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Category

4,910 results for efl1

Page 2 of 99

(R64-2-1)chrXIV:328483G>A

(Saccharomyces cerevisiae)

Allele/Variant

Source: NC_001146.8:g.328483G>A

Genes: RIA1 (Sce)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: synonymous_variant

Diseases: Not Available

Variant Name: (R64-2-1)chrXIV:328483G>A

Gene Synonyms: EFL1

(R64-2-1)chrXIV:330041A>T

(Saccharomyces cerevisiae)

Allele/Variant

Source: NC_001146.8:g.330041A>T

Genes: RIA1 (Sce)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: synonymous_variant

Diseases: Not Available

Variant Name: (R64-2-1)chrXIV:330041A>T

Gene Synonyms: EFL1

(R64-2-1)chrXIV:328022C>T

(Saccharomyces cerevisiae)

Allele/Variant

Source: NC_001146.8:g.328022C>T

Genes: RIA1 (Sce)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: synonymous_variant

Diseases: Not Available

Variant Name: (R64-2-1)chrXIV:328022C>T

Gene Synonyms: EFL1

(R64-2-1)chrXIV:326625C>G

(Saccharomyces cerevisiae)

Allele/Variant

Source: NC_001146.8:g.326625C>G

Genes: RIA1 (Sce)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intergenic_variant

Diseases: Not Available

Variant Name: (R64-2-1)chrXIV:326625C>G

Gene Synonyms: EFL1

(R64-2-1)chrXIV:329339A>G

(Saccharomyces cerevisiae)

Allele/Variant

Source: NC_001146.8:g.329339A>G

Genes: RIA1 (Sce)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: synonymous_variant

Diseases: Not Available

Variant Name: (R64-2-1)chrXIV:329339A>G

Gene Synonyms: EFL1

(R64-2-1)chrXIV:328328C>A

(Saccharomyces cerevisiae)

Allele/Variant

Source: NC_001146.8:g.328328C>A

Genes: RIA1 (Sce)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant

Diseases: Not Available

Variant Name: (R64-2-1)chrXIV:328328C>A

Gene Synonyms: EFL1

(R64-2-1)chrXIV:327674T>C

(Saccharomyces cerevisiae)

Allele/Variant

Source: NC_001146.8:g.327674T>C

Genes: RIA1 (Sce)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: synonymous_variant

Diseases: Not Available

Variant Name: (R64-2-1)chrXIV:327674T>C

Gene Synonyms: EFL1

(R64-2-1)chrXIV:328673A>G

(Saccharomyces cerevisiae)

Allele/Variant

Source: NC_001146.8:g.328673A>G

Genes: RIA1 (Sce)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: synonymous_variant

Diseases: Not Available

Variant Name: (R64-2-1)chrXIV:328673A>G

Gene Synonyms: EFL1

(R64-2-1)chrXIV:328880C>T

(Saccharomyces cerevisiae)

Allele/Variant

Source: NC_001146.8:g.328880C>T

Genes: RIA1 (Sce)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: synonymous_variant

Diseases: Not Available

Variant Name: (R64-2-1)chrXIV:328880C>T

Gene Synonyms: EFL1

(R64-2-1)chrXIV:329033C>T

(Saccharomyces cerevisiae)

Allele/Variant

Source: NC_001146.8:g.329033C>T

Genes: RIA1 (Sce)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant

Diseases: Not Available

Variant Name: (R64-2-1)chrXIV:329033C>T

Gene Synonyms: EFL1

(R64-2-1)chrXIV:326711G>A

(Saccharomyces cerevisiae)

Allele/Variant

Source: NC_001146.8:g.326711G>A

Genes: RIA1 (Sce)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intergenic_variant

Diseases: Not Available

Variant Name: (R64-2-1)chrXIV:326711G>A

Gene Synonyms: EFL1

(R64-2-1)chrXIV:329212T>G

(Saccharomyces cerevisiae)

Allele/Variant

Source: NC_001146.8:g.329212T>G

Genes: RIA1 (Sce)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: synonymous_variant

Diseases: Not Available

Variant Name: (R64-2-1)chrXIV:329212T>G

Gene Synonyms: EFL1

sa30883

(Danio rerio)

Allele/Variant

Source: ZFIN:ZDB-ALT-160601-681

Genes: efl1 (Dre)

Synonyms: Not Available

Variant Type: point_mutation

Molecular Consequence: stop_gained

Diseases: Not Available

Variant Name: Not Available

Genes: efl1 (Dre)

(GRCh38)1:155131383A>G

(Homo sapiens)

Allele/Variant

Source: rs146875946

Genes: EFNA1 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)1:155131383A>G

Gene Synonyms: EFL1

(GRCh38)1:155131529C>T

(Homo sapiens)

Allele/Variant

Source: rs779806956

Genes: EFNA1 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)1:155131529C>T

Gene Synonyms: EFL1

(GRCh38)1:155133751A>G

(Homo sapiens)

Allele/Variant

Source: rs4745

Genes: EFNA1 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)1:155133751A>G

Gene Synonyms: EFL1

(GRCh38)1:155131556C>G

(Homo sapiens)

Allele/Variant

Source: rs1444026141

Genes: EFNA1 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)1:155131556C>G

Gene Synonyms: EFL1

(GRCh38)1:155131371A>T

(Homo sapiens)

Allele/Variant

Source: NC_000001.11:g.155131371A>T

Genes: EFNA1 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)1:155131371A>T

Gene Synonyms: EFL1

(GRCh38)1:155133973T>C

(Homo sapiens)

Allele/Variant

Source: rs771450050

Genes: EFNA1 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)1:155133973T>C

Gene Synonyms: EFL1

(GRCh38)1:155134023T>C

(Homo sapiens)

Allele/Variant

Source: rs2102473665

Genes: EFNA1 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)1:155134023T>C

Gene Synonyms: EFL1

(GRCh38)1:155131391A>G

(Homo sapiens)

Allele/Variant

Source: rs374457600

Genes: EFNA1 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)1:155131391A>G

Gene Synonyms: EFL1

(GRCh38)1:155133752C>A

(Homo sapiens)

Allele/Variant

Source: rs1664299539

Genes: EFNA1 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)1:155133752C>A

Gene Synonyms: EFL1

(GRCh38)1:155133771C>T

(Homo sapiens)

Allele/Variant

Source: rs1475793891

Genes: EFNA1 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)1:155133771C>T

Gene Synonyms: EFL1

sa34011

(Danio rerio)

Allele/Variant

Source: ZFIN:ZDB-ALT-160601-2804

Genes: efl1 (Dre)

Synonyms: Not Available

Variant Type: point_mutation

Molecular Consequence: splice_donor_variant

Diseases: Not Available

Variant Name: Not Available

Genes: efl1 (Dre)

sa20868

(Danio rerio)

Allele/Variant

Source: ZFIN:ZDB-ALT-131217-15570

Genes: efl1 (Dre)

Synonyms: Not Available

Variant Type: point_mutation

Molecular Consequence: splice_donor_variant

Diseases: Not Available

Variant Name: Not Available

Genes: efl1 (Dre)

sa12887

(Danio rerio)

Allele/Variant

Source: ZFIN:ZDB-ALT-130411-2563

Genes: efl1 (Dre)

Synonyms: Not Available

Variant Type: point_mutation

Molecular Consequence: splice_donor_variant

Diseases: Not Available

Variant Name: Not Available

Genes: efl1 (Dre)

cytosol

Gene Ontology

Source: GO:0005829

Synonyms: Not Available

Branch: cellular component

Genes: efl1 (Dre)...EFL1 (Hsa)...Efl1 (Rno)...Efl1 (Mmu)

Genes Annotated with this GO Term (10000)

nucleotide binding

Gene Ontology

Source: GO:0000166

Synonyms: Not Available

Branch: molecular function

Genes: efl1 (Dre)...EFL1 (Hsa)

Genes Annotated with this GO Term (10000)

translation

Gene Ontology

Source: GO:0006412

Synonyms:

protein anabolism
protein biosynthesis

Branch: biological process

Genes: efl1 (Dre)...EFL1 (Hsa)

Genes Annotated with this GO Term (3634)

protein binding

Gene Ontology

Source: GO:0005515

Synonyms:

glycoprotein binding
protein amino acid binding

Branch: molecular function

Genes: EFL1 (Hsa)

Genes Annotated with this GO Term (10000)

(GRCh38)15:82238289A>G

(Homo sapiens)

Allele/Variant

Source: rs1972460

Genes: EFL1 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: non_coding_transcript_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)15:82238289A>G

(GRCh38)15:82240485C>T

(Homo sapiens)

Allele/Variant

Source: rs767883960

Genes: EFL1 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)15:82240485C>T

(GRCh38)15:82240509A>T

(Homo sapiens)

Allele/Variant

Source: NC_000015.10:g.82240509A>T

Genes: EFL1 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)15:82240509A>T

(GRCh38)15:82241348G>C

(Homo sapiens)

Allele/Variant

Source: rs751585204

Genes: EFL1 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant

Diseases: Not Available

Variant Name: (GRCh38)15:82241348G>C

(GRCh38)15:82252689A>C

(Homo sapiens)

Allele/Variant

Source: rs372509575

Genes: EFL1 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: non_coding_transcript_variant, splice_donor_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)15:82252689A>C

(GRCh38)15:82151520C>T

(Homo sapiens)

Allele/Variant

Source: rs775222060

Genes: EFL1 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant

Diseases: Not Available

Variant Name: (GRCh38)15:82151520C>T

(GRCh38)15:82130517T>C

(Homo sapiens)

Allele/Variant

Source: rs780836068

Genes: EFL1 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant

Diseases: Not Available

Variant Name: (GRCh38)15:82130517T>C

(GRCh38)15:82151560A>C

(Homo sapiens)

Allele/Variant

Source: NC_000015.10:g.82151560A>C

Genes: EFL1 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)15:82151560A>C

(GRCh38)15:82151487G>A

(Homo sapiens)

Allele/Variant

Source: rs189569278

Genes: EFL1 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant

Diseases: Not Available

Variant Name: (GRCh38)15:82151487G>A

(GRCh38)15:82151519G>A

(Homo sapiens)

Allele/Variant

Source: rs376049108

Genes: EFL1 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)15:82151519G>A

(GRCh38)15:82151615C>G

(Homo sapiens)

Allele/Variant

Source: rs1024438888

Genes: EFL1 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)15:82151615C>G

(GRCh38)15:82152401C>T

(Homo sapiens)

Allele/Variant

Source: rs568840186

Genes: EFL1 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)15:82152401C>T

(GRCh38)15:82163917T>C

(Homo sapiens)

Allele/Variant

Source: rs760435290

Genes: EFL1 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant

Diseases: Not Available

Variant Name: (GRCh38)15:82163917T>C

(GRCh38)15:82151483C>T

(Homo sapiens)

Allele/Variant

Source: rs78664413

Genes: EFL1 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)15:82151483C>T

(GRCh38)15:82130460G>A

(Homo sapiens)

Allele/Variant

Source: rs752615261

Genes: EFL1 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant

Diseases: Not Available

Variant Name: (GRCh38)15:82130460G>A

(GRCh38)15:82151526T>C

(Homo sapiens)

Allele/Variant

Source: rs900621884

Genes: EFL1 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant

Diseases: Not Available

Variant Name: (GRCh38)15:82151526T>C

(GRCh38)15:82138748C>A

(Homo sapiens)

Allele/Variant

Source: rs371564001

Genes: EFL1 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant

Diseases: Not Available

Variant Name: (GRCh38)15:82138748C>A

(GRCh38)15:82151571T>C

(Homo sapiens)

Allele/Variant

Source: rs780082234

Genes: EFL1 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant

Diseases: Not Available

Variant Name: (GRCh38)15:82151571T>C

(GRCh38)15:82151670T>C

(Homo sapiens)

Allele/Variant

Source: rs371159786

Genes: EFL1 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant

Diseases: Not Available

Variant Name: (GRCh38)15:82151670T>C

(GRCh38)15:82152194G>A

(Homo sapiens)

Allele/Variant

Source: rs1330065864

Genes: EFL1 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: stop_gained, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)15:82152194G>A

Page 2 of 99