Incidental Mutation 'IGL01291:Ceacam23'
ID 72931
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 # IGL01291
Quality Score
Status
Chromosome 7
Chromosomal Location 17605692-17652935 bp(+) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) T to A at 17639041 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: 39 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acacb T A 5: 114,363,931 (GRCm39) F1464Y probably benign Het
Adgrg6 G A 10: 14,286,274 (GRCm39) A1114V possibly damaging Het
Agl A G 3: 116,566,438 (GRCm39) I975T possibly damaging Het
Arhgef11 T C 3: 87,640,481 (GRCm39) W1213R probably benign Het
Ccar1 T A 10: 62,592,428 (GRCm39) E708V probably damaging Het
Cilp T C 9: 65,186,265 (GRCm39) S787P possibly damaging Het
Col5a1 T A 2: 27,861,456 (GRCm39) probably benign Het
Col6a3 G A 1: 90,730,014 (GRCm39) T1157I probably damaging Het
Dock3 T C 9: 106,835,599 (GRCm39) probably benign Het
Dusp19 A G 2: 80,454,618 (GRCm39) T113A probably benign Het
Dync1h1 A C 12: 110,615,538 (GRCm39) Y2957S probably benign Het
Fcho1 A T 8: 72,165,191 (GRCm39) L422Q probably benign Het
Gca T A 2: 62,520,787 (GRCm39) Y210* probably null Het
Gpnmb T C 6: 49,032,615 (GRCm39) V513A probably benign Het
Irx4 A G 13: 73,415,786 (GRCm39) T192A probably damaging Het
Isca1 T C 13: 59,906,785 (GRCm39) T54A probably benign Het
L3mbtl1 T C 2: 162,812,100 (GRCm39) V715A probably benign Het
Lama1 G A 17: 68,045,865 (GRCm39) D257N probably damaging Het
Lgr5 T C 10: 115,314,439 (GRCm39) H166R probably damaging Het
M6pr A G 6: 122,289,218 (GRCm39) R9G probably benign Het
Or8k30 G A 2: 86,339,513 (GRCm39) A237T possibly damaging Het
Pank4 T C 4: 155,059,103 (GRCm39) M412T probably damaging Het
Psd A G 19: 46,303,186 (GRCm39) V100A possibly damaging Het
Rab11fip3 T C 17: 26,235,087 (GRCm39) T28A probably damaging Het
Rnpepl1 A T 1: 92,847,468 (GRCm39) D685V probably benign Het
Rrad T C 8: 105,357,283 (GRCm39) E88G probably benign Het
Sdk2 T A 11: 113,733,906 (GRCm39) M846L probably benign Het
Sparcl1 A T 5: 104,242,581 (GRCm39) V36E possibly damaging Het
Srrm4 C T 5: 116,605,628 (GRCm39) E210K unknown Het
Stk25 A T 1: 93,551,145 (GRCm39) probably null Het
Tacr3 A T 3: 134,635,810 (GRCm39) Y338F probably damaging Het
Tap2 A T 17: 34,428,184 (GRCm39) Q286L probably benign Het
Tbce A T 13: 14,184,325 (GRCm39) probably benign Het
Tubgcp5 C A 7: 55,458,277 (GRCm39) A396E possibly damaging Het
Ube2o T C 11: 116,430,960 (GRCm39) D980G probably damaging Het
Vmn1r86 T C 7: 12,836,433 (GRCm39) M98V probably benign Het
Vmn2r58 T A 7: 41,513,935 (GRCm39) H236L probably benign Het
Zfp521 T C 18: 13,950,303 (GRCm39) H1217R probably damaging Het
Zfyve1 A T 12: 83,601,779 (GRCm39) F110I probably benign 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
IGL01135:Ceacam23 APN 7 17,636,396 (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 2013-10-07