Incidental Mutation 'IGL02109:Ano10'
ID281143
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Ano10
Ensembl Gene ENSMUSG00000037949
Gene Nameanoctamin 10
SynonymsTmem16k
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.108) question?
Stock #IGL02109
Quality Score
Status
Chromosome9
Chromosomal Location122175874-122294423 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) C to T at 122261342 bp
ZygosityHeterozygous
Amino Acid Change Glutamic Acid to Lysine at position 302 (E302K)
Ref Sequence ENSEMBL: ENSMUSP00000150161 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000042546] [ENSMUST00000214283] [ENSMUST00000214409] [ENSMUST00000214507] [ENSMUST00000216081] [ENSMUST00000216670]
Predicted Effect probably damaging
Transcript: ENSMUST00000042546
AA Change: E302K

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000045214
Gene: ENSMUSG00000037949
AA Change: E302K

DomainStartEndE-ValueType
Pfam:Anoctamin 200 628 2.2e-115 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000214283
AA Change: E302K

PolyPhen 2 Score 0.995 (Sensitivity: 0.68; Specificity: 0.97)
Predicted Effect probably damaging
Transcript: ENSMUST00000214409
AA Change: E244K

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
Predicted Effect probably damaging
Transcript: ENSMUST00000214507
AA Change: E110K

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
Predicted Effect probably benign
Transcript: ENSMUST00000216081
Predicted Effect probably damaging
Transcript: ENSMUST00000216670
AA Change: E302K

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Coding Region Coverage
Validation Efficiency
MGI Phenotype FUNCTION: This gene encodes a member of the anoctamin family, which in mammals is comprised of 10 members. Anoctamin proteins are proposed to have eight transmembrane domains with both termini facing the cytoplasm and a C-terminal domain of unknown function. While some members have been characterized as calcium-activated chloride channels, this protein is reported to inhibit anion conductance. Alternative splicing results in multiple transcript variants that encode different protein isoforms. [provided by RefSeq, Dec 2012]
PHENOTYPE: Mice homozygous for a knock-out allele fail to exhibit calcium-activated chloride ion secretion in the jejunum. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 28 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ank1 T A 8: 23,096,184 N427K probably damaging Het
Arl3 T A 19: 46,542,346 probably benign Het
Clec14a T A 12: 58,268,148 E229D probably benign Het
Ctbp1 T C 5: 33,266,968 D26G probably damaging Het
Flt3 G T 5: 147,350,681 H671N probably benign Het
Fras1 A G 5: 96,700,523 D1799G probably benign Het
Il20ra G A 10: 19,759,505 G498D possibly damaging Het
Kcnu1 T G 8: 25,937,699 L348R possibly damaging Het
Lrpprc A T 17: 84,726,570 L999* probably null Het
Myt1 T G 2: 181,815,617 probably benign Het
N4bp2 C T 5: 65,798,134 T467M probably damaging Het
Nup98 T C 7: 102,183,486 T355A probably benign Het
Ocstamp A T 2: 165,397,336 V310E possibly damaging Het
Olfr1285 T G 2: 111,408,493 noncoding transcript Het
Olfr147 T C 9: 38,403,086 F71L possibly damaging Het
Plcb1 C A 2: 134,786,559 H9Q probably damaging Het
Plxna4 T A 6: 32,215,641 Q795L probably benign Het
Pms1 A G 1: 53,207,409 S324P probably damaging Het
Pnldc1 G T 17: 12,905,538 H143Q probably benign Het
Ppp1r12b A G 1: 134,872,805 probably null Het
Ryr3 A G 2: 112,949,157 F250L probably benign Het
Scgn T C 13: 23,953,965 D241G possibly damaging Het
St8sia4 T C 1: 95,660,892 I73V possibly damaging Het
Tle3 T A 9: 61,413,050 C595S probably damaging Het
Tmem209 T C 6: 30,497,945 Y117C probably damaging Het
Tshr T A 12: 91,537,992 I568N probably damaging Het
Ttll10 C T 4: 156,047,480 D22N probably benign Het
Ttn A T 2: 76,809,858 V13802E probably damaging Het
Other mutations in Ano10
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00545:Ano10 APN 9 122261356 missense possibly damaging 0.96
IGL00886:Ano10 APN 9 122271324 missense probably benign 0.01
IGL00932:Ano10 APN 9 122251231 nonsense probably null
IGL01613:Ano10 APN 9 122259540 missense possibly damaging 0.75
IGL02397:Ano10 APN 9 122261392 missense probably damaging 1.00
IGL02512:Ano10 APN 9 122272474 missense possibly damaging 0.50
IGL03216:Ano10 APN 9 122257061 missense probably damaging 1.00
arna UTSW 9 122259564 missense possibly damaging 0.77
R0624:Ano10 UTSW 9 122259595 splice site probably benign
R1669:Ano10 UTSW 9 122257183 missense possibly damaging 0.94
R1801:Ano10 UTSW 9 122253030 missense probably damaging 1.00
R2511:Ano10 UTSW 9 122258945 missense probably damaging 0.99
R3836:Ano10 UTSW 9 122263763 missense possibly damaging 0.58
R4027:Ano10 UTSW 9 122252928 splice site probably benign
R4151:Ano10 UTSW 9 122261535 nonsense probably null
R4590:Ano10 UTSW 9 122257165 missense probably benign 0.22
R4651:Ano10 UTSW 9 122261115 nonsense probably null
R4652:Ano10 UTSW 9 122261115 nonsense probably null
R4676:Ano10 UTSW 9 122263787 missense probably damaging 0.98
R5026:Ano10 UTSW 9 122272559 nonsense probably null
R5281:Ano10 UTSW 9 122261486 missense probably damaging 1.00
R5401:Ano10 UTSW 9 122261290 missense probably damaging 1.00
R6269:Ano10 UTSW 9 122261242 missense probably damaging 0.99
R6449:Ano10 UTSW 9 122201688 intron probably benign
R6702:Ano10 UTSW 9 122259564 missense possibly damaging 0.77
R7010:Ano10 UTSW 9 122253124 missense probably damaging 1.00
R7384:Ano10 UTSW 9 122176343 missense unknown
R7584:Ano10 UTSW 9 122275531 missense probably benign
Posted On2015-04-16