Incidental Mutation 'R0899:Scnn1b'
| ID |
83794 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Scnn1b
|
| Ensembl Gene |
ENSMUSG00000030873 |
| Gene Name |
sodium channel, nonvoltage-gated 1 beta |
| Synonyms |
ENaC beta |
| MMRRC Submission |
039059-MU
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R0899 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
7 |
| Chromosomal Location |
121464261-121517737 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to A
at 121516938 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Glycine to Serine
at position 525
(G525S)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000033161
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000033161]
[ENSMUST00000205438]
[ENSMUST00000205520]
|
| AlphaFold |
Q9WU38 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000033161
AA Change: G525S
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000033161
Gene: ENSMUSG00000030873
AA Change: G525S
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:ASC
|
29 |
541 |
2.4e-93 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000205438
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000205520
|
| Coding Region Coverage |
- 1x: 99.7%
- 3x: 99.0%
- 10x: 97.2%
- 20x: 93.6%
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Nonvoltage-gated, amiloride-sensitive, sodium channels control fluid and electrolyte transport across epithelia in many organs. These channels are heteromeric complexes consisting of 3 subunits: alpha, beta, and gamma. This gene encodes the beta subunit, and mutations in this gene have been associated with pseudohypoaldosteronism type 1 (PHA1), and Liddle syndrome. [provided by RefSeq, Apr 2009]
PHENOTYPE: Homozygous mutation of this gene results in death shortly after birth, decreased serum sodium levels but higher urine sodium levels and increased serum potassium and chloride levels but lower potassium urine levels. Another homozygous mutation exhibits no abnormal phenotype. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 38 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 5031439G07Rik |
T |
C |
15: 84,833,459 (GRCm39) |
K442E |
probably damaging |
Het |
| Adamts1 |
G |
A |
16: 85,594,940 (GRCm39) |
R340* |
probably null |
Het |
| Afg3l2 |
T |
C |
18: 67,556,047 (GRCm39) |
N428S |
possibly damaging |
Het |
| Aqp12 |
G |
A |
1: 92,934,332 (GRCm39) |
D70N |
probably damaging |
Het |
| Astn1 |
T |
A |
1: 158,338,679 (GRCm39) |
C475* |
probably null |
Het |
| Atp2b1 |
G |
A |
10: 98,852,893 (GRCm39) |
|
probably null |
Het |
| Cbln2 |
T |
C |
18: 86,734,877 (GRCm39) |
S217P |
possibly damaging |
Het |
| Ces2h |
T |
C |
8: 105,741,182 (GRCm39) |
L58P |
probably damaging |
Het |
| Cfap43 |
C |
T |
19: 47,736,433 (GRCm39) |
G1353R |
possibly damaging |
Het |
| Crcp |
A |
G |
5: 130,088,672 (GRCm39) |
M91V |
probably benign |
Het |
| Cubn |
A |
G |
2: 13,367,139 (GRCm39) |
V1577A |
possibly damaging |
Het |
| Dthd1 |
A |
G |
5: 63,000,271 (GRCm39) |
H531R |
probably benign |
Het |
| Fam120a |
G |
T |
13: 49,039,219 (GRCm39) |
A979E |
possibly damaging |
Het |
| Fam3d |
A |
G |
14: 8,364,863 (GRCm38) |
I16T |
probably damaging |
Het |
| Fat2 |
C |
T |
11: 55,147,051 (GRCm39) |
G3982S |
probably damaging |
Het |
| Fbxo44 |
C |
G |
4: 148,240,726 (GRCm39) |
R220S |
probably damaging |
Het |
| Fcnb |
T |
A |
2: 27,966,791 (GRCm39) |
K247N |
probably damaging |
Het |
| Gtf2a1l |
A |
G |
17: 88,976,152 (GRCm39) |
N5S |
|
Het |
| Htr3a |
T |
A |
9: 48,812,752 (GRCm39) |
D229V |
possibly damaging |
Het |
| Ipo11 |
A |
C |
13: 107,037,324 (GRCm39) |
L173* |
probably null |
Het |
| Jam3 |
C |
A |
9: 27,010,253 (GRCm39) |
G244W |
probably damaging |
Het |
| Lypd11 |
C |
T |
7: 24,422,737 (GRCm39) |
R112H |
probably benign |
Het |
| Mrpl52 |
C |
T |
14: 54,664,541 (GRCm39) |
R12* |
probably null |
Het |
| Myo15a |
A |
G |
11: 60,368,011 (GRCm39) |
Y257C |
possibly damaging |
Het |
| Myocd |
G |
A |
11: 65,086,018 (GRCm39) |
P215L |
possibly damaging |
Het |
| Ndst1 |
T |
C |
18: 60,840,954 (GRCm39) |
T243A |
probably benign |
Het |
| Obox5 |
A |
T |
7: 15,492,800 (GRCm39) |
T252S |
probably benign |
Het |
| Or5m13b |
A |
G |
2: 85,753,731 (GRCm39) |
T40A |
probably benign |
Het |
| Or6c75 |
T |
C |
10: 129,337,301 (GRCm39) |
F183L |
probably damaging |
Het |
| Or7g34 |
A |
C |
9: 19,477,843 (GRCm39) |
V276G |
probably damaging |
Het |
| Osbpl1a |
T |
C |
18: 12,890,747 (GRCm39) |
S377G |
possibly damaging |
Het |
| Pfkl |
A |
G |
10: 77,841,273 (GRCm39) |
|
probably null |
Het |
| Prdm16 |
A |
T |
4: 154,613,366 (GRCm39) |
N20K |
probably damaging |
Het |
| Prkd1 |
A |
G |
12: 50,431,976 (GRCm39) |
I589T |
probably damaging |
Het |
| Tktl2 |
G |
A |
8: 66,964,999 (GRCm39) |
V186M |
probably damaging |
Het |
| Ttn |
A |
G |
2: 76,718,329 (GRCm39) |
|
probably benign |
Het |
| Wap |
T |
C |
11: 6,586,725 (GRCm39) |
T125A |
probably benign |
Het |
| Wdr86 |
C |
T |
5: 24,923,005 (GRCm39) |
R229Q |
probably benign |
Het |
|
| Other mutations in Scnn1b |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01021:Scnn1b
|
APN |
7 |
121,517,259 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01108:Scnn1b
|
APN |
7 |
121,513,555 (GRCm39) |
splice site |
probably null |
|
|
IGL02191:Scnn1b
|
APN |
7 |
121,516,736 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02197:Scnn1b
|
APN |
7 |
121,502,113 (GRCm39) |
missense |
probably null |
0.89 |
|
IGL02355:Scnn1b
|
APN |
7 |
121,516,770 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02362:Scnn1b
|
APN |
7 |
121,516,770 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02554:Scnn1b
|
APN |
7 |
121,516,746 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02834:Scnn1b
|
APN |
7 |
121,511,285 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0266:Scnn1b
|
UTSW |
7 |
121,511,698 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0494:Scnn1b
|
UTSW |
7 |
121,498,681 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0849:Scnn1b
|
UTSW |
7 |
121,511,698 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0872:Scnn1b
|
UTSW |
7 |
121,513,553 (GRCm39) |
critical splice donor site |
probably null |
|
|
R1386:Scnn1b
|
UTSW |
7 |
121,501,711 (GRCm39) |
missense |
possibly damaging |
0.60 |
|
R1406:Scnn1b
|
UTSW |
7 |
121,501,767 (GRCm39) |
critical splice donor site |
probably null |
|
|
R1406:Scnn1b
|
UTSW |
7 |
121,501,767 (GRCm39) |
critical splice donor site |
probably null |
|
|
R1662:Scnn1b
|
UTSW |
7 |
121,501,551 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1782:Scnn1b
|
UTSW |
7 |
121,517,184 (GRCm39) |
missense |
probably benign |
|
|
R1829:Scnn1b
|
UTSW |
7 |
121,502,068 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1861:Scnn1b
|
UTSW |
7 |
121,513,484 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1928:Scnn1b
|
UTSW |
7 |
121,509,670 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4016:Scnn1b
|
UTSW |
7 |
121,513,555 (GRCm39) |
splice site |
probably null |
|
|
R4192:Scnn1b
|
UTSW |
7 |
121,501,962 (GRCm39) |
missense |
possibly damaging |
0.63 |
|
R4504:Scnn1b
|
UTSW |
7 |
121,511,698 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4745:Scnn1b
|
UTSW |
7 |
121,501,509 (GRCm39) |
missense |
probably benign |
0.03 |
|
R4888:Scnn1b
|
UTSW |
7 |
121,502,110 (GRCm39) |
missense |
probably benign |
0.06 |
|
R4941:Scnn1b
|
UTSW |
7 |
121,511,231 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5121:Scnn1b
|
UTSW |
7 |
121,502,110 (GRCm39) |
missense |
probably benign |
0.06 |
|
R6379:Scnn1b
|
UTSW |
7 |
121,514,551 (GRCm39) |
missense |
probably benign |
0.10 |
|
R6516:Scnn1b
|
UTSW |
7 |
121,511,335 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6650:Scnn1b
|
UTSW |
7 |
121,502,043 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R6730:Scnn1b
|
UTSW |
7 |
121,502,100 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7151:Scnn1b
|
UTSW |
7 |
121,517,109 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8670:Scnn1b
|
UTSW |
7 |
121,498,472 (GRCm39) |
missense |
probably benign |
0.06 |
|
R8675:Scnn1b
|
UTSW |
7 |
121,498,474 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8930:Scnn1b
|
UTSW |
7 |
121,502,067 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8932:Scnn1b
|
UTSW |
7 |
121,502,067 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9170:Scnn1b
|
UTSW |
7 |
121,511,326 (GRCm39) |
missense |
probably benign |
0.32 |
|
R9204:Scnn1b
|
UTSW |
7 |
121,498,522 (GRCm39) |
missense |
probably benign |
0.20 |
|
R9339:Scnn1b
|
UTSW |
7 |
121,511,254 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R9466:Scnn1b
|
UTSW |
7 |
121,502,013 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9696:Scnn1b
|
UTSW |
7 |
121,498,462 (GRCm39) |
start codon destroyed |
probably damaging |
0.99 |
|
R9709:Scnn1b
|
UTSW |
7 |
121,509,693 (GRCm39) |
missense |
probably benign |
|
|
| Predicted Primers |
PCR Primer
(F):5'- AGCCAACAATGTAAGTGTGGGTGTG -3'
(R):5'- GGCCTAATGAAACGAGGCACTGAC -3'
Sequencing Primer
(F):5'- GTGTGCCTGGTGTGTGG -3'
(R):5'- AGCCTCAGGGAGTCATAGTTG -3'
|
| Posted On |
2013-11-08 |
Incidental Mutation