Incidental Mutation 'IGL03066:Myg1'
ID |
409718 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Myg1
|
Ensembl Gene |
ENSMUSG00000001285 |
Gene Name |
melanocyte proliferating gene 1 |
Synonyms |
Gamm1 |
Accession Numbers |
|
Essential gene? |
Possibly non essential
(E-score: 0.255)
|
Stock # |
IGL03066
|
Quality Score |
|
Status
|
|
Chromosome |
15 |
Chromosomal Location |
102240144-102246574 bp(+) (GRCm39) |
Type of Mutation |
unclassified |
DNA Base Change (assembly) |
G to A
at 102242801 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000001331]
[ENSMUST00000001335]
[ENSMUST00000041208]
[ENSMUST00000062492]
[ENSMUST00000113682]
[ENSMUST00000165671]
[ENSMUST00000166658]
[ENSMUST00000170627]
[ENSMUST00000228959]
[ENSMUST00000165717]
|
AlphaFold |
Q9JK81 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000001331
|
SMART Domains |
Protein: ENSMUSP00000001331 Gene: ENSMUSG00000001285
Domain | Start | End | E-Value | Type |
Pfam:UPF0160
|
41 |
161 |
4.8e-54 |
PFAM |
Pfam:UPF0160
|
158 |
312 |
1.3e-59 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000001335
|
SMART Domains |
Protein: ENSMUSP00000001335 Gene: ENSMUSG00000001289
Domain | Start | End | E-Value | Type |
SCOP:d1fxkc_
|
12 |
58 |
4e-3 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000041208
|
SMART Domains |
Protein: ENSMUSP00000044604 Gene: ENSMUSG00000036678
Domain | Start | End | E-Value | Type |
WD40
|
136 |
179 |
3.7e0 |
SMART |
WD40
|
181 |
221 |
4.75e1 |
SMART |
WD40
|
232 |
273 |
1.17e-5 |
SMART |
WD40
|
278 |
315 |
2.66e0 |
SMART |
Blast:WD40
|
319 |
357 |
2e-15 |
BLAST |
low complexity region
|
534 |
545 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000062492
|
SMART Domains |
Protein: ENSMUSP00000126970 Gene: ENSMUSG00000001289
Domain | Start | End | E-Value | Type |
Pfam:Prefoldin
|
1 |
75 |
2.2e-20 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000113682
|
SMART Domains |
Protein: ENSMUSP00000109312 Gene: ENSMUSG00000001285
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
20 |
N/A |
INTRINSIC |
Pfam:UPF0160
|
45 |
365 |
1.5e-143 |
PFAM |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000164019
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000164961
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000171733
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000170078
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000170713
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000171244
|
SMART Domains |
Protein: ENSMUSP00000129494 Gene: ENSMUSG00000001285
Domain | Start | End | E-Value | Type |
Pfam:UPF0160
|
41 |
209 |
1.7e-76 |
PFAM |
Pfam:UPF0160
|
204 |
306 |
3.3e-43 |
PFAM |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000168805
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000170281
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000168547
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000229589
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000165671
|
SMART Domains |
Protein: ENSMUSP00000128526 Gene: ENSMUSG00000001289
Domain | Start | End | E-Value | Type |
Pfam:Prefoldin
|
1 |
75 |
2.2e-20 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000166658
|
SMART Domains |
Protein: ENSMUSP00000129178 Gene: ENSMUSG00000001289
Domain | Start | End | E-Value | Type |
Pfam:Prefoldin
|
22 |
143 |
8.6e-32 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000170627
|
SMART Domains |
Protein: ENSMUSP00000131245 Gene: ENSMUSG00000001289
Domain | Start | End | E-Value | Type |
Pfam:Prefoldin
|
7 |
99 |
4.6e-22 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000230239
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000228959
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000165717
|
SMART Domains |
Protein: ENSMUSP00000132441 Gene: ENSMUSG00000001289
Domain | Start | End | E-Value | Type |
Pfam:Prefoldin
|
1 |
72 |
1.4e-20 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000230406
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000231099
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000230812
|
Coding Region Coverage |
|
Validation Efficiency |
|
MGI Phenotype |
PHENOTYPE: Mice homozygous for a null mutation display no gross abnormalities but altered sex-dependent anxiety-like behaviors in different tests. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Brd4 |
A |
C |
17: 32,418,062 (GRCm39) |
|
probably benign |
Het |
Cd209d |
C |
A |
8: 3,928,437 (GRCm39) |
|
probably null |
Het |
Cela2a |
T |
A |
4: 141,548,765 (GRCm39) |
I124F |
probably damaging |
Het |
Cemip2 |
G |
A |
19: 21,801,207 (GRCm39) |
D775N |
possibly damaging |
Het |
Cnot2 |
A |
T |
10: 116,335,262 (GRCm39) |
N245K |
probably benign |
Het |
Cpt2 |
A |
G |
4: 107,765,183 (GRCm39) |
F148L |
probably benign |
Het |
Ctsj |
A |
C |
13: 61,152,302 (GRCm39) |
H21Q |
possibly damaging |
Het |
Cul4a |
A |
G |
8: 13,183,776 (GRCm39) |
N388S |
probably benign |
Het |
Dnah12 |
A |
G |
14: 26,418,553 (GRCm39) |
D147G |
probably benign |
Het |
Dnhd1 |
A |
G |
7: 105,369,089 (GRCm39) |
T4287A |
probably damaging |
Het |
Dock10 |
C |
A |
1: 80,562,758 (GRCm39) |
C534F |
probably benign |
Het |
Efcab14 |
A |
G |
4: 115,596,001 (GRCm39) |
E49G |
probably benign |
Het |
Fancm |
G |
T |
12: 65,171,888 (GRCm39) |
E86* |
probably null |
Het |
Galnt17 |
A |
T |
5: 130,929,486 (GRCm39) |
S440R |
probably benign |
Het |
Hectd4 |
T |
A |
5: 121,503,116 (GRCm39) |
Y4362N |
possibly damaging |
Het |
Lctl |
T |
G |
9: 64,025,017 (GRCm39) |
M1R |
probably null |
Het |
Llgl1 |
A |
G |
11: 60,596,860 (GRCm39) |
T154A |
possibly damaging |
Het |
Mink1 |
G |
T |
11: 70,499,715 (GRCm39) |
V750F |
probably benign |
Het |
Mroh7 |
A |
G |
4: 106,549,595 (GRCm39) |
V950A |
possibly damaging |
Het |
Or4x11 |
A |
T |
2: 89,867,778 (GRCm39) |
I172F |
probably damaging |
Het |
Or6b2b |
T |
A |
1: 92,419,305 (GRCm39) |
R57S |
probably damaging |
Het |
Or7d10 |
A |
G |
9: 19,831,667 (GRCm39) |
H54R |
probably benign |
Het |
Pask |
A |
T |
1: 93,258,588 (GRCm39) |
S253R |
probably benign |
Het |
Pkd1 |
C |
A |
17: 24,805,208 (GRCm39) |
H3253Q |
probably damaging |
Het |
Pkd1l2 |
G |
A |
8: 117,792,484 (GRCm39) |
T436I |
probably benign |
Het |
Rapgef4 |
A |
G |
2: 71,971,523 (GRCm39) |
|
probably benign |
Het |
Rnf169 |
G |
T |
7: 99,574,760 (GRCm39) |
R612S |
possibly damaging |
Het |
Sclt1 |
A |
T |
3: 41,672,278 (GRCm39) |
D104E |
probably benign |
Het |
Shh |
G |
T |
5: 28,666,369 (GRCm39) |
D172E |
probably damaging |
Het |
Sil1 |
G |
T |
18: 35,402,259 (GRCm39) |
|
probably benign |
Het |
Slc19a3 |
A |
G |
1: 82,992,557 (GRCm39) |
I388T |
probably damaging |
Het |
Spink5 |
A |
G |
18: 44,149,457 (GRCm39) |
Y946C |
probably damaging |
Het |
Sulf1 |
A |
T |
1: 12,878,168 (GRCm39) |
I219F |
probably damaging |
Het |
Tcf3 |
T |
C |
10: 80,248,879 (GRCm39) |
D529G |
probably damaging |
Het |
Txnip |
G |
A |
3: 96,466,934 (GRCm39) |
E203K |
probably damaging |
Het |
Ubc |
G |
T |
5: 125,465,327 (GRCm39) |
|
probably benign |
Het |
Ubxn4 |
A |
T |
1: 128,188,591 (GRCm39) |
|
probably null |
Het |
Usp16 |
T |
C |
16: 87,268,721 (GRCm39) |
V284A |
probably damaging |
Het |
Vmn2r6 |
T |
A |
3: 64,472,574 (GRCm39) |
N49I |
probably damaging |
Het |
Ythdf1 |
A |
T |
2: 180,553,339 (GRCm39) |
I292N |
probably damaging |
Het |
Zfp128 |
A |
G |
7: 12,624,044 (GRCm39) |
I137M |
probably benign |
Het |
|
Other mutations in Myg1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01369:Myg1
|
APN |
15 |
102,242,773 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02188:Myg1
|
APN |
15 |
102,245,876 (GRCm39) |
missense |
probably benign |
0.08 |
IGL02373:Myg1
|
APN |
15 |
102,245,268 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02885:Myg1
|
APN |
15 |
102,240,594 (GRCm39) |
missense |
probably damaging |
1.00 |
R0583:Myg1
|
UTSW |
15 |
102,246,225 (GRCm39) |
nonsense |
probably null |
|
R0631:Myg1
|
UTSW |
15 |
102,240,284 (GRCm39) |
missense |
probably benign |
0.00 |
R0835:Myg1
|
UTSW |
15 |
102,240,537 (GRCm39) |
missense |
probably damaging |
1.00 |
R1016:Myg1
|
UTSW |
15 |
102,242,786 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1466:Myg1
|
UTSW |
15 |
102,245,825 (GRCm39) |
missense |
probably damaging |
1.00 |
R1466:Myg1
|
UTSW |
15 |
102,245,825 (GRCm39) |
missense |
probably damaging |
1.00 |
R1757:Myg1
|
UTSW |
15 |
102,240,264 (GRCm39) |
missense |
probably benign |
|
R2400:Myg1
|
UTSW |
15 |
102,246,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R2428:Myg1
|
UTSW |
15 |
102,246,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R2429:Myg1
|
UTSW |
15 |
102,246,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R2431:Myg1
|
UTSW |
15 |
102,246,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R2997:Myg1
|
UTSW |
15 |
102,245,945 (GRCm39) |
missense |
probably null |
1.00 |
R3683:Myg1
|
UTSW |
15 |
102,246,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R3826:Myg1
|
UTSW |
15 |
102,246,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R3827:Myg1
|
UTSW |
15 |
102,246,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R3829:Myg1
|
UTSW |
15 |
102,246,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R4923:Myg1
|
UTSW |
15 |
102,240,288 (GRCm39) |
missense |
probably benign |
|
R5363:Myg1
|
UTSW |
15 |
102,246,259 (GRCm39) |
missense |
probably benign |
0.00 |
R5419:Myg1
|
UTSW |
15 |
102,245,397 (GRCm39) |
missense |
probably damaging |
0.99 |
R9389:Myg1
|
UTSW |
15 |
102,245,372 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Posted On |
2016-08-02 |