Incidental Mutation 'R1828:Hao1'
ID 206982
Institutional Source Beutler Lab
Gene Symbol Hao1
Ensembl Gene ENSMUSG00000027261
Gene Name hydroxyacid oxidase 1, liver
Synonyms Gox1, Hao-1, GOX
MMRRC Submission 039855-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.070) question?
Stock # R1828 (G1)
Quality Score 225
Status Not validated
Chromosome 2
Chromosomal Location 134339281-134396272 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 134372584 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Arginine to Serine at position 141 (R141S)
Ref Sequence ENSEMBL: ENSMUSP00000028704 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000028704]
AlphaFold Q9WU19
Predicted Effect probably benign
Transcript: ENSMUST00000028704
AA Change: R141S

PolyPhen 2 Score 0.085 (Sensitivity: 0.93; Specificity: 0.85)
SMART Domains Protein: ENSMUSP00000028704
Gene: ENSMUSG00000027261
AA Change: R141S

DomainStartEndE-ValueType
Pfam:FMN_dh 15 362 9.1e-140 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000140794
Coding Region Coverage
  • 1x: 97.4%
  • 3x: 96.9%
  • 10x: 95.2%
  • 20x: 92.0%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene is one of three related genes that have 2-hydroxyacid oxidase activity yet differ in encoded protein amino acid sequence, tissue expression and substrate preference. Subcellular location of the encoded protein is the peroxisome. Specifically, this gene is expressed primarily in liver and pancreas and the encoded protein is most active on glycolate, a two-carbon substrate. The protein is also active on 2-hydroxy fatty acids. The transcript detected at high levels in pancreas may represent an alternatively spliced form or the use of a multiple near-consensus upstream polyadenylation site. [provided by RefSeq, Jul 2008]
PHENOTYPE: Electrophoretic variants are known for this locus. The a allele determines a fast migrating band in BALB/c, CBA/H, C3H/He and C57BL/6; the b allele, a slow band in NZC; the c allele, the fastest band in DBA/Li, NFS/N, STS, 101/H and 129. [provided by MGI curators]
Allele List at MGI

All alleles(3) : Targeted, other(2) Gene trapped(1)

Other mutations in this stock
Total: 80 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
9130008F23Rik T C 17: 41,190,962 (GRCm39) T156A probably benign Het
9230106D20Rik A T 10: 19,536,065 (GRCm39) noncoding transcript Het
Abca3 A G 17: 24,585,171 (GRCm39) D144G probably benign Het
Anxa2 T A 9: 69,390,260 (GRCm39) L121Q probably damaging Het
Anxa7 A T 14: 20,512,732 (GRCm39) I267N probably damaging Het
Asb14 A T 14: 26,633,797 (GRCm39) D334V possibly damaging Het
Batf3 A G 1: 190,830,714 (GRCm39) N20S probably benign Het
Bub1b A G 2: 118,468,920 (GRCm39) H895R probably benign Het
C1qtnf12 G A 4: 156,050,160 (GRCm39) probably null Het
Cars1 T C 7: 143,130,385 (GRCm39) I294V probably damaging Het
Ccdc142 G A 6: 83,084,462 (GRCm39) A527T probably damaging Het
Ccdc168 A T 1: 44,096,234 (GRCm39) N1621K possibly damaging Het
Ccdc92 T C 5: 124,913,242 (GRCm39) N96D probably benign Het
Ceacam18 T A 7: 43,288,880 (GRCm39) D210E probably benign Het
Cenpe A G 3: 134,952,257 (GRCm39) T1373A probably damaging Het
Cfap161 T G 7: 83,440,932 (GRCm39) probably null Het
Cimip4 T C 15: 78,270,588 (GRCm39) Y60C possibly damaging Het
Cldn19 A G 4: 119,112,990 (GRCm39) D74G probably benign Het
Clec12a A G 6: 129,330,762 (GRCm39) T115A probably damaging Het
Cox7a2l T A 17: 83,811,397 (GRCm39) Q78L probably benign Het
Crot T C 5: 9,019,080 (GRCm39) N491S probably benign Het
Cspg4b T A 13: 113,505,342 (GRCm39) L2157Q probably damaging Het
Ctr9 A G 7: 110,643,165 (GRCm39) probably null Het
Cyp4f14 T G 17: 33,130,209 (GRCm39) D190A probably damaging Het
D630039A03Rik C T 4: 57,910,240 (GRCm39) V191I probably benign Het
Dnah10 A T 5: 124,838,343 (GRCm39) N1124I probably benign Het
Duox1 T A 2: 122,177,861 (GRCm39) Y1548* probably null Het
Epdr1 G A 13: 19,778,773 (GRCm39) Q6* probably null Het
Erbin A G 13: 103,996,577 (GRCm39) probably null Het
Ero1a A T 14: 45,525,217 (GRCm39) I436K probably damaging Het
Exph5 A T 9: 53,287,941 (GRCm39) Q1674L possibly damaging Het
Fat4 A T 3: 39,037,607 (GRCm39) Y3753F probably damaging Het
Gaa T C 11: 119,174,098 (GRCm39) V763A probably damaging Het
Golim4 G A 3: 75,809,745 (GRCm39) T216I probably damaging Het
Gpr83 G T 9: 14,779,629 (GRCm39) C269F possibly damaging Het
Gtf2f2 A G 14: 76,245,143 (GRCm39) probably null Het
Gtf3c5 T C 2: 28,469,694 (GRCm39) Y70C probably damaging Het
Hecw2 T C 1: 53,965,182 (GRCm39) D548G probably benign Het
Hr G A 14: 70,809,477 (GRCm39) probably null Het
Hrg A C 16: 22,774,853 (GRCm39) E161A probably damaging Het
Hydin A T 8: 111,237,526 (GRCm39) N1933I probably benign Het
Itpr2 A G 6: 146,229,830 (GRCm39) L1255P probably damaging Het
Kcnma1 C A 14: 23,380,997 (GRCm39) D903Y probably damaging Het
Kif5c T C 2: 49,570,252 (GRCm39) probably null Het
Mgat5b C A 11: 116,868,614 (GRCm39) H512Q probably damaging Het
Mtmr4 T C 11: 87,502,943 (GRCm39) V999A probably benign Het
Mttp G T 3: 137,813,041 (GRCm39) Q545K probably damaging Het
Ncstn CAGCTCCACGAAG CAG 1: 171,899,038 (GRCm39) probably null Het
Nexn A G 3: 151,948,405 (GRCm39) I386T probably damaging Het
Nrip3 A G 7: 109,365,763 (GRCm39) S85P probably benign Het
Nxpe2 T C 9: 48,237,914 (GRCm39) T114A probably damaging Het
Olr1 T C 6: 129,465,895 (GRCm39) N37S possibly damaging Het
Or14j5 C T 17: 38,161,966 (GRCm39) A161V probably benign Het
Or4b1d A G 2: 89,968,931 (GRCm39) L184S probably damaging Het
Or4c105 A T 2: 88,648,402 (GRCm39) I296F probably benign Het
Or55b3 A G 7: 102,126,720 (GRCm39) L119P probably damaging Het
Or5p80 G T 7: 108,229,855 (GRCm39) V219F possibly damaging Het
Pax4 T C 6: 28,443,446 (GRCm39) Y290C probably benign Het
Pcdhb2 T A 18: 37,429,038 (GRCm39) V337D probably damaging Het
Pglyrp4 T C 3: 90,640,310 (GRCm39) Y187H probably damaging Het
Pi4ka A G 16: 17,098,614 (GRCm39) M2017T probably benign Het
Pkdrej T C 15: 85,703,483 (GRCm39) T818A possibly damaging Het
Pxk C T 14: 8,151,507 (GRCm38) R441* probably null Het
Pygm T C 19: 6,447,637 (GRCm39) I648T possibly damaging Het
Rab4a A T 8: 124,550,565 (GRCm39) K15I probably damaging Het
Rasa3 T C 8: 13,635,035 (GRCm39) E428G probably benign Het
Rnf182 G A 13: 43,822,010 (GRCm39) W187* probably null Het
Rpl3 C T 15: 79,964,591 (GRCm39) V222M possibly damaging Het
Rtl9 C T X: 141,886,011 (GRCm39) S1141F possibly damaging Het
S100a11 A T 3: 93,433,428 (GRCm39) I91F probably benign Het
Sfswap C T 5: 129,590,148 (GRCm39) T215I probably damaging Het
Slit2 A G 5: 48,461,372 (GRCm39) D1456G probably damaging Het
Tex19.2 C T 11: 121,008,317 (GRCm39) V44I probably benign Het
Tmem127 G A 2: 127,098,094 (GRCm39) probably null Het
Tpd52 G T 3: 9,012,579 (GRCm39) N59K probably damaging Het
Trpc3 G A 3: 36,692,695 (GRCm39) P766S possibly damaging Het
Usp17la T A 7: 104,510,331 (GRCm39) V312D probably damaging Het
Xirp2 A G 2: 67,345,582 (GRCm39) N2608D possibly damaging Het
Zfp764l1 T A 7: 126,991,081 (GRCm39) H302L probably damaging Het
Zscan25 C A 5: 145,227,858 (GRCm39) H507Q possibly damaging Het
Other mutations in Hao1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00465:Hao1 APN 2 134,396,190 (GRCm39) missense probably damaging 0.99
IGL00886:Hao1 APN 2 134,365,079 (GRCm39) missense probably benign 0.00
IGL00954:Hao1 APN 2 134,340,181 (GRCm39) missense possibly damaging 0.87
IGL01472:Hao1 APN 2 134,396,150 (GRCm39) missense probably benign 0.04
IGL01570:Hao1 APN 2 134,396,120 (GRCm39) missense probably damaging 0.97
3-1:Hao1 UTSW 2 134,342,916 (GRCm39) critical splice donor site probably null
R0928:Hao1 UTSW 2 134,347,536 (GRCm39) missense possibly damaging 0.54
R0948:Hao1 UTSW 2 134,372,693 (GRCm39) missense probably damaging 1.00
R1204:Hao1 UTSW 2 134,364,947 (GRCm39) nonsense probably null
R1748:Hao1 UTSW 2 134,340,238 (GRCm39) missense possibly damaging 0.67
R1827:Hao1 UTSW 2 134,372,584 (GRCm39) missense probably benign 0.09
R1917:Hao1 UTSW 2 134,364,980 (GRCm39) missense probably benign 0.02
R2054:Hao1 UTSW 2 134,340,178 (GRCm39) synonymous silent
R2070:Hao1 UTSW 2 134,372,535 (GRCm39) missense probably damaging 1.00
R3831:Hao1 UTSW 2 134,364,925 (GRCm39) missense probably damaging 1.00
R3833:Hao1 UTSW 2 134,364,925 (GRCm39) missense probably damaging 1.00
R3960:Hao1 UTSW 2 134,364,903 (GRCm39) critical splice donor site probably null
R4509:Hao1 UTSW 2 134,364,964 (GRCm39) missense probably damaging 0.99
R4635:Hao1 UTSW 2 134,365,072 (GRCm39) missense probably damaging 1.00
R4662:Hao1 UTSW 2 134,364,947 (GRCm39) nonsense probably null
R4716:Hao1 UTSW 2 134,347,540 (GRCm39) missense probably damaging 1.00
R6161:Hao1 UTSW 2 134,347,545 (GRCm39) missense probably benign 0.06
R6374:Hao1 UTSW 2 134,365,024 (GRCm39) missense probably benign 0.14
R6799:Hao1 UTSW 2 134,372,685 (GRCm39) missense probably damaging 1.00
R6876:Hao1 UTSW 2 134,343,069 (GRCm39) missense probably benign 0.00
R7305:Hao1 UTSW 2 134,390,121 (GRCm39) missense probably benign 0.00
R7554:Hao1 UTSW 2 134,372,538 (GRCm39) missense possibly damaging 0.78
R7585:Hao1 UTSW 2 134,343,076 (GRCm39) missense probably damaging 1.00
R7920:Hao1 UTSW 2 134,390,172 (GRCm39) missense probably damaging 1.00
R8528:Hao1 UTSW 2 134,364,913 (GRCm39) missense probably damaging 1.00
R9426:Hao1 UTSW 2 134,347,555 (GRCm39) missense probably benign 0.00
R9475:Hao1 UTSW 2 134,390,181 (GRCm39) missense probably benign 0.00
R9479:Hao1 UTSW 2 134,396,204 (GRCm39) missense probably benign 0.00
R9792:Hao1 UTSW 2 134,372,552 (GRCm39) missense possibly damaging 0.70
R9793:Hao1 UTSW 2 134,372,552 (GRCm39) missense possibly damaging 0.70
R9795:Hao1 UTSW 2 134,372,552 (GRCm39) missense possibly damaging 0.70
Predicted Primers PCR Primer
(F):5'- AACAGATTCTGGAAGTGGCCC -3'
(R):5'- CCCTTGAATGAAACACTAGTCTTAGG -3'

Sequencing Primer
(F):5'- TTCTGGAAGTGGCCCATGAAAG -3'
(R):5'- AGGAGGGACTGTGCTAGGTCTAC -3'
Posted On 2014-06-23