Version: 8.0.0
Date: Tue Jan 28 2025
690 results for lrat
Allele/Variant

Lratem5Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7301727
Genes: Lrat (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Lrat (Mmu)
Genes: Lrat (Mmu)
Symbol: Lratem5Gpt

Lrattm1Bok

(Mus musculus)
Allele/Variant
Source: MGI:3777016
Genes: Lrat (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Lrat (Mmu)
Genes: Lrat (Mmu)
Symbol: Lrattm1Bok

Lrattm1(cre/ERT2)Jhe

(Mus musculus)
Allele/Variant
Source: MGI:7764730
Genes: Lrat (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Lrat (Mmu)
Genes: Lrat (Mmu)
Symbol: Lrattm1(cre/ERT2)Jhe
Construct Regulatory Region: Lrat (Mmu)
Constructs: Lrat< construct

Lrattm1(KOMP)Vlcg

(Mus musculus)
Allele/Variant
Source: MGI:4415406
Genes: Lrat (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Lrat (Mmu)
Genes: Lrat (Mmu)
Symbol: Lrattm1(KOMP)Vlcg

Lratem1(cre)Smoc

(Mus musculus)
Allele/Variant
Source: MGI:6514033
Genes: Lrat (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Lrat (Mmu)
Genes: Lrat (Mmu)
Symbol: Lratem1(cre)Smoc
Construct Regulatory Region: Lrat (Mmu)
Constructs: Lrat< construct

Lrattm1.1(KOMP)Vlcg

(Mus musculus)
Allele/Variant
Source: MGI:5708196
Genes: Lrat (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Lrat (Mmu)
Genes: Lrat (Mmu)
Symbol: Lrattm1.1(KOMP)Vlcg

lratb.1_unrecovered

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-091027-24
Genes: lratb.1 (Dre)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: lratb.1_unrecovered (Dre)
Genes: lratb.1 (Dre)
Symbol: lratb.1_unrecovered

Lrattm1.1Bok

(Mus musculus)
Allele/Variant
Source: MGI:3777017
Genes: Lrat (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Lrat (Mmu)
Genes: Lrat (Mmu)
Symbol: Lrattm1.1Bok

Lratem2Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7301726
Genes: Lrat (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Lrat (Mmu)
Genes: Lrat (Mmu)
Symbol: Lratem2Gpt

Lratem1(icre)Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7301725
Genes: Lrat (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Lrat (Mmu)
Genes: Lrat (Mmu)
Symbol: Lratem1(icre)Gpt
Construct Regulatory Region: Lrat (Mmu)
Constructs: Lrat< construct

Lratd2em1(IMPC)Ccpcz

(Mus musculus)
Allele/Variant
Source: MGI:6316150
Genes: Lratd2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Lratd2 (Mmu)
Genes: Lratd2 (Mmu)
Symbol: Lratd2em1(IMPC)Ccpcz

Lrattm1Kpal

(Mus musculus)
Allele/Variant
Source: MGI:3038935
Genes: Lrat (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Leber congenital amaurosis 14
Variant Name: Not Available
Symbol: Lrat (Mmu)
Genes: Lrat (Mmu)
Symbol: Lrattm1Kpal

Lrattm1Log

(Mus musculus)
Allele/Variant
Source: MGI:3612421
Genes: Lrat (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Lrat (Mmu)
Genes: Lrat (Mmu)
Symbol: Lrattm1Log

zko489b

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-171115-413
Genes: lrata (Dre)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: lrat
Genes: lrata (Dre)

la013604Tg

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-120806-8390
Genes: lrata (Dre)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: lrat
Genes: lrata (Dre)

c601Tg

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-230828-3
Genes: lratd2a (Dre)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Genes: lratd2a (Dre)

fh260

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-080325-4
Genes: lratb.1 (Dre)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Genes: lratb.1 (Dre)

zko215a

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-171115-171
Genes: lratb.2 (Dre)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Genes: lratb.2 (Dre)

la021366Tg

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-120806-9097
Genes: lratb.1 (Dre)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Genes: lratb.1 (Dre)

zko215b

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-171115-172
Genes: lratb.2 (Dre)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Genes: lratb.2 (Dre)

Tg(Lrat-cre)1Rshw

(Mus musculus)
Allele/Variant
Source: MGI:5545650
Genes: Not Available
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Tg(Lrat-cre)1Rshw
Construct Regulatory Region: Lrat
Constructs: Tg(Lrat-cre)1Rshw construct

sa10285

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-130411-260
Genes: lratb.2 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: lratb.2 (Dre)

sa37079

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-160601-5107
Genes: lratd1 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: lratd1 (Dre)

sa1600

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-120411-211
Genes: lratb.1 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: lratb.1 (Dre)

(GRCh38)4:154744109C>G

(Homo sapiens)
Allele/Variant
Source: rs886059159
Genes: LRAT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:154744109C>G

(GRCh38)4:154744392C>T

(Homo sapiens)
Allele/Variant
Source: NC_000004.12:g.154744392C>T
Genes: LRAT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:154744392C>T

(GRCh38)4:154744485G>C

(Homo sapiens)
Allele/Variant
Source: NC_000004.12:g.154744485G>C
Genes: LRAT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:154744485G>C

(GRCh38)4:154744845G>T

(Homo sapiens)
Allele/Variant
Source: rs375365480
Genes: LRAT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:154744845G>T

(GRCh38)4:154750417C>A

(Homo sapiens)
Allele/Variant
Source: rs572110901
Genes: LRAT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)4:154750417C>A

(GRCh38)4:154750474T>G

(Homo sapiens)
Allele/Variant
Source: rs12507608
Genes: LRAT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)4:154750474T>G

(GRCh38)4:154751990A>G

(Homo sapiens)
Allele/Variant
Source: rs745679958
Genes: LRAT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)4:154751990A>G

(GRCh38)4:154744395G>A

(Homo sapiens)
Allele/Variant
Source: rs1191239917
Genes: LRAT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:154744395G>A

(GRCh38)4:154744409G>A

(Homo sapiens)
Allele/Variant
Source: rs1732833730
Genes: LRAT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:154744409G>A

(GRCh38)4:154744531C>T

(Homo sapiens)
Allele/Variant
Source: rs775838916
Genes: LRAT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:154744531C>T

(GRCh38)4:154744497C>T

(Homo sapiens)
Allele/Variant
Source: rs762402395
Genes: LRAT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:154744497C>T

(GRCh38)4:154744843C>T

(Homo sapiens)
Allele/Variant
Source: rs145355018
Genes: LRAT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:154744843C>T

(GRCh38)4:154744737C>G

(Homo sapiens)
Allele/Variant
Source: rs572457198
Genes: LRAT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:154744737C>G

(GRCh38)4:154751358G>C

(Homo sapiens)
Allele/Variant
Source: rs940106140
Genes: LRAT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)4:154751358G>C

(GRCh38)4:154751458C>T

(Homo sapiens)
Allele/Variant
Source: rs1046783706
Genes: LRAT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)4:154751458C>T

(GRCh38)4:154751594C>T

(Homo sapiens)
Allele/Variant
Source: rs538201546
Genes: LRAT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)4:154751594C>T

(GRCh38)4:154749217T>C

(Homo sapiens)
Allele/Variant
Source: rs763149722
Genes: LRAT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)4:154749217T>C

(GRCh38)4:154751554G>A

(Homo sapiens)
Allele/Variant
Source: rs886059170
Genes: LRAT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)4:154751554G>A

(GRCh38)4:154751991A>G

(Homo sapiens)
Allele/Variant
Source: rs1733006832
Genes: LRAT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)4:154751991A>G

(GRCh38)4:154752906A>G

(Homo sapiens)
Allele/Variant
Source: rs886059178
Genes: LRAT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)4:154752906A>G

(GRCh38)4:154744229A>C

(Homo sapiens)
Allele/Variant
Source: rs886059161
Genes: LRAT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:154744229A>C

(GRCh38)4:154744415C>T

(Homo sapiens)
Allele/Variant
Source: rs1042443674
Genes: LRAT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:154744415C>T

(GRCh38)4:154744470C>T

(Homo sapiens)
Allele/Variant
Source: rs1367430236
Genes: LRAT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:154744470C>T

(GRCh38)4:154744746G>A

(Homo sapiens)
Allele/Variant
Source: rs1412729929
Genes: LRAT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:154744746G>A

(GRCh38)4:154744787A>G

(Homo sapiens)
Allele/Variant
Source: rs1470351055
Genes: LRAT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:154744787A>G

(GRCh38)4:154744799G>A

(Homo sapiens)
Allele/Variant
Source: rs878853351
Genes: LRAT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:154744799G>A