Incidental Mutation 'IGL01805:Mucl3'
ID 155641
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Mucl3
Ensembl Gene ENSMUSG00000073408
Gene Name mucin like 3
Synonyms LOC268949, Dpcr1
Accession Numbers
Essential gene? Probably non essential (E-score: 0.052) question?
Stock # IGL01805
Quality Score
Status
Chromosome 17
Chromosomal Location 35946647-35954587 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 35948535 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Serine at position 355 (T355S)
Ref Sequence ENSEMBL: ENSMUSP00000093120 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000095467] [ENSMUST00000174521]
AlphaFold Q3TNW5
Predicted Effect possibly damaging
Transcript: ENSMUST00000095467
AA Change: T355S

PolyPhen 2 Score 0.617 (Sensitivity: 0.87; Specificity: 0.91)
SMART Domains Protein: ENSMUSP00000093120
Gene: ENSMUSG00000073408
AA Change: T355S

DomainStartEndE-ValueType
signal peptide 1 27 N/A INTRINSIC
transmembrane domain 428 450 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000174521
SMART Domains Protein: ENSMUSP00000134221
Gene: ENSMUSG00000090509

DomainStartEndE-ValueType
Pfam:SFTA2 80 117 9.2e-18 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000174534
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 28 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700019D03Rik T C 1: 52,964,677 (GRCm39) D17G possibly damaging Het
Adam28 G T 14: 68,879,540 (GRCm39) S169R probably benign Het
Aox1 T C 1: 58,120,672 (GRCm39) M855T possibly damaging Het
Apc C A 18: 34,451,271 (GRCm39) N2688K probably benign Het
Arhgap23 T A 11: 97,383,428 (GRCm39) probably benign Het
Bpifa6 A G 2: 153,826,832 (GRCm39) T66A probably benign Het
C1qtnf1 T A 11: 118,338,993 (GRCm39) L221Q probably damaging Het
Ccdc175 T A 12: 72,176,003 (GRCm39) probably benign Het
Ccl1 C A 11: 82,068,958 (GRCm39) M26I possibly damaging Het
Dnah10 T A 5: 124,860,985 (GRCm39) F2123I probably damaging Het
Fancm T C 12: 65,160,635 (GRCm39) probably null Het
Fstl4 C A 11: 53,077,184 (GRCm39) A647E probably damaging Het
Hmgb4 G T 4: 128,154,015 (GRCm39) probably benign Het
Hr A T 14: 70,802,737 (GRCm39) probably benign Het
Ilrun C T 17: 27,986,880 (GRCm39) probably benign Het
Kcna4 G T 2: 107,126,843 (GRCm39) V526L probably damaging Het
Mas1 T C 17: 13,061,117 (GRCm39) Y102C probably damaging Het
Mul1 C T 4: 138,166,974 (GRCm39) P343S possibly damaging Het
Obscn T C 11: 59,023,422 (GRCm39) S652G probably damaging Het
Or8g55 T C 9: 39,785,075 (GRCm39) F168S probably damaging Het
Pjvk A T 2: 76,487,858 (GRCm39) N250I probably benign Het
Pkd2 T C 5: 104,630,959 (GRCm39) I461T probably benign Het
Psen2 T C 1: 180,057,403 (GRCm39) probably null Het
Ralb T C 1: 119,403,725 (GRCm39) E81G probably benign Het
Slc15a4 T C 5: 127,685,900 (GRCm39) T261A possibly damaging Het
Vmn2r77 G A 7: 86,460,395 (GRCm39) V574M probably benign Het
Xrn2 A G 2: 146,870,063 (GRCm39) I251V probably damaging Het
Zfp974 G A 7: 27,611,689 (GRCm39) probably benign Het
Other mutations in Mucl3
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00476:Mucl3 APN 17 35,948,994 (GRCm39) missense possibly damaging 0.46
IGL01321:Mucl3 APN 17 35,947,758 (GRCm39) missense probably damaging 0.98
IGL02320:Mucl3 APN 17 35,948,332 (GRCm39) missense probably benign 0.00
R1869:Mucl3 UTSW 17 35,949,305 (GRCm39) missense possibly damaging 0.82
R4570:Mucl3 UTSW 17 35,948,883 (GRCm39) missense possibly damaging 0.66
R4858:Mucl3 UTSW 17 35,948,468 (GRCm39) missense possibly damaging 0.74
R5592:Mucl3 UTSW 17 35,954,535 (GRCm39) missense probably damaging 0.99
R5733:Mucl3 UTSW 17 35,949,102 (GRCm39) missense probably benign 0.00
R7422:Mucl3 UTSW 17 35,949,312 (GRCm39) missense probably benign 0.00
R7689:Mucl3 UTSW 17 35,948,969 (GRCm39) missense possibly damaging 0.83
R7780:Mucl3 UTSW 17 35,947,874 (GRCm39) missense possibly damaging 0.95
R8079:Mucl3 UTSW 17 35,949,084 (GRCm39) missense unknown
R8320:Mucl3 UTSW 17 35,954,530 (GRCm39) missense probably benign 0.22
R8337:Mucl3 UTSW 17 35,948,486 (GRCm39) missense possibly damaging 0.95
R8867:Mucl3 UTSW 17 35,948,872 (GRCm39) missense probably benign 0.27
R9734:Mucl3 UTSW 17 35,949,233 (GRCm39) missense probably benign 0.07
Posted On 2014-02-04