Incidental Mutation 'IGL00094:Ceacam14'
ID 1530
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Ceacam14
Ensembl Gene ENSMUSG00000023185
Gene Name CEA cell adhesion molecule 14
Synonyms 1600021E03Rik, 1600025E09Rik
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL00094
Quality Score
Status
Chromosome 7
Chromosomal Location 17546607-17549552 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 17548062 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Isoleucine at position 51 (V51I)
Ref Sequence ENSEMBL: ENSMUSP00000023953 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000023953]
AlphaFold Q78Y72
Predicted Effect probably damaging
Transcript: ENSMUST00000023953
AA Change: V51I

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000023953
Gene: ENSMUSG00000023185
AA Change: V51I

DomainStartEndE-ValueType
low complexity region 18 29 N/A INTRINSIC
IG_like 40 141 6.35e0 SMART
IG_like 158 261 2.73e1 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 61 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aacs T A 5: 125,591,254 (GRCm39) N547K probably benign Het
Abca13 A G 11: 9,247,443 (GRCm39) T2397A probably benign Het
Abcc1 A G 16: 14,288,398 (GRCm39) N1341S probably null Het
Adcy9 T A 16: 4,122,446 (GRCm39) I535L probably benign Het
Akap6 A G 12: 53,187,763 (GRCm39) S1726G possibly damaging Het
Ap3d1 T C 10: 80,577,813 (GRCm39) M5V probably benign Het
Ash1l T A 3: 88,889,019 (GRCm39) N299K probably benign Het
B3gnt2 C T 11: 22,786,151 (GRCm39) V346I probably benign Het
Cfap69 T C 5: 5,634,682 (GRCm39) D812G probably damaging Het
Cfap97d1 A G 11: 101,881,646 (GRCm39) E114G possibly damaging Het
Chrna9 T C 5: 66,126,600 (GRCm39) V118A probably benign Het
Cpsf7 A G 19: 10,517,151 (GRCm39) R418G probably damaging Het
Csnk1g3 T C 18: 54,052,075 (GRCm39) Y215H probably damaging Het
Dcaf5 A C 12: 80,386,097 (GRCm39) N676K probably benign Het
Dld A T 12: 31,385,576 (GRCm39) M255K probably benign Het
Esr2 A T 12: 76,180,670 (GRCm39) L417H probably damaging Het
Fsip2 T A 2: 82,820,730 (GRCm39) S5488T probably benign Het
Gatb A T 3: 85,509,227 (GRCm39) I130L possibly damaging Het
Gbp9 T C 5: 105,229,130 (GRCm39) K506E probably benign Het
Hkdc1 T C 10: 62,229,568 (GRCm39) N703S probably damaging Het
Itgb3 T A 11: 104,524,410 (GRCm39) V182E probably damaging Het
Itih4 A T 14: 30,617,426 (GRCm39) Y582F probably damaging Het
Lancl2 T A 6: 57,701,522 (GRCm39) probably benign Het
Lgals3 A G 14: 47,622,175 (GRCm39) K197R probably benign Het
Lipe T C 7: 25,082,977 (GRCm39) T767A probably damaging Het
Lrp2 T A 2: 69,338,123 (GRCm39) D1219V probably damaging Het
Lrriq3 T A 3: 154,806,698 (GRCm39) C116S probably benign Het
Mcm5 T G 8: 75,851,573 (GRCm39) probably null Het
Mtpn G T 6: 35,499,711 (GRCm39) T31K probably damaging Het
Mycbp2 A T 14: 103,460,486 (GRCm39) Y1494N probably damaging Het
Nbeal1 G T 1: 60,274,350 (GRCm39) E498* probably null Het
Nos1 T G 5: 118,048,165 (GRCm39) S657A probably damaging Het
Nr3c1 A T 18: 39,561,661 (GRCm39) probably null Het
Or12e7 T A 2: 87,288,271 (GRCm39) V254E probably damaging Het
Or13a17 A T 7: 140,271,349 (GRCm39) H177L probably damaging Het
Or4c127 T A 2: 89,833,365 (GRCm39) I205N possibly damaging Het
Or7g32 T A 9: 19,408,155 (GRCm39) I37N probably damaging Het
Or8g20 T C 9: 39,395,944 (GRCm39) I202V probably benign Het
Or8s8 T G 15: 98,354,299 (GRCm39) V36G possibly damaging Het
Or9i1 A T 19: 13,839,150 (GRCm39) probably benign Het
Osbp2 T G 11: 3,661,848 (GRCm39) S735R probably benign Het
Otop3 A T 11: 115,235,279 (GRCm39) T304S probably benign Het
Pcdhac2 A T 18: 37,278,128 (GRCm39) L369F probably damaging Het
Pick1 T C 15: 79,131,457 (GRCm39) probably benign Het
Prlhr A T 19: 60,456,119 (GRCm39) V149E probably damaging Het
Prss12 G A 3: 123,280,598 (GRCm39) probably benign Het
Rab19 A T 6: 39,365,132 (GRCm39) probably benign Het
Ralgapb T C 2: 158,262,776 (GRCm39) W5R probably damaging Het
Rfx4 T A 10: 84,676,063 (GRCm39) L44Q probably damaging Het
Scube2 T C 7: 109,407,661 (GRCm39) T760A probably damaging Het
Shcbp1 A C 8: 4,804,258 (GRCm39) Y145* probably null Het
Snx31 T A 15: 36,545,761 (GRCm39) probably null Het
Spopl A T 2: 23,427,643 (GRCm39) V163E possibly damaging Het
Sqor T C 2: 122,629,463 (GRCm39) I107T probably damaging Het
Tcte1 T C 17: 45,845,854 (GRCm39) F153L probably damaging Het
Tnfrsf11b T A 15: 54,123,238 (GRCm39) H121L probably damaging Het
Tnip1 G T 11: 54,831,643 (GRCm39) Y10* probably null Het
Tnxb G T 17: 34,904,603 (GRCm39) G1123C probably damaging Het
Wdr62 T C 7: 29,942,948 (GRCm39) E515G probably benign Het
Zfand1 A T 3: 10,413,590 (GRCm39) D32E probably null Het
Zfp112 A C 7: 23,821,668 (GRCm39) T3P probably damaging Het
Other mutations in Ceacam14
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0452:Ceacam14 UTSW 7 17,549,248 (GRCm39) missense probably benign
R1613:Ceacam14 UTSW 7 17,547,973 (GRCm39) splice site probably benign
R1990:Ceacam14 UTSW 7 17,549,290 (GRCm39) nonsense probably null
R2153:Ceacam14 UTSW 7 17,548,153 (GRCm39) missense probably benign 0.00
R3887:Ceacam14 UTSW 7 17,548,063 (GRCm39) missense probably damaging 1.00
R4724:Ceacam14 UTSW 7 17,547,975 (GRCm39) critical splice acceptor site probably null
R5323:Ceacam14 UTSW 7 17,549,402 (GRCm39) makesense probably null
R5454:Ceacam14 UTSW 7 17,548,110 (GRCm39) missense probably damaging 1.00
R5696:Ceacam14 UTSW 7 17,548,267 (GRCm39) missense probably damaging 0.97
R6318:Ceacam14 UTSW 7 17,548,237 (GRCm39) missense probably damaging 1.00
R6763:Ceacam14 UTSW 7 17,549,268 (GRCm39) missense probably benign 0.04
R7607:Ceacam14 UTSW 7 17,548,246 (GRCm39) missense possibly damaging 0.95
R7789:Ceacam14 UTSW 7 17,548,096 (GRCm39) missense probably damaging 0.99
R8946:Ceacam14 UTSW 7 17,547,999 (GRCm39) missense probably benign 0.01
R9781:Ceacam14 UTSW 7 17,549,082 (GRCm39) missense possibly damaging 0.60
Posted On 2011-07-12