Incidental Mutation 'IGL01540:Ceacam12'
ID90137
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Ceacam12
Ensembl Gene ENSMUSG00000030366
Gene Namecarcinoembryonic antigen-related cell adhesion molecule 12
SynonymsCeacam12-C1, Ceacam12-C3, 1600031J20Rik
Accession Numbers
Is this an essential gene? Non essential (E-score: 0.000) question?
Stock #IGL01540
Quality Score
Status
Chromosome7
Chromosomal Location18065929-18077986 bp(+) (GRCm38)
Type of Mutationintron
DNA Base Change (assembly) T to C at 18071802 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000104127 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000032520] [ENSMUST00000108483] [ENSMUST00000108487]
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
4932415D10Rik A T 10: 82,284,182 H4331Q possibly damaging Het
4933425L06Rik T C 13: 105,082,253 S32P possibly damaging Het
Adgrb3 A G 1: 25,112,171 probably null Het
Cyp2j13 A T 4: 96,068,722 probably benign Het
Golim4 T G 3: 75,886,740 E538A possibly damaging Het
Gstcd A T 3: 132,986,414 V580D probably damaging Het
Hspg2 A G 4: 137,519,706 T1115A probably damaging Het
Maea T C 5: 33,358,566 S18P probably benign Het
Mertk T C 2: 128,783,967 L674P probably damaging Het
Nol8 A T 13: 49,661,670 Q400L probably benign Het
Olfr1416 A G 1: 92,480,480 L47P probably damaging Het
Olfr516 G T 7: 108,845,680 T110N probably damaging Het
Pycard T A 7: 127,992,830 D113V probably benign Het
S100z G A 13: 95,477,353 T83M probably damaging Het
Sacs A G 14: 61,191,635 D381G possibly damaging Het
Tbpl2 T C 2: 24,094,973 H53R probably benign Het
Tlr6 T C 5: 64,955,286 R93G probably damaging Het
Trabd A G 15: 89,084,795 E172G probably benign Het
Vrk3 A G 7: 44,767,144 H277R probably damaging Het
Zfp512 T C 5: 31,473,496 V338A probably damaging Het
Other mutations in Ceacam12
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00577:Ceacam12 APN 7 18067261 missense probably damaging 1.00
IGL01483:Ceacam12 APN 7 18067521 missense probably benign 0.07
IGL01505:Ceacam12 APN 7 18067432 missense probably damaging 0.98
R0033:Ceacam12 UTSW 7 18069460 splice site probably benign
R0033:Ceacam12 UTSW 7 18069460 splice site probably benign
R1816:Ceacam12 UTSW 7 18071765 synonymous probably null
R4227:Ceacam12 UTSW 7 18071753 missense probably benign 0.01
R4382:Ceacam12 UTSW 7 18066034 start gained probably benign
R4541:Ceacam12 UTSW 7 18071723 missense probably benign
R4651:Ceacam12 UTSW 7 18067434 missense probably damaging 1.00
R4652:Ceacam12 UTSW 7 18067434 missense probably damaging 1.00
R4831:Ceacam12 UTSW 7 18077380 splice site probably null
R5351:Ceacam12 UTSW 7 18067234 missense probably damaging 1.00
R5357:Ceacam12 UTSW 7 18077459 nonsense probably null
R5779:Ceacam12 UTSW 7 18069154 missense probably benign 0.29
R5893:Ceacam12 UTSW 7 18069374 missense probably damaging 1.00
R5946:Ceacam12 UTSW 7 18069206 missense probably damaging 1.00
R6151:Ceacam12 UTSW 7 18069105 missense probably benign 0.01
R6175:Ceacam12 UTSW 7 18067387 missense probably damaging 1.00
R6346:Ceacam12 UTSW 7 18069401 missense probably damaging 0.99
R6491:Ceacam12 UTSW 7 18069260 missense probably damaging 1.00
R6591:Ceacam12 UTSW 7 18069224 missense possibly damaging 0.53
R6691:Ceacam12 UTSW 7 18069224 missense possibly damaging 0.53
Posted On2013-12-03