Incidental Mutation 'IGL01314:Ceacam5'
ID 73801
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 # IGL01314
Quality Score
Status
Chromosome 7
Chromosomal Location 17447163-17495057 bp(+) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) T to A at 17481181 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Stop codon at position 309 (Y309*)
Ref Sequence ENSEMBL: ENSMUSP00000080582 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000081907]
AlphaFold Q3UKK2
Predicted Effect probably null
Transcript: ENSMUST00000081907
AA Change: Y309*
SMART Domains Protein: ENSMUSP00000080582
Gene: ENSMUSG00000008789
AA Change: Y309*

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: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adamts12 C T 15: 11,071,939 (GRCm39) A161V probably benign Het
Bptf A T 11: 106,945,679 (GRCm39) V2520E probably damaging Het
C87436 T C 6: 86,434,837 (GRCm39) F395S probably damaging Het
Capn1 T C 19: 6,040,014 (GRCm39) probably benign Het
Clasp2 A G 9: 113,735,195 (GRCm39) D1011G possibly damaging Het
Csmd3 A G 15: 47,713,151 (GRCm39) Y1608H probably damaging Het
Dcaf1 T C 9: 106,711,390 (GRCm39) I77T probably benign Het
Dcdc2a T C 13: 25,286,587 (GRCm39) L170P probably damaging Het
Ddx28 A G 8: 106,737,212 (GRCm39) F282S probably damaging Het
Egf A G 3: 129,479,909 (GRCm39) I497T probably benign Het
Emsy A G 7: 98,242,662 (GRCm39) V1159A probably benign Het
Hk3 C A 13: 55,154,876 (GRCm39) probably benign Het
Htt A G 5: 35,036,200 (GRCm39) D2049G probably benign Het
Inpp5d C A 1: 87,611,472 (GRCm39) S45* probably null Het
Irf8 A G 8: 121,480,119 (GRCm39) Y119C probably damaging Het
Klk1b4 T C 7: 43,860,600 (GRCm39) probably null Het
Macf1 A G 4: 123,380,513 (GRCm39) S1273P probably damaging Het
Man2c1 A T 9: 57,049,103 (GRCm39) H867L probably benign Het
Mgat4e T C 1: 134,469,187 (GRCm39) T286A probably damaging Het
Mug2 T C 6: 122,058,238 (GRCm39) F1267L possibly damaging Het
Necab1 T A 4: 15,005,079 (GRCm39) E128D probably damaging Het
Or10ak9 G A 4: 118,726,328 (GRCm39) V117I probably benign Het
Pds5a A G 5: 65,772,637 (GRCm39) V1322A probably benign Het
Poc1b C T 10: 98,965,503 (GRCm39) T144I probably damaging Het
Prcc T A 3: 87,777,387 (GRCm39) N196Y probably damaging Het
Psma5 G A 3: 108,187,111 (GRCm39) V237M possibly damaging Het
Rap1gds1 A G 3: 138,756,322 (GRCm39) L11P probably damaging Het
Rapgef3 A G 15: 97,646,104 (GRCm39) F132S probably damaging Het
Rgs13 T G 1: 144,047,179 (GRCm39) D14A probably benign Het
Rlig1 A C 10: 100,409,473 (GRCm39) D313E probably damaging Het
Stxbp4 A G 11: 90,512,475 (GRCm39) probably benign Het
Tcerg1 C A 18: 42,706,374 (GRCm39) A1017D probably damaging Het
Tent5c T C 3: 100,380,490 (GRCm39) K89E probably benign Het
Tmem79 T C 3: 88,239,883 (GRCm39) I276V possibly damaging Het
Tmem94 C A 11: 115,680,835 (GRCm39) H113N probably damaging Het
Vil1 G A 1: 74,467,397 (GRCm39) D715N probably damaging Het
Vmn2r96 A G 17: 18,803,226 (GRCm39) T187A probably benign Het
Zfhx4 T A 3: 5,478,154 (GRCm39) S3590T 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
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
IGL03395:Ceacam5 APN 7 17,479,304 (GRCm39) splice site probably benign
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 2013-10-07