Version: 8.0.0Date: Tue Jan 28 2025
Category
Plekhm3
(Mus musculus)Gene
Name: pleckstrin homology domain containing, family M, member 3
Synonyms: RGD1307151, A230102O09Rik, pleckstrin homology domain containing, family M, member 1-like, 9430067K14Rik, AI449570, RIKEN cDNA A230102O09 gene, RIKEN cDNA 9430067K14 gene, expressed sequence AI449570, Dapr, Plekhm1l
Source: MGI:2443627
Biotype: protein coding gene
Symbol: Plekhm3 (Mmu)
Symbol: Plekhm3
Automated Gene Synopsis: Orthologous to human PLEKHM3 (pleckstrin homology domain containing M3).
Strict Orthology Symbols: plekhm3
PLEKHM3
(Homo sapiens)Gene
Name: pleckstrin homology domain containing M3
Synonyms: DAPR, FLJ41210, pleckstrin homology domain containing, family M, member 1-like, differentiation associated protein, PLEKHM1L, DKFZp686O04200, pleckstrin homology domain-containing family M member 3, PH domain-containing family M member 3, pleckstrin homology domain containing, family M, member 3
Source: HGNC:34006
Biotype: protein coding gene
Symbol: PLEKHM3 (Hsa)
Symbol: PLEKHM3
Strict Orthology Symbols: plekhm3
plekhm3
(Danio rerio)Gene
Name: pleckstrin homology domain containing, family M, member 3
Synonyms: si:dkey-159b16.1
Source: ZFIN:ZDB-GENE-070912-382
Biotype: protein coding gene
Symbol: plekhm3 (Dre)
Symbol: plekhm3
Automated Gene Synopsis: Orthologous to human PLEKHM3 (pleckstrin homology domain containing M3).
Strict Orthology Symbols: plekhm3
Plekhm3
(Rattus norvegicus)Gene
Name: pleckstrin homology domain containing M3
Synonyms: RGD1307151, pleckstrin homology domain containing, family M, member 1-like, differentiation associated protein, similar to CG6613-PA, pleckstrin homology domain-containing family M member 3, pleckstrin homology domain containing, family M, member 3, LOC316455, Dapr, Plekhm1l
Source: RGD:1307151
Biotype: protein coding gene
Symbol: Plekhm3 (Rno)
Symbol: Plekhm3
Gene Synopsis: Orthologous to human PLEKHM3 (pleckstrin homology domain containing M3); INTERACTS WITH 17alpha-ethynylestradiol
Automated Gene Synopsis: Orthologous to human PLEKHM3 (pleckstrin homology domain containing M3).
Strict Orthology Symbols: plekhm3
plekhm3
(Xenopus tropicalis)Gene
Name: pleckstrin homology domain containing M3
Synonyms: pleckstrin homology domain containing M3, plekhm3
Source: Xenbase:XB-GENE-5825075
Biotype: gene
Symbol: plekhm3
Symbol: plekhm3 (Xtr)
Automated Gene Synopsis: Orthologous to human PLEKHM3 (pleckstrin homology domain containing M3).
Synonyms: plekhm3...plekhm3...plekhm3
Strict Orthology Symbols: plekhm3
plekhm3.S
(Xenopus laevis)Gene
Name: pleckstrin homology domain containing M3
Synonyms: plekhm3.S, pleckstrin homology domain containing M3
Source: Xenbase:XB-GENE-17341418
Biotype: gene
Symbol: plekhm3.S (Xla)
Automated Gene Synopsis: Orthologous to human PLEKHM3 (pleckstrin homology domain containing M3).
Strict Orthology Symbols: plekhm3
Symbol: plekhm3.S
plekhm3.L
(Xenopus laevis)Gene
Name: pleckstrin homology domain containing M3
Synonyms: pleckstrin homology domain containing M3, plekhm3.L
Source: Xenbase:XB-GENE-5825077
Biotype: gene
Symbol: plekhm3.L (Xla)
Automated Gene Synopsis: Orthologous to human PLEKHM3 (pleckstrin homology domain containing M3).
Strict Orthology Symbols: plekhm3
Symbol: plekhm3.L
cup-14
(Caenorhabditis elegans)Gene
Name: Coelomocyte UPtake-defective 14
Synonyms: Y51H1A.2, CELE_Y51H1A.2
Source: WB:WBGene00013093
Biotype: protein coding gene
Strict Orthology Symbols: plekhm3
Plekhm1
(Drosophila melanogaster)Gene
Name: Pleckstrin homology and RUN domain containing M1
Synonyms: CG6613, Plekhm1
Source: FB:FBgn0034694
Biotype: protein coding gene
Strict Orthology Symbols: plekhm3
Gene Ontology
Source: GO:0045445
Synonyms:
- myoblast cell differentiation
Branch: biological process
Genes: Plekhm3 (Rno)...Plekhm3 (Mmu)...PLEKHM3 (Hsa)
Gene Ontology
Source: GO:0005794
Synonyms:
- Golgi
- Golgi complex
Branch: cellular component
Genes: Plekhm3 (Rno)...PLEKHM3 (Hsa)...Plekhm3 (Mmu)
sa17447
(Danio rerio)Allele/Variant
Source: ZFIN:ZDB-ALT-131217-13567
Genes: plekhm3 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: plekhm3 (Dre)
sa34662
(Danio rerio)Allele/Variant
Source: ZFIN:ZDB-ALT-160601-3297
Genes: plekhm3 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: plekhm3 (Dre)
sa13274
(Danio rerio)Allele/Variant
Source: ZFIN:ZDB-ALT-130411-2917
Genes: plekhm3 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: plekhm3 (Dre)
Gene Ontology
Source: GO:0046872
Synonyms:
- heavy metal binding
- metal binding
Branch: molecular function
Genes: Plekhm3 (Rno)...PLEKHM3 (Hsa)...Plekhm3 (Mmu)...plekhm3 (Dre)
Gene Ontology
Source: GO:0005886
Synonyms:
- bacterial inner membrane
- cell membrane
Branch: cellular component
Genes: Plekhm3 (Rno)...PLEKHM3 (Hsa)...Plekhm3 (Mmu)
Gene Ontology
Source: GO:0005737
Synonyms: Not Available
Branch: cellular component
Genes: PLEKHM3 (Hsa)...Plekhm3 (Rno)...Plekhm3 (Mmu)
Gene Ontology
Source: GO:0005515
Synonyms:
- glycoprotein binding
- protein amino acid binding
Branch: molecular function
Genes: Plekhm3 (Mmu)
(GRCh38)2:208001495C>T
(Homo sapiens)Allele/Variant
Source: rs950859081
Genes: PLEKHM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:208001495C>T
(GRCh38)2:207861255T>C
(Homo sapiens)Allele/Variant
Source: rs762422346
Genes: PLEKHM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)2:207861255T>C
(GRCh38)2:207976701G>A
(Homo sapiens)Allele/Variant
Source: rs200046449
Genes: PLEKHM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)2:207976701G>A
(GRCh38)2:207977062C>T
(Homo sapiens)Allele/Variant
Source: rs868708982
Genes: PLEKHM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:207977062C>T
(GRCh38)2:207977526T>C
(Homo sapiens)Allele/Variant
Source: rs771200556
Genes: PLEKHM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)2:207977526T>C
(GRCh38)2:207946402G>A
(Homo sapiens)Allele/Variant
Source: rs202021467
Genes: PLEKHM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:207946402G>A
(GRCh38)2:207977196G>A
(Homo sapiens)Allele/Variant
Source: rs1163987591
Genes: PLEKHM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)2:207977196G>A
(GRCh38)2:208001057T>G
(Homo sapiens)Allele/Variant
Source: rs537974055
Genes: PLEKHM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:208001057T>G
(GRCh38)2:207828443G>C
(Homo sapiens)Allele/Variant
Source: rs781575909
Genes: PLEKHM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:207828443G>C
(GRCh38)2:207861130G>A
(Homo sapiens)Allele/Variant
Source: rs778046594
Genes: PLEKHM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:207861130G>A
(GRCh38)2:207861153C>T
(Homo sapiens)Allele/Variant
Source: rs1266904915
Genes: PLEKHM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)2:207861153C>T
(GRCh38)2:207977109A>G
(Homo sapiens)Allele/Variant
Source: NC_000002.12:g.207977109A>G
Genes: PLEKHM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)2:207977109A>G
(GRCh38)2:207976777T>C
(Homo sapiens)Allele/Variant
Source: rs779273690
Genes: PLEKHM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:207976777T>C
(GRCh38)2:207976731G>C
(Homo sapiens)Allele/Variant
Source: rs762229483
Genes: PLEKHM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:207976731G>C
(GRCh38)2:207976975C>A
(Homo sapiens)Allele/Variant
Source: NC_000002.12:g.207976975C>A
Genes: PLEKHM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:207976975C>A
(GRCh38)2:207977554T>C
(Homo sapiens)Allele/Variant
Source: rs1417145488
Genes: PLEKHM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)2:207977554T>C
(GRCh38)2:208001176G>T
(Homo sapiens)Allele/Variant
Source: rs180671227
Genes: PLEKHM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:208001176G>T
(GRCh38)2:208001603A>C
(Homo sapiens)Allele/Variant
Source: rs1559278439
Genes: PLEKHM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:208001603A>C
(GRCh38)2:207976764C>T
(Homo sapiens)Allele/Variant
Source: rs753970574
Genes: PLEKHM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)2:207976764C>T
(GRCh38)2:207977322G>A
(Homo sapiens)Allele/Variant
Source: rs756408624
Genes: PLEKHM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)2:207977322G>A
(GRCh38)2:207931019A>C
(Homo sapiens)Allele/Variant
Source: NC_000002.12:g.207931019A>C
Genes: PLEKHM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)2:207931019A>C
(GRCh38)2:207976776T>C
(Homo sapiens)Allele/Variant
Source: rs1173496556
Genes: PLEKHM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)2:207976776T>C
(GRCh38)2:207977125G>C
(Homo sapiens)Allele/Variant
Source: rs746708061
Genes: PLEKHM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:207977125G>C
(GRCh38)2:207976875C>T
(Homo sapiens)Allele/Variant
Source: rs369158949
Genes: PLEKHM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)2:207976875C>T
(GRCh38)2:207861116A>C
(Homo sapiens)Allele/Variant
Source: rs200896303
Genes: PLEKHM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:207861116A>C
(GRCh38)2:207861117A>G
(Homo sapiens)Allele/Variant
Source: rs1296865966
Genes: PLEKHM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)2:207861117A>G
(GRCh38)2:208001515A>C
(Homo sapiens)Allele/Variant
Source: rs756976770
Genes: PLEKHM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:208001515A>C
(GRCh38)2:208001479A>G
(Homo sapiens)Allele/Variant
Source: rs772528902
Genes: PLEKHM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:208001479A>G
(GRCh38)2:207861107G>C
(Homo sapiens)Allele/Variant
Source: NC_000002.12:g.207861107G>C
Genes: PLEKHM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:207861107G>C
(GRCh38)2:207976887C>T
(Homo sapiens)Allele/Variant
Source: rs765459423
Genes: PLEKHM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)2:207976887C>T
(GRCh38)2:207946437C>T
(Homo sapiens)Allele/Variant
Source: rs2105968903
Genes: PLEKHM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, stop_retained_variant
Diseases: Not Available
Variant Name: (GRCh38)2:207946437C>T
(GRCh38)2:207976855T>A
(Homo sapiens)Allele/Variant
Source: rs1691329154
Genes: PLEKHM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:207976855T>A