Incidental Mutation 'R6927:Cd300ld2'
ID 541173
Institutional Source Beutler Lab
Gene Symbol Cd300ld2
Ensembl Gene ENSMUSG00000089753
Gene Name CD300 molecule like family member D2
Synonyms Gm11709
MMRRC Submission 045044-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R6927 (G1)
Quality Score 225.009
Status Validated
Chromosome 11
Chromosomal Location 114901161-114907019 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 114904619 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Arginine to Tryptophan at position 83 (R83W)
Ref Sequence ENSEMBL: ENSMUSP00000102188 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000092463] [ENSMUST00000106578]
AlphaFold A2A7W0
Predicted Effect probably damaging
Transcript: ENSMUST00000092463
AA Change: R83W

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000090120
Gene: ENSMUSG00000089753
AA Change: R83W

DomainStartEndE-ValueType
signal peptide 1 18 N/A INTRINSIC
IG 25 124 2.11e-2 SMART
Predicted Effect probably damaging
Transcript: ENSMUST00000106578
AA Change: R83W

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000102188
Gene: ENSMUSG00000089753
AA Change: R83W

DomainStartEndE-ValueType
signal peptide 1 18 N/A INTRINSIC
IG 25 124 2.11e-2 SMART
low complexity region 131 201 N/A INTRINSIC
low complexity region 202 222 N/A INTRINSIC
transmembrane domain 240 262 N/A INTRINSIC
Meta Mutation Damage Score 0.6467 question?
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.0%
  • 20x: 96.1%
Validation Efficiency 98% (57/58)
Allele List at MGI
Other mutations in this stock
Total: 57 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcc10 A T 17: 46,635,317 (GRCm39) W229R probably damaging Het
Adck2 T C 6: 39,560,998 (GRCm39) probably null Het
Ahi1 A T 10: 20,930,968 (GRCm39) N936I probably damaging Het
Ass1 T C 2: 31,404,813 (GRCm39) S365P probably damaging Het
Atp9b T C 18: 80,935,072 (GRCm39) K208E possibly damaging Het
Bag6 G A 17: 35,364,898 (GRCm39) probably null Het
Bptf A T 11: 106,945,421 (GRCm39) V2491E probably damaging Het
Chrnd T C 1: 87,126,434 (GRCm39) F396L probably damaging Het
Cyp3a13 G A 5: 137,893,546 (GRCm39) P439S probably damaging Het
Dnhd1 C A 7: 105,364,770 (GRCm39) H4279N probably damaging Het
Fam118a T C 15: 84,929,038 (GRCm39) probably null Het
Fan1 T A 7: 64,022,234 (GRCm39) N340Y probably damaging Het
Fasn T A 11: 120,699,115 (GRCm39) D2386V probably benign Het
Fat1 G A 8: 45,477,532 (GRCm39) V2170I probably benign Het
Fdps T C 3: 89,000,958 (GRCm39) R374G probably benign Het
Fhl5 T C 4: 25,213,681 (GRCm39) D85G probably benign Het
Flvcr1 T C 1: 190,757,861 (GRCm39) M144V possibly damaging Het
Gask1b T C 3: 79,848,769 (GRCm39) I505T probably damaging Het
Gpr31b A G 17: 13,270,765 (GRCm39) S135P probably damaging Het
Hey2 A T 10: 30,710,413 (GRCm39) D113E probably benign Het
Hoxc5 T A 15: 102,923,807 (GRCm39) I201N probably damaging Het
Ighv1-50 A T 12: 115,083,794 (GRCm39) W3R probably damaging Het
Impa1 A G 3: 10,380,348 (GRCm39) I208T probably benign Het
Iqcj T C 3: 67,954,624 (GRCm39) L43P possibly damaging Het
Itga10 T C 3: 96,564,030 (GRCm39) F895L probably damaging Het
Kdm4b T C 17: 56,706,435 (GRCm39) C850R probably damaging Het
Krt25 A T 11: 99,208,205 (GRCm39) I341N probably damaging Het
L3mbtl3 T A 10: 26,168,567 (GRCm39) R621* probably null Het
Lipm T C 19: 34,078,563 (GRCm39) probably benign Het
Macrod2 A T 2: 142,098,441 (GRCm39) D286V probably damaging Het
Mad2l2 T A 4: 148,225,411 (GRCm39) V27E possibly damaging Het
Map4k4 T A 1: 40,050,842 (GRCm39) H768Q probably benign Het
Mgat4d A G 8: 84,081,496 (GRCm39) N83S probably benign Het
Nucb1 C T 7: 45,148,282 (GRCm39) R141H possibly damaging Het
Or2t46 A G 11: 58,472,491 (GRCm39) K274E possibly damaging Het
Pcdhga2 A C 18: 37,803,719 (GRCm39) D521A probably damaging Het
Pcnx1 T C 12: 81,964,586 (GRCm39) V251A probably benign Het
Pdf A T 8: 107,774,833 (GRCm39) M133K probably damaging Het
Piezo2 A G 18: 63,166,057 (GRCm39) F2058S probably damaging Het
Plekhb2 T A 1: 34,915,982 (GRCm39) probably null Het
Ppp2r3d G C 9: 101,052,547 (GRCm39) H221D probably damaging Het
Prl2c5 A T 13: 13,357,503 (GRCm39) probably null Het
Puf60 T A 15: 75,947,663 (GRCm39) M49L probably benign Het
Rdh16f1 T C 10: 127,624,561 (GRCm39) V133A probably benign Het
Robo2 T A 16: 73,778,946 (GRCm39) D389V probably damaging Het
Slc22a23 G T 13: 34,528,362 (GRCm39) A140D probably benign Het
Slc25a42 A G 8: 70,641,573 (GRCm39) L136P probably damaging Het
Slc36a3 T A 11: 55,020,519 (GRCm39) M284L probably damaging Het
Tas2r115 T A 6: 132,714,895 (GRCm39) I19F probably damaging Het
Tmc2 A G 2: 130,103,300 (GRCm39) H812R probably benign Het
Vmn2r26 A G 6: 124,016,057 (GRCm39) S174G possibly damaging Het
Vstm4 T A 14: 32,585,959 (GRCm39) probably null Het
Vwc2 C A 11: 11,104,250 (GRCm39) P261T probably damaging Het
Zfhx3 C G 8: 109,683,453 (GRCm39) H3631D unknown Het
Zfp335 A G 2: 164,735,640 (GRCm39) C1105R probably damaging Het
Zfp488 A G 14: 33,692,755 (GRCm39) L136P probably benign Het
Zzef1 G A 11: 72,803,983 (GRCm39) R2575H probably damaging Het
Other mutations in Cd300ld2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01012:Cd300ld2 APN 11 114,903,123 (GRCm39) missense probably benign 0.23
IGL01450:Cd300ld2 APN 11 114,903,369 (GRCm39) unclassified probably benign
IGL01452:Cd300ld2 APN 11 114,903,428 (GRCm39) unclassified probably benign
IGL02086:Cd300ld2 APN 11 114,903,384 (GRCm39) unclassified probably benign
IGL02111:Cd300ld2 APN 11 114,903,219 (GRCm39) unclassified probably benign
IGL02505:Cd300ld2 APN 11 114,904,513 (GRCm39) missense probably benign 0.11
IGL02517:Cd300ld2 APN 11 114,901,249 (GRCm39) missense possibly damaging 0.53
IGL02836:Cd300ld2 APN 11 114,904,576 (GRCm39) missense probably benign 0.07
IGL03081:Cd300ld2 APN 11 114,903,368 (GRCm39) unclassified probably benign
PIT4486001:Cd300ld2 UTSW 11 114,903,257 (GRCm39) small deletion probably benign
R0579:Cd300ld2 UTSW 11 114,903,125 (GRCm39) missense probably benign 0.23
R1065:Cd300ld2 UTSW 11 114,904,586 (GRCm39) missense probably damaging 1.00
R1393:Cd300ld2 UTSW 11 114,903,404 (GRCm39) unclassified probably benign
R1481:Cd300ld2 UTSW 11 114,903,459 (GRCm39) missense probably benign 0.36
R1583:Cd300ld2 UTSW 11 114,904,603 (GRCm39) missense probably benign 0.06
R1755:Cd300ld2 UTSW 11 114,904,601 (GRCm39) missense probably benign 0.01
R1865:Cd300ld2 UTSW 11 114,903,444 (GRCm39) unclassified probably benign
R4018:Cd300ld2 UTSW 11 114,903,330 (GRCm39) unclassified probably benign
R5516:Cd300ld2 UTSW 11 114,903,270 (GRCm39) unclassified probably benign
R6065:Cd300ld2 UTSW 11 114,903,428 (GRCm39) unclassified probably benign
R7874:Cd300ld2 UTSW 11 114,903,257 (GRCm39) small deletion probably benign
R7883:Cd300ld2 UTSW 11 114,903,257 (GRCm39) small deletion probably benign
R8044:Cd300ld2 UTSW 11 114,904,545 (GRCm39) nonsense probably null
R8263:Cd300ld2 UTSW 11 114,903,192 (GRCm39) missense unknown
R8306:Cd300ld2 UTSW 11 114,904,648 (GRCm39) missense probably benign 0.04
R8424:Cd300ld2 UTSW 11 114,903,257 (GRCm39) small deletion probably benign
R8808:Cd300ld2 UTSW 11 114,903,257 (GRCm39) small deletion probably benign
R8847:Cd300ld2 UTSW 11 114,903,257 (GRCm39) small deletion probably benign
R9090:Cd300ld2 UTSW 11 114,904,550 (GRCm39) missense probably damaging 1.00
R9176:Cd300ld2 UTSW 11 114,904,772 (GRCm39) nonsense probably null
R9271:Cd300ld2 UTSW 11 114,904,550 (GRCm39) missense probably damaging 1.00
R9494:Cd300ld2 UTSW 11 114,901,249 (GRCm39) missense possibly damaging 0.53
R9564:Cd300ld2 UTSW 11 114,903,257 (GRCm39) small deletion probably benign
R9720:Cd300ld2 UTSW 11 114,903,118 (GRCm39) critical splice donor site probably null
R9727:Cd300ld2 UTSW 11 114,903,257 (GRCm39) small deletion probably benign
Predicted Primers PCR Primer
(F):5'- CTTGGCAGGACAAATACAGTAGAC -3'
(R):5'- ATCCAGTCACAGGTCCAGAG -3'

Sequencing Primer
(F):5'- AGGACCCTTGATACTTCACCAGG -3'
(R):5'- TCACAGGTCCAGAGGAGGTG -3'
Posted On 2018-11-28