Incidental Mutation 'IGL02321:Gm4781'
ID 288221
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm4781
Ensembl Gene ENSMUSG00000090987
Gene Name predicted gene 4781
Synonyms
Accession Numbers
Essential gene? Not available question?
Stock # IGL02321
Quality Score
Status
Chromosome 10
Chromosomal Location 100396413-100397063 bp(-) (GRCm38)
Type of Mutation exon
DNA Base Change (assembly) T to A at 100396890 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000167995
SMART Domains Protein: ENSMUSP00000132273
Gene: ENSMUSG00000090987

DomainStartEndE-ValueType
Pfam:FYTT 1 52 6e-8 PFAM
RRM 87 159 9.63e-17 SMART
coiled coil region 209 261 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 43 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2410089E03Rik A G 15: 8,216,572 E1476G probably benign Het
Acsf3 C T 8: 122,780,114 R49C possibly damaging Het
Alg2 T C 4: 47,474,249 Y13C probably benign Het
Apoa4 A G 9: 46,242,920 D273G probably damaging Het
Axl C T 7: 25,758,769 V854I probably damaging Het
BC117090 A G 16: 36,323,026 probably benign Het
Bicral A G 17: 46,811,947 S673P probably benign Het
C87499 A G 4: 88,630,103 S22P probably benign Het
Camkk2 A G 5: 122,764,127 S40P probably damaging Het
Ccdc39 A G 3: 33,816,958 probably benign Het
Ccdc87 A G 19: 4,841,031 E517G probably damaging Het
Cd22 A G 7: 30,869,883 S603P probably damaging Het
Cdk5rap3 A T 11: 96,913,465 C21S probably damaging Het
Chml G A 1: 175,692,334 P68L possibly damaging Het
Ephb3 T C 16: 21,214,389 V41A probably damaging Het
Hip1r A T 5: 123,999,890 I760F probably damaging Het
Hyal5 T C 6: 24,891,615 L476P probably benign Het
Isyna1 A G 8: 70,596,270 N333S probably damaging Het
Kcnmb1 A T 11: 33,970,091 probably benign Het
Mark4 T C 7: 19,426,389 T649A probably benign Het
Mgat1 T C 11: 49,261,709 F340L probably benign Het
Mical1 G A 10: 41,486,664 E932K possibly damaging Het
Mmaa T G 8: 79,274,130 Y233S probably damaging Het
Ntsr1 G T 2: 180,538,834 probably null Het
Olfr1394 T G 11: 49,160,775 Y254D probably damaging Het
Orm2 T C 4: 63,362,992 Y56H probably damaging Het
Pex26 C T 6: 121,193,509 probably benign Het
Pik3r4 C T 9: 105,644,478 A81V probably benign Het
Prr14l G T 5: 32,827,807 T1448K probably benign Het
Ralgapa2 A T 2: 146,412,816 Y799* probably null Het
Ryr1 A C 7: 29,078,696 L2132R probably damaging Het
Sec23b T C 2: 144,579,405 probably null Het
Sirt5 C T 13: 43,379,688 T164I probably damaging Het
Slc9c1 T C 16: 45,556,614 V429A probably benign Het
Spen T C 4: 141,517,130 D198G unknown Het
Syne2 A G 12: 75,918,999 N832D possibly damaging Het
Traf7 C A 17: 24,513,046 C193F possibly damaging Het
Vmn1r191 T A 13: 22,178,898 R229* probably null Het
Vps53 C T 11: 76,048,538 D680N possibly damaging Het
Wbp1l G T 19: 46,654,310 G234V probably benign Het
Wdfy3 A T 5: 101,922,609 S1098T probably damaging Het
Yod1 T A 1: 130,718,951 D188E probably damaging Het
Zbtb25 T C 12: 76,350,133 D105G probably damaging Het
Other mutations in Gm4781
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02583:Gm4781 APN 10 100396645 exon noncoding transcript
R0731:Gm4781 UTSW 10 100396777 exon noncoding transcript
R1686:Gm4781 UTSW 10 100396975 exon noncoding transcript
R1836:Gm4781 UTSW 10 100396720 exon noncoding transcript
R2147:Gm4781 UTSW 10 100396552 exon noncoding transcript
R4647:Gm4781 UTSW 10 100397000 exon noncoding transcript
R5036:Gm4781 UTSW 10 100396989 exon noncoding transcript
R5039:Gm4781 UTSW 10 100396989 exon noncoding transcript
R5777:Gm4781 UTSW 10 100396969 exon noncoding transcript
R5793:Gm4781 UTSW 10 100396667 exon noncoding transcript
R5966:Gm4781 UTSW 10 100396952 exon noncoding transcript
R6180:Gm4781 UTSW 10 100396487 exon noncoding transcript
R8227:Gm4781 UTSW 10 100396562 missense noncoding transcript
Posted On 2015-04-16