Incidental Mutation 'IGL01774:Fabp12'
ID 154054
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Fabp12
Ensembl Gene ENSMUSG00000027530
Gene Name fatty acid binding protein 12
Synonyms 1700008G05Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.056) question?
Stock # IGL01774
Quality Score
Status
Chromosome 3
Chromosomal Location 10309269-10366243 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to C at 10312754 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Asparagine to Lysine at position 89 (N89K)
Ref Sequence ENSEMBL: ENSMUSP00000131101 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000029043] [ENSMUST00000117917] [ENSMUST00000119761] [ENSMUST00000172126]
AlphaFold Q9DAK4
Predicted Effect probably benign
Transcript: ENSMUST00000029043
AA Change: N89K

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)
SMART Domains Protein: ENSMUSP00000029043
Gene: ENSMUSG00000027530
AA Change: N89K

DomainStartEndE-ValueType
Pfam:Lipocalin 6 132 1.4e-25 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000117917
AA Change: N89K

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)
SMART Domains Protein: ENSMUSP00000112464
Gene: ENSMUSG00000027530
AA Change: N89K

DomainStartEndE-ValueType
Pfam:Lipocalin 6 132 1.4e-25 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000119761
AA Change: N89K

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)
SMART Domains Protein: ENSMUSP00000112958
Gene: ENSMUSG00000027530
AA Change: N89K

DomainStartEndE-ValueType
Pfam:Lipocalin 6 132 1.4e-25 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000172126
AA Change: N89K

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)
SMART Domains Protein: ENSMUSP00000131101
Gene: ENSMUSG00000027530
AA Change: N89K

DomainStartEndE-ValueType
Pfam:Lipocalin 6 132 1.4e-25 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 36 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca16 A G 7: 120,077,058 (GRCm39) D708G probably damaging Het
Abca16 T C 7: 120,021,024 (GRCm39) probably benign Het
Abcc5 T C 16: 20,197,207 (GRCm39) D674G probably damaging Het
Abr A G 11: 76,355,125 (GRCm39) probably benign Het
Arfgef3 A G 10: 18,619,363 (GRCm39) I4T possibly damaging Het
Btla A G 16: 45,070,911 (GRCm39) N290S possibly damaging Het
Catip C A 1: 74,407,642 (GRCm39) R325S probably damaging Het
Cep120 A G 18: 53,839,902 (GRCm39) L786P possibly damaging Het
Cnot8 A G 11: 58,006,133 (GRCm39) I221V probably benign Het
Eloc A T 1: 16,716,013 (GRCm39) D37E probably benign Het
Ficd G T 5: 113,877,073 (GRCm39) R416L probably damaging Het
Frmd3 T C 4: 74,106,075 (GRCm39) Y574H probably damaging Het
Frmd4a T C 2: 4,540,047 (GRCm39) probably benign Het
Gatc G A 5: 115,479,076 (GRCm39) Q45* probably null Het
Gm5414 T C 15: 101,535,410 (GRCm39) D225G probably benign Het
Itpkc G T 7: 26,911,795 (GRCm39) A592E probably benign Het
Kl G T 5: 150,911,948 (GRCm39) V566L probably benign Het
Lpin1 T A 12: 16,608,477 (GRCm39) D545V probably damaging Het
Mtcl1 T C 17: 66,692,880 (GRCm39) Y483C probably damaging Het
Neb C T 2: 52,112,982 (GRCm39) W67* probably null Het
Nrarp T C 2: 25,071,298 (GRCm39) V59A possibly damaging Het
Nuf2 G A 1: 169,333,641 (GRCm39) T345M probably benign Het
Or52n20 T C 7: 104,320,149 (GRCm39) I80T probably benign Het
Pacs2 T A 12: 113,020,462 (GRCm39) H278Q probably benign Het
Pot1a T C 6: 25,753,276 (GRCm39) K420R probably benign Het
Rag2 A G 2: 101,460,392 (GRCm39) Y234C probably damaging Het
Ralgds C T 2: 28,440,554 (GRCm39) Q88* probably null Het
Rictor T C 15: 6,799,258 (GRCm39) S365P probably damaging Het
Slco1a1 G A 6: 141,871,339 (GRCm39) Q276* probably null Het
Tas2r134 C T 2: 51,518,160 (GRCm39) T213I probably benign Het
Tecpr1 A G 5: 144,148,358 (GRCm39) I349T probably damaging Het
Tnxb T C 17: 34,907,813 (GRCm39) S1286P probably damaging Het
Trafd1 A G 5: 121,513,113 (GRCm39) V375A possibly damaging Het
Vmn2r110 T A 17: 20,803,889 (GRCm39) I229L probably benign Het
Vnn1 T C 10: 23,776,608 (GRCm39) Y320H probably benign Het
Zfp990 T C 4: 145,263,518 (GRCm39) V172A probably benign Het
Other mutations in Fabp12
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00551:Fabp12 APN 3 10,311,115 (GRCm39) splice site probably benign
IGL00957:Fabp12 APN 3 10,315,273 (GRCm39) critical splice acceptor site probably null
IGL01822:Fabp12 APN 3 10,311,082 (GRCm39) nonsense probably null
IGL02047:Fabp12 APN 3 10,312,778 (GRCm39) splice site probably benign
IGL02164:Fabp12 APN 3 10,311,075 (GRCm39) missense probably damaging 0.99
IGL03108:Fabp12 APN 3 10,315,114 (GRCm39) missense probably benign 0.12
R0501:Fabp12 UTSW 3 10,315,203 (GRCm39) missense probably benign 0.00
R0647:Fabp12 UTSW 3 10,311,096 (GRCm39) missense possibly damaging 0.55
R1134:Fabp12 UTSW 3 10,312,731 (GRCm39) missense probably benign 0.17
R2020:Fabp12 UTSW 3 10,315,209 (GRCm39) missense probably benign 0.00
R5269:Fabp12 UTSW 3 10,315,167 (GRCm39) missense probably benign 0.12
R7434:Fabp12 UTSW 3 10,312,738 (GRCm39) missense probably benign 0.10
R9022:Fabp12 UTSW 3 10,317,333 (GRCm39) missense probably damaging 1.00
Posted On 2014-02-04