Incidental Mutation 'IGL02948:Fam162b'
ID 364817
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Fam162b
Ensembl Gene ENSMUSG00000019909
Gene Name family with sequence similarity 162, member B
Synonyms 9430073N08Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.064) question?
Stock # IGL02948
Quality Score
Status
Chromosome 10
Chromosomal Location 51461512-51466613 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 51463392 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Methionine to Valine at position 92 (M92V)
Ref Sequence ENSEMBL: ENSMUSP00000020064 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000020064]
AlphaFold Q9CX19
Predicted Effect probably damaging
Transcript: ENSMUST00000020064
AA Change: M92V

PolyPhen 2 Score 0.995 (Sensitivity: 0.68; Specificity: 0.97)
SMART Domains Protein: ENSMUSP00000020064
Gene: ENSMUSG00000019909
AA Change: M92V

DomainStartEndE-ValueType
Pfam:DUF1075 15 154 3.8e-56 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 54 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aass A T 6: 23,094,318 (GRCm39) probably benign Het
Ano3 A T 2: 110,527,363 (GRCm39) probably benign Het
Arpp21 T C 9: 112,005,268 (GRCm39) Y193C probably damaging Het
Atm G A 9: 53,364,740 (GRCm39) probably benign Het
Ceacam13 C T 7: 17,744,988 (GRCm39) probably benign Het
Cenpi T A X: 133,250,017 (GRCm39) C599S possibly damaging Het
Clec7a A C 6: 129,442,441 (GRCm39) D195E possibly damaging Het
Cnksr1 T C 4: 133,962,417 (GRCm39) probably null Het
Cntn1 A G 15: 92,143,891 (GRCm39) T285A probably benign Het
Dusp4 G T 8: 35,285,726 (GRCm39) G329V probably damaging Het
Emb C A 13: 117,409,602 (GRCm39) probably benign Het
Esyt1 A T 10: 128,355,040 (GRCm39) S496T probably damaging Het
Evpl T C 11: 116,112,648 (GRCm39) T1681A probably damaging Het
Fam131b A C 6: 42,297,926 (GRCm39) probably benign Het
Fbxw2 T C 2: 34,695,723 (GRCm39) *455W probably null Het
Gm12886 A G 4: 121,280,234 (GRCm39) L14P unknown Het
Gpc4 A T X: 51,163,178 (GRCm39) V235E probably damaging Het
Gss A G 2: 155,419,541 (GRCm39) L170P probably damaging Het
Hbs1l C T 10: 21,217,610 (GRCm39) probably benign Het
Hhatl T C 9: 121,618,857 (GRCm39) M92V probably benign Het
Hhla1 A T 15: 65,814,542 (GRCm39) L194H probably damaging Het
Hivep2 C A 10: 14,004,757 (GRCm39) R452S probably benign Het
Homer2 C A 7: 81,299,393 (GRCm39) W24L probably damaging Het
Lhcgr A T 17: 89,050,050 (GRCm39) L492H probably damaging Het
Lrba C A 3: 86,217,691 (GRCm39) probably null Het
Lrp2 G T 2: 69,318,181 (GRCm39) P2090Q probably damaging Het
Lyl1 C T 8: 85,429,300 (GRCm39) P3L possibly damaging Het
Madd T A 2: 90,973,172 (GRCm39) M1497L probably benign Het
Naprt C T 15: 75,764,206 (GRCm39) R336Q probably damaging Het
Nars1 A G 18: 64,638,266 (GRCm39) C266R possibly damaging Het
Or10v1 T A 19: 11,874,145 (GRCm39) Y253* probably null Het
Or5k8 T A 16: 58,644,451 (GRCm39) Q207L probably benign Het
Pard3 A T 8: 128,032,975 (GRCm39) T190S probably benign Het
Pstpip2 A G 18: 77,942,507 (GRCm39) N86S probably benign Het
Ptgfrn T C 3: 100,980,135 (GRCm39) T402A probably benign Het
Rnf130 T C 11: 49,943,598 (GRCm39) probably benign Het
Ropn1l T C 15: 31,451,325 (GRCm39) D53G possibly damaging Het
Rps6ka2 G A 17: 7,521,849 (GRCm39) probably null Het
Rtn2 T C 7: 19,027,036 (GRCm39) S17P probably damaging Het
Shank2 T C 7: 143,963,373 (GRCm39) V327A probably benign Het
Slc22a16 T G 10: 40,449,958 (GRCm39) Y131* probably null Het
Slc28a2 T A 2: 122,288,458 (GRCm39) M583K possibly damaging Het
Slco1a6 G T 6: 142,078,961 (GRCm39) probably null Het
Slfn8 T A 11: 82,894,078 (GRCm39) I854F probably damaging Het
Strip1 T C 3: 107,520,582 (GRCm39) R823G probably benign Het
Stxbp2 A T 8: 3,691,971 (GRCm39) I538F probably benign Het
Tcl1b5 C T 12: 105,145,273 (GRCm39) T79M probably benign Het
Tmem104 G T 11: 115,088,122 (GRCm39) A36S probably damaging Het
Trim55 T A 3: 19,725,116 (GRCm39) L211Q probably damaging Het
Trim80 T C 11: 115,332,419 (GRCm39) W204R possibly damaging Het
Ttbk1 G A 17: 46,757,256 (GRCm39) T1126I probably benign Het
Ubqln2 C T X: 152,282,692 (GRCm39) Q415* probably null Het
Unc13a C T 8: 72,103,193 (GRCm39) R931H possibly damaging Het
Utp4 T A 8: 107,621,273 (GRCm39) S17T probably benign Het
Other mutations in Fam162b
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00567:Fam162b APN 10 51,466,390 (GRCm39) missense possibly damaging 0.94
R0709:Fam162b UTSW 10 51,463,347 (GRCm39) missense probably damaging 1.00
R1185:Fam162b UTSW 10 51,466,439 (GRCm39) missense probably benign
R1185:Fam162b UTSW 10 51,466,439 (GRCm39) missense probably benign
R1185:Fam162b UTSW 10 51,466,439 (GRCm39) missense probably benign
R1505:Fam162b UTSW 10 51,463,298 (GRCm39) missense probably damaging 1.00
R1735:Fam162b UTSW 10 51,463,307 (GRCm39) missense probably damaging 1.00
R1961:Fam162b UTSW 10 51,466,430 (GRCm39) missense probably benign 0.00
R2401:Fam162b UTSW 10 51,463,314 (GRCm39) missense probably damaging 0.99
R6059:Fam162b UTSW 10 51,466,403 (GRCm39) missense probably benign 0.28
R6196:Fam162b UTSW 10 51,463,506 (GRCm39) splice site probably null
R6284:Fam162b UTSW 10 51,461,598 (GRCm39) missense probably damaging 0.99
R6625:Fam162b UTSW 10 51,466,391 (GRCm39) missense probably damaging 1.00
R7324:Fam162b UTSW 10 51,466,282 (GRCm39) splice site probably null
R7380:Fam162b UTSW 10 51,466,572 (GRCm39) start gained probably benign
R8945:Fam162b UTSW 10 51,466,469 (GRCm39) missense probably benign 0.02
R9415:Fam162b UTSW 10 51,466,155 (GRCm39) critical splice donor site probably null
Posted On 2015-12-18