Version: 8.1.0Date: Fri Apr 18 2025
Category
ATP5MF-PTCD1
(Homo sapiens)Gene
Name: ATP5MF-PTCD1 readthrough
Synonyms: FLJ56092, ATP5J2-PTCD1, ATP5J2-PTCD1 fusion protein, ATP5J2-PTCD1 read-through transcript, ATP5J2-PTCD1 readthrough
Source: HGNC:38844
Biotype: protein coding gene
Symbol: ATP5MF-PTCD1 (Hsa)
Symbol: ATP5MF-PTCD1
Ptcd1
(Rattus norvegicus)Gene
Name: pentatricopeptide repeat domain 1
Synonyms: pentatricopeptide repeat-containing protein 1, mitochondrial, LOC304278
Source: RGD:1311473
Biotype: protein coding gene
Strict Orthology Symbols: ATP5MF-PTCD1
Gene Ontology
Source: GO:0006754
Synonyms:
- ATP anabolism
- ATP biosynthesis
Branch: biological process
Genes: ATP5MF-PTCD1 (Hsa)
Gene Ontology
Source: GO:0045259
Synonyms:
- F1-F0 complex
- hydrogen-translocating F-type ATPase complex
Branch: cellular component
Genes: ATP5MF-PTCD1 (Hsa)
Gene Ontology
Source: GO:1902600
Synonyms:
- ATP hydrolysis coupled proton transport
- hydrogen ion transmembrane transport
Branch: biological process
Genes: ATP5MF-PTCD1 (Hsa)
Gene Ontology
Source: GO:0005759
Synonyms:
- mitochondrial lumen
- mitochondrial stroma
Branch: cellular component
Genes: ATP5MF-PTCD1 (Hsa)
Gene Ontology
Source: GO:0005743
Synonyms:
- inner mitochondrial membrane
- inner mitochondrion membrane
Branch: cellular component
Genes: ATP5MF-PTCD1 (Hsa)
Gene Ontology
Source: GO:0005739
Synonyms:
- mitochondria
Branch: cellular component
Genes: ATP5MF-PTCD1 (Hsa)
(GRCh38)7:99434854C>T
(Homo sapiens)Allele/Variant
Source: rs534734137
Genes: ATP5MF-PTCD1 (Hsa), PTCD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:99434854C>T
(GRCh38)7:99434935C>T
(Homo sapiens)Allele/Variant
Source: rs776982093
Genes: ATP5MF-PTCD1 (Hsa), PTCD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:99434935C>T
(GRCh38)7:99435112G>A
(Homo sapiens)Allele/Variant
Source: rs34452317
Genes: ATP5MF-PTCD1 (Hsa), PTCD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:99435112G>A
(GRCh38)7:99424829G>A
(Homo sapiens)Allele/Variant
Source: rs375045061
Genes: ATP5MF-PTCD1 (Hsa), PTCD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)7:99424829G>A
(GRCh38)7:99434927C>T
(Homo sapiens)Allele/Variant
Source: rs780586921
Genes: ATP5MF-PTCD1 (Hsa), PTCD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:99434927C>T
(GRCh38)7:99434936G>A
(Homo sapiens)Allele/Variant
Source: rs150504114
Genes: ATP5MF-PTCD1 (Hsa), PTCD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:99434936G>A
(GRCh38)7:99434948G>A
(Homo sapiens)Allele/Variant
Source: rs201365604
Genes: ATP5MF-PTCD1 (Hsa), PTCD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:99434948G>A
(GRCh38)7:99435054C>G
(Homo sapiens)Allele/Variant
Source: rs114565866
Genes: ATP5MF-PTCD1 (Hsa), PTCD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:99435054C>G
(GRCh38)7:99425257G>T
(Homo sapiens)Allele/Variant
Source: rs80070442
Genes: ATP5MF-PTCD1 (Hsa), PTCD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:99425257G>T
(GRCh38)7:99425448G>A
(Homo sapiens)Allele/Variant
Source: rs150731740
Genes: ATP5MF-PTCD1 (Hsa), PTCD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)7:99425448G>A
(GRCh38)7:99434801T>G
(Homo sapiens)Allele/Variant
Source: rs368346878
Genes: ATP5MF-PTCD1 (Hsa), PTCD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:99434801T>G
(GRCh38)7:99420071C>T
(Homo sapiens)Allele/Variant
Source: rs199655168
Genes: ATP5MF-PTCD1 (Hsa), PTCD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)7:99420071C>T
(GRCh38)7:99425298G>A
(Homo sapiens)Allele/Variant
Source: rs143293943
Genes: ATP5MF-PTCD1 (Hsa), PTCD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)7:99425298G>A
(GRCh38)7:99425550C>T
(Homo sapiens)Allele/Variant
Source: NC_000007.14:g.99425550C>T
Genes: ATP5MF-PTCD1 (Hsa), PTCD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)7:99425550C>T
(GRCh38)7:99435071C>G
(Homo sapiens)Allele/Variant
Source: rs753255115
Genes: ATP5MF-PTCD1 (Hsa), PTCD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:99435071C>G
(GRCh38)7:99435139C>A
(Homo sapiens)Allele/Variant
Source: rs142290155
Genes: ATP5MF-PTCD1 (Hsa), PTCD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:99435139C>A
(GRCh38)7:99435197T>C
(Homo sapiens)Allele/Variant
Source: rs535812037
Genes: ATP5MF-PTCD1 (Hsa), PTCD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:99435197T>C
(GRCh38)7:99420136T>C
(Homo sapiens)Allele/Variant
Source: rs772306071
Genes: ATP5MF-PTCD1 (Hsa), PTCD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)7:99420136T>C
(GRCh38)7:99435010G>A
(Homo sapiens)Allele/Variant
Source: rs758848789
Genes: ATP5MF-PTCD1 (Hsa), PTCD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:99435010G>A
(GRCh38)7:99424939G>C
(Homo sapiens)Allele/Variant
Source: rs551907449
Genes: ATP5MF-PTCD1 (Hsa), PTCD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)7:99424939G>C
(GRCh38)7:99434903A>C
(Homo sapiens)Allele/Variant
Source: rs749966548
Genes: ATP5MF-PTCD1 (Hsa), PTCD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:99434903A>C
(GRCh38)7:99429804C>T
(Homo sapiens)Allele/Variant
Source: NC_000007.14:g.99429804C>T
Genes: ATP5MF-PTCD1 (Hsa), PTCD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:99429804C>T
(GRCh38)7:99434863T>C
(Homo sapiens)Allele/Variant
Source: rs761648024
Genes: ATP5MF-PTCD1 (Hsa), PTCD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:99434863T>C
(GRCh38)7:99425250C>T
(Homo sapiens)Allele/Variant
Source: rs147045279
Genes: ATP5MF-PTCD1 (Hsa), PTCD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)7:99425250C>T
(GRCh38)7:99423912T>A
(Homo sapiens)Allele/Variant
Source: rs781654991
Genes: ATP5MF-PTCD1 (Hsa), PTCD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)7:99423912T>A
(GRCh38)7:99423950T>G
(Homo sapiens)Allele/Variant
Source: rs772006873
Genes: ATP5MF-PTCD1 (Hsa), PTCD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)7:99423950T>G
(GRCh38)7:99429742T>C
(Homo sapiens)Allele/Variant
Source: rs1399778210
Genes: ATP5MF-PTCD1 (Hsa), PTCD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:99429742T>C
(GRCh38)7:99429117G>A
(Homo sapiens)Allele/Variant
Source: rs140372739
Genes: ATP5MF-PTCD1 (Hsa), PTCD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:99429117G>A
(GRCh38)7:99429672G>C
(Homo sapiens)Allele/Variant
Source: rs201764292
Genes: ATP5MF-PTCD1 (Hsa), PTCD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:99429672G>C
(GRCh38)7:99425034C>G
(Homo sapiens)Allele/Variant
Source: rs748559296
Genes: ATP5MF-PTCD1 (Hsa), PTCD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)7:99425034C>G
(GRCh38)7:99419986C>T
(Homo sapiens)Allele/Variant
Source: rs930154607
Genes: ATP5MF-PTCD1 (Hsa), PTCD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)7:99419986C>T
(GRCh38)7:99424919C>T
(Homo sapiens)Allele/Variant
Source: rs139956151
Genes: ATP5MF-PTCD1 (Hsa), PTCD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)7:99424919C>T
(GRCh38)7:99425129A>G
(Homo sapiens)Allele/Variant
Source: rs148440637
Genes: ATP5MF-PTCD1 (Hsa), PTCD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)7:99425129A>G
(GRCh38)7:99425543C>G
(Homo sapiens)Allele/Variant
Source: rs771084548
Genes: ATP5MF-PTCD1 (Hsa), PTCD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)7:99425543C>G
(GRCh38)7:99435178T>C
(Homo sapiens)Allele/Variant
Source: rs140634486
Genes: ATP5MF-PTCD1 (Hsa), PTCD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:99435178T>C
(GRCh38)7:99435212C>A
(Homo sapiens)Allele/Variant
Source: rs150342946
Genes: ATP5MF-PTCD1 (Hsa), PTCD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:99435212C>A
(GRCh38)7:99433303T>C
(Homo sapiens)Allele/Variant
Source: rs111989725
Genes: ATP5MF-PTCD1 (Hsa), PTCD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:99433303T>C
(GRCh38)7:99434905C>A
(Homo sapiens)Allele/Variant
Source: rs148051918
Genes: ATP5MF-PTCD1 (Hsa), PTCD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:99434905C>A
(GRCh38)7:99434848C>T
(Homo sapiens)Allele/Variant
Source: rs138669812
Genes: ATP5MF-PTCD1 (Hsa), PTCD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:99434848C>T
(GRCh38)7:99435085A>C
(Homo sapiens)Allele/Variant
Source: rs745338035
Genes: ATP5MF-PTCD1 (Hsa), PTCD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:99435085A>C
(GRCh38)7:99425006G>A
(Homo sapiens)Allele/Variant
Source: rs377292526
Genes: ATP5MF-PTCD1 (Hsa), PTCD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)7:99425006G>A
(GRCh38)7:99425060G>A
(Homo sapiens)Allele/Variant
Source: rs535281099
Genes: ATP5MF-PTCD1 (Hsa), PTCD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)7:99425060G>A