Incidental Mutation 'IGL00163:Minar1'
ID 28103
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Minar1
Ensembl Gene ENSMUSG00000039313
Gene Name membrane integral NOTCH2 associated receptor 1
Synonyms DD1, AF529169
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL00163
Quality Score
Status
Chromosome 9
Chromosomal Location 89469269-89505178 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) A to T at 89473150 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000140942 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000044491] [ENSMUST00000191465]
AlphaFold Q8K3V7
Predicted Effect probably benign
Transcript: ENSMUST00000044491
SMART Domains Protein: ENSMUSP00000046111
Gene: ENSMUSG00000039313

DomainStartEndE-ValueType
low complexity region 508 522 N/A INTRINSIC
Pfam:UPF0258 760 915 8.7e-73 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000191465
SMART Domains Protein: ENSMUSP00000140942
Gene: ENSMUSG00000039313

DomainStartEndE-ValueType
low complexity region 508 522 N/A INTRINSIC
Pfam:UPF0258 759 854 6.1e-38 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 49 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930553M12Rik G A 4: 88,786,310 (GRCm39) Q103* probably null Het
4933406P04Rik C A 10: 20,186,970 (GRCm39) probably benign Het
Adgrg6 T C 10: 14,343,194 (GRCm39) E251G probably damaging Het
Ago2 T C 15: 72,998,302 (GRCm39) H292R probably benign Het
Akr1c6 T C 13: 4,498,977 (GRCm39) probably benign Het
Arhgap24 T A 5: 103,008,265 (GRCm39) M62K possibly damaging Het
Bicd1 A G 6: 149,451,888 (GRCm39) H834R possibly damaging Het
Ccdc77 G T 6: 120,306,045 (GRCm39) probably benign Het
Cdadc1 G T 14: 59,818,818 (GRCm39) H337N probably damaging Het
Cep192 A G 18: 68,013,871 (GRCm39) T2424A possibly damaging Het
Cep78 T C 19: 15,946,504 (GRCm39) T443A probably benign Het
Chrna1 T A 2: 73,400,986 (GRCm39) E181D probably benign Het
Dmxl1 G A 18: 49,984,534 (GRCm39) D177N probably damaging Het
Eif3h T A 15: 51,650,195 (GRCm39) I330F probably damaging Het
Fam184b T C 5: 45,697,091 (GRCm39) E691G probably benign Het
Fastkd1 T A 2: 69,537,893 (GRCm39) S230C probably benign Het
Gipc2 T C 3: 151,843,215 (GRCm39) I141V probably damaging Het
Hsd17b2 A T 8: 118,485,410 (GRCm39) D291V probably damaging Het
Itpr2 G A 6: 146,292,334 (GRCm39) A420V possibly damaging Het
Jag1 C T 2: 136,927,952 (GRCm39) probably null Het
Mmp1b T A 9: 7,387,946 (GRCm39) Y16F probably benign Het
Muc4 G T 16: 32,754,090 (GRCm38) R1322M probably benign Het
Myo9b T C 8: 71,801,379 (GRCm39) I1179T probably benign Het
Nos1ap A G 1: 170,342,175 (GRCm39) probably benign Het
Npc1l1 A T 11: 6,174,199 (GRCm39) V702E probably damaging Het
Or13d1 G A 4: 52,971,058 (GRCm39) V146M possibly damaging Het
Or1j21 A G 2: 36,684,012 (GRCm39) I255V probably benign Het
Or2ag17 T A 7: 106,389,796 (GRCm39) R137S probably benign Het
Or2y10 A C 11: 49,454,747 (GRCm39) probably benign Het
Or4c31 A T 2: 88,291,696 (GRCm39) Y4F probably benign Het
Or4f7 A C 2: 111,644,126 (GRCm39) probably benign Het
Osmr A T 15: 6,873,926 (GRCm39) L157* probably null Het
Pdzph1 T C 17: 59,281,791 (GRCm39) T164A possibly damaging Het
Ptn T C 6: 36,720,424 (GRCm39) K43E probably benign Het
Rbm45 T C 2: 76,209,051 (GRCm39) V340A probably damaging Het
Rnf5 C T 17: 34,821,083 (GRCm39) G83E probably damaging Het
Scin G T 12: 40,126,971 (GRCm39) Q459K probably benign Het
Serpina5 C A 12: 104,071,479 (GRCm39) A362D probably damaging Het
Tex47 T A 5: 7,355,468 (GRCm39) Y216* probably null Het
Tll1 A T 8: 64,469,170 (GRCm39) H984Q probably benign Het
Tmem259 A G 10: 79,815,568 (GRCm39) V81A probably benign Het
Tns3 A T 11: 8,401,066 (GRCm39) S1077R probably benign Het
Trgv3 G A 13: 19,427,381 (GRCm39) S88N probably benign Het
Ttc17 A G 2: 94,153,428 (GRCm39) probably benign Het
Tubgcp2 T C 7: 139,610,935 (GRCm39) T149A possibly damaging Het
Ulk1 G A 5: 110,935,738 (GRCm39) A25V probably damaging Het
Vps13d T C 4: 144,895,110 (GRCm39) E378G probably damaging Het
Vsig10 A G 5: 117,476,479 (GRCm39) N311S probably benign Het
Zfp511 T C 7: 139,617,429 (GRCm39) Y144H possibly damaging Het
Other mutations in Minar1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00089:Minar1 APN 9 89,483,853 (GRCm39) missense probably benign 0.02
IGL00336:Minar1 APN 9 89,485,196 (GRCm39) missense probably damaging 1.00
IGL01608:Minar1 APN 9 89,478,551 (GRCm39) missense probably benign 0.15
IGL01818:Minar1 APN 9 89,483,366 (GRCm39) missense probably damaging 0.99
IGL02012:Minar1 APN 9 89,483,491 (GRCm39) missense probably benign 0.01
IGL02259:Minar1 APN 9 89,484,412 (GRCm39) missense possibly damaging 0.93
IGL02894:Minar1 APN 9 89,485,155 (GRCm39) missense probably damaging 0.99
IGL03008:Minar1 APN 9 89,478,731 (GRCm39) missense probably damaging 1.00
IGL02988:Minar1 UTSW 9 89,484,792 (GRCm39) missense probably benign 0.02
R0410:Minar1 UTSW 9 89,484,256 (GRCm39) missense probably damaging 0.97
R0825:Minar1 UTSW 9 89,485,332 (GRCm39) nonsense probably null
R0883:Minar1 UTSW 9 89,484,470 (GRCm39) missense probably benign 0.05
R0989:Minar1 UTSW 9 89,484,088 (GRCm39) missense probably damaging 0.99
R1376:Minar1 UTSW 9 89,473,299 (GRCm39) missense probably damaging 1.00
R1376:Minar1 UTSW 9 89,473,299 (GRCm39) missense probably damaging 1.00
R1632:Minar1 UTSW 9 89,484,413 (GRCm39) missense probably damaging 0.96
R1804:Minar1 UTSW 9 89,485,152 (GRCm39) missense possibly damaging 0.91
R1974:Minar1 UTSW 9 89,483,256 (GRCm39) missense probably damaging 1.00
R2151:Minar1 UTSW 9 89,484,221 (GRCm39) missense possibly damaging 0.53
R2882:Minar1 UTSW 9 89,484,855 (GRCm39) missense possibly damaging 0.86
R2909:Minar1 UTSW 9 89,473,331 (GRCm39) missense probably damaging 1.00
R3961:Minar1 UTSW 9 89,483,963 (GRCm39) missense probably damaging 1.00
R3962:Minar1 UTSW 9 89,483,963 (GRCm39) missense probably damaging 1.00
R3963:Minar1 UTSW 9 89,483,963 (GRCm39) missense probably damaging 1.00
R4676:Minar1 UTSW 9 89,483,606 (GRCm39) missense probably damaging 1.00
R4778:Minar1 UTSW 9 89,485,155 (GRCm39) missense probably damaging 1.00
R4931:Minar1 UTSW 9 89,483,705 (GRCm39) missense probably benign 0.05
R5300:Minar1 UTSW 9 89,485,252 (GRCm39) missense probably damaging 1.00
R5702:Minar1 UTSW 9 89,473,208 (GRCm39) missense probably benign 0.22
R5759:Minar1 UTSW 9 89,483,125 (GRCm39) missense probably benign 0.01
R6187:Minar1 UTSW 9 89,473,220 (GRCm39) missense probably damaging 1.00
R7320:Minar1 UTSW 9 89,483,679 (GRCm39) missense probably benign
R7542:Minar1 UTSW 9 89,483,964 (GRCm39) missense probably damaging 1.00
R7552:Minar1 UTSW 9 89,483,888 (GRCm39) missense probably benign 0.00
R8826:Minar1 UTSW 9 89,483,234 (GRCm39) missense probably damaging 1.00
R9181:Minar1 UTSW 9 89,485,394 (GRCm39) start codon destroyed probably null 1.00
R9220:Minar1 UTSW 9 89,484,398 (GRCm39) missense probably damaging 1.00
R9560:Minar1 UTSW 9 89,484,531 (GRCm39) missense probably benign 0.00
R9666:Minar1 UTSW 9 89,484,072 (GRCm39) missense probably benign 0.06
U24488:Minar1 UTSW 9 89,485,100 (GRCm39) missense probably damaging 1.00
Z1177:Minar1 UTSW 9 89,485,215 (GRCm39) missense probably damaging 1.00
Posted On 2013-04-17