820 results for lhx8

Lhx8

(Rattus norvegicus)
Gene
Name: LIM homeobox 8
Synonyms: LIM/homeobox protein Lhx8, MGC109530, LOC365963, LIM homeobox protein 8, Lhx7
Source: RGD:1308749
Biotype: protein coding gene
Symbol: Lhx8 (Rno)
Symbol: Lhx8
Gene Synopsis: Orthologous to human LHX8 (LIM homeobox 8); INTERACTS WITH 1-naphthyl isothiocyanate; 17beta-estradiol
Automated Gene Synopsis: Orthologous to human LHX8 (LIM homeobox 8).
Synonyms: LIM/homeobox protein Lhx8
Strict Orthology Symbols: lhx8

Lhx8

(Mus musculus)
Gene
Name: LIM homeobox protein 8
Synonyms: L3, Lhx7
Source: MGI:1096343
Biotype: protein coding gene
Symbol: Lhx8 (Mmu)
Symbol: Lhx8
Automated Gene Synopsis: Orthologous to human LHX8 (LIM homeobox 8).
Strict Orthology Symbols: lhx8
Alleles: Lhx8 (Mmu)...Lhx8 (Mmu)...Lhx8 (Mmu)...Lhx8 (Mmu)...Lhx8 (Mmu)

LHX8

(Homo sapiens)
Gene
Name: LIM homeobox 8
Synonyms: LIM/homeobox protein Lhx8, LIM-homeodomain protein Lhx8, LIM homeobox protein 8, Lhx7
Source: HGNC:28838
Biotype: protein coding gene
Symbol: LHX8 (Hsa)
Symbol: LHX8
Synonyms: LIM/homeobox protein Lhx8...LIM-homeodomain protein Lhx8
Strict Orthology Symbols: lhx8

lhx8

(Xenopus tropicalis)
Gene
Name: LIM homeobox 8
Synonyms: x-Lhx7, LIM homeobox 8, lhx7, lhx8
Source: Xenbase:XB-GENE-494997
Biotype: gene
Symbol: lhx8 (Xtr)
Symbol: lhx8
Automated Gene Synopsis: Orthologous to human LHX8 (LIM homeobox 8).
Synonyms: lhx8...lhx8...lhx8
Strict Orthology Symbols: lhx8.L...lhx8a...Lhx8...lhx8.S...LHX8

lhx8a

(Danio rerio)
Gene
Name: LIM homeobox 8a
Synonyms: wu:fk78g12, fk78g12, cb875, lhx7, lhx8
Source: ZFIN:ZDB-GENE-031008-2
Biotype: protein coding gene
Symbol: lhx8a (Dre)
Automated Gene Synopsis: Orthologous to human LHX8 (LIM homeobox 8).
Synonyms: lhx8...lhx8...lhx8
Strict Orthology Symbols: lhx8
Symbol: lhx8a

LHX8-AS1

(Homo sapiens)
Gene
Name: LHX8 antisense RNA 1
Synonyms: Not Available
Source: HGNC:41213
Biotype: ncRNA gene
Symbol: LHX8-AS1 (Hsa)
Symbol: LHX8-AS1

lhx8.L

(Xenopus laevis)
Gene
Name: LIM homeobox 8
Synonyms: x-Lhx7, lhx8.L, LIM homeobox 8, lhx7
Source: Xenbase:XB-GENE-866406
Biotype: gene
Symbol: lhx8.L (Xla)
Automated Gene Synopsis: Orthologous to human LHX8 (LIM homeobox 8).
Strict Orthology Symbols: lhx8
Symbol: lhx8.L

lhx8.S

(Xenopus laevis)
Gene
Name: LIM homeobox 8
Synonyms: x-Lhx7, LIM homeobox 8, lhx7, lhx8.S
Source: Xenbase:XB-GENE-17335912
Biotype: gene
Symbol: lhx8.S (Xla)
Automated Gene Synopsis: Orthologous to human LHX8 (LIM homeobox 8).
Strict Orthology Symbols: lhx8
Symbol: lhx8.S

lhx8b

(Danio rerio)
Gene
Name: LIM homeobox 8b
Synonyms: si:dkey-267j14.2
Source: ZFIN:ZDB-GENE-081105-153
Biotype: protein coding gene
Symbol: lhx8b (Dre)
Symbol: lhx8b

Lhx8em2Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7301637
Genes: Lhx8 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Lhx8 (Mmu)
Genes: Lhx8 (Mmu)
Symbol: Lhx8em2Gpt

Lhx8tm1Awan

(Mus musculus)
Allele/Variant
Source: MGI:3588411
Genes: Lhx8 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Lhx8 (Mmu)
Genes: Lhx8 (Mmu)
Symbol: Lhx8tm1Awan

Lhx8tm1Lmgd

(Mus musculus)
Allele/Variant
Source: MGI:2182594
Genes: Lhx8 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Lhx8 (Mmu)
Genes: Lhx8 (Mmu)
Symbol: Lhx8tm1Lmgd

Lhx8tm1Vpa

(Mus musculus)
Allele/Variant
Source: MGI:3603531
Genes: Lhx8 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Lhx8 (Mmu)
Genes: Lhx8 (Mmu)
Symbol: Lhx8tm1Vpa

Lhx8tm1(cre)Grsr

(Mus musculus)
Allele/Variant
Source: MGI:5564768
Genes: Lhx8 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Lhx8 (Mmu)
Genes: Lhx8 (Mmu)
Symbol: Lhx8tm1(cre)Grsr
Construct Regulatory Region: Lhx8 (Mmu)
Constructs: Lhx8< construct

Lhx8tm2.1Vpa

(Mus musculus)
Allele/Variant
Source: MGI:5314801
Genes: Lhx8 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Lhx8 (Mmu)
Genes: Lhx8 (Mmu)
Symbol: Lhx8tm2.1Vpa

Id: MGI:5314802
Synonyms: Not Available
Symbol: Lhx8/Lhx8 Tmem163/0 [background:] involves: 129P2/OlaHsd * 129S4
Genes: Lhx8 (Mmu)
Alleles: Lhx8 (Mmu)
Name: Lhx8/Lhx8 Tmem163/0 [background:] involves: 129P2/OlaHsd * 129S4

Id: MGI:5314803
Synonyms: Not Available
Symbol: Lhx8/Lhx8 Tg(Chat-cre)GM24Gsat/0 [background:] involves: 129P2/OlaHsd * 129S4/SvJae
Genes: Lhx8 (Mmu)
Alleles: Lhx8 (Mmu)
Name: Lhx8/Lhx8 Tg(Chat-cre)GM24Gsat/0 [background:] involves: 129P2/OlaHsd * 129S4/SvJae

Id: MGI:3607081
Synonyms: Not Available
Symbol: Lhx8/Lhx8 [background:] B6.Cg-Lhx8 (Mmu)
Genes: Lhx8 (Mmu)
Alleles: Lhx8 (Mmu)
Name: Lhx8/Lhx8 [background:] B6.Cg-Lhx8

Id: MGI:7259843
Synonyms: Not Available
Symbol: Lhx8/Lhx8 [background:] involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6 (
Genes: Lhx8 (Mmu)
Alleles: Lhx8 (Mmu)
Name: Lhx8/Lhx8 [background:] involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6

Id: MGI:3590315
Synonyms: Not Available
Symbol: Lhx8/Lhx8 [background:] involves: 129S2/SvPas * C57BL/6J (Mmu)
Genes: Lhx8 (Mmu)
Alleles: Lhx8 (Mmu)
Name: Lhx8/Lhx8 [background:] involves: 129S2/SvPas * C57BL/6J

Id: MGI:7259871
Synonyms: Not Available
Symbol: Lhx8/Lhx8 [background:] involves: 129 * C57BL/6 (Mmu)
Genes: Lhx8 (Mmu)
Alleles: Lhx8 (Mmu)
Name: Lhx8/Lhx8 [background:] involves: 129 * C57BL/6

High-Throughput (HTP) Dataset Index metadata provided by MGI
ID: ArrayExpress:GSE109473
Tags: WT vs. mutant, developmental stage, genotype
Summary: Following proliferation of oogonia inmammals, great numbers of germ cells are discarded, primarily by apoptosis, while the remainder form primordial follicles (the ovarian reserve) that determine fertility and reproductive lifespan. More massive, rapid, and essentially total loss of oocytes, however, occurs when the transcription factor Lhx8 is ablated--though the cause and mechanism of germ cell loss from the Lhx8-/- ovaries has been unknown. We found that Lhx8-/- ovaries maintain the same number of germ cells throughout embryonic development; rapid decrease in the pool of oocytes starts shortly before birth. The loss results from activation of autophagy, which becomes overwhelming within the first postnatal week, with extracellular matrix proteins filling the space previously occupied by follicles to produce a fibrotic ovary. Associated with this process, as early as a few days before birth, Lhx8-/- oocytes failed to repair DNA damage--which normally occurs when meiosis is initiated during embryonic development; and DNA damage repair genes were downregulated throughout the oocyte short lifespan. Based on gene expression analyses and morphological changes, we propose a model in which lineage-restricted failure of DNA repair triggers germ cell autophagy, causing premature depletion of the ovarian reserve in Lhx8-/- mice Gonadal tissue was obtained from postnatal day 0 (P0) and P7 wildtype (WT) and Lhx8 knockout (KO) mice, with three biological replicates per genotype and time point.
Symbol: Lhx8 ablation leads to massive autophagy of mouse oocytes associated with DNA damage
Name: Lhx8 ablation leads to massive autophagy of mouse oocytes associated with DNA damage

Id: MGI:3040868
Synonyms: Not Available
Symbol: Lhx8/Lhx8 [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 (Mmu)
Genes: Lhx8 (Mmu)
Alleles: Lhx8 (Mmu)
Name: Lhx8/Lhx8 [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6

lim-4

(Caenorhabditis elegans)
Gene
Name: LIM domain family 4
Synonyms: ZC64.4, CELE_ZC64.4, nss-1
Source: WB:WBGene00002987
Biotype: protein coding gene
Automated Gene Synopsis: Orthologous to human LHX6 (LIM homeobox 6) and LHX8 (LIM homeobox 8).
Strict Orthology Symbols: lhx8

Awh

(Drosophila melanogaster)
Gene
Name: Arrowhead
Synonyms: l(3)63Ea, lethal(3)63Ea, awh, l(3)63Ea/Awh, l(3)64Ea, l(3)SH9, CG1072, arrowhead, l63Ea
Source: FB:FBgn0013751
Biotype: protein coding gene
Automated Gene Synopsis: Orthologous to human LHX6 (LIM homeobox 6) and LHX8 (LIM homeobox 8).
Strict Orthology Symbols: lhx8

PXL1

(Saccharomyces cerevisiae)
Gene
Name: PaXillin-Like protein
Synonyms: YKR090W
Source: SGD:S000001798
Biotype: protein coding gene
Strict Orthology Symbols: lhx8

Source: GO:0021884
Synonyms: Not Available
Branch: biological process
Genes: Lhx8 (Mmu)...Lhx8 (Rno)...lhx8a (Dre)...LHX8 (Hsa)

Source: GO:0021879
Synonyms: Not Available
Branch: biological process
Genes: Lhx8 (Mmu)...Lhx8 (Rno)...LHX8 (Hsa)

la014804Tg

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-120806-8532
Genes: lhx8a (Dre)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: lhx8
Genes: lhx8a (Dre)

Source: GO:0001674
Synonyms:
  • female germ-cell nucleus
Branch: cellular component
Genes: Lhx8 (Mmu)...Lhx8 (Rno)...LHX8 (Hsa)

High-Throughput (HTP) Dataset Index metadata provided by MGI
ID: ArrayExpress:E-GEOD-7774, GEO:GSE7774
Tags: WT vs. mutant
Summary: Lhx8 is a homeobox gene expressed in oocytes and critical in oogenesis. Lhx8 deficiency leads to rapid loss of postnatal oocytes. Early oocyte differentiation is poorly understood. We hypothesized that lack of Lhx8 perturbs global expression of genes preferentially expressed in oocytes. We compared Lhx8 knockout and wild type ovaries using Affymetrix 430 2.0 microarray platform. Experiment Overall Design: Each array was hybridized with cRNA produced from pooled total RNA from at least 25 specimens. The experiment was performed with 3 replicates. The results from these three arrays was compared to arrays hybridized with cRNA produced from pooled total RNA from at least 25 wild type specimens of the same genetic background.
Symbol: Transcription profiling of mouse ovaries from Lhx8 Null newborns
Name: Transcription profiling of mouse ovaries from Lhx8 Null newborns

High-Throughput (HTP) Dataset Index metadata provided by MGI
ID: ArrayExpress:GSE139966
Tags: WT vs. mutant, developmental stage, genotype
Summary: Germ-cell transcription factors control gene networks that regulate primordial follicle formation and oocyte differentiation during early, postnatal mouse oogenesis. Taking advantage of gene-edited mice lacking transcription factors expressed in female germ cells, we analyzed global gene expression profiles in perinatal ovaries from wildtype, FiglaNull, Lhx8Null and SohlhNull mice. Figla deficiency dysregulates expression of meiosis-related genes (e.g., Sycp3, Rad51 and Msy2) and a variety of genes (e.g., Nobox, Lhx8, Taf4b, Sohlh1, Sohlh2 and Gdf9) associated with oocyte growth and differentiation. The absence of FIGLA significantly impedes meiotic progression, causes DNA damage and results in oocyte apoptosis. Moreover, we find that FIGLA and other transcriptional regulators (e.g., NOBOX, LHX8, SOHLH1 and SOHLH2) are co-expressed in the same subset of germ cells in perinatal ovaries and Figla ablation dramatically disrupts KIT, NOBOX, LHX8, SOHLH1 and SOHLH2 expression. In addition, not only do FIGLA, SOHLH1 and LHX8 cross-regulate each other, they also cooperate by direct interaction with each during early oocyte development and share downstream gene targets. Thus, our findings substantiate a major role for FIGLA, LHX8 and SOHLH1 as multifunctional regulators of networks necessary for oocyte maintenance and differentiation during early folliculogenesis. RNA-seq was performed using embryonic day 18.5 (E18.5) or postnatal day 0 (P0) ovaires between control and Figla knockout mice in order to identify the differentially expressed genes. RNA-seq was performed using P0 ovaires between control and Lhx8 knockout mice in order to identify the differentially expressed genes.
Symbol: FIGLA, LHX8 and SOHLH1 transcription factor networks regulate mouse oocyte growth and differentiation
Name: FIGLA, LHX8 and SOHLH1 transcription factor networks regulate mouse oocyte growth and differentiation

Source: GO:0008585
Synonyms:
  • ovarian development
  • ovary development
Branch: biological process
Genes: Lhx8 (Mmu)...Lhx8 (Rno)...LHX8 (Hsa)

Tg(Lhx8-EGFP)MJ80Gsat

(Mus musculus)
Allele/Variant
Source: MGI:4940659
Genes: Not Available
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Tg(Lhx8-EGFP)MJ80Gsat

Source: GO:0042475
Synonyms:
  • odontogenesis of dentine-containing teeth
  • odontogenesis of dentine-containing tooth
Branch: biological process
Genes: Lhx8 (Mmu)...Lhx8 (Rno)...LHX8 (Hsa)

Gene Ontology
Source: GO:0007611
Synonyms: Not Available
Branch: biological process
Genes: Lhx8 (Mmu)...Lhx8 (Rno)...LHX8 (Hsa)

Tg(Lhx8-icre)1Kess

(Mus musculus)
Allele/Variant
Source: MGI:7490134
Genes: Not Available
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Tg(Lhx8-icre)1Kess
Construct Regulatory Region: Lhx8 (Mmu)

High-Throughput (HTP) Dataset Index metadata provided by MGI
ID: ArrayExpress:GSE99049
Tags: WT vs. mutant, genotype
Summary: In the mammalian cortex, about 60% of GABAergic interneurons, mainly including parvalbumin-expressing (PV+) and somatostatin (SST+) interneurons are generated from the medial ganglionic eminence (MGE) in the subpallium and tangentially migrate to the cortex. Here we analyze the role of the Sp9 transcription factor in regulating the development of MGE-derived cortical interneurons. We show that SP9 is widely expressed in the MGE subventricular zone (SVZ) and in MGE-derived migrating interneurons. By analyzing Sp9 null and conditional mutant mice, we demonstrate that Sp9 promotes MGE progenitor proliferation in the SVZ and is required for the normal patterning of tangential migration and the laminar distribution of MGE-derived cortical GABAergic interneurons. Loss of Sp9 function results in a ~50% reduction of MGE-derived cortical interneurons, an ectopic aggregation of MGE-derived neurons in the embryonic ventral telencephalon, and an increased ratio of SST+/PV+ cortical interneurons. Finally, we provide evidence that Sp9 regulates MGE derived cortical interneuron development through promoting expression of the Lhx6 and Lhx8 transcription factors. Medial ganglionic eminence mRNA profiles of embryonic 12.5 wild type (WT) and sp9 null mutant mice were generated by deep sequencing, in triplicate, using using an illumina high-seq 2500

Source: GO:0030182
Synonyms: Not Available
Branch: biological process
Genes: Lhx8 (Mmu)...Lhx8 (Rno)...LHX8 (Hsa)...lhx8a (Dre)

High-Throughput (HTP) Dataset Index metadata provided by MGI
ID: ArrayExpress:E-GEOD-71285, GEO:GSE71285
Tags: WT vs. mutant, genotype
Summary: We used laser capture microdissection to isolate maxillary arch mesenchyme from E10.5 embryos. This tissue was collected from both control (3x) and Lhx6-/-;Lhx8-/- mutant (3x) samples. Transcriptional profiling was performed using Affymetrix GeneChip Mouse Genome 430 2.0 arrays. The mutant mice are of mixed genetic background of C57BL/6J, 129 and CD-1 strains. The head of E10.5 embryos was collected and embedded in Optimal Cutting Temperature resin (Tissue-Tek) by flash freezing on dry ice. The frozen sections were collected on polyethylene naphthalate membrane slides (Leica). Leica LMD6000 Laser Micro-Dissection System was used to cut out the normal expression domain of Lhx6 and Lhx8 in the maxillary arch mesenchyme. The tissue was collected from the entire antero-posterior extent of the maxillary arches. Total RNA was extracted using RNeasy Micro Kit (Qiagen). Subsequent steps of transcriptional profiling were performed by the New York University Genome Technology Center, beginning with the amplification of RNA by Ovation Nano Amplification system (NuGen). RNA samples from three wild-type and three Lhx6-/-;Lhx8-/- mutantmutant embryos, all somite count- and sex-matched (females), were analyzed with Affymetrix GeneChip Mouse Genome 430 2.0 arrays. A list of Lhx-regulated genes were generated from the microarray result based on the following criteria: fold change in the average expression between wild types and Lhx6-/-;Lhx8-/- mutant mutants is >1.5, the difference is statistically significant (P < 0.05) and the average intensity of the probe signal is >100 for wild-type and/or mutant samples. The resulting list of 212 genes was used for a gene ontology analysis with DAVID (27,28).

(GRCh38)1:75141078G>C

(Homo sapiens)
Allele/Variant
Source: NC_000001.11:g.75141078G>C
Genes: LHX8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:75141078G>C
Gene Synonyms: LIM/homeobox protein Lhx8...LIM-homeodomain protein Lhx8

(GRCh38)1:75143870C>T

(Homo sapiens)
Allele/Variant
Source: rs147867930
Genes: LHX8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:75143870C>T
Gene Synonyms: LIM/homeobox protein Lhx8...LIM-homeodomain protein Lhx8

(GRCh38)1:75136633C>T

(Homo sapiens)
Allele/Variant
Source: rs376772505
Genes: LHX8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:75136633C>T
Gene Synonyms: LIM/homeobox protein Lhx8...LIM-homeodomain protein Lhx8

(GRCh38)1:75143937G>C

(Homo sapiens)
Allele/Variant
Source: rs943066714
Genes: LHX8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:75143937G>C
Gene Synonyms: LIM/homeobox protein Lhx8...LIM-homeodomain protein Lhx8

(GRCh38)1:75143147G>A

(Homo sapiens)
Allele/Variant
Source: NC_000001.11:g.75143147G>A
Genes: LHX8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:75143147G>A
Gene Synonyms: LIM/homeobox protein Lhx8...LIM-homeodomain protein Lhx8

(GRCh38)1:75143857G>T

(Homo sapiens)
Allele/Variant
Source: rs753429679
Genes: LHX8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:75143857G>T
Gene Synonyms: LIM/homeobox protein Lhx8...LIM-homeodomain protein Lhx8

(GRCh38)1:75156895G>T

(Homo sapiens)
Allele/Variant
Source: rs79714503
Genes: LHX8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:75156895G>T
Gene Synonyms: LIM/homeobox protein Lhx8...LIM-homeodomain protein Lhx8

(GRCh38)1:75157080G>C

(Homo sapiens)
Allele/Variant
Source: rs1476916587
Genes: LHX8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:75157080G>C
Gene Synonyms: LIM/homeobox protein Lhx8...LIM-homeodomain protein Lhx8

(GRCh38)1:75143169C>T

(Homo sapiens)
Allele/Variant
Source: rs12084309
Genes: LHX8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:75143169C>T
Gene Synonyms: LIM/homeobox protein Lhx8...LIM-homeodomain protein Lhx8

(GRCh38)1:75137237G>A

(Homo sapiens)
Allele/Variant
Source: rs149422695
Genes: LHX8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:75137237G>A
Gene Synonyms: LIM/homeobox protein Lhx8...LIM-homeodomain protein Lhx8