622 results for CHKB-CPT1B

CHKB-CPT1B

(Homo sapiens)
Gene
Name: CHKB-CPT1B readthrough (NMD candidate)
Synonyms: CPTI-M, CPT1-M, CHKL-CPT1B, FLJ56256, KIAA1670, CPT1B, MGC149140
Source: HGNC:41998
Biotype: ncRNA gene
Symbol: CHKB-CPT1B (Hsa)
Symbol: CHKB-CPT1B

Gm44502

(Mus musculus)
Gene
Name: predicted readthrough transcript (NMD candidate), 44502
Synonyms: ChkbCpt1b, cDNA sequence BC090627, Chkb-Cpt1b, BC090627, Chkbcpt1b, Chkb-Cpt1b readthrough transcript (NMD candidate)
Source: MGI:3846135
Biotype: protein coding gene
Synonyms: Chkb-Cpt1b...Chkb-Cpt1b...Chkb-Cpt1b readthrough transcript (NMD candidate)...Chkb-Cpt1b...Chkb-Cpt1b readthrough transcript (NMD candidate)

Source: GO:0008654
Synonyms:
  • phospholipid anabolism
  • phospholipid biosynthesis
Branch: biological process
Genes: CHKB-CPT1B (Hsa)

Allele/Variant
Source: rs237496061
Genes: Gm44502 (Mmu), Cpt1b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:89307394C>T
Gene Synonyms: Chkb-Cpt1b...Chkb-Cpt1b readthrough transcript (NMD candidate)

Allele/Variant
Source: rs241998246
Genes: Gm44502 (Mmu), Cpt1b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:89307650G>T
Gene Synonyms: Chkb-Cpt1b...Chkb-Cpt1b readthrough transcript (NMD candidate)

Allele/Variant
Source: rs231069114
Genes: Gm44502 (Mmu), Cpt1b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:89307805C>T
Gene Synonyms: Chkb-Cpt1b...Chkb-Cpt1b readthrough transcript (NMD candidate)

Allele/Variant
Source: rs223721618
Genes: Gm44502 (Mmu), Cpt1b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:89303895G>A
Gene Synonyms: Chkb-Cpt1b...Chkb-Cpt1b readthrough transcript (NMD candidate)

Allele/Variant
Source: rs258684980
Genes: Gm44502 (Mmu), Cpt1b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)15:89304364C>A
Gene Synonyms: Chkb-Cpt1b...Chkb-Cpt1b readthrough transcript (NMD candidate)

Allele/Variant
Source: rs230160418
Genes: Gm44502 (Mmu), Cpt1b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:89304499C>T
Gene Synonyms: Chkb-Cpt1b...Chkb-Cpt1b readthrough transcript (NMD candidate)

Allele/Variant
Source: rs212165250
Genes: Gm44502 (Mmu), Cpt1b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:89304533T>A
Gene Synonyms: Chkb-Cpt1b...Chkb-Cpt1b readthrough transcript (NMD candidate)

Allele/Variant
Source: rs222961748
Genes: Gm44502 (Mmu), Cpt1b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)15:89304909G>A
Gene Synonyms: Chkb-Cpt1b...Chkb-Cpt1b readthrough transcript (NMD candidate)

Allele/Variant
Source: rs584318712
Genes: Gm44502 (Mmu), Cpt1b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:89305152A>G
Gene Synonyms: Chkb-Cpt1b...Chkb-Cpt1b readthrough transcript (NMD candidate)

Allele/Variant
Source: rs246328497
Genes: Gm44502 (Mmu), Cpt1b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)15:89300736C>T
Gene Synonyms: Chkb-Cpt1b...Chkb-Cpt1b readthrough transcript (NMD candidate)

Allele/Variant
Source: rs232547678
Genes: Gm44502 (Mmu), Cpt1b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)15:89300733G>T
Gene Synonyms: Chkb-Cpt1b...Chkb-Cpt1b readthrough transcript (NMD candidate)

Allele/Variant
Source: rs583103395
Genes: Gm44502 (Mmu), Cpt1b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:89301700C>A
Gene Synonyms: Chkb-Cpt1b...Chkb-Cpt1b readthrough transcript (NMD candidate)

Allele/Variant
Source: rs251288794
Genes: Gm44502 (Mmu), Cpt1b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:89301804A>G
Gene Synonyms: Chkb-Cpt1b...Chkb-Cpt1b readthrough transcript (NMD candidate)

Allele/Variant
Source: rs107632418
Genes: Gm44502 (Mmu), Cpt1b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:89301909A>C
Gene Synonyms: Chkb-Cpt1b...Chkb-Cpt1b readthrough transcript (NMD candidate)

Allele/Variant
Source: rs260970625
Genes: Gm44502 (Mmu), Cpt1b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:89301932A>G
Gene Synonyms: Chkb-Cpt1b...Chkb-Cpt1b readthrough transcript (NMD candidate)

Allele/Variant
Source: rs248505703
Genes: Gm44502 (Mmu), Cpt1b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:89301937C>T
Gene Synonyms: Chkb-Cpt1b...Chkb-Cpt1b readthrough transcript (NMD candidate)

Allele/Variant
Source: rs31987124
Genes: Gm44502 (Mmu), Cpt1b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:89302240C>T
Gene Synonyms: Chkb-Cpt1b...Chkb-Cpt1b readthrough transcript (NMD candidate)

Allele/Variant
Source: rs214827192
Genes: Gm44502 (Mmu), Cpt1b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:89302306G>T
Gene Synonyms: Chkb-Cpt1b...Chkb-Cpt1b readthrough transcript (NMD candidate)

Allele/Variant
Source: rs258045311
Genes: Gm44502 (Mmu), Cpt1b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:89302653C>T
Gene Synonyms: Chkb-Cpt1b...Chkb-Cpt1b readthrough transcript (NMD candidate)

Allele/Variant
Source: rs235036800
Genes: Gm44502 (Mmu), Cpt1b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)15:89303433G>A
Gene Synonyms: Chkb-Cpt1b...Chkb-Cpt1b readthrough transcript (NMD candidate)

Allele/Variant
Source: rs232676839
Genes: Gm44502 (Mmu), Cpt1b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:89302191C>T
Gene Synonyms: Chkb-Cpt1b...Chkb-Cpt1b readthrough transcript (NMD candidate)

Allele/Variant
Source: rs234555229
Genes: Gm44502 (Mmu), Cpt1b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:89302385C>T
Gene Synonyms: Chkb-Cpt1b...Chkb-Cpt1b readthrough transcript (NMD candidate)

Allele/Variant
Source: rs242958173
Genes: Gm44502 (Mmu), Cpt1b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:89302419C>T
Gene Synonyms: Chkb-Cpt1b...Chkb-Cpt1b readthrough transcript (NMD candidate)

Allele/Variant
Source: rs235157034
Genes: Gm44502 (Mmu), Cpt1b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:89302467C>T
Gene Synonyms: Chkb-Cpt1b...Chkb-Cpt1b readthrough transcript (NMD candidate)

Allele/Variant
Source: rs262484594
Genes: Gm44502 (Mmu), Cpt1b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)15:89303543C>T
Gene Synonyms: Chkb-Cpt1b...Chkb-Cpt1b readthrough transcript (NMD candidate)

Allele/Variant
Source: rs265193874
Genes: Gm44502 (Mmu), Cpt1b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:89304226C>T
Gene Synonyms: Chkb-Cpt1b...Chkb-Cpt1b readthrough transcript (NMD candidate)

Allele/Variant
Source: rs229017477
Genes: Gm44502 (Mmu), Cpt1b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:89305433C>T
Gene Synonyms: Chkb-Cpt1b...Chkb-Cpt1b readthrough transcript (NMD candidate)

Allele/Variant
Source: rs240165492
Genes: Gm44502 (Mmu), Cpt1b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:89305832C>T
Gene Synonyms: Chkb-Cpt1b...Chkb-Cpt1b readthrough transcript (NMD candidate)

Allele/Variant
Source: rs248541736
Genes: Gm44502 (Mmu), Cpt1b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:89306057C>T
Gene Synonyms: Chkb-Cpt1b...Chkb-Cpt1b readthrough transcript (NMD candidate)

Allele/Variant
Source: rs33858577
Genes: Gm44502 (Mmu), Cpt1b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:89306105C>T
Gene Synonyms: Chkb-Cpt1b...Chkb-Cpt1b readthrough transcript (NMD candidate)

Allele/Variant
Source: rs262906456
Genes: Gm44502 (Mmu), Cpt1b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)15:89300770G>A
Gene Synonyms: Chkb-Cpt1b...Chkb-Cpt1b readthrough transcript (NMD candidate)

Allele/Variant
Source: rs228772892
Genes: Gm44502 (Mmu), Cpt1b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)15:89300837G>A
Gene Synonyms: Chkb-Cpt1b...Chkb-Cpt1b readthrough transcript (NMD candidate)

Allele/Variant
Source: rs583904444
Genes: Gm44502 (Mmu), Cpt1b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)15:89301004C>T
Gene Synonyms: Chkb-Cpt1b...Chkb-Cpt1b readthrough transcript (NMD candidate)

Allele/Variant
Source: rs238435479
Genes: Gm44502 (Mmu), Cpt1b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:89301194G>T
Gene Synonyms: Chkb-Cpt1b...Chkb-Cpt1b readthrough transcript (NMD candidate)

Allele/Variant
Source: rs248904160
Genes: Gm44502 (Mmu), Cpt1b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:89301593G>T
Gene Synonyms: Chkb-Cpt1b...Chkb-Cpt1b readthrough transcript (NMD candidate)

Allele/Variant
Source: rs243323957
Genes: Gm44502 (Mmu), Cpt1b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:89301850A>C
Gene Synonyms: Chkb-Cpt1b...Chkb-Cpt1b readthrough transcript (NMD candidate)

Allele/Variant
Source: rs216688535
Genes: Gm44502 (Mmu), Cpt1b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:89302420A>G
Gene Synonyms: Chkb-Cpt1b...Chkb-Cpt1b readthrough transcript (NMD candidate)

Allele/Variant
Source: rs251331085
Genes: Gm44502 (Mmu), Cpt1b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:89302475A>G
Gene Synonyms: Chkb-Cpt1b...Chkb-Cpt1b readthrough transcript (NMD candidate)

Allele/Variant
Source: rs584912030
Genes: Gm44502 (Mmu), Cpt1b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:89302588A>G
Gene Synonyms: Chkb-Cpt1b...Chkb-Cpt1b readthrough transcript (NMD candidate)

Allele/Variant
Source: rs238385278
Genes: Gm44502 (Mmu), Cpt1b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:89302774T>C
Gene Synonyms: Chkb-Cpt1b...Chkb-Cpt1b readthrough transcript (NMD candidate)

Allele/Variant
Source: rs32084857
Genes: Gm44502 (Mmu), Cpt1b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:89301471C>T
Gene Synonyms: Chkb-Cpt1b...Chkb-Cpt1b readthrough transcript (NMD candidate)

Allele/Variant
Source: rs221906750
Genes: Gm44502 (Mmu), Cpt1b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:89301597C>T
Gene Synonyms: Chkb-Cpt1b...Chkb-Cpt1b readthrough transcript (NMD candidate)

Allele/Variant
Source: rs225458262
Genes: Gm44502 (Mmu), Cpt1b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:89301816G>A
Gene Synonyms: Chkb-Cpt1b...Chkb-Cpt1b readthrough transcript (NMD candidate)

Allele/Variant
Source: rs238291420
Genes: Gm44502 (Mmu), Cpt1b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:89301911T>C
Gene Synonyms: Chkb-Cpt1b...Chkb-Cpt1b readthrough transcript (NMD candidate)

Allele/Variant
Source: rs263002348
Genes: Gm44502 (Mmu), Cpt1b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:89301939T>C
Gene Synonyms: Chkb-Cpt1b...Chkb-Cpt1b readthrough transcript (NMD candidate)

Allele/Variant
Source: rs3164881
Genes: Gm44502 (Mmu), Cpt1b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:89303829T>C
Gene Synonyms: Chkb-Cpt1b...Chkb-Cpt1b readthrough transcript (NMD candidate)

Allele/Variant
Source: rs222623256
Genes: Gm44502 (Mmu), Cpt1b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:89304021T>C
Gene Synonyms: Chkb-Cpt1b...Chkb-Cpt1b readthrough transcript (NMD candidate)