Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
Species
Category
Variant Type
Molecular Consequence
Genes
Construct Knockdown Component
Construct Regulatory Region
Allele/Variant
PlapHMS05685
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0325954
Genes: Not Available
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Plap
Construct Knockdown Component: Plap (Dme)
Symbol: PlapHMS05685
PlapKK102839
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0259233
Genes: Not Available
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Plap
Construct Knockdown Component: Plap (Dme)
Symbol: PlapKK102839
PlapU6.NIG.sgRNA
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0379113
Genes: Not Available
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Plap
Construct Knockdown Component: Plap (Dme)
Symbol: PlapU6.NIG.sgRNA
PlapJF01611
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0245851
Genes: Not Available
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Plap
Construct Knockdown Component: Plap (Dme)
Symbol: PlapJF01611
PlapGD11535
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0208092
Genes: Not Available
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Plap
Construct Knockdown Component: Plap (Dme)
Symbol: PlapGD11535
Constructs: UAS-PlapRNAi...UAS-Plap[RNAi]
PlapNIG.5105R
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0274524
Genes: Not Available
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Plap
Construct Knockdown Component: Plap (Dme)
Symbol: PlapNIG.5105R
PlapEY10786
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0160006
Genes: Plap (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: Not Available
Symbol: Plap
Gene Synonyms: plap
Genes: Plap (Dme)
Symbol: PlapEY10786
PlapSK6
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0383424
Genes: Plap (Dme)
Synonyms: Not Available
Variant Type: deletion
Molecular Consequence: frameshift_variant
Diseases: Not Available
Variant Name: Not Available
Symbol: Plap
Gene Synonyms: plap
Genes: Plap (Dme)
Symbol: PlapSK6
Plapd09025
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0160005
Genes: Plap (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: Not Available
Symbol: Plap
Gene Synonyms: plap
Genes: Plap (Dme)
Symbol: Plapd09025
Papolaem1(IMPC)J
(Mus musculus)Allele/Variant
Source: MGI:6314387
Genes: Papola (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: Plap
Papolaem1Gpt
(Mus musculus)Allele/Variant
Source: MGI:7303857
Genes: Papola (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: Plap
Plaaem1Smoc
(Mus musculus)Allele/Variant
Source: MGI:7291690
Genes: Plaa (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: Plap
Plaatm2.1Chopa
(Mus musculus)Allele/Variant
Source: MGI:7539702
Genes: Plaa (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: Plap
Plaaem1Gpt
(Mus musculus)Allele/Variant
Source: MGI:7304324
Genes: Plaa (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: Plap
Plaaem1(IMPC)Kmpc
(Mus musculus)Allele/Variant
Source: MGI:6336130
Genes: Plaa (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: Plap
Plaatm1.1Chopa
(Mus musculus)Allele/Variant
Source: MGI:6343219
Genes: Plaa (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: Plap
Plaaem1Pmi
(Mus musculus)Allele/Variant
Source: MGI:5828117
Genes: Plaa (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: Plap
Plaatm1(NCOM)Cmhd
(Mus musculus)Allele/Variant
Source: MGI:4880046
Genes: Plaa (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: Plap
(GRCh38)9:26920272A>T
(Homo sapiens)Allele/Variant
Source: rs766216764
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26920272A>T
Gene Synonyms: PLAP
(GRCh38)9:26905525G>T
(Homo sapiens)Allele/Variant
Source: rs960134042
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26905525G>T
Gene Synonyms: PLAP
(GRCh38)9:26905528T>G
(Homo sapiens)Allele/Variant
Source: rs1824200336
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26905528T>G
Gene Synonyms: PLAP
(GRCh38)9:26905573A>T
(Homo sapiens)Allele/Variant
Source: rs752278393
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26905573A>T
Gene Synonyms: PLAP
(GRCh38)9:26905811C>G
(Homo sapiens)Allele/Variant
Source: rs1049445907
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26905811C>G
Gene Synonyms: PLAP
(GRCh38)9:26905965T>C
(Homo sapiens)Allele/Variant
Source: rs1385484105
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26905965T>C
Gene Synonyms: PLAP
(GRCh38)9:26928198G>A
(Homo sapiens)Allele/Variant
Source: rs566272935
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26928198G>A
Gene Synonyms: PLAP
(GRCh38)9:26947033C>T
(Homo sapiens)Allele/Variant
Source: rs1455722084
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26947033C>T
Gene Synonyms: PLAP
(GRCh38)9:26947061G>A
(Homo sapiens)Allele/Variant
Source: rs1825754982
Genes: PLAA (Hsa), IFT74 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26947061G>A
Gene Synonyms: PLAP
(GRCh38)9:26913898G>A
(Homo sapiens)Allele/Variant
Source: rs370264645
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26913898G>A
Gene Synonyms: PLAP
(GRCh38)9:26923359A>C
(Homo sapiens)Allele/Variant
Source: rs1824835966
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26923359A>C
Gene Synonyms: PLAP
(GRCh38)9:26923361T>G
(Homo sapiens)Allele/Variant
Source: rs529320124
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26923361T>G
Gene Synonyms: PLAP
(GRCh38)9:26923367G>T
(Homo sapiens)Allele/Variant
Source: rs1824836492
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26923367G>T
Gene Synonyms: PLAP
(GRCh38)9:26905544A>G
(Homo sapiens)Allele/Variant
Source: rs2131360575
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26905544A>G
Gene Synonyms: PLAP
(GRCh38)9:26906020T>C
(Homo sapiens)Allele/Variant
Source: NC_000009.12:g.26906020T>C
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26906020T>C
Gene Synonyms: PLAP
(GRCh38)9:26906093G>T
(Homo sapiens)Allele/Variant
Source: rs750356765
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26906093G>T
Gene Synonyms: PLAP
(GRCh38)9:26928112T>C
(Homo sapiens)Allele/Variant
Source: rs750196251
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26928112T>C
Gene Synonyms: PLAP
(GRCh38)9:26928395T>C
(Homo sapiens)Allele/Variant
Source: rs1251664115
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26928395T>C
Gene Synonyms: PLAP
(GRCh38)9:26935157A>C
(Homo sapiens)Allele/Variant
Source: rs757313107
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26935157A>C
Gene Synonyms: PLAP
(GRCh38)9:26946947G>C
(Homo sapiens)Allele/Variant
Source: rs368369595
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26946947G>C
Gene Synonyms: PLAP
(GRCh38)9:26910382T>G
(Homo sapiens)Allele/Variant
Source: NC_000009.12:g.26910382T>G
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26910382T>G
Gene Synonyms: PLAP
(GRCh38)9:26910425G>A
(Homo sapiens)Allele/Variant
Source: rs1241511703
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, stop_gained, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26910425G>A
Gene Synonyms: PLAP
(GRCh38)9:26913871G>T
(Homo sapiens)Allele/Variant
Source: rs747382266
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26913871G>T
Gene Synonyms: PLAP
(GRCh38)9:26913885A>G
(Homo sapiens)Allele/Variant
Source: rs1438160394
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26913885A>G
Gene Synonyms: PLAP
(GRCh38)9:26913897C>T
(Homo sapiens)Allele/Variant
Source: rs139288553
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26913897C>T
Gene Synonyms: PLAP
(GRCh38)9:26917078A>G
(Homo sapiens)Allele/Variant
Source: rs141342759
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26917078A>G
Gene Synonyms: PLAP
(GRCh38)9:26923236G>A
(Homo sapiens)Allele/Variant
Source: rs75789871
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26923236G>A
Gene Synonyms: PLAP
(GRCh38)9:26923253T>C
(Homo sapiens)Allele/Variant
Source: rs2131386997
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26923253T>C
Gene Synonyms: PLAP
(GRCh38)9:26923296A>G
(Homo sapiens)Allele/Variant
Source: rs1379209247
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26923296A>G
Gene Synonyms: PLAP
(GRCh38)9:26923308T>G
(Homo sapiens)Allele/Variant
Source: NC_000009.12:g.26923308T>G
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26923308T>G
Gene Synonyms: PLAP
(GRCh38)9:26907841A>G
(Homo sapiens)Allele/Variant
Source: rs1227890958
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26907841A>G
Gene Synonyms: PLAP
(GRCh38)9:26907856C>T
(Homo sapiens)Allele/Variant
Source: NC_000009.12:g.26907856C>T
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, stop_gained, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26907856C>T
Gene Synonyms: PLAP