Version: 8.0.0
Date: Tue Jan 28 2025
22 results for vatl

atp6v0c

(Xenopus tropicalis)
Gene
Name: ATPase, H+ transporting, lysosomal 16kDa, V0 subunit c
Synonyms: xduct, atpl, ductin, atp6v0c, vatl, atp6c, atp6l, vma3, ATPase, H+ transporting, lysosomal 16kDa, V0 subunit c
Source: Xenbase:XB-GENE-981790
Biotype: gene
Synonyms: vatl...vatl...vatl

atp6v0c.S

(Xenopus laevis)
Gene
Name: ATPase, H+ transporting, lysosomal 16kDa, V0 subunit c
Synonyms: xduct, atpl, ductin, vatl, atp6c, atp6v0c.S, atp6l, vma3, ATPase, H+ transporting, lysosomal 16kDa, V0 subunit c
Source: Xenbase:XB-GENE-17342706
Biotype: gene
Synonyms: vatl...vatl...vatl

atp6v0c.L

(Xenopus laevis)
Gene
Name: ATPase, H+ transporting, lysosomal 16kDa, V0 subunit c
Synonyms: xduct, atpl, atp6v0c.L, ductin, vatl, atp6c, ATPase, H+ transporting, lysosomal 16kDa, V0 subunit c, vma3, atp6l
Source: Xenbase:XB-GENE-981796
Biotype: gene
Synonyms: vatl...vatl...vatl

ATP6V0C

(Homo sapiens)
Gene
Name: ATPase H+ transporting V0 subunit c
Synonyms: Vma3, V-type proton ATPase 16 kDa proteolipid subunit, VPPC, ATP6L, V-type proton ATPase 16 kDa proteolipid subunit c, vacuolar H+ ATPase proton channel subunit, vacuolar ATP synthase 16 kDa proteolipid subunit, VATL, ATPase, H+ transporting, lysosomal 16kDa, V0 subunit c, EPEO3, vacuolar proton pump 16 kDa proteolipid subunit, ATP6C, ATPL, vacuolar proton pump 16 kDa proteolipid subunit c, V-ATPase subunit c, V-ATPase 16 kDa proteolipid subunit, vacuolar proton pump, 16 kDa subunit, H(+)-transporting two-sector ATPase, 16 kDa subunit, V-ATPase 16 kDa proteolipid subunit c
Source: HGNC:855
Biotype: protein coding gene
Synonyms: VATL...VATL

(GRCh38)16:2519391A>T

(Homo sapiens)
Allele/Variant
Source: NC_000016.10:g.2519391A>T
Genes: ATP6V0C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)16:2519391A>T
Gene Synonyms: VATL

(GRCh38)16:2519310C>G

(Homo sapiens)
Allele/Variant
Source: rs2065895527
Genes: ATP6V0C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:2519310C>G
Gene Synonyms: VATL

(GRCh38)16:2519744A>T

(Homo sapiens)
Allele/Variant
Source: rs2065899210
Genes: ATP6V0C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_lost
Diseases: Not Available
Variant Name: (GRCh38)16:2519744A>T
Gene Synonyms: VATL

(GRCh38)16:2519722G>A

(Homo sapiens)
Allele/Variant
Source: NC_000016.10:g.2519722G>A
Genes: ATP6V0C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:2519722G>A
Gene Synonyms: VATL

(GRCh38)16:2519725C>T

(Homo sapiens)
Allele/Variant
Source: NC_000016.10:g.2519725C>T
Genes: ATP6V0C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:2519725C>T
Gene Synonyms: VATL

(GRCh38)16:2519701G>T

(Homo sapiens)
Allele/Variant
Source: NC_000016.10:g.2519701G>T
Genes: ATP6V0C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:2519701G>T
Gene Synonyms: VATL

(GRCh38)16:2519686T>C

(Homo sapiens)
Allele/Variant
Source: NC_000016.10:g.2519686T>C
Genes: ATP6V0C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:2519686T>C
Gene Synonyms: VATL

(GRCh38)16:2519681T>C

(Homo sapiens)
Allele/Variant
Source: NC_000016.10:g.2519681T>C
Genes: ATP6V0C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:2519681T>C
Gene Synonyms: VATL

(GRCh38)16:2519326G>C

(Homo sapiens)
Allele/Variant
Source: NC_000016.10:g.2519326G>C
Genes: ATP6V0C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:2519326G>C
Gene Synonyms: VATL

(GRCh38)16:2519654G>C

(Homo sapiens)
Allele/Variant
Source: NC_000016.10:g.2519654G>C
Genes: ATP6V0C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)16:2519654G>C
Gene Synonyms: VATL

(GRCh38)16:2514158G>T

(Homo sapiens)
Allele/Variant
Source: NC_000016.10:g.2514158G>T
Genes: ATP6V0C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:2514158G>T
Gene Synonyms: VATL

(GRCh38)16:2519551C>T

(Homo sapiens)
Allele/Variant
Source: NC_000016.10:g.2519551C>T
Genes: ATP6V0C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)16:2519551C>T
Gene Synonyms: VATL

(GRCh38)16:2519560G>A

(Homo sapiens)
Allele/Variant
Source: NC_000016.10:g.2519560G>A
Genes: ATP6V0C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)16:2519560G>A
Gene Synonyms: VATL

(GRCh38)16:2519572G>A

(Homo sapiens)
Allele/Variant
Source: NC_000016.10:g.2519572G>A
Genes: ATP6V0C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)16:2519572G>A
Gene Synonyms: VATL

(GRCh38)16:2514182G>A

(Homo sapiens)
Allele/Variant
Source: NC_000016.10:g.2514182G>A
Genes: ATP6V0C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:2514182G>A
Gene Synonyms: VATL

(GRCh38)16:2519560G>C

(Homo sapiens)
Allele/Variant
Source: NC_000016.10:g.2519560G>C
Genes: ATP6V0C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)16:2519560G>C
Gene Synonyms: VATL

(GRCh38)16:2519689G>C

(Homo sapiens)
Allele/Variant
Source: rs2065898758
Genes: ATP6V0C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:2519689G>C
Gene Synonyms: VATL

(GRCh38)16:2514167G>A

(Homo sapiens)
Allele/Variant
Source: NC_000016.10:g.2514167G>A
Genes: ATP6V0C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:2514167G>A
Gene Synonyms: VATL