Incidental Mutation 'IGL01717:Gigyf1'
ID 104963
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gigyf1
Ensembl Gene ENSMUSG00000029714
Gene Name GRB10 interacting GYF protein 1
Synonyms Perq1
Accession Numbers
Essential gene? Possibly essential (E-score: 0.531) question?
Stock # IGL01717
Quality Score
Status
Chromosome 5
Chromosomal Location 137516810-137526197 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 137523953 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Glutamic Acid at position 1041 (V1041E)
Ref Sequence ENSEMBL: ENSMUSP00000031727 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000031726] [ENSMUST00000031727] [ENSMUST00000111020] [ENSMUST00000111023] [ENSMUST00000111027] [ENSMUST00000111038] [ENSMUST00000140139] [ENSMUST00000170293] [ENSMUST00000143495] [ENSMUST00000150063] [ENSMUST00000132525] [ENSMUST00000168746]
AlphaFold Q99MR1
Predicted Effect probably benign
Transcript: ENSMUST00000031726
SMART Domains Protein: ENSMUSP00000031726
Gene: ENSMUSG00000029713

DomainStartEndE-ValueType
low complexity region 3 17 N/A INTRINSIC
WD40 44 83 1.05e-7 SMART
WD40 86 125 3.96e-3 SMART
WD40 132 170 1.57e-6 SMART
WD40 173 212 2.98e-7 SMART
WD40 215 254 2.1e-7 SMART
WD40 257 298 1.72e-3 SMART
WD40 301 340 2.04e-5 SMART
Predicted Effect probably damaging
Transcript: ENSMUST00000031727
AA Change: V1041E

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000031727
Gene: ENSMUSG00000029714
AA Change: V1041E

DomainStartEndE-ValueType
low complexity region 17 32 N/A INTRINSIC
low complexity region 69 87 N/A INTRINSIC
low complexity region 114 129 N/A INTRINSIC
low complexity region 253 269 N/A INTRINSIC
low complexity region 323 352 N/A INTRINSIC
low complexity region 360 379 N/A INTRINSIC
coiled coil region 424 450 N/A INTRINSIC
GYF 477 532 1.6e-25 SMART
low complexity region 534 543 N/A INTRINSIC
low complexity region 553 576 N/A INTRINSIC
low complexity region 597 613 N/A INTRINSIC
coiled coil region 671 735 N/A INTRINSIC
low complexity region 748 759 N/A INTRINSIC
low complexity region 826 837 N/A INTRINSIC
low complexity region 848 877 N/A INTRINSIC
low complexity region 881 893 N/A INTRINSIC
coiled coil region 957 984 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000111020
SMART Domains Protein: ENSMUSP00000106649
Gene: ENSMUSG00000029713

DomainStartEndE-ValueType
WD40 1 39 2.65e-4 SMART
WD40 42 81 3.96e-3 SMART
WD40 88 126 1.57e-6 SMART
WD40 129 168 2.98e-7 SMART
WD40 171 210 2.1e-7 SMART
WD40 213 254 1.72e-3 SMART
WD40 257 296 2.04e-5 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000111023
SMART Domains Protein: ENSMUSP00000106652
Gene: ENSMUSG00000029713

DomainStartEndE-ValueType
WD40 1 39 2.65e-4 SMART
WD40 42 81 3.96e-3 SMART
WD40 88 126 1.57e-6 SMART
WD40 129 168 2.98e-7 SMART
WD40 171 210 2.1e-7 SMART
WD40 213 254 1.72e-3 SMART
WD40 257 296 2.04e-5 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000111027
SMART Domains Protein: ENSMUSP00000106656
Gene: ENSMUSG00000029713

DomainStartEndE-ValueType
low complexity region 23 41 N/A INTRINSIC
low complexity region 45 59 N/A INTRINSIC
WD40 86 125 1.05e-7 SMART
WD40 128 167 3.96e-3 SMART
WD40 174 212 1.57e-6 SMART
WD40 215 254 2.98e-7 SMART
WD40 257 296 2.1e-7 SMART
WD40 299 340 1.72e-3 SMART
WD40 343 382 2.04e-5 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000111038
SMART Domains Protein: ENSMUSP00000106667
Gene: ENSMUSG00000029711

DomainStartEndE-ValueType
signal peptide 1 23 N/A INTRINSIC
Pfam:EPO_TPO 30 191 2.8e-69 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000125868
Predicted Effect noncoding transcript
Transcript: ENSMUST00000167225
Predicted Effect noncoding transcript
Transcript: ENSMUST00000142252
Predicted Effect noncoding transcript
Transcript: ENSMUST00000144667
Predicted Effect noncoding transcript
Transcript: ENSMUST00000185075
Predicted Effect noncoding transcript
Transcript: ENSMUST00000145238
Predicted Effect probably benign
Transcript: ENSMUST00000140139
SMART Domains Protein: ENSMUSP00000121942
Gene: ENSMUSG00000029713

DomainStartEndE-ValueType
low complexity region 3 17 N/A INTRINSIC
WD40 44 83 1.05e-7 SMART
WD40 86 125 3.96e-3 SMART
WD40 132 170 1.57e-6 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000170293
SMART Domains Protein: ENSMUSP00000128038
Gene: ENSMUSG00000029713

DomainStartEndE-ValueType
WD40 1 39 2.65e-4 SMART
WD40 42 81 3.96e-3 SMART
WD40 88 126 1.57e-6 SMART
WD40 129 168 2.98e-7 SMART
WD40 171 210 2.1e-7 SMART
WD40 213 254 1.72e-3 SMART
WD40 257 296 2.04e-5 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000143495
SMART Domains Protein: ENSMUSP00000126823
Gene: ENSMUSG00000029713

DomainStartEndE-ValueType
Pfam:WD40 1 25 3.8e-3 PFAM
WD40 32 70 1.57e-6 SMART
WD40 73 112 2.98e-7 SMART
WD40 115 154 2.1e-7 SMART
WD40 157 198 1.72e-3 SMART
WD40 201 240 2.04e-5 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000150063
SMART Domains Protein: ENSMUSP00000129353
Gene: ENSMUSG00000029713

DomainStartEndE-ValueType
low complexity region 3 17 N/A INTRINSIC
WD40 44 83 1.05e-7 SMART
WD40 86 125 3.96e-3 SMART
WD40 132 170 1.57e-6 SMART
WD40 173 212 2.98e-7 SMART
WD40 215 254 2.1e-7 SMART
WD40 257 298 1.72e-3 SMART
WD40 301 340 2.04e-5 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000132525
SMART Domains Protein: ENSMUSP00000119725
Gene: ENSMUSG00000029713

DomainStartEndE-ValueType
low complexity region 3 17 N/A INTRINSIC
WD40 44 83 1.05e-7 SMART
WD40 86 125 3.96e-3 SMART
WD40 132 170 1.57e-6 SMART
WD40 173 212 2.98e-7 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000168746
SMART Domains Protein: ENSMUSP00000132908
Gene: ENSMUSG00000029713

DomainStartEndE-ValueType
Pfam:WD40 1 25 3.8e-3 PFAM
WD40 32 70 1.57e-6 SMART
WD40 73 112 2.98e-7 SMART
WD40 115 154 2.1e-7 SMART
WD40 157 198 1.72e-3 SMART
WD40 201 240 2.04e-5 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aif1 A T 17: 35,390,531 (GRCm39) M73K probably damaging Het
Alk T C 17: 72,910,377 (GRCm39) I110V probably benign Het
Aoah T C 13: 21,184,147 (GRCm39) S404P probably damaging Het
Bhlhe41 A G 6: 145,808,763 (GRCm39) S350P possibly damaging Het
Bltp1 A G 3: 37,088,885 (GRCm39) S4112G probably benign Het
Capn12 A G 7: 28,588,530 (GRCm39) D540G probably benign Het
Chd6 A G 2: 160,807,179 (GRCm39) Y2012H possibly damaging Het
Col1a1 A G 11: 94,841,603 (GRCm39) T1284A unknown Het
Col24a1 T C 3: 145,230,018 (GRCm39) probably benign Het
Col4a5 T A X: 140,422,234 (GRCm39) V1070D unknown Het
Col6a5 T C 9: 105,817,472 (GRCm39) T280A unknown Het
Dicer1 A T 12: 104,669,046 (GRCm39) L1212* probably null Het
Gm4978 C T 9: 69,358,155 (GRCm39) probably benign Het
Gnai1 A G 5: 18,496,459 (GRCm39) probably null Het
Golgb1 C T 16: 36,735,864 (GRCm39) R1704* probably null Het
Incenp A G 19: 9,870,629 (GRCm39) probably benign Het
Lrrc39 A T 3: 116,373,146 (GRCm39) probably benign Het
Man2a2 T C 7: 80,017,113 (GRCm39) K319E probably damaging Het
Neb T C 2: 52,079,879 (GRCm39) D83G probably damaging Het
Osbpl6 T C 2: 76,418,938 (GRCm39) I732T probably damaging Het
Pacs1 T A 19: 5,218,000 (GRCm39) K130N probably damaging Het
Pappa2 A G 1: 158,684,702 (GRCm39) probably null Het
Pole2 T C 12: 69,260,623 (GRCm39) M186V probably damaging Het
Rwdd4a T C 8: 47,997,140 (GRCm39) probably benign Het
Sel1l3 A G 5: 53,357,510 (GRCm39) Y161H probably damaging Het
Sf3a2 C T 10: 80,640,526 (GRCm39) Q446* probably null Het
Slc26a3 T C 12: 31,513,476 (GRCm39) I466T probably benign Het
Slc29a4 A T 5: 142,704,501 (GRCm39) I348F probably damaging Het
Tbl1xr1 A G 3: 22,247,335 (GRCm39) probably benign Het
Tlr5 A T 1: 182,802,963 (GRCm39) I756F probably damaging Het
Ttn A T 2: 76,560,748 (GRCm39) L29218I probably damaging Het
Ttn T A 2: 76,560,746 (GRCm39) L29218F probably damaging Het
Other mutations in Gigyf1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00230:Gigyf1 APN 5 137,521,007 (GRCm39) unclassified probably benign
IGL00326:Gigyf1 APN 5 137,517,210 (GRCm39) utr 5 prime probably benign
IGL00935:Gigyf1 APN 5 137,523,096 (GRCm39) missense possibly damaging 0.95
IGL02090:Gigyf1 APN 5 137,523,826 (GRCm39) splice site probably null
IGL02354:Gigyf1 APN 5 137,517,989 (GRCm39) splice site probably benign
IGL02361:Gigyf1 APN 5 137,517,989 (GRCm39) splice site probably benign
IGL03370:Gigyf1 APN 5 137,523,952 (GRCm39) missense possibly damaging 0.93
PIT4354001:Gigyf1 UTSW 5 137,522,366 (GRCm39) missense unknown
R1415:Gigyf1 UTSW 5 137,517,478 (GRCm39) splice site probably null
R1764:Gigyf1 UTSW 5 137,520,770 (GRCm39) unclassified probably benign
R2259:Gigyf1 UTSW 5 137,518,594 (GRCm39) missense possibly damaging 0.93
R2260:Gigyf1 UTSW 5 137,518,594 (GRCm39) missense possibly damaging 0.93
R4656:Gigyf1 UTSW 5 137,523,477 (GRCm39) nonsense probably null
R4717:Gigyf1 UTSW 5 137,523,494 (GRCm39) missense probably damaging 1.00
R4732:Gigyf1 UTSW 5 137,523,032 (GRCm39) missense probably benign 0.39
R4733:Gigyf1 UTSW 5 137,523,032 (GRCm39) missense probably benign 0.39
R4942:Gigyf1 UTSW 5 137,523,952 (GRCm39) missense possibly damaging 0.93
R5338:Gigyf1 UTSW 5 137,521,422 (GRCm39) unclassified probably benign
R5503:Gigyf1 UTSW 5 137,521,729 (GRCm39) unclassified probably benign
R5790:Gigyf1 UTSW 5 137,522,517 (GRCm39) unclassified probably benign
R5888:Gigyf1 UTSW 5 137,523,959 (GRCm39) missense probably damaging 1.00
R5955:Gigyf1 UTSW 5 137,521,769 (GRCm39) splice site probably null
R6544:Gigyf1 UTSW 5 137,523,321 (GRCm39) missense probably damaging 1.00
R7227:Gigyf1 UTSW 5 137,522,085 (GRCm39) missense unknown
R7493:Gigyf1 UTSW 5 137,523,795 (GRCm39) missense probably damaging 0.98
R7660:Gigyf1 UTSW 5 137,519,231 (GRCm39) missense probably benign 0.23
R7959:Gigyf1 UTSW 5 137,522,581 (GRCm39) missense probably damaging 1.00
R8026:Gigyf1 UTSW 5 137,523,740 (GRCm39) missense probably damaging 1.00
R8159:Gigyf1 UTSW 5 137,520,457 (GRCm39) missense unknown
R8552:Gigyf1 UTSW 5 137,521,401 (GRCm39) unclassified probably benign
R8936:Gigyf1 UTSW 5 137,523,469 (GRCm39) missense probably damaging 0.99
R9622:Gigyf1 UTSW 5 137,522,926 (GRCm39) nonsense probably null
Posted On 2014-01-21