Incidental Mutation 'IGL01807:Atf1'
ID 155719
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Atf1
Ensembl Gene ENSMUSG00000023027
Gene Name activating transcription factor 1
Synonyms
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL01807
Quality Score
Status
Chromosome 15
Chromosomal Location 100125729-100159129 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) T to C at 100149945 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000132907 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000023769] [ENSMUST00000163855] [ENSMUST00000165804] [ENSMUST00000168103] [ENSMUST00000169408] [ENSMUST00000172154] [ENSMUST00000171869]
AlphaFold P81269
Predicted Effect probably benign
Transcript: ENSMUST00000023769
SMART Domains Protein: ENSMUSP00000023769
Gene: ENSMUSG00000023027

DomainStartEndE-ValueType
Pfam:pKID 43 83 3.9e-21 PFAM
BRLZ 209 266 3.28e-10 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000163855
Predicted Effect probably benign
Transcript: ENSMUST00000165804
SMART Domains Protein: ENSMUSP00000127969
Gene: ENSMUSG00000023027

DomainStartEndE-ValueType
Pfam:pKID 46 76 1.9e-19 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000166435
SMART Domains Protein: ENSMUSP00000127985
Gene: ENSMUSG00000023027

DomainStartEndE-ValueType
low complexity region 76 92 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000168103
Predicted Effect probably benign
Transcript: ENSMUST00000169408
Predicted Effect probably benign
Transcript: ENSMUST00000172154
SMART Domains Protein: ENSMUSP00000132907
Gene: ENSMUSG00000023027

DomainStartEndE-ValueType
Pfam:pKID 43 83 2.5e-20 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000171869
SMART Domains Protein: ENSMUSP00000131278
Gene: ENSMUSG00000023027

DomainStartEndE-ValueType
Pfam:pKID 43 67 5.2e-12 PFAM
Coding Region Coverage
Validation Efficiency
MGI Phenotype PHENOTYPE: Homozygous mutation of this gene does not result in a phenotype. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 31 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcc9 G T 6: 142,551,640 (GRCm39) L1223M probably damaging Het
Ano7 A G 1: 93,330,418 (GRCm39) E814G possibly damaging Het
Bco2 T C 9: 50,457,158 (GRCm39) probably benign Het
Birc6 A G 17: 74,938,032 (GRCm39) I2625V probably benign Het
Bub1 A G 2: 127,654,897 (GRCm39) S545P probably benign Het
Cacna1i T A 15: 80,258,348 (GRCm39) I1173N probably damaging Het
Ccdc175 T C 12: 72,206,616 (GRCm39) E210G probably benign Het
Ccl2 G A 11: 81,926,513 (GRCm39) G9D possibly damaging Het
Chmp2b T A 16: 65,337,091 (GRCm39) T189S probably benign Het
Col4a1 A T 8: 11,297,056 (GRCm39) probably benign Het
Ecm1 A G 3: 95,643,891 (GRCm39) S236P probably damaging Het
Epha8 A G 4: 136,658,993 (GRCm39) V887A probably benign Het
Fam227a T C 15: 79,533,856 (GRCm39) M36V probably benign Het
Fbxo15 T A 18: 84,999,506 (GRCm39) probably benign Het
Mtmr4 A G 11: 87,494,976 (GRCm39) I423V possibly damaging Het
Ngly1 C T 14: 16,290,873 (GRCm38) L452F probably benign Het
Or52u1 T A 7: 104,237,091 (GRCm39) W27R probably damaging Het
Or5ac15 T C 16: 58,939,936 (GRCm39) T166A possibly damaging Het
Pak2 T C 16: 31,856,097 (GRCm39) K247E probably damaging Het
Pola2 A G 19: 6,003,187 (GRCm39) probably benign Het
Ppp1r9a C T 6: 5,158,248 (GRCm39) Q1219* probably null Het
Rasgrf1 T C 9: 89,873,566 (GRCm39) I625T probably damaging Het
Rpap1 T C 2: 119,613,189 (GRCm39) T120A possibly damaging Het
Scin T C 12: 40,134,288 (GRCm39) Y252C probably damaging Het
Slc5a9 A T 4: 111,734,737 (GRCm39) *686R probably null Het
Smc1b T A 15: 84,980,946 (GRCm39) D774V probably damaging Het
Uba6 C T 5: 86,270,270 (GRCm39) R838Q probably damaging Het
Ulk4 A G 9: 121,084,251 (GRCm39) S105P probably damaging Het
Vwa3a G A 7: 120,374,729 (GRCm39) probably null Het
Xirp2 A G 2: 67,345,375 (GRCm39) T2539A probably benign Het
Zfpm2 T C 15: 40,616,452 (GRCm39) probably null Het
Other mutations in Atf1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02172:Atf1 APN 15 100,152,322 (GRCm39) missense probably damaging 0.99
IGL02718:Atf1 APN 15 100,152,100 (GRCm39) missense probably damaging 1.00
R0426:Atf1 UTSW 15 100,130,708 (GRCm39) missense possibly damaging 0.66
R1393:Atf1 UTSW 15 100,130,647 (GRCm39) missense possibly damaging 0.66
R1965:Atf1 UTSW 15 100,152,052 (GRCm39) missense probably benign 0.12
R1968:Atf1 UTSW 15 100,152,395 (GRCm39) critical splice donor site probably null
R4913:Atf1 UTSW 15 100,149,979 (GRCm39) splice site probably null
R5837:Atf1 UTSW 15 100,152,265 (GRCm39) missense probably damaging 1.00
R6064:Atf1 UTSW 15 100,150,029 (GRCm39) missense probably benign 0.24
R6230:Atf1 UTSW 15 100,130,705 (GRCm39) missense possibly damaging 0.46
R7625:Atf1 UTSW 15 100,152,158 (GRCm39) splice site probably null
R8094:Atf1 UTSW 15 100,143,170 (GRCm39) missense probably damaging 1.00
Posted On 2014-02-04