Incidental Mutation 'R3106:Ceacam5'
ID 263055
Institutional Source Beutler Lab
Gene Symbol Ceacam5
Ensembl Gene ENSMUSG00000008789
Gene Name CEA cell adhesion molecule 5
Synonyms Psg30, 1600029H12Rik
MMRRC Submission 040580-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.055) question?
Stock # R3106 (G1)
Quality Score 225
Status Validated
Chromosome 7
Chromosomal Location 17447163-17495057 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 17481248 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Histidine at position 332 (Y332H)
Ref Sequence ENSEMBL: ENSMUSP00000080582 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000081907]
AlphaFold Q3UKK2
Predicted Effect probably benign
Transcript: ENSMUST00000081907
AA Change: Y332H

PolyPhen 2 Score 0.056 (Sensitivity: 0.94; Specificity: 0.84)
SMART Domains Protein: ENSMUSP00000080582
Gene: ENSMUSG00000008789
AA Change: Y332H

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
Meta Mutation Damage Score 0.2178 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.4%
  • 20x: 95.7%
Validation Efficiency 100% (53/53)
Allele List at MGI
Other mutations in this stock
Total: 53 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca15 A T 7: 119,995,856 (GRCm39) E1331V possibly damaging Het
Adam22 A G 5: 8,167,583 (GRCm39) probably null Het
Adamts17 T A 7: 66,774,820 (GRCm39) S980T probably damaging Het
Adarb1 C A 10: 77,157,591 (GRCm39) K285N probably damaging Het
Atp5f1c A G 2: 10,068,276 (GRCm39) S160P probably benign Het
Baz2a AGCGGCGGTACTTGCGGG AG 10: 127,960,946 (GRCm39) probably null Het
Btf3 T G 13: 98,447,496 (GRCm39) E145D probably benign Het
Ccdc184 G T 15: 98,066,482 (GRCm39) A96S probably damaging Het
Ccdc191 T C 16: 43,751,573 (GRCm39) F301S probably damaging Het
Clip2 T C 5: 134,551,918 (GRCm39) K68R probably benign Het
Cntln C T 4: 84,875,406 (GRCm39) T280M possibly damaging Het
Col6a3 T C 1: 90,744,024 (GRCm39) R515G probably damaging Het
Ctnnal1 G A 4: 56,813,246 (GRCm39) L662F probably benign Het
Dennd3 C A 15: 73,436,973 (GRCm39) S118* probably null Het
Dgkg T A 16: 22,394,091 (GRCm39) T321S probably damaging Het
Dzip1l A T 9: 99,524,625 (GRCm39) K249* probably null Het
Dzip1l A G 9: 99,529,174 (GRCm39) E301G probably benign Het
Emc10 G A 7: 44,142,616 (GRCm39) R109W probably damaging Het
Ezh1 A C 11: 101,086,468 (GRCm39) C575W probably damaging Het
Fam187b A G 7: 30,676,665 (GRCm39) D58G probably benign Het
Galnt4 T C 10: 98,945,243 (GRCm39) Y323H probably benign Het
Grm1 A G 10: 10,955,601 (GRCm39) S228P probably benign Het
H1f2 G T 13: 23,922,883 (GRCm39) A18S unknown Het
Hnf4g T G 3: 3,717,916 (GRCm39) S388R probably benign Het
Il1rap A G 16: 26,541,502 (GRCm39) E581G probably benign Het
Lemd2 C A 17: 27,420,644 (GRCm39) L256F probably damaging Het
Mnd1 C A 3: 84,041,416 (GRCm39) C62F probably benign Het
Nphs1 C A 7: 30,166,965 (GRCm39) S724* probably null Het
Or4g17 A G 2: 111,209,840 (GRCm39) N165S probably benign Het
Or5w13 T C 2: 87,523,849 (GRCm39) I126V probably damaging Het
Osgep T C 14: 51,154,286 (GRCm39) T225A probably benign Het
Pan3 T C 5: 147,476,189 (GRCm39) probably benign Het
Pld3 A G 7: 27,235,212 (GRCm39) probably null Het
Plekha7 C T 7: 115,763,639 (GRCm39) R321K probably benign Het
Plekhg5 C T 4: 152,196,635 (GRCm39) T694M probably damaging Het
Pramel31 T C 4: 144,088,246 (GRCm39) V14A probably benign Het
Ptpn20 A G 14: 33,334,253 (GRCm39) I44V probably benign Het
Ptprj T A 2: 90,270,975 (GRCm39) H1251L probably damaging Het
Sbspon T C 1: 15,962,806 (GRCm39) E24G probably benign Het
Sfmbt1 G A 14: 30,539,753 (GRCm39) C847Y probably damaging Het
Sparcl1 T C 5: 104,241,203 (GRCm39) T74A probably benign Het
Sppl2b A G 10: 80,703,325 (GRCm39) E529G probably benign Het
Stradb C A 1: 59,031,450 (GRCm39) H212Q possibly damaging Het
Tkfc G T 19: 10,574,357 (GRCm39) C198* probably null Het
Tm4sf4 C T 3: 57,345,043 (GRCm39) R150C possibly damaging Het
Tmem212 T C 3: 27,939,019 (GRCm39) S156G probably damaging Het
Tmem51 T C 4: 141,765,035 (GRCm39) N8D probably damaging Het
Tmigd1 A G 11: 76,801,124 (GRCm39) T204A possibly damaging Het
Trp53bp1 A G 2: 121,067,133 (GRCm39) L531S probably damaging Het
Tsga10 G A 1: 37,840,872 (GRCm39) L445F probably damaging Het
Urb1 C T 16: 90,592,331 (GRCm39) V310I probably damaging Het
Vmn2r129 T A 4: 156,685,730 (GRCm39) noncoding transcript Het
Wdr19 T C 5: 65,359,966 (GRCm39) S24P probably benign 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
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
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
Predicted Primers PCR Primer
(F):5'- TCACCCTTTGCAAGTCAAGATCG -3'
(R):5'- GCAATGGGAAAGTCAATATGTCTAG -3'

Sequencing Primer
(F):5'- GAATCACTTCCTCAGAATGTTGCTG -3'
(R):5'- AGTTCCTTCTAGACAGTTCAGTG -3'
Posted On 2015-02-05