Incidental Mutation 'R6264:H2-Aa'
ID 506914
Institutional Source Beutler Lab
Gene Symbol H2-Aa
Ensembl Gene ENSMUSG00000036594
Gene Name histocompatibility 2, class II antigen A, alpha
Synonyms Ia1, I-Aalpha, H-2Aa, A alpha, Aalpha, Ia-1
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R6264 (G1)
Quality Score 225.009
Status Not validated
Chromosome 17
Chromosomal Location 34501718-34506797 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 34502172 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Proline at position 250 (S250P)
Ref Sequence ENSEMBL: ENSMUSP00000046105 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000040655] [ENSMUST00000174751]
AlphaFold no structure available at present
PDB Structure CRYSTAL STRUCTURE OF CLASS II MHC MOLECULE IAb BOUND TO EALPHA3K PEPTIDE [X-RAY DIFFRACTION]
Crystal structure of murine class II MHC I-Ab in complex with a human CLIP peptide [X-RAY DIFFRACTION]
Crystal structure of mouse MHC class II I-Ab/3K peptide complexed with mouse TCR B3K506 [X-RAY DIFFRACTION]
Crystal structure of mouse MHC class II I-Ab/3K peptide complexed with mouse TCR YAe62 [X-RAY DIFFRACTION]
Crystal structure of mouse MHC class II I-Ab/3K peptide complexed with mouse TCR 2W20 [X-RAY DIFFRACTION]
Crystal Structure of 809.B5 TCR complexed with MHC Class II I-Ab/3k peptide [X-RAY DIFFRACTION]
J809.B5 TCR bound to IAb/3K [X-RAY DIFFRACTION]
J809.B5 Y31A TCR bound to IAb3K [X-RAY DIFFRACTION]
14.C6 TCR complexed with MHC class II I-Ab/3K peptide [X-RAY DIFFRACTION]
Predicted Effect probably damaging
Transcript: ENSMUST00000040655
AA Change: S250P

PolyPhen 2 Score 0.975 (Sensitivity: 0.76; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000046105
Gene: ENSMUSG00000036594
AA Change: S250P

DomainStartEndE-ValueType
MHC_II_alpha 31 111 1.83e-45 SMART
IGc1 129 200 2.51e-27 SMART
Pfam:C1-set_C 203 255 2.1e-30 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000165139
Predicted Effect noncoding transcript
Transcript: ENSMUST00000173944
Predicted Effect probably benign
Transcript: ENSMUST00000174751
AA Change: S167P

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)
SMART Domains Protein: ENSMUSP00000133399
Gene: ENSMUSG00000036594
AA Change: S167P

DomainStartEndE-ValueType
signal peptide 1 23 N/A INTRINSIC
IGc1 46 117 2.51e-27 SMART
low complexity region 141 158 N/A INTRINSIC
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.7%
  • 10x: 98.5%
  • 20x: 96.1%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] HLA-DQA1 belongs to the HLA class II alpha chain paralogues. The class II molecule is a heterodimer consisting of an alpha (DQA) and a beta chain (DQB), both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells (APC: B Lymphocytes, dendritic cells, macrophages). The alpha chain is approximately 33-35 kDa. It is encoded by 5 exons; exon 1 encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, and exon 4 encodes the transmembrane domain and the cytoplasmic tail. Within the DQ molecule both the alpha chain and the beta chain contain the polymorphisms specifying the peptide binding specificities, resulting in up to four different molecules. Typing for these polymorphisms is routinely done for bone marrow transplantation. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a knock-out allele lack cell surface expression of MHC class II molecules on macrophages and show decreased CD4-positive T cell number, increased CD8-positive T cell number, thymus hyperplasia, enlarged lymph nodes, and altered splenocyte response to staphylococcal enterotoxin B. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 60 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcc3 A G 11: 94,264,824 (GRCm39) Y175H probably damaging Het
Agtpbp1 A T 13: 59,598,114 (GRCm39) V1165D possibly damaging Het
Ahsg A G 16: 22,717,611 (GRCm39) D224G probably benign Het
Akap11 T C 14: 78,749,861 (GRCm39) D842G possibly damaging Het
Anln T C 9: 22,245,413 (GRCm39) N186D possibly damaging Het
Aqr A G 2: 113,940,445 (GRCm39) Y1234H probably damaging Het
Ccdc162 A G 10: 41,570,464 (GRCm39) F7S probably benign Het
Cltc T C 11: 86,596,084 (GRCm39) Y1222C probably damaging Het
Coro2a C T 4: 46,562,912 (GRCm39) V81I probably damaging Het
Cpa5 T C 6: 30,613,984 (GRCm39) V42A probably damaging Het
D2hgdh A G 1: 93,754,177 (GRCm39) Y50C probably damaging Het
Ddx6 A G 9: 44,540,049 (GRCm39) N326D probably damaging Het
Dedd2 A G 7: 24,903,215 (GRCm39) L248P possibly damaging Het
Frem3 T A 8: 81,341,832 (GRCm39) I1375N probably damaging Het
Gm12185 T C 11: 48,807,002 (GRCm39) N63S probably benign Het
Hbs1l T C 10: 21,243,656 (GRCm39) S667P possibly damaging Het
Hc T A 2: 34,896,285 (GRCm39) probably null Het
Hoxd4 A T 2: 74,557,729 (GRCm39) Y36F possibly damaging Het
Ifi207 A G 1: 173,555,111 (GRCm39) V864A probably damaging Het
Igsf10 T A 3: 59,235,928 (GRCm39) T1418S possibly damaging Het
Klhl41 T C 2: 69,510,176 (GRCm39) probably null Het
Lman2l T C 1: 36,477,850 (GRCm39) N162S probably damaging Het
Lrr1 T G 12: 69,215,655 (GRCm39) V9G probably damaging Het
Marchf5 T C 19: 37,198,140 (GRCm39) I127T probably damaging Het
Med12l T C 3: 59,163,423 (GRCm39) L1350P probably damaging Het
Mmp25 G A 17: 23,849,768 (GRCm39) A541V possibly damaging Het
Myh10 T A 11: 68,636,241 (GRCm39) I210N probably benign Het
Myo5c A G 9: 75,182,836 (GRCm39) N825S probably benign Het
Nav3 T C 10: 109,524,694 (GRCm39) T2312A probably damaging Het
Ndrg4 G T 8: 96,436,396 (GRCm39) R208L probably damaging Het
Nell2 G A 15: 95,244,706 (GRCm39) P464S probably damaging Het
Nrxn3 T A 12: 90,299,011 (GRCm39) Y374N probably damaging Het
Oprd1 A C 4: 131,841,365 (GRCm39) C198G possibly damaging Het
Pik3ca T C 3: 32,494,863 (GRCm39) probably null Het
Plin4 T G 17: 56,411,787 (GRCm39) D748A possibly damaging Het
Pramel23 T G 4: 143,425,722 (GRCm39) T74P possibly damaging Het
Prkg2 T G 5: 99,082,223 (GRCm39) K52Q probably benign Het
Ptprk A T 10: 28,442,669 (GRCm39) E890D probably damaging Het
Rab27b T C 18: 70,122,659 (GRCm39) D100G probably damaging Het
Ranbp6 T C 19: 29,790,026 (GRCm39) T109A probably benign Het
Rarb T A 14: 16,818,819 (GRCm38) M17L probably benign Het
Rasgrf2 T C 13: 92,167,293 (GRCm39) H260R probably damaging Het
Rec8 T A 14: 55,856,636 (GRCm39) D109E probably damaging Het
Scd4 C A 19: 44,327,398 (GRCm39) S158* probably null Het
Scn7a T A 2: 66,505,870 (GRCm39) E1673V possibly damaging Het
Sit1 A T 4: 43,482,651 (GRCm39) D169E possibly damaging Het
Slc16a14 G T 1: 84,885,130 (GRCm39) Q470K probably benign Het
Slc43a2 T A 11: 75,457,900 (GRCm39) C392S possibly damaging Het
Smg1 A G 7: 117,765,310 (GRCm39) probably benign Het
Sstr2 A T 11: 113,515,932 (GRCm39) I284F probably damaging Het
Tep1 C T 14: 51,082,970 (GRCm39) V1013M probably damaging Het
Tmem120b T G 5: 123,253,763 (GRCm39) L232R probably damaging Het
Tmem9b C A 7: 109,344,612 (GRCm39) V75F probably damaging Het
Trappc3 A G 4: 126,167,731 (GRCm39) S97G probably damaging Het
Ube3c T C 5: 29,795,829 (GRCm39) F73L probably damaging Het
Vmn1r127 C A 7: 21,052,930 (GRCm39) C286F probably benign Het
Vmn1r44 T C 6: 89,870,652 (GRCm39) S133P probably benign Het
Vps8 C T 16: 21,378,099 (GRCm39) Q635* probably null Het
Vwa8 A G 14: 79,324,252 (GRCm39) E1185G possibly damaging Het
Zfp354c G A 11: 50,706,274 (GRCm39) T267I probably benign Het
Other mutations in H2-Aa
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00089:H2-Aa APN 17 34,503,504 (GRCm39) missense probably damaging 1.00
citation UTSW 17 34,506,651 (GRCm39) splice site probably null
reference UTSW 17 34,502,794 (GRCm39) missense probably damaging 1.00
G1citation:H2-Aa UTSW 17 34,506,651 (GRCm39) splice site probably null
R1556:H2-Aa UTSW 17 34,503,390 (GRCm39) missense possibly damaging 0.94
R1901:H2-Aa UTSW 17 34,502,207 (GRCm39) missense possibly damaging 0.65
R2144:H2-Aa UTSW 17 34,502,801 (GRCm39) missense probably damaging 1.00
R4816:H2-Aa UTSW 17 34,502,794 (GRCm39) missense probably damaging 1.00
R5607:H2-Aa UTSW 17 34,502,816 (GRCm39) missense possibly damaging 0.89
R5608:H2-Aa UTSW 17 34,502,816 (GRCm39) missense possibly damaging 0.89
R6822:H2-Aa UTSW 17 34,506,651 (GRCm39) splice site probably null
R6917:H2-Aa UTSW 17 34,502,681 (GRCm39) missense probably damaging 1.00
R7052:H2-Aa UTSW 17 34,503,484 (GRCm39) missense possibly damaging 0.50
R7116:H2-Aa UTSW 17 34,502,601 (GRCm39) nonsense probably null
R8168:H2-Aa UTSW 17 34,506,695 (GRCm39) missense possibly damaging 0.83
R8257:H2-Aa UTSW 17 34,502,211 (GRCm39) missense probably damaging 0.97
R8264:H2-Aa UTSW 17 34,506,709 (GRCm39) missense probably benign 0.18
R8682:H2-Aa UTSW 17 34,502,734 (GRCm39) missense possibly damaging 0.75
R9667:H2-Aa UTSW 17 34,502,295 (GRCm39) missense probably benign
X0063:H2-Aa UTSW 17 34,506,785 (GRCm39) unclassified probably benign
Predicted Primers PCR Primer
(F):5'- AACACACTGTGCCAGGTCAC -3'
(R):5'- ACATGAACATACTCCCTTCTGACTC -3'

Sequencing Primer
(F):5'- CTGAAGAGGGACACACGCCTG -3'
(R):5'- CTAAAACTTCTCTTTCTCAGAACCTG -3'
Posted On 2018-03-15