Incidental Mutation 'R0060:Colec10'
ID 16370
Institutional Source Beutler Lab
Gene Symbol Colec10
Ensembl Gene ENSMUSG00000038591
Gene Name collectin sub-family member 10
Synonyms CL-L1
MMRRC Submission 038353-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R0060 (G1)
Quality Score
Status Validated
Chromosome 15
Chromosomal Location 54274170-54329754 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) G to A at 54302542 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000037867 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000036737]
AlphaFold Q8CF98
Predicted Effect probably benign
Transcript: ENSMUST00000036737
SMART Domains Protein: ENSMUSP00000037867
Gene: ENSMUSG00000038591

DomainStartEndE-ValueType
signal peptide 1 27 N/A INTRINSIC
Pfam:Collagen 44 96 1.4e-9 PFAM
Pfam:Collagen 65 123 4.3e-10 PFAM
CLECT 148 271 1.09e-16 SMART
Coding Region Coverage
  • 1x: 90.4%
  • 3x: 88.3%
  • 10x: 83.8%
  • 20x: 78.1%
Validation Efficiency 94% (74/79)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the C-lectin family, proteins that possess collagen-like sequences and carbohydrate recognition domains. The other members of this family are secreted proteins and bind to carbohydrate antigens on microorganisms facilitating their recognition and removal. This gene product is a cytosolic protein, a characteristic that suggests that it may have different biological functions than other C-lectins. [provided by RefSeq, Jul 2008]
Allele List at MGI
Other mutations in this stock
Total: 52 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1810065E05Rik A C 11: 58,313,008 (GRCm39) probably benign Het
4930432E11Rik A G 7: 29,273,595 (GRCm39) noncoding transcript Het
A630091E08Rik A G 7: 98,192,875 (GRCm39) noncoding transcript Het
Abca8a T C 11: 109,961,306 (GRCm39) T539A probably damaging Het
Adam34 A T 8: 44,128,920 (GRCm39) probably benign Het
Ankrd60 A T 2: 173,414,406 (GRCm39) M1K probably null Het
Cald1 T C 6: 34,692,394 (GRCm39) probably benign Het
Capn7 T C 14: 31,087,561 (GRCm39) probably benign Het
Cd109 G A 9: 78,610,389 (GRCm39) E1145K probably damaging Het
Celsr1 A T 15: 85,806,399 (GRCm39) V2353D probably damaging Het
Cep135 A T 5: 76,769,197 (GRCm39) I616F probably benign Het
Cep162 T A 9: 87,119,878 (GRCm39) probably benign Het
Cep350 C T 1: 155,804,372 (GRCm39) D904N probably damaging Het
Cep85 T C 4: 133,894,611 (GRCm39) D65G probably damaging Het
Cfdp1 T C 8: 112,566,986 (GRCm39) probably benign Het
Chl1 T A 6: 103,688,019 (GRCm39) probably benign Het
Crxos A G 7: 15,632,448 (GRCm39) T40A possibly damaging Het
Dnhd1 A G 7: 105,317,721 (GRCm39) D472G probably damaging Het
Dpp6 C A 5: 27,803,817 (GRCm39) N254K probably damaging Het
Eps8l3 T C 3: 107,786,857 (GRCm39) L11S probably damaging Het
Flad1 G A 3: 89,309,552 (GRCm39) R515* probably null Het
Fzd5 T C 1: 64,774,835 (GRCm39) T309A probably benign Het
Gm19685 T C 17: 61,075,418 (GRCm39) Het
Gsdme A G 6: 50,198,009 (GRCm39) I317T possibly damaging Het
H2bc1 A T 13: 24,117,928 (GRCm39) I71N possibly damaging Het
Incenp A G 19: 9,862,823 (GRCm39) probably benign Het
Itgad T C 7: 127,802,158 (GRCm39) S979P probably damaging Het
Kat2b T C 17: 53,961,571 (GRCm39) V557A probably damaging Het
Lamc1 A T 1: 153,117,614 (GRCm39) probably benign Het
Lgi4 G A 7: 30,762,996 (GRCm39) G157D probably damaging Het
Mga T C 2: 119,791,442 (GRCm39) probably null Het
Nubpl T C 12: 52,357,470 (GRCm39) probably benign Het
Or2b4 T C 17: 38,116,891 (GRCm39) L285P probably damaging Het
Or5be3 T C 2: 86,864,118 (GRCm39) Y149C probably damaging Het
Or8c20 C T 9: 38,260,808 (GRCm39) S143F probably benign Het
Peak1 A T 9: 56,135,107 (GRCm39) I78K probably damaging Het
Prune2 T A 19: 16,981,097 (GRCm39) F85I probably damaging Het
Rbm11 G T 16: 75,395,667 (GRCm39) D113Y probably damaging Het
Rif1 C T 2: 52,001,129 (GRCm39) R1528C probably damaging Het
Sema4d A G 13: 51,859,293 (GRCm39) probably benign Het
Slc30a4 T A 2: 122,527,104 (GRCm39) T381S probably benign Het
Slf2 G T 19: 44,936,443 (GRCm39) G696V probably damaging Het
Suv39h2 T C 2: 3,465,953 (GRCm39) Y134C probably damaging Het
Tmem273 C A 14: 32,528,726 (GRCm39) probably benign Het
Tmem89 T A 9: 108,744,485 (GRCm39) V126D probably damaging Het
Trf T C 9: 103,098,121 (GRCm39) T46A probably benign Het
Trmt6 C T 2: 132,648,689 (GRCm39) R415Q possibly damaging Het
Trp53bp1 T C 2: 121,035,006 (GRCm39) K1625E probably damaging Het
Usp6nl T A 2: 6,445,701 (GRCm39) D559E probably benign Het
Wdr75 A G 1: 45,855,777 (GRCm39) D476G probably benign Het
Wrap53 A C 11: 69,454,256 (GRCm39) L261V possibly damaging Het
Zcchc4 T A 5: 52,964,420 (GRCm39) I292N possibly damaging Het
Other mutations in Colec10
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01313:Colec10 APN 15 54,323,157 (GRCm39) missense probably damaging 0.98
BB002:Colec10 UTSW 15 54,325,767 (GRCm39) missense probably damaging 0.97
BB012:Colec10 UTSW 15 54,325,767 (GRCm39) missense probably damaging 0.97
R0004:Colec10 UTSW 15 54,274,271 (GRCm39) missense possibly damaging 0.57
R0060:Colec10 UTSW 15 54,302,542 (GRCm39) splice site probably benign
R0827:Colec10 UTSW 15 54,325,980 (GRCm39) missense probably damaging 1.00
R1238:Colec10 UTSW 15 54,325,835 (GRCm39) missense possibly damaging 0.75
R1551:Colec10 UTSW 15 54,325,658 (GRCm39) missense probably damaging 1.00
R2371:Colec10 UTSW 15 54,325,796 (GRCm39) missense possibly damaging 0.84
R4023:Colec10 UTSW 15 54,325,947 (GRCm39) missense probably damaging 1.00
R4024:Colec10 UTSW 15 54,325,947 (GRCm39) missense probably damaging 1.00
R4628:Colec10 UTSW 15 54,323,127 (GRCm39) missense possibly damaging 0.68
R5893:Colec10 UTSW 15 54,274,185 (GRCm39) missense probably benign 0.18
R6062:Colec10 UTSW 15 54,323,203 (GRCm39) missense possibly damaging 0.93
R6489:Colec10 UTSW 15 54,325,609 (GRCm39) splice site probably null
R6775:Colec10 UTSW 15 54,298,419 (GRCm39) missense possibly damaging 0.95
R6928:Colec10 UTSW 15 54,326,002 (GRCm39) missense probably damaging 1.00
R7124:Colec10 UTSW 15 54,325,767 (GRCm39) missense probably damaging 0.97
R7925:Colec10 UTSW 15 54,325,767 (GRCm39) missense probably damaging 0.97
R8208:Colec10 UTSW 15 54,325,696 (GRCm39) missense possibly damaging 0.62
R8363:Colec10 UTSW 15 54,274,238 (GRCm39) missense probably benign
R8691:Colec10 UTSW 15 54,298,420 (GRCm39) missense probably benign 0.01
R9495:Colec10 UTSW 15 54,325,761 (GRCm39) missense probably damaging 0.97
R9712:Colec10 UTSW 15 54,323,180 (GRCm39) missense possibly damaging 0.77
RF003:Colec10 UTSW 15 54,325,787 (GRCm39) missense possibly damaging 0.50
Posted On 2013-01-20