Incidental Mutation 'R1270:C4a'
ID 151292
Institutional Source Beutler Lab
Gene Symbol C4a
Ensembl Gene ENSMUSG00000015451
Gene Name complement C4A (Rodgers blood group)
Synonyms Slp
MMRRC Submission 039336-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.142) question?
Stock # R1270 (G1)
Quality Score 193
Status Validated
Chromosome 17
Chromosomal Location 35028069-35042436 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) A to G at 35033505 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000015595
Predicted Effect noncoding transcript
Transcript: ENSMUST00000159539
Predicted Effect noncoding transcript
Transcript: ENSMUST00000159669
Predicted Effect noncoding transcript
Transcript: ENSMUST00000160309
Predicted Effect noncoding transcript
Transcript: ENSMUST00000160528
Predicted Effect noncoding transcript
Transcript: ENSMUST00000160657
Predicted Effect noncoding transcript
Transcript: ENSMUST00000160679
Predicted Effect noncoding transcript
Transcript: ENSMUST00000161121
Predicted Effect noncoding transcript
Transcript: ENSMUST00000161797
Predicted Effect noncoding transcript
Transcript: ENSMUST00000162133
Meta Mutation Damage Score 0.0869 question?
Coding Region Coverage
  • 1x: 98.9%
  • 3x: 98.1%
  • 10x: 95.5%
  • 20x: 89.7%
Validation Efficiency 97% (36/37)
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcc3 C T 11: 94,248,210 (GRCm39) R1129Q probably damaging Het
Adam7 T A 14: 68,765,118 (GRCm39) K93M probably damaging Het
Aldh1a2 T G 9: 71,188,988 (GRCm39) L301V probably benign Het
Alg9 A G 9: 50,698,872 (GRCm39) probably benign Het
Aspg C T 12: 112,082,881 (GRCm39) T187I probably damaging Het
Bltp1 T A 3: 37,006,333 (GRCm39) H1662Q probably damaging Het
Cdh2 T G 18: 16,760,614 (GRCm39) probably benign Het
Ceacam1 T C 7: 25,165,739 (GRCm39) probably null Het
Cep250 G A 2: 155,832,601 (GRCm39) V1509I probably benign Het
D130043K22Rik T C 13: 25,041,321 (GRCm39) S248P probably benign Het
Dgkd A T 1: 87,861,847 (GRCm39) M801L probably damaging Het
Edc4 A G 8: 106,617,896 (GRCm39) E1152G possibly damaging Het
Enkd1 A G 8: 106,430,533 (GRCm39) I334T probably damaging Het
Gli3 C T 13: 15,898,329 (GRCm39) A803V probably benign Het
Glrx3 A G 7: 137,055,143 (GRCm39) N95S probably benign Het
Ints2 C T 11: 86,123,911 (GRCm39) G626R probably damaging Het
Kank2 A T 9: 21,684,056 (GRCm39) N724K probably damaging Het
Kctd20 A G 17: 29,185,905 (GRCm39) D416G possibly damaging Het
Lmtk3 A G 7: 45,443,252 (GRCm39) E645G probably damaging Het
Mrgpra9 A T 7: 46,902,531 (GRCm39) probably null Het
Muc1 T A 3: 89,139,414 (GRCm39) Y605N probably damaging Het
Or4a47 C T 2: 89,665,666 (GRCm39) V208M possibly damaging Het
Or8g17 A C 9: 38,930,543 (GRCm39) I98R possibly damaging Het
Prx T A 7: 27,218,355 (GRCm39) I952N probably damaging Het
Shf G A 2: 122,199,163 (GRCm39) P51S probably damaging Het
Skint5 A T 4: 113,799,856 (GRCm39) Y90* probably null Het
Swt1 A T 1: 151,260,142 (GRCm39) N752K probably benign Het
Taar1 T C 10: 23,796,431 (GRCm39) V43A probably damaging Het
Tenm2 T C 11: 35,932,486 (GRCm39) N1702D probably damaging Het
Tff2 C T 17: 31,363,143 (GRCm39) probably null Het
Trim2 G A 3: 84,074,984 (GRCm39) A686V probably damaging Het
Ube2q2l A T 6: 136,378,785 (GRCm39) I15N probably damaging Het
Other mutations in C4a
AlleleSourceChrCoordTypePredicted EffectPPH Score
R4366:C4a UTSW 17 35,033,885 (GRCm39) unclassified noncoding transcript
R4652:C4a UTSW 17 35,029,108 (GRCm39) exon noncoding transcript
R4681:C4a UTSW 17 35,036,075 (GRCm39) unclassified noncoding transcript
R4818:C4a UTSW 17 35,035,975 (GRCm39) unclassified noncoding transcript
Predicted Primers PCR Primer
(F):5'- AAGAACAGAGCACGGCTTCCTTAC -3'
(R):5'- AGCATTTTCTCCAGCCAAGCCC -3'

Sequencing Primer
(F):5'- ACGGCTTCCTTACCACTCTG -3'
(R):5'- CCCTCCGCTCTAGGCTG -3'
Posted On 2014-01-29