Incidental Mutation 'IGL02966:Fam78b'
ID365572
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Fam78b
Ensembl Gene ENSMUSG00000060568
Gene Namefamily with sequence similarity 78, member B
SynonymsC030014K22Rik, C030020L09Rik
Accession Numbers
Is this an essential gene? Possibly non essential (E-score: 0.274) question?
Stock #IGL02966
Quality Score
Status
Chromosome1
Chromosomal Location167001417-167091302 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) G to T at 167078888 bp
ZygosityHeterozygous
Amino Acid Change Leucine to Phenylalanine at position 205 (L205F)
Ref Sequence ENSEMBL: ENSMUSP00000139628 (fasta)
Predicted Effect probably benign
Transcript: ENSMUST00000122929
AA Change: L200F

PolyPhen 2 Score 0.059 (Sensitivity: 0.94; Specificity: 0.84)
Predicted Effect probably damaging
Transcript: ENSMUST00000126198
AA Change: L205F

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
Predicted Effect probably benign
Transcript: ENSMUST00000128373
AA Change: L197F

PolyPhen 2 Score 0.059 (Sensitivity: 0.94; Specificity: 0.84)
Predicted Effect probably damaging
Transcript: ENSMUST00000156025
AA Change: L205F

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
Predicted Effect probably damaging
Transcript: ENSMUST00000165874
AA Change: L205F

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
Predicted Effect probably damaging
Transcript: ENSMUST00000190081
AA Change: L205F

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 59 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930595M18Rik A T X: 81,419,711 Y797N possibly damaging Het
Actbl2 G A 13: 111,255,572 G147E probably damaging Het
Adam18 A T 8: 24,611,149 probably benign Het
Ahcyl2 G A 6: 29,880,557 V175I probably benign Het
Alox12 T A 11: 70,250,085 T375S probably damaging Het
Batf2 C A 19: 6,171,789 Q210K probably damaging Het
Bicd1 T C 6: 149,483,996 S76P probably damaging Het
Bphl A T 13: 34,063,997 H251L probably damaging Het
C130074G19Rik C A 1: 184,882,746 E82D probably damaging Het
Calu A T 6: 29,356,585 K39* probably null Het
Capns1 T C 7: 30,192,193 D142G probably damaging Het
Ccr8 T C 9: 120,094,140 V107A probably damaging Het
Cep170b G A 12: 112,736,444 G447D possibly damaging Het
Chat C T 14: 32,448,946 V199M probably damaging Het
Cntnap1 G T 11: 101,184,749 V918L probably damaging Het
Cyp27a1 A G 1: 74,732,090 T145A probably benign Het
Dgkq T A 5: 108,656,421 probably null Het
Dnhd1 A G 7: 105,720,741 I4458V probably benign Het
Enpp1 T A 10: 24,660,274 E409D probably damaging Het
Foxr2 C A X: 153,130,681 R183S probably damaging Het
Ganc T C 2: 120,433,648 S361P probably damaging Het
Gfra4 C A 2: 131,042,640 A15S possibly damaging Het
Gm8011 A T 14: 42,466,000 D145V unknown Het
Gnb4 A G 3: 32,585,223 V307A probably benign Het
Hdac4 A T 1: 92,054,945 V17E possibly damaging Het
Herc6 G A 6: 57,583,333 probably null Het
Hivep3 A G 4: 120,132,186 T1945A probably benign Het
Ica1l A T 1: 60,010,139 N218K probably damaging Het
Kmt2b A T 7: 30,575,462 L1939Q probably benign Het
Lrrc40 G A 3: 158,041,665 probably benign Het
March8 C T 6: 116,403,538 R117C probably damaging Het
Megf6 T C 4: 154,253,777 S327P probably damaging Het
Mocos T G 18: 24,676,611 C424G probably damaging Het
Mrpl50 A G 4: 49,521,014 W14R probably benign Het
Mysm1 A T 4: 94,975,286 D23E probably benign Het
Naa35 T A 13: 59,586,271 D34E probably benign Het
Nid1 A G 13: 13,482,221 I646V probably benign Het
Nupr1 T C 7: 126,624,901 probably benign Het
Olfr1449 A T 19: 12,934,800 I21F probably benign Het
Olfr171 G T 16: 19,624,301 H266Q probably damaging Het
Olfr875 T G 9: 37,773,586 L309R probably benign Het
Pcbp2 A C 15: 102,484,249 probably benign Het
Pde8b T C 13: 95,095,648 Q158R probably damaging Het
Pdzd8 T C 19: 59,300,859 Y703C probably damaging Het
Plxnb3 T C X: 73,765,283 S885P probably benign Het
Poc1b T A 10: 99,144,314 C136S probably damaging Het
Pole2 T C 12: 69,209,875 D292G probably damaging Het
Prpf39 T C 12: 65,042,779 V97A probably benign Het
Rbbp8 T A 18: 11,705,812 H183Q possibly damaging Het
Scn2a C T 2: 65,701,844 T600M possibly damaging Het
Spata32 T C 11: 103,208,803 Q292R possibly damaging Het
Sugp1 T C 8: 70,071,108 probably benign Het
Sult3a1 A C 10: 33,877,273 probably benign Het
Tpm3-rs7 C T 14: 113,315,378 Q235* probably null Het
Trbv2 A T 6: 41,047,751 T34S possibly damaging Het
Tssk6 A G 8: 69,902,885 Y193C probably benign Het
Ttn T C 2: 76,708,458 K34676R possibly damaging Het
Ugt3a2 T C 15: 9,370,068 Y433H probably damaging Het
Wdhd1 T C 14: 47,241,644 K1072E possibly damaging Het
Other mutations in Fam78b
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL03128:Fam78b APN 1 167078941 missense probably damaging 1.00
IGL03258:Fam78b APN 1 167078754 missense probably damaging 1.00
pacer UTSW 1 167078709 missense probably damaging 1.00
PIT1430001:Fam78b UTSW 1 167001744 missense probably benign 0.12
R1443:Fam78b UTSW 1 167078760 missense probably damaging 0.96
R1475:Fam78b UTSW 1 167001777 missense probably damaging 1.00
R1729:Fam78b UTSW 1 167001630 missense possibly damaging 0.83
R1883:Fam78b UTSW 1 167001602 missense probably benign
R2118:Fam78b UTSW 1 167078709 missense probably damaging 1.00
R2121:Fam78b UTSW 1 167078709 missense probably damaging 1.00
R2122:Fam78b UTSW 1 167078709 missense probably damaging 1.00
R2124:Fam78b UTSW 1 167078709 missense probably damaging 1.00
R2168:Fam78b UTSW 1 167078650 missense probably damaging 1.00
R4152:Fam78b UTSW 1 167078800 missense probably benign 0.19
R4167:Fam78b UTSW 1 167001732 missense possibly damaging 0.67
R4439:Fam78b UTSW 1 167078922 missense probably damaging 0.99
R4441:Fam78b UTSW 1 167078922 missense probably damaging 0.99
R4795:Fam78b UTSW 1 167078647 missense probably benign 0.01
R4796:Fam78b UTSW 1 167078647 missense probably benign 0.01
R6268:Fam78b UTSW 1 167078553 missense probably damaging 1.00
R6817:Fam78b UTSW 1 167078850 missense possibly damaging 0.94
Posted On2015-12-18