Incidental Mutation 'IGL01398:Zdhhc14'
| ID |
79540 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Zdhhc14
|
| Ensembl Gene |
ENSMUSG00000034265 |
| Gene Name |
zinc finger, DHHC domain containing 14 |
| Synonyms |
New1cp, B530001K09Rik |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.080)
|
| Stock # |
IGL01398
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
17 |
| Chromosomal Location |
5542832-5804086 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 5762738 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Threonine
at position 214
(I214T)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000086589
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000089185]
|
| AlphaFold |
Q8BQQ1 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000089185
AA Change: I214T
PolyPhen 2
Score 0.903 (Sensitivity: 0.82; Specificity: 0.94)
|
| SMART Domains |
Protein: ENSMUSP00000086589
Gene: ENSMUSG00000034265
AA Change: I214T
| Domain | Start | End | E-Value | Type |
|---|
|
transmembrane domain
|
62 |
81 |
N/A |
INTRINSIC |
|
transmembrane domain
|
91 |
110 |
N/A |
INTRINSIC |
|
Pfam:zf-DHHC
|
160 |
289 |
1.8e-38 |
PFAM |
|
low complexity region
|
351 |
365 |
N/A |
INTRINSIC |
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 28 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Acap1 |
T |
C |
11: 69,772,548 (GRCm39) |
D521G |
probably damaging |
Het |
| Apol11b |
G |
A |
15: 77,522,219 (GRCm39) |
T26M |
probably damaging |
Het |
| Best2 |
T |
A |
8: 85,735,956 (GRCm39) |
Y326F |
probably damaging |
Het |
| Clca3a1 |
T |
C |
3: 144,722,512 (GRCm39) |
T287A |
possibly damaging |
Het |
| Cyp26a1 |
C |
T |
19: 37,686,395 (GRCm39) |
T13I |
probably damaging |
Het |
| Dhcr7 |
T |
C |
7: 143,395,056 (GRCm39) |
S188P |
probably damaging |
Het |
| Eml3 |
T |
G |
19: 8,911,598 (GRCm39) |
|
probably benign |
Het |
| Faf1 |
A |
T |
4: 109,593,793 (GRCm39) |
I124F |
probably damaging |
Het |
| Fkbp9 |
T |
A |
6: 56,837,790 (GRCm39) |
|
probably benign |
Het |
| Foxq1 |
G |
A |
13: 31,743,434 (GRCm39) |
D179N |
probably damaging |
Het |
| Frem1 |
C |
T |
4: 82,868,599 (GRCm39) |
V1443M |
possibly damaging |
Het |
| Gpnmb |
T |
A |
6: 49,027,365 (GRCm39) |
M363K |
probably benign |
Het |
| Grm3 |
T |
C |
5: 9,535,762 (GRCm39) |
|
probably benign |
Het |
| Ints3 |
A |
G |
3: 90,300,130 (GRCm39) |
L929P |
probably damaging |
Het |
| Myh11 |
T |
A |
16: 14,019,964 (GRCm39) |
I1823F |
probably damaging |
Het |
| Nudt9 |
T |
C |
5: 104,212,979 (GRCm39) |
*351Q |
probably null |
Het |
| Or2ak6 |
A |
T |
11: 58,592,593 (GRCm39) |
H22L |
probably benign |
Het |
| Or4c107 |
C |
T |
2: 88,789,193 (GRCm39) |
P128S |
probably damaging |
Het |
| Or8k38 |
A |
T |
2: 86,488,032 (GRCm39) |
F257I |
probably damaging |
Het |
| Pgr15l |
C |
T |
X: 96,121,785 (GRCm39) |
T392I |
probably benign |
Het |
| Sdk1 |
C |
A |
5: 141,923,332 (GRCm39) |
L318I |
probably benign |
Het |
| Sult1c2 |
C |
A |
17: 54,269,180 (GRCm39) |
V279L |
possibly damaging |
Het |
| Tek |
T |
C |
4: 94,738,014 (GRCm39) |
I688T |
probably damaging |
Het |
| Telo2 |
A |
T |
17: 25,324,748 (GRCm39) |
D477E |
probably benign |
Het |
| Ubr3 |
T |
A |
2: 69,789,997 (GRCm39) |
Y884N |
probably damaging |
Het |
| Upf3a |
C |
A |
8: 13,836,221 (GRCm39) |
H92Q |
probably damaging |
Het |
| Vmn2r51 |
C |
T |
7: 9,836,341 (GRCm39) |
E147K |
probably benign |
Het |
| Vps54 |
A |
G |
11: 21,245,403 (GRCm39) |
|
probably benign |
Het |
|
| Other mutations in Zdhhc14 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00419:Zdhhc14
|
APN |
17 |
5,802,959 (GRCm39) |
splice site |
probably benign |
|
|
IGL00909:Zdhhc14
|
APN |
17 |
5,803,067 (GRCm39) |
missense |
probably benign |
|
|
IGL00964:Zdhhc14
|
APN |
17 |
5,762,756 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01483:Zdhhc14
|
APN |
17 |
5,762,733 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL02185:Zdhhc14
|
APN |
17 |
5,803,157 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL02801:Zdhhc14
|
APN |
17 |
5,777,094 (GRCm39) |
splice site |
probably null |
|
|
R0189:Zdhhc14
|
UTSW |
17 |
5,775,539 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R0304:Zdhhc14
|
UTSW |
17 |
5,775,611 (GRCm39) |
splice site |
probably benign |
|
|
R0648:Zdhhc14
|
UTSW |
17 |
5,543,877 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1017:Zdhhc14
|
UTSW |
17 |
5,543,924 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1595:Zdhhc14
|
UTSW |
17 |
5,543,831 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2416:Zdhhc14
|
UTSW |
17 |
5,803,283 (GRCm39) |
missense |
probably benign |
|
|
R3420:Zdhhc14
|
UTSW |
17 |
5,803,366 (GRCm39) |
makesense |
probably null |
|
|
R3421:Zdhhc14
|
UTSW |
17 |
5,803,366 (GRCm39) |
makesense |
probably null |
|
|
R4063:Zdhhc14
|
UTSW |
17 |
5,802,983 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4088:Zdhhc14
|
UTSW |
17 |
5,777,131 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5359:Zdhhc14
|
UTSW |
17 |
5,543,821 (GRCm39) |
missense |
probably benign |
|
|
R6236:Zdhhc14
|
UTSW |
17 |
5,543,918 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7029:Zdhhc14
|
UTSW |
17 |
5,698,186 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R7350:Zdhhc14
|
UTSW |
17 |
5,777,151 (GRCm39) |
missense |
probably benign |
0.44 |
|
R7873:Zdhhc14
|
UTSW |
17 |
5,762,729 (GRCm39) |
missense |
probably benign |
0.37 |
|
R8247:Zdhhc14
|
UTSW |
17 |
5,736,031 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8492:Zdhhc14
|
UTSW |
17 |
5,762,689 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8865:Zdhhc14
|
UTSW |
17 |
5,775,570 (GRCm39) |
missense |
possibly damaging |
0.58 |
|
R8969:Zdhhc14
|
UTSW |
17 |
5,775,555 (GRCm39) |
missense |
probably benign |
0.12 |
|
R9133:Zdhhc14
|
UTSW |
17 |
5,803,283 (GRCm39) |
missense |
probably benign |
|
|
R9291:Zdhhc14
|
UTSW |
17 |
5,698,237 (GRCm39) |
missense |
probably benign |
0.02 |
|
R9433:Zdhhc14
|
UTSW |
17 |
5,781,779 (GRCm39) |
missense |
probably benign |
0.03 |
|
| Posted On |
2013-11-05 |
Incidental Mutation