Version: 8.0.0
Date: Tue Jan 28 2025
8,186 results for loxhd1

LOXHD1

(Homo sapiens)
Gene
Name: lipoxygenase homology PLAT domains 1
Synonyms: LH2D1, FLJ32670, lipoxygenase homology domains 1, lipoxygenase homology domain-containing protein 1, DFNB77
Source: HGNC:26521
Biotype: protein coding gene
Symbol: LOXHD1 (Hsa)
Symbol: LOXHD1
Strict Orthology Symbols: loxhd1.L...loxhd1b...Loxhd1...loxhd1a

Loxhd1

(Mus musculus)
Gene
Name: lipoxygenase homology domains 1
Synonyms: RIKEN cDNA 1700096C21 gene, sba, 1700096C21Rik, samba
Source: MGI:1914609
Biotype: protein coding gene
Symbol: Loxhd1 (Mmu)
Symbol: Loxhd1
Automated Gene Synopsis: Orthologous to human LOXHD1 (lipoxygenase homology PLAT domains 1).
Strict Orthology Symbols: LOXHD1...loxhd1b...Loxhd1...loxhd1a
Alleles: Loxhd1 (Mmu)...Loxhd1 (Mmu)...Loxhd1 (Mmu)...Loxhd1 (Mmu)...Loxhd1 (Mmu)

Loxhd1

(Rattus norvegicus)
Gene
Name: lipoxygenase homology PLAT domains 1
Synonyms: similar to lipoxygenase homology domains 1, LOC291427, lipoxygenase homology domains 1, lipoxygenase homology domain-containing protein 1
Source: RGD:1304815
Biotype: protein coding gene
Symbol: Loxhd1 (Rno)
Symbol: Loxhd1
Gene Synopsis: Orthologous to human LOXHD1 (lipoxygenase homology PLAT domains 1); INTERACTS WITH 2,3,7,8-tetrachlorodibenzodioxine
Automated Gene Synopsis: Orthologous to human LOXHD1 (lipoxygenase homology PLAT domains 1).
Strict Orthology Symbols: LOXHD1...loxhd1b...Loxhd1...loxhd1a

loxhd1b

(Danio rerio)
Gene
Name: lipoxygenase homology PLAT domains 1b
Synonyms: si:dkey-210e6.2
Source: ZFIN:ZDB-GENE-081104-370
Biotype: protein coding gene
Symbol: loxhd1b (Dre)
Automated Gene Synopsis: Orthologous to human LOXHD1 (lipoxygenase homology PLAT domains 1).
Strict Orthology Symbols: LOXHD1...Loxhd1
Symbol: loxhd1b

loxhd1a

(Danio rerio)
Gene
Name: lipoxygenase homology PLAT domains 1a
Synonyms: si:ch211-14i19.1, loxhd1
Source: ZFIN:ZDB-GENE-091112-20
Biotype: protein coding gene
Symbol: loxhd1a (Dre)
Automated Gene Synopsis: Orthologous to human LOXHD1 (lipoxygenase homology PLAT domains 1).
Synonyms: loxhd1...loxhd1...loxhd1
Strict Orthology Symbols: LOXHD1...Loxhd1
Symbol: loxhd1a

loxhd1

(Xenopus tropicalis)
Gene
Name: lipoxygenase homology PLAT domains 1
Synonyms: lh2d1, LOC108705494, dfnb77, lipoxygenase homology PLAT domains 1, loxhd1
Source: Xenbase:XB-GENE-6467524
Biotype: gene
Symbol: loxhd1 (Xtr)
Symbol: loxhd1
Synonyms: loxhd1...loxhd1...loxhd1
Strict Orthology Symbols: loxhd1.L

loxhd1.L

(Xenopus laevis)
Gene
Name: lipoxygenase homology PLAT domains 1
Synonyms: loxhd1.L, lh2d1, dfnb77, LOC108705494, lipoxygenase homology PLAT domains 1
Source: Xenbase:XB-GENE-17332055
Biotype: gene
Symbol: loxhd1.L (Xla)
Automated Gene Synopsis: Orthologous to human LOXHD1 (lipoxygenase homology PLAT domains 1).
Strict Orthology Symbols: loxhd1
Symbol: loxhd1.L

Loxhd1sba

(Mus musculus)
Allele/Variant
Source: MGI:3708447
Genes: Loxhd1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Loxhd1 (Mmu)
Genes: Loxhd1 (Mmu)
Symbol: Loxhd1sba

Loxhd1mpc231H

(Mus musculus)
Allele/Variant
Source: MGI:5792077
Genes: Loxhd1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Loxhd1 (Mmu)
Genes: Loxhd1 (Mmu)
Symbol: Loxhd1mpc231H

Loxhd1tm1.1Ngt

(Mus musculus)
Allele/Variant
Source: MGI:6696448
Genes: Loxhd1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Loxhd1 (Mmu)
Genes: Loxhd1 (Mmu)
Symbol: Loxhd1tm1.1Ngt

Loxhd1em1Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7301705
Genes: Loxhd1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Loxhd1 (Mmu)
Genes: Loxhd1 (Mmu)
Symbol: Loxhd1em1Gpt

Loxhd1mpc188H

(Mus musculus)
Allele/Variant
Source: MGI:5792020
Genes: Loxhd1 (Mmu)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: Not Available
Symbol: Loxhd1 (Mmu)
Genes: Loxhd1 (Mmu)
Symbol: Loxhd1mpc188H

Loxhd1mpc188H/Loxhd1mpc188H [background:] involves: BALB/c * C3H/HeH * C57BL/6J

(Mus musculus)
Model
Id: MGI:5792354
Synonyms: Not Available
Symbol: Loxhd1/Loxhd1 [background:] involves: BALB/c * C3H/HeH * C57BL/6J (Mmu)
Genes: Loxhd1 (Mmu)
Alleles: Loxhd1 (Mmu)
Name: Loxhd1/Loxhd1 [background:] involves: BALB/c * C3H/HeH * C57BL/6J

Loxhd1sba/Loxhd1sba [background:] involves: C57BL/6J

(Mus musculus)
Model
Id: MGI:3709046
Synonyms: Not Available
Symbol: Loxhd1/Loxhd1 [background:] involves: C57BL/6J (Mmu)
Genes: Loxhd1 (Mmu)
Alleles: Loxhd1 (Mmu)
Name: Loxhd1/Loxhd1 [background:] involves: C57BL/6J

Loxhd1mpc231H/Loxhd1mpc231H [background:] involves: BALB/c * C3H/HeH * C57BL/6J

(Mus musculus)
Model
Id: MGI:5792355
Synonyms: Not Available
Symbol: Loxhd1/Loxhd1 [background:] involves: BALB/c * C3H/HeH * C57BL/6J (Mmu)
Genes: Loxhd1 (Mmu)
Alleles: Loxhd1 (Mmu)
Name: Loxhd1/Loxhd1 [background:] involves: BALB/c * C3H/HeH * C57BL/6J

F27C1.11

(Caenorhabditis elegans)
Gene
Name: Doublecortin domain-containing protein
Synonyms: CELE_F27C1.11
Source: WB:WBGene00017858
Biotype: protein coding gene
Gene Synopsis: Is an ortholog of human LOXHD1 (lipoxygenase homology PLAT domains 1).
Automated Gene Synopsis: Orthologous to human LOXHD1 (lipoxygenase homology PLAT domains 1).
Strict Orthology Symbols: LOXHD1...Loxhd1

autosomal recessive nonsyndromic deafness 77

Disease
Source: DOID:0110525
Definition: An autosomal recessive nonsyndromic deafness that is characterized by postlingual onset with moderate to profound, progressive hearing loss and has_material_basis_in mutation in the LOXHD1 gene on chromosome 18q21.
Genes: loxhd1b (Dre)...loxhd1.L (Xla)...Loxhd1 (Rno)...Loxhd1 (Mmu)...LOXHD1 (Hsa)

Fuchs' endothelial dystrophy

Disease
Source: DOID:11555
Definition: A corneal dystrophy characterized by accumulation of focal outgrowths (guttae) and thickening of Descemet's membrane, leading to corneal edema and loss of vision.
Genes: loxhd1.L (Xla)...loxhd1b (Dre)...LOXHD1 (Hsa)...loxhd1a (Dre)...Loxhd1 (Rno)

orofacial cleft

Disease
Source: DOID:0050567
Definition: A physical disorder that is characterized by cleft lip and/or cleft palate that result in feeding, speech and hearing problems caused by failures during development.
Genes: loxhd1b (Dre)...LOXHD1 (Hsa)...Loxhd1 (Rno)...Loxhd1 (Mmu)...loxhd1a (Dre)

stereocilium

Gene Ontology
Source: GO:0032420
Synonyms: Not Available
Branch: cellular component
Genes: LOXHD1 (Hsa)...Loxhd1 (Rno)...Loxhd1 (Mmu)

sensory perception of sound

Gene Ontology
Source: GO:0007605
Synonyms:
  • hearing
  • perception of sound
Branch: biological process
Genes: Loxhd1 (Rno)...Loxhd1 (Mmu)...LOXHD1 (Hsa)

cell projection

Gene Ontology
Source: GO:0042995
Synonyms:
  • cell process
  • cellular process
Branch: cellular component
Genes: LOXHD1 (Hsa)

sa41097

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-160601-7164
Genes: loxhd1b (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: loxhd1b (Dre)

sa31624

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-160601-1148
Genes: loxhd1b (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: Not Available
Genes: loxhd1b (Dre)

biological_process

Gene Ontology
Source: GO:0008150
Synonyms:
  • biological process
  • physiological process
Branch: biological process
Genes: Loxhd1 (Rno)

(GRCh38)18:46560063A>C

(Homo sapiens)
Allele/Variant
Source: rs2365338
Genes: LOXHD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)18:46560063A>C

(GRCh38)18:46560072G>A

(Homo sapiens)
Allele/Variant
Source: rs763038988
Genes: LOXHD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)18:46560072G>A

(GRCh38)18:46592589G>A

(Homo sapiens)
Allele/Variant
Source: NC_000018.10:g.46592589G>A
Genes: LOXHD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)18:46592589G>A

(GRCh38)18:46563234G>A

(Homo sapiens)
Allele/Variant
Source: rs886053834
Genes: LOXHD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)18:46563234G>A

(GRCh38)18:46592575G>A

(Homo sapiens)
Allele/Variant
Source: rs189622061
Genes: LOXHD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)18:46592575G>A

(GRCh38)18:46601200C>T

(Homo sapiens)
Allele/Variant
Source: rs780454307
Genes: LOXHD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)18:46601200C>T

(GRCh38)18:46518218A>T

(Homo sapiens)
Allele/Variant
Source: NC_000018.10:g.46518218A>T
Genes: LOXHD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)18:46518218A>T

(GRCh38)18:46477511C>T

(Homo sapiens)
Allele/Variant
Source: rs115835484
Genes: LOXHD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)18:46477511C>T

(GRCh38)18:46477888C>T

(Homo sapiens)
Allele/Variant
Source: rs766184517
Genes: LOXHD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)18:46477888C>T

(GRCh38)18:46477644C>T

(Homo sapiens)
Allele/Variant
Source: rs955408829
Genes: LOXHD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)18:46477644C>T

(GRCh38)18:46572164T>C

(Homo sapiens)
Allele/Variant
Source: NC_000018.10:g.46572164T>C
Genes: LOXHD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, splice_acceptor_variant
Diseases: Not Available
Variant Name: (GRCh38)18:46572164T>C

(GRCh38)18:46563238G>A

(Homo sapiens)
Allele/Variant
Source: rs578232367
Genes: LOXHD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)18:46563238G>A

(GRCh38)18:46560082C>T

(Homo sapiens)
Allele/Variant
Source: rs537227442
Genes: LOXHD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, splice_donor_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)18:46560082C>T

(GRCh38)18:46594365A>G

(Homo sapiens)
Allele/Variant
Source: rs1203046811
Genes: LOXHD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)18:46594365A>G

(GRCh38)18:46601283G>T

(Homo sapiens)
Allele/Variant
Source: rs2144283144
Genes: LOXHD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)18:46601283G>T

(GRCh38)18:46594590C>T

(Homo sapiens)
Allele/Variant
Source: rs328144
Genes: LOXHD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)18:46594590C>T

(GRCh38)18:46601215A>G

(Homo sapiens)
Allele/Variant
Source: rs1599040620
Genes: LOXHD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, splice_donor_variant
Diseases: Not Available
Variant Name: (GRCh38)18:46601215A>G

(GRCh38)18:46593651G>C

(Homo sapiens)
Allele/Variant
Source: rs750264813
Genes: LOXHD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)18:46593651G>C

(GRCh38)18:46593660A>T

(Homo sapiens)
Allele/Variant
Source: rs755819004
Genes: LOXHD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)18:46593660A>T

(GRCh38)18:46593714A>G

(Homo sapiens)
Allele/Variant
Source: NC_000018.10:g.46593714A>G
Genes: LOXHD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)18:46593714A>G

(GRCh38)18:46533262C>T

(Homo sapiens)
Allele/Variant
Source: rs2144266552
Genes: LOXHD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)18:46533262C>T

(GRCh38)18:46533271A>G

(Homo sapiens)
Allele/Variant
Source: NC_000018.10:g.46533271A>G
Genes: LOXHD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)18:46533271A>G

(GRCh38)18:46538145A>G

(Homo sapiens)
Allele/Variant
Source: NC_000018.10:g.46538145A>G
Genes: LOXHD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)18:46538145A>G

(GRCh38)18:46538171G>A

(Homo sapiens)
Allele/Variant
Source: NC_000018.10:g.46538171G>A
Genes: LOXHD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)18:46538171G>A

(GRCh38)18:46547070G>C

(Homo sapiens)
Allele/Variant
Source: NC_000018.10:g.46547070G>C
Genes: LOXHD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)18:46547070G>C