Incidental Mutation 'IGL02709:Dennd6b'
ID 304512
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Dennd6b
Ensembl Gene ENSMUSG00000015377
Gene Name DENN domain containing 6B
Synonyms Fam116b, 1700027J05Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.142) question?
Stock # IGL02709
Quality Score
Status
Chromosome 15
Chromosomal Location 89066416-89080699 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) A to T at 89075125 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000155612 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000078953] [ENSMUST00000229755]
AlphaFold Q9D9V7
Predicted Effect probably benign
Transcript: ENSMUST00000078953
SMART Domains Protein: ENSMUSP00000077978
Gene: ENSMUSG00000015377

DomainStartEndE-ValueType
low complexity region 4 31 N/A INTRINSIC
Pfam:Avl9 42 181 1.1e-8 PFAM
Pfam:DENN 148 344 1.2e-8 PFAM
Pfam:SPA 248 358 6.7e-16 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000229416
Predicted Effect probably benign
Transcript: ENSMUST00000229755
Predicted Effect noncoding transcript
Transcript: ENSMUST00000229935
Predicted Effect noncoding transcript
Transcript: ENSMUST00000230111
Predicted Effect noncoding transcript
Transcript: ENSMUST00000230823
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 46 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aadacl2fm2 A G 3: 59,654,619 (GRCm39) Y151C probably damaging Het
Aco1 G A 4: 40,180,199 (GRCm39) V367M possibly damaging Het
Acsm5 G A 7: 119,134,041 (GRCm39) W274* probably null Het
Ago1 G A 4: 126,347,433 (GRCm39) Q135* probably null Het
Bmpr1b A T 3: 141,562,314 (GRCm39) L291Q probably damaging Het
Cdcp1 A G 9: 123,002,879 (GRCm39) Y731H probably damaging Het
Clrn2 A G 5: 45,617,495 (GRCm39) N122S probably damaging Het
Col4a3 G T 1: 82,656,833 (GRCm39) G751W unknown Het
Ctsc C T 7: 87,957,347 (GRCm39) A294V probably damaging Het
Cyp26a1 T C 19: 37,688,426 (GRCm39) L316P probably damaging Het
Dnah10 T A 5: 124,850,809 (GRCm39) Y1659* probably null Het
Dspp A C 5: 104,325,116 (GRCm39) D493A unknown Het
Dyrk1a C T 16: 94,486,102 (GRCm39) A445V probably benign Het
E030025P04Rik C A 11: 109,030,324 (GRCm39) probably benign Het
Ecpas A G 4: 58,872,699 (GRCm39) S201P possibly damaging Het
Foxd4 T C 19: 24,876,973 (GRCm39) H409R probably damaging Het
Fubp3 A G 2: 31,485,343 (GRCm39) probably benign Het
Herc1 A G 9: 66,404,962 (GRCm39) K4511E probably damaging Het
Ifna1 A G 4: 88,768,523 (GRCm39) D67G probably benign Het
Map1lc3b T A 8: 122,322,768 (GRCm39) L82Q probably damaging Het
Mcc A T 18: 44,578,877 (GRCm39) S844T possibly damaging Het
Mccc1 A T 3: 36,044,888 (GRCm39) *85K probably null Het
Memo1 G A 17: 74,552,027 (GRCm39) L90F probably damaging Het
Mfrp A G 9: 44,014,561 (GRCm39) H236R probably benign Het
Mmrn1 G A 6: 60,950,030 (GRCm39) D327N probably damaging Het
Mycbp2 T C 14: 103,392,697 (GRCm39) E3178G probably damaging Het
Pcsk9 A G 4: 106,304,886 (GRCm39) probably benign Het
Pros1 T C 16: 62,719,308 (GRCm39) L110P probably damaging Het
Reck A G 4: 43,913,791 (GRCm39) Y215C probably damaging Het
Ripk4 T C 16: 97,544,766 (GRCm39) D627G probably damaging Het
Rnf144a G T 12: 26,371,009 (GRCm39) H151N probably damaging Het
Slc39a9 T A 12: 80,713,421 (GRCm39) H106Q probably damaging Het
Stab2 A G 10: 86,682,029 (GRCm39) probably benign Het
Sympk T G 7: 18,781,463 (GRCm39) H806Q probably benign Het
Tars2 C A 3: 95,649,383 (GRCm39) probably benign Het
Thap3 T A 4: 152,070,169 (GRCm39) H75L probably damaging Het
Trappc8 T C 18: 20,970,235 (GRCm39) I918M possibly damaging Het
Ube2j2 T C 4: 156,041,788 (GRCm39) V249A probably damaging Het
Ubqln3 T G 7: 103,790,543 (GRCm39) T516P probably benign Het
Unc13c A G 9: 73,466,238 (GRCm39) S1810P probably benign Het
Vmn1r4 T A 6: 56,933,524 (GRCm39) Y9* probably null Het
Vmn1r89 T A 7: 12,954,131 (GRCm39) M221K probably damaging Het
Vmn2r1 G T 3: 64,012,355 (GRCm39) V739F probably benign Het
Vmn2r25 C T 6: 123,816,723 (GRCm39) R286Q possibly damaging Het
Vmn2r91 T A 17: 18,325,711 (GRCm39) Y110N possibly damaging Het
Zbtb48 T C 4: 152,105,851 (GRCm39) H418R probably damaging Het
Other mutations in Dennd6b
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL03109:Dennd6b APN 15 89,069,188 (GRCm39) utr 3 prime probably benign
IGL03133:Dennd6b APN 15 89,072,726 (GRCm39) critical splice acceptor site probably null
P0016:Dennd6b UTSW 15 89,071,180 (GRCm39) missense probably benign
PIT4791001:Dennd6b UTSW 15 89,070,955 (GRCm39) critical splice donor site probably null
R0025:Dennd6b UTSW 15 89,070,386 (GRCm39) missense probably benign 0.11
R0025:Dennd6b UTSW 15 89,070,386 (GRCm39) missense probably benign 0.11
R0268:Dennd6b UTSW 15 89,080,432 (GRCm39) missense probably benign 0.01
R0344:Dennd6b UTSW 15 89,080,432 (GRCm39) missense probably benign 0.01
R0391:Dennd6b UTSW 15 89,071,417 (GRCm39) missense probably damaging 1.00
R1453:Dennd6b UTSW 15 89,073,075 (GRCm39) missense probably damaging 0.99
R1655:Dennd6b UTSW 15 89,080,543 (GRCm39) missense unknown
R1670:Dennd6b UTSW 15 89,069,540 (GRCm39) intron probably benign
R1765:Dennd6b UTSW 15 89,074,506 (GRCm39) nonsense probably null
R1968:Dennd6b UTSW 15 89,074,544 (GRCm39) missense possibly damaging 0.63
R3692:Dennd6b UTSW 15 89,071,030 (GRCm39) splice site probably benign
R4344:Dennd6b UTSW 15 89,072,866 (GRCm39) missense probably benign 0.00
R4736:Dennd6b UTSW 15 89,069,795 (GRCm39) missense probably benign 0.00
R5030:Dennd6b UTSW 15 89,080,454 (GRCm39) missense possibly damaging 0.82
R5058:Dennd6b UTSW 15 89,071,553 (GRCm39) missense possibly damaging 0.69
R5509:Dennd6b UTSW 15 89,069,225 (GRCm39) missense probably damaging 1.00
R6005:Dennd6b UTSW 15 89,072,371 (GRCm39) missense possibly damaging 0.91
R6160:Dennd6b UTSW 15 89,073,024 (GRCm39) missense probably damaging 0.97
R6535:Dennd6b UTSW 15 89,070,570 (GRCm39) missense probably damaging 1.00
R6646:Dennd6b UTSW 15 89,070,387 (GRCm39) missense probably damaging 0.99
R7098:Dennd6b UTSW 15 89,072,890 (GRCm39) missense probably damaging 1.00
R7169:Dennd6b UTSW 15 89,073,055 (GRCm39) missense possibly damaging 0.80
R7381:Dennd6b UTSW 15 89,070,376 (GRCm39) missense possibly damaging 0.84
R7706:Dennd6b UTSW 15 89,069,447 (GRCm39) missense probably benign 0.19
R8070:Dennd6b UTSW 15 89,069,576 (GRCm39) missense probably benign 0.29
R8803:Dennd6b UTSW 15 89,070,383 (GRCm39) missense probably benign 0.01
R8927:Dennd6b UTSW 15 89,069,780 (GRCm39) frame shift probably null
R9291:Dennd6b UTSW 15 89,071,590 (GRCm39) missense possibly damaging 0.95
X0063:Dennd6b UTSW 15 89,069,623 (GRCm39) missense probably damaging 1.00
Posted On 2015-04-16