Incidental Mutation 'R5751:Adam6a'
ID 446014
Institutional Source Beutler Lab
Gene Symbol Adam6a
Ensembl Gene ENSMUSG00000043945
Gene Name a disintegrin and metallopeptidase domain 6A
Synonyms Adam6
MMRRC Submission 043201-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.072) question?
Stock # R5751 (G1)
Quality Score 225
Status Not validated
Chromosome 12
Chromosomal Location 113507528-113510034 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 113508447 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Glutamic Acid at position 273 (D273E)
Ref Sequence ENSEMBL: ENSMUSP00000059315 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000053086]
AlphaFold B2RSY5
Predicted Effect possibly damaging
Transcript: ENSMUST00000053086
AA Change: D273E

PolyPhen 2 Score 0.792 (Sensitivity: 0.85; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000059315
Gene: ENSMUSG00000043945
AA Change: D273E

DomainStartEndE-ValueType
Pfam:Pep_M12B_propep 30 167 6.9e-17 PFAM
Pfam:Reprolysin 222 407 4e-15 PFAM
DISIN 427 502 1.63e-33 SMART
ACR 503 640 7.46e-62 SMART
transmembrane domain 704 726 N/A INTRINSIC
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.6%
  • 10x: 97.3%
  • 20x: 95.3%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 37 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acacb A G 5: 114,368,893 (GRCm39) T1704A possibly damaging Het
Adgrv1 T A 13: 81,670,355 (GRCm39) L1610F probably damaging Het
Ago2 C T 15: 73,000,172 (GRCm39) probably null Het
Apob T A 12: 8,062,619 (GRCm39) Y87* probably null Het
Aqp7 G A 4: 41,035,510 (GRCm39) T115I probably benign Het
Atp7b A G 8: 22,508,144 (GRCm39) V599A probably damaging Het
Dnah1 T A 14: 31,032,863 (GRCm39) I391F probably benign Het
Emc2 A G 15: 43,360,453 (GRCm39) probably null Het
Gbp9 G T 5: 105,229,124 (GRCm39) Q508K probably benign Het
Grpel1 C T 5: 36,626,811 (GRCm39) T31M probably benign Het
Gtf3c4 C T 2: 28,717,511 (GRCm39) A790T probably damaging Het
Hmcn1 A G 1: 150,449,305 (GRCm39) C115R probably damaging Het
Ik G A 18: 36,886,566 (GRCm39) R346H probably benign Het
Ldc1 A C 4: 130,114,234 (GRCm39) V61G probably benign Het
Lhx3 A G 2: 26,091,173 (GRCm39) S379P probably benign Het
Mocs1 A G 17: 49,756,766 (GRCm39) probably null Het
Mycbp2 C A 14: 103,385,986 (GRCm39) V3457F probably damaging Het
Or14j7 A T 17: 38,234,861 (GRCm39) I135L probably benign Het
Or4a2 A T 2: 89,248,031 (GRCm39) I242N probably damaging Het
Or5an6 G A 19: 12,371,780 (GRCm39) R51K probably benign Het
Orc5 C T 5: 22,704,969 (GRCm39) probably null Het
Phf20 T C 2: 156,109,261 (GRCm39) S203P probably benign Het
Pkd1l1 T C 11: 8,817,204 (GRCm39) S1815G possibly damaging Het
Pnpla7 T C 2: 24,871,790 (GRCm39) V11A probably damaging Het
Ranbp2 T C 10: 58,300,086 (GRCm39) probably null Het
Ranbp3l A G 15: 9,063,169 (GRCm39) D326G probably damaging Het
Rsph4a C T 10: 33,781,789 (GRCm39) A213V probably damaging Het
Sema3b A G 9: 107,476,913 (GRCm39) S570P probably benign Het
Spata31d1b T A 13: 59,866,787 (GRCm39) C1312S probably benign Het
Sphkap G T 1: 83,253,618 (GRCm39) T1377K probably benign Het
Stk32a A T 18: 43,438,085 (GRCm39) R195W possibly damaging Het
Tacr2 T C 10: 62,088,769 (GRCm39) I58T probably damaging Het
Tmem200c A T 17: 69,147,547 (GRCm39) K43N probably damaging Het
Tnik T C 3: 28,648,241 (GRCm39) M431T probably benign Het
Uckl1 A G 2: 181,216,245 (GRCm39) S167P possibly damaging Het
Vmn2r90 A G 17: 17,954,128 (GRCm39) Y764C probably damaging Het
Zan C T 5: 137,408,423 (GRCm39) probably null Het
Other mutations in Adam6a
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00580:Adam6a APN 12 113,508,845 (GRCm39) missense probably benign 0.00
IGL00896:Adam6a APN 12 113,509,030 (GRCm39) missense possibly damaging 0.56
IGL01146:Adam6a APN 12 113,507,840 (GRCm39) missense probably damaging 1.00
IGL01285:Adam6a APN 12 113,509,893 (GRCm39) makesense probably null
IGL01839:Adam6a APN 12 113,508,242 (GRCm39) missense probably benign 0.03
IGL01906:Adam6a APN 12 113,507,951 (GRCm39) missense probably benign 0.19
IGL02306:Adam6a APN 12 113,509,343 (GRCm39) missense possibly damaging 0.93
IGL03146:Adam6a APN 12 113,509,144 (GRCm39) missense probably damaging 1.00
IGL03176:Adam6a APN 12 113,509,822 (GRCm39) missense probably benign 0.00
IGL03365:Adam6a APN 12 113,507,765 (GRCm39) missense possibly damaging 0.86
IGL03373:Adam6a APN 12 113,509,172 (GRCm39) missense possibly damaging 0.55
PIT4802001:Adam6a UTSW 12 113,509,078 (GRCm39) missense probably damaging 1.00
R0091:Adam6a UTSW 12 113,507,849 (GRCm39) missense possibly damaging 0.46
R0149:Adam6a UTSW 12 113,509,369 (GRCm39) missense probably damaging 1.00
R0348:Adam6a UTSW 12 113,508,337 (GRCm39) missense probably damaging 0.99
R0376:Adam6a UTSW 12 113,508,310 (GRCm39) missense probably damaging 1.00
R1471:Adam6a UTSW 12 113,508,013 (GRCm39) missense probably damaging 1.00
R1474:Adam6a UTSW 12 113,508,069 (GRCm39) missense possibly damaging 0.66
R1553:Adam6a UTSW 12 113,508,835 (GRCm39) missense probably damaging 1.00
R1679:Adam6a UTSW 12 113,508,376 (GRCm39) missense probably benign 0.00
R1808:Adam6a UTSW 12 113,508,334 (GRCm39) missense probably benign 0.00
R1826:Adam6a UTSW 12 113,509,742 (GRCm39) missense possibly damaging 0.46
R1856:Adam6a UTSW 12 113,508,923 (GRCm39) missense probably damaging 1.00
R1916:Adam6a UTSW 12 113,509,556 (GRCm39) missense probably benign
R2011:Adam6a UTSW 12 113,508,998 (GRCm39) missense probably benign 0.09
R2049:Adam6a UTSW 12 113,508,049 (GRCm39) missense probably benign 0.17
R2364:Adam6a UTSW 12 113,508,250 (GRCm39) missense probably benign 0.05
R3820:Adam6a UTSW 12 113,507,798 (GRCm39) missense probably benign 0.00
R4119:Adam6a UTSW 12 113,508,194 (GRCm39) missense probably benign 0.06
R4540:Adam6a UTSW 12 113,508,119 (GRCm39) missense probably damaging 1.00
R4627:Adam6a UTSW 12 113,508,569 (GRCm39) missense probably benign
R4665:Adam6a UTSW 12 113,507,992 (GRCm39) missense possibly damaging 0.64
R4859:Adam6a UTSW 12 113,509,609 (GRCm39) missense probably damaging 1.00
R4997:Adam6a UTSW 12 113,508,991 (GRCm39) missense probably damaging 1.00
R5270:Adam6a UTSW 12 113,507,747 (GRCm39) missense possibly damaging 0.46
R5775:Adam6a UTSW 12 113,509,886 (GRCm39) missense possibly damaging 0.47
R5863:Adam6a UTSW 12 113,507,987 (GRCm39) missense probably benign 0.01
R6154:Adam6a UTSW 12 113,509,292 (GRCm39) missense probably benign 0.11
R6313:Adam6a UTSW 12 113,508,670 (GRCm39) missense possibly damaging 0.56
R6316:Adam6a UTSW 12 113,509,196 (GRCm39) missense probably benign 0.27
R6706:Adam6a UTSW 12 113,508,886 (GRCm39) missense probably benign 0.00
R6845:Adam6a UTSW 12 113,507,717 (GRCm39) missense possibly damaging 0.96
R7134:Adam6a UTSW 12 113,508,655 (GRCm39) missense probably benign 0.04
R7179:Adam6a UTSW 12 113,509,291 (GRCm39) missense probably benign 0.02
R7206:Adam6a UTSW 12 113,509,654 (GRCm39) missense probably damaging 1.00
R7230:Adam6a UTSW 12 113,509,202 (GRCm39) missense probably damaging 1.00
R7296:Adam6a UTSW 12 113,509,192 (GRCm39) missense probably damaging 1.00
R7676:Adam6a UTSW 12 113,508,196 (GRCm39) missense probably benign 0.00
R7730:Adam6a UTSW 12 113,507,660 (GRCm39) missense possibly damaging 0.86
R7743:Adam6a UTSW 12 113,508,152 (GRCm39) missense probably benign
R7841:Adam6a UTSW 12 113,509,078 (GRCm39) missense probably damaging 1.00
R8356:Adam6a UTSW 12 113,509,757 (GRCm39) missense probably benign 0.08
R8531:Adam6a UTSW 12 113,508,917 (GRCm39) missense probably damaging 1.00
R9568:Adam6a UTSW 12 113,508,020 (GRCm39) missense possibly damaging 0.74
R9624:Adam6a UTSW 12 113,509,070 (GRCm39) missense probably damaging 1.00
R9679:Adam6a UTSW 12 113,509,542 (GRCm39) missense probably benign 0.00
R9680:Adam6a UTSW 12 113,509,484 (GRCm39) nonsense probably null
X0027:Adam6a UTSW 12 113,508,863 (GRCm39) missense probably benign 0.01
Z1176:Adam6a UTSW 12 113,508,941 (GRCm39) missense possibly damaging 0.92
Predicted Primers PCR Primer
(F):5'- AATATGCAGATGGAGCTCCC -3'
(R):5'- TGACCAAGACAAATTAGGGCTG -3'

Sequencing Primer
(F):5'- TGGAGCTCCCAGACTATCTAGTAAG -3'
(R):5'- TTAGGGCTGAGGGAGAACATATACTC -3'
Posted On 2016-11-21