Incidental Mutation 'IGL02224:Phf11b'
ID285283
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Phf11b
Ensembl Gene ENSMUSG00000091649
Gene NamePHD finger protein 11B
SynonymsGm4902
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.189) question?
Stock #IGL02224
Quality Score
Status
Chromosome14
Chromosomal Location59320964-59341351 bp(-) (GRCm38)
Type of Mutationsplice site
DNA Base Change (assembly) A to T at 59326066 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000127857 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000166121]
Predicted Effect probably benign
Transcript: ENSMUST00000166121
SMART Domains Protein: ENSMUSP00000127857
Gene: ENSMUSG00000091649

DomainStartEndE-ValueType
PHD 92 143 1.55e-1 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 37 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Akr1c12 T A 13: 4,279,290 T23S probably damaging Het
Alpk3 G A 7: 81,076,868 probably benign Het
Atp8b3 A G 10: 80,525,976 probably benign Het
Atr C T 9: 95,878,629 R1051C probably damaging Het
B4galt2 T C 4: 117,876,913 D309G probably benign Het
C130026L21Rik A G 5: 111,582,425 noncoding transcript Het
Cadm3 A G 1: 173,338,061 I344T possibly damaging Het
Cd101 T C 3: 101,017,002 T370A probably benign Het
Col6a5 A T 9: 105,864,335 S2462T probably damaging Het
Csf3r A T 4: 126,043,539 N739Y probably benign Het
Ensa T C 3: 95,628,679 S108P probably benign Het
Fancd2 T A 6: 113,568,320 probably null Het
Fbp1 T A 13: 62,888,007 T13S probably damaging Het
Flrt2 C A 12: 95,780,028 T380K possibly damaging Het
Gpatch11 T C 17: 78,841,093 probably benign Het
Hagh A G 17: 24,852,887 D29G probably damaging Het
Hmmr T C 11: 40,710,004 Q513R unknown Het
Hoxb8 T C 11: 96,283,155 S65P probably benign Het
Il4ra T C 7: 125,570,099 probably benign Het
Lbp A G 2: 158,306,749 N27S probably damaging Het
Msh4 G A 3: 153,890,185 T76I possibly damaging Het
Nfat5 T C 8: 107,344,815 V281A probably benign Het
Olfr1115 C T 2: 87,252,477 S180F probably benign Het
Olfr1140 T A 2: 87,746,413 C72* probably null Het
Olfr1181 C T 2: 88,423,708 probably null Het
Olfr1459 T A 19: 13,145,756 K301M probably damaging Het
Olfr272 A T 4: 52,911,392 V134D probably damaging Het
Pik3c2a A G 7: 116,363,340 probably benign Het
Prdx1 T A 4: 116,691,867 F66L probably damaging Het
Prss39 A G 1: 34,499,378 H108R probably damaging Het
Spta1 C A 1: 174,217,689 probably benign Het
Tmem87b A G 2: 128,834,207 I297V possibly damaging Het
Vmn1r191 T C 13: 22,178,898 R229G probably damaging Het
Vmn2r113 A T 17: 22,955,986 R524* probably null Het
Washc2 T A 6: 116,220,569 D254E possibly damaging Het
Zfp318 C T 17: 46,396,810 R265* probably null Het
Zfp773 T C 7: 7,132,976 H207R probably benign Het
Other mutations in Phf11b
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00560:Phf11b APN 14 59324875 missense probably damaging 1.00
IGL01116:Phf11b APN 14 59323182 missense probably benign 0.02
IGL01446:Phf11b APN 14 59341291 missense probably benign 0.02
IGL03062:Phf11b APN 14 59324924 missense probably damaging 1.00
PIT4131001:Phf11b UTSW 14 59323162 splice site probably benign
R1795:Phf11b UTSW 14 59328105 missense probably benign 0.00
R3774:Phf11b UTSW 14 59326057 missense probably benign 0.45
R4553:Phf11b UTSW 14 59341285 missense probably benign 0.10
R5460:Phf11b UTSW 14 59331264 missense probably benign 0.01
R5620:Phf11b UTSW 14 59321504 missense probably benign 0.01
R5985:Phf11b UTSW 14 59321578 missense possibly damaging 0.52
R5990:Phf11b UTSW 14 59324926 missense possibly damaging 0.57
R6775:Phf11b UTSW 14 59338645 missense probably benign 0.14
R6836:Phf11b UTSW 14 59328123 missense possibly damaging 0.81
R7197:Phf11b UTSW 14 59326058 missense probably benign 0.06
R8043:Phf11b UTSW 14 59331273 missense probably benign 0.35
Posted On2015-04-16