Incidental Mutation 'R3771:Adam26b'
ID 273275
Institutional Source Beutler Lab
Gene Symbol Adam26b
Ensembl Gene ENSMUSG00000063900
Gene Name a disintegrin and metallopeptidase domain 26B
Synonyms
MMRRC Submission 040747-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.063) question?
Stock # R3771 (G1)
Quality Score 225
Status Validated
Chromosome 8
Chromosomal Location 43972901-43981174 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 43973751 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Valine at position 417 (D417V)
Ref Sequence ENSEMBL: ENSMUSP00000079032 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000080135]
AlphaFold Q6IMH6
Predicted Effect probably damaging
Transcript: ENSMUST00000080135
AA Change: D417V

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000079032
Gene: ENSMUSG00000063900
AA Change: D417V

DomainStartEndE-ValueType
signal peptide 1 22 N/A INTRINSIC
Pfam:Pep_M12B_propep 29 147 4.9e-18 PFAM
Pfam:Reprolysin_5 193 364 4.8e-15 PFAM
Pfam:Reprolysin_4 194 380 1.3e-8 PFAM
Pfam:Reprolysin 195 385 9.9e-50 PFAM
Pfam:Reprolysin_2 215 377 3.9e-15 PFAM
Pfam:Reprolysin_3 219 340 2e-15 PFAM
DISIN 401 476 5.88e-40 SMART
ACR 477 613 7.69e-64 SMART
low complexity region 631 642 N/A INTRINSIC
transmembrane domain 670 692 N/A INTRINSIC
Meta Mutation Damage Score 0.6467 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.3%
  • 20x: 95.3%
Validation Efficiency 99% (69/70)
Allele List at MGI
Other mutations in this stock
Total: 65 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aanat G T 11: 116,487,697 (GRCm39) G132V probably damaging Het
Abcb11 T A 2: 69,159,720 (GRCm39) probably benign Het
Ank1 T C 8: 23,613,913 (GRCm39) S1482P probably benign Het
Aoc1l2 T C 6: 48,908,130 (GRCm39) Y377H probably damaging Het
Armc2 C T 10: 41,798,223 (GRCm39) V768M probably damaging Het
Ascc3 C T 10: 50,596,814 (GRCm39) probably benign Het
Birc6 T A 17: 74,925,424 (GRCm39) probably benign Het
Cd109 CATTTATTTATTTATTTATTTATTTATTTATTTAT CATTTATTTATTTATTTATTTATTTATTTATTTATTTAT 9: 78,619,782 (GRCm39) probably benign Het
Cdh12 A T 15: 21,578,640 (GRCm39) probably benign Het
Chd1 A G 17: 17,594,913 (GRCm39) D16G probably damaging Het
Clstn2 A G 9: 97,464,615 (GRCm39) I180T probably damaging Het
Cxcr6 A G 9: 123,639,550 (GRCm39) I184V probably benign Het
Dagla G A 19: 10,225,831 (GRCm39) P778S possibly damaging Het
Ddx19b T C 8: 111,747,613 (GRCm39) K107R probably benign Het
Dpyd G A 3: 119,205,927 (GRCm39) probably null Het
Elf1 T C 14: 79,804,650 (GRCm39) V105A possibly damaging Het
Fam13a T G 6: 58,964,171 (GRCm39) K87T probably benign Het
Fap C A 2: 62,363,354 (GRCm39) S359I probably damaging Het
Fbxo39 T C 11: 72,208,041 (GRCm39) I131T possibly damaging Het
Fmn1 T G 2: 113,412,463 (GRCm39) S996A probably damaging Het
Gm5866 T C 5: 52,740,088 (GRCm39) noncoding transcript Het
Hmcn2 C T 2: 31,250,908 (GRCm39) T790M probably damaging Het
Irf2bp2 T C 8: 127,318,550 (GRCm39) K339E probably damaging Het
Kat6b A G 14: 21,567,166 (GRCm39) D75G probably damaging Het
Kcnab3 A G 11: 69,219,389 (GRCm39) T127A probably damaging Het
Kdm5b G T 1: 134,541,083 (GRCm39) C725F probably damaging Het
Lrp5 G A 19: 3,662,330 (GRCm39) R173C probably damaging Het
Lrrn3 T A 12: 41,502,869 (GRCm39) I483L probably damaging Het
Man2c1 C A 9: 57,047,661 (GRCm39) probably benign Het
Med23 G T 10: 24,778,099 (GRCm39) G810C probably damaging Het
Nhlrc4 T A 17: 26,162,367 (GRCm39) K127* probably null Het
Numb T C 12: 83,846,350 (GRCm39) D344G probably damaging Het
Nup210l T G 3: 90,027,201 (GRCm39) Y194* probably null Het
Ogg1 T C 6: 113,310,804 (GRCm39) V317A possibly damaging Het
Or1o2 T A 17: 37,542,356 (GRCm39) I302F possibly damaging Het
Or6c69c A G 10: 129,911,143 (GRCm39) Y288C probably damaging Het
Pclo A T 5: 14,589,422 (GRCm39) probably null Het
Pnpt1 T C 11: 29,088,174 (GRCm39) M195T probably benign Het
Polr3c T A 3: 96,633,170 (GRCm39) T43S probably damaging Het
Ptprs T C 17: 56,735,978 (GRCm39) T152A possibly damaging Het
Rasl10b A T 11: 83,309,349 (GRCm39) T134S probably benign Het
Rin2 C T 2: 145,702,366 (GRCm39) T354I probably benign Het
Rnf39 T C 17: 37,258,121 (GRCm39) W96R probably damaging Het
Ros1 G T 10: 52,005,087 (GRCm39) A949E probably damaging Het
Rwdd2a A C 9: 86,456,214 (GRCm39) N130T possibly damaging Het
Scn9a T C 2: 66,313,992 (GRCm39) N1909D probably benign Het
Shisal1 A T 15: 84,290,886 (GRCm39) Y120* probably null Het
Ska3 C T 14: 58,047,534 (GRCm39) V334I probably benign Het
Srebf2 A G 15: 82,066,309 (GRCm39) K579R probably benign Het
Sun1 A G 5: 139,224,575 (GRCm39) probably benign Het
Tc2n T A 12: 101,660,833 (GRCm39) Q133L possibly damaging Het
Tecta T C 9: 42,242,292 (GRCm39) T2094A probably damaging Het
Tex2 T C 11: 106,437,720 (GRCm39) D650G unknown Het
Trio A G 15: 27,748,177 (GRCm39) S2492P probably damaging Het
Ttn T C 2: 76,601,711 (GRCm39) T16872A probably benign Het
Ugcg T C 4: 59,189,690 (GRCm39) F16S probably benign Het
Usp16 T C 16: 87,255,571 (GRCm39) M1T probably null Het
Vmn1r60 C A 7: 5,547,710 (GRCm39) C130F possibly damaging Het
Vmn2r101 A G 17: 19,809,919 (GRCm39) D235G probably benign Het
Vpreb3 A T 10: 75,775,800 (GRCm39) V26E probably benign Het
Vps39 C T 2: 120,172,497 (GRCm39) V179I possibly damaging Het
Xrn2 T C 2: 146,903,207 (GRCm39) V765A probably benign Het
Zfp251 A G 15: 76,737,836 (GRCm39) I414T possibly damaging Het
Zfp426 A T 9: 20,384,413 (GRCm39) probably null Het
Zfp61 T C 7: 23,995,406 (GRCm39) M1V probably null Het
Other mutations in Adam26b
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00703:Adam26b APN 8 43,973,216 (GRCm39) missense probably damaging 1.00
IGL00806:Adam26b APN 8 43,974,379 (GRCm39) missense probably damaging 1.00
IGL00984:Adam26b APN 8 43,973,410 (GRCm39) missense possibly damaging 0.86
IGL01081:Adam26b APN 8 43,972,975 (GRCm39) missense probably benign 0.00
IGL01783:Adam26b APN 8 43,974,798 (GRCm39) missense probably benign 0.30
IGL02021:Adam26b APN 8 43,972,909 (GRCm39) missense probably benign
IGL02707:Adam26b APN 8 43,972,895 (GRCm39) utr 3 prime probably benign
IGL03112:Adam26b APN 8 43,974,549 (GRCm39) missense probably benign
R0195:Adam26b UTSW 8 43,973,307 (GRCm39) missense probably damaging 0.99
R0453:Adam26b UTSW 8 43,973,387 (GRCm39) missense probably benign 0.00
R0562:Adam26b UTSW 8 43,973,408 (GRCm39) missense probably benign 0.36
R0645:Adam26b UTSW 8 43,973,524 (GRCm39) missense probably damaging 1.00
R0763:Adam26b UTSW 8 43,973,601 (GRCm39) missense probably damaging 1.00
R1697:Adam26b UTSW 8 43,974,000 (GRCm39) missense probably damaging 0.98
R1739:Adam26b UTSW 8 43,974,714 (GRCm39) missense probably damaging 1.00
R1751:Adam26b UTSW 8 43,972,948 (GRCm39) missense probably benign 0.00
R1767:Adam26b UTSW 8 43,972,948 (GRCm39) missense probably benign 0.00
R1994:Adam26b UTSW 8 43,973,676 (GRCm39) missense probably benign 0.44
R3747:Adam26b UTSW 8 43,974,234 (GRCm39) missense probably benign 0.07
R3748:Adam26b UTSW 8 43,974,234 (GRCm39) missense probably benign 0.07
R3750:Adam26b UTSW 8 43,974,234 (GRCm39) missense probably benign 0.07
R4027:Adam26b UTSW 8 43,973,409 (GRCm39) missense probably benign 0.09
R4652:Adam26b UTSW 8 43,974,375 (GRCm39) missense possibly damaging 0.49
R4790:Adam26b UTSW 8 43,973,764 (GRCm39) missense probably benign 0.19
R4859:Adam26b UTSW 8 43,973,296 (GRCm39) missense possibly damaging 0.80
R5059:Adam26b UTSW 8 43,973,637 (GRCm39) missense probably damaging 1.00
R5191:Adam26b UTSW 8 43,973,028 (GRCm39) missense probably damaging 1.00
R5540:Adam26b UTSW 8 43,974,654 (GRCm39) missense probably damaging 1.00
R5568:Adam26b UTSW 8 43,973,529 (GRCm39) missense probably benign 0.00
R5886:Adam26b UTSW 8 43,973,310 (GRCm39) missense possibly damaging 0.72
R5935:Adam26b UTSW 8 43,974,335 (GRCm39) missense probably benign 0.00
R5983:Adam26b UTSW 8 43,974,378 (GRCm39) missense probably damaging 1.00
R6544:Adam26b UTSW 8 43,974,818 (GRCm39) missense probably damaging 0.98
R6610:Adam26b UTSW 8 43,974,190 (GRCm39) missense probably damaging 1.00
R6668:Adam26b UTSW 8 43,973,727 (GRCm39) missense possibly damaging 0.72
R6966:Adam26b UTSW 8 43,974,472 (GRCm39) missense possibly damaging 0.51
R7545:Adam26b UTSW 8 43,974,750 (GRCm39) missense probably damaging 0.98
R7596:Adam26b UTSW 8 43,973,237 (GRCm39) missense probably benign
R7634:Adam26b UTSW 8 43,974,034 (GRCm39) missense probably benign
R7657:Adam26b UTSW 8 43,974,579 (GRCm39) missense possibly damaging 0.95
R7692:Adam26b UTSW 8 43,973,832 (GRCm39) missense probably benign 0.00
R7769:Adam26b UTSW 8 43,974,732 (GRCm39) missense probably benign 0.00
R7912:Adam26b UTSW 8 43,973,245 (GRCm39) missense probably benign 0.13
R7918:Adam26b UTSW 8 43,974,138 (GRCm39) missense probably benign 0.14
R8286:Adam26b UTSW 8 43,972,998 (GRCm39) missense probably benign 0.05
R8897:Adam26b UTSW 8 43,974,009 (GRCm39) missense possibly damaging 0.91
R8922:Adam26b UTSW 8 43,973,216 (GRCm39) missense probably damaging 1.00
R9075:Adam26b UTSW 8 43,973,405 (GRCm39) missense probably benign 0.07
R9225:Adam26b UTSW 8 43,973,453 (GRCm39) nonsense probably null
X0066:Adam26b UTSW 8 43,973,041 (GRCm39) missense probably damaging 0.97
Z1088:Adam26b UTSW 8 43,973,634 (GRCm39) missense probably damaging 0.99
Z1177:Adam26b UTSW 8 43,974,459 (GRCm39) missense probably benign 0.03
Z1177:Adam26b UTSW 8 43,973,735 (GRCm39) missense probably benign 0.24
Predicted Primers PCR Primer
(F):5'- TCACCACTGCAAGGGATTCC -3'
(R):5'- CTGTCTAATGGCCCCATATAAAAC -3'

Sequencing Primer
(F):5'- ACTGCAAGGGATTCCGTCTG -3'
(R):5'- TGGCCCCATATAAAACAAATTCTC -3'
Posted On 2015-03-25