Incidental Mutation 'R0265:Ano8'
ID 34856
Institutional Source Beutler Lab
Gene Symbol Ano8
Ensembl Gene ENSMUSG00000034863
Gene Name anoctamin 8
Synonyms Tmem16h
MMRRC Submission 038491-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R0265 (G1)
Quality Score 122
Status Validated
Chromosome 8
Chromosomal Location 71928663-71938607 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) T to C at 71933168 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000123665 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000093450] [ENSMUST00000124745] [ENSMUST00000138892] [ENSMUST00000213382] [ENSMUST00000147642]
AlphaFold Q6PB70
Predicted Effect unknown
Transcript: ENSMUST00000093450
AA Change: N708S
SMART Domains Protein: ENSMUSP00000091157
Gene: ENSMUSG00000034863
AA Change: N708S

DomainStartEndE-ValueType
low complexity region 14 31 N/A INTRINSIC
low complexity region 73 84 N/A INTRINSIC
Pfam:Anoctamin 237 874 3e-149 PFAM
coiled coil region 881 919 N/A INTRINSIC
low complexity region 948 964 N/A INTRINSIC
low complexity region 974 988 N/A INTRINSIC
low complexity region 1042 1056 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000124745
SMART Domains Protein: ENSMUSP00000121042
Gene: ENSMUSG00000074247

DomainStartEndE-ValueType
Pfam:DDA1 3 65 6e-34 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000130098
Predicted Effect noncoding transcript
Transcript: ENSMUST00000135052
Predicted Effect probably benign
Transcript: ENSMUST00000138892
Predicted Effect noncoding transcript
Transcript: ENSMUST00000146677
Predicted Effect noncoding transcript
Transcript: ENSMUST00000213016
Predicted Effect noncoding transcript
Transcript: ENSMUST00000212768
Predicted Effect unknown
Transcript: ENSMUST00000213382
AA Change: N752S
Predicted Effect probably benign
Transcript: ENSMUST00000147642
SMART Domains Protein: ENSMUSP00000123665
Gene: ENSMUSG00000074247

DomainStartEndE-ValueType
Pfam:DDA1 3 52 1.2e-23 PFAM
low complexity region 84 98 N/A INTRINSIC
Meta Mutation Damage Score 0.0756 question?
Coding Region Coverage
  • 1x: 98.5%
  • 3x: 97.4%
  • 10x: 95.6%
  • 20x: 92.0%
Validation Efficiency 99% (83/84)
Allele List at MGI
Other mutations in this stock
Total: 82 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca14 A G 7: 119,822,850 (GRCm39) I321V probably benign Het
Adcy7 A G 8: 89,051,391 (GRCm39) D837G probably damaging Het
Aldh1a1 T A 19: 20,617,440 (GRCm39) Y457* probably null Het
Alox5 T C 6: 116,397,323 (GRCm39) Y287C probably benign Het
Ap3b1 A G 13: 94,630,189 (GRCm39) K815E unknown Het
Atp11a A T 8: 12,906,930 (GRCm39) probably benign Het
Atp6v0a1 A T 11: 100,939,341 (GRCm39) D702V possibly damaging Het
Cacna1b T A 2: 24,651,856 (GRCm39) N108Y probably damaging Het
Ccdc57 G C 11: 120,812,637 (GRCm39) A39G probably benign Het
Cdhr1 A T 14: 36,803,333 (GRCm39) V581D probably benign Het
Cfap20dc T G 14: 8,431,667 (GRCm38) Y655S probably damaging Het
Cyp2b23 A G 7: 26,372,304 (GRCm39) probably benign Het
D430041D05Rik G C 2: 103,998,295 (GRCm39) P1836R probably damaging Het
Ddit4l C T 3: 137,330,048 (GRCm39) probably benign Het
Dnah8 A T 17: 30,909,245 (GRCm39) I1024F probably benign Het
Dync2i1 T C 12: 116,221,026 (GRCm39) probably benign Het
Edc3 T A 9: 57,634,621 (GRCm39) F213I probably damaging Het
Edrf1 G A 7: 133,258,774 (GRCm39) D717N probably damaging Het
Efna5 G A 17: 62,958,068 (GRCm39) P63S probably damaging Het
Elapor2 T C 5: 9,484,681 (GRCm39) L486P probably damaging Het
Entpd3 A G 9: 120,387,547 (GRCm39) Y248C probably damaging Het
Flcn G A 11: 59,686,635 (GRCm39) Q373* probably null Het
Fry T C 5: 150,358,241 (GRCm39) V1908A probably damaging Het
Gabrg3 A T 7: 57,031,365 (GRCm39) Y58* probably null Het
Gabrp A T 11: 33,502,614 (GRCm39) Y417N probably damaging Het
Golga2 C A 2: 32,194,964 (GRCm39) probably null Het
Grip2 C A 6: 91,750,773 (GRCm39) probably null Het
Gsx2 A G 5: 75,237,729 (GRCm39) Y227C probably damaging Het
H2ac1 T C 13: 24,118,632 (GRCm39) V63A probably benign Het
Hif3a T C 7: 16,769,793 (GRCm39) *665W probably null Het
Hsd3b1 C A 3: 98,760,089 (GRCm39) V301L probably damaging Het
Ifitm5 T C 7: 140,529,921 (GRCm39) probably benign Het
Inpp4a A T 1: 37,418,067 (GRCm39) D498V probably damaging Het
Itga1 A T 13: 115,128,995 (GRCm39) D554E probably benign Het
Itk G A 11: 46,280,285 (GRCm39) probably benign Het
Kdm3b T A 18: 34,928,716 (GRCm39) probably benign Het
Klhl6 A G 16: 19,766,984 (GRCm39) V470A probably benign Het
Lamb3 T A 1: 193,002,839 (GRCm39) W95R probably damaging Het
Lbhd2 T A 12: 111,376,676 (GRCm39) I41N probably damaging Het
Lrp4 A T 2: 91,321,015 (GRCm39) S1014C probably damaging Het
Ltbp2 C T 12: 84,832,743 (GRCm39) probably null Het
Map3k19 A G 1: 127,749,919 (GRCm39) I1144T possibly damaging Het
Mfsd10 T C 5: 34,792,507 (GRCm39) probably benign Het
Mocos A G 18: 24,799,333 (GRCm39) D189G probably benign Het
Mvb12a T A 8: 71,999,654 (GRCm39) F224L probably damaging Het
Myo15a A T 11: 60,405,723 (GRCm39) probably null Het
Nos2 A T 11: 78,828,428 (GRCm39) H249L probably damaging Het
Notum A G 11: 120,549,160 (GRCm39) M184T probably benign Het
Nvl C A 1: 180,962,395 (GRCm39) D192Y probably damaging Het
Or10j3 A G 1: 173,031,484 (GRCm39) K187R probably benign Het
Or4f57 T C 2: 111,790,839 (GRCm39) Y193C probably damaging Het
Or5ac22 A T 16: 59,135,434 (GRCm39) F112Y probably damaging Het
Or5m12 T A 2: 85,734,591 (GRCm39) N269I probably benign Het
Or8k27 C A 2: 86,276,303 (GRCm39) V8L probably benign Het
Osgin1 A G 8: 120,172,396 (GRCm39) I397V possibly damaging Het
Otulin A G 15: 27,616,510 (GRCm39) V123A probably damaging Het
P4ha1 A G 10: 59,184,081 (GRCm39) Y181C probably damaging Het
Pcdhgc5 A T 18: 37,954,403 (GRCm39) D559V probably damaging Het
Phf2 T C 13: 48,982,270 (GRCm39) N151S unknown Het
Plxnc1 C A 10: 94,648,991 (GRCm39) G1263C probably benign Het
Rad51ap1 A G 6: 126,901,160 (GRCm39) *338Q probably null Het
Raver1 A G 9: 20,986,955 (GRCm39) S676P probably benign Het
Rfx8 T C 1: 39,727,737 (GRCm39) E196G possibly damaging Het
Rreb1 A T 13: 38,100,131 (GRCm39) K187* probably null Het
Rxfp1 T C 3: 79,574,961 (GRCm39) T217A probably benign Het
Rxra T C 2: 27,642,442 (GRCm39) L305P probably damaging Het
Sardh T C 2: 27,117,078 (GRCm39) probably benign Het
Skor2 A T 18: 76,964,293 (GRCm39) E952D probably damaging Het
Slc22a29 A T 19: 8,147,334 (GRCm39) S343T probably benign Het
Sorbs2 T C 8: 46,238,374 (GRCm39) probably benign Het
Supt7l C T 5: 31,673,262 (GRCm39) V329I probably benign Het
Taar2 G A 10: 23,817,393 (GRCm39) R311H probably benign Het
Tac1 T C 6: 7,559,165 (GRCm39) probably benign Het
Tcn2 A T 11: 3,872,044 (GRCm39) V361D probably damaging Het
Tm2d3 G A 7: 65,347,582 (GRCm39) A170T possibly damaging Het
Tnks G A 8: 35,307,124 (GRCm39) R1142* probably null Het
Ttll7 C A 3: 146,649,915 (GRCm39) Y648* probably null Het
Umod G T 7: 119,065,296 (GRCm39) Q578K probably benign Het
Upf2 G A 2: 6,032,015 (GRCm39) probably benign Het
Vmn2r92 C T 17: 18,388,219 (GRCm39) A408V probably damaging Het
Washc5 A G 15: 59,210,809 (GRCm39) I1013T probably benign Het
Zfp704 C A 3: 9,630,217 (GRCm39) R48L probably damaging Het
Other mutations in Ano8
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00338:Ano8 APN 8 71,936,902 (GRCm39) splice site probably benign
IGL00501:Ano8 APN 8 71,931,793 (GRCm39) critical splice donor site probably null
IGL01380:Ano8 APN 8 71,933,453 (GRCm39) unclassified probably benign
IGL02138:Ano8 APN 8 71,937,486 (GRCm39) missense probably damaging 0.99
IGL02516:Ano8 APN 8 71,937,721 (GRCm39) missense probably damaging 1.00
IGL02675:Ano8 APN 8 71,936,184 (GRCm39) missense probably damaging 0.99
IGL02995:Ano8 APN 8 71,935,761 (GRCm39) missense possibly damaging 0.72
H8786:Ano8 UTSW 8 71,931,388 (GRCm39) unclassified probably benign
R0282:Ano8 UTSW 8 71,933,258 (GRCm39) unclassified probably benign
R0518:Ano8 UTSW 8 71,931,902 (GRCm39) missense probably benign 0.39
R0521:Ano8 UTSW 8 71,931,902 (GRCm39) missense probably benign 0.39
R1028:Ano8 UTSW 8 71,933,615 (GRCm39) small deletion probably benign
R1147:Ano8 UTSW 8 71,934,661 (GRCm39) missense probably damaging 1.00
R1147:Ano8 UTSW 8 71,934,661 (GRCm39) missense probably damaging 1.00
R1748:Ano8 UTSW 8 71,931,602 (GRCm39) unclassified probably benign
R1852:Ano8 UTSW 8 71,936,131 (GRCm39) missense probably damaging 0.99
R4161:Ano8 UTSW 8 71,935,281 (GRCm39) missense probably damaging 1.00
R4192:Ano8 UTSW 8 71,935,936 (GRCm39) missense probably damaging 1.00
R4274:Ano8 UTSW 8 71,931,385 (GRCm39) unclassified probably benign
R4834:Ano8 UTSW 8 71,936,939 (GRCm39) missense probably damaging 1.00
R4961:Ano8 UTSW 8 71,935,640 (GRCm39) missense probably damaging 1.00
R5252:Ano8 UTSW 8 71,935,261 (GRCm39) missense probably damaging 1.00
R5553:Ano8 UTSW 8 71,937,641 (GRCm39) splice site probably null
R5598:Ano8 UTSW 8 71,935,221 (GRCm39) missense probably damaging 1.00
R5695:Ano8 UTSW 8 71,935,887 (GRCm39) missense probably damaging 0.98
R5994:Ano8 UTSW 8 71,937,478 (GRCm39) missense probably damaging 1.00
R6019:Ano8 UTSW 8 71,935,024 (GRCm39) missense probably damaging 1.00
R6153:Ano8 UTSW 8 71,933,441 (GRCm39) unclassified probably benign
R6405:Ano8 UTSW 8 71,935,674 (GRCm39) missense probably damaging 1.00
R6516:Ano8 UTSW 8 71,934,424 (GRCm39) splice site probably null
R6539:Ano8 UTSW 8 71,937,127 (GRCm39) missense probably damaging 1.00
R7194:Ano8 UTSW 8 71,935,007 (GRCm39) missense possibly damaging 0.66
R7204:Ano8 UTSW 8 71,931,669 (GRCm39) missense probably benign 0.39
R7340:Ano8 UTSW 8 71,935,655 (GRCm39) missense probably damaging 0.99
R7365:Ano8 UTSW 8 71,937,754 (GRCm39) missense probably damaging 1.00
R7417:Ano8 UTSW 8 71,933,477 (GRCm39) missense unknown
R7486:Ano8 UTSW 8 71,937,642 (GRCm39) critical splice donor site probably null
R7644:Ano8 UTSW 8 71,937,474 (GRCm39) missense probably damaging 0.98
R7709:Ano8 UTSW 8 71,934,933 (GRCm39) missense probably damaging 1.00
R7719:Ano8 UTSW 8 71,935,784 (GRCm39) missense possibly damaging 0.82
R8040:Ano8 UTSW 8 71,934,812 (GRCm39) missense probably benign 0.26
R8219:Ano8 UTSW 8 71,933,357 (GRCm39) missense unknown
R8355:Ano8 UTSW 8 71,933,210 (GRCm39) unclassified probably benign
R8401:Ano8 UTSW 8 71,936,011 (GRCm39) missense probably damaging 1.00
R8713:Ano8 UTSW 8 71,937,721 (GRCm39) missense probably damaging 1.00
R8755:Ano8 UTSW 8 71,935,724 (GRCm39) missense probably benign 0.11
R8871:Ano8 UTSW 8 71,931,944 (GRCm39) missense probably benign 0.39
R8903:Ano8 UTSW 8 71,934,834 (GRCm39) critical splice acceptor site probably null
R8990:Ano8 UTSW 8 71,929,201 (GRCm39) missense unknown
R9037:Ano8 UTSW 8 71,937,088 (GRCm39) missense probably damaging 1.00
R9379:Ano8 UTSW 8 71,936,178 (GRCm39) missense probably benign 0.28
R9432:Ano8 UTSW 8 71,933,561 (GRCm39) missense unknown
R9492:Ano8 UTSW 8 71,934,784 (GRCm39) missense possibly damaging 0.66
R9609:Ano8 UTSW 8 71,933,726 (GRCm39) missense unknown
X0026:Ano8 UTSW 8 71,931,801 (GRCm39) unclassified probably benign
Predicted Primers PCR Primer
(F):5'- TCCCGAGTAGCAGTCTCATACCTG -3'
(R):5'- GGTGTGTTTACTCTGGCCGAAGAAG -3'

Sequencing Primer
(F):5'- gggaatggaagccaggac -3'
(R):5'- TCTGGCCGAAGAAGACGATG -3'
Posted On 2013-05-09