Incidental Mutation 'IGL03247:Fam159a'
ID414432
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Fam159a
Ensembl Gene ENSMUSG00000059816
Gene Namefamily with sequence similarity 159, member A
SynonymsOTTMUSG00000008243
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.087) question?
Stock #IGL03247
Quality Score
Status
Chromosome4
Chromosomal Location108367777-108383349 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to T at 108367901 bp
ZygosityHeterozygous
Amino Acid Change Cysteine to Serine at position 155 (C155S)
Ref Sequence ENSEMBL: ENSMUSP00000060463 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000053157]
Predicted Effect probably benign
Transcript: ENSMUST00000053157
AA Change: C155S

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
SMART Domains Protein: ENSMUSP00000060463
Gene: ENSMUSG00000059816
AA Change: C155S

DomainStartEndE-ValueType
transmembrane domain 56 90 N/A INTRINSIC
low complexity region 131 139 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adcy4 T A 14: 55,770,096 I926F probably damaging Het
Agap3 A G 5: 24,487,822 N418D probably damaging Het
Alms1 T C 6: 85,678,597 V3375A possibly damaging Het
Ankrd6 T A 4: 32,860,441 M1L possibly damaging Het
Aox4 A G 1: 58,264,367 D1188G probably damaging Het
Car2 T A 3: 14,887,939 L47Q probably damaging Het
Catsper2 A G 2: 121,410,200 V107A probably benign Het
Catsperg2 T C 7: 29,717,048 N313S possibly damaging Het
Dolk T C 2: 30,285,511 Y174C probably damaging Het
Erfe A G 1: 91,370,425 E219G probably benign Het
Ern2 T C 7: 122,171,671 E733G probably benign Het
Fam228a A G 12: 4,737,734 F13S probably damaging Het
Fancd2 T C 6: 113,568,208 V829A probably benign Het
Gid4 C A 11: 60,432,343 T87N probably benign Het
H2-Ob A G 17: 34,243,492 K152R probably benign Het
Ifna2 T A 4: 88,683,377 T135S probably benign Het
Il1rapl2 G A X: 138,789,680 G298D probably damaging Het
Mbd1 T A 18: 74,274,754 L174* probably null Het
Mga T A 2: 119,935,513 D1341E possibly damaging Het
Mmp12 T A 9: 7,348,631 M54K probably benign Het
Mphosph8 T A 14: 56,678,820 probably null Het
Mrps23 A G 11: 88,210,096 probably benign Het
Necab1 C T 4: 14,960,046 M300I probably benign Het
Nid2 G A 14: 19,779,620 D660N probably damaging Het
Olfr693 T A 7: 106,677,547 H313L probably benign Het
Olfr824 T A 10: 130,126,715 E114V probably damaging Het
P2ry13 A T 3: 59,209,592 V255D possibly damaging Het
Peak1 C T 9: 56,257,930 E905K probably damaging Het
Picalm C A 7: 90,194,291 Q550K probably benign Het
Rnf103 T A 6: 71,510,305 V640E possibly damaging Het
Sec31b T G 19: 44,518,940 K817N possibly damaging Het
Skint2 C A 4: 112,626,026 H209Q probably benign Het
Skint5 T C 4: 113,940,808 S193G probably damaging Het
Tacr3 A G 3: 134,930,091 probably benign Het
Tek A G 4: 94,865,443 M1041V possibly damaging Het
Tm4sf1 A G 3: 57,293,015 S89P possibly damaging Het
Tusc3 T A 8: 39,130,777 N299K possibly damaging Het
Washc4 T C 10: 83,564,463 S418P probably benign Het
Other mutations in Fam159a
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02578:Fam159a APN 4 108368028 missense probably benign 0.02
R4028:Fam159a UTSW 4 108383215 nonsense probably null
R4029:Fam159a UTSW 4 108383215 nonsense probably null
R4030:Fam159a UTSW 4 108383215 nonsense probably null
R4890:Fam159a UTSW 4 108367801 missense probably benign
R4911:Fam159a UTSW 4 108377461 missense probably benign 0.11
R6190:Fam159a UTSW 4 108367855 missense probably damaging 1.00
R6647:Fam159a UTSW 4 108368027 missense probably benign 0.00
R7128:Fam159a UTSW 4 108367903 missense probably benign
R8557:Fam159a UTSW 4 108367888 missense probably benign 0.37
Posted On2016-08-02