Incidental Mutation 'IGL03256:Frk'
| ID |
414656 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Frk
|
| Ensembl Gene |
ENSMUSG00000019779 |
| Gene Name |
fyn-related kinase |
| Synonyms |
BSK/IYK, GTK |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.190)
|
| Stock # |
IGL03256
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
10 |
| Chromosomal Location |
34359395-34487274 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 34483838 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Valine
at position 400
(I400V)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000130289
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000019913]
[ENSMUST00000170771]
|
| AlphaFold |
Q922K9 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000019913
AA Change: I400V
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
| SMART Domains |
Protein: ENSMUSP00000019913
Gene: ENSMUSG00000019779
AA Change: I400V
| Domain | Start | End | E-Value | Type |
|---|
|
SH3
|
52 |
116 |
2.76e-19 |
SMART |
|
SH2
|
121 |
206 |
4.97e-37 |
SMART |
|
TyrKc
|
241 |
494 |
8.58e-137 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000170771
AA Change: I400V
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
| SMART Domains |
Protein: ENSMUSP00000130289
Gene: ENSMUSG00000019779
AA Change: I400V
| Domain | Start | End | E-Value | Type |
|---|
|
SH3
|
52 |
116 |
2.76e-19 |
SMART |
|
SH2
|
121 |
206 |
4.97e-37 |
SMART |
|
TyrKc
|
241 |
494 |
8.58e-137 |
SMART |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000215594
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene belongs to the TYR family of protein kinases. This tyrosine kinase is a nuclear protein and may function during G1 and S phase of the cell cycle and suppress growth. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a targeted null mutation do not exhibit increased susceptibility to spontaneous tumors nor increased sensitivity to inoizing radiation. Epithelial tissues appear similar to controls, but circulating levels of T3 were significantly reduced. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 50 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1700030K09Rik |
C |
T |
8: 73,199,043 (GRCm39) |
T150I |
probably benign |
Het |
| Adam2 |
T |
C |
14: 66,291,280 (GRCm39) |
N333D |
probably benign |
Het |
| Aifm3 |
G |
A |
16: 17,324,174 (GRCm39) |
R578Q |
probably benign |
Het |
| Arid2 |
C |
A |
15: 96,268,643 (GRCm39) |
Q919K |
probably benign |
Het |
| Atp6v1a |
T |
C |
16: 43,931,451 (GRCm39) |
|
probably benign |
Het |
| Bicd1 |
A |
T |
6: 149,415,083 (GRCm39) |
T599S |
probably benign |
Het |
| Bltp1 |
T |
C |
3: 36,960,832 (GRCm39) |
|
probably benign |
Het |
| Catsperg2 |
T |
A |
7: 29,409,299 (GRCm39) |
R601W |
probably damaging |
Het |
| Clca3a2 |
A |
C |
3: 144,792,153 (GRCm39) |
S369R |
possibly damaging |
Het |
| Cyfip1 |
T |
G |
7: 55,557,182 (GRCm39) |
V795G |
possibly damaging |
Het |
| Ddb1 |
A |
G |
19: 10,599,225 (GRCm39) |
T544A |
probably benign |
Het |
| Defb43 |
T |
C |
14: 63,255,329 (GRCm39) |
I54T |
probably damaging |
Het |
| Dera |
A |
G |
6: 137,756,643 (GRCm39) |
M89V |
probably benign |
Het |
| Fam227b |
T |
A |
2: 125,830,923 (GRCm39) |
K427I |
probably damaging |
Het |
| Gk5 |
T |
A |
9: 96,011,106 (GRCm39) |
L72H |
probably damaging |
Het |
| Gprc6a |
T |
A |
10: 51,504,445 (GRCm39) |
Y133F |
possibly damaging |
Het |
| Hecw1 |
A |
G |
13: 14,455,069 (GRCm39) |
L662P |
probably damaging |
Het |
| Hecw1 |
G |
T |
13: 14,455,070 (GRCm39) |
L662M |
probably benign |
Het |
| Il12b |
T |
A |
11: 44,298,757 (GRCm39) |
S71T |
probably benign |
Het |
| Kdm2a |
A |
T |
19: 4,395,538 (GRCm39) |
|
probably benign |
Het |
| Lhfpl6 |
A |
G |
3: 52,950,974 (GRCm39) |
R83G |
possibly damaging |
Het |
| Magel2 |
C |
A |
7: 62,030,162 (GRCm39) |
T1022K |
unknown |
Het |
| Mycbp2 |
C |
A |
14: 103,426,025 (GRCm39) |
V2367F |
possibly damaging |
Het |
| Nap1l3 |
C |
T |
X: 121,305,905 (GRCm39) |
G271D |
probably benign |
Het |
| Nars2 |
T |
A |
7: 96,689,117 (GRCm39) |
D346E |
possibly damaging |
Het |
| Nek11 |
T |
A |
9: 105,121,613 (GRCm39) |
E435D |
probably damaging |
Het |
| Nfam1 |
C |
T |
15: 82,894,611 (GRCm39) |
G205R |
probably benign |
Het |
| Or10aa1 |
T |
C |
1: 173,869,774 (GRCm39) |
L86P |
probably damaging |
Het |
| Or1e35 |
A |
T |
11: 73,797,522 (GRCm39) |
N265K |
probably benign |
Het |
| Or5b118 |
T |
A |
19: 13,448,631 (GRCm39) |
M99K |
probably damaging |
Het |
| Otud3 |
G |
A |
4: 138,636,928 (GRCm39) |
R78W |
probably damaging |
Het |
| Oxct2a |
C |
T |
4: 123,216,758 (GRCm39) |
A208T |
probably damaging |
Het |
| Pcdh11x |
A |
T |
X: 119,310,607 (GRCm39) |
E683D |
probably benign |
Het |
| Phtf2 |
C |
A |
5: 21,008,250 (GRCm39) |
V144L |
probably damaging |
Het |
| Pkn2 |
T |
C |
3: 142,509,311 (GRCm39) |
|
probably null |
Het |
| Puf60 |
T |
A |
15: 75,942,445 (GRCm39) |
D459V |
possibly damaging |
Het |
| Ralgapa2 |
A |
G |
2: 146,302,632 (GRCm39) |
|
probably null |
Het |
| Rapgef6 |
A |
C |
11: 54,548,255 (GRCm39) |
Q813P |
probably damaging |
Het |
| Rsf1 |
A |
T |
7: 97,328,211 (GRCm39) |
D1071V |
possibly damaging |
Het |
| Sctr |
T |
C |
1: 119,959,289 (GRCm39) |
|
probably benign |
Het |
| Serpini1 |
A |
G |
3: 75,526,481 (GRCm39) |
I244M |
probably benign |
Het |
| Tada2a |
C |
A |
11: 83,978,018 (GRCm39) |
|
probably benign |
Het |
| Tada3 |
A |
T |
6: 113,352,092 (GRCm39) |
H112Q |
possibly damaging |
Het |
| Tnxb |
T |
A |
17: 34,907,694 (GRCm39) |
L1246Q |
probably damaging |
Het |
| Txndc16 |
T |
C |
14: 45,389,353 (GRCm39) |
N449S |
probably damaging |
Het |
| Usp34 |
T |
A |
11: 23,370,090 (GRCm39) |
Y1771* |
probably null |
Het |
| Vav2 |
A |
T |
2: 27,161,912 (GRCm39) |
|
probably null |
Het |
| Virma |
T |
C |
4: 11,542,207 (GRCm39) |
|
probably benign |
Het |
| Vmn1r78 |
T |
A |
7: 11,886,725 (GRCm39) |
I112N |
probably damaging |
Het |
| Vnn3 |
A |
T |
10: 23,727,698 (GRCm39) |
|
probably benign |
Het |
|
| Other mutations in Frk |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00337:Frk
|
APN |
10 |
34,360,239 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL01402:Frk
|
APN |
10 |
34,423,381 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02197:Frk
|
APN |
10 |
34,360,330 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02289:Frk
|
APN |
10 |
34,360,362 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02618:Frk
|
APN |
10 |
34,459,960 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
IGL02885:Frk
|
APN |
10 |
34,360,067 (GRCm39) |
missense |
probably benign |
0.03 |
|
R0299:Frk
|
UTSW |
10 |
34,360,367 (GRCm39) |
critical splice donor site |
probably null |
|
|
R0697:Frk
|
UTSW |
10 |
34,483,833 (GRCm39) |
missense |
probably benign |
0.12 |
|
R1033:Frk
|
UTSW |
10 |
34,484,454 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1583:Frk
|
UTSW |
10 |
34,467,806 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
R1793:Frk
|
UTSW |
10 |
34,483,878 (GRCm39) |
missense |
probably benign |
0.05 |
|
R2248:Frk
|
UTSW |
10 |
34,484,527 (GRCm39) |
missense |
probably benign |
0.10 |
|
R3084:Frk
|
UTSW |
10 |
34,483,950 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3086:Frk
|
UTSW |
10 |
34,483,950 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3765:Frk
|
UTSW |
10 |
34,360,001 (GRCm39) |
start codon destroyed |
probably null |
0.98 |
|
R3766:Frk
|
UTSW |
10 |
34,360,001 (GRCm39) |
start codon destroyed |
probably null |
0.98 |
|
R3906:Frk
|
UTSW |
10 |
34,460,052 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4163:Frk
|
UTSW |
10 |
34,467,868 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R4486:Frk
|
UTSW |
10 |
34,484,377 (GRCm39) |
missense |
probably benign |
0.10 |
|
R4591:Frk
|
UTSW |
10 |
34,481,829 (GRCm39) |
missense |
probably benign |
0.03 |
|
R4821:Frk
|
UTSW |
10 |
34,360,233 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5070:Frk
|
UTSW |
10 |
34,360,280 (GRCm39) |
nonsense |
probably null |
|
|
R6172:Frk
|
UTSW |
10 |
34,467,961 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6572:Frk
|
UTSW |
10 |
34,459,963 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6619:Frk
|
UTSW |
10 |
34,481,835 (GRCm39) |
missense |
probably benign |
0.22 |
|
R7307:Frk
|
UTSW |
10 |
34,467,934 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7486:Frk
|
UTSW |
10 |
34,423,292 (GRCm39) |
nonsense |
probably null |
|
|
R7916:Frk
|
UTSW |
10 |
34,360,021 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
R8341:Frk
|
UTSW |
10 |
34,462,279 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8675:Frk
|
UTSW |
10 |
34,484,493 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8801:Frk
|
UTSW |
10 |
34,423,402 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
R9608:Frk
|
UTSW |
10 |
34,481,873 (GRCm39) |
critical splice donor site |
probably null |
|
|
Z1177:Frk
|
UTSW |
10 |
34,460,001 (GRCm39) |
missense |
probably benign |
|
|
| Posted On |
2016-08-02 |
Incidental Mutation