Incidental Mutation 'IGL01094:Tm4sf19'
ID 52911
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Tm4sf19
Ensembl Gene ENSMUSG00000079625
Gene Name transmembrane 4 L six family member 19
Synonyms EG277203
Accession Numbers
Essential gene? Probably non essential (E-score: 0.072) question?
Stock # IGL01094
Quality Score
Status
Chromosome 16
Chromosomal Location 32219324-32227045 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 32224772 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Asparagine to Serine at position 40 (N40S)
Ref Sequence ENSEMBL: ENSMUSP00000110802 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000115149]
AlphaFold E9Q9H8
Predicted Effect possibly damaging
Transcript: ENSMUST00000115149
AA Change: N40S

PolyPhen 2 Score 0.633 (Sensitivity: 0.87; Specificity: 0.91)
SMART Domains Protein: ENSMUSP00000110802
Gene: ENSMUSG00000079625
AA Change: N40S

DomainStartEndE-ValueType
Pfam:L6_membrane 9 204 1.1e-57 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000194813
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 27 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adss2 A T 1: 177,612,508 (GRCm39) H80Q probably damaging Het
Ahi1 A G 10: 20,847,959 (GRCm39) N456D probably damaging Het
Alpk2 T G 18: 65,439,673 (GRCm39) E573D probably damaging Het
Axin2 G A 11: 108,814,501 (GRCm39) V130M probably damaging Het
Cadm4 T C 7: 24,202,184 (GRCm39) L341P possibly damaging Het
Col20a1 G A 2: 180,641,559 (GRCm39) C625Y probably damaging Het
Col6a3 T G 1: 90,731,655 (GRCm39) I1533L possibly damaging Het
Dusp10 A T 1: 183,769,697 (GRCm39) probably null Het
Dysf T A 6: 84,171,368 (GRCm39) I1837N probably damaging Het
Fbxw19 A G 9: 109,322,614 (GRCm39) S119P probably benign Het
Il22ra1 C A 4: 135,478,395 (GRCm39) P489T possibly damaging Het
Il7r A T 15: 9,508,085 (GRCm39) N412K possibly damaging Het
Kdr A T 5: 76,122,420 (GRCm39) Y502N probably benign Het
Med12l T A 3: 59,001,076 (GRCm39) L713H probably damaging Het
Nfxl1 A G 5: 72,707,771 (GRCm39) probably benign Het
Or4a70 A G 2: 89,324,182 (GRCm39) V158A probably benign Het
Piezo1 T A 8: 123,208,877 (GRCm39) E2495D probably damaging Het
Pkhd1l1 T C 15: 44,410,325 (GRCm39) F2611L probably benign Het
Pld2 T C 11: 70,432,132 (GRCm39) C84R probably damaging Het
Prss3l A G 6: 41,420,357 (GRCm39) V123A possibly damaging Het
Scfd2 G T 5: 74,691,707 (GRCm39) P192T possibly damaging Het
Tmc2 T C 2: 130,102,086 (GRCm39) probably benign Het
Tmem217 T C 17: 29,745,566 (GRCm39) R55G probably benign Het
Unc80 A G 1: 66,734,592 (GRCm39) D3205G possibly damaging Het
Vps13c A G 9: 67,793,566 (GRCm39) N440D probably damaging Het
Wdr35 T C 12: 9,055,838 (GRCm39) probably benign Het
Zfp110 T A 7: 12,583,723 (GRCm39) H790Q probably damaging Het
Other mutations in Tm4sf19
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02468:Tm4sf19 APN 16 32,226,533 (GRCm39) splice site probably benign
IGL02573:Tm4sf19 APN 16 32,226,678 (GRCm39) missense possibly damaging 0.88
IGL02938:Tm4sf19 APN 16 32,224,733 (GRCm39) missense probably damaging 0.98
R1306:Tm4sf19 UTSW 16 32,226,720 (GRCm39) missense probably damaging 1.00
R1450:Tm4sf19 UTSW 16 32,226,781 (GRCm39) missense probably damaging 1.00
R1522:Tm4sf19 UTSW 16 32,224,820 (GRCm39) missense possibly damaging 0.61
R1895:Tm4sf19 UTSW 16 32,226,500 (GRCm39) missense probably damaging 1.00
R4407:Tm4sf19 UTSW 16 32,226,712 (GRCm39) missense possibly damaging 0.77
R5527:Tm4sf19 UTSW 16 32,226,739 (GRCm39) missense probably damaging 1.00
R6166:Tm4sf19 UTSW 16 32,226,681 (GRCm39) missense probably damaging 1.00
R6949:Tm4sf19 UTSW 16 32,224,676 (GRCm39) missense probably benign 0.01
R7269:Tm4sf19 UTSW 16 32,224,814 (GRCm39) missense probably damaging 0.98
R7316:Tm4sf19 UTSW 16 32,226,466 (GRCm39) missense possibly damaging 0.82
R7993:Tm4sf19 UTSW 16 32,226,458 (GRCm39) missense possibly damaging 0.90
Z1177:Tm4sf19 UTSW 16 32,224,741 (GRCm39) missense probably damaging 1.00
Posted On 2013-06-21