Incidental Mutation 'IGL02142:Ms4a20'
ID 281623
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 # IGL02142
Quality Score
Status
Chromosome 19
Chromosomal Location 11074180-11108240 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) G to A at 11087695 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamine to Stop codon at position 79 (Q79*)
Ref Sequence ENSEMBL: ENSMUSP00000025635 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000025635]
AlphaFold G5E851
Predicted Effect probably null
Transcript: ENSMUST00000025635
AA Change: Q79*
SMART Domains Protein: ENSMUSP00000025635
Gene: ENSMUSG00000024729
AA Change: Q79*

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: ENSMUST00000188756
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 62 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca4 T C 3: 121,963,575 (GRCm39) S2060P probably benign Het
Abcg4 A G 9: 44,189,014 (GRCm39) F426S probably benign Het
Actn1 C T 12: 80,222,929 (GRCm39) probably null Het
Adgrd1 T A 5: 129,208,648 (GRCm39) H251Q probably benign Het
Adgrg3 C T 8: 95,766,483 (GRCm39) P385S probably damaging Het
Ampd2 G T 3: 107,987,660 (GRCm39) probably benign Het
Arhgap42 A G 9: 9,155,360 (GRCm39) S86P probably damaging Het
Art5 C T 7: 101,747,123 (GRCm39) E121K probably null Het
Atad5 G A 11: 79,985,023 (GRCm39) E37K probably benign Het
Atp13a5 A G 16: 29,053,315 (GRCm39) V1084A probably benign Het
Cfap44 T C 16: 44,241,507 (GRCm39) I626T probably benign Het
Col16a1 T A 4: 129,945,440 (GRCm39) probably null Het
Defa22 T G 8: 21,653,130 (GRCm39) C81G possibly damaging Het
Dnm2 A G 9: 21,411,649 (GRCm39) Y622C probably damaging Het
Efna5 T A 17: 62,914,340 (GRCm39) L201F unknown Het
Elac1 T C 18: 73,871,991 (GRCm39) R335G probably benign Het
Enpp5 T C 17: 44,396,468 (GRCm39) V460A probably benign Het
Esr2 A G 12: 76,169,969 (GRCm39) V453A probably benign Het
Fam210b T A 2: 172,194,497 (GRCm39) probably benign Het
Fcgr1 T C 3: 96,191,893 (GRCm39) Y305C probably benign Het
Fcrlb A G 1: 170,736,248 (GRCm39) V176A probably damaging Het
Gabrq T A X: 71,879,783 (GRCm39) V256E possibly damaging Het
Gba1 T C 3: 89,113,148 (GRCm39) L193P probably damaging Het
Gm10717 C T 9: 3,025,616 (GRCm39) S67L probably benign Het
Helq A G 5: 100,930,960 (GRCm39) F597L probably benign Het
Hrh1 A T 6: 114,457,204 (GRCm39) I162L probably damaging Het
Jph1 A T 1: 17,161,884 (GRCm39) F259L probably damaging Het
Kdm2b C T 5: 123,085,898 (GRCm39) E238K probably damaging Het
Kdm4c T A 4: 74,225,253 (GRCm39) probably null Het
Kif13a T C 13: 46,925,011 (GRCm39) T308A probably benign Het
Lars1 C T 18: 42,360,345 (GRCm39) V704M probably benign Het
Lcmt2 A G 2: 120,969,394 (GRCm39) L343P possibly damaging Het
Lhfpl1 A G X: 144,123,733 (GRCm39) F125L probably benign Het
Lmbrd2 C A 15: 9,186,772 (GRCm39) D582E probably damaging Het
Lrrn2 T A 1: 132,866,983 (GRCm39) S683T possibly damaging Het
Macf1 T C 4: 123,365,842 (GRCm39) D1408G probably benign Het
Magi3 T C 3: 103,923,219 (GRCm39) K1166R probably benign Het
Marchf5 T C 19: 37,197,892 (GRCm39) probably benign Het
Naa25 A G 5: 121,564,825 (GRCm39) Q555R possibly damaging Het
Npat A G 9: 53,481,207 (GRCm39) T1005A probably benign Het
Nt5c3 G A 6: 56,863,670 (GRCm39) A108V probably damaging Het
Ocrl T A X: 47,024,995 (GRCm39) M322K probably damaging Het
Odad2 C A 18: 7,214,601 (GRCm39) W733C probably damaging Het
Or8g2 A G 9: 39,821,935 (GRCm39) T279A possibly damaging Het
Psg23 A T 7: 18,344,345 (GRCm39) V370E probably benign Het
Rassf2 A T 2: 131,838,353 (GRCm39) M311K possibly damaging Het
Rhobtb3 A G 13: 76,025,614 (GRCm39) Y501H probably damaging Het
Rpl4 A G 9: 64,083,488 (GRCm39) D179G possibly damaging Het
Scn2a T A 2: 65,546,182 (GRCm39) I915N probably damaging Het
Scn3a T A 2: 65,356,965 (GRCm39) T160S possibly damaging Het
Slx4ip T G 2: 136,909,942 (GRCm39) N242K possibly damaging Het
Spidr T A 16: 15,865,945 (GRCm39) Q288L probably benign Het
Sun1 A T 5: 139,216,918 (GRCm39) H255L possibly damaging Het
Tacc1 C T 8: 25,665,233 (GRCm39) G51S probably damaging Het
Tet2 T A 3: 133,185,900 (GRCm39) N1179I possibly damaging Het
Tgfbrap1 T C 1: 43,101,752 (GRCm39) Y349C probably damaging Het
Tnrc6a T C 7: 122,751,414 (GRCm39) probably benign Het
Trim32 T C 4: 65,532,736 (GRCm39) L431P probably damaging Het
Vmn1r35 A G 6: 66,656,334 (GRCm39) L112S probably damaging Het
Vmn2r100 A C 17: 19,742,583 (GRCm39) H319P probably damaging Het
Wdr20rt A G 12: 65,274,039 (GRCm39) T328A probably benign Het
Zbtb17 T C 4: 141,192,293 (GRCm39) Y413H probably benign Het
Other mutations in Ms4a20
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02182:Ms4a20 APN 19 11,074,436 (GRCm39) splice site probably benign
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