Incidental Mutation 'IGL01540:Ceacam12'
ID 90137
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Ceacam12
Ensembl Gene ENSMUSG00000030366
Gene Name CEA cell adhesion molecule 12
Synonyms Ceacam12-C1, Ceacam12-C3, 1600031J20Rik
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL01540
Quality Score
Status
Chromosome 7
Chromosomal Location 17799854-17811911 bp(+) (GRCm39)
Type of Mutation intron
DNA Base Change (assembly) T to C at 17805727 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000104127 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000032520] [ENSMUST00000108483] [ENSMUST00000108487]
AlphaFold Q3UKP4
Predicted Effect probably benign
Transcript: ENSMUST00000032520
SMART Domains Protein: ENSMUSP00000032520
Gene: ENSMUSG00000030366

DomainStartEndE-ValueType
IG 40 141 7.77e-1 SMART
IG_like 159 260 4.78e1 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000108483
SMART Domains Protein: ENSMUSP00000104123
Gene: ENSMUSG00000030366

DomainStartEndE-ValueType
IG 40 141 7.77e-1 SMART
IG_like 159 260 4.78e1 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000108487
SMART Domains Protein: ENSMUSP00000104127
Gene: ENSMUSG00000030366

DomainStartEndE-ValueType
IG 40 141 7.77e-1 SMART
IG_like 159 260 4.78e1 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000205637
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 20 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgrb3 A G 1: 25,151,252 (GRCm39) probably null Het
Cyp2j13 A T 4: 95,956,959 (GRCm39) probably benign Het
Golim4 T G 3: 75,794,047 (GRCm39) E538A possibly damaging Het
Gstcd A T 3: 132,692,175 (GRCm39) V580D probably damaging Het
Hspg2 A G 4: 137,247,017 (GRCm39) T1115A probably damaging Het
Maea T C 5: 33,515,910 (GRCm39) S18P probably benign Het
Mertk T C 2: 128,625,887 (GRCm39) L674P probably damaging Het
Nol8 A T 13: 49,815,146 (GRCm39) Q400L probably benign Het
Nt5el T C 13: 105,218,761 (GRCm39) S32P possibly damaging Het
Or10a3b G T 7: 108,444,887 (GRCm39) T110N probably damaging Het
Or6b2 A G 1: 92,408,202 (GRCm39) L47P probably damaging Het
Pycard T A 7: 127,592,002 (GRCm39) D113V probably benign Het
S100z G A 13: 95,613,861 (GRCm39) T83M probably damaging Het
Sacs A G 14: 61,429,084 (GRCm39) D381G possibly damaging Het
Spata31h1 A T 10: 82,120,016 (GRCm39) H4331Q possibly damaging Het
Tbpl2 T C 2: 23,984,985 (GRCm39) H53R probably benign Het
Tlr6 T C 5: 65,112,629 (GRCm39) R93G probably damaging Het
Trabd A G 15: 88,968,998 (GRCm39) E172G probably benign Het
Vrk3 A G 7: 44,416,568 (GRCm39) H277R probably damaging Het
Zfp512 T C 5: 31,630,840 (GRCm39) V338A probably damaging Het
Other mutations in Ceacam12
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00577:Ceacam12 APN 7 17,801,186 (GRCm39) missense probably damaging 1.00
IGL01483:Ceacam12 APN 7 17,801,446 (GRCm39) missense probably benign 0.07
IGL01505:Ceacam12 APN 7 17,801,357 (GRCm39) missense probably damaging 0.98
R0033:Ceacam12 UTSW 7 17,803,385 (GRCm39) splice site probably benign
R0033:Ceacam12 UTSW 7 17,803,385 (GRCm39) splice site probably benign
R1816:Ceacam12 UTSW 7 17,805,690 (GRCm39) splice site probably null
R4227:Ceacam12 UTSW 7 17,805,678 (GRCm39) missense probably benign 0.01
R4382:Ceacam12 UTSW 7 17,799,959 (GRCm39) start gained probably benign
R4541:Ceacam12 UTSW 7 17,805,648 (GRCm39) missense probably benign
R4651:Ceacam12 UTSW 7 17,801,359 (GRCm39) missense probably damaging 1.00
R4652:Ceacam12 UTSW 7 17,801,359 (GRCm39) missense probably damaging 1.00
R4831:Ceacam12 UTSW 7 17,811,305 (GRCm39) splice site probably null
R5351:Ceacam12 UTSW 7 17,801,159 (GRCm39) missense probably damaging 1.00
R5357:Ceacam12 UTSW 7 17,811,384 (GRCm39) nonsense probably null
R5779:Ceacam12 UTSW 7 17,803,079 (GRCm39) missense probably benign 0.29
R5893:Ceacam12 UTSW 7 17,803,299 (GRCm39) missense probably damaging 1.00
R5946:Ceacam12 UTSW 7 17,803,131 (GRCm39) missense probably damaging 1.00
R6151:Ceacam12 UTSW 7 17,803,030 (GRCm39) missense probably benign 0.01
R6175:Ceacam12 UTSW 7 17,801,312 (GRCm39) missense probably damaging 1.00
R6346:Ceacam12 UTSW 7 17,803,326 (GRCm39) missense probably damaging 0.99
R6491:Ceacam12 UTSW 7 17,803,185 (GRCm39) missense probably damaging 1.00
R6591:Ceacam12 UTSW 7 17,803,149 (GRCm39) missense possibly damaging 0.53
R6691:Ceacam12 UTSW 7 17,803,149 (GRCm39) missense possibly damaging 0.53
R8822:Ceacam12 UTSW 7 17,803,378 (GRCm39) critical splice donor site probably benign
R9232:Ceacam12 UTSW 7 17,803,341 (GRCm39) missense probably benign
R9279:Ceacam12 UTSW 7 17,801,177 (GRCm39) missense probably damaging 1.00
R9372:Ceacam12 UTSW 7 17,803,229 (GRCm39) missense probably benign 0.40
Z1177:Ceacam12 UTSW 7 17,801,440 (GRCm39) missense probably damaging 1.00
Posted On 2013-12-03