Incidental Mutation 'IGL02793:Hyal6'
ID 359830
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Hyal6
Ensembl Gene ENSMUSG00000029679
Gene Name hyaluronoglucosaminidase 6
Synonyms Hyal-ps1, 4932701A20Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.062) question?
Stock # IGL02793
Quality Score
Status
Chromosome 6
Chromosomal Location 24733244-24745451 bp(+) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) A to T at 24734378 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Lysine to Stop codon at position 104 (K104*)
Ref Sequence ENSEMBL: ENSMUSP00000031690 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000031690]
AlphaFold Q9D4E9
Predicted Effect probably null
Transcript: ENSMUST00000031690
AA Change: K104*
SMART Domains Protein: ENSMUSP00000031690
Gene: ENSMUSG00000029679
AA Change: K104*

DomainStartEndE-ValueType
signal peptide 1 24 N/A INTRINSIC
Pfam:Glyco_hydro_56 30 363 4.8e-136 PFAM
EGF 365 438 6.02e0 SMART
transmembrane domain 457 479 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 39 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcb11 T C 2: 69,122,293 (GRCm39) I397V possibly damaging Het
Bco2 A T 9: 50,455,834 (GRCm39) V173E probably damaging Het
Bdnf T C 2: 109,554,196 (GRCm39) V150A probably damaging Het
Cdh15 T A 8: 123,587,721 (GRCm39) V215E probably damaging Het
Col6a2 A T 10: 76,432,144 (GRCm39) I1003N possibly damaging Het
Daam2 A C 17: 49,771,056 (GRCm39) I887S probably damaging Het
Dnajb13 C T 7: 100,156,648 (GRCm39) D143N probably damaging Het
Fabp3-ps1 T A 10: 86,567,943 (GRCm39) probably benign Het
Gid4 G A 11: 60,323,256 (GRCm39) R116Q probably benign Het
Hectd2 A G 19: 36,564,821 (GRCm39) E34G probably damaging Het
Il1b A G 2: 129,209,171 (GRCm39) I153T probably benign Het
Kdm3b A G 18: 34,962,072 (GRCm39) M1499V probably damaging Het
Kntc1 C A 5: 123,916,340 (GRCm39) probably null Het
Lmbr1 A G 5: 29,497,186 (GRCm39) S72P probably damaging Het
Lrrc2 T C 9: 110,808,695 (GRCm39) probably null Het
Map2k5 T C 9: 63,164,321 (GRCm39) I328V probably benign Het
Mphosph9 T A 5: 124,421,800 (GRCm39) probably null Het
Mpp4 C T 1: 59,175,993 (GRCm39) probably null Het
Ndrg3 A G 2: 156,791,952 (GRCm39) probably null Het
Ndufa10 A C 1: 92,397,639 (GRCm39) Y136D probably damaging Het
Or10ak9 A T 4: 118,726,794 (GRCm39) D271V probably damaging Het
Or2b7 T A 13: 21,740,172 (GRCm39) S7C probably damaging Het
Or4a72 T C 2: 89,405,896 (GRCm39) Y58C probably damaging Het
Or8g34 A G 9: 39,372,802 (GRCm39) E22G probably benign Het
Rab18 T C 18: 6,788,474 (GRCm39) probably benign Het
Rad1 T C 15: 10,493,365 (GRCm39) I264T probably benign Het
Rhbdf1 A G 11: 32,163,293 (GRCm39) V393A possibly damaging Het
Rrp12 A G 19: 41,860,005 (GRCm39) L1025P probably damaging Het
Rtca A G 3: 116,286,726 (GRCm39) F302S probably damaging Het
Slc9b1 T A 3: 135,080,167 (GRCm39) probably benign Het
Sspo A T 6: 48,464,828 (GRCm39) probably benign Het
Ssrp1 T A 2: 84,871,264 (GRCm39) I257N probably damaging Het
Sval2 A C 6: 41,838,795 (GRCm39) Y11S probably benign Het
Tcl1b2 T C 12: 105,120,358 (GRCm39) *118Q probably null Het
Thsd7b A G 1: 129,879,130 (GRCm39) Y989C probably damaging Het
Tlr4 A C 4: 66,757,681 (GRCm39) H158P probably damaging Het
Vmn2r42 T C 7: 8,197,852 (GRCm39) T256A probably benign Het
Xdh T C 17: 74,207,576 (GRCm39) E927G probably damaging Het
Yap1 T C 9: 7,973,907 (GRCm39) N178S probably benign Het
Other mutations in Hyal6
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01351:Hyal6 APN 6 24,734,178 (GRCm39) missense probably damaging 1.00
IGL02269:Hyal6 APN 6 24,740,858 (GRCm39) missense probably damaging 0.97
IGL02729:Hyal6 APN 6 24,734,694 (GRCm39) missense probably damaging 1.00
IGL02943:Hyal6 APN 6 24,743,438 (GRCm39) missense probably damaging 0.99
IGL03351:Hyal6 APN 6 24,743,428 (GRCm39) missense probably damaging 1.00
R0481:Hyal6 UTSW 6 24,743,417 (GRCm39) missense probably damaging 1.00
R0517:Hyal6 UTSW 6 24,734,852 (GRCm39) missense probably benign
R0853:Hyal6 UTSW 6 24,734,072 (GRCm39) missense probably benign
R1182:Hyal6 UTSW 6 24,743,416 (GRCm39) missense probably damaging 1.00
R1401:Hyal6 UTSW 6 24,743,434 (GRCm39) missense probably damaging 1.00
R1780:Hyal6 UTSW 6 24,734,031 (GRCm39) splice site probably benign
R1858:Hyal6 UTSW 6 24,740,857 (GRCm39) missense probably benign 0.01
R2011:Hyal6 UTSW 6 24,734,723 (GRCm39) missense possibly damaging 0.69
R3441:Hyal6 UTSW 6 24,734,592 (GRCm39) missense probably benign
R4819:Hyal6 UTSW 6 24,734,965 (GRCm39) nonsense probably null
R5357:Hyal6 UTSW 6 24,734,517 (GRCm39) missense probably benign 0.05
R5648:Hyal6 UTSW 6 24,734,235 (GRCm39) missense possibly damaging 0.61
R5717:Hyal6 UTSW 6 24,743,690 (GRCm39) missense probably benign 0.15
R5884:Hyal6 UTSW 6 24,743,368 (GRCm39) missense probably damaging 1.00
R6657:Hyal6 UTSW 6 24,734,757 (GRCm39) missense possibly damaging 0.61
R6826:Hyal6 UTSW 6 24,734,371 (GRCm39) missense probably damaging 1.00
R7178:Hyal6 UTSW 6 24,734,834 (GRCm39) missense probably benign 0.28
R7531:Hyal6 UTSW 6 24,740,786 (GRCm39) missense possibly damaging 0.46
R7630:Hyal6 UTSW 6 24,734,583 (GRCm39) missense probably damaging 1.00
R7787:Hyal6 UTSW 6 24,743,735 (GRCm39) missense probably damaging 0.99
R7851:Hyal6 UTSW 6 24,734,497 (GRCm39) missense probably benign 0.05
R8132:Hyal6 UTSW 6 24,740,827 (GRCm39) missense possibly damaging 0.80
R8200:Hyal6 UTSW 6 24,734,565 (GRCm39) missense probably benign 0.01
R8294:Hyal6 UTSW 6 24,734,378 (GRCm39) missense possibly damaging 0.53
R8300:Hyal6 UTSW 6 24,734,087 (GRCm39) missense probably benign
R8509:Hyal6 UTSW 6 24,734,605 (GRCm39) missense probably damaging 1.00
R8705:Hyal6 UTSW 6 24,734,673 (GRCm39) missense probably benign 0.01
R8917:Hyal6 UTSW 6 24,734,103 (GRCm39) missense possibly damaging 0.96
R9133:Hyal6 UTSW 6 24,734,585 (GRCm39) missense possibly damaging 0.61
R9149:Hyal6 UTSW 6 24,734,151 (GRCm39) missense probably benign 0.02
R9325:Hyal6 UTSW 6 24,743,455 (GRCm39) missense probably damaging 1.00
R9515:Hyal6 UTSW 6 24,734,929 (GRCm39) nonsense probably null
X0019:Hyal6 UTSW 6 24,734,666 (GRCm39) missense probably damaging 1.00
Posted On 2015-12-18