Incidental Mutation 'IGL01884:Lce1f'
ID 179068
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Lce1f
Ensembl Gene ENSMUSG00000042124
Gene Name late cornified envelope 1F
Synonyms 1110055J05Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.108) question?
Stock # IGL01884
Quality Score
Status
Chromosome 3
Chromosomal Location 92626003-92627657 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) G to T at 92626608 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Cysteine to Stop codon at position 16 (C16*)
Ref Sequence ENSEMBL: ENSMUSP00000037349 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000047153]
AlphaFold B9EJP6
Predicted Effect probably null
Transcript: ENSMUST00000047153
AA Change: C16*
SMART Domains Protein: ENSMUSP00000037349
Gene: ENSMUSG00000042124
AA Change: C16*

DomainStartEndE-ValueType
Pfam:LCE 25 66 3.3e-13 PFAM
Pfam:LCE 64 124 3.6e-12 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 23 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1190005I06Rik G A 8: 121,335,774 (GRCm39) probably benign Het
Col11a1 G A 3: 113,860,191 (GRCm39) G206R unknown Het
Cyp2e1 T C 7: 140,353,663 (GRCm39) Y426H probably benign Het
Fcrl1 A G 3: 87,292,044 (GRCm39) K68E probably damaging Het
Gabbr2 A G 4: 46,875,711 (GRCm39) V137A probably damaging Het
Gm10718 A T 9: 3,025,118 (GRCm39) Y194F probably benign Het
Gm21738 G A 14: 19,416,979 (GRCm38) S144L probably benign Het
Hacd1 G A 2: 14,040,593 (GRCm39) P221S probably damaging Het
Kndc1 C T 7: 139,494,110 (GRCm39) T535I probably damaging Het
Lrba C T 3: 86,217,719 (GRCm39) A543V possibly damaging Het
Lrp1b A T 2: 41,174,225 (GRCm39) C676* probably null Het
Mocos A G 18: 24,816,273 (GRCm39) K617E probably damaging Het
Muc5b A G 7: 141,421,820 (GRCm39) probably benign Het
Mylk A T 16: 34,809,247 (GRCm39) probably benign Het
Naip2 A G 13: 100,325,329 (GRCm39) probably benign Het
Or6c76 A G 10: 129,612,697 (GRCm39) K320E probably benign Het
Pcdhb5 C T 18: 37,454,387 (GRCm39) P256S probably benign Het
Rbl2 A G 8: 91,823,464 (GRCm39) E464G probably damaging Het
Rfc1 A T 5: 65,431,803 (GRCm39) L769Q possibly damaging Het
Setd7 T C 3: 51,450,132 (GRCm39) Y98C possibly damaging Het
Tbc1d8 A G 1: 39,415,526 (GRCm39) Y920H probably damaging Het
Tcte1 T C 17: 45,850,735 (GRCm39) probably null Het
Vmn2r129 C T 4: 156,690,549 (GRCm39) noncoding transcript Het
Other mutations in Lce1f
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01359:Lce1f APN 3 92,626,491 (GRCm39) nonsense probably null
R1499:Lce1f UTSW 3 92,626,276 (GRCm39) missense unknown
R5728:Lce1f UTSW 3 92,626,652 (GRCm39) missense unknown
R8285:Lce1f UTSW 3 92,626,238 (GRCm39) missense unknown
R9356:Lce1f UTSW 3 92,626,272 (GRCm39) small deletion probably benign
Z1088:Lce1f UTSW 3 92,626,561 (GRCm39) missense unknown
Z1177:Lce1f UTSW 3 92,626,505 (GRCm39) missense unknown
Posted On 2014-05-07