Incidental Mutation 'IGL01135:Ceacam23'
ID 51631
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Ceacam23
Ensembl Gene ENSMUSG00000078793
Gene Name CEA cell adhesion moleculen23
Synonyms Gm5155
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL01135
Quality Score
Status
Chromosome 7
Chromosomal Location 17605692-17652935 bp(+) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) A to T at 17636396 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold A0A3Q4EGJ1
Predicted Effect noncoding transcript
Transcript: ENSMUST00000072381
SMART Domains Protein: ENSMUSP00000072218
Gene: ENSMUSG00000078793

DomainStartEndE-ValueType
IG 40 141 2.27e-2 SMART
IG_like 160 261 2.73e1 SMART
IG_like 277 378 6.69e0 SMART
IG_like 397 498 4.07e1 SMART
IG_like 514 615 6.52e0 SMART
IG_like 634 735 1.05e1 SMART
IG 753 853 1.28e-1 SMART
IGc2 869 933 3.82e-9 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1110038F14Rik G A 15: 76,834,475 (GRCm39) V124I probably damaging Het
5730507C01Rik G A 12: 18,583,375 (GRCm39) R145H possibly damaging Het
Acox3 T A 5: 35,746,096 (GRCm39) V93E probably benign Het
Ankar T C 1: 72,704,378 (GRCm39) N848S probably benign Het
Blzf1 A G 1: 164,131,499 (GRCm39) probably benign Het
Cc2d1a G T 8: 84,870,033 (GRCm39) H161N probably benign Het
Cfap206 C T 4: 34,721,562 (GRCm39) S162N probably damaging Het
Ckmt1 A C 2: 121,191,631 (GRCm39) D267A probably damaging Het
Dtl G T 1: 191,280,442 (GRCm39) T364K probably damaging Het
Fat1 T A 8: 45,477,877 (GRCm39) F2308I probably damaging Het
Fbxo41 A T 6: 85,454,890 (GRCm39) S673T probably benign Het
Flnb G A 14: 7,909,736 (GRCm38) V1397I probably benign Het
Gdi2 A G 13: 3,598,855 (GRCm39) probably benign Het
Grik3 C T 4: 125,526,208 (GRCm39) T147I probably benign Het
Htr1a T C 13: 105,581,792 (GRCm39) V344A possibly damaging Het
Isg20l2 A T 3: 87,839,068 (GRCm39) D93V probably damaging Het
Kcnt2 T C 1: 140,282,293 (GRCm39) probably null Het
Mfsd4b3-ps A G 10: 39,824,068 (GRCm39) M64T probably benign Het
Nox3 T A 17: 3,746,527 (GRCm39) probably benign Het
Or2ag12 C T 7: 106,277,400 (GRCm39) A98T probably benign Het
Pikfyve T A 1: 65,290,794 (GRCm39) N1204K probably damaging Het
Pou4f3 C T 18: 42,529,031 (GRCm39) Q325* probably null Het
Rap1a T A 3: 105,639,351 (GRCm39) T103S probably benign Het
Rfc4 G A 16: 22,934,526 (GRCm39) R165C probably damaging Het
Smtnl1 A G 2: 84,649,231 (GRCm39) S8P probably benign Het
Syt17 C T 7: 117,981,270 (GRCm39) G351S possibly damaging Het
Tcf20 T A 15: 82,738,101 (GRCm39) M1117L probably benign Het
Tent5a A G 9: 85,208,652 (GRCm39) V57A probably damaging Het
Tgfbr3 A T 5: 107,362,894 (GRCm39) H39Q probably damaging Het
Trdmt1 T C 2: 13,526,071 (GRCm39) probably null Het
Twf2 A G 9: 106,090,027 (GRCm39) I127V probably benign Het
Unc13c A G 9: 73,392,175 (GRCm39) V2059A probably damaging Het
Other mutations in Ceacam23
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00480:Ceacam23 APN 7 17,644,622 (GRCm39) missense probably benign 0.32
IGL01085:Ceacam23 APN 7 17,649,616 (GRCm39) missense possibly damaging 0.71
IGL01291:Ceacam23 APN 7 17,639,041 (GRCm39) exon noncoding transcript
IGL02252:Ceacam23 APN 7 17,644,457 (GRCm39) missense possibly damaging 0.93
IGL03243:Ceacam23 APN 7 17,652,574 (GRCm39) exon noncoding transcript
R0113:Ceacam23 UTSW 7 17,642,873 (GRCm39) exon noncoding transcript
R0833:Ceacam23 UTSW 7 17,638,906 (GRCm39) missense possibly damaging 0.95
R0836:Ceacam23 UTSW 7 17,638,906 (GRCm39) missense possibly damaging 0.95
R1462:Ceacam23 UTSW 7 17,649,516 (GRCm39) exon noncoding transcript
R1473:Ceacam23 UTSW 7 17,639,016 (GRCm39) exon noncoding transcript
R1817:Ceacam23 UTSW 7 17,607,255 (GRCm39) exon noncoding transcript
R1905:Ceacam23 UTSW 7 17,607,477 (GRCm39) exon noncoding transcript
R2362:Ceacam23 UTSW 7 17,636,398 (GRCm39) exon noncoding transcript
R3721:Ceacam23 UTSW 7 17,636,663 (GRCm39) missense probably benign 0.41
R4305:Ceacam23 UTSW 7 17,639,118 (GRCm39) missense probably benign 0.19
R4567:Ceacam23 UTSW 7 17,642,891 (GRCm39) missense probably damaging 0.97
R4587:Ceacam23 UTSW 7 17,620,149 (GRCm39) missense possibly damaging 0.47
R4691:Ceacam23 UTSW 7 17,642,891 (GRCm39) missense possibly damaging 0.93
R4989:Ceacam23 UTSW 7 17,639,143 (GRCm39) splice site probably null
R5023:Ceacam23 UTSW 7 17,636,631 (GRCm39) missense probably damaging 1.00
R5024:Ceacam23 UTSW 7 17,644,607 (GRCm39) missense probably benign 0.06
R5274:Ceacam23 UTSW 7 17,649,642 (GRCm39) splice site probably null
R5279:Ceacam23 UTSW 7 17,607,214 (GRCm39) splice site noncoding transcript
R5304:Ceacam23 UTSW 7 17,636,617 (GRCm39) missense probably benign 0.06
R5312:Ceacam23 UTSW 7 17,643,067 (GRCm39) missense probably damaging 1.00
R5899:Ceacam23 UTSW 7 17,651,369 (GRCm39) missense possibly damaging 0.92
Posted On 2013-06-21