Incidental Mutation 'IGL03305:Npy6r'
ID 416361
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Npy6r
Ensembl Gene ENSMUSG00000038071
Gene Name neuropeptide Y receptor Y6
Synonyms
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL03305
Quality Score
Status
Chromosome 18
Chromosomal Location 44403194-44410767 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 44408921 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Cysteine at position 114 (Y114C)
Ref Sequence ENSEMBL: ENSMUSP00000040797 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000042747]
AlphaFold Q61212
Predicted Effect probably damaging
Transcript: ENSMUST00000042747
AA Change: Y114C

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000040797
Gene: ENSMUSG00000038071
AA Change: Y114C

DomainStartEndE-ValueType
low complexity region 33 41 N/A INTRINSIC
Pfam:7tm_1 52 318 3.5e-51 PFAM
Coding Region Coverage
Validation Efficiency
MGI Phenotype PHENOTYPE: Mice homozygous for a reporter allele exhibit enhanced performance on the rotarod test. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 12 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A330008L17Rik T A 8: 100,146,462 (GRCm39) probably benign Het
Akap3 G A 6: 126,841,728 (GRCm39) V116I probably benign Het
B4galt5 T C 2: 167,147,703 (GRCm39) D224G probably damaging Het
Bmpr1b G T 3: 141,548,785 (GRCm39) probably benign Het
Chmp2a T C 7: 12,766,082 (GRCm39) K137E possibly damaging Het
Cpeb1 T C 7: 81,011,464 (GRCm39) K159R probably benign Het
Dhx36 G A 3: 62,408,257 (GRCm39) Q194* probably null Het
Gm4922 T A 10: 18,659,232 (GRCm39) K497* probably null Het
Grid1 A G 14: 34,973,664 (GRCm39) N247S probably damaging Het
Ppl A G 16: 4,911,097 (GRCm39) V785A possibly damaging Het
Tmprss11d T C 5: 86,474,279 (GRCm39) H88R probably damaging Het
Wdr64 G A 1: 175,583,152 (GRCm39) V373M possibly damaging Het
Other mutations in Npy6r
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00227:Npy6r APN 18 44,409,511 (GRCm39) missense probably damaging 1.00
IGL00767:Npy6r APN 18 44,409,385 (GRCm39) missense probably benign 0.01
IGL01103:Npy6r APN 18 44,408,585 (GRCm39) missense probably benign 0.15
IGL02085:Npy6r APN 18 44,408,998 (GRCm39) missense probably damaging 1.00
IGL02653:Npy6r APN 18 44,409,694 (GRCm39) makesense probably null
R0588:Npy6r UTSW 18 44,408,888 (GRCm39) missense possibly damaging 0.94
R1993:Npy6r UTSW 18 44,409,575 (GRCm39) missense probably damaging 1.00
R2039:Npy6r UTSW 18 44,409,070 (GRCm39) missense probably benign
R2567:Npy6r UTSW 18 44,408,888 (GRCm39) missense possibly damaging 0.68
R4572:Npy6r UTSW 18 44,408,984 (GRCm39) missense probably benign 0.03
R4584:Npy6r UTSW 18 44,409,262 (GRCm39) missense probably damaging 1.00
R4611:Npy6r UTSW 18 44,409,468 (GRCm39) missense probably damaging 1.00
R4741:Npy6r UTSW 18 44,408,791 (GRCm39) missense probably damaging 1.00
R5145:Npy6r UTSW 18 44,409,686 (GRCm39) missense probably benign 0.04
R5603:Npy6r UTSW 18 44,409,652 (GRCm39) missense probably damaging 1.00
R5610:Npy6r UTSW 18 44,409,061 (GRCm39) missense probably benign
R6030:Npy6r UTSW 18 44,409,149 (GRCm39) missense probably benign 0.02
R6030:Npy6r UTSW 18 44,409,149 (GRCm39) missense probably benign 0.02
R6083:Npy6r UTSW 18 44,409,559 (GRCm39) missense probably damaging 0.99
R6364:Npy6r UTSW 18 44,409,578 (GRCm39) missense possibly damaging 0.86
R7146:Npy6r UTSW 18 44,408,788 (GRCm39) missense probably benign 0.30
R7178:Npy6r UTSW 18 44,409,551 (GRCm39) missense probably damaging 1.00
R7180:Npy6r UTSW 18 44,409,223 (GRCm39) missense probably benign
R7203:Npy6r UTSW 18 44,408,999 (GRCm39) missense probably damaging 1.00
R7448:Npy6r UTSW 18 44,409,260 (GRCm39) missense probably damaging 1.00
R8425:Npy6r UTSW 18 44,409,070 (GRCm39) missense probably benign 0.03
R8845:Npy6r UTSW 18 44,408,606 (GRCm39) missense probably benign
R9389:Npy6r UTSW 18 44,408,759 (GRCm39) missense probably damaging 1.00
Posted On 2016-08-02