Incidental Mutation 'IGL01106:Mcoln3'
| ID |
50745 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Mcoln3
|
| Ensembl Gene |
ENSMUSG00000036853 |
| Gene Name |
mucolipin 3 |
| Synonyms |
Va, varitint-waddler, TRPML3, 6720490O21Rik |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.183)
|
| Stock # |
IGL01106
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
3 |
| Chromosomal Location |
145823205-145847561 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 145843019 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Threonine to Alanine
at position 368
(T368A)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000038801
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000039450]
|
| AlphaFold |
Q8R4F0 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000039450
AA Change: T368A
PolyPhen 2
Score 0.006 (Sensitivity: 0.97; Specificity: 0.75)
|
| SMART Domains |
Protein: ENSMUSP00000038801
Gene: ENSMUSG00000036853
AA Change: T368A
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
24 |
29 |
N/A |
INTRINSIC |
|
transmembrane domain
|
286 |
308 |
N/A |
INTRINSIC |
|
transmembrane domain
|
335 |
357 |
N/A |
INTRINSIC |
|
Pfam:PKD_channel
|
360 |
508 |
3.5e-15 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000146689
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes one of members of the mucolipin cation channel proteins. Mutation studies of the highly similar protein in mice have shown that the protein is found in cochlea hair cells, and mutant mice show early-onset hearing loss and balance problems. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2011]
PHENOTYPE: Heterozygotes show normal/diluted/white hair patches, circling, hyperactivity, deafness, and reduced fertility. Homozygotes are white with small patches of color and show severe behavioral abnormalities, poor postnatal viability and are nearly infertile. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 29 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Atg13 |
T |
C |
2: 91,526,297 (GRCm39) |
D12G |
probably damaging |
Het |
| Cmya5 |
A |
G |
13: 93,221,120 (GRCm39) |
L3163P |
probably damaging |
Het |
| Cntn2 |
A |
G |
1: 132,449,622 (GRCm39) |
|
probably benign |
Het |
| Ddx23 |
C |
T |
15: 98,548,821 (GRCm39) |
R327Q |
probably benign |
Het |
| Dlec1 |
G |
A |
9: 118,931,853 (GRCm39) |
E91K |
probably benign |
Het |
| Fam13c |
T |
C |
10: 70,284,646 (GRCm39) |
|
probably null |
Het |
| Fbn1 |
T |
C |
2: 125,193,626 (GRCm39) |
T1398A |
possibly damaging |
Het |
| Frem1 |
T |
C |
4: 82,840,494 (GRCm39) |
T1793A |
probably benign |
Het |
| Gprc5b |
T |
C |
7: 118,583,084 (GRCm39) |
K262E |
probably benign |
Het |
| Hadh |
A |
T |
3: 131,034,619 (GRCm39) |
Y226N |
possibly damaging |
Het |
| Herc1 |
T |
A |
9: 66,383,720 (GRCm39) |
|
probably benign |
Het |
| Ikbke |
A |
G |
1: 131,187,792 (GRCm39) |
|
probably benign |
Het |
| Iqcg |
T |
A |
16: 32,855,970 (GRCm39) |
I202L |
possibly damaging |
Het |
| Kank3 |
G |
A |
17: 34,036,375 (GRCm39) |
G81E |
probably damaging |
Het |
| Kcna3 |
A |
G |
3: 106,945,180 (GRCm39) |
E481G |
possibly damaging |
Het |
| Kdm1a |
A |
G |
4: 136,299,639 (GRCm39) |
|
probably benign |
Het |
| Klhdc8a |
A |
T |
1: 132,232,438 (GRCm39) |
S321C |
probably benign |
Het |
| Kntc1 |
A |
G |
5: 123,900,666 (GRCm39) |
K255E |
probably benign |
Het |
| Lhfpl4 |
T |
A |
6: 113,170,824 (GRCm39) |
T121S |
probably benign |
Het |
| Lsm11 |
G |
A |
11: 45,824,490 (GRCm39) |
Q346* |
probably null |
Het |
| Nlrp4g |
A |
T |
9: 124,350,452 (GRCm38) |
|
noncoding transcript |
Het |
| Nol8 |
A |
G |
13: 49,807,957 (GRCm39) |
I58V |
possibly damaging |
Het |
| Or5al6 |
C |
T |
2: 85,976,560 (GRCm39) |
V173M |
probably benign |
Het |
| Phactr4 |
A |
G |
4: 132,098,116 (GRCm39) |
F384S |
probably benign |
Het |
| Prkg1 |
T |
A |
19: 30,562,678 (GRCm39) |
I509L |
probably benign |
Het |
| Rims1 |
T |
A |
1: 22,449,671 (GRCm39) |
D1019V |
probably damaging |
Het |
| Sclt1 |
T |
C |
3: 41,629,754 (GRCm39) |
|
probably benign |
Het |
| Sntg2 |
T |
A |
12: 30,307,987 (GRCm39) |
K233* |
probably null |
Het |
| Syt5 |
T |
C |
7: 4,544,156 (GRCm39) |
T295A |
probably damaging |
Het |
|
| Other mutations in Mcoln3 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00508:Mcoln3
|
APN |
3 |
145,839,683 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01712:Mcoln3
|
APN |
3 |
145,834,019 (GRCm39) |
unclassified |
probably benign |
|
|
IGL02115:Mcoln3
|
APN |
3 |
145,843,056 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02116:Mcoln3
|
APN |
3 |
145,839,664 (GRCm39) |
missense |
probably benign |
0.29 |
|
P4717OSA:Mcoln3
|
UTSW |
3 |
145,830,504 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0463:Mcoln3
|
UTSW |
3 |
145,846,331 (GRCm39) |
nonsense |
probably null |
|
|
R1981:Mcoln3
|
UTSW |
3 |
145,846,345 (GRCm39) |
nonsense |
probably null |
|
|
R2056:Mcoln3
|
UTSW |
3 |
145,833,979 (GRCm39) |
missense |
probably benign |
0.01 |
|
R3000:Mcoln3
|
UTSW |
3 |
145,839,662 (GRCm39) |
missense |
possibly damaging |
0.62 |
|
R4366:Mcoln3
|
UTSW |
3 |
145,846,247 (GRCm39) |
missense |
possibly damaging |
0.76 |
|
R4667:Mcoln3
|
UTSW |
3 |
145,836,959 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4950:Mcoln3
|
UTSW |
3 |
145,845,274 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R5457:Mcoln3
|
UTSW |
3 |
145,833,877 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6302:Mcoln3
|
UTSW |
3 |
145,830,527 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6353:Mcoln3
|
UTSW |
3 |
145,836,909 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6632:Mcoln3
|
UTSW |
3 |
145,833,942 (GRCm39) |
missense |
probably benign |
|
|
R6915:Mcoln3
|
UTSW |
3 |
145,843,011 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
R7790:Mcoln3
|
UTSW |
3 |
145,845,247 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7838:Mcoln3
|
UTSW |
3 |
145,845,230 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7861:Mcoln3
|
UTSW |
3 |
145,830,546 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R8348:Mcoln3
|
UTSW |
3 |
145,836,974 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8509:Mcoln3
|
UTSW |
3 |
145,830,647 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8708:Mcoln3
|
UTSW |
3 |
145,846,276 (GRCm39) |
nonsense |
probably null |
|
|
R8838:Mcoln3
|
UTSW |
3 |
145,845,126 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8861:Mcoln3
|
UTSW |
3 |
145,845,159 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8981:Mcoln3
|
UTSW |
3 |
145,827,554 (GRCm39) |
missense |
probably benign |
|
|
Z1176:Mcoln3
|
UTSW |
3 |
145,846,221 (GRCm39) |
missense |
probably benign |
0.00 |
|
| Posted On |
2013-06-21 |
Incidental Mutation