Incidental Mutation 'IGL01311:Kcnrg'
| ID |
73688 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Kcnrg
|
| Ensembl Gene |
ENSMUSG00000046168 |
| Gene Name |
potassium channel regulator |
| Synonyms |
LOC328424, E030012H22Rik |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.249)
|
| Stock # |
IGL01311
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
14 |
| Chromosomal Location |
61844906-61850275 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 61849274 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Leucine to Proline
at position 245
(L245P)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000055327
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000051184]
[ENSMUST00000225582]
|
| AlphaFold |
Q2TUM3 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000051184
AA Change: L245P
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000055327
Gene: ENSMUSG00000046168
AA Change: L245P
| Domain | Start | End | E-Value | Type |
|---|
|
BTB
|
5 |
106 |
8.7e-7 |
SMART |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000182259
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000182325
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000182768
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000183054
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000183066
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000225582
|
| 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 protein which regulates the activity of voltage-gated potassium channels. This gene is on chromosome 13 and overlaps the gene for tripartite motif containing 13 on the same strand. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2012]
|
| Allele List at MGI |
All alleles(1) : Gene trapped(1) |
| Other mutations in this stock |
Total: 36 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Arap1 |
A |
T |
7: 101,037,343 (GRCm39) |
K457* |
probably null |
Het |
| Arhgef10 |
C |
A |
8: 15,041,054 (GRCm39) |
|
probably null |
Het |
| Becn1 |
C |
T |
11: 101,182,342 (GRCm39) |
G281S |
probably damaging |
Het |
| Borcs8 |
A |
G |
8: 70,617,818 (GRCm39) |
S59G |
probably damaging |
Het |
| Brd10 |
C |
T |
19: 29,731,420 (GRCm39) |
V531I |
probably benign |
Het |
| Capn5 |
C |
A |
7: 97,811,130 (GRCm39) |
R53L |
probably damaging |
Het |
| Cdk5 |
C |
T |
5: 24,624,593 (GRCm39) |
|
probably null |
Het |
| Cnksr1 |
A |
G |
4: 133,957,777 (GRCm39) |
L434P |
probably damaging |
Het |
| Col22a1 |
C |
T |
15: 71,845,486 (GRCm39) |
|
probably benign |
Het |
| Fn1 |
T |
C |
1: 71,667,299 (GRCm39) |
D811G |
probably damaging |
Het |
| Haus3 |
G |
A |
5: 34,324,988 (GRCm39) |
Q224* |
probably null |
Het |
| Jakmip2 |
A |
G |
18: 43,690,389 (GRCm39) |
|
probably benign |
Het |
| Jam3 |
T |
G |
9: 27,010,019 (GRCm39) |
T296P |
probably damaging |
Het |
| Kif1b |
A |
G |
4: 149,305,059 (GRCm39) |
L909P |
probably damaging |
Het |
| Klrc3 |
T |
C |
6: 129,618,375 (GRCm39) |
D136G |
probably damaging |
Het |
| Lrrc37 |
T |
A |
11: 103,425,502 (GRCm39) |
R1450S |
unknown |
Het |
| Ltf |
T |
C |
9: 110,860,080 (GRCm39) |
|
probably benign |
Het |
| Meig1 |
A |
T |
2: 3,410,245 (GRCm39) |
V85D |
possibly damaging |
Het |
| Mrgprb2 |
T |
A |
7: 48,201,746 (GRCm39) |
E326D |
probably benign |
Het |
| Nlrp2 |
T |
A |
7: 5,322,238 (GRCm39) |
D65V |
possibly damaging |
Het |
| Or4c100 |
T |
C |
2: 88,356,104 (GRCm39) |
F59S |
possibly damaging |
Het |
| Or52h7 |
T |
C |
7: 104,214,036 (GRCm39) |
Y203H |
probably damaging |
Het |
| Padi2 |
G |
A |
4: 140,644,948 (GRCm39) |
V61I |
probably benign |
Het |
| Pkd1l1 |
T |
C |
11: 8,851,174 (GRCm39) |
S753G |
possibly damaging |
Het |
| Ppp4r3b |
T |
C |
11: 29,144,591 (GRCm39) |
S314P |
probably benign |
Het |
| Serpina3i |
T |
C |
12: 104,233,946 (GRCm39) |
S305P |
probably damaging |
Het |
| Slc16a4 |
G |
T |
3: 107,199,821 (GRCm39) |
V23F |
possibly damaging |
Het |
| Slc25a34 |
G |
A |
4: 141,348,747 (GRCm39) |
T239I |
possibly damaging |
Het |
| Srebf2 |
T |
C |
15: 82,076,404 (GRCm39) |
|
probably benign |
Het |
| Tasor2 |
A |
G |
13: 3,625,885 (GRCm39) |
V1355A |
possibly damaging |
Het |
| Tcf12 |
A |
T |
9: 71,765,938 (GRCm39) |
|
probably benign |
Het |
| Tnpo3 |
T |
C |
6: 29,586,077 (GRCm39) |
E171G |
possibly damaging |
Het |
| Ubr4 |
A |
G |
4: 139,206,356 (GRCm39) |
H4864R |
possibly damaging |
Het |
| Vmn2r108 |
A |
T |
17: 20,682,939 (GRCm39) |
L755* |
probably null |
Het |
| Zfp292 |
C |
T |
4: 34,807,961 (GRCm39) |
M1699I |
probably benign |
Het |
| Zmynd8 |
T |
C |
2: 165,647,129 (GRCm39) |
D880G |
probably damaging |
Het |
|
| Other mutations in Kcnrg |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00595:Kcnrg
|
APN |
14 |
61,845,359 (GRCm39) |
missense |
probably damaging |
1.00 |
|
D4216:Kcnrg
|
UTSW |
14 |
61,849,242 (GRCm39) |
nonsense |
probably null |
|
|
R1081:Kcnrg
|
UTSW |
14 |
61,845,163 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R1346:Kcnrg
|
UTSW |
14 |
61,849,144 (GRCm39) |
missense |
probably benign |
0.31 |
|
R3147:Kcnrg
|
UTSW |
14 |
61,845,140 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4690:Kcnrg
|
UTSW |
14 |
61,849,176 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4820:Kcnrg
|
UTSW |
14 |
61,845,386 (GRCm39) |
missense |
probably benign |
0.39 |
|
R5068:Kcnrg
|
UTSW |
14 |
61,845,266 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5914:Kcnrg
|
UTSW |
14 |
61,849,280 (GRCm39) |
missense |
probably benign |
|
|
R7234:Kcnrg
|
UTSW |
14 |
61,845,531 (GRCm39) |
missense |
unknown |
|
|
R8232:Kcnrg
|
UTSW |
14 |
61,845,386 (GRCm39) |
missense |
probably benign |
0.39 |
|
R8821:Kcnrg
|
UTSW |
14 |
61,844,981 (GRCm39) |
missense |
possibly damaging |
0.55 |
|
R9442:Kcnrg
|
UTSW |
14 |
61,845,009 (GRCm39) |
small deletion |
probably benign |
|
|
R9475:Kcnrg
|
UTSW |
14 |
61,845,106 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R9633:Kcnrg
|
UTSW |
14 |
61,845,009 (GRCm39) |
small deletion |
probably benign |
|
|
R9634:Kcnrg
|
UTSW |
14 |
61,845,009 (GRCm39) |
small deletion |
probably benign |
|
|
R9703:Kcnrg
|
UTSW |
14 |
61,845,009 (GRCm39) |
small deletion |
probably benign |
|
|
| Posted On |
2013-10-07 |
Incidental Mutation