs370803858
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85244847G>A

(GRCh38)12:85153694G>C

(Homo sapiens)
Allele/Variant
Source: NC_000012.12:g.85153694G>C
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85153694G>C

(GRCh38)12:85244814C>T

(Homo sapiens)
Allele/Variant
Source: rs376086109
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85244814C>T

(GRCh38)12:85055945A>G

(Homo sapiens)
Allele/Variant
Source: rs539161034
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85055945A>G