Incidental Mutation 'IGL01766:Znhit3'
ID 153683
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Znhit3
Ensembl Gene ENSMUSG00000020526
Gene Name zinc finger, HIT type 3
Synonyms Trip3
Accession Numbers
Essential gene? Probably essential (E-score: 0.791) question?
Stock # IGL01766
Quality Score
Status
Chromosome 11
Chromosomal Location 84801776-84807192 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) G to T at 84806959 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000099484 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000093969] [ENSMUST00000103195]
AlphaFold Q9CQK1
Predicted Effect probably benign
Transcript: ENSMUST00000093969
SMART Domains Protein: ENSMUSP00000091502
Gene: ENSMUSG00000020527

DomainStartEndE-ValueType
MYSc 29 759 4.07e-219 SMART
IQ 760 782 1.74e1 SMART
IQ 783 804 1.97e0 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000103195
SMART Domains Protein: ENSMUSP00000099484
Gene: ENSMUSG00000020526

DomainStartEndE-ValueType
Pfam:zf-HIT 7 36 9.3e-13 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000127838
Predicted Effect noncoding transcript
Transcript: ENSMUST00000136656
Predicted Effect noncoding transcript
Transcript: ENSMUST00000144552
Predicted Effect noncoding transcript
Transcript: ENSMUST00000156046
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
9330159F19Rik A G 10: 29,100,557 (GRCm39) D310G probably benign Het
Ahnak A G 19: 8,977,482 (GRCm39) T7A unknown Het
Arhgap21 T A 2: 20,854,448 (GRCm39) D1648V possibly damaging Het
Cd274 T C 19: 29,362,810 (GRCm39) *291Q probably null Het
Ceacam1 G A 7: 25,171,420 (GRCm39) S348L probably damaging Het
Dcaf13 T C 15: 38,982,145 (GRCm39) V37A probably benign Het
Degs1 A T 1: 182,106,660 (GRCm39) F200I probably damaging Het
Dock4 G T 12: 40,496,378 (GRCm39) E8* probably null Het
Dsc2 G A 18: 20,179,399 (GRCm39) P223L possibly damaging Het
Exo1 A G 1: 175,719,587 (GRCm39) T171A possibly damaging Het
Gen1 C T 12: 11,306,895 (GRCm39) D92N probably damaging Het
Gm572 A T 4: 148,739,352 (GRCm39) H60L possibly damaging Het
Gucy2c T C 6: 136,692,971 (GRCm39) T719A probably benign Het
Heatr5a T C 12: 51,936,447 (GRCm39) S1575G probably benign Het
Hspa12a T C 19: 58,787,899 (GRCm39) E641G probably damaging Het
Itgb4 G A 11: 115,879,752 (GRCm39) V635I probably damaging Het
Luzp1 T C 4: 136,270,084 (GRCm39) I769T possibly damaging Het
Map2k5 C T 9: 63,284,509 (GRCm39) A11T probably benign Het
Myo9b A G 8: 71,743,161 (GRCm39) E74G probably damaging Het
Myom1 T C 17: 71,384,283 (GRCm39) V666A probably damaging Het
Or1e29 T A 11: 73,667,901 (GRCm39) N84I probably benign Het
Or2n1 G T 17: 38,486,577 (GRCm39) V201L probably benign Het
Or5ak4 A G 2: 85,161,945 (GRCm39) L99S probably benign Het
Or6c69 A G 10: 129,747,649 (GRCm39) F166S probably damaging Het
Plekhg1 A G 10: 3,823,400 (GRCm39) T123A probably damaging Het
Polrmt T C 10: 79,572,402 (GRCm39) E1077G possibly damaging Het
Ptprh A G 7: 4,583,915 (GRCm39) W226R probably benign Het
Robo1 A G 16: 72,801,553 (GRCm39) H1059R probably benign Het
Sesn1 A G 10: 41,774,365 (GRCm39) T306A probably benign Het
Sox14 T A 9: 99,757,169 (GRCm39) H190L probably damaging Het
Spag8 G T 4: 43,653,209 (GRCm39) probably benign Het
Tomm40 T C 7: 19,437,007 (GRCm39) H20R possibly damaging Het
Other mutations in Znhit3
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01391:Znhit3 APN 11 84,802,283 (GRCm39) utr 3 prime probably benign
R4133:Znhit3 UTSW 11 84,807,139 (GRCm39) missense probably benign 0.03
R4625:Znhit3 UTSW 11 84,802,316 (GRCm39) missense probably damaging 0.99
R4700:Znhit3 UTSW 11 84,807,155 (GRCm39) missense probably benign 0.20
R5792:Znhit3 UTSW 11 84,806,910 (GRCm39) splice site probably null
Z1177:Znhit3 UTSW 11 84,804,076 (GRCm39) missense probably damaging 1.00
Posted On 2014-02-04