Version: 8.0.0
Date: Tue Jan 28 2025
8 results for groa

CXCL1

(Homo sapiens)
Gene
Name: C-X-C motif chemokine ligand 1
Synonyms: GRO1 oncogene (melanoma growth-stimulating activity), fibroblast secretory protein, FSP, MGSA-a, SCYB1, NAP-3, melanoma growth stimulating activity, alpha, MGSA alpha, MGSA, GRO1, GRO1 oncogene (melanoma growth stimulating activity, alpha), melanoma growth stimulatory activity alpha, growth-regulated alpha protein, chemokine (C-X-C motif) ligand 1 (melanoma growth stimulating activity, alpha), GROa, GRO-alpha(1-73), neutrophil-activating protein 3, C-X-C motif chemokine 1
Source: HGNC:4602
Biotype: protein coding gene
Synonyms: GROa...GROa

(GRCh38)4:73869752G>A

(Homo sapiens)
Allele/Variant
Source: rs186092967
Genes: CXCL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:73869752G>A
Gene Synonyms: GROa

(GRCh38)4:73869777C>T

(Homo sapiens)
Allele/Variant
Source: rs145342393
Genes: CXCL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:73869777C>T
Gene Synonyms: GROa

(GRCh38)4:73869498C>T

(Homo sapiens)
Allele/Variant
Source: NC_000004.12:g.73869498C>T
Genes: CXCL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:73869498C>T
Gene Synonyms: GROa

(GRCh38)4:73869698C>G

(Homo sapiens)
Allele/Variant
Source: NC_000004.12:g.73869698C>G
Genes: CXCL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:73869698C>G
Gene Synonyms: GROa

(GRCh38)4:73869716C>A

(Homo sapiens)
Allele/Variant
Source: rs200234866
Genes: CXCL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:73869716C>A
Gene Synonyms: GROa

(GRCh38)4:73869738T>C

(Homo sapiens)
Allele/Variant
Source: rs201545979
Genes: CXCL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:73869738T>C
Gene Synonyms: GROa

(GRCh38)4:73869751C>G

(Homo sapiens)
Allele/Variant
Source: rs201293315
Genes: CXCL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:73869751C>G
Gene Synonyms: GROa