Incidental Mutation 'IGL00903:Zfas1'
ID 26834
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Zfas1
Ensembl Gene ENSMUSG00000074578
Gene Name zinc finger, NFX1-type containing 1, antisense RNA 1
Synonyms Zfos1, 1500012F01Rik
Accession Numbers
Essential gene? Not available question?
Stock # IGL00903
Quality Score
Status
Chromosome 2
Chromosomal Location 166904854-166907782 bp(+) (GRCm39)
Type of Mutation critical splice donor site (6 bp from exon)
DNA Base Change (assembly) G to T at 166907406 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s): [ENSMUST00000048988] [ENSMUST00000128676]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000048988
SMART Domains Protein: ENSMUSP00000049404
Gene: ENSMUSG00000039501

DomainStartEndE-ValueType
Pfam:AAA_11 590 855 2.2e-17 PFAM
Pfam:AAA_19 597 684 1.7e-10 PFAM
Pfam:AAA_11 829 1033 1.4e-18 PFAM
Pfam:AAA_12 1044 1228 3.7e-42 PFAM
internal_repeat_2 1281 1374 1.33e-7 PROSPERO
internal_repeat_1 1292 1410 1.32e-16 PROSPERO
low complexity region 1422 1433 N/A INTRINSIC
internal_repeat_1 1434 1547 1.32e-16 PROSPERO
internal_repeat_2 1453 1555 1.33e-7 PROSPERO
Predicted Effect noncoding transcript
Transcript: ENSMUST00000104327
Predicted Effect noncoding transcript
Transcript: ENSMUST00000104377
Predicted Effect noncoding transcript
Transcript: ENSMUST00000104510
Predicted Effect probably benign
Transcript: ENSMUST00000125674
SMART Domains Protein: ENSMUSP00000127947
Gene: ENSMUSG00000074578

DomainStartEndE-ValueType
low complexity region 2 13 N/A INTRINSIC
transmembrane domain 52 74 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000125841
Predicted Effect noncoding transcript
Transcript: ENSMUST00000189909
Predicted Effect noncoding transcript
Transcript: ENSMUST00000184735
Predicted Effect noncoding transcript
Transcript: ENSMUST00000135967
Predicted Effect noncoding transcript
Transcript: ENSMUST00000136378
Predicted Effect noncoding transcript
Transcript: ENSMUST00000145859
Predicted Effect noncoding transcript
Transcript: ENSMUST00000143587
Predicted Effect probably benign
Transcript: ENSMUST00000128676
SMART Domains Protein: ENSMUSP00000121598
Gene: ENSMUSG00000039501

DomainStartEndE-ValueType
Pfam:AAA_11 590 837 1.8e-17 PFAM
Pfam:AAA_19 597 684 3.4e-11 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 27 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Arsk A G 13: 76,246,487 (GRCm39) probably null Het
As3mt A G 19: 46,700,673 (GRCm39) I159V probably benign Het
Atpsckmt T C 15: 31,606,261 (GRCm39) V73A possibly damaging Het
Ctsll3 C A 13: 60,948,075 (GRCm39) V201L probably benign Het
Dapk1 T C 13: 60,909,211 (GRCm39) Y1275H probably damaging Het
Erap1 G A 13: 74,821,826 (GRCm39) R727H probably benign Het
Fcrl6 T A 1: 172,426,674 (GRCm39) T91S probably benign Het
Gvin1 T C 7: 105,757,377 (GRCm39) E2364G probably benign Het
Hacd3 T C 9: 64,911,535 (GRCm39) probably benign Het
Hcls1 T A 16: 36,776,383 (GRCm39) probably null Het
Igf2r C T 17: 12,902,754 (GRCm39) R2432H possibly damaging Het
Kif27 C A 13: 58,492,486 (GRCm39) V218F possibly damaging Het
Klhl20 T C 1: 160,918,076 (GRCm39) Y70C probably benign Het
Krt86 C T 15: 101,371,741 (GRCm39) H104Y probably benign Het
Lcn12 G T 2: 25,383,332 (GRCm39) N15K possibly damaging Het
Mrgpra1 T C 7: 46,985,326 (GRCm39) M118V probably benign Het
Nacad G T 11: 6,550,632 (GRCm39) T853K probably damaging Het
Nos3 A T 5: 24,574,860 (GRCm39) Q293L probably damaging Het
Prkca C T 11: 107,874,800 (GRCm39) V381M probably damaging Het
Ptcd3 A G 6: 71,884,828 (GRCm39) F37S possibly damaging Het
Ptgs2 A G 1: 149,980,175 (GRCm39) Y371C probably damaging Het
Pygl T C 12: 70,254,516 (GRCm39) Y143C probably damaging Het
Samhd1 A G 2: 156,949,343 (GRCm39) probably benign Het
Scube1 T A 15: 83,587,702 (GRCm39) H89L probably damaging Het
Tmem59l G A 8: 70,938,315 (GRCm39) probably benign Het
Vmn2r108 A G 17: 20,682,774 (GRCm39) V810A probably damaging Het
Vmn2r61 T G 7: 41,949,935 (GRCm39) F785C probably damaging Het
Posted On 2013-04-17