Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: Lcn2 (Mmu)
Lcn2tm1.1Bara
(Mus musculus)Allele/Variant
Source: MGI:5645260
Genes: Lcn2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Lcn2em1Cya
(Mus musculus)Allele/Variant
Source: MGI:7584767
Genes: Lcn2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Lcn2tm1Aade
(Mus musculus)Allele/Variant
Source: MGI:3525578
Genes: Lcn2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Lcn2em1Gpt
(Mus musculus)Allele/Variant
Source: MGI:7301558
Genes: Lcn2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Lcn2tm2Bara
(Mus musculus)Allele/Variant
Source: MGI:5703928
Genes: Lcn2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Lcn2tm1.1Bga
(Mus musculus)Allele/Variant
Source: MGI:6155602
Genes: Lcn2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Lcn2em5Gpt
(Mus musculus)Allele/Variant
Source: MGI:7301559
Genes: Lcn2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Lcn2em2Cya
(Mus musculus)Allele/Variant
Source: MGI:7584768
Genes: Lcn2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Lcn2tm1.2Bara
(Mus musculus)Allele/Variant
Source: MGI:5645261
Genes: Lcn2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Lcn2tm1a(KOMP)Wtsi
(Mus musculus)Allele/Variant
Source: MGI:5302289
Genes: Lcn2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Lcn2tm1Smoc
(Mus musculus)Allele/Variant
Source: MGI:7290793
Genes: Lcn2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Lcn2tm1Mrgr
(Mus musculus)Allele/Variant
Source: MGI:5052158
Genes: Lcn2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Lcn2tm1b(KOMP)Wtsi
(Mus musculus)Allele/Variant
Source: MGI:5588291
Genes: Lcn2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Lcn2tm1Mak
(Mus musculus)Allele/Variant
Source: MGI:3620000
Genes: Lcn2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Lcn2tm1Hmhl
(Mus musculus)Allele/Variant
Source: MGI:7427378
Genes: Lcn2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
(GRCm39)2:32276685C>T
(Mus musculus)Allele/Variant
Source: rs228496819
Genes: Lcn2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:32276685C>T
(GRCm39)2:32277799C>T
(Mus musculus)Allele/Variant
Source: rs28236192
Genes: Lcn2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:32277799C>T
(GRCm39)2:32275576G>A
(Mus musculus)Allele/Variant
Source: rs28236196
Genes: Lcn2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:32275576G>A
(GRCm39)2:32275879A>G
(Mus musculus)Allele/Variant
Source: rs28236194
Genes: Lcn2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:32275879A>G
(GRCm39)2:32276468T>G
(Mus musculus)Allele/Variant
Source: rs28236193
Genes: Lcn2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:32276468T>G
(GRCm39)2:32276545G>C
(Mus musculus)Allele/Variant
Source: rs242387848
Genes: Lcn2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:32276545G>C
(GRCm39)2:32274679A>G
(Mus musculus)Allele/Variant
Source: rs251843130
Genes: Lcn2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)2:32274679A>G
(GRCm39)2:32275120A>G
(Mus musculus)Allele/Variant
Source: rs252538137
Genes: Lcn2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:32275120A>G
(GRCm39)2:32275631T>A
(Mus musculus)Allele/Variant
Source: rs231875975
Genes: Lcn2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:32275631T>A
(GRCm39)2:32276057T>A
(Mus musculus)Allele/Variant
Source: rs237400585
Genes: Lcn2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:32276057T>A
(GRCm39)2:32277976G>A
(Mus musculus)Allele/Variant
Source: rs235678981
Genes: Lcn2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCm39)2:32277976G>A
(GRCm39)2:32277219C>T
(Mus musculus)Allele/Variant
Source: rs230903679
Genes: Lcn2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:32277219C>T
(GRCm39)2:32276914G>C
(Mus musculus)Allele/Variant
Source: rs245965631
Genes: Lcn2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:32276914G>C
(GRCm39)2:32277517C>T
(Mus musculus)Allele/Variant
Source: rs235704312
Genes: Lcn2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:32277517C>T
(GRCm39)2:32276655C>T
(Mus musculus)Allele/Variant
Source: rs253917461
Genes: Lcn2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:32276655C>T
(GRCm39)2:32275189C>G
(Mus musculus)Allele/Variant
Source: rs240212211
Genes: Lcn2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:32275189C>G
(GRCm39)2:32276868T>C
(Mus musculus)Allele/Variant
Source: rs259558183
Genes: Lcn2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:32276868T>C
(GRCm39)2:32275265G>A
(Mus musculus)Allele/Variant
Source: rs28236197
Genes: Lcn2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:32275265G>A
(GRCm39)2:32275425C>T
(Mus musculus)Allele/Variant
Source: rs13461545
Genes: Lcn2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:32275425C>T
(GRCm39)2:32275794C>T
(Mus musculus)Allele/Variant
Source: rs245930307
Genes: Lcn2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)2:32275794C>T
(GRCm39)2:32277274C>T
(Mus musculus)Allele/Variant
Source: rs249760241
Genes: Lcn2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:32277274C>T
(GRCm39)2:32277458A>G
(Mus musculus)Allele/Variant
Source: rs235564459
Genes: Lcn2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:32277458A>G
(GRCm39)2:32274875A>G
(Mus musculus)Allele/Variant
Source: rs13461542
Genes: Lcn2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)2:32274875A>G
(GRCm39)2:32275458C>T
(Mus musculus)Allele/Variant
Source: rs223860059
Genes: Lcn2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, coding_sequence_variant, incomplete_terminal_codon_variant
Diseases: Not Available
Variant Name: (GRCm39)2:32275458C>T
(GRCm39)2:32275676G>A
(Mus musculus)Allele/Variant
Source: rs228963150
Genes: Lcn2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:32275676G>A
(GRCm39)2:32276907T>G
(Mus musculus)Allele/Variant
Source: rs227965303
Genes: Lcn2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:32276907T>G
(GRCm39)2:32275705C>T
(Mus musculus)Allele/Variant
Source: rs28236195
Genes: Lcn2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:32275705C>T
(GRCm39)2:32278074T>A
(Mus musculus)Allele/Variant
Source: rs253272049
Genes: Lcn2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCm39)2:32278074T>A
(GRCm39)2:32278157T>C
(Mus musculus)Allele/Variant
Source: rs237443244
Genes: Lcn2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:32278157T>C
(GRCm39)2:32275255C>A
(Mus musculus)Allele/Variant
Source: rs258003847
Genes: Lcn2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:32275255C>A
(GRCm39)2:32277899T>C
(Mus musculus)Allele/Variant
Source: rs243700561
Genes: Lcn2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)2:32277899T>C
(GRCm39)2:32277129C>T
(Mus musculus)Allele/Variant
Source: rs13461546
Genes: Lcn2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)2:32277129C>T
(GRCm39)2:32278079G>C
(Mus musculus)Allele/Variant
Source: rs216229714
Genes: Lcn2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCm39)2:32278079G>C
(GRCm39)2:32278171T>C
(Mus musculus)Allele/Variant
Source: rs47201711
Genes: Lcn2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:32278171T>C
(GRCm39)2:32274990C>T
(Mus musculus)Allele/Variant
Source: rs231901279
Genes: Lcn2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:32274990C>T