Incidental Mutation 'IGL02182:Ms4a20'
ID 283297
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Ms4a20
Ensembl Gene ENSMUSG00000024729
Gene Name membrane-spanning 4-domains, subfamily A, member 20
Synonyms 1700017D01Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.069) question?
Stock # IGL02182
Quality Score
Status
Chromosome 19
Chromosomal Location 11074180-11108240 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) A to T at 11074436 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000025635 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000025635]
AlphaFold G5E851
Predicted Effect probably benign
Transcript: ENSMUST00000025635
SMART Domains Protein: ENSMUSP00000025635
Gene: ENSMUSG00000024729

DomainStartEndE-ValueType
Pfam:CD20 18 118 2.4e-8 PFAM
transmembrane domain 130 152 N/A INTRINSIC
low complexity region 169 185 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000186376
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adam34 T A 8: 44,104,790 (GRCm39) N285I probably benign Het
Adprh T C 16: 38,267,838 (GRCm39) H149R probably benign Het
Ahctf1 A G 1: 179,580,643 (GRCm39) V1853A probably benign Het
Ank1 T C 8: 23,603,868 (GRCm39) V905A possibly damaging Het
Atp10b T G 11: 43,139,774 (GRCm39) L1234R probably damaging Het
Bco1 G A 8: 117,859,805 (GRCm39) A503T probably damaging Het
Clxn T A 16: 14,738,659 (GRCm39) D163E probably damaging Het
Cpz T A 5: 35,675,066 (GRCm39) Y61F probably damaging Het
Dnah8 T A 17: 31,013,737 (GRCm39) M3826K possibly damaging Het
Dtd2 A G 12: 52,046,492 (GRCm39) S116P probably benign Het
Eml5 T C 12: 98,768,581 (GRCm39) D1498G probably damaging Het
Fat4 T C 3: 38,944,695 (GRCm39) V1196A probably damaging Het
Gm15557 T C 2: 155,783,737 (GRCm39) D405G probably damaging Het
Lpp C T 16: 24,580,895 (GRCm39) R204W probably damaging Het
Mfsd11 T A 11: 116,764,740 (GRCm39) V388E possibly damaging Het
Or10a3m A G 7: 108,313,075 (GRCm39) T160A probably benign Het
Or52b4 A G 7: 102,184,775 (GRCm39) I274V probably benign Het
Pik3cg A T 12: 32,255,272 (GRCm39) D238E possibly damaging Het
Plcb3 T C 19: 6,946,988 (GRCm39) H9R probably benign Het
Ppp3cc A C 14: 70,462,473 (GRCm39) V388G probably benign Het
Ranbp2 T A 10: 58,321,582 (GRCm39) C2626* probably null Het
Resp18 T C 1: 75,250,615 (GRCm39) T155A probably benign Het
Ror2 C T 13: 53,264,764 (GRCm39) S764N probably damaging Het
Scarb2 C T 5: 92,601,913 (GRCm39) S327N probably damaging Het
Secisbp2l T A 2: 125,589,497 (GRCm39) I684F probably damaging Het
Slc39a6 T C 18: 24,734,347 (GRCm39) D114G probably damaging Het
Smap1 T A 1: 23,898,180 (GRCm39) E85D probably damaging Het
Tas2r121 T A 6: 132,677,133 (GRCm39) I280F probably damaging Het
Uhrf2 T C 19: 30,016,609 (GRCm39) V86A probably benign Het
Vip A T 10: 5,593,561 (GRCm39) Y91F probably benign Het
Zfp318 C T 17: 46,707,736 (GRCm39) R265* probably null Het
Zfp618 G A 4: 63,013,798 (GRCm39) probably benign Het
Other mutations in Ms4a20
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02142:Ms4a20 APN 19 11,087,695 (GRCm39) nonsense probably null
IGL03156:Ms4a20 APN 19 11,083,114 (GRCm39) missense possibly damaging 0.80
R0189:Ms4a20 UTSW 19 11,074,311 (GRCm39) missense possibly damaging 0.46
R0218:Ms4a20 UTSW 19 11,093,801 (GRCm39) nonsense probably null
R0464:Ms4a20 UTSW 19 11,089,801 (GRCm39) missense probably damaging 1.00
R0617:Ms4a20 UTSW 19 11,089,764 (GRCm39) missense probably damaging 1.00
R1171:Ms4a20 UTSW 19 11,089,741 (GRCm39) missense probably damaging 0.97
R2341:Ms4a20 UTSW 19 11,083,157 (GRCm39) missense probably benign
R5099:Ms4a20 UTSW 19 11,089,825 (GRCm39) critical splice acceptor site probably null
R5330:Ms4a20 UTSW 19 11,069,222 (GRCm39) unclassified probably benign
R5331:Ms4a20 UTSW 19 11,069,222 (GRCm39) unclassified probably benign
R5341:Ms4a20 UTSW 19 11,087,745 (GRCm39) intron probably benign
R6109:Ms4a20 UTSW 19 11,079,276 (GRCm39) missense possibly damaging 0.66
R6177:Ms4a20 UTSW 19 11,083,114 (GRCm39) missense possibly damaging 0.53
R6970:Ms4a20 UTSW 19 11,089,678 (GRCm39) critical splice donor site probably null
R7038:Ms4a20 UTSW 19 11,087,675 (GRCm39) missense probably benign
R7584:Ms4a20 UTSW 19 11,087,725 (GRCm39) missense possibly damaging 0.94
R7752:Ms4a20 UTSW 19 11,079,224 (GRCm39) missense probably benign 0.02
R7854:Ms4a20 UTSW 19 11,089,741 (GRCm39) missense probably benign 0.01
R8261:Ms4a20 UTSW 19 11,087,707 (GRCm39) missense probably damaging 0.97
R8723:Ms4a20 UTSW 19 11,083,055 (GRCm39) missense probably damaging 0.99
R9027:Ms4a20 UTSW 19 11,083,055 (GRCm39) missense probably damaging 0.99
R9264:Ms4a20 UTSW 19 11,093,830 (GRCm39) start codon destroyed probably benign 0.14
X0019:Ms4a20 UTSW 19 11,083,156 (GRCm39) missense probably benign 0.00
Posted On 2015-04-16