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)
|
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
Domain | Start | End | E-Value | Type |
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
Domain | Start | End | E-Value | Type |
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
Domain | Start | End | E-Value | Type |
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
Domain | Start | End | E-Value | Type |
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
Domain | Start | End | E-Value | Type |
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
Domain | Start | End | E-Value | Type |
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
Domain | Start | End | E-Value | Type |
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
Domain | Start | End | E-Value | Type |
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
Domain | Start | End | E-Value | Type |
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
Domain | Start | End | E-Value | Type |
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
Domain | Start | End | E-Value | Type |
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
Domain | Start | End | E-Value | Type |
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
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
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 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH 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 |