Incidental Mutation 'IGL02903:Fam159b'
ID 363708
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Fam159b
Ensembl Gene ENSMUSG00000042655
Gene Name family with sequence similarity 159, member B
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.059) question?
Stock # IGL02903
Quality Score
Chromosome 13
Chromosomal Location 104845283-104863893 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) T to A at 104863610 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Phenylalanine at position 35 (Y35F)
Ref Sequence ENSEMBL: ENSMUSP00000042302 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000043061]
AlphaFold Q9D1Y9
Predicted Effect probably benign
Transcript: ENSMUST00000043061
AA Change: Y35F

PolyPhen 2 Score 0.034 (Sensitivity: 0.95; Specificity: 0.82)
SMART Domains Protein: ENSMUSP00000042302
Gene: ENSMUSG00000042655
AA Change: Y35F

Pfam:Shisa 6 57 3.5e-11 PFAM
transmembrane domain 60 94 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000223913
Predicted Effect noncoding transcript
Transcript: ENSMUST00000225969
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 37 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2410089E03Rik G T 15: 8,269,778 R3150M unknown Het
2410089E03Rik G T 15: 8,269,779 R3150S unknown Het
4931417E11Rik A G 6: 73,469,120 Y149H probably damaging Het
Alox5 T G 6: 116,420,335 N296T probably damaging Het
Anks6 C T 4: 47,045,004 E301K probably damaging Het
Astn1 A G 1: 158,688,550 S1237G probably damaging Het
Atf6 G A 1: 170,799,714 P394S probably benign Het
Atp4a G A 7: 30,715,919 M321I probably benign Het
C4bp G A 1: 130,655,985 T82I probably damaging Het
Cask A T X: 13,552,447 probably benign Het
Cenpf A T 1: 189,646,876 S2906T probably damaging Het
Cfl1 T C 19: 5,492,800 F103L probably benign Het
Chrnb3 A T 8: 27,386,806 T83S probably damaging Het
Cmtr2 A G 8: 110,222,878 T607A probably benign Het
Cts7 A T 13: 61,356,626 probably benign Het
Dgkz A T 2: 91,939,962 Y514N possibly damaging Het
Dmrtc1b T A X: 102,713,567 L206Q probably benign Het
Dus3l C T 17: 56,768,363 L397F probably damaging Het
Gm13089 A T 4: 143,699,166 M69K probably benign Het
Gm6356 C T 14: 6,973,735 G27E probably damaging Het
Hkdc1 C T 10: 62,400,191 probably null Het
Kcmf1 A T 6: 72,858,883 V21E possibly damaging Het
Kcnh4 T A 11: 100,757,654 T75S possibly damaging Het
Lemd2 A G 17: 27,193,210 probably benign Het
Magee1 G T X: 105,123,339 R910L probably damaging Het
Mcm3ap T C 10: 76,471,258 probably benign Het
Mfsd4b3 T A 10: 39,947,643 E207V possibly damaging Het
Olfr1354 A G 10: 78,917,416 D192G probably damaging Het
Olfr697 A G 7: 106,741,710 S75P probably damaging Het
Pappa T C 4: 65,261,980 V1026A probably damaging Het
Paxip1 A G 5: 27,748,872 L942P probably damaging Het
Ppp1r12b A T 1: 134,955,649 L45Q probably benign Het
Ptprq T C 10: 107,666,586 T824A possibly damaging Het
Rfwd3 T C 8: 111,278,229 T574A probably benign Het
Rsbn1 T C 3: 103,928,569 S308P probably damaging Het
Smr2 A T 5: 88,108,630 I56F probably benign Het
Wdfy4 C T 14: 33,109,650 R873H probably damaging Het
Other mutations in Fam159b
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0666:Fam159b UTSW 13 104858354 missense possibly damaging 0.91
R1401:Fam159b UTSW 13 104863605 missense probably damaging 1.00
R1448:Fam159b UTSW 13 104845962 missense probably benign 0.00
R3015:Fam159b UTSW 13 104858391 missense possibly damaging 0.85
R6855:Fam159b UTSW 13 104863706 missense probably benign
R7085:Fam159b UTSW 13 104858306 missense probably benign 0.01
R7167:Fam159b UTSW 13 104863658 missense probably damaging 1.00
R9653:Fam159b UTSW 13 104863788 start gained probably benign
Posted On 2015-12-18