Incidental Mutation 'IGL03395:Ceacam5'
ID 421237
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Ceacam5
Ensembl Gene ENSMUSG00000008789
Gene Name CEA cell adhesion molecule 5
Synonyms Psg30, 1600029H12Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.055) question?
Stock # IGL03395
Quality Score
Status
Chromosome 7
Chromosomal Location 17447163-17495057 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) T to C at 17479304 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000080582 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000081907]
AlphaFold Q3UKK2
Predicted Effect probably benign
Transcript: ENSMUST00000081907
SMART Domains Protein: ENSMUSP00000080582
Gene: ENSMUSG00000008789

DomainStartEndE-ValueType
IG 40 141 4.46e-1 SMART
IG_like 160 261 2.96e1 SMART
IG_like 277 378 5.86e0 SMART
IG_like 397 496 4.07e1 SMART
IG 514 615 2.64e0 SMART
IG_like 634 735 2.81e1 SMART
IG 753 853 1.72e-2 SMART
IGc2 869 933 1.28e-10 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adam11 A G 11: 102,663,746 (GRCm39) D308G probably damaging Het
Adgrg3 A T 8: 95,761,701 (GRCm39) I155F probably damaging Het
Ado T C 10: 67,384,368 (GRCm39) Y79C probably benign Het
Aox1 T C 1: 58,107,884 (GRCm39) probably benign Het
Bicd2 T A 13: 49,528,734 (GRCm39) D165E probably damaging Het
Ccdc124 A C 8: 71,321,251 (GRCm39) M163R probably benign Het
Cenpq A G 17: 41,234,449 (GRCm39) L247P probably damaging Het
Crat A G 2: 30,294,978 (GRCm39) V479A probably benign Het
Egfr T C 11: 16,860,261 (GRCm39) probably benign Het
Elapor2 A T 5: 9,472,359 (GRCm39) Q352L probably damaging Het
Emc9 C T 14: 55,822,197 (GRCm39) A72T probably benign Het
Fbxo5 G A 10: 5,751,935 (GRCm39) S226F probably benign Het
Gm42688 A C 6: 83,085,352 (GRCm39) E737D possibly damaging Het
Got1l1 G T 8: 27,690,885 (GRCm39) H54Q probably benign Het
Grid2 G A 6: 63,886,053 (GRCm39) V150I possibly damaging Het
Klc4 C T 17: 46,943,789 (GRCm39) V506M probably damaging Het
Lrrc8c A G 5: 105,754,495 (GRCm39) N90S probably benign Het
Lrrk2 T A 15: 91,681,617 (GRCm39) probably null Het
Mbd6 G A 10: 127,119,286 (GRCm39) R950C probably damaging Het
Nol11 A G 11: 107,066,548 (GRCm39) V414A probably benign Het
Or7e178 A T 9: 20,225,847 (GRCm39) M123K probably damaging Het
Pcnt T C 10: 76,272,325 (GRCm39) E177G possibly damaging Het
Pcnx2 G T 8: 126,614,262 (GRCm39) D396E probably benign Het
Pcyt2 A T 11: 120,503,876 (GRCm39) probably null Het
Pds5a T C 5: 65,809,792 (GRCm39) D390G possibly damaging Het
Pik3r2 T C 8: 71,224,999 (GRCm39) T155A probably benign Het
Rab31 T A 17: 66,003,362 (GRCm39) H95L probably benign Het
Rfx5 C T 3: 94,865,113 (GRCm39) R259* probably null Het
Slc6a17 T C 3: 107,384,622 (GRCm39) D285G probably damaging Het
Spats2l A T 1: 57,977,175 (GRCm39) I318F probably damaging Het
Spef1l G T 7: 139,556,589 (GRCm39) probably benign Het
Tcf12 A G 9: 71,783,304 (GRCm39) S361P probably damaging Het
Other mutations in Ceacam5
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00419:Ceacam5 APN 7 17,493,481 (GRCm39) nonsense probably null
IGL00981:Ceacam5 APN 7 17,479,458 (GRCm39) missense probably benign 0.08
IGL01314:Ceacam5 APN 7 17,481,181 (GRCm39) nonsense probably null
IGL01329:Ceacam5 APN 7 17,479,534 (GRCm39) missense probably damaging 0.98
IGL01389:Ceacam5 APN 7 17,481,300 (GRCm39) missense probably damaging 0.96
IGL01418:Ceacam5 APN 7 17,479,524 (GRCm39) missense probably damaging 1.00
IGL02418:Ceacam5 APN 7 17,493,359 (GRCm39) missense possibly damaging 0.71
IGL02734:Ceacam5 APN 7 17,484,737 (GRCm39) missense probably damaging 1.00
IGL03220:Ceacam5 APN 7 17,494,653 (GRCm39) missense probably damaging 1.00
IGL03377:Ceacam5 APN 7 17,449,056 (GRCm39) missense probably benign 0.15
IGL03054:Ceacam5 UTSW 7 17,493,379 (GRCm39) missense possibly damaging 0.71
R0456:Ceacam5 UTSW 7 17,494,776 (GRCm39) missense possibly damaging 0.63
R0624:Ceacam5 UTSW 7 17,448,888 (GRCm39) missense probably benign 0.03
R0847:Ceacam5 UTSW 7 17,491,762 (GRCm39) missense possibly damaging 0.71
R0879:Ceacam5 UTSW 7 17,491,627 (GRCm39) missense probably benign 0.16
R0945:Ceacam5 UTSW 7 17,481,269 (GRCm39) missense probably damaging 1.00
R1382:Ceacam5 UTSW 7 17,486,090 (GRCm39) missense probably benign 0.33
R1474:Ceacam5 UTSW 7 17,481,159 (GRCm39) missense probably damaging 1.00
R1526:Ceacam5 UTSW 7 17,484,620 (GRCm39) missense probably damaging 1.00
R1793:Ceacam5 UTSW 7 17,481,320 (GRCm39) missense probably benign 0.01
R1851:Ceacam5 UTSW 7 17,448,835 (GRCm39) nonsense probably null
R1907:Ceacam5 UTSW 7 17,486,309 (GRCm39) missense possibly damaging 0.85
R1913:Ceacam5 UTSW 7 17,493,502 (GRCm39) nonsense probably null
R1990:Ceacam5 UTSW 7 17,491,805 (GRCm39) missense probably damaging 0.99
R1999:Ceacam5 UTSW 7 17,481,172 (GRCm39) missense possibly damaging 0.66
R2336:Ceacam5 UTSW 7 17,481,300 (GRCm39) missense probably benign 0.28
R2355:Ceacam5 UTSW 7 17,479,560 (GRCm39) missense probably damaging 1.00
R3106:Ceacam5 UTSW 7 17,481,248 (GRCm39) missense probably benign 0.06
R3423:Ceacam5 UTSW 7 17,491,562 (GRCm39) missense possibly damaging 0.52
R3432:Ceacam5 UTSW 7 17,448,901 (GRCm39) missense probably benign 0.06
R3686:Ceacam5 UTSW 7 17,494,748 (GRCm39) missense possibly damaging 0.94
R3713:Ceacam5 UTSW 7 17,493,263 (GRCm39) missense possibly damaging 0.52
R3878:Ceacam5 UTSW 7 17,484,506 (GRCm39) missense probably damaging 1.00
R4214:Ceacam5 UTSW 7 17,486,076 (GRCm39) missense probably benign 0.00
R4335:Ceacam5 UTSW 7 17,486,054 (GRCm39) missense probably benign
R4725:Ceacam5 UTSW 7 17,494,602 (GRCm39) missense probably benign 0.26
R4823:Ceacam5 UTSW 7 17,491,669 (GRCm39) missense possibly damaging 0.71
R4833:Ceacam5 UTSW 7 17,486,183 (GRCm39) missense probably benign
R4986:Ceacam5 UTSW 7 17,491,758 (GRCm39) missense possibly damaging 0.85
R5099:Ceacam5 UTSW 7 17,479,513 (GRCm39) missense probably damaging 0.96
R5365:Ceacam5 UTSW 7 17,493,473 (GRCm39) missense probably damaging 0.98
R5522:Ceacam5 UTSW 7 17,449,005 (GRCm39) missense probably benign
R5605:Ceacam5 UTSW 7 17,481,161 (GRCm39) missense probably benign 0.03
R6199:Ceacam5 UTSW 7 17,448,810 (GRCm39) missense probably benign 0.00
R6222:Ceacam5 UTSW 7 17,479,472 (GRCm39) missense probably benign 0.15
R6320:Ceacam5 UTSW 7 17,481,123 (GRCm39) missense probably damaging 1.00
R6464:Ceacam5 UTSW 7 17,481,391 (GRCm39) critical splice donor site probably null
R6521:Ceacam5 UTSW 7 17,484,756 (GRCm39) critical splice donor site probably null
R6568:Ceacam5 UTSW 7 17,479,416 (GRCm39) missense probably damaging 1.00
R6573:Ceacam5 UTSW 7 17,447,372 (GRCm39) start codon destroyed probably null 0.70
R6814:Ceacam5 UTSW 7 17,486,212 (GRCm39) nonsense probably null
R6872:Ceacam5 UTSW 7 17,486,212 (GRCm39) nonsense probably null
R6930:Ceacam5 UTSW 7 17,484,759 (GRCm39) splice site probably null
R7071:Ceacam5 UTSW 7 17,484,577 (GRCm39) missense possibly damaging 0.49
R7121:Ceacam5 UTSW 7 17,479,462 (GRCm39) missense probably benign 0.29
R7174:Ceacam5 UTSW 7 17,491,839 (GRCm39) critical splice donor site probably null
R7187:Ceacam5 UTSW 7 17,493,410 (GRCm39) missense possibly damaging 0.85
R7355:Ceacam5 UTSW 7 17,481,312 (GRCm39) missense probably damaging 1.00
R7411:Ceacam5 UTSW 7 17,484,678 (GRCm39) missense probably damaging 0.99
R7462:Ceacam5 UTSW 7 17,494,764 (GRCm39) missense probably damaging 1.00
R7612:Ceacam5 UTSW 7 17,493,341 (GRCm39) missense possibly damaging 0.86
R7803:Ceacam5 UTSW 7 17,493,317 (GRCm39) missense probably damaging 0.98
R7943:Ceacam5 UTSW 7 17,479,491 (GRCm39) missense probably benign 0.26
R8342:Ceacam5 UTSW 7 17,486,171 (GRCm39) missense possibly damaging 0.53
R8356:Ceacam5 UTSW 7 17,479,624 (GRCm39) missense possibly damaging 0.68
R8426:Ceacam5 UTSW 7 17,493,266 (GRCm39) missense possibly damaging 0.51
R8456:Ceacam5 UTSW 7 17,479,624 (GRCm39) missense possibly damaging 0.68
R8534:Ceacam5 UTSW 7 17,484,671 (GRCm39) missense probably benign 0.20
R8815:Ceacam5 UTSW 7 17,493,285 (GRCm39) missense possibly damaging 0.85
R8871:Ceacam5 UTSW 7 17,494,827 (GRCm39) missense probably benign 0.12
R9021:Ceacam5 UTSW 7 17,448,877 (GRCm39) missense possibly damaging 0.48
R9157:Ceacam5 UTSW 7 17,493,419 (GRCm39) missense possibly damaging 0.71
R9199:Ceacam5 UTSW 7 17,479,350 (GRCm39) missense probably benign 0.16
R9372:Ceacam5 UTSW 7 17,481,267 (GRCm39) missense possibly damaging 0.84
R9579:Ceacam5 UTSW 7 17,479,561 (GRCm39) missense probably damaging 1.00
R9605:Ceacam5 UTSW 7 17,493,520 (GRCm39) missense probably damaging 0.98
R9719:Ceacam5 UTSW 7 17,491,835 (GRCm39) missense probably damaging 0.97
X0020:Ceacam5 UTSW 7 17,494,834 (GRCm39) missense probably damaging 1.00
Posted On 2016-08-02