Incidental Mutation 'IGL02490:Ftmt'
ID295574
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Ftmt
Ensembl Gene ENSMUSG00000024510
Gene Nameferritin mitochondrial
SynonymsMtF, 4930447C24Rik, mitochondrial ferritin, Fth3
Accession Numbers
Is this an essential gene? Non essential (E-score: 0.000) question?
Stock #IGL02490
Quality Score
Status
Chromosome18
Chromosomal Location52331536-52332986 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to C at 52331688 bp
ZygosityHeterozygous
Amino Acid Change Arginine to Serine at position 25 (R25S)
Ref Sequence ENSEMBL: ENSMUSP00000025388 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000025388]
Predicted Effect probably benign
Transcript: ENSMUST00000025388
AA Change: R25S

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000025388
Gene: ENSMUSG00000024510
AA Change: R25S

DomainStartEndE-ValueType
Pfam:Ferritin 73 214 1.3e-37 PFAM
Coding Region Coverage
Validation Efficiency
MGI Phenotype PHENOTYPE: Mice homozygous for a knock-out allele do not exhibit any overt phenotype. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 58 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4933427D06Rik A G 6: 89,101,577 noncoding transcript Het
Adam5 A T 8: 24,781,704 Y562* probably null Het
Akr1d1 T C 6: 37,558,488 V269A probably damaging Het
Anks4b A G 7: 120,174,018 T34A probably damaging Het
Arhgef40 A G 14: 51,989,195 N232S probably damaging Het
Cdc40 C T 10: 40,841,771 V379I probably benign Het
Cdc45 C T 16: 18,798,729 M200I probably benign Het
Cdh13 A G 8: 119,095,323 D307G probably damaging Het
Ces1h A G 8: 93,356,999 probably null Het
Chchd6 T A 6: 89,384,674 H249L possibly damaging Het
Cul1 T C 6: 47,514,886 V392A probably damaging Het
Cwc15 A T 9: 14,502,024 D34V probably damaging Het
Cyp2c39 T C 19: 39,539,002 I264T probably damaging Het
Dapk1 A G 13: 60,749,334 D789G probably damaging Het
Dcdc2a T A 13: 25,107,652 Y207N probably damaging Het
Efcab1 T A 16: 14,916,946 V60E probably benign Het
Flt3 T A 5: 147,331,296 N960Y probably damaging Het
Fmn1 C T 2: 113,529,472 probably benign Het
Foxm1 T A 6: 128,373,351 C400* probably null Het
Guca1b T C 17: 47,389,265 probably benign Het
Hectd4 A T 5: 121,318,613 K680N possibly damaging Het
Hephl1 C A 9: 15,053,685 R1138L probably benign Het
Il1rl2 T A 1: 40,356,812 probably benign Het
Ints2 A T 11: 86,233,183 I593K possibly damaging Het
Iqcg T A 16: 33,035,567 K213* probably null Het
Kif1b T A 4: 149,204,208 S1259C probably benign Het
Klc1 C T 12: 111,781,776 T371M possibly damaging Het
Loxl4 T C 19: 42,604,830 T301A probably benign Het
Lrrc40 T C 3: 158,062,699 L497P probably damaging Het
Masp2 C T 4: 148,607,943 R298W possibly damaging Het
Myo5a A T 9: 75,136,455 Y242F probably damaging Het
Nup98 A G 7: 102,152,366 V784A probably damaging Het
Olfr1138 T C 2: 87,737,955 Y123C probably damaging Het
Osbpl1a G T 18: 12,882,284 probably benign Het
Pcdh10 A G 3: 45,380,487 Y412C probably damaging Het
Pfkfb2 T A 1: 130,700,852 Y339F probably damaging Het
Plcb2 T C 2: 118,719,760 N172D probably damaging Het
Plec T C 15: 76,189,263 Y517C probably damaging Het
Plod2 G T 9: 92,586,842 A207S probably benign Het
Plxdc1 A T 11: 97,954,778 D229E probably benign Het
Ppp3cb A G 14: 20,531,658 probably null Het
Procr T C 2: 155,753,432 L52P probably damaging Het
Psme2b G T 11: 48,946,119 probably benign Het
Rgs22 G A 15: 36,054,847 A727V probably damaging Het
Rock2 T A 12: 16,948,563 W277R probably damaging Het
Rpl26 A G 11: 68,904,390 D112G probably damaging Het
Rxfp1 C A 3: 79,652,167 probably null Het
Sdr39u1 G A 14: 55,898,341 P98L probably damaging Het
Sgms1 T C 19: 32,160,143 K8E probably damaging Het
Stk31 T C 6: 49,417,535 V277A probably benign Het
Trav15-1-dv6-1 A C 14: 53,560,131 E79A probably benign Het
Ttll6 A T 11: 96,156,720 D715V possibly damaging Het
Ush2a T C 1: 188,810,364 S3376P probably damaging Het
Vmn2r109 T A 17: 20,540,984 T704S possibly damaging Het
Zfp27 T A 7: 29,894,935 H535L possibly damaging Het
Zfp609 A T 9: 65,703,968 V571D possibly damaging Het
Zfp874a A T 13: 67,442,700 Y288* probably null Het
Zfp993 T C 4: 146,657,617 S133P probably damaging Het
Other mutations in Ftmt
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01290:Ftmt APN 18 52332113 missense probably damaging 0.96
IGL01678:Ftmt APN 18 52332134 missense probably damaging 0.98
IGL02111:Ftmt APN 18 52332053 missense possibly damaging 0.77
IGL02472:Ftmt APN 18 52331840 missense possibly damaging 0.92
IGL03181:Ftmt APN 18 52331881 missense probably damaging 0.97
R4867:Ftmt UTSW 18 52332053 missense possibly damaging 0.77
R4899:Ftmt UTSW 18 52331586 start gained probably benign
R6238:Ftmt UTSW 18 52332235 missense probably damaging 0.99
R6699:Ftmt UTSW 18 52331665 missense possibly damaging 0.87
R7057:Ftmt UTSW 18 52332108 missense probably benign 0.04
R7270:Ftmt UTSW 18 52332019 missense probably benign 0.10
Posted On2015-04-16