Incidental Mutation 'IGL01805:Mucl3'
ID |
155641 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Mucl3
|
Ensembl Gene |
ENSMUSG00000073408 |
Gene Name |
mucin like 3 |
Synonyms |
LOC268949, Dpcr1 |
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.052)
|
Stock # |
IGL01805
|
Quality Score |
|
Status
|
|
Chromosome |
17 |
Chromosomal Location |
35946647-35954587 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to A
at 35948535 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Threonine to Serine
at position 355
(T355S)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000093120
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000095467]
[ENSMUST00000174521]
|
AlphaFold |
Q3TNW5 |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000095467
AA Change: T355S
PolyPhen 2
Score 0.617 (Sensitivity: 0.87; Specificity: 0.91)
|
SMART Domains |
Protein: ENSMUSP00000093120 Gene: ENSMUSG00000073408 AA Change: T355S
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
27 |
N/A |
INTRINSIC |
transmembrane domain
|
428 |
450 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000174521
|
SMART Domains |
Protein: ENSMUSP00000134221 Gene: ENSMUSG00000090509
Domain | Start | End | E-Value | Type |
Pfam:SFTA2
|
80 |
117 |
9.2e-18 |
PFAM |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000174534
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 28 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700019D03Rik |
T |
C |
1: 52,964,677 (GRCm39) |
D17G |
possibly damaging |
Het |
Adam28 |
G |
T |
14: 68,879,540 (GRCm39) |
S169R |
probably benign |
Het |
Aox1 |
T |
C |
1: 58,120,672 (GRCm39) |
M855T |
possibly damaging |
Het |
Apc |
C |
A |
18: 34,451,271 (GRCm39) |
N2688K |
probably benign |
Het |
Arhgap23 |
T |
A |
11: 97,383,428 (GRCm39) |
|
probably benign |
Het |
Bpifa6 |
A |
G |
2: 153,826,832 (GRCm39) |
T66A |
probably benign |
Het |
C1qtnf1 |
T |
A |
11: 118,338,993 (GRCm39) |
L221Q |
probably damaging |
Het |
Ccdc175 |
T |
A |
12: 72,176,003 (GRCm39) |
|
probably benign |
Het |
Ccl1 |
C |
A |
11: 82,068,958 (GRCm39) |
M26I |
possibly damaging |
Het |
Dnah10 |
T |
A |
5: 124,860,985 (GRCm39) |
F2123I |
probably damaging |
Het |
Fancm |
T |
C |
12: 65,160,635 (GRCm39) |
|
probably null |
Het |
Fstl4 |
C |
A |
11: 53,077,184 (GRCm39) |
A647E |
probably damaging |
Het |
Hmgb4 |
G |
T |
4: 128,154,015 (GRCm39) |
|
probably benign |
Het |
Hr |
A |
T |
14: 70,802,737 (GRCm39) |
|
probably benign |
Het |
Ilrun |
C |
T |
17: 27,986,880 (GRCm39) |
|
probably benign |
Het |
Kcna4 |
G |
T |
2: 107,126,843 (GRCm39) |
V526L |
probably damaging |
Het |
Mas1 |
T |
C |
17: 13,061,117 (GRCm39) |
Y102C |
probably damaging |
Het |
Mul1 |
C |
T |
4: 138,166,974 (GRCm39) |
P343S |
possibly damaging |
Het |
Obscn |
T |
C |
11: 59,023,422 (GRCm39) |
S652G |
probably damaging |
Het |
Or8g55 |
T |
C |
9: 39,785,075 (GRCm39) |
F168S |
probably damaging |
Het |
Pjvk |
A |
T |
2: 76,487,858 (GRCm39) |
N250I |
probably benign |
Het |
Pkd2 |
T |
C |
5: 104,630,959 (GRCm39) |
I461T |
probably benign |
Het |
Psen2 |
T |
C |
1: 180,057,403 (GRCm39) |
|
probably null |
Het |
Ralb |
T |
C |
1: 119,403,725 (GRCm39) |
E81G |
probably benign |
Het |
Slc15a4 |
T |
C |
5: 127,685,900 (GRCm39) |
T261A |
possibly damaging |
Het |
Vmn2r77 |
G |
A |
7: 86,460,395 (GRCm39) |
V574M |
probably benign |
Het |
Xrn2 |
A |
G |
2: 146,870,063 (GRCm39) |
I251V |
probably damaging |
Het |
Zfp974 |
G |
A |
7: 27,611,689 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Mucl3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00476:Mucl3
|
APN |
17 |
35,948,994 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL01321:Mucl3
|
APN |
17 |
35,947,758 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02320:Mucl3
|
APN |
17 |
35,948,332 (GRCm39) |
missense |
probably benign |
0.00 |
R1869:Mucl3
|
UTSW |
17 |
35,949,305 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4570:Mucl3
|
UTSW |
17 |
35,948,883 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4858:Mucl3
|
UTSW |
17 |
35,948,468 (GRCm39) |
missense |
possibly damaging |
0.74 |
R5592:Mucl3
|
UTSW |
17 |
35,954,535 (GRCm39) |
missense |
probably damaging |
0.99 |
R5733:Mucl3
|
UTSW |
17 |
35,949,102 (GRCm39) |
missense |
probably benign |
0.00 |
R7422:Mucl3
|
UTSW |
17 |
35,949,312 (GRCm39) |
missense |
probably benign |
0.00 |
R7689:Mucl3
|
UTSW |
17 |
35,948,969 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7780:Mucl3
|
UTSW |
17 |
35,947,874 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8079:Mucl3
|
UTSW |
17 |
35,949,084 (GRCm39) |
missense |
unknown |
|
R8320:Mucl3
|
UTSW |
17 |
35,954,530 (GRCm39) |
missense |
probably benign |
0.22 |
R8337:Mucl3
|
UTSW |
17 |
35,948,486 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8867:Mucl3
|
UTSW |
17 |
35,948,872 (GRCm39) |
missense |
probably benign |
0.27 |
R9734:Mucl3
|
UTSW |
17 |
35,949,233 (GRCm39) |
missense |
probably benign |
0.07 |
|
Posted On |
2014-02-04 |