Incidental Mutation 'IGL02589:Idnk'
ID 299683
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Idnk
Ensembl Gene ENSMUSG00000050002
Gene Name idnK gluconokinase homolog (E. coli)
Synonyms 5133401N09Rik
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL02589
Quality Score
Status
Chromosome 13
Chromosomal Location 58305463-58312507 bp(+) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) G to T at 58311239 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000153324 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000051490] [ENSMUST00000109868] [ENSMUST00000225236] [ENSMUST00000226010]
AlphaFold Q8R0J8
Predicted Effect probably benign
Transcript: ENSMUST00000051490
SMART Domains Protein: ENSMUSP00000060218
Gene: ENSMUSG00000050002

DomainStartEndE-ValueType
Pfam:AAA_17 6 138 8.7e-8 PFAM
Pfam:SKI 13 183 1.3e-13 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000109868
SMART Domains Protein: ENSMUSP00000105494
Gene: ENSMUSG00000050002

DomainStartEndE-ValueType
Pfam:AAA_17 6 75 8.4e-11 PFAM
Pfam:SKI 13 60 2.9e-12 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000225236
Predicted Effect probably benign
Transcript: ENSMUST00000226010
Coding Region Coverage
Validation Efficiency
MGI Phenotype PHENOTYPE: Female mice homozygous for a targeted mutation exhibit impaired learning/memory during trace aversive conditioning, and both males and females show decreased tear production. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 43 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A2ml1 T G 6: 128,558,463 (GRCm39) I5L probably benign Het
Ang6 A G 14: 44,239,419 (GRCm39) I103T possibly damaging Het
Arhgdib A G 6: 136,910,576 (GRCm39) probably benign Het
Atp13a2 C T 4: 140,733,722 (GRCm39) T1037M probably damaging Het
Bptf T C 11: 107,002,357 (GRCm39) N252D possibly damaging Het
Capn2 T C 1: 182,311,913 (GRCm39) Y387C probably damaging Het
Cdc27 T G 11: 104,396,470 (GRCm39) D817A probably benign Het
Cdc45 C T 16: 18,617,479 (GRCm39) M200I probably benign Het
Cntnap3 T G 13: 64,940,244 (GRCm39) I318L probably benign Het
Cog6 A T 3: 52,914,691 (GRCm39) L255Q probably damaging Het
Ect2l T A 10: 18,016,342 (GRCm39) probably benign Het
Ercc5 T C 1: 44,203,209 (GRCm39) V282A probably damaging Het
Fras1 A G 5: 96,917,372 (GRCm39) D3464G probably damaging Het
Gabrg1 A T 5: 70,999,495 (GRCm39) L18* probably null Het
Ggcx T C 6: 72,406,131 (GRCm39) Y586H probably damaging Het
Gm5796 A T 14: 15,379,030 (GRCm39) K24* probably null Het
Gnb4 C T 3: 32,643,998 (GRCm39) V187M probably damaging Het
Gpt2 C T 8: 86,242,795 (GRCm39) Q276* probably null Het
Igkv3-9 A G 6: 70,565,683 (GRCm39) D94G possibly damaging Het
Ipo8 C A 6: 148,711,405 (GRCm39) L294F probably damaging Het
Itgad A T 7: 127,780,883 (GRCm39) D157V probably damaging Het
Kcnab3 A T 11: 69,222,928 (GRCm39) I392L probably benign Het
Kdm3b A G 18: 34,945,471 (GRCm39) S761G possibly damaging Het
Kif21a G A 15: 90,869,489 (GRCm39) T454M probably damaging Het
Lta4h A G 10: 93,310,793 (GRCm39) N441S probably benign Het
Man2a1 A G 17: 64,986,773 (GRCm39) E595G probably benign Het
Micos13 T C 17: 56,915,856 (GRCm39) E66G probably benign Het
Mvd T C 8: 123,164,773 (GRCm39) probably benign Het
Notch2 A G 3: 98,011,663 (GRCm39) probably null Het
Phf20l1 G T 15: 66,487,481 (GRCm39) probably benign Het
Rdm1 A G 11: 101,518,831 (GRCm39) S13G possibly damaging Het
Rnf123 G A 9: 107,945,501 (GRCm39) R390* probably null Het
Scn4a G T 11: 106,218,958 (GRCm39) D953E probably benign Het
Sh2b1 A G 7: 126,068,440 (GRCm39) I457T probably benign Het
Srrm1 G A 4: 135,052,415 (GRCm39) P658L unknown Het
Tagap C A 17: 8,152,504 (GRCm39) T563K possibly damaging Het
Ugt1a7c T C 1: 88,023,360 (GRCm39) I173T probably benign Het
Unc79 C T 12: 103,139,755 (GRCm39) A2370V probably damaging Het
Vmn2r102 T A 17: 19,901,480 (GRCm39) C536S probably damaging Het
Vmn2r53 G A 7: 12,315,872 (GRCm39) T649I possibly damaging Het
Whrn G A 4: 63,336,334 (GRCm39) Q301* probably null Het
Zfp1007 T A 5: 109,826,386 (GRCm39) H62L possibly damaging Het
Zfp518a G A 19: 40,903,061 (GRCm39) G997R probably damaging Het
Other mutations in Idnk
AlleleSourceChrCoordTypePredicted EffectPPH Score
R1773:Idnk UTSW 13 58,305,526 (GRCm39) missense probably damaging 0.96
R4648:Idnk UTSW 13 58,310,683 (GRCm39) missense probably benign 0.05
R4908:Idnk UTSW 13 58,311,267 (GRCm39) missense probably benign 0.00
R6523:Idnk UTSW 13 58,311,457 (GRCm39) missense probably damaging 1.00
R6947:Idnk UTSW 13 58,308,055 (GRCm39) splice site probably null
Posted On 2015-04-16