Incidental Mutation 'IGL01595:Krt79'
| ID |
93385 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Krt79
|
| Ensembl Gene |
ENSMUSG00000061397 |
| Gene Name |
keratin 79 |
| Synonyms |
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
IGL01595
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
15 |
| Chromosomal Location |
101837767-101848759 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to G
at 101840206 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Glutamic Acid to Alanine
at position 330
(E330A)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000023799
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000023799]
|
| AlphaFold |
Q8VED5 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000023799
AA Change: E330A
PolyPhen 2
Score 0.983 (Sensitivity: 0.75; Specificity: 0.96)
|
| SMART Domains |
Protein: ENSMUSP00000023799
Gene: ENSMUSG00000061397
AA Change: E330A
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Keratin_2_head
|
15 |
98 |
6.6e-11 |
PFAM |
|
Pfam:Keratin_2_head
|
73 |
135 |
1.2e-21 |
PFAM |
|
Filament
|
138 |
452 |
7.12e-159 |
SMART |
|
low complexity region
|
474 |
500 |
N/A |
INTRINSIC |
|
low complexity region
|
519 |
530 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000229195
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000230273
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000230441
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Keratins are intermediate filament proteins responsible for the structural integrity of epithelial cells and are subdivided into epithelial keratins and hair keratins. This gene encodes an epithelial keratin that is expressed in skeletal muscle, skin and scalp. The type II keratins are clustered in a region of chromosome 12q13.[provided by RefSeq, Jun 2009]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 35 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Acbd5 |
A |
G |
2: 22,968,181 (GRCm39) |
M111V |
probably damaging |
Het |
| Adamts14 |
A |
T |
10: 61,041,252 (GRCm39) |
H819Q |
probably damaging |
Het |
| Adamts7 |
T |
A |
9: 90,075,359 (GRCm39) |
N1072K |
probably benign |
Het |
| Ahnak |
T |
A |
19: 8,980,865 (GRCm39) |
Y716* |
probably null |
Het |
| Arfgef3 |
T |
C |
10: 18,470,660 (GRCm39) |
K1702E |
possibly damaging |
Het |
| BB014433 |
C |
A |
8: 15,092,499 (GRCm39) |
|
probably null |
Het |
| Bdnf |
A |
T |
2: 109,554,273 (GRCm39) |
K176* |
probably null |
Het |
| C2cd5 |
C |
T |
6: 142,963,748 (GRCm39) |
R879H |
probably damaging |
Het |
| Capn11 |
T |
A |
17: 45,950,360 (GRCm39) |
H327L |
probably benign |
Het |
| Ccdc68 |
A |
G |
18: 70,089,117 (GRCm39) |
N220S |
probably benign |
Het |
| Cftr |
T |
C |
6: 18,198,238 (GRCm39) |
|
probably benign |
Het |
| Clca3a2 |
G |
A |
3: 144,793,768 (GRCm39) |
L296F |
probably damaging |
Het |
| Cubn |
A |
T |
2: 13,330,027 (GRCm39) |
L2618Q |
probably benign |
Het |
| Gfi1b |
A |
G |
2: 28,501,429 (GRCm39) |
|
probably null |
Het |
| Gpr37 |
G |
T |
6: 25,669,572 (GRCm39) |
T424N |
probably damaging |
Het |
| Kank3 |
G |
A |
17: 34,038,154 (GRCm39) |
|
probably null |
Het |
| Kcnh5 |
T |
C |
12: 74,945,101 (GRCm39) |
Q716R |
probably benign |
Het |
| Kntc1 |
G |
A |
5: 123,941,758 (GRCm39) |
M1817I |
probably benign |
Het |
| Mapk15 |
C |
A |
15: 75,867,129 (GRCm39) |
P82Q |
probably benign |
Het |
| Myh15 |
A |
T |
16: 48,993,312 (GRCm39) |
D1649V |
probably damaging |
Het |
| Myo1d |
T |
C |
11: 80,566,936 (GRCm39) |
I326V |
probably benign |
Het |
| Nek9 |
A |
T |
12: 85,361,194 (GRCm39) |
W504R |
probably damaging |
Het |
| Nlrp4c |
T |
A |
7: 6,069,111 (GRCm39) |
C337* |
probably null |
Het |
| Nup160 |
A |
G |
2: 90,560,081 (GRCm39) |
N1269D |
probably damaging |
Het |
| Or52e3 |
A |
G |
7: 102,869,558 (GRCm39) |
D211G |
probably damaging |
Het |
| Or56b2 |
T |
C |
7: 104,337,285 (GRCm39) |
M21T |
possibly damaging |
Het |
| Or8c10 |
T |
C |
9: 38,279,346 (GRCm39) |
V168A |
probably benign |
Het |
| Pde6a |
A |
G |
18: 61,414,599 (GRCm39) |
M36V |
probably damaging |
Het |
| Perp |
A |
G |
10: 18,731,407 (GRCm39) |
Q122R |
probably damaging |
Het |
| S100a7a |
T |
C |
3: 90,565,107 (GRCm39) |
Y101H |
probably benign |
Het |
| Sbk2 |
C |
A |
7: 4,960,712 (GRCm39) |
V153L |
possibly damaging |
Het |
| Serpinb7 |
A |
T |
1: 107,356,052 (GRCm39) |
N25I |
probably damaging |
Het |
| Tbx5 |
A |
T |
5: 119,978,903 (GRCm39) |
D105V |
probably damaging |
Het |
| Trip6 |
T |
A |
5: 137,311,675 (GRCm39) |
T101S |
probably benign |
Het |
| Ush2a |
T |
A |
1: 188,386,921 (GRCm39) |
|
probably null |
Het |
|
| Other mutations in Krt79 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00516:Krt79
|
APN |
15 |
101,848,601 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL00546:Krt79
|
APN |
15 |
101,838,308 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02193:Krt79
|
APN |
15 |
101,848,340 (GRCm39) |
missense |
possibly damaging |
0.59 |
|
R0639:Krt79
|
UTSW |
15 |
101,839,983 (GRCm39) |
nonsense |
probably null |
|
|
R0980:Krt79
|
UTSW |
15 |
101,846,442 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1839:Krt79
|
UTSW |
15 |
101,846,373 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R4624:Krt79
|
UTSW |
15 |
101,848,241 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R4745:Krt79
|
UTSW |
15 |
101,839,119 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5203:Krt79
|
UTSW |
15 |
101,838,175 (GRCm39) |
missense |
unknown |
|
|
R5382:Krt79
|
UTSW |
15 |
101,839,875 (GRCm39) |
missense |
probably benign |
0.09 |
|
R5568:Krt79
|
UTSW |
15 |
101,838,220 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6902:Krt79
|
UTSW |
15 |
101,840,314 (GRCm39) |
missense |
probably benign |
0.08 |
|
R6916:Krt79
|
UTSW |
15 |
101,844,605 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6998:Krt79
|
UTSW |
15 |
101,846,307 (GRCm39) |
missense |
probably benign |
|
|
R7009:Krt79
|
UTSW |
15 |
101,839,876 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7663:Krt79
|
UTSW |
15 |
101,840,278 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R8161:Krt79
|
UTSW |
15 |
101,839,137 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R8184:Krt79
|
UTSW |
15 |
101,838,187 (GRCm39) |
missense |
unknown |
|
|
R8206:Krt79
|
UTSW |
15 |
101,848,705 (GRCm39) |
start gained |
probably null |
|
|
R8705:Krt79
|
UTSW |
15 |
101,846,441 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8993:Krt79
|
UTSW |
15 |
101,839,441 (GRCm39) |
intron |
probably benign |
|
|
R9055:Krt79
|
UTSW |
15 |
101,839,922 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9322:Krt79
|
UTSW |
15 |
101,840,245 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R9456:Krt79
|
UTSW |
15 |
101,839,904 (GRCm39) |
missense |
probably benign |
0.02 |
|
R9495:Krt79
|
UTSW |
15 |
101,840,288 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9514:Krt79
|
UTSW |
15 |
101,840,288 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9533:Krt79
|
UTSW |
15 |
101,848,417 (GRCm39) |
missense |
possibly damaging |
0.55 |
|
R9560:Krt79
|
UTSW |
15 |
101,846,277 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9705:Krt79
|
UTSW |
15 |
101,839,196 (GRCm39) |
missense |
probably benign |
|
|
R9706:Krt79
|
UTSW |
15 |
101,839,196 (GRCm39) |
missense |
probably benign |
|
|
R9707:Krt79
|
UTSW |
15 |
101,839,196 (GRCm39) |
missense |
probably benign |
|
|
R9714:Krt79
|
UTSW |
15 |
101,839,196 (GRCm39) |
missense |
probably benign |
|
|
R9750:Krt79
|
UTSW |
15 |
101,839,196 (GRCm39) |
missense |
probably benign |
|
|
R9751:Krt79
|
UTSW |
15 |
101,839,196 (GRCm39) |
missense |
probably benign |
|
|
R9753:Krt79
|
UTSW |
15 |
101,839,196 (GRCm39) |
missense |
probably benign |
|
|
R9772:Krt79
|
UTSW |
15 |
101,839,196 (GRCm39) |
missense |
probably benign |
|
|
| Posted On |
2013-12-09 |
Incidental Mutation