Incidental Mutation 'R0735:H2-Q7'
ID68255
Institutional Source Beutler Lab
Gene Symbol H2-Q7
Ensembl Gene ENSMUSG00000060550
Gene Namehistocompatibility 2, Q region locus 7
SynonymsPed, Qa7, Qa-7, H-2Q7
MMRRC Submission 038916-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.191) question?
Stock #R0735 (G1)
Quality Score157
Status Not validated
Chromosome17
Chromosomal Location35439155-35443773 bp(+) (GRCm38)
Type of Mutationcritical splice donor site (2 bp from exon)
DNA Base Change (assembly) T to G at 35440186 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000112297 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000071951] [ENSMUST00000076256] [ENSMUST00000078205] [ENSMUST00000116598]
Predicted Effect probably null
Transcript: ENSMUST00000071951
SMART Domains Protein: ENSMUSP00000071843
Gene: ENSMUSG00000060550

DomainStartEndE-ValueType
signal peptide 1 21 N/A INTRINSIC
Pfam:MHC_I 22 200 3e-97 PFAM
IGc1 219 290 7.68e-23 SMART
transmembrane domain 308 330 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000076256
SMART Domains Protein: ENSMUSP00000075606
Gene: ENSMUSG00000060550

DomainStartEndE-ValueType
signal peptide 1 21 N/A INTRINSIC
Pfam:MHC_I 22 200 3.3e-98 PFAM
IGc1 219 290 7.68e-23 SMART
low complexity region 310 325 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000078205
SMART Domains Protein: ENSMUSP00000077335
Gene: ENSMUSG00000060550

DomainStartEndE-ValueType
signal peptide 1 21 N/A INTRINSIC
Pfam:MHC_I 22 200 1.9e-97 PFAM
IGc1 219 290 7.68e-23 SMART
Predicted Effect probably null
Transcript: ENSMUST00000116598
SMART Domains Protein: ENSMUSP00000112297
Gene: ENSMUSG00000060550

DomainStartEndE-ValueType
signal peptide 1 21 N/A INTRINSIC
Pfam:MHC_I 22 200 8.5e-98 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000173016
Predicted Effect noncoding transcript
Transcript: ENSMUST00000173788
Coding Region Coverage
  • 1x: 99.5%
  • 3x: 98.7%
  • 10x: 96.7%
  • 20x: 91.8%
Validation Efficiency 95% (73/77)
MGI Phenotype PHENOTYPE: This locus controls a widely distributed lymphocyte antigen recognized by monoclonal antibody, serology or CTL assay. Using all assays, antigen is present (allele a) in C57BL/6, DBA/1, DBA/2 and SWR and absent (allele b) in AKR, C3H and BALB/c. Other strain allele typings were assay-dependent. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 69 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
9930021J03Rik A T 19: 29,717,638 I1552K possibly damaging Het
Actr8 T A 14: 29,989,712 M405K probably benign Het
Adam10 G A 9: 70,748,251 V334I possibly damaging Het
Adgra2 G T 8: 27,117,318 G686C probably damaging Het
Akap11 A T 14: 78,510,078 I1623N probably damaging Het
Astn1 A T 1: 158,472,389 T100S possibly damaging Het
B3galt1 A C 2: 68,118,579 I213L possibly damaging Het
B4galnt4 A G 7: 141,064,323 K101E probably benign Het
Camsap2 A G 1: 136,292,888 S324P probably damaging Het
Chrnb4 A G 9: 55,043,800 S60P probably damaging Het
Cpne1 A G 2: 156,078,750 probably null Het
Cubn G A 2: 13,491,689 probably benign Het
Cul7 T A 17: 46,663,190 L1467H probably damaging Het
Cxcl15 T C 5: 90,801,294 M106T probably benign Het
Cyp2c23 A T 19: 44,016,810 M140K probably damaging Het
Dgke A G 11: 89,060,075 F104S probably benign Het
Dhx36 T A 3: 62,472,729 M849L probably benign Het
Dnah7a C T 1: 53,544,511 E1522K possibly damaging Het
Edil3 G T 13: 89,177,178 V219F probably damaging Het
Egln1 A G 8: 124,948,495 V187A possibly damaging Het
Fam193a T C 5: 34,439,378 I455T possibly damaging Het
Fdft1 A T 14: 63,163,420 I88N probably damaging Het
Fem1c G A 18: 46,505,160 R592C probably benign Het
Frs2 T A 10: 117,074,582 S292C probably damaging Het
Gm15448 T C 7: 3,821,782 T533A possibly damaging Het
Gpr107 T A 2: 31,171,994 F145I probably benign Het
Gpr153 T A 4: 152,279,373 C83* probably null Het
Hsp90b1 A T 10: 86,695,748 probably benign Het
Kcnk1 C A 8: 126,025,289 N211K probably damaging Het
Klb T C 5: 65,379,727 V800A probably benign Het
Lat2 T C 5: 134,606,783 Y59C probably damaging Het
Mlkl A T 8: 111,327,801 probably benign Het
Mroh2a G A 1: 88,243,950 R770Q probably damaging Het
Mtbp T A 15: 55,562,942 C93* probably null Het
Myo7a A G 7: 98,081,180 probably benign Het
Myt1 G A 2: 181,807,387 probably benign Het
Ogfrl1 T C 1: 23,375,754 Q224R possibly damaging Het
Olfr418 A G 1: 173,271,002 T276A probably benign Het
Olfr661 A T 7: 104,688,819 H268L probably damaging Het
Osbpl2 A G 2: 180,150,290 probably benign Het
Plb1 C T 5: 32,284,920 T252M possibly damaging Het
Ptpro T A 6: 137,443,594 V1007D probably damaging Het
Rbsn T C 6: 92,189,693 T657A probably benign Het
Rims4 C T 2: 163,863,929 V262M possibly damaging Het
Rps6kb2 C A 19: 4,157,883 S348I probably benign Het
Rsrp1 C T 4: 134,924,257 R111W unknown Het
Ryr3 T C 2: 112,732,982 T2933A probably benign Het
Scara5 A G 14: 65,731,019 D247G possibly damaging Het
Slc7a11 C T 3: 50,424,096 S231N probably benign Het
Sod2 A T 17: 13,010,564 N91Y probably damaging Het
Spesp1 A T 9: 62,272,685 S314T probably benign Het
St3gal1 C A 15: 67,113,687 M39I probably benign Het
Stat6 A T 10: 127,658,241 I646F probably damaging Het
Tdrd1 A T 19: 56,865,978 K1119* probably null Het
Thbs2 A G 17: 14,679,815 I600T probably benign Het
Tor1a A G 2: 30,963,838 V160A probably damaging Het
Trdmt1 T G 2: 13,523,438 D104A probably benign Het
Trim58 T C 11: 58,651,393 V393A probably benign Het
Trip4 C T 9: 65,884,918 probably benign Het
Trip6 T C 5: 137,310,821 E341G probably benign Het
Ttn T A 2: 76,715,195 I32595F probably damaging Het
Ubr4 T A 4: 139,428,028 probably null Het
Ush2a G A 1: 188,864,693 V3877I probably benign Het
Vmn1r29 G T 6: 58,307,732 G146C probably damaging Het
Vmn2r53 A G 7: 12,581,780 V704A probably benign Het
Vmn2r7 C T 3: 64,716,367 M268I probably benign Het
Wnt7b G A 15: 85,537,495 T248M probably damaging Het
Xab2 G A 8: 3,613,649 P394S possibly damaging Het
Zfp663 A G 2: 165,359,075 V13A probably damaging Het
Other mutations in H2-Q7
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0839:H2-Q7 UTSW 17 35439712 missense probably damaging 1.00
R1737:H2-Q7 UTSW 17 35439626 missense probably damaging 1.00
R1831:H2-Q7 UTSW 17 35439699 missense probably benign 0.00
R1832:H2-Q7 UTSW 17 35439699 missense probably benign 0.00
R1833:H2-Q7 UTSW 17 35439699 missense probably benign 0.00
R2047:H2-Q7 UTSW 17 35440147 missense probably damaging 1.00
R4498:H2-Q7 UTSW 17 35439530 missense probably damaging 1.00
R4657:H2-Q7 UTSW 17 35442759 missense possibly damaging 0.86
R4784:H2-Q7 UTSW 17 35439938 missense probably damaging 1.00
R5387:H2-Q7 UTSW 17 35439542 missense probably damaging 1.00
R5499:H2-Q7 UTSW 17 35439940 nonsense probably null
R6410:H2-Q7 UTSW 17 35440176 missense probably benign 0.13
R6457:H2-Q7 UTSW 17 35439679 missense probably damaging 1.00
R6720:H2-Q7 UTSW 17 35442678 missense probably benign 0.05
R6943:H2-Q7 UTSW 17 35439584 missense probably benign 0.30
R7069:H2-Q7 UTSW 17 35440031 missense probably damaging 0.98
R7086:H2-Q7 UTSW 17 35439485 missense probably damaging 1.00
R7303:H2-Q7 UTSW 17 35440061 missense probably benign 0.13
R7520:H2-Q7 UTSW 17 35442710 missense probably benign 0.04
R7603:H2-Q7 UTSW 17 35439963 missense probably damaging 1.00
R7747:H2-Q7 UTSW 17 35440061 missense probably benign 0.13
Z1177:H2-Q7 UTSW 17 35439162 start gained probably benign
Z1177:H2-Q7 UTSW 17 35442500 missense probably damaging 0.99
Predicted Primers PCR Primer
(F):5'- CGATTACATCGCCCTGAACGAAGAC -3'
(R):5'- ACACACTCAGCAGGATAGCAGTGG -3'

Sequencing Primer
(F):5'- CCTGAAAACGTGGACGGC -3'
(R):5'- ATGGCTGACAGATGCTGC -3'
Posted On2013-09-03