Incidental Mutation 'IGL01736:Ceacam10'
ID 105697
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Ceacam10
Ensembl Gene ENSMUSG00000054169
Gene Name CEA cell adhesion molecule 10
Synonyms Bgp3, Cea10
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL01736
Quality Score
Status
Chromosome 7
Chromosomal Location 24476631-24484082 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 24480535 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Cysteine at position 102 (Y102C)
Ref Sequence ENSEMBL: ENSMUSP00000146217 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000038069] [ENSMUST00000206847]
AlphaFold no structure available at present
Predicted Effect unknown
Transcript: ENSMUST00000038069
AA Change: Y222C
SMART Domains Protein: ENSMUSP00000037036
Gene: ENSMUSG00000054169
AA Change: Y222C

DomainStartEndE-ValueType
IG_like 42 141 1.23e1 SMART
low complexity region 142 151 N/A INTRINSIC
IG_like 160 261 4.41e1 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000206380
Predicted Effect probably damaging
Transcript: ENSMUST00000206847
AA Change: Y102C

PolyPhen 2 Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)
Predicted Effect probably benign
Transcript: ENSMUST00000206850
Coding Region Coverage
Validation Efficiency
MGI Phenotype PHENOTYPE: Animals homozygous for a mutation in this gene are fertile and viable. However, a small but significant 23% reduction in litter size was observed in homozygous matings. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 42 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acacb A G 5: 114,326,503 (GRCm39) T290A possibly damaging Het
Apip G A 2: 102,917,486 (GRCm39) V62M probably damaging Het
Appbp2 T C 11: 85,105,143 (GRCm39) K141R possibly damaging Het
Arhgef18 T A 8: 3,501,624 (GRCm39) probably benign Het
B3galt2 A G 1: 143,522,583 (GRCm39) T240A probably benign Het
Bivm A T 1: 44,180,973 (GRCm39) N385I probably damaging Het
Brd4 A T 17: 32,417,649 (GRCm39) probably benign Het
Cage1 T C 13: 38,206,789 (GRCm39) D352G possibly damaging Het
Diaph3 T C 14: 87,156,282 (GRCm39) D677G probably benign Het
Dis3l T C 9: 64,226,536 (GRCm39) probably null Het
Dnah6 C T 6: 73,165,360 (GRCm39) V582M probably benign Het
Fndc3b A G 3: 27,521,552 (GRCm39) L541P probably damaging Het
Folh1 T C 7: 86,391,444 (GRCm39) T384A possibly damaging Het
Gdpd3 T C 7: 126,365,695 (GRCm39) L18P probably damaging Het
Grxcr2 T A 18: 42,132,047 (GRCm39) K7N probably damaging Het
Gulo A G 14: 66,234,325 (GRCm39) F246L probably benign Het
Inpp4b A T 8: 82,723,968 (GRCm39) D500V probably benign Het
Ints4 C T 7: 97,175,849 (GRCm39) L647F probably benign Het
Kif17 T A 4: 138,013,876 (GRCm39) L264Q possibly damaging Het
Kif21a T C 15: 90,843,948 (GRCm39) N1104S possibly damaging Het
Ly6e T G 15: 74,830,546 (GRCm39) L132R probably benign Het
Mis18bp1 T A 12: 65,185,452 (GRCm39) H905L probably damaging Het
Nr2f2 A G 7: 70,004,446 (GRCm39) S269P probably damaging Het
Or2b2b C A 13: 21,858,787 (GRCm39) C109F probably benign Het
Or2o1 G A 11: 49,051,354 (GRCm39) C171Y probably damaging Het
Or5d46 T A 2: 88,170,771 (GRCm39) N287K probably damaging Het
Pde8b T C 13: 95,166,910 (GRCm39) I757V probably damaging Het
Psg23 A T 7: 18,346,122 (GRCm39) I191N possibly damaging Het
Slc12a4 A T 8: 106,672,475 (GRCm39) probably null Het
Snph A T 2: 151,436,093 (GRCm39) Y209* probably null Het
Tnfaip3 T C 10: 18,882,649 (GRCm39) H256R probably damaging Het
Tnip3 T A 6: 65,573,107 (GRCm39) probably benign Het
Ttc3 T A 16: 94,243,386 (GRCm39) F1130Y probably damaging Het
Twnk T G 19: 44,998,627 (GRCm39) V515G probably damaging Het
Usp24 T A 4: 106,280,658 (GRCm39) I2324K probably benign Het
Vwa7 T C 17: 35,238,827 (GRCm39) F305S probably damaging Het
Ythdc2 A T 18: 44,983,735 (GRCm39) Q567L probably damaging Het
Zbtb11 T A 16: 55,818,523 (GRCm39) I649K probably damaging Het
Zbtb49 T C 5: 38,358,204 (GRCm39) Y683C probably damaging Het
Zfhx4 A T 3: 5,309,152 (GRCm39) M793L possibly damaging Het
Zmym6 T G 4: 127,002,437 (GRCm39) I556R probably damaging Het
Zswim8 C T 14: 20,764,780 (GRCm39) P717S probably benign Het
Other mutations in Ceacam10
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02538:Ceacam10 APN 7 24,477,908 (GRCm39) missense probably damaging 1.00
R0040:Ceacam10 UTSW 7 24,477,689 (GRCm39) missense probably damaging 1.00
R0040:Ceacam10 UTSW 7 24,477,689 (GRCm39) missense probably damaging 1.00
R0254:Ceacam10 UTSW 7 24,477,733 (GRCm39) missense probably damaging 0.96
R0396:Ceacam10 UTSW 7 24,480,439 (GRCm39) missense probably damaging 1.00
R0567:Ceacam10 UTSW 7 24,477,834 (GRCm39) missense probably damaging 1.00
R1694:Ceacam10 UTSW 7 24,480,491 (GRCm39) missense probably benign 0.27
R2069:Ceacam10 UTSW 7 24,477,797 (GRCm39) missense probably damaging 1.00
R4425:Ceacam10 UTSW 7 24,480,433 (GRCm39) missense possibly damaging 0.68
R4748:Ceacam10 UTSW 7 24,480,477 (GRCm39) missense probably benign 0.01
R7292:Ceacam10 UTSW 7 24,477,775 (GRCm39) missense probably damaging 1.00
R7359:Ceacam10 UTSW 7 24,480,432 (GRCm39) missense unknown
R7664:Ceacam10 UTSW 7 24,477,757 (GRCm39) missense probably benign 0.05
R7736:Ceacam10 UTSW 7 24,480,636 (GRCm39) missense unknown
R8296:Ceacam10 UTSW 7 24,480,513 (GRCm39) missense unknown
R9625:Ceacam10 UTSW 7 24,476,705 (GRCm39) missense probably damaging 1.00
X0052:Ceacam10 UTSW 7 24,480,450 (GRCm39) missense probably benign 0.00
Posted On 2014-01-21