Incidental Mutation 'R4816:Dsg1a'
ID 369858
Institutional Source Beutler Lab
Gene Symbol Dsg1a
Ensembl Gene ENSMUSG00000069441
Gene Name desmoglein 1 alpha
Synonyms Dsg1
MMRRC Submission 042434-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.084) question?
Stock # R4816 (G1)
Quality Score 225
Status Validated
Chromosome 18
Chromosomal Location 20443930-20476410 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 20466779 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Serine at position 550 (T550S)
Ref Sequence ENSEMBL: ENSMUSP00000076393 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000077146]
AlphaFold Q61495
Predicted Effect probably benign
Transcript: ENSMUST00000077146
AA Change: T550S

PolyPhen 2 Score 0.104 (Sensitivity: 0.93; Specificity: 0.86)
SMART Domains Protein: ENSMUSP00000076393
Gene: ENSMUSG00000069441
AA Change: T550S

DomainStartEndE-ValueType
signal peptide 1 23 N/A INTRINSIC
CA 70 155 3.45e-14 SMART
CA 179 267 3.11e-21 SMART
CA 290 384 6.29e-8 SMART
CA 407 485 6.44e-1 SMART
low complexity region 573 584 N/A INTRINSIC
low complexity region 590 598 N/A INTRINSIC
Pfam:Cadherin_C 659 781 1.6e-10 PFAM
low complexity region 786 799 N/A INTRINSIC
internal_repeat_1 823 888 9.56e-6 PROSPERO
internal_repeat_1 908 975 9.56e-6 PROSPERO
low complexity region 983 1004 N/A INTRINSIC
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.4%
  • 10x: 96.5%
  • 20x: 93.0%
Validation Efficiency 97% (113/116)
MGI Phenotype FUNCTION: This gene encodes a member of the cadherin family of proteins that forms an integral transmembrane component of desmosomes, the multiprotein complexes involved in cell adhesion, organization of the cytoskeleton, cell sorting and cell signaling. The encoded preproprotein undergoes proteolytic processing to generate a mature, functional protein. This gene is located in a cluster of desmosomal cadherin genes on chromosome 18. [provided by RefSeq, Jan 2016]
Allele List at MGI
Other mutations in this stock
Total: 107 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcc8 C A 7: 45,754,131 (GRCm39) A1562S probably benign Het
Adam30 C A 3: 98,070,061 (GRCm39) D631E possibly damaging Het
Adgrv1 T C 13: 81,676,793 (GRCm39) T2013A probably damaging Het
Ark2n A T 18: 77,740,995 (GRCm39) probably null Het
Baiap3 T A 17: 25,466,269 (GRCm39) probably benign Het
Bicra T C 7: 15,722,831 (GRCm39) T229A possibly damaging Het
C1qbp A G 11: 70,873,190 (GRCm39) probably benign Het
C2cd3 C A 7: 100,040,226 (GRCm39) T265K probably benign Het
Cacna1s T A 1: 136,043,007 (GRCm39) I1331K possibly damaging Het
Cdadc1 AGACGGA AGA 14: 59,806,440 (GRCm39) probably null Het
Cdcp2 A G 4: 106,963,969 (GRCm39) Y273C probably damaging Het
Cdh23 A C 10: 60,244,856 (GRCm39) V1013G possibly damaging Het
Celf3 T A 3: 94,386,529 (GRCm39) I39N probably damaging Het
Cep152 A C 2: 125,405,674 (GRCm39) S1619R probably damaging Het
Cfap36 A G 11: 29,195,108 (GRCm39) I42T probably damaging Het
Cfap61 G T 2: 145,985,020 (GRCm39) V955L probably damaging Het
Cit G A 5: 116,046,750 (GRCm39) D388N probably damaging Het
Clca3a2 T C 3: 144,516,613 (GRCm39) M328V probably benign Het
Cntn4 A T 6: 106,527,458 (GRCm39) I447L probably benign Het
Csmd3 T C 15: 47,721,330 (GRCm39) T1538A possibly damaging Het
Cstf1 A G 2: 172,214,905 (GRCm39) K9E probably damaging Het
Dip2c T A 13: 9,625,186 (GRCm39) M560K probably benign Het
Dtnb A G 12: 3,799,505 (GRCm39) E460G probably damaging Het
Dus1l GAGGTAAG GAG 11: 120,680,584 (GRCm39) probably benign Het
Efl1 T A 7: 82,320,927 (GRCm39) V120E probably damaging Het
Fbxl13 T C 5: 21,689,001 (GRCm39) Y769C probably benign Het
Fcho2 T C 13: 98,942,874 (GRCm39) Y22C probably damaging Het
Flacc1 G A 1: 58,709,567 (GRCm39) A196V probably benign Het
Gbp3 T C 3: 142,273,335 (GRCm39) V294A probably damaging Het
Gls A G 1: 52,239,104 (GRCm39) probably benign Het
Gm15130 A T 2: 110,965,714 (GRCm39) probably benign Het
Gm6185 A T 1: 161,040,728 (GRCm39) noncoding transcript Het
Gpr171 T A 3: 59,005,517 (GRCm39) H86L probably damaging Het
Gpr179 T C 11: 97,230,074 (GRCm39) T694A probably damaging Het
H2-Aa A T 17: 34,502,794 (GRCm39) V124E probably damaging Het
H2bc13 A G 13: 21,900,135 (GRCm39) M60T probably benign Het
H2-M5 A G 17: 37,300,309 (GRCm39) probably benign Het
Igf2r A T 17: 12,902,984 (GRCm39) N2355K probably damaging Het
Il9r A C 11: 32,142,654 (GRCm39) S295A possibly damaging Het
Ipo9 T C 1: 135,334,288 (GRCm39) T313A probably benign Het
Kalrn C T 16: 34,334,389 (GRCm39) probably benign Het
Lama3 G A 18: 12,610,661 (GRCm39) V1175M possibly damaging Het
Lhpp T A 7: 132,272,104 (GRCm39) C242* probably null Het
Lipe A G 7: 25,079,568 (GRCm39) S1013P probably damaging Het
Lrrc25 C T 8: 71,070,726 (GRCm39) T169I probably benign Het
Lrrc39 T C 3: 116,362,515 (GRCm39) probably null Het
Lrrd1 T A 5: 3,901,126 (GRCm39) L477* probably null Het
Lrriq4 A G 3: 30,714,196 (GRCm39) I515V possibly damaging Het
Magel2 A G 7: 62,030,840 (GRCm39) Y1248C unknown Het
Maml1 G T 11: 50,149,162 (GRCm39) N859K possibly damaging Het
Mdm1 A T 10: 117,982,782 (GRCm39) H139L possibly damaging Het
Mef2d C T 3: 88,075,397 (GRCm39) P420S possibly damaging Het
Mgat4b A G 11: 50,101,848 (GRCm39) K38E probably benign Het
Mtmr4 T C 11: 87,494,923 (GRCm39) V405A probably damaging Het
Naip5 G A 13: 100,356,195 (GRCm39) T1140M probably benign Het
Naip5 T C 13: 100,356,204 (GRCm39) Q1137R probably benign Het
Naip5 G A 13: 100,356,189 (GRCm39) S1142F probably benign Het
Nfe2l3 T C 6: 51,433,604 (GRCm39) S239P probably damaging Het
Nlrp3 A G 11: 59,439,127 (GRCm39) I235V probably benign Het
Nyap2 T A 1: 81,219,028 (GRCm39) L318Q probably damaging Het
Nynrin G A 14: 56,109,458 (GRCm39) V1522M probably damaging Het
Oog3 A G 4: 143,885,731 (GRCm39) L289P probably damaging Het
Or52n20 C T 7: 104,319,942 (GRCm39) P11L probably benign Het
Or5b107 A G 19: 13,142,488 (GRCm39) I37V probably benign Het
Or6c69b T C 10: 129,627,308 (GRCm39) D50G probably damaging Het
Or8b12b T A 9: 37,684,726 (GRCm39) M257K possibly damaging Het
Or9g20 A T 2: 85,630,391 (GRCm39) N74K probably benign Het
Pax6 T C 2: 105,514,129 (GRCm39) probably benign Het
Pbrm1 G A 14: 30,832,405 (GRCm39) R1441K probably benign Het
Pcdha9 C T 18: 37,132,511 (GRCm39) R527W probably damaging Het
Pcdhb17 T C 18: 37,620,450 (GRCm39) S747P probably benign Het
Pcnx3 A C 19: 5,738,023 (GRCm39) probably null Het
Pds5a A T 5: 65,808,632 (GRCm39) V413E probably damaging Het
Phpt1 G T 2: 25,464,332 (GRCm39) probably benign Het
Phykpl A G 11: 51,483,780 (GRCm39) E220G probably benign Het
Pias2 T C 18: 77,193,587 (GRCm39) probably null Het
Pkhd1 T A 1: 20,269,639 (GRCm39) I3302L probably damaging Het
Poli A G 18: 70,655,822 (GRCm39) L241P probably damaging Het
Ppm1h T A 10: 122,515,284 (GRCm39) I65N possibly damaging Het
Ptpn14 T C 1: 189,588,997 (GRCm39) L954P probably damaging Het
Pxk T G 14: 8,136,893 (GRCm38) M138R probably damaging Het
Rasl11b G T 5: 74,359,058 (GRCm39) D188Y probably damaging Het
Rtraf A G 14: 19,872,644 (GRCm39) F59S probably benign Het
Sanbr A C 11: 23,565,243 (GRCm39) I248S possibly damaging Het
Serpinb5 G T 1: 106,800,069 (GRCm39) L86F probably damaging Het
Setdb2 G A 14: 59,651,095 (GRCm39) T412I probably benign Het
Shank2 C A 7: 143,606,043 (GRCm39) N75K probably damaging Het
Shank3 T A 15: 89,427,318 (GRCm39) I791N probably damaging Het
Slc25a13 T A 6: 6,114,274 (GRCm39) M213L possibly damaging Het
Slc25a21 T C 12: 56,760,623 (GRCm39) Y298C probably damaging Het
Slc34a2 A G 5: 53,226,362 (GRCm39) N495S probably damaging Het
Smc2 A G 4: 52,451,231 (GRCm39) T292A probably benign Het
Spag9 T C 11: 93,939,425 (GRCm39) probably benign Het
Tas2r113 C T 6: 132,870,745 (GRCm39) P258S probably benign Het
Tbkbp1 T C 11: 97,029,567 (GRCm39) S530G probably benign Het
Tenm2 A G 11: 35,918,117 (GRCm39) V1881A probably damaging Het
Tm9sf1 C T 14: 55,878,606 (GRCm39) R262Q possibly damaging Het
Tmcc3 G T 10: 94,414,646 (GRCm39) G147V possibly damaging Het
Trim38 A T 13: 23,972,264 (GRCm39) E195V probably damaging Het
Try5 T C 6: 41,290,349 (GRCm39) Y45C probably benign Het
Umad1 A C 6: 8,457,462 (GRCm39) probably benign Het
Vmn2r105 T C 17: 20,428,953 (GRCm39) I708V probably benign Het
Zc3h12d A T 10: 7,743,711 (GRCm39) S494C probably damaging Het
Zeb2 A G 2: 44,887,780 (GRCm39) S382P probably damaging Het
Zfc3h1 A G 10: 115,251,599 (GRCm39) S1304G probably benign Het
Zfp287 G T 11: 62,605,074 (GRCm39) T611K probably damaging Het
Zfp534 G A 4: 147,758,743 (GRCm39) T642I possibly damaging Het
Other mutations in Dsg1a
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01064:Dsg1a APN 18 20,473,263 (GRCm39) missense probably damaging 1.00
IGL01148:Dsg1a APN 18 20,453,982 (GRCm39) missense probably damaging 0.97
IGL01534:Dsg1a APN 18 20,474,053 (GRCm39) missense probably benign 0.06
IGL01566:Dsg1a APN 18 20,469,840 (GRCm39) splice site probably benign
IGL01582:Dsg1a APN 18 20,461,905 (GRCm39) missense probably null 1.00
IGL01913:Dsg1a APN 18 20,455,293 (GRCm39) missense probably damaging 1.00
IGL01926:Dsg1a APN 18 20,466,641 (GRCm39) missense possibly damaging 0.60
IGL02102:Dsg1a APN 18 20,465,089 (GRCm39) missense probably benign 0.01
IGL02900:Dsg1a APN 18 20,461,713 (GRCm39) splice site probably benign
IGL02937:Dsg1a APN 18 20,464,591 (GRCm39) missense possibly damaging 0.93
IGL02962:Dsg1a APN 18 20,473,381 (GRCm39) missense possibly damaging 0.92
IGL03003:Dsg1a APN 18 20,469,876 (GRCm39) missense probably benign 0.43
PIT4687001:Dsg1a UTSW 18 20,464,755 (GRCm39) missense probably benign 0.16
R0126:Dsg1a UTSW 18 20,473,935 (GRCm39) missense probably benign 0.00
R0200:Dsg1a UTSW 18 20,473,995 (GRCm39) missense probably benign 0.00
R0284:Dsg1a UTSW 18 20,464,684 (GRCm39) missense probably damaging 0.98
R0394:Dsg1a UTSW 18 20,466,807 (GRCm39) missense probably damaging 1.00
R0543:Dsg1a UTSW 18 20,473,920 (GRCm39) missense probably damaging 1.00
R0656:Dsg1a UTSW 18 20,468,949 (GRCm39) splice site probably benign
R0733:Dsg1a UTSW 18 20,471,725 (GRCm39) missense probably damaging 0.97
R0750:Dsg1a UTSW 18 20,473,210 (GRCm39) missense probably benign 0.10
R1300:Dsg1a UTSW 18 20,465,206 (GRCm39) missense probably benign 0.19
R1501:Dsg1a UTSW 18 20,465,076 (GRCm39) missense probably damaging 1.00
R1523:Dsg1a UTSW 18 20,455,374 (GRCm39) missense probably damaging 0.99
R1673:Dsg1a UTSW 18 20,464,561 (GRCm39) missense probably damaging 1.00
R1980:Dsg1a UTSW 18 20,471,707 (GRCm39) missense probably damaging 1.00
R2102:Dsg1a UTSW 18 20,466,830 (GRCm39) missense probably damaging 1.00
R2132:Dsg1a UTSW 18 20,473,854 (GRCm39) missense probably damaging 1.00
R2299:Dsg1a UTSW 18 20,473,207 (GRCm39) missense probably damaging 1.00
R2426:Dsg1a UTSW 18 20,469,861 (GRCm39) missense probably damaging 0.96
R3031:Dsg1a UTSW 18 20,473,549 (GRCm39) missense probably damaging 1.00
R4044:Dsg1a UTSW 18 20,457,087 (GRCm39) missense probably damaging 1.00
R4075:Dsg1a UTSW 18 20,473,127 (GRCm39) missense possibly damaging 0.53
R4644:Dsg1a UTSW 18 20,473,785 (GRCm39) missense probably benign 0.04
R4661:Dsg1a UTSW 18 20,473,590 (GRCm39) missense probably damaging 0.99
R5221:Dsg1a UTSW 18 20,457,071 (GRCm39) missense possibly damaging 0.64
R5257:Dsg1a UTSW 18 20,453,988 (GRCm39) missense probably damaging 1.00
R5360:Dsg1a UTSW 18 20,474,011 (GRCm39) missense probably damaging 0.96
R5547:Dsg1a UTSW 18 20,469,097 (GRCm39) critical splice donor site probably null
R5702:Dsg1a UTSW 18 20,469,922 (GRCm39) critical splice donor site probably null
R5987:Dsg1a UTSW 18 20,464,599 (GRCm39) missense probably damaging 1.00
R6108:Dsg1a UTSW 18 20,473,304 (GRCm39) missense probably benign 0.19
R6170:Dsg1a UTSW 18 20,469,043 (GRCm39) missense probably damaging 0.99
R7018:Dsg1a UTSW 18 20,461,795 (GRCm39) missense possibly damaging 0.48
R7201:Dsg1a UTSW 18 20,461,368 (GRCm39) missense probably damaging 0.98
R7730:Dsg1a UTSW 18 20,464,768 (GRCm39) missense possibly damaging 0.77
R7814:Dsg1a UTSW 18 20,471,572 (GRCm39) splice site probably null
R8185:Dsg1a UTSW 18 20,473,669 (GRCm39) missense probably damaging 1.00
R8297:Dsg1a UTSW 18 20,465,090 (GRCm39) missense probably benign 0.02
R8377:Dsg1a UTSW 18 20,466,831 (GRCm39) missense probably damaging 1.00
R8409:Dsg1a UTSW 18 20,473,208 (GRCm39) missense probably damaging 1.00
R8775:Dsg1a UTSW 18 20,473,564 (GRCm39) missense probably damaging 0.98
R8775-TAIL:Dsg1a UTSW 18 20,473,564 (GRCm39) missense probably damaging 0.98
R8818:Dsg1a UTSW 18 20,473,599 (GRCm39) missense possibly damaging 0.87
R8821:Dsg1a UTSW 18 20,453,365 (GRCm39) missense probably damaging 0.96
R8831:Dsg1a UTSW 18 20,453,365 (GRCm39) missense probably damaging 0.96
R9030:Dsg1a UTSW 18 20,473,549 (GRCm39) missense probably damaging 1.00
R9205:Dsg1a UTSW 18 20,473,228 (GRCm39) missense probably damaging 1.00
R9239:Dsg1a UTSW 18 20,473,750 (GRCm39) missense probably damaging 1.00
R9410:Dsg1a UTSW 18 20,464,590 (GRCm39) missense possibly damaging 0.50
Predicted Primers PCR Primer
(F):5'- AACTTAGTGGCACTGGCTGG -3'
(R):5'- GGAACAACTGGTTAGGCAATGC -3'

Sequencing Primer
(F):5'- AGTGGCACTGGCTGGGTAAC -3'
(R):5'- CTGGTTAGGCAATGCTTATAGACAC -3'
Posted On 2016-02-04