Version: 8.1.0
Date: Fri Apr 18 2025
1,430 results for epn4

clint1a

(Danio rerio)
Gene
Name: clathrin interactor 1a
Synonyms: wu:fc12e09, wu:fa05f05, enth, wu:fb97f11, kiaa0171, zgc:103447, clint1, enthoprotin, epn4
Source: ZFIN:ZDB-GENE-030131-2590
Biotype: protein coding gene
Synonyms: epn4...epn4...epn4

clint1.S

(Xenopus laevis)
Gene
Name: clathrin interactor 1
Synonyms: epnr, enth, clint, clathrin interactor 1, clint1-b, clint1.S, clint1-a, epsinr, epn4
Source: Xenbase:XB-GENE-6255326
Biotype: gene
Synonyms: epn4...epn4...epn4

clint1

(Xenopus tropicalis)
Gene
Name: clathrin interactor 1
Synonyms: epnr, enth, clint, clathrin interactor 1, clint1-b, clint1, clint1-a, epsinr, epn4
Source: Xenbase:XB-GENE-1013621
Biotype: gene
Synonyms: epn4...epn4...epn4

Clint1

(Rattus norvegicus)
Gene
Name: clathrin interactor 1
Synonyms: Epn4, Clint, epsin 4, enthoprotin, Enth
Source: RGD:1303328
Biotype: protein coding gene
Synonyms: Epn4...Epn4

clint1.L

(Xenopus laevis)
Gene
Name: clathrin interactor 1
Synonyms: epnr, enth, clint, clathrin interactor 1, clint1-b, clint1-a, clint1.L, epsinr, epn4
Source: Xenbase:XB-GENE-1013624
Biotype: gene
Synonyms: epn4...epn4...epn4

CLINT1

(Homo sapiens)
Gene
Name: clathrin interactor 1
Synonyms: FLJ46753, clathrin-interacting protein localized in the trans-Golgi region, epsin-related protein, enthoprotin, KIAA0171, epsin-4, EPNR, EPN4, CLINT, clathrin interacting protein localized in the trans-Golgi region, epsin 4, epsinR, ENTH
Source: HGNC:23186
Biotype: protein coding gene
Synonyms: EPN4...EPN4

Clint1

(Mus musculus)
Gene
Name: clathrin interactor 1
Synonyms: Epn4, mKIAA0171, Clint, RIKEN cDNA C530049I24 gene, expressed sequence AW537616, C530049I24Rik, AI642036, AW537616, Enth, expressed sequence AI642036
Source: MGI:2144243
Biotype: protein coding gene
Synonyms: Epn4...Epn4

hi2558Tg

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-040728-4
Genes: clint1a (Dre)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: epn4

hi1520Tg

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-040728-2
Genes: clint1a (Dre)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: epn4

Clint1em1(IMPC)Mbp

(Mus musculus)
Allele/Variant
Source: MGI:7484790
Genes: Clint1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: Epn4

Clint1em1Smoc

(Mus musculus)
Allele/Variant
Source: MGI:7289028
Genes: Clint1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: Epn4

Clint1tm1a(EUCOMM)Hmgu

(Mus musculus)
Allele/Variant
Source: MGI:4881976
Genes: Clint1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: Epn4

Clint1em1Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7297112
Genes: Clint1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: Epn4

(GRCh38)5:157789503A>G

(Homo sapiens)
Allele/Variant
Source: rs373698096
Genes: CLINT1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:157789503A>G
Gene Synonyms: EPN4

(GRCh38)5:157787765C>T

(Homo sapiens)
Allele/Variant
Source: rs759387255
Genes: CLINT1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)5:157787765C>T
Gene Synonyms: EPN4

(GRCh38)5:157787930A>T

(Homo sapiens)
Allele/Variant
Source: NC_000005.10:g.157787930A>T
Genes: CLINT1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)5:157787930A>T
Gene Synonyms: EPN4

(GRCh38)5:157789521T>C

(Homo sapiens)
Allele/Variant
Source: rs1247930185
Genes: CLINT1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:157789521T>C
Gene Synonyms: EPN4

(GRCh38)5:157787860T>C

(Homo sapiens)
Allele/Variant
Source: rs202225711
Genes: CLINT1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)5:157787860T>C
Gene Synonyms: EPN4

(GRCh38)5:157789423G>A

(Homo sapiens)
Allele/Variant
Source: NC_000005.10:g.157789423G>A
Genes: CLINT1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)5:157789423G>A
Gene Synonyms: EPN4

(GRCh38)5:157791840G>C

(Homo sapiens)
Allele/Variant
Source: rs1761920411
Genes: CLINT1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:157791840G>C
Gene Synonyms: EPN4

(GRCh38)5:157787899T>C

(Homo sapiens)
Allele/Variant
Source: rs753045326
Genes: CLINT1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)5:157787899T>C
Gene Synonyms: EPN4

(GRCh38)5:157806071G>A

(Homo sapiens)
Allele/Variant
Source: rs780997030
Genes: CLINT1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:157806071G>A
Gene Synonyms: EPN4

(GRCh38)5:157809683C>T

(Homo sapiens)
Allele/Variant
Source: rs932482029
Genes: CLINT1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:157809683C>T
Gene Synonyms: EPN4

(GRCh38)5:157809725T>C

(Homo sapiens)
Allele/Variant
Source: NC_000005.10:g.157809725T>C
Genes: CLINT1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:157809725T>C
Gene Synonyms: EPN4

(GRCh38)5:157791846G>C

(Homo sapiens)
Allele/Variant
Source: NC_000005.10:g.157791846G>C
Genes: CLINT1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:157791846G>C
Gene Synonyms: EPN4

(GRCh38)5:157806059A>T

(Homo sapiens)
Allele/Variant
Source: rs1329599129
Genes: CLINT1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:157806059A>T
Gene Synonyms: EPN4

(GRCh38)5:157813159C>T

(Homo sapiens)
Allele/Variant
Source: rs760291166
Genes: CLINT1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:157813159C>T
Gene Synonyms: EPN4

(GRCh38)5:157814287G>C

(Homo sapiens)
Allele/Variant
Source: NC_000005.10:g.157814287G>C
Genes: CLINT1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:157814287G>C
Gene Synonyms: EPN4

(GRCh38)5:157791980C>T

(Homo sapiens)
Allele/Variant
Source: NC_000005.10:g.157791980C>T
Genes: CLINT1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, stop_gained
Diseases: Not Available
Variant Name: (GRCh38)5:157791980C>T
Gene Synonyms: EPN4

(GRCh38)5:157791986G>T

(Homo sapiens)
Allele/Variant
Source: rs777820202
Genes: CLINT1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:157791986G>T
Gene Synonyms: EPN4

(GRCh38)5:157813080A>G

(Homo sapiens)
Allele/Variant
Source: NC_000005.10:g.157813080A>G
Genes: CLINT1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:157813080A>G
Gene Synonyms: EPN4

(GRCh38)5:157791941G>T

(Homo sapiens)
Allele/Variant
Source: NC_000005.10:g.157791941G>T
Genes: CLINT1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:157791941G>T
Gene Synonyms: EPN4

(GRCh38)5:157805891G>A

(Homo sapiens)
Allele/Variant
Source: rs368145773
Genes: CLINT1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:157805891G>A
Gene Synonyms: EPN4

(GRCh38)5:157813221T>C

(Homo sapiens)
Allele/Variant
Source: rs566963901
Genes: CLINT1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:157813221T>C
Gene Synonyms: EPN4

(GRCh38)5:157787747T>C

(Homo sapiens)
Allele/Variant
Source: rs772805192
Genes: CLINT1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)5:157787747T>C
Gene Synonyms: EPN4

(GRCh38)5:157787855T>G

(Homo sapiens)
Allele/Variant
Source: NC_000005.10:g.157787855T>G
Genes: CLINT1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)5:157787855T>G
Gene Synonyms: EPN4

(GRCh38)5:157787818G>C

(Homo sapiens)
Allele/Variant
Source: NC_000005.10:g.157787818G>C
Genes: CLINT1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)5:157787818G>C
Gene Synonyms: EPN4

(GRCh38)5:157787828G>A

(Homo sapiens)
Allele/Variant
Source: rs1489956886
Genes: CLINT1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)5:157787828G>A
Gene Synonyms: EPN4

(GRCh38)5:157789417T>C

(Homo sapiens)
Allele/Variant
Source: rs762597450
Genes: CLINT1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)5:157789417T>C
Gene Synonyms: EPN4

(GRCh38)5:157789525G>C

(Homo sapiens)
Allele/Variant
Source: rs772066913
Genes: CLINT1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:157789525G>C
Gene Synonyms: EPN4

(GRCh38)5:157806074G>A

(Homo sapiens)
Allele/Variant
Source: NC_000005.10:g.157806074G>A
Genes: CLINT1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:157806074G>A
Gene Synonyms: EPN4

(GRCh38)5:157791884G>A

(Homo sapiens)
Allele/Variant
Source: rs771442603
Genes: CLINT1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:157791884G>A
Gene Synonyms: EPN4

(GRCh38)5:157789376C>G

(Homo sapiens)
Allele/Variant
Source: rs375467930
Genes: CLINT1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)5:157789376C>G
Gene Synonyms: EPN4

(GRCh38)5:157803687G>T

(Homo sapiens)
Allele/Variant
Source: rs933526917
Genes: CLINT1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:157803687G>T
Gene Synonyms: EPN4

(GRCh38)5:157805888T>G

(Homo sapiens)
Allele/Variant
Source: rs375245097
Genes: CLINT1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:157805888T>G
Gene Synonyms: EPN4

(mRatBN7.2)10:30303788G>C

(Rattus norvegicus)
Allele/Variant
Source: rs105413103
Genes: Clint1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:30303788G>C
Gene Synonyms: Epn4

(mRatBN7.2)10:30305336T>G

(Rattus norvegicus)
Allele/Variant
Source: rs196970181
Genes: Clint1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:30305336T>G
Gene Synonyms: Epn4

(mRatBN7.2)10:30342938G>A

(Rattus norvegicus)
Allele/Variant
Source: rs105968409
Genes: Clint1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:30342938G>A
Gene Synonyms: Epn4

(mRatBN7.2)10:30347385T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3321715275
Genes: Clint1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:30347385T>C
Gene Synonyms: Epn4

(mRatBN7.2)10:30324777G>A

(Rattus norvegicus)
Allele/Variant
Source: rs105556118
Genes: Clint1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:30324777G>A
Gene Synonyms: Epn4