Incidental Mutation 'IGL00089:Adgre4'
ID 778
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Adgre4
Ensembl Gene ENSMUSG00000032915
Gene Name adhesion G protein-coupled receptor E4
Synonyms EGF-TM7, Gpr127, FIRE, Emr4, D17Ertd479e
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL00089
Quality Score
Status
Chromosome 17
Chromosomal Location 56056984-56160662 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) A to T at 56098915 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000025004 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000025004]
AlphaFold Q91ZE5
Predicted Effect probably benign
Transcript: ENSMUST00000025004
SMART Domains Protein: ENSMUSP00000025004
Gene: ENSMUSG00000032915

DomainStartEndE-ValueType
signal peptide 1 36 N/A INTRINSIC
Blast:EGF_like 38 76 2e-10 BLAST
Pfam:EGF_CA 77 117 3.6e-9 PFAM
GPS 288 338 4.03e-12 SMART
Pfam:7tm_2 343 588 5.7e-57 PFAM
low complexity region 613 628 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 80 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A430033K04Rik T C 5: 138,645,854 (GRCm39) S580P probably damaging Het
Abca12 T A 1: 71,342,700 (GRCm39) I927F possibly damaging Het
Abca8a A G 11: 109,941,765 (GRCm39) V1168A possibly damaging Het
Abcc1 T A 16: 14,278,847 (GRCm39) N1052K probably benign Het
Adamts13 C A 2: 26,895,373 (GRCm39) Q1155K probably benign Het
Ahsa2 T C 11: 23,446,837 (GRCm39) E42G probably damaging Het
Ankk1 T G 9: 49,333,200 (GRCm39) I95L probably benign Het
Anpep A T 7: 79,491,734 (GRCm39) L89Q probably damaging Het
Arl5a T C 2: 52,306,083 (GRCm39) N83S probably benign Het
Atp11b A G 3: 35,863,525 (GRCm39) probably null Het
Atp6v0a2 T C 5: 124,798,841 (GRCm39) F849L probably benign Het
BC106179 A G 16: 23,043,022 (GRCm39) probably benign Het
Bcl2a1c T C 9: 114,159,608 (GRCm39) *129Q probably null Het
C2cd5 T C 6: 142,963,671 (GRCm39) I888V probably null Het
Calb2 A T 8: 110,872,303 (GRCm39) L227Q probably damaging Het
Ccp110 G T 7: 118,321,647 (GRCm39) C434F possibly damaging Het
Cd209c A T 8: 3,990,339 (GRCm39) C160S probably damaging Het
Chmp1a A G 8: 123,935,758 (GRCm39) probably null Het
Col6a6 T A 9: 105,635,390 (GRCm39) probably null Het
Cyld T A 8: 89,432,085 (GRCm39) C28S probably benign Het
Dapk1 A T 13: 60,908,854 (GRCm39) I1156F probably benign Het
Dennd1a A T 2: 38,133,454 (GRCm39) Y16* probably null Het
Dennd3 T G 15: 73,438,982 (GRCm39) S1117A probably benign Het
Dgka A T 10: 128,568,955 (GRCm39) D203E probably damaging Het
Dhx15 G T 5: 52,324,117 (GRCm39) L392I probably damaging Het
Dnah10 A G 5: 124,823,680 (GRCm39) D567G probably benign Het
Eaf1 T A 14: 31,226,483 (GRCm39) probably null Het
Efnb2 T C 8: 8,710,589 (GRCm39) D9G probably benign Het
Fcrla A T 1: 170,755,067 (GRCm39) C15S probably benign Het
Flt3 T C 5: 147,291,686 (GRCm39) N588S probably damaging Het
Garre1 A T 7: 33,945,412 (GRCm39) probably benign Het
Gm10146 A T 10: 78,229,307 (GRCm39) noncoding transcript Het
Gnpat T C 8: 125,603,653 (GRCm39) probably benign Het
Golm2 T C 2: 121,741,274 (GRCm39) probably benign Het
Gpr39 A C 1: 125,800,468 (GRCm39) R406S probably benign Het
H2-Aa T C 17: 34,503,504 (GRCm39) H31R probably damaging Het
Helz2 G T 2: 180,871,495 (GRCm39) R2706S probably damaging Het
Hip1r T A 5: 124,127,798 (GRCm39) probably null Het
Hnf4g A G 3: 3,713,142 (GRCm39) T239A probably benign Het
Hps5 A T 7: 46,425,362 (GRCm39) I413N probably damaging Het
Hspg2 G A 4: 137,256,131 (GRCm39) G1413R probably damaging Het
Itgax T G 7: 127,734,498 (GRCm39) M352R probably damaging Het
Katna1 T A 10: 7,638,568 (GRCm39) M433K probably damaging Het
Kcna4 T G 2: 107,126,207 (GRCm39) S314A probably damaging Het
Kif13b C T 14: 64,907,142 (GRCm39) T42I possibly damaging Het
Krt78 G A 15: 101,855,945 (GRCm39) T622I probably benign Het
Krt86 T A 15: 101,374,396 (GRCm39) M263K possibly damaging Het
Lap3 A G 5: 45,663,511 (GRCm39) probably benign Het
Lepr A T 4: 101,672,232 (GRCm39) R1085S probably benign Het
Lmcd1 A G 6: 112,306,769 (GRCm39) I314V probably benign Het
Luc7l2 T C 6: 38,585,105 (GRCm39) probably benign Het
Mcm2 T A 6: 88,870,383 (GRCm39) M117L probably benign Het
Mdh2 T C 5: 135,815,138 (GRCm39) Y133H probably damaging Het
Minar1 C T 9: 89,483,853 (GRCm39) V515I probably benign Het
Mlkl T A 8: 112,046,060 (GRCm39) R317* probably null Het
Mrps34 T C 17: 25,114,344 (GRCm39) L68P probably damaging Het
Muc4 G A 16: 32,754,086 (GRCm38) G1321R probably benign Het
Myo18a A G 11: 77,738,764 (GRCm39) E1299G probably damaging Het
Nlrp14 T C 7: 106,791,709 (GRCm39) L139P possibly damaging Het
Nudcd2 A G 11: 40,627,413 (GRCm39) D86G probably damaging Het
Or10u4 T A 10: 129,801,673 (GRCm39) R293W probably damaging Het
Or4c107 T A 2: 88,789,110 (GRCm39) I100N probably damaging Het
Or4f62 A T 2: 111,986,412 (GRCm39) M39L probably benign Het
Patj T C 4: 98,353,343 (GRCm39) F629L probably damaging Het
Rad23a A G 8: 85,562,524 (GRCm39) F280L probably damaging Het
Ralgapa1 C A 12: 55,769,558 (GRCm39) G811V probably damaging Het
St18 A G 1: 6,872,796 (GRCm39) D177G probably benign Het
Sult1c2 A C 17: 54,140,147 (GRCm39) Y159* probably null Het
Surf6 T A 2: 26,783,081 (GRCm39) probably null Het
Susd6 T G 12: 80,916,841 (GRCm39) probably benign Het
Sypl2 G A 3: 108,133,742 (GRCm39) probably benign Het
Ubr5 A T 15: 37,984,280 (GRCm39) F2289Y probably damaging Het
Vcl T C 14: 21,037,071 (GRCm39) I223T probably benign Het
Vmn1r234 C T 17: 21,449,860 (GRCm39) T258I possibly damaging Het
Vmn2r58 T A 7: 41,513,854 (GRCm39) K263M possibly damaging Het
Vmo1 A T 11: 70,404,424 (GRCm39) N192K probably damaging Het
Wrnip1 A G 13: 33,000,312 (GRCm39) N440D probably damaging Het
Zc3h4 T C 7: 16,156,159 (GRCm39) Y264H unknown Het
Zfp639 T G 3: 32,573,902 (GRCm39) probably null Het
Zfp831 T C 2: 174,488,078 (GRCm39) Y918H possibly damaging Het
Other mutations in Adgre4
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00228:Adgre4 APN 17 56,109,135 (GRCm39) missense probably damaging 1.00
IGL00572:Adgre4 APN 17 56,127,648 (GRCm39) missense probably benign 0.00
IGL01404:Adgre4 APN 17 56,104,639 (GRCm39) missense possibly damaging 0.63
IGL01420:Adgre4 APN 17 56,106,785 (GRCm39) splice site probably benign
IGL01501:Adgre4 APN 17 56,109,002 (GRCm39) splice site probably benign
IGL01510:Adgre4 APN 17 56,125,760 (GRCm39) critical splice donor site probably null
IGL01554:Adgre4 APN 17 56,124,090 (GRCm39) missense probably damaging 1.00
IGL01607:Adgre4 APN 17 56,101,748 (GRCm39) splice site probably benign
IGL01767:Adgre4 APN 17 56,104,740 (GRCm39) missense probably benign 0.19
IGL02253:Adgre4 APN 17 56,067,573 (GRCm39) missense probably benign 0.01
IGL02358:Adgre4 APN 17 56,150,209 (GRCm39) missense probably benign 0.15
IGL02466:Adgre4 APN 17 56,121,188 (GRCm39) missense probably benign 0.42
IGL03057:Adgre4 APN 17 56,106,602 (GRCm39) splice site probably benign
R0070:Adgre4 UTSW 17 56,109,154 (GRCm39) missense probably damaging 0.98
R0070:Adgre4 UTSW 17 56,109,154 (GRCm39) missense probably damaging 0.98
R0111:Adgre4 UTSW 17 56,124,073 (GRCm39) missense possibly damaging 0.92
R0311:Adgre4 UTSW 17 56,109,010 (GRCm39) missense probably benign 0.36
R0366:Adgre4 UTSW 17 56,099,001 (GRCm39) nonsense probably null
R0415:Adgre4 UTSW 17 56,159,288 (GRCm39) missense probably benign 0.03
R0465:Adgre4 UTSW 17 56,092,137 (GRCm39) splice site probably benign
R0619:Adgre4 UTSW 17 56,127,679 (GRCm39) missense possibly damaging 0.52
R0685:Adgre4 UTSW 17 56,099,035 (GRCm39) missense probably benign 0.05
R0724:Adgre4 UTSW 17 56,159,281 (GRCm39) missense probably benign 0.00
R0835:Adgre4 UTSW 17 56,106,637 (GRCm39) missense probably damaging 1.00
R1330:Adgre4 UTSW 17 56,085,814 (GRCm39) missense probably benign 0.36
R1452:Adgre4 UTSW 17 56,091,996 (GRCm39) missense probably benign 0.35
R1960:Adgre4 UTSW 17 56,098,497 (GRCm39) missense probably benign
R1961:Adgre4 UTSW 17 56,098,497 (GRCm39) missense probably benign
R2046:Adgre4 UTSW 17 56,085,847 (GRCm39) missense possibly damaging 0.82
R2421:Adgre4 UTSW 17 56,085,872 (GRCm39) missense probably benign 0.10
R2570:Adgre4 UTSW 17 56,085,878 (GRCm39) missense possibly damaging 0.54
R3162:Adgre4 UTSW 17 56,109,218 (GRCm39) splice site probably benign
R4222:Adgre4 UTSW 17 56,092,121 (GRCm39) missense probably damaging 1.00
R4526:Adgre4 UTSW 17 56,092,016 (GRCm39) nonsense probably null
R4631:Adgre4 UTSW 17 56,121,305 (GRCm39) missense probably null 1.00
R4689:Adgre4 UTSW 17 56,109,096 (GRCm39) missense probably damaging 1.00
R4701:Adgre4 UTSW 17 56,091,971 (GRCm39) missense probably damaging 1.00
R4792:Adgre4 UTSW 17 56,098,491 (GRCm39) missense probably benign 0.00
R5205:Adgre4 UTSW 17 56,101,727 (GRCm39) nonsense probably null
R5210:Adgre4 UTSW 17 56,092,029 (GRCm39) missense probably damaging 0.97
R5358:Adgre4 UTSW 17 56,125,758 (GRCm39) missense probably benign 0.00
R5873:Adgre4 UTSW 17 56,159,282 (GRCm39) missense probably benign 0.13
R6025:Adgre4 UTSW 17 56,099,013 (GRCm39) missense probably benign 0.00
R6257:Adgre4 UTSW 17 56,109,133 (GRCm39) missense possibly damaging 0.87
R6426:Adgre4 UTSW 17 56,109,196 (GRCm39) missense probably benign 0.18
R6440:Adgre4 UTSW 17 56,101,744 (GRCm39) critical splice donor site probably null
R6484:Adgre4 UTSW 17 56,109,036 (GRCm39) missense possibly damaging 0.52
R6680:Adgre4 UTSW 17 56,098,959 (GRCm39) missense probably benign 0.09
R7086:Adgre4 UTSW 17 56,127,649 (GRCm39) missense probably benign 0.00
R7442:Adgre4 UTSW 17 56,159,340 (GRCm39) missense probably benign 0.04
R7467:Adgre4 UTSW 17 56,098,952 (GRCm39) missense probably benign 0.00
R7875:Adgre4 UTSW 17 56,099,016 (GRCm39) missense probably benign 0.00
R8007:Adgre4 UTSW 17 56,121,233 (GRCm39) missense probably damaging 0.99
R8096:Adgre4 UTSW 17 56,127,700 (GRCm39) missense probably damaging 1.00
R8172:Adgre4 UTSW 17 56,104,769 (GRCm39) missense probably benign 0.00
R8512:Adgre4 UTSW 17 56,125,760 (GRCm39) critical splice donor site probably null
R8972:Adgre4 UTSW 17 56,109,189 (GRCm39) missense probably damaging 1.00
R9018:Adgre4 UTSW 17 56,098,993 (GRCm39) missense probably benign 0.00
R9049:Adgre4 UTSW 17 56,092,094 (GRCm39) missense probably benign 0.05
S24628:Adgre4 UTSW 17 56,159,288 (GRCm39) missense probably benign 0.03
X0010:Adgre4 UTSW 17 56,121,308 (GRCm39) missense probably damaging 1.00
Z1177:Adgre4 UTSW 17 56,121,152 (GRCm39) critical splice acceptor site probably null
Posted On 2011-07-12