Incidental Mutation 'IGL02572:Hsf5'
ID 299072
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Hsf5
Ensembl Gene ENSMUSG00000070345
Gene Name heat shock transcription factor family member 5
Synonyms LOC327992
Accession Numbers
Essential gene? Probably non essential (E-score: 0.203) question?
Stock # IGL02572
Quality Score
Status
Chromosome 11
Chromosomal Location 87507990-87550368 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) A to G at 87522521 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000091488 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000093956]
AlphaFold Q5ND04
Predicted Effect probably benign
Transcript: ENSMUST00000093956
SMART Domains Protein: ENSMUSP00000091488
Gene: ENSMUSG00000070345

DomainStartEndE-ValueType
HSF 11 153 2.35e-9 SMART
Blast:HSF 163 423 1e-149 BLAST
low complexity region 442 457 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 55 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A630001G21Rik T C 1: 85,652,892 (GRCm39) N92S probably damaging Het
Abca2 T C 2: 25,323,329 (GRCm39) L99P possibly damaging Het
Adam19 T A 11: 46,022,548 (GRCm39) Y500* probably null Het
Amy1 A T 3: 113,358,722 (GRCm39) probably benign Het
Aox3 T C 1: 58,197,526 (GRCm39) I624T probably damaging Het
Atad3a C T 4: 155,838,041 (GRCm39) D244N possibly damaging Het
Atp5mf C A 5: 145,124,047 (GRCm39) probably benign Het
Bbof1 G A 12: 84,475,139 (GRCm39) D443N probably damaging Het
Bod1l G A 5: 41,978,573 (GRCm39) Q914* probably null Het
C330011M18Rik A G 8: 84,793,208 (GRCm39) probably benign Het
Cgref1 A G 5: 31,090,911 (GRCm39) V301A probably benign Het
Coa6 T C 8: 127,149,480 (GRCm39) Y19H probably damaging Het
Cop1 T A 1: 159,136,448 (GRCm39) probably benign Het
Dmrta1 T C 4: 89,579,795 (GRCm39) S252P probably benign Het
Dnaaf5 T G 5: 139,170,384 (GRCm39) S484A probably benign Het
Dspp A T 5: 104,324,935 (GRCm39) S433C probably damaging Het
Efcab5 G A 11: 77,028,714 (GRCm39) R206* probably null Het
Epop A T 11: 97,519,027 (GRCm39) S361T probably benign Het
Fat3 T A 9: 15,871,802 (GRCm39) T3530S probably benign Het
Flvcr1 A G 1: 190,757,843 (GRCm39) Y108H probably damaging Het
Fsip2 T G 2: 82,822,347 (GRCm39) S6027A probably benign Het
Galnt14 A G 17: 73,842,262 (GRCm39) L209P probably damaging Het
Hif3a C A 7: 16,784,513 (GRCm39) R25L probably null Het
Il22ra2 A T 10: 19,502,492 (GRCm39) T104S probably benign Het
Klrk1 A G 6: 129,592,316 (GRCm39) S138P probably damaging Het
Lrp5 G T 19: 3,664,283 (GRCm39) Q815K probably benign Het
Morn4 A G 19: 42,064,886 (GRCm39) probably benign Het
Nlrp14 T A 7: 106,781,929 (GRCm39) Y375* probably null Het
Nsd1 T A 13: 55,443,943 (GRCm39) M1714K probably damaging Het
Or2aj6 T A 16: 19,443,848 (GRCm39) M1L probably benign Het
Or5aq7 G A 2: 86,938,710 (GRCm39) T7I possibly damaging Het
Or6c213 T A 10: 129,574,735 (GRCm39) D17V possibly damaging Het
Pappa2 C T 1: 158,678,786 (GRCm39) A877T probably benign Het
Pcsk2 G A 2: 143,532,262 (GRCm39) A137T probably damaging Het
Piezo1 A G 8: 123,212,044 (GRCm39) V2054A probably benign Het
Rad52 A G 6: 119,892,188 (GRCm39) probably benign Het
Rnf123 G A 9: 107,945,501 (GRCm39) R390* probably null Het
Rusf1 A T 7: 127,889,752 (GRCm39) probably benign Het
Sbno1 A G 5: 124,519,740 (GRCm39) probably benign Het
Scrn1 C T 6: 54,489,186 (GRCm39) D312N probably benign Het
Sin3b A G 8: 73,471,109 (GRCm39) Q352R probably benign Het
Slc25a28 A G 19: 43,652,885 (GRCm39) Y259H probably damaging Het
Sppl2a T C 2: 126,768,216 (GRCm39) M151V probably benign Het
Srrm1 G A 4: 135,052,415 (GRCm39) P658L unknown Het
Stra8 G A 6: 34,916,094 (GRCm39) D280N probably damaging Het
Thbs2 A T 17: 14,897,275 (GRCm39) D744E possibly damaging Het
Tiparp A G 3: 65,439,310 (GRCm39) T27A probably benign Het
Tmem38a T C 8: 73,333,818 (GRCm39) F99S probably damaging Het
Tmod3 T C 9: 75,416,667 (GRCm39) T222A probably benign Het
Tnn A G 1: 159,913,677 (GRCm39) I1272T probably damaging Het
Tnpo1 A T 13: 98,985,667 (GRCm39) I829N probably damaging Het
Trpm5 A T 7: 142,641,613 (GRCm39) probably benign Het
Ttn A G 2: 76,598,215 (GRCm39) V19566A probably damaging Het
V1ra8 A G 6: 90,180,040 (GRCm39) D81G probably damaging Het
Zdhhc20 A G 14: 58,127,564 (GRCm39) V25A probably benign Het
Other mutations in Hsf5
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00514:Hsf5 APN 11 87,513,922 (GRCm39) missense probably damaging 0.99
IGL01726:Hsf5 APN 11 87,526,951 (GRCm39) missense probably benign 0.22
IGL02480:Hsf5 APN 11 87,522,483 (GRCm39) missense possibly damaging 0.67
IGL03113:Hsf5 APN 11 87,548,190 (GRCm39) missense probably benign 0.03
R0015:Hsf5 UTSW 11 87,548,161 (GRCm39) missense probably benign
R0015:Hsf5 UTSW 11 87,548,161 (GRCm39) missense probably benign
R1381:Hsf5 UTSW 11 87,528,995 (GRCm39) missense probably benign
R1807:Hsf5 UTSW 11 87,548,168 (GRCm39) missense probably benign 0.04
R1838:Hsf5 UTSW 11 87,526,881 (GRCm39) missense probably benign 0.45
R2187:Hsf5 UTSW 11 87,529,010 (GRCm39) missense possibly damaging 0.51
R3930:Hsf5 UTSW 11 87,522,508 (GRCm39) missense probably damaging 1.00
R3931:Hsf5 UTSW 11 87,522,508 (GRCm39) missense probably damaging 1.00
R4420:Hsf5 UTSW 11 87,548,130 (GRCm39) missense probably benign 0.02
R4423:Hsf5 UTSW 11 87,522,460 (GRCm39) missense probably damaging 0.99
R4744:Hsf5 UTSW 11 87,513,617 (GRCm39) missense probably benign 0.02
R4795:Hsf5 UTSW 11 87,526,446 (GRCm39) missense probably benign 0.18
R5862:Hsf5 UTSW 11 87,513,817 (GRCm39) missense probably damaging 0.96
R6232:Hsf5 UTSW 11 87,508,120 (GRCm39) missense probably benign 0.05
R6234:Hsf5 UTSW 11 87,508,120 (GRCm39) missense probably benign 0.05
R6609:Hsf5 UTSW 11 87,526,779 (GRCm39) missense probably damaging 0.99
R7821:Hsf5 UTSW 11 87,528,954 (GRCm39) missense probably benign 0.04
R7989:Hsf5 UTSW 11 87,526,450 (GRCm39) missense probably benign 0.07
R9299:Hsf5 UTSW 11 87,526,770 (GRCm39) missense probably benign
R9419:Hsf5 UTSW 11 87,528,935 (GRCm39) missense probably benign 0.02
R9752:Hsf5 UTSW 11 87,513,709 (GRCm39) missense probably benign 0.22
Z1177:Hsf5 UTSW 11 87,528,959 (GRCm39) nonsense probably null
Posted On 2015-04-16