Incidental Mutation 'IGL03101:Rps6kb1'
| ID |
418728 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Rps6kb1
|
| Ensembl Gene |
ENSMUSG00000020516 |
| Gene Name |
ribosomal protein S6 kinase, polypeptide 1 |
| Synonyms |
S6K1, 2610318I15Rik, p70S6K1, p70/85s6k, p70s6k |
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.953)
|
| Stock # |
IGL03101
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
11 |
| Chromosomal Location |
86389697-86435631 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 86393708 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Tyrosine to Cysteine
at position 474
(Y474C)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000119715
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000020827]
[ENSMUST00000154617]
|
| AlphaFold |
Q8BSK8 |
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000020824
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000020827
|
| SMART Domains |
Protein: ENSMUSP00000020827
Gene: ENSMUSG00000020521
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
92 |
104 |
N/A |
INTRINSIC |
|
transmembrane domain
|
125 |
147 |
N/A |
INTRINSIC |
|
transmembrane domain
|
168 |
190 |
N/A |
INTRINSIC |
|
transmembrane domain
|
210 |
232 |
N/A |
INTRINSIC |
|
transmembrane domain
|
244 |
266 |
N/A |
INTRINSIC |
|
transmembrane domain
|
281 |
303 |
N/A |
INTRINSIC |
|
RING
|
335 |
372 |
1.67e-6 |
SMART |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000149392
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000154617
AA Change: Y474C
PolyPhen 2
Score 0.232 (Sensitivity: 0.91; Specificity: 0.88)
|
| SMART Domains |
Protein: ENSMUSP00000119715
Gene: ENSMUSG00000020516
AA Change: Y474C
| Domain | Start | End | E-Value | Type |
|---|
|
S_TKc
|
91 |
352 |
8.24e-107 |
SMART |
|
S_TK_X
|
353 |
415 |
9.2e-27 |
SMART |
|
| 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 a member of the ribosomal S6 kinase family of serine/threonine kinases. The encoded protein responds to mTOR (mammalian target of rapamycin) signaling to promote protein synthesis, cell growth, and cell proliferation. Activity of this gene has been associated with human cancer. Alternatively spliced transcript variants have been observed. The use of alternative translation start sites results in isoforms with longer or shorter N-termini which may differ in their subcellular localizations. There are two pseudogenes for this gene on chromosome 17. [provided by RefSeq, Jan 2013]
PHENOTYPE: Homozygotes for a targeted null mutation exhibit reduced prenatal growth, glucose intolerance, and hypoinsulinemia associated with diminished pancreatic beta cell size. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 32 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| AA474408 |
A |
T |
7: 109,660,177 (GRCm39) |
|
probably benign |
Het |
| Abcc1 |
T |
A |
16: 14,207,732 (GRCm39) |
V23D |
probably damaging |
Het |
| Adam8 |
G |
T |
7: 139,568,456 (GRCm39) |
N260K |
possibly damaging |
Het |
| Ap3b1 |
A |
T |
13: 94,591,906 (GRCm39) |
I457L |
probably benign |
Het |
| Apaf1 |
T |
C |
10: 90,867,421 (GRCm39) |
N808S |
possibly damaging |
Het |
| Arhgef26 |
A |
G |
3: 62,327,082 (GRCm39) |
T532A |
possibly damaging |
Het |
| Cfap65 |
G |
T |
1: 74,967,592 (GRCm39) |
T162N |
possibly damaging |
Het |
| Clec12b |
A |
G |
6: 129,356,480 (GRCm39) |
|
probably null |
Het |
| Creb3 |
T |
C |
4: 43,563,081 (GRCm39) |
V60A |
probably benign |
Het |
| Cyp11b1 |
A |
G |
15: 74,707,703 (GRCm39) |
F469L |
probably benign |
Het |
| Defb28 |
A |
T |
2: 152,362,047 (GRCm39) |
E69V |
possibly damaging |
Het |
| Etnppl |
T |
C |
3: 130,415,967 (GRCm39) |
L118S |
probably damaging |
Het |
| Fsip1 |
T |
C |
2: 118,072,144 (GRCm39) |
Y213C |
probably damaging |
Het |
| Glb1l2 |
A |
G |
9: 26,676,421 (GRCm39) |
W480R |
probably damaging |
Het |
| Herc1 |
A |
T |
9: 66,395,279 (GRCm39) |
M4205L |
probably benign |
Het |
| Kif5a |
A |
T |
10: 127,071,478 (GRCm39) |
|
probably benign |
Het |
| Lmbrd2 |
C |
T |
15: 9,186,695 (GRCm39) |
R557C |
probably damaging |
Het |
| Map4k3 |
A |
G |
17: 80,963,284 (GRCm39) |
|
probably null |
Het |
| Npc1 |
A |
G |
18: 12,331,596 (GRCm39) |
I858T |
probably benign |
Het |
| Or7e173 |
T |
C |
9: 19,938,725 (GRCm39) |
T170A |
probably benign |
Het |
| Pecam1 |
A |
G |
11: 106,588,177 (GRCm39) |
V92A |
probably damaging |
Het |
| Rbm43 |
A |
T |
2: 51,816,757 (GRCm39) |
I70N |
probably benign |
Het |
| Slco2a1 |
G |
A |
9: 102,954,205 (GRCm39) |
G459R |
possibly damaging |
Het |
| Snca |
T |
A |
6: 60,804,595 (GRCm39) |
|
probably benign |
Het |
| Spata31f1e |
T |
C |
4: 42,793,424 (GRCm39) |
D236G |
possibly damaging |
Het |
| Stap2 |
T |
A |
17: 56,309,029 (GRCm39) |
I113F |
probably damaging |
Het |
| Tas2r140 |
T |
C |
6: 40,468,764 (GRCm39) |
M198T |
probably benign |
Het |
| Trim9 |
T |
C |
12: 70,393,428 (GRCm39) |
E172G |
probably damaging |
Het |
| Ttll7 |
T |
C |
3: 146,602,445 (GRCm39) |
V81A |
possibly damaging |
Het |
| Vmn2r103 |
A |
G |
17: 19,993,782 (GRCm39) |
Y53C |
probably damaging |
Het |
| Vmn2r22 |
C |
A |
6: 123,614,295 (GRCm39) |
A432S |
probably benign |
Het |
| Zfp943 |
T |
C |
17: 22,211,156 (GRCm39) |
S81P |
probably damaging |
Het |
|
| Other mutations in Rps6kb1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01010:Rps6kb1
|
APN |
11 |
86,393,592 (GRCm39) |
missense |
probably benign |
|
|
IGL02707:Rps6kb1
|
APN |
11 |
86,426,236 (GRCm39) |
critical splice donor site |
probably null |
|
|
IGL03331:Rps6kb1
|
APN |
11 |
86,423,656 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Cobb
|
UTSW |
11 |
86,410,757 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R0025:Rps6kb1
|
UTSW |
11 |
86,402,413 (GRCm39) |
critical splice donor site |
probably null |
|
|
R1797:Rps6kb1
|
UTSW |
11 |
86,393,634 (GRCm39) |
nonsense |
probably null |
|
|
R1931:Rps6kb1
|
UTSW |
11 |
86,423,647 (GRCm39) |
missense |
possibly damaging |
0.52 |
|
R2214:Rps6kb1
|
UTSW |
11 |
86,424,896 (GRCm39) |
missense |
possibly damaging |
0.71 |
|
R3196:Rps6kb1
|
UTSW |
11 |
86,397,633 (GRCm39) |
missense |
probably benign |
0.01 |
|
R3699:Rps6kb1
|
UTSW |
11 |
86,423,620 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4171:Rps6kb1
|
UTSW |
11 |
86,435,405 (GRCm39) |
missense |
possibly damaging |
0.68 |
|
R4291:Rps6kb1
|
UTSW |
11 |
86,410,702 (GRCm39) |
intron |
probably benign |
|
|
R4685:Rps6kb1
|
UTSW |
11 |
86,410,713 (GRCm39) |
splice site |
probably null |
|
|
R4727:Rps6kb1
|
UTSW |
11 |
86,435,484 (GRCm39) |
splice site |
probably null |
|
|
R4728:Rps6kb1
|
UTSW |
11 |
86,435,484 (GRCm39) |
splice site |
probably null |
|
|
R5450:Rps6kb1
|
UTSW |
11 |
86,423,663 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5648:Rps6kb1
|
UTSW |
11 |
86,403,697 (GRCm39) |
missense |
possibly damaging |
0.54 |
|
R5796:Rps6kb1
|
UTSW |
11 |
86,402,677 (GRCm39) |
missense |
probably benign |
0.26 |
|
R5955:Rps6kb1
|
UTSW |
11 |
86,404,431 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7080:Rps6kb1
|
UTSW |
11 |
86,397,666 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7450:Rps6kb1
|
UTSW |
11 |
86,393,657 (GRCm39) |
missense |
probably benign |
0.11 |
|
R7709:Rps6kb1
|
UTSW |
11 |
86,404,148 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8084:Rps6kb1
|
UTSW |
11 |
86,426,262 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8366:Rps6kb1
|
UTSW |
11 |
86,402,655 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8723:Rps6kb1
|
UTSW |
11 |
86,410,757 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R9192:Rps6kb1
|
UTSW |
11 |
86,404,381 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9484:Rps6kb1
|
UTSW |
11 |
86,408,443 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9525:Rps6kb1
|
UTSW |
11 |
86,410,746 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
| Posted On |
2016-08-02 |
Incidental Mutation