Incidental Mutation 'R6787:Ddhd1'
| ID |
543674 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Ddhd1
|
| Ensembl Gene |
ENSMUSG00000037697 |
| Gene Name |
DDHD domain containing 1 |
| Synonyms |
4921528E07Rik, 9630061G18Rik |
| MMRRC Submission |
044901-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R6787 (G1)
|
| Quality Score |
77.0075 |
|
Status
|
Validated
|
| Chromosome |
14 |
| Chromosomal Location |
45830628-45895600 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 45894976 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Threonine to Alanine
at position 165
(T165A)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000118848
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000051310]
[ENSMUST00000087320]
[ENSMUST00000111828]
[ENSMUST00000149286]
[ENSMUST00000226301]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000051310
AA Change: T165A
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
| SMART Domains |
Protein: ENSMUSP00000050088
Gene: ENSMUSG00000037697
AA Change: T165A
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
28 |
39 |
N/A |
INTRINSIC |
|
low complexity region
|
95 |
111 |
N/A |
INTRINSIC |
|
low complexity region
|
118 |
141 |
N/A |
INTRINSIC |
|
low complexity region
|
183 |
201 |
N/A |
INTRINSIC |
|
low complexity region
|
206 |
217 |
N/A |
INTRINSIC |
|
low complexity region
|
284 |
297 |
N/A |
INTRINSIC |
|
Blast:DDHD
|
450 |
573 |
6e-67 |
BLAST |
|
DDHD
|
595 |
842 |
1.49e-100 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000087320
AA Change: T165A
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
| SMART Domains |
Protein: ENSMUSP00000084577
Gene: ENSMUSG00000037697
AA Change: T165A
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
28 |
39 |
N/A |
INTRINSIC |
|
low complexity region
|
95 |
111 |
N/A |
INTRINSIC |
|
low complexity region
|
118 |
141 |
N/A |
INTRINSIC |
|
low complexity region
|
183 |
201 |
N/A |
INTRINSIC |
|
low complexity region
|
206 |
217 |
N/A |
INTRINSIC |
|
low complexity region
|
284 |
297 |
N/A |
INTRINSIC |
|
Blast:DDHD
|
484 |
607 |
1e-66 |
BLAST |
|
DDHD
|
629 |
904 |
3.75e-106 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000111828
AA Change: T165A
PolyPhen 2
Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
|
| SMART Domains |
Protein: ENSMUSP00000107459
Gene: ENSMUSG00000037697
AA Change: T165A
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
28 |
39 |
N/A |
INTRINSIC |
|
low complexity region
|
95 |
111 |
N/A |
INTRINSIC |
|
low complexity region
|
118 |
141 |
N/A |
INTRINSIC |
|
low complexity region
|
183 |
201 |
N/A |
INTRINSIC |
|
low complexity region
|
206 |
217 |
N/A |
INTRINSIC |
|
low complexity region
|
284 |
297 |
N/A |
INTRINSIC |
|
Blast:DDHD
|
450 |
573 |
8e-67 |
BLAST |
|
DDHD
|
595 |
870 |
3.75e-106 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000149286
AA Change: T165A
PolyPhen 2
Score 0.011 (Sensitivity: 0.96; Specificity: 0.78)
|
| SMART Domains |
Protein: ENSMUSP00000118848
Gene: ENSMUSG00000037697
AA Change: T165A
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
28 |
39 |
N/A |
INTRINSIC |
|
low complexity region
|
95 |
111 |
N/A |
INTRINSIC |
|
low complexity region
|
118 |
141 |
N/A |
INTRINSIC |
|
low complexity region
|
183 |
201 |
N/A |
INTRINSIC |
|
low complexity region
|
206 |
217 |
N/A |
INTRINSIC |
|
low complexity region
|
284 |
297 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000226301
|
| Meta Mutation Damage Score |
0.0913 |
| Coding Region Coverage |
- 1x: 99.9%
- 3x: 99.7%
- 10x: 98.6%
- 20x: 96.3%
|
| Validation Efficiency |
96% (51/53) |
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene is a member of the intracellular phospholipase A1 gene family. The protein encoded by this gene preferentially hydrolyzes phosphatidic acid. It is a cytosolic protein with some mitochondrial localization, and is thought to be involved in the regulation of mitochondrial dynamics. Overexpression of this gene causes fragmentation of the tubular structures in mitochondria, while depletion of the gene results in mitochondrial tubule elongation. Deletion of this gene in male mice caused fertility defects, resulting from disruption in the organization of the mitochondria during spermiogenesis. In humans, mutations in this gene have been associated with hereditary spastic paraplegia (HSP), also known as Strumpell-Lorrain disease, or, familial spastic paraparesis (FSP). This inherited disorder is characterized by progressive weakness and spasticity of the legs. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Aug 2015]
PHENOTYPE: Mice homozygous for a null allele show reduced testis weight, oligozoospermia, teratozoospermia, and male subfertility. Sperm defects include a disorganized mitochondrial structure, an abnormal gap between the middle and principal pieces, and hairpin flagellum leading to impaired sperm motility. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 52 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 2700097O09Rik |
G |
A |
12: 55,126,768 (GRCm39) |
T32I |
probably benign |
Het |
| 4930486L24Rik |
T |
A |
13: 61,000,922 (GRCm39) |
I205L |
probably benign |
Het |
| Aatk |
C |
T |
11: 119,901,508 (GRCm39) |
V963M |
probably damaging |
Het |
| Adra1b |
C |
A |
11: 43,726,242 (GRCm39) |
R225L |
probably damaging |
Het |
| Adrb1 |
T |
C |
19: 56,711,021 (GRCm39) |
V73A |
probably damaging |
Het |
| Akt3 |
A |
T |
1: 176,877,756 (GRCm39) |
Y337* |
probably null |
Het |
| BC035947 |
G |
T |
1: 78,475,527 (GRCm39) |
P335Q |
possibly damaging |
Het |
| C2cd3 |
T |
C |
7: 100,104,553 (GRCm39) |
F2189L |
probably benign |
Het |
| Capn9 |
A |
G |
8: 125,342,924 (GRCm39) |
I635V |
probably benign |
Het |
| Cep55 |
T |
A |
19: 38,046,374 (GRCm39) |
D42E |
probably benign |
Het |
| Cftr |
T |
A |
6: 18,274,607 (GRCm39) |
Y878* |
probably null |
Het |
| Clpb |
A |
T |
7: 101,312,866 (GRCm39) |
|
probably benign |
Het |
| Cpeb3 |
T |
C |
19: 37,022,089 (GRCm39) |
I569V |
possibly damaging |
Het |
| Cpne6 |
A |
T |
14: 55,752,701 (GRCm39) |
D297V |
probably damaging |
Het |
| Fam98b |
T |
C |
2: 117,093,402 (GRCm39) |
|
probably null |
Het |
| Frem2 |
T |
C |
3: 53,561,744 (GRCm39) |
N921S |
probably benign |
Het |
| Gbf1 |
T |
A |
19: 46,260,211 (GRCm39) |
V1039E |
probably benign |
Het |
| Gmip |
A |
G |
8: 70,266,436 (GRCm39) |
E212G |
probably damaging |
Het |
| Gpcpd1 |
C |
T |
2: 132,379,758 (GRCm39) |
|
probably benign |
Het |
| Gtf2ird1 |
A |
T |
5: 134,392,766 (GRCm39) |
N796K |
probably damaging |
Het |
| Hadhb |
T |
C |
5: 30,360,247 (GRCm39) |
|
probably benign |
Het |
| Itga4 |
T |
A |
2: 79,119,609 (GRCm39) |
S472T |
probably damaging |
Het |
| Kcna4 |
G |
A |
2: 107,125,670 (GRCm39) |
E135K |
possibly damaging |
Het |
| Kmt2c |
G |
T |
5: 25,480,737 (GRCm39) |
|
probably null |
Het |
| Lama1 |
T |
C |
17: 68,091,020 (GRCm39) |
I1620T |
unknown |
Het |
| Lins1 |
A |
G |
7: 66,363,902 (GRCm39) |
E594G |
probably benign |
Het |
| Lrrc38 |
T |
A |
4: 143,096,364 (GRCm39) |
M225K |
probably benign |
Het |
| Mphosph9 |
A |
G |
5: 124,399,090 (GRCm39) |
I975T |
probably damaging |
Het |
| Mrgprh |
T |
C |
17: 13,095,874 (GRCm39) |
F38S |
probably benign |
Het |
| Myo1h |
G |
A |
5: 114,458,714 (GRCm39) |
G150R |
probably damaging |
Het |
| Oas2 |
T |
G |
5: 120,876,863 (GRCm39) |
I391L |
possibly damaging |
Het |
| Or4a70 |
T |
A |
2: 89,324,378 (GRCm39) |
R93* |
probably null |
Het |
| Or5p72 |
T |
C |
7: 108,021,889 (GRCm39) |
I37T |
possibly damaging |
Het |
| Or6c3b |
T |
A |
10: 129,527,391 (GRCm39) |
D173V |
possibly damaging |
Het |
| Or7e178 |
T |
C |
9: 20,247,221 (GRCm39) |
D14G |
probably benign |
Het |
| Pdcd5 |
T |
C |
7: 35,342,063 (GRCm39) |
T182A |
probably damaging |
Het |
| Pdlim7 |
T |
C |
13: 55,656,810 (GRCm39) |
D48G |
probably damaging |
Het |
| Polr3b |
A |
C |
10: 84,464,489 (GRCm39) |
|
probably null |
Het |
| Psmd5 |
C |
T |
2: 34,747,649 (GRCm39) |
|
probably null |
Het |
| Rsf1 |
GGCG |
GGCGACGGCCGCG |
7: 97,229,113 (GRCm39) |
|
probably benign |
Homo |
| Sdhb |
T |
C |
4: 140,703,501 (GRCm39) |
Y208H |
probably damaging |
Het |
| Serinc5 |
G |
A |
13: 92,842,740 (GRCm39) |
V397I |
possibly damaging |
Het |
| Sik2 |
A |
T |
9: 50,909,834 (GRCm39) |
M73K |
possibly damaging |
Het |
| Slc41a1 |
A |
G |
1: 131,770,487 (GRCm39) |
|
probably null |
Het |
| Slco1a1 |
T |
C |
6: 141,882,213 (GRCm39) |
I119V |
probably benign |
Het |
| Srd5a1 |
T |
C |
13: 69,759,418 (GRCm39) |
|
probably benign |
Het |
| Stab2 |
T |
C |
10: 86,754,948 (GRCm39) |
I1111V |
probably benign |
Het |
| Stxbp6 |
G |
T |
12: 44,949,779 (GRCm39) |
|
probably null |
Het |
| Tbc1d19 |
A |
G |
5: 53,992,591 (GRCm39) |
|
probably null |
Het |
| Tnxb |
A |
T |
17: 34,929,710 (GRCm39) |
T2815S |
probably benign |
Het |
| Txnip |
T |
A |
3: 96,467,623 (GRCm39) |
I363N |
probably damaging |
Het |
| Zfp442 |
A |
T |
2: 150,251,499 (GRCm39) |
N134K |
possibly damaging |
Het |
|
| Other mutations in Ddhd1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01318:Ddhd1
|
APN |
14 |
45,854,008 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01635:Ddhd1
|
APN |
14 |
45,867,037 (GRCm39) |
missense |
probably null |
0.98 |
|
IGL02176:Ddhd1
|
APN |
14 |
45,854,057 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02698:Ddhd1
|
APN |
14 |
45,842,663 (GRCm39) |
unclassified |
probably benign |
|
|
IGL03052:Ddhd1
|
UTSW |
14 |
45,858,240 (GRCm39) |
missense |
probably damaging |
1.00 |
|
PIT4434001:Ddhd1
|
UTSW |
14 |
45,848,062 (GRCm39) |
missense |
possibly damaging |
0.62 |
|
R0037:Ddhd1
|
UTSW |
14 |
45,847,967 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0105:Ddhd1
|
UTSW |
14 |
45,848,147 (GRCm39) |
missense |
probably benign |
0.37 |
|
R0165:Ddhd1
|
UTSW |
14 |
45,833,049 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1237:Ddhd1
|
UTSW |
14 |
45,839,107 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1401:Ddhd1
|
UTSW |
14 |
45,842,508 (GRCm39) |
critical splice donor site |
probably null |
|
|
R1574:Ddhd1
|
UTSW |
14 |
45,833,004 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1574:Ddhd1
|
UTSW |
14 |
45,833,004 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1582:Ddhd1
|
UTSW |
14 |
45,842,566 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R2070:Ddhd1
|
UTSW |
14 |
45,848,081 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2307:Ddhd1
|
UTSW |
14 |
45,846,447 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2417:Ddhd1
|
UTSW |
14 |
45,894,729 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3756:Ddhd1
|
UTSW |
14 |
45,894,720 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3756:Ddhd1
|
UTSW |
14 |
45,848,030 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4541:Ddhd1
|
UTSW |
14 |
45,860,313 (GRCm39) |
nonsense |
probably null |
|
|
R4737:Ddhd1
|
UTSW |
14 |
45,866,278 (GRCm39) |
intron |
probably benign |
|
|
R5105:Ddhd1
|
UTSW |
14 |
45,894,864 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5810:Ddhd1
|
UTSW |
14 |
45,840,164 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5898:Ddhd1
|
UTSW |
14 |
45,840,125 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6217:Ddhd1
|
UTSW |
14 |
45,856,971 (GRCm39) |
splice site |
probably null |
|
|
R6218:Ddhd1
|
UTSW |
14 |
45,851,633 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6671:Ddhd1
|
UTSW |
14 |
45,894,689 (GRCm39) |
frame shift |
probably null |
|
|
R7049:Ddhd1
|
UTSW |
14 |
45,840,138 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7150:Ddhd1
|
UTSW |
14 |
45,895,263 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7213:Ddhd1
|
UTSW |
14 |
45,895,210 (GRCm39) |
missense |
probably benign |
0.41 |
|
R7261:Ddhd1
|
UTSW |
14 |
45,894,688 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7522:Ddhd1
|
UTSW |
14 |
45,895,104 (GRCm39) |
missense |
possibly damaging |
0.47 |
|
R7920:Ddhd1
|
UTSW |
14 |
45,894,927 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R8736:Ddhd1
|
UTSW |
14 |
45,836,642 (GRCm39) |
missense |
probably benign |
0.30 |
|
R8880:Ddhd1
|
UTSW |
14 |
45,846,430 (GRCm39) |
missense |
probably benign |
|
|
R9140:Ddhd1
|
UTSW |
14 |
45,894,918 (GRCm39) |
missense |
probably benign |
0.12 |
|
R9393:Ddhd1
|
UTSW |
14 |
45,894,685 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9398:Ddhd1
|
UTSW |
14 |
45,895,117 (GRCm39) |
missense |
possibly damaging |
0.60 |
|
R9399:Ddhd1
|
UTSW |
14 |
45,895,117 (GRCm39) |
missense |
possibly damaging |
0.60 |
|
R9502:Ddhd1
|
UTSW |
14 |
45,894,679 (GRCm39) |
missense |
possibly damaging |
0.75 |
|
R9687:Ddhd1
|
UTSW |
14 |
45,848,190 (GRCm39) |
missense |
probably damaging |
0.97 |
|
Z1177:Ddhd1
|
UTSW |
14 |
45,895,051 (GRCm39) |
missense |
possibly damaging |
0.63 |
|
| Predicted Primers |
PCR Primer
(F):5'- CTCCTTGAGTGACATCCACC -3'
(R):5'- TCGTCGTTGCGCTACTACAG -3'
Sequencing Primer
(F):5'- TGAGTGACATCCACCTCGTAG -3'
(R):5'- CTACTACAGCGAGGGCGAG -3'
|
| Posted On |
2019-05-03 |
Incidental Mutation