Incidental Mutation 'R8295:H2-Ab1'
ID 638907
Institutional Source Beutler Lab
Gene Symbol H2-Ab1
Ensembl Gene ENSMUSG00000073421
Gene Name histocompatibility 2, class II antigen A, beta 1
Synonyms H-2Ab, Ia2, H2-Ab, IAb, Ia-2, Abeta, I-Abeta, A beta, Rmcs1, I-A
MMRRC Submission 067714-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R8295 (G1)
Quality Score 225.009
Status Not validated
Chromosome 17
Chromosomal Location 34482201-34488392 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 34483816 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Phenylalanine at position 59 (Y59F)
Ref Sequence ENSEMBL: ENSMUSP00000041008 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000040828]
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: ENSMUST00000040828
AA Change: Y59F

PolyPhen 2 Score 0.994 (Sensitivity: 0.69; Specificity: 0.97)
SMART Domains Protein: ENSMUSP00000041008
Gene: ENSMUSG00000073421
AA Change: Y59F

DomainStartEndE-ValueType
low complexity region 7 22 N/A INTRINSIC
MHC_II_beta 40 114 1.53e-47 SMART
IGc1 140 211 8.47e-34 SMART
transmembrane domain 228 247 N/A INTRINSIC
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 99.1%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] HLA-DQB1 belongs to the HLA class II beta chain paralogs. This 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 beta chain is approximately 26-28 kDa and it contains six exons. Exon 1 encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and exon 5 encodes 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. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2011]
PHENOTYPE: Homozygotes for targeted null mutations exhibit depletion of mature CD4+ T cells, deficiency in cell-mediated immune responses, and increased susceptibility to viral infections. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 34 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca15 T G 7: 119,974,188 (GRCm39) I915S probably benign Het
Abcf2 CAT CATAAT 5: 24,781,589 (GRCm39) probably benign Het
Ahdc1 T A 4: 132,788,762 (GRCm39) M1K probably null Het
Akr1c12 T G 13: 4,322,355 (GRCm39) D229A probably benign Het
Ankfn1 C T 11: 89,302,923 (GRCm39) V32M probably benign Het
C7 A T 15: 5,018,327 (GRCm39) C839S probably damaging Het
Card6 TTGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGCGGATGAGAGGGCTTAGCATGGGAGGACTG TTGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGCGGATGAGAGGGCTTAGCATGGGAGGACTG 15: 5,128,173 (GRCm39) probably benign Het
Ccdc110 A G 8: 46,396,416 (GRCm39) D769G probably damaging Het
Clk2 G T 3: 89,080,766 (GRCm39) D251Y probably damaging Het
Dlx1 C A 2: 71,362,726 (GRCm39) P211Q probably benign Het
Dock8 G A 19: 25,100,600 (GRCm39) A703T probably benign Het
Eif2d T A 1: 131,085,988 (GRCm39) L161Q probably benign Het
Epha8 G T 4: 136,665,897 (GRCm39) L420M probably damaging Het
Fndc3a T C 14: 72,789,959 (GRCm39) I1079V probably benign Het
Gm21886 ACTCACTGAGGCCTGCAGACAGTAGGTGCTCACTGAGGCCTGCAGACAGTAGGTGCTCACTGAGGCCTGCAGACAGTAGGTGCTCACTGAGACCTGCAGACAGTAGGTGCTCACTGAGACCTGCAGACAGTAGGTGCTCACTGAGG ACTCACTGAGGCCTGCAGACAGTAGGTGCTCACTGAGGCCTGCAGACAGTAGGTGCTCACTGAGACCTGCAGACAGTAGGTGCTCACTGAGACCTGCAGACAGTAGGTGCTCACTGAGG 18: 80,133,040 (GRCm39) probably benign Het
Gtf3c1 A G 7: 125,262,234 (GRCm39) V1104A probably benign Het
Ints2 T C 11: 86,115,914 (GRCm39) T772A probably damaging Het
Kcnh4 A G 11: 100,640,523 (GRCm39) V501A probably benign Het
Ltbp1 A T 17: 75,486,184 (GRCm39) T70S probably benign Het
Obox2 A G 7: 15,131,247 (GRCm39) T118A probably benign Het
Or52ab4 C T 7: 102,987,474 (GRCm39) T71I probably benign Het
Or8k17 T C 2: 86,066,916 (GRCm39) M88V probably benign Het
Pih1d2 C T 9: 50,532,379 (GRCm39) H146Y probably damaging Het
Pou2af1 C T 9: 51,144,305 (GRCm39) S73F possibly damaging Het
Rnase2a T A 14: 51,493,096 (GRCm39) I90L probably benign Het
S100a16 T A 3: 90,449,336 (GRCm39) C4S probably benign Het
Sprr1a T C 3: 92,391,849 (GRCm39) K51E possibly damaging Het
Tmem168 A T 6: 13,602,850 (GRCm39) M172K probably damaging Het
Tnrc6b T C 15: 80,797,565 (GRCm39) S1371P probably damaging Het
Trav21-dv12 T A 14: 54,113,510 (GRCm39) L13* probably null Het
Vmn1r234 T A 17: 21,449,101 (GRCm39) V5D probably benign Het
Vmn2r18 A G 5: 151,508,621 (GRCm39) C168R probably damaging Het
Vmn2r90 C T 17: 17,948,358 (GRCm39) P535S probably benign Het
Zfp595 A G 13: 67,464,764 (GRCm39) C503R possibly damaging Het
Other mutations in H2-Ab1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00418:H2-Ab1 APN 17 34,486,549 (GRCm39) missense probably damaging 1.00
IGL01941:H2-Ab1 APN 17 34,486,408 (GRCm39) nonsense probably null
IGL02826:H2-Ab1 APN 17 34,483,885 (GRCm39) missense probably damaging 0.98
R0479:H2-Ab1 UTSW 17 34,483,942 (GRCm39) missense possibly damaging 0.68
R0815:H2-Ab1 UTSW 17 34,486,328 (GRCm39) missense probably damaging 0.99
R0863:H2-Ab1 UTSW 17 34,486,328 (GRCm39) missense probably damaging 0.99
R1796:H2-Ab1 UTSW 17 34,486,346 (GRCm39) missense probably damaging 0.99
R2875:H2-Ab1 UTSW 17 34,482,286 (GRCm39) start codon destroyed probably benign 0.21
R4042:H2-Ab1 UTSW 17 34,483,834 (GRCm39) missense probably benign
R4687:H2-Ab1 UTSW 17 34,483,783 (GRCm39) missense probably damaging 0.99
R4761:H2-Ab1 UTSW 17 34,486,474 (GRCm39) missense probably damaging 0.98
R4787:H2-Ab1 UTSW 17 34,486,441 (GRCm39) missense possibly damaging 0.92
R5111:H2-Ab1 UTSW 17 34,486,456 (GRCm39) missense probably damaging 0.96
R5155:H2-Ab1 UTSW 17 34,486,358 (GRCm39) missense possibly damaging 0.89
R5194:H2-Ab1 UTSW 17 34,488,352 (GRCm39) utr 3 prime probably benign
R6869:H2-Ab1 UTSW 17 34,486,537 (GRCm39) missense probably damaging 1.00
R7037:H2-Ab1 UTSW 17 34,486,963 (GRCm39) missense probably damaging 0.99
R7054:H2-Ab1 UTSW 17 34,482,316 (GRCm39) missense probably benign 0.41
R7250:H2-Ab1 UTSW 17 34,486,481 (GRCm39) missense probably damaging 1.00
R9205:H2-Ab1 UTSW 17 34,483,981 (GRCm39) missense probably damaging 1.00
R9253:H2-Ab1 UTSW 17 34,486,378 (GRCm39) missense probably damaging 1.00
R9321:H2-Ab1 UTSW 17 34,486,969 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TTCCTTACCCCGGGTCGAAC -3'
(R):5'- AACCGCTTCTGACAGGACC -3'

Sequencing Primer
(F):5'- GCGAAGAGACTGCCCGG -3'
(R):5'- AAGGAGGCCATGCAGCTC -3'
Posted On 2020-07-28