Incidental Mutation 'R0588:Zdhhc7'
ID |
55840 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Zdhhc7
|
Ensembl Gene |
ENSMUSG00000031823 |
Gene Name |
zinc finger, DHHC domain containing 7 |
Synonyms |
|
MMRRC Submission |
038778-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.090)
|
Stock # |
R0588 (G1)
|
Quality Score |
190 |
Status
|
Validated
|
Chromosome |
8 |
Chromosomal Location |
120807834-120828211 bp(-) (GRCm39) |
Type of Mutation |
intron |
DNA Base Change (assembly) |
A to G
at 120810106 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000118564
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000034280]
[ENSMUST00000127664]
|
AlphaFold |
Q91WU6 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000034280
|
SMART Domains |
Protein: ENSMUSP00000034280 Gene: ENSMUSG00000031823
Domain | Start | End | E-Value | Type |
low complexity region
|
25 |
31 |
N/A |
INTRINSIC |
transmembrane domain
|
39 |
61 |
N/A |
INTRINSIC |
transmembrane domain
|
76 |
98 |
N/A |
INTRINSIC |
Pfam:zf-DHHC
|
129 |
258 |
9.8e-38 |
PFAM |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000124044
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000127664
|
SMART Domains |
Protein: ENSMUSP00000118564 Gene: ENSMUSG00000092329
Domain | Start | End | E-Value | Type |
Pfam:Glycos_transf_2
|
104 |
287 |
7.4e-31 |
PFAM |
Pfam:Glyco_transf_7C
|
261 |
331 |
4.9e-8 |
PFAM |
RICIN
|
406 |
531 |
9.28e-27 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000141886
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000150444
|
Meta Mutation Damage Score |
0.0898 |
Coding Region Coverage |
- 1x: 99.4%
- 3x: 98.8%
- 10x: 97.4%
- 20x: 94.8%
|
Validation Efficiency |
100% (25/25) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 24 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc9 |
T |
A |
6: 142,548,787 (GRCm39) |
K1299* |
probably null |
Het |
Adamts2 |
G |
T |
11: 50,667,491 (GRCm39) |
W476C |
probably damaging |
Het |
Ankrd13c |
T |
C |
3: 157,711,454 (GRCm39) |
F525L |
probably damaging |
Het |
Arg1 |
T |
C |
10: 24,796,522 (GRCm39) |
S102G |
probably damaging |
Het |
Atp2a3 |
A |
T |
11: 72,863,850 (GRCm39) |
D192V |
possibly damaging |
Het |
Cabin1 |
T |
C |
10: 75,581,171 (GRCm39) |
E385G |
possibly damaging |
Het |
Cacna1h |
A |
T |
17: 25,606,538 (GRCm39) |
D1020E |
probably damaging |
Het |
Calcb |
C |
T |
7: 114,319,361 (GRCm39) |
H48Y |
probably benign |
Het |
Crtc1 |
A |
G |
8: 70,892,199 (GRCm39) |
S4P |
probably damaging |
Het |
Dcaf6 |
A |
G |
1: 165,247,792 (GRCm39) |
I147T |
possibly damaging |
Het |
Ears2 |
T |
C |
7: 121,643,514 (GRCm39) |
|
probably benign |
Het |
Fas |
T |
C |
19: 34,304,540 (GRCm39) |
V267A |
probably damaging |
Het |
Fus |
T |
C |
7: 127,584,746 (GRCm39) |
L84P |
probably damaging |
Het |
Fyb1 |
T |
C |
15: 6,609,940 (GRCm39) |
V171A |
probably benign |
Het |
Gdap2 |
T |
A |
3: 100,077,317 (GRCm39) |
M1K |
probably null |
Het |
Gprc5b |
T |
A |
7: 118,583,218 (GRCm39) |
Q217L |
probably benign |
Het |
Lrrc69 |
A |
G |
4: 14,704,001 (GRCm39) |
I273T |
possibly damaging |
Het |
Map4k4 |
C |
A |
1: 40,044,024 (GRCm39) |
Q556K |
possibly damaging |
Het |
Npy6r |
T |
A |
18: 44,408,888 (GRCm39) |
V103E |
possibly damaging |
Het |
Or5b24 |
A |
G |
19: 12,912,111 (GRCm39) |
Y3C |
probably benign |
Het |
Shisa9 |
A |
G |
16: 12,085,638 (GRCm39) |
T416A |
probably damaging |
Het |
Slc26a9 |
C |
A |
1: 131,681,749 (GRCm39) |
|
probably benign |
Het |
Sostdc1 |
G |
T |
12: 36,367,020 (GRCm39) |
|
probably benign |
Het |
St18 |
T |
A |
1: 6,887,962 (GRCm39) |
F510L |
probably damaging |
Het |
|
Other mutations in Zdhhc7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01757:Zdhhc7
|
APN |
8 |
120,814,662 (GRCm39) |
missense |
probably benign |
|
IGL01988:Zdhhc7
|
APN |
8 |
120,809,329 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03407:Zdhhc7
|
APN |
8 |
120,812,131 (GRCm39) |
missense |
probably damaging |
0.98 |
R0362:Zdhhc7
|
UTSW |
8 |
120,813,386 (GRCm39) |
missense |
probably null |
0.32 |
R0629:Zdhhc7
|
UTSW |
8 |
120,814,785 (GRCm39) |
missense |
possibly damaging |
0.60 |
R1224:Zdhhc7
|
UTSW |
8 |
120,809,311 (GRCm39) |
missense |
probably benign |
|
R1317:Zdhhc7
|
UTSW |
8 |
120,811,639 (GRCm39) |
missense |
probably benign |
0.04 |
R1796:Zdhhc7
|
UTSW |
8 |
120,812,157 (GRCm39) |
missense |
probably benign |
0.04 |
R5891:Zdhhc7
|
UTSW |
8 |
120,811,639 (GRCm39) |
missense |
probably benign |
0.04 |
R6495:Zdhhc7
|
UTSW |
8 |
120,813,395 (GRCm39) |
missense |
probably benign |
0.19 |
R6711:Zdhhc7
|
UTSW |
8 |
120,810,066 (GRCm39) |
missense |
probably benign |
0.04 |
R6833:Zdhhc7
|
UTSW |
8 |
120,811,663 (GRCm39) |
missense |
probably damaging |
1.00 |
R7083:Zdhhc7
|
UTSW |
8 |
120,812,166 (GRCm39) |
missense |
probably damaging |
1.00 |
R7743:Zdhhc7
|
UTSW |
8 |
120,813,467 (GRCm39) |
missense |
possibly damaging |
0.49 |
R9368:Zdhhc7
|
UTSW |
8 |
120,814,494 (GRCm39) |
missense |
probably damaging |
1.00 |
R9401:Zdhhc7
|
UTSW |
8 |
120,813,425 (GRCm39) |
missense |
probably benign |
0.44 |
|
Predicted Primers |
PCR Primer
(F):5'- TCTGAGACCCACTGAGTTCTGACC -3'
(R):5'- GCTTGCCTGCCATTGTAAAGCTCTG -3'
Sequencing Primer
(F):5'- GGAACTATGCTGCCCCAATG -3'
(R):5'- TATAGTCCCCAGTGCGGTAAG -3'
|
Posted On |
2013-07-11 |