Incidental Mutation 'IGL03305:Gm4922'
ID 416366
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm4922
Ensembl Gene ENSMUSG00000044624
Gene Name predicted gene 4922
Synonyms
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL03305
Quality Score
Status
Chromosome 10
Chromosomal Location 18655475-18662541 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) T to A at 18659232 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Lysine to Stop codon at position 497 (K497*)
Ref Sequence ENSEMBL: ENSMUSP00000149756 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000055107] [ENSMUST00000216654]
AlphaFold Q8C0N0
Predicted Effect probably null
Transcript: ENSMUST00000055107
AA Change: K497*
SMART Domains Protein: ENSMUSP00000055273
Gene: ENSMUSG00000044624
AA Change: K497*

DomainStartEndE-ValueType
low complexity region 3 13 N/A INTRINSIC
S_TKc 28 275 1.92e-75 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000215162
Predicted Effect probably null
Transcript: ENSMUST00000216654
AA Change: K497*
Coding Region Coverage
Validation Efficiency
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
Grid1 A G 14: 34,973,664 (GRCm39) N247S probably damaging Het
Npy6r A G 18: 44,408,921 (GRCm39) Y114C 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 Gm4922
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01810:Gm4922 APN 10 18,659,795 (GRCm39) missense probably benign 0.20
IGL01818:Gm4922 APN 10 18,660,701 (GRCm39) missense unknown
IGL01931:Gm4922 APN 10 18,660,042 (GRCm39) missense probably benign 0.01
IGL02021:Gm4922 APN 10 18,660,225 (GRCm39) missense probably damaging 1.00
IGL02573:Gm4922 APN 10 18,659,423 (GRCm39) missense probably benign 0.05
R0149:Gm4922 UTSW 10 18,659,289 (GRCm39) missense probably benign 0.10
R0361:Gm4922 UTSW 10 18,659,289 (GRCm39) missense probably benign 0.10
R0564:Gm4922 UTSW 10 18,659,813 (GRCm39) missense possibly damaging 0.66
R1079:Gm4922 UTSW 10 18,660,086 (GRCm39) missense probably damaging 0.97
R1163:Gm4922 UTSW 10 18,659,469 (GRCm39) missense possibly damaging 0.83
R1164:Gm4922 UTSW 10 18,659,469 (GRCm39) missense possibly damaging 0.83
R1398:Gm4922 UTSW 10 18,659,496 (GRCm39) missense possibly damaging 0.65
R1458:Gm4922 UTSW 10 18,659,640 (GRCm39) nonsense probably null
R1867:Gm4922 UTSW 10 18,660,211 (GRCm39) missense possibly damaging 0.73
R1994:Gm4922 UTSW 10 18,659,388 (GRCm39) missense probably benign 0.10
R2146:Gm4922 UTSW 10 18,659,264 (GRCm39) missense probably benign
R2437:Gm4922 UTSW 10 18,659,829 (GRCm39) missense probably benign 0.00
R3551:Gm4922 UTSW 10 18,660,244 (GRCm39) missense probably benign 0.01
R3939:Gm4922 UTSW 10 18,660,362 (GRCm39) missense probably damaging 1.00
R4580:Gm4922 UTSW 10 18,659,432 (GRCm39) missense probably benign 0.00
R4602:Gm4922 UTSW 10 18,660,007 (GRCm39) nonsense probably null
R4704:Gm4922 UTSW 10 18,660,567 (GRCm39) missense probably benign 0.20
R4790:Gm4922 UTSW 10 18,659,916 (GRCm39) missense possibly damaging 0.58
R5478:Gm4922 UTSW 10 18,659,885 (GRCm39) missense probably benign
R5510:Gm4922 UTSW 10 18,659,745 (GRCm39) missense probably benign 0.00
R5694:Gm4922 UTSW 10 18,660,035 (GRCm39) missense possibly damaging 0.76
R6080:Gm4922 UTSW 10 18,660,500 (GRCm39) missense probably damaging 1.00
R6869:Gm4922 UTSW 10 18,660,263 (GRCm39) missense probably damaging 1.00
R6923:Gm4922 UTSW 10 18,659,616 (GRCm39) missense probably damaging 1.00
R7667:Gm4922 UTSW 10 18,660,096 (GRCm39) missense probably damaging 1.00
R8198:Gm4922 UTSW 10 18,659,340 (GRCm39) missense probably benign 0.00
R8270:Gm4922 UTSW 10 18,659,760 (GRCm39) missense probably benign 0.00
R8310:Gm4922 UTSW 10 18,659,536 (GRCm39) missense probably benign 0.09
R9454:Gm4922 UTSW 10 18,660,329 (GRCm39) missense probably damaging 1.00
Posted On 2016-08-02