Incidental Mutation 'R4634:Marveld2'
| ID |
349416 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Marveld2
|
| Ensembl Gene |
ENSMUSG00000021636 |
| Gene Name |
MARVEL (membrane-associating) domain containing 2 |
| Synonyms |
Tric, Tric-a, Tric-b, Tric-c, Tricellulin, Mrvldc2 |
| MMRRC Submission |
042009-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R4634 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
13 |
| Chromosomal Location |
100732465-100753479 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 100748447 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Tyrosine to Histidine
at position 211
(Y211H)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000153294
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000022137]
[ENSMUST00000163163]
[ENSMUST00000168772]
[ENSMUST00000225754]
|
| AlphaFold |
Q3UZP0 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000022137
AA Change: Y211H
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000022137
Gene: ENSMUSG00000021636
AA Change: Y211H
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
2 |
13 |
N/A |
INTRINSIC |
|
low complexity region
|
46 |
57 |
N/A |
INTRINSIC |
|
Pfam:MARVEL
|
182 |
358 |
4.1e-20 |
PFAM |
|
low complexity region
|
423 |
434 |
N/A |
INTRINSIC |
|
Pfam:Occludin_ELL
|
443 |
545 |
2.7e-35 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000163163
|
| SMART Domains |
Protein: ENSMUSP00000129990
Gene: ENSMUSG00000021636
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
25 |
53 |
N/A |
INTRINSIC |
|
low complexity region
|
146 |
157 |
N/A |
INTRINSIC |
|
Pfam:Occludin_ELL
|
166 |
268 |
4.2e-36 |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000168772
AA Change: Y211H
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000126438
Gene: ENSMUSG00000021636
AA Change: Y211H
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
2 |
13 |
N/A |
INTRINSIC |
|
low complexity region
|
46 |
57 |
N/A |
INTRINSIC |
|
Pfam:MARVEL
|
182 |
358 |
3.6e-20 |
PFAM |
|
low complexity region
|
423 |
434 |
N/A |
INTRINSIC |
|
Pfam:Occludin_ELL
|
443 |
545 |
6.6e-33 |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000225754
AA Change: Y211H
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| Meta Mutation Damage Score |
0.7282 |
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.5%
- 10x: 97.1%
- 20x: 94.7%
|
| Validation Efficiency |
98% (40/41) |
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a membrane protein found at the tight junctions between epithelial cells. The encoded protein helps establish epithelial barriers such as those in the organ of Corti, where these barriers are required for normal hearing. Defects in this gene are a cause of deafness autosomal recessive type 49 (DFNB49). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011]
PHENOTYPE: Mice homozygous for a knock-in mutation fisplay syndromic deafness with rapid progressive degeneration of the hair cells, increased body and organ weights and abnormal tricellular tight junctions. However, vestibular function is intact. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 31 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adgrb1 |
A |
G |
15: 74,456,278 (GRCm39) |
|
probably benign |
Het |
| Atm |
T |
C |
9: 53,443,033 (GRCm39) |
T77A |
probably benign |
Het |
| Brd8 |
T |
C |
18: 34,741,537 (GRCm39) |
M311V |
possibly damaging |
Het |
| Cand2 |
T |
A |
6: 115,774,948 (GRCm39) |
I1052N |
probably damaging |
Het |
| Ccdc121 |
G |
A |
5: 31,645,435 (GRCm39) |
R396Q |
probably benign |
Het |
| Ceacam16 |
T |
A |
7: 19,592,531 (GRCm39) |
M126L |
probably benign |
Het |
| Chd3 |
TGCTGCCGCTGCCGC |
TGCTGCCGCTGCCGCTGCCGC |
11: 69,253,013 (GRCm39) |
|
probably benign |
Het |
| Cln8 |
C |
T |
8: 14,944,842 (GRCm39) |
T52I |
probably damaging |
Het |
| Cops2 |
C |
A |
2: 125,682,400 (GRCm39) |
D194Y |
probably damaging |
Het |
| Csf1 |
C |
T |
3: 107,656,483 (GRCm39) |
V71M |
probably damaging |
Het |
| Dip2b |
T |
C |
15: 100,058,372 (GRCm39) |
F183S |
probably damaging |
Het |
| Ears2 |
T |
A |
7: 121,643,832 (GRCm39) |
K375N |
probably benign |
Het |
| Fbn1 |
C |
A |
2: 125,185,981 (GRCm39) |
G1596C |
probably damaging |
Het |
| Fscn2 |
A |
T |
11: 120,258,546 (GRCm39) |
D390V |
possibly damaging |
Het |
| Gm42669 |
A |
T |
5: 107,656,079 (GRCm39) |
I781F |
possibly damaging |
Het |
| Gprin1 |
G |
T |
13: 54,885,871 (GRCm39) |
P801Q |
probably damaging |
Het |
| Hira |
C |
A |
16: 18,765,150 (GRCm39) |
S609R |
probably damaging |
Het |
| Htt |
G |
T |
5: 35,033,292 (GRCm39) |
K1853N |
probably benign |
Het |
| Kif2c |
T |
C |
4: 117,035,437 (GRCm39) |
I4V |
probably benign |
Het |
| Myd88 |
G |
A |
9: 119,167,175 (GRCm39) |
|
probably null |
Het |
| Nup153 |
A |
T |
13: 46,840,706 (GRCm39) |
N967K |
possibly damaging |
Het |
| Or4a76 |
A |
C |
2: 89,460,516 (GRCm39) |
I242S |
possibly damaging |
Het |
| Peg10 |
GC |
GCTCC |
6: 4,756,452 (GRCm39) |
|
probably benign |
Het |
| Rabepk |
A |
G |
2: 34,670,752 (GRCm39) |
M228T |
probably damaging |
Het |
| Rcn3 |
T |
A |
7: 44,738,092 (GRCm39) |
D92V |
probably damaging |
Het |
| Sec1 |
T |
A |
7: 45,328,297 (GRCm39) |
Y250F |
probably damaging |
Het |
| Slc39a4 |
T |
C |
15: 76,498,693 (GRCm39) |
T334A |
probably benign |
Het |
| Trip11 |
G |
T |
12: 101,803,875 (GRCm39) |
T1669K |
probably damaging |
Het |
| Ttbk2 |
A |
G |
2: 120,570,673 (GRCm39) |
L1091P |
probably damaging |
Het |
| Vmn1r231 |
A |
G |
17: 21,110,660 (GRCm39) |
V85A |
possibly damaging |
Het |
| Zfp280b |
T |
C |
10: 75,874,663 (GRCm39) |
C181R |
probably benign |
Het |
|
| Other mutations in Marveld2 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00565:Marveld2
|
APN |
13 |
100,737,401 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
IGL00573:Marveld2
|
APN |
13 |
100,734,367 (GRCm39) |
splice site |
probably benign |
|
|
R1569:Marveld2
|
UTSW |
13 |
100,737,506 (GRCm39) |
missense |
probably benign |
0.32 |
|
R1884:Marveld2
|
UTSW |
13 |
100,737,129 (GRCm39) |
missense |
probably benign |
0.15 |
|
R1958:Marveld2
|
UTSW |
13 |
100,733,858 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2249:Marveld2
|
UTSW |
13 |
100,748,599 (GRCm39) |
missense |
probably benign |
|
|
R2258:Marveld2
|
UTSW |
13 |
100,748,978 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2259:Marveld2
|
UTSW |
13 |
100,748,978 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2260:Marveld2
|
UTSW |
13 |
100,748,978 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2473:Marveld2
|
UTSW |
13 |
100,733,829 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R3918:Marveld2
|
UTSW |
13 |
100,748,401 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4010:Marveld2
|
UTSW |
13 |
100,747,936 (GRCm39) |
splice site |
probably null |
|
|
R4089:Marveld2
|
UTSW |
13 |
100,736,988 (GRCm39) |
missense |
probably benign |
0.04 |
|
R4775:Marveld2
|
UTSW |
13 |
100,753,303 (GRCm39) |
unclassified |
probably benign |
|
|
R4961:Marveld2
|
UTSW |
13 |
100,748,431 (GRCm39) |
missense |
probably benign |
0.12 |
|
R5424:Marveld2
|
UTSW |
13 |
100,748,695 (GRCm39) |
missense |
probably benign |
|
|
R5546:Marveld2
|
UTSW |
13 |
100,737,446 (GRCm39) |
missense |
probably benign |
0.14 |
|
R5900:Marveld2
|
UTSW |
13 |
100,748,176 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5977:Marveld2
|
UTSW |
13 |
100,748,197 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R6177:Marveld2
|
UTSW |
13 |
100,733,886 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7409:Marveld2
|
UTSW |
13 |
100,747,984 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7484:Marveld2
|
UTSW |
13 |
100,748,068 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8142:Marveld2
|
UTSW |
13 |
100,737,448 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R9063:Marveld2
|
UTSW |
13 |
100,748,653 (GRCm39) |
missense |
probably benign |
0.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- ATGCCAAGCACCAGGATAATAATG -3'
(R):5'- GCACCTTTAATTCCCAGCACG -3'
Sequencing Primer
(F):5'- TGGTGGTGATCCAAGCCAATC -3'
(R):5'- AGATGCCATGTTTGCCCACG -3'
|
| Posted On |
2015-10-08 |
Incidental Mutation