Incidental Mutation 'IGL00502:Foxk2'
ID 4451
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Foxk2
Ensembl Gene ENSMUSG00000039275
Gene Name forkhead box K2
Synonyms 1110054H05Rik, Ilf1, 5730434B08Rik
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL00502
Quality Score
Status
Chromosome 11
Chromosomal Location 121150816-121200722 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) A to G at 121187925 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000101719 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000106113]
AlphaFold Q3UCQ1
Predicted Effect probably benign
Transcript: ENSMUST00000106113
SMART Domains Protein: ENSMUSP00000101719
Gene: ENSMUSG00000039275

DomainStartEndE-ValueType
low complexity region 2 32 N/A INTRINSIC
FHA 47 119 9.96e-10 SMART
FH 247 338 2.2e-52 SMART
low complexity region 440 465 N/A INTRINSIC
low complexity region 486 498 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000151492
Predicted Effect noncoding transcript
Transcript: ENSMUST00000153579
Coding Region Coverage
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene contains a fork head DNA binding domain. This protein can bind to the purine-rich motifs of the HIV long terminal repeat (LTR), and to the similar purine-rich motif in the interleukin 2 (IL2) promoter. It may be involved in the regulation of viral and cellular promoter elements. [provided by RefSeq, Jul 2008]
Allele List at MGI
Other mutations in this stock
Total: 36 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adamts20 A T 15: 94,301,278 (GRCm39) I82N probably damaging Het
Ampd2 A T 3: 107,984,712 (GRCm39) L422H probably damaging Het
Angptl2 T A 2: 33,118,406 (GRCm39) V60E probably damaging Het
Ano3 G A 2: 110,601,395 (GRCm39) probably benign Het
Arhgap40 A G 2: 158,373,078 (GRCm39) D112G probably benign Het
Bcorl1 T G X: 47,494,919 (GRCm39) V1730G probably damaging Het
Btrc A T 19: 45,515,704 (GRCm39) E553V probably damaging Het
Cacna1b A T 2: 24,541,212 (GRCm39) Y1323* probably null Het
Ccdc146 A G 5: 21,506,420 (GRCm39) C674R possibly damaging Het
Ccdc170 A G 10: 4,496,836 (GRCm39) D458G probably damaging Het
Cfap57 T A 4: 118,438,198 (GRCm39) M898L probably benign Het
Crybg1 C T 10: 43,834,309 (GRCm39) V1961I probably damaging Het
Dsp T C 13: 38,381,822 (GRCm39) S2257P probably damaging Het
Dytn A G 1: 63,717,999 (GRCm39) V12A probably benign Het
Galnt2l T C 8: 125,054,837 (GRCm39) M204T probably damaging Het
Gfi1b G A 2: 28,504,797 (GRCm39) Q70* probably null Het
Gsdmc T C 15: 63,676,270 (GRCm39) T58A probably benign Het
Hikeshi G A 7: 89,572,818 (GRCm39) T26I probably benign Het
Mpdz T C 4: 81,287,960 (GRCm39) D433G probably damaging Het
Ndufb5 T A 3: 32,799,048 (GRCm39) V55D probably damaging Het
Nostrin T C 2: 69,014,336 (GRCm39) S431P probably benign Het
Pdcd1lg2 A T 19: 29,423,462 (GRCm39) T169S possibly damaging Het
Plekha7 A T 7: 115,734,419 (GRCm39) M1006K probably damaging Het
Rgs6 A T 12: 83,098,097 (GRCm39) I94F probably benign Het
Rims2 A T 15: 39,370,380 (GRCm39) D938V probably damaging Het
Slc4a8 A G 15: 100,705,319 (GRCm39) T842A possibly damaging Het
Spata21 C A 4: 140,838,675 (GRCm39) probably null Het
Stk32a C T 18: 43,443,510 (GRCm39) T229I possibly damaging Het
Tent4b C T 8: 88,978,886 (GRCm39) Q63* probably null Het
Trim33 C T 3: 103,237,498 (GRCm39) P185S probably benign Het
Tspoap1 A G 11: 87,668,647 (GRCm39) probably null Het
Vcan A G 13: 89,840,438 (GRCm39) V742A probably benign Het
Vrtn A T 12: 84,695,837 (GRCm39) I196F probably benign Het
Wasf1 A T 10: 40,796,293 (GRCm39) I8F probably damaging Het
Ythdc2 A G 18: 44,980,879 (GRCm39) I491M probably damaging Het
Zfp292 T C 4: 34,809,775 (GRCm39) T1095A possibly damaging Het
Other mutations in Foxk2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00339:Foxk2 APN 11 121,190,560 (GRCm39) missense probably damaging 1.00
IGL02619:Foxk2 APN 11 121,190,402 (GRCm39) splice site probably benign
IGL03067:Foxk2 APN 11 121,176,394 (GRCm39) missense possibly damaging 0.87
R1843:Foxk2 UTSW 11 121,176,363 (GRCm39) missense probably benign 0.01
R2153:Foxk2 UTSW 11 121,151,213 (GRCm39) missense probably benign 0.08
R2847:Foxk2 UTSW 11 121,151,317 (GRCm39) small insertion probably benign
R3770:Foxk2 UTSW 11 121,151,317 (GRCm39) small insertion probably benign
R4024:Foxk2 UTSW 11 121,176,439 (GRCm39) missense possibly damaging 0.67
R6958:Foxk2 UTSW 11 121,190,563 (GRCm39) missense probably benign 0.16
R6968:Foxk2 UTSW 11 121,151,308 (GRCm39) missense possibly damaging 0.87
R7558:Foxk2 UTSW 11 121,178,884 (GRCm39) missense probably benign 0.00
R7736:Foxk2 UTSW 11 121,190,473 (GRCm39) missense possibly damaging 0.92
R7902:Foxk2 UTSW 11 121,190,553 (GRCm39) missense probably benign
Posted On 2012-04-20