Version: 8.1.0
Date: Fri Apr 18 2025
583 results for nupl2

nup42

(Danio rerio)
Gene
Name: nucleoporin 42
Synonyms: nupl2, zgc:77724
Source: ZFIN:ZDB-GENE-040426-2292
Biotype: protein coding gene
Synonyms: nupl2...nupl2...nupl2

nup42

(Xenopus tropicalis)
Gene
Name: nucleoporin 42
Synonyms: nup42, nlp_1, nlp-1, nupl2, nucleoporin 42
Source: Xenbase:XB-GENE-6258607
Biotype: gene
Synonyms: nupl2...nupl2...nupl2

nup42.L

(Xenopus laevis)
Gene
Name: nucleoporin 42
Synonyms: nup42.L, nlp_1, nlp-1, nupl2, nucleoporin 42
Source: Xenbase:XB-GENE-6254296
Biotype: gene
Synonyms: nupl2...nupl2...nupl2

Nup42

(Mus musculus)
Gene
Name: nucleoporin 42
Synonyms: AV116043, expressed sequence AV116043, nucleoporin like 2, CG1, Nupl2, RGD1560934
Source: MGI:2387631
Biotype: protein coding gene
Synonyms: Nupl2...Nupl2

NUP42

(Homo sapiens)
Gene
Name: nucleoporin 42
Synonyms: nucleoporin NUP42, NLP_1, CG1, nucleoporin hCG1, nucleoporin-like protein 2, nucleoporin-like protein 1, H_RG271G13.9, UIP1, hCG1, NUP42 homolog, NLP-1, nucleoporin like 2, NLP1, NUPL2
Source: HGNC:17010
Biotype: protein coding gene
Synonyms: NUPL2...NUPL2

Nup42

(Rattus norvegicus)
Gene
Name: nucleoporin 42
Synonyms: nucleoporin NUP42, nucleoporin like 2, LOC499974, Nupl2, nucleoporin-like protein 2, RGD1560934, similar to nucleoporin like 2
Source: RGD:1560934
Biotype: protein coding gene
Synonyms: Nupl2...Nupl2

Nup42em1Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7303344
Genes: Nup42 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: Nupl2

(GRCh38)7:23182089G>A

(Homo sapiens)
Allele/Variant
Source: rs977948600
Genes: NUP42 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:23182089G>A
Gene Synonyms: NUPL2

(GRCh38)7:23182158G>A

(Homo sapiens)
Allele/Variant
Source: rs1331551680
Genes: NUP42 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:23182158G>A
Gene Synonyms: NUPL2

(GRCh38)7:23185081C>T

(Homo sapiens)
Allele/Variant
Source: rs757786096
Genes: NUP42 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:23185081C>T
Gene Synonyms: NUPL2

(GRCh38)7:23200306G>A

(Homo sapiens)
Allele/Variant
Source: rs1239044039
Genes: NUP42 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:23200306G>A
Gene Synonyms: NUPL2

(GRCh38)7:23182128G>A

(Homo sapiens)
Allele/Variant
Source: rs762887774
Genes: NUP42 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:23182128G>A
Gene Synonyms: NUPL2

(GRCh38)7:23200249C>A

(Homo sapiens)
Allele/Variant
Source: rs766463707
Genes: NUP42 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:23200249C>A
Gene Synonyms: NUPL2

(GRCh38)7:23200687A>C

(Homo sapiens)
Allele/Variant
Source: rs750817913
Genes: NUP42 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:23200687A>C
Gene Synonyms: NUPL2

(GRCh38)7:23200707C>T

(Homo sapiens)
Allele/Variant
Source: rs267601462
Genes: NUP42 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:23200707C>T
Gene Synonyms: NUPL2

(GRCh38)7:23185229G>T

(Homo sapiens)
Allele/Variant
Source: rs144835773
Genes: NUP42 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:23185229G>T
Gene Synonyms: NUPL2

(GRCh38)7:23185244A>T

(Homo sapiens)
Allele/Variant
Source: NC_000007.14:g.23185244A>T
Genes: NUP42 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:23185244A>T
Gene Synonyms: NUPL2

(GRCh38)7:23182159C>T

(Homo sapiens)
Allele/Variant
Source: rs764949484
Genes: NUP42 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:23182159C>T
Gene Synonyms: NUPL2

(GRCh38)7:23200350C>G

(Homo sapiens)
Allele/Variant
Source: rs773653043
Genes: NUP42 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:23200350C>G
Gene Synonyms: NUPL2

(GRCh38)7:23200636C>T

(Homo sapiens)
Allele/Variant
Source: rs1326581633
Genes: NUP42 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:23200636C>T
Gene Synonyms: NUPL2

(GRCh38)7:23182122C>A

(Homo sapiens)
Allele/Variant
Source: rs765112038
Genes: NUP42 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:23182122C>A
Gene Synonyms: NUPL2

(GRCh38)7:23185133G>A

(Homo sapiens)
Allele/Variant
Source: rs149868774
Genes: NUP42 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:23185133G>A
Gene Synonyms: NUPL2

(GRCh38)7:23185290G>A

(Homo sapiens)
Allele/Variant
Source: rs145269225
Genes: NUP42 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:23185290G>A
Gene Synonyms: NUPL2

(GRCh38)7:23182092A>G

(Homo sapiens)
Allele/Variant
Source: rs779252589
Genes: NUP42 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:23182092A>G
Gene Synonyms: NUPL2

(GRCh38)7:23185154G>C

(Homo sapiens)
Allele/Variant
Source: rs1554295346
Genes: NUP42 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:23185154G>C
Gene Synonyms: NUPL2

(GRCh38)7:23185082G>A

(Homo sapiens)
Allele/Variant
Source: rs781615275
Genes: NUP42 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:23185082G>A
Gene Synonyms: NUPL2

(GRCh38)7:23187072T>C

(Homo sapiens)
Allele/Variant
Source: rs536538587
Genes: NUP42 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, start_lost
Diseases: Not Available
Variant Name: (GRCh38)7:23187072T>C
Gene Synonyms: NUPL2

(GRCh38)7:23196689G>A

(Homo sapiens)
Allele/Variant
Source: rs769693804
Genes: NUP42 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:23196689G>A
Gene Synonyms: NUPL2

(GRCh38)7:23200405T>G

(Homo sapiens)
Allele/Variant
Source: NC_000007.14:g.23200405T>G
Genes: NUP42 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:23200405T>G
Gene Synonyms: NUPL2

(GRCh38)7:23200483G>C

(Homo sapiens)
Allele/Variant
Source: rs80001203
Genes: NUP42 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:23200483G>C
Gene Synonyms: NUPL2

(GRCh38)7:23200503G>A

(Homo sapiens)
Allele/Variant
Source: rs201148821
Genes: NUP42 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:23200503G>A
Gene Synonyms: NUPL2

(GRCh38)7:23200623A>G

(Homo sapiens)
Allele/Variant
Source: rs376366312
Genes: NUP42 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:23200623A>G
Gene Synonyms: NUPL2

(GRCh38)7:23200657T>G

(Homo sapiens)
Allele/Variant
Source: rs1429376986
Genes: NUP42 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:23200657T>G
Gene Synonyms: NUPL2

(GRCh38)7:23200734C>A

(Homo sapiens)
Allele/Variant
Source: rs180753026
Genes: NUP42 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:23200734C>A
Gene Synonyms: NUPL2

(GRCh38)7:23185213A>G

(Homo sapiens)
Allele/Variant
Source: rs776285163
Genes: NUP42 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:23185213A>G
Gene Synonyms: NUPL2

(GRCh38)7:23196705A>T

(Homo sapiens)
Allele/Variant
Source: rs751114640
Genes: NUP42 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:23196705A>T
Gene Synonyms: NUPL2

(GRCh38)7:23200491A>G

(Homo sapiens)
Allele/Variant
Source: rs1786183141
Genes: NUP42 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:23200491A>G
Gene Synonyms: NUPL2

(GRCh38)7:23185115A>T

(Homo sapiens)
Allele/Variant
Source: rs150791680
Genes: NUP42 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:23185115A>T
Gene Synonyms: NUPL2

(GRCh38)7:23185132A>G

(Homo sapiens)
Allele/Variant
Source: rs773074996
Genes: NUP42 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:23185132A>G
Gene Synonyms: NUPL2

sa36745

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-160601-4852
Genes: nup42 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: nupl2

(GRCm39)5:24370641A>C

(Mus musculus)
Allele/Variant
Source: rs237939200
Genes: Nup42 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)5:24370641A>C
Gene Synonyms: Nupl2

(GRCm39)5:24375042G>T

(Mus musculus)
Allele/Variant
Source: rs237079235
Genes: Nup42 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)5:24375042G>T
Gene Synonyms: Nupl2

(GRCm39)5:24375226C>T

(Mus musculus)
Allele/Variant
Source: rs240048662
Genes: Nup42 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)5:24375226C>T
Gene Synonyms: Nupl2

(GRCm39)5:24375254A>C

(Mus musculus)
Allele/Variant
Source: rs257061571
Genes: Nup42 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)5:24375254A>C
Gene Synonyms: Nupl2

(GRCm39)5:24375420C>A

(Mus musculus)
Allele/Variant
Source: rs578960945
Genes: Nup42 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)5:24375420C>A
Gene Synonyms: Nupl2

(GRCm39)5:24375427T>C

(Mus musculus)
Allele/Variant
Source: rs264770279
Genes: Nup42 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)5:24375427T>C
Gene Synonyms: Nupl2

(GRCm39)5:24376309G>A

(Mus musculus)
Allele/Variant
Source: rs215375847
Genes: Nup42 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)5:24376309G>A
Gene Synonyms: Nupl2

(GRCm39)5:24377346C>G

(Mus musculus)
Allele/Variant
Source: rs252537870
Genes: Nup42 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)5:24377346C>G
Gene Synonyms: Nupl2

(GRCm39)5:24381170G>T

(Mus musculus)
Allele/Variant
Source: rs213287272
Genes: Nup42 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)5:24381170G>T
Gene Synonyms: Nupl2

(GRCm39)5:24381200T>C

(Mus musculus)
Allele/Variant
Source: rs215930303
Genes: Nup42 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)5:24381200T>C
Gene Synonyms: Nupl2