Incidental Mutation 'R3794:Ceacam13'
ID 272686
Institutional Source Beutler Lab
Gene Symbol Ceacam13
Ensembl Gene ENSMUSG00000057195
Gene Name CEA cell adhesion molecule 13
Synonyms Ceacam13-C2, Ceacam13-C1, 1600025J19Rik, 1600012K03Rik
MMRRC Submission 040756-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.051) question?
Stock # R3794 (G1)
Quality Score 225
Status Validated
Chromosome 7
Chromosomal Location 17743814-17753145 bp(+) (GRCm39)
Type of Mutation makesense
DNA Base Change (assembly) A to G at 17747340 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Stop codon to Tryptophan at position 264 (*264W)
Ref Sequence ENSEMBL: ENSMUSP00000080404 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000081703] [ENSMUST00000108488]
AlphaFold Q9DAT7
Predicted Effect probably null
Transcript: ENSMUST00000081703
AA Change: *264W
SMART Domains Protein: ENSMUSP00000080404
Gene: ENSMUSG00000057195
AA Change: *264W

DomainStartEndE-ValueType
IG_like 40 143 1.37e1 SMART
IG_like 158 261 8.97e0 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000108488
SMART Domains Protein: ENSMUSP00000104128
Gene: ENSMUSG00000057195

DomainStartEndE-ValueType
IG_like 40 143 1.37e1 SMART
IG_like 158 261 8.97e0 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000175466
Meta Mutation Damage Score 0.9755 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.7%
  • 10x: 97.4%
  • 20x: 95.4%
Validation Efficiency 97% (37/38)
Allele List at MGI
Other mutations in this stock
Total: 34 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adcy6 C T 15: 98,496,824 (GRCm39) V482I probably damaging Het
Adgrv1 T A 13: 81,431,486 (GRCm39) M1L probably damaging Het
Dennd5b A T 6: 149,002,715 (GRCm39) D31E possibly damaging Het
Dip2c T C 13: 9,654,597 (GRCm39) V706A probably damaging Het
Enpp3 T C 10: 24,707,630 (GRCm39) probably null Het
Exoc4 T G 6: 33,452,932 (GRCm39) V474G probably benign Het
F2rl1 A G 13: 95,649,719 (GRCm39) Y388H unknown Het
Fasl T C 1: 161,609,306 (GRCm39) R17G probably benign Het
Htr1a G A 13: 105,580,852 (GRCm39) V31M possibly damaging Het
Inpp4b T C 8: 82,759,845 (GRCm39) V445A probably damaging Het
Itih3 T C 14: 30,640,351 (GRCm39) Y319C probably damaging Het
Katnip A G 7: 125,419,261 (GRCm39) N476S probably benign Het
Kmt2d T C 15: 98,735,240 (GRCm39) probably benign Het
Mobp A T 9: 119,997,033 (GRCm39) K55* probably null Het
Ndufaf5 T A 2: 140,044,843 (GRCm39) M279K possibly damaging Het
Nlrc3 T C 16: 3,765,739 (GRCm39) I1057V probably benign Het
Or10al7 A G 17: 38,365,786 (GRCm39) Y224H probably damaging Het
Or4c112 G T 2: 88,853,770 (GRCm39) H192Q probably benign Het
Piezo2 C T 18: 63,214,864 (GRCm39) R1257Q probably damaging Het
Pigv A G 4: 133,392,502 (GRCm39) S223P possibly damaging Het
Pkdcc A G 17: 83,531,382 (GRCm39) T464A probably damaging Het
Polr2k A G 15: 36,175,193 (GRCm39) I18V probably damaging Het
Pon3 A G 6: 5,221,578 (GRCm39) Y351H probably benign Het
Rsf1 ATGGCG ATGGCGACGGTGGCG 7: 97,229,111 (GRCm39) probably benign Het
Scaf8 A G 17: 3,240,524 (GRCm39) E632G probably damaging Het
Smurf1 A G 5: 144,837,985 (GRCm39) probably null Het
Tex16 T G X: 111,150,375 (GRCm39) M1R probably null Het
Tln1 G T 4: 43,536,295 (GRCm39) A1999D probably damaging Het
Trgv5 A T 13: 19,376,694 (GRCm39) H47L probably benign Het
Ttn C T 2: 76,772,781 (GRCm39) V2405I possibly damaging Het
Vps13d G A 4: 144,812,007 (GRCm39) probably benign Het
Xrcc1 A G 7: 24,269,985 (GRCm39) T469A probably benign Het
Zfp287 G T 11: 62,605,070 (GRCm39) H612Q probably damaging Het
Zfp352 C T 4: 90,113,386 (GRCm39) H509Y probably damaging Het
Other mutations in Ceacam13
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00791:Ceacam13 APN 7 17,747,278 (GRCm39) missense possibly damaging 0.59
IGL01617:Ceacam13 APN 7 17,745,308 (GRCm39) missense possibly damaging 0.53
IGL02948:Ceacam13 APN 7 17,744,988 (GRCm39) splice site probably benign
R1508:Ceacam13 UTSW 7 17,744,996 (GRCm39) missense possibly damaging 0.89
R4882:Ceacam13 UTSW 7 17,746,997 (GRCm39) missense probably benign 0.20
R6859:Ceacam13 UTSW 7 17,747,032 (GRCm39) missense probably damaging 1.00
R8081:Ceacam13 UTSW 7 17,747,113 (GRCm39) missense probably damaging 1.00
R8742:Ceacam13 UTSW 7 17,743,934 (GRCm39) missense probably damaging 0.96
R8745:Ceacam13 UTSW 7 17,743,934 (GRCm39) missense probably damaging 0.96
R9471:Ceacam13 UTSW 7 17,753,012 (GRCm39) makesense probably null
R9473:Ceacam13 UTSW 7 17,747,281 (GRCm39) missense probably benign 0.00
Predicted Primers PCR Primer
(F):5'- ATTCAACCACTCTGGGGTATGC -3'
(R):5'- GAGCTGAGTTTGACATCATTGG -3'

Sequencing Primer
(F):5'- CCACTCTGGGGTATGCATATTATGAC -3'
(R):5'- GGACTGAGTTACCATACTACTGTC -3'
Posted On 2015-03-25