Incidental Mutation 'IGL01645:Gm5422'
ID 102634
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm5422
Ensembl Gene ENSMUSG00000039684
Gene Name predicted pseudogene 5422
Synonyms
Accession Numbers
Essential gene? Probably essential (E-score: 0.915) question?
Stock # IGL01645
Quality Score
Status
Chromosome 10
Chromosomal Location 31124133-31127039 bp(+) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) A to T at 31126069 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000050717
SMART Domains Protein: ENSMUSP00000135967
Gene: ENSMUSG00000039684

DomainStartEndE-ValueType
low complexity region 44 61 N/A INTRINSIC
Pfam:PC_rep 438 474 6.8e-9 PFAM
Pfam:PC_rep 475 509 1.1e-8 PFAM
SCOP:d1gw5a_ 603 760 4e-4 SMART
PDB:4CR4|Z 648 901 1e-50 PDB
Predicted Effect noncoding transcript
Transcript: ENSMUST00000216161
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 47 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcc8 C T 7: 45,764,477 (GRCm39) C1156Y possibly damaging Het
Armh4 T C 14: 50,011,011 (GRCm39) E232G probably damaging Het
Atp8b1 G A 18: 64,679,184 (GRCm39) H766Y probably benign Het
Cacna2d1 C A 5: 16,217,389 (GRCm39) probably null Het
Card11 T A 5: 140,863,778 (GRCm39) T987S probably benign Het
Dennd2b T A 7: 109,126,841 (GRCm39) K540* probably null Het
Dmxl2 A T 9: 54,286,017 (GRCm39) Y2723N possibly damaging Het
Dnah11 T A 12: 118,150,733 (GRCm39) I342F possibly damaging Het
Dnajc10 A G 2: 80,170,871 (GRCm39) H454R possibly damaging Het
Dpy19l3 T C 7: 35,394,763 (GRCm39) T592A probably benign Het
Eea1 T A 10: 95,825,451 (GRCm39) S49T probably damaging Het
Esd T A 14: 74,987,159 (GRCm39) N294K probably benign Het
Fmo3 A G 1: 162,791,575 (GRCm39) V234A possibly damaging Het
Folh1 A G 7: 86,391,435 (GRCm39) F420L probably damaging Het
Gabra1 T C 11: 42,026,389 (GRCm39) N301S probably damaging Het
Gorab A T 1: 163,214,000 (GRCm39) L310Q possibly damaging Het
Gsdme A G 6: 50,228,316 (GRCm39) Y51H probably damaging Het
Hrob T C 11: 102,146,012 (GRCm39) L96P probably damaging Het
Itpr1 T C 6: 108,450,560 (GRCm39) I1964T possibly damaging Het
Lmbr1 A G 5: 29,440,053 (GRCm39) L410P probably damaging Het
Lrrc37a T C 11: 103,395,090 (GRCm39) R112G probably benign Het
Mrgpra6 T C 7: 46,835,681 (GRCm39) T247A probably benign Het
Mroh4 A G 15: 74,483,207 (GRCm39) probably benign Het
Mycbpap T C 11: 94,394,293 (GRCm39) probably null Het
Myoz2 T A 3: 122,827,881 (GRCm39) K12N probably damaging Het
Odad2 T C 18: 7,268,491 (GRCm39) S343G probably benign Het
Or1d2 T C 11: 74,256,359 (GRCm39) I288T possibly damaging Het
P3h1 T G 4: 119,093,980 (GRCm39) F212V probably damaging Het
Pcnx2 T C 8: 126,614,656 (GRCm39) D265G probably damaging Het
Pkd1l3 C T 8: 110,361,934 (GRCm39) T992I possibly damaging Het
Prss58 T C 6: 40,874,244 (GRCm39) D144G probably damaging Het
Pth2 T A 7: 44,830,764 (GRCm39) L29Q possibly damaging Het
Rab1b A C 19: 5,154,962 (GRCm39) probably benign Het
Rasa2 A T 9: 96,464,834 (GRCm39) C190* probably null Het
Scn9a T C 2: 66,317,986 (GRCm39) K1501E possibly damaging Het
Selenoi A G 5: 30,462,821 (GRCm39) probably benign Het
Slc11a2 T C 15: 100,286,999 (GRCm39) N558S probably benign Het
Sox10 T C 15: 79,040,539 (GRCm39) I173V probably benign Het
Sra1 A C 18: 36,804,526 (GRCm39) F476C probably damaging Het
Tmem119 T A 5: 113,933,409 (GRCm39) K131* probably null Het
Trim12c T A 7: 103,994,261 (GRCm39) K198* probably null Het
Ttn A G 2: 76,681,904 (GRCm39) probably benign Het
Unc119b C T 5: 115,265,371 (GRCm39) V154I probably benign Het
Usp47 T A 7: 111,654,069 (GRCm39) S108R probably damaging Het
Vmn1r15 T A 6: 57,235,547 (GRCm39) C138* probably null Het
Vmn1r191 T C 13: 22,363,614 (GRCm39) I47V probably benign Het
Wnt3 C T 11: 103,703,204 (GRCm39) A229V probably benign Het
Other mutations in Gm5422
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01306:Gm5422 APN 10 31,125,432 (GRCm39) exon noncoding transcript
IGL01569:Gm5422 APN 10 31,125,897 (GRCm39) exon noncoding transcript
IGL02273:Gm5422 APN 10 31,126,003 (GRCm39) exon noncoding transcript
IGL02603:Gm5422 APN 10 31,125,436 (GRCm39) exon noncoding transcript
IGL02928:Gm5422 APN 10 31,126,250 (GRCm39) exon noncoding transcript
IGL03003:Gm5422 APN 10 31,126,840 (GRCm39) exon noncoding transcript
IGL03274:Gm5422 APN 10 31,126,348 (GRCm39) exon noncoding transcript
IGL03297:Gm5422 APN 10 31,125,727 (GRCm39) exon noncoding transcript
ANU23:Gm5422 UTSW 10 31,125,432 (GRCm39) exon noncoding transcript
R0010:Gm5422 UTSW 10 31,125,750 (GRCm39) exon noncoding transcript
R0506:Gm5422 UTSW 10 31,126,318 (GRCm39) exon noncoding transcript
R0560:Gm5422 UTSW 10 31,125,240 (GRCm39) exon noncoding transcript
R0573:Gm5422 UTSW 10 31,126,156 (GRCm39) exon noncoding transcript
R0652:Gm5422 UTSW 10 31,125,277 (GRCm39) exon noncoding transcript
R1210:Gm5422 UTSW 10 31,126,719 (GRCm39) intron noncoding transcript
R1259:Gm5422 UTSW 10 31,125,111 (GRCm39) exon noncoding transcript
R1352:Gm5422 UTSW 10 31,126,731 (GRCm39) intron noncoding transcript
R1631:Gm5422 UTSW 10 31,125,802 (GRCm39) exon noncoding transcript
R1707:Gm5422 UTSW 10 31,124,458 (GRCm39) exon noncoding transcript
R1893:Gm5422 UTSW 10 31,125,609 (GRCm39) exon noncoding transcript
R2011:Gm5422 UTSW 10 31,124,764 (GRCm39) exon noncoding transcript
R2132:Gm5422 UTSW 10 31,124,929 (GRCm39) exon noncoding transcript
R3427:Gm5422 UTSW 10 31,124,842 (GRCm39) exon noncoding transcript
R3772:Gm5422 UTSW 10 31,124,510 (GRCm39) exon noncoding transcript
R4703:Gm5422 UTSW 10 31,125,608 (GRCm39) exon noncoding transcript
R5539:Gm5422 UTSW 10 31,124,646 (GRCm39) exon noncoding transcript
R5603:Gm5422 UTSW 10 31,126,840 (GRCm39) exon noncoding transcript
R5660:Gm5422 UTSW 10 31,126,048 (GRCm39) exon noncoding transcript
R6124:Gm5422 UTSW 10 31,125,396 (GRCm39) exon noncoding transcript
R6178:Gm5422 UTSW 10 31,125,688 (GRCm39) exon noncoding transcript
R8263:Gm5422 UTSW 10 31,125,099 (GRCm39) missense noncoding transcript
Posted On 2014-01-21