Incidental Mutation 'IGL02712:Angel1'
ID 304631
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Angel1
Ensembl Gene ENSMUSG00000021257
Gene Name angel homolog 1
Synonyms 1110030H02Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.164) question?
Stock # IGL02712
Quality Score
Status
Chromosome 12
Chromosomal Location 86747276-86773234 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) A to G at 86769613 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000021682 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000021682]
AlphaFold Q8VCU0
Predicted Effect probably benign
Transcript: ENSMUST00000021682
SMART Domains Protein: ENSMUSP00000021682
Gene: ENSMUSG00000021257

DomainStartEndE-ValueType
signal peptide 1 16 N/A INTRINSIC
Pfam:Exo_endo_phos 245 653 4.1e-40 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000163388
Predicted Effect noncoding transcript
Transcript: ENSMUST00000171293
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 40 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Arhgef33 T A 17: 80,667,802 (GRCm39) V289D probably damaging Het
Cabp5 A G 7: 13,137,271 (GRCm39) M93V probably damaging Het
Ces1a A C 8: 93,762,668 (GRCm39) V201G probably damaging Het
Cisd1 A G 10: 71,172,181 (GRCm39) F34L probably benign Het
Cyp26a1 T C 19: 37,688,426 (GRCm39) L316P probably damaging Het
Ddx39a A G 8: 84,448,386 (GRCm39) I213V probably benign Het
Ddx59 A T 1: 136,367,519 (GRCm39) N542I probably benign Het
Dytn T C 1: 63,703,581 (GRCm39) T233A probably benign Het
Fbxo7 A G 10: 85,860,302 (GRCm39) T49A possibly damaging Het
Fmnl2 C A 2: 52,926,510 (GRCm39) probably benign Het
Golga2 G T 2: 32,194,225 (GRCm39) K610N probably damaging Het
Hipk4 T C 7: 27,228,060 (GRCm39) Y269H probably damaging Het
Ifi209 T C 1: 173,470,267 (GRCm39) V285A possibly damaging Het
Ifna1 A G 4: 88,768,523 (GRCm39) D67G probably benign Het
Map3k13 T G 16: 21,724,005 (GRCm39) V329G probably damaging Het
Mrm3 T C 11: 76,134,683 (GRCm39) W29R possibly damaging Het
Nherf1 T C 11: 115,068,060 (GRCm39) V200A possibly damaging Het
Nos1ap T C 1: 170,156,820 (GRCm39) I213V possibly damaging Het
Nphp4 C T 4: 152,640,732 (GRCm39) T1033M probably damaging Het
Nr5a2 T C 1: 136,868,266 (GRCm39) probably null Het
Nrcam A G 12: 44,620,610 (GRCm39) Y885C probably damaging Het
Odr4 A G 1: 150,262,107 (GRCm39) probably null Het
Or1e17 T C 11: 73,831,756 (GRCm39) V228A probably benign Het
Or8b57 T C 9: 40,004,082 (GRCm39) H60R probably damaging Het
Ovgp1 T A 3: 105,893,829 (GRCm39) probably benign Het
Pdzd2 T C 15: 12,376,113 (GRCm39) S1341G probably benign Het
Pld2 T G 11: 70,447,905 (GRCm39) L856R probably benign Het
Plod1 A G 4: 148,003,344 (GRCm39) F494L possibly damaging Het
Pnkd T A 1: 74,389,027 (GRCm39) S233T possibly damaging Het
Rnf144b T C 13: 47,393,255 (GRCm39) I198T probably damaging Het
Rsc1a1 G T 4: 141,412,376 (GRCm39) Q179K probably benign Het
Slc5a10 C T 11: 61,598,632 (GRCm39) W249* probably null Het
Spata32 T G 11: 103,098,973 (GRCm39) probably benign Het
Stk4 T A 2: 163,938,817 (GRCm39) H228Q probably damaging Het
Szt2 T A 4: 118,242,030 (GRCm39) Q1592L probably benign Het
Tnc T A 4: 63,893,493 (GRCm39) I1598F probably damaging Het
Togaram2 A T 17: 72,011,749 (GRCm39) D476V probably benign Het
Ttll6 T G 11: 96,030,601 (GRCm39) probably benign Het
Vmn2r118 A G 17: 55,899,655 (GRCm39) S750P probably benign Het
Zswim5 C T 4: 116,842,892 (GRCm39) T879I probably damaging Het
Other mutations in Angel1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01678:Angel1 APN 12 86,763,800 (GRCm39) missense probably benign
IGL02738:Angel1 APN 12 86,752,060 (GRCm39) missense probably benign 0.10
R0521:Angel1 UTSW 12 86,769,681 (GRCm39) missense probably benign 0.01
R0626:Angel1 UTSW 12 86,764,487 (GRCm39) critical splice donor site probably null
R1929:Angel1 UTSW 12 86,749,093 (GRCm39) missense probably damaging 1.00
R4291:Angel1 UTSW 12 86,767,057 (GRCm39) missense probably damaging 1.00
R4292:Angel1 UTSW 12 86,767,057 (GRCm39) missense probably damaging 1.00
R4295:Angel1 UTSW 12 86,767,057 (GRCm39) missense probably damaging 1.00
R4450:Angel1 UTSW 12 86,768,698 (GRCm39) missense probably damaging 1.00
R4726:Angel1 UTSW 12 86,768,649 (GRCm39) missense probably damaging 0.99
R7097:Angel1 UTSW 12 86,773,158 (GRCm39) missense probably damaging 0.98
R7284:Angel1 UTSW 12 86,767,298 (GRCm39) missense probably damaging 1.00
R7616:Angel1 UTSW 12 86,764,510 (GRCm39) missense probably benign 0.00
R7984:Angel1 UTSW 12 86,767,068 (GRCm39) missense probably benign 0.33
R9010:Angel1 UTSW 12 86,770,153 (GRCm39) missense possibly damaging 0.78
Posted On 2015-04-16