Incidental Mutation 'IGL01669:Ceacam18'
ID 103402
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Ceacam18
Ensembl Gene ENSMUSG00000030472
Gene Name CEA cell adhesion molecule 18
Synonyms 2010110O04Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.052) question?
Stock # IGL01669
Quality Score
Status
Chromosome 7
Chromosomal Location 43284131-43298719 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 43294939 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glycine to Glutamic Acid at position 333 (G333E)
Ref Sequence ENSEMBL: ENSMUSP00000032663 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000032663]
AlphaFold Q9D871
Predicted Effect probably damaging
Transcript: ENSMUST00000032663
AA Change: G333E

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000032663
Gene: ENSMUSG00000030472
AA Change: G333E

DomainStartEndE-ValueType
signal peptide 1 28 N/A INTRINSIC
IG_like 36 135 1.03e2 SMART
IG_like 148 226 5.56e0 SMART
IGc2 248 305 5.24e-7 SMART
transmembrane domain 334 356 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 40 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acsl4 G T X: 141,126,184 (GRCm39) D313E probably damaging Het
Aifm3 A C 16: 17,321,405 (GRCm39) K453T probably benign Het
Anks1b T C 10: 90,733,100 (GRCm39) probably benign Het
Arfgef1 T C 1: 10,229,840 (GRCm39) D1287G probably damaging Het
Bcl3 G A 7: 19,546,416 (GRCm39) Q140* probably null Het
Bnipl T G 3: 95,150,045 (GRCm39) R316S probably damaging Het
Cacna1i T A 15: 80,275,958 (GRCm39) H1916Q probably benign Het
Ccdc171 C T 4: 83,599,432 (GRCm39) A749V probably damaging Het
Cul7 G T 17: 46,969,641 (GRCm39) M969I possibly damaging Het
Cylc2 A G 4: 51,228,360 (GRCm39) T144A probably benign Het
Cyp2c50 A T 19: 40,086,495 (GRCm39) H294L probably damaging Het
D430041D05Rik T C 2: 104,085,306 (GRCm39) K1081R probably damaging Het
D930020B18Rik A G 10: 121,519,866 (GRCm39) K456R probably benign Het
Drd2 A G 9: 49,313,389 (GRCm39) N186S possibly damaging Het
Fanci A T 7: 79,098,925 (GRCm39) E1306D probably benign Het
Fbxl21 T A 13: 56,675,522 (GRCm39) probably benign Het
Galk2 T A 2: 125,729,807 (GRCm39) Y63N probably damaging Het
Git2 T C 5: 114,905,166 (GRCm39) D97G probably damaging Het
Gm8258 T A 5: 104,923,940 (GRCm39) noncoding transcript Het
Irf4 G T 13: 30,941,454 (GRCm39) S270I probably damaging Het
Itgb3 C A 11: 104,524,216 (GRCm39) probably benign Het
Itpr2 A C 6: 146,081,727 (GRCm39) I2299R probably damaging Het
Lig4 T C 8: 10,023,673 (GRCm39) I36V probably benign Het
Nedd9 A G 13: 41,492,111 (GRCm39) V133A probably damaging Het
Nup133 A C 8: 124,665,869 (GRCm39) Y185* probably null Het
Or51b6b A T 7: 103,310,194 (GRCm39) F88I probably benign Het
Or5d14 T C 2: 87,880,128 (GRCm39) Y280C possibly damaging Het
Or6c3 A G 10: 129,309,080 (GRCm39) H173R probably damaging Het
Pgbd5 T A 8: 125,101,138 (GRCm39) T373S possibly damaging Het
Ppp1r8 T C 4: 132,555,480 (GRCm39) E246G probably benign Het
Rmnd5b C T 11: 51,518,727 (GRCm39) V89M probably damaging Het
Rnf123 T C 9: 107,935,555 (GRCm39) I969V probably damaging Het
Ror2 A G 13: 53,265,124 (GRCm39) I656T probably damaging Het
Sgsm1 T C 5: 113,411,356 (GRCm39) E503G probably benign Het
Smgc T A 15: 91,744,882 (GRCm39) S381T possibly damaging Het
Tlr4 T G 4: 66,759,504 (GRCm39) F766V possibly damaging Het
Tnc T C 4: 63,918,938 (GRCm39) T1162A probably damaging Het
Usp39 A G 6: 72,315,476 (GRCm39) V156A probably damaging Het
Zdhhc5 A G 2: 84,521,538 (GRCm39) Y352H probably damaging Het
Zfp646 A G 7: 127,478,137 (GRCm39) T105A probably benign Het
Other mutations in Ceacam18
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00426:Ceacam18 APN 7 43,288,780 (GRCm39) missense probably benign 0.00
IGL00585:Ceacam18 APN 7 43,286,435 (GRCm39) missense possibly damaging 0.90
R0001:Ceacam18 UTSW 7 43,286,300 (GRCm39) missense possibly damaging 0.58
R0227:Ceacam18 UTSW 7 43,288,815 (GRCm39) missense probably damaging 1.00
R1524:Ceacam18 UTSW 7 43,288,779 (GRCm39) missense possibly damaging 0.95
R1647:Ceacam18 UTSW 7 43,288,689 (GRCm39) missense possibly damaging 0.78
R1768:Ceacam18 UTSW 7 43,297,918 (GRCm39) missense probably benign 0.00
R1828:Ceacam18 UTSW 7 43,288,880 (GRCm39) missense probably benign 0.19
R3751:Ceacam18 UTSW 7 43,291,372 (GRCm39) missense probably damaging 1.00
R4870:Ceacam18 UTSW 7 43,291,328 (GRCm39) missense probably damaging 1.00
R5259:Ceacam18 UTSW 7 43,286,536 (GRCm39) critical splice donor site probably null
R5358:Ceacam18 UTSW 7 43,286,497 (GRCm39) missense possibly damaging 0.57
R5368:Ceacam18 UTSW 7 43,291,458 (GRCm39) missense probably benign 0.08
R5810:Ceacam18 UTSW 7 43,286,382 (GRCm39) missense probably benign 0.00
R5817:Ceacam18 UTSW 7 43,291,265 (GRCm39) missense probably benign 0.07
R5835:Ceacam18 UTSW 7 43,286,382 (GRCm39) missense probably benign 0.00
R7113:Ceacam18 UTSW 7 43,291,400 (GRCm39) missense probably benign
R7138:Ceacam18 UTSW 7 43,288,706 (GRCm39) missense possibly damaging 0.80
R7275:Ceacam18 UTSW 7 43,291,308 (GRCm39) missense probably damaging 1.00
R7502:Ceacam18 UTSW 7 43,286,298 (GRCm39) missense probably damaging 0.99
R8849:Ceacam18 UTSW 7 43,294,967 (GRCm39) missense probably benign 0.00
R9119:Ceacam18 UTSW 7 43,288,909 (GRCm39) missense probably benign
R9347:Ceacam18 UTSW 7 43,294,915 (GRCm39) missense possibly damaging 0.70
R9663:Ceacam18 UTSW 7 43,288,764 (GRCm39) missense probably damaging 1.00
Posted On 2014-01-21