Incidental Mutation 'IGL03047:Odf2'
ID |
408954 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Odf2
|
Ensembl Gene |
ENSMUSG00000026790 |
Gene Name |
outer dense fiber of sperm tails 2 |
Synonyms |
cenexin, MMTEST29 |
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
IGL03047 (G1)
|
Quality Score |
|
Status
|
|
Chromosome |
2 |
Chromosomal Location |
29779233-29821758 bp(+) (GRCm39) |
Type of Mutation |
splice site |
DNA Base Change (assembly) |
A to T
at 29810907 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000139390
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000028128]
[ENSMUST00000046571]
[ENSMUST00000113755]
[ENSMUST00000113756]
[ENSMUST00000113757]
[ENSMUST00000113759]
[ENSMUST00000113762]
[ENSMUST00000113763]
[ENSMUST00000113765]
[ENSMUST00000184845]
[ENSMUST00000113767]
[ENSMUST00000113764]
|
AlphaFold |
A3KGV1 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000028128
|
SMART Domains |
Protein: ENSMUSP00000028128 Gene: ENSMUSG00000026790
Domain | Start | End | E-Value | Type |
coiled coil region
|
125 |
197 |
N/A |
INTRINSIC |
internal_repeat_1
|
248 |
284 |
1.04e-5 |
PROSPERO |
internal_repeat_1
|
447 |
481 |
1.04e-5 |
PROSPERO |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000046571
|
SMART Domains |
Protein: ENSMUSP00000049272 Gene: ENSMUSG00000026790
Domain | Start | End | E-Value | Type |
internal_repeat_2
|
120 |
138 |
1.77e-5 |
PROSPERO |
coiled coil region
|
139 |
211 |
N/A |
INTRINSIC |
internal_repeat_2
|
218 |
236 |
1.77e-5 |
PROSPERO |
internal_repeat_1
|
262 |
298 |
8.12e-7 |
PROSPERO |
internal_repeat_1
|
461 |
495 |
8.12e-7 |
PROSPERO |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000113755
|
SMART Domains |
Protein: ENSMUSP00000109384 Gene: ENSMUSG00000026790
Domain | Start | End | E-Value | Type |
coiled coil region
|
139 |
211 |
N/A |
INTRINSIC |
internal_repeat_1
|
262 |
298 |
2.12e-5 |
PROSPERO |
internal_repeat_1
|
461 |
495 |
2.12e-5 |
PROSPERO |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000113756
|
SMART Domains |
Protein: ENSMUSP00000109385 Gene: ENSMUSG00000026790
Domain | Start | End | E-Value | Type |
internal_repeat_2
|
120 |
138 |
1.77e-5 |
PROSPERO |
coiled coil region
|
139 |
211 |
N/A |
INTRINSIC |
internal_repeat_2
|
218 |
236 |
1.77e-5 |
PROSPERO |
internal_repeat_1
|
262 |
298 |
8.12e-7 |
PROSPERO |
internal_repeat_1
|
461 |
495 |
8.12e-7 |
PROSPERO |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000113757
|
SMART Domains |
Protein: ENSMUSP00000109386 Gene: ENSMUSG00000026790
Domain | Start | End | E-Value | Type |
internal_repeat_2
|
101 |
119 |
9.13e-6 |
PROSPERO |
coiled coil region
|
120 |
192 |
N/A |
INTRINSIC |
internal_repeat_2
|
199 |
217 |
9.13e-6 |
PROSPERO |
internal_repeat_1
|
243 |
279 |
3.83e-7 |
PROSPERO |
internal_repeat_1
|
442 |
476 |
3.83e-7 |
PROSPERO |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000113759
|
SMART Domains |
Protein: ENSMUSP00000109388 Gene: ENSMUSG00000026790
Domain | Start | End | E-Value | Type |
internal_repeat_2
|
120 |
138 |
1.82e-5 |
PROSPERO |
coiled coil region
|
139 |
211 |
N/A |
INTRINSIC |
internal_repeat_2
|
218 |
236 |
1.82e-5 |
PROSPERO |
internal_repeat_1
|
262 |
299 |
1.55e-6 |
PROSPERO |
internal_repeat_1
|
462 |
496 |
1.55e-6 |
PROSPERO |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000113762
|
SMART Domains |
Protein: ENSMUSP00000109391 Gene: ENSMUSG00000026790
Domain | Start | End | E-Value | Type |
coiled coil region
|
144 |
216 |
N/A |
INTRINSIC |
internal_repeat_1
|
267 |
303 |
1.9e-5 |
PROSPERO |
internal_repeat_1
|
466 |
500 |
1.9e-5 |
PROSPERO |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000113763
|
SMART Domains |
Protein: ENSMUSP00000109392 Gene: ENSMUSG00000026790
Domain | Start | End | E-Value | Type |
coiled coil region
|
125 |
197 |
N/A |
INTRINSIC |
internal_repeat_1
|
248 |
284 |
1.04e-5 |
PROSPERO |
internal_repeat_1
|
447 |
481 |
1.04e-5 |
PROSPERO |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000113765
|
SMART Domains |
Protein: ENSMUSP00000109394 Gene: ENSMUSG00000026790
Domain | Start | End | E-Value | Type |
internal_repeat_2
|
125 |
143 |
1.66e-5 |
PROSPERO |
coiled coil region
|
144 |
216 |
N/A |
INTRINSIC |
internal_repeat_2
|
223 |
241 |
1.66e-5 |
PROSPERO |
internal_repeat_1
|
267 |
303 |
7.56e-7 |
PROSPERO |
internal_repeat_1
|
466 |
500 |
7.56e-7 |
PROSPERO |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000184845
|
SMART Domains |
Protein: ENSMUSP00000139390 Gene: ENSMUSG00000026790
Domain | Start | End | E-Value | Type |
coiled coil region
|
139 |
211 |
N/A |
INTRINSIC |
internal_repeat_1
|
262 |
298 |
3.95e-5 |
PROSPERO |
internal_repeat_1
|
461 |
495 |
3.95e-5 |
PROSPERO |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000113767
|
SMART Domains |
Protein: ENSMUSP00000109396 Gene: ENSMUSG00000026790
Domain | Start | End | E-Value | Type |
low complexity region
|
9 |
23 |
N/A |
INTRINSIC |
coiled coil region
|
188 |
260 |
N/A |
INTRINSIC |
internal_repeat_1
|
311 |
347 |
3e-5 |
PROSPERO |
internal_repeat_1
|
510 |
544 |
3e-5 |
PROSPERO |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000113764
|
SMART Domains |
Protein: ENSMUSP00000109393 Gene: ENSMUSG00000026790
Domain | Start | End | E-Value | Type |
coiled coil region
|
125 |
197 |
N/A |
INTRINSIC |
internal_repeat_1
|
248 |
284 |
1.04e-5 |
PROSPERO |
internal_repeat_1
|
447 |
481 |
1.04e-5 |
PROSPERO |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000152026
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000152503
|
Coding Region Coverage |
- 1x: 0.0%
- 3x: 0.0%
- 10x: 0.0%
- 20x: 0.0%
|
Validation Efficiency |
98% (41/42) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The outer dense fibers are cytoskeletal structures that surround the axoneme in the middle piece and principal piece of the sperm tail. The fibers function in maintaining the elastic structure and recoil of the sperm tail as well as in protecting the tail from shear forces during epididymal transport and ejaculation. Defects in the outer dense fibers lead to abnormal sperm morphology and infertility. This gene encodes one of the major outer dense fiber proteins. Alternative splicing results in multiple transcript variants. The longer transcripts, also known as 'Cenexins', encode proteins with a C-terminal extension that are differentially targeted to somatic centrioles and thought to be crucial for the formation of microtubule organizing centers. [provided by RefSeq, Oct 2010] PHENOTYPE: Mice homozygous for a gene trapped allele exhibit embryonic lethality before implantation and transmission ratio distortion while all heterozygous males display normal development and fertility. Males heterozygous for other alleles are either infertile orshow reduced fertility. [provided by MGI curators]
|
Allele List at MGI |
All alleles(18) : Gene trapped(18) |
Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2900092C05Rik |
T |
A |
7: 12,246,568 (GRCm39) |
H21Q |
possibly damaging |
Het |
4933427D14Rik |
A |
G |
11: 72,057,552 (GRCm39) |
I749T |
possibly damaging |
Het |
Adam22 |
A |
G |
5: 8,132,220 (GRCm39) |
S869P |
probably damaging |
Het |
Add3 |
A |
G |
19: 53,231,022 (GRCm39) |
T566A |
probably benign |
Het |
Asic3 |
A |
C |
5: 24,618,788 (GRCm39) |
M27L |
probably benign |
Het |
Atp2c1 |
T |
A |
9: 105,398,206 (GRCm39) |
|
probably benign |
Het |
Cabin1 |
A |
T |
10: 75,535,934 (GRCm39) |
|
probably benign |
Het |
Ccr7 |
C |
T |
11: 99,036,160 (GRCm39) |
R254H |
probably benign |
Het |
Cdk2ap1 |
G |
T |
5: 124,486,753 (GRCm39) |
A63E |
possibly damaging |
Het |
Cfap70 |
T |
C |
14: 20,498,646 (GRCm39) |
T14A |
possibly damaging |
Het |
Cldn11 |
T |
A |
3: 31,217,256 (GRCm39) |
F141L |
probably damaging |
Het |
Comp |
G |
T |
8: 70,827,559 (GRCm39) |
A107S |
possibly damaging |
Het |
Cyp2b23 |
A |
T |
7: 26,380,892 (GRCm39) |
|
probably benign |
Het |
Cyp2c68 |
T |
G |
19: 39,722,904 (GRCm39) |
I215L |
probably benign |
Het |
Cyp4f17 |
T |
A |
17: 32,743,023 (GRCm39) |
I232K |
possibly damaging |
Het |
Dram2 |
T |
G |
3: 106,480,345 (GRCm39) |
F219L |
probably damaging |
Het |
Fam186a |
G |
A |
15: 99,843,589 (GRCm39) |
A885V |
unknown |
Het |
Fbxo42 |
A |
G |
4: 140,926,853 (GRCm39) |
T378A |
possibly damaging |
Het |
Frmpd1 |
T |
A |
4: 45,283,993 (GRCm39) |
V938E |
probably damaging |
Het |
Gramd1c |
C |
A |
16: 43,808,610 (GRCm39) |
L489F |
probably damaging |
Het |
Il17ra |
T |
C |
6: 120,458,187 (GRCm39) |
I446T |
probably damaging |
Het |
Il36g |
G |
A |
2: 24,082,719 (GRCm39) |
A165T |
probably damaging |
Het |
Kcne4 |
G |
T |
1: 78,795,495 (GRCm39) |
V48F |
possibly damaging |
Het |
Ly6g6c |
T |
A |
17: 35,288,325 (GRCm39) |
|
probably null |
Het |
Mars2 |
A |
G |
1: 55,278,032 (GRCm39) |
Y545C |
probably benign |
Het |
Mmp12 |
T |
G |
9: 7,357,797 (GRCm39) |
|
probably benign |
Het |
Mthfd1l |
T |
A |
10: 3,930,409 (GRCm39) |
|
probably benign |
Het |
Nop14 |
C |
T |
5: 34,817,358 (GRCm39) |
R11K |
possibly damaging |
Het |
Npas3 |
T |
A |
12: 53,878,470 (GRCm39) |
|
probably benign |
Het |
Or2y1d |
A |
G |
11: 49,321,794 (GRCm39) |
M164V |
probably benign |
Het |
Or5p73 |
T |
C |
7: 108,064,983 (GRCm39) |
S151P |
probably damaging |
Het |
Or5w16 |
A |
G |
2: 87,577,338 (GRCm39) |
Y266C |
possibly damaging |
Het |
Or6s1 |
A |
G |
14: 51,308,613 (GRCm39) |
I79T |
possibly damaging |
Het |
Otud7b |
T |
C |
3: 96,058,301 (GRCm39) |
|
probably benign |
Het |
Plcg1 |
T |
C |
2: 160,596,799 (GRCm39) |
Y747H |
probably damaging |
Het |
Runx1t1 |
G |
A |
4: 13,865,882 (GRCm39) |
V357I |
probably damaging |
Het |
Seh1l |
C |
G |
18: 67,922,520 (GRCm39) |
T291R |
probably damaging |
Het |
Speer4c1 |
A |
C |
5: 15,919,214 (GRCm39) |
|
probably benign |
Het |
Sulf2 |
G |
T |
2: 165,922,814 (GRCm39) |
|
probably null |
Het |
Tent4a |
C |
A |
13: 69,651,030 (GRCm39) |
D369Y |
probably damaging |
Het |
Tex14 |
C |
T |
11: 87,427,530 (GRCm39) |
S1174F |
probably damaging |
Het |
Tm9sf4 |
A |
G |
2: 153,003,326 (GRCm39) |
|
probably benign |
Het |
Vmn2r7 |
G |
A |
3: 64,614,639 (GRCm39) |
H392Y |
possibly damaging |
Het |
Zfhx4 |
T |
A |
3: 5,308,793 (GRCm39) |
V673D |
probably damaging |
Het |
|
Other mutations in Odf2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01472:Odf2
|
APN |
2 |
29,783,071 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01511:Odf2
|
APN |
2 |
29,804,321 (GRCm39) |
splice site |
probably benign |
|
IGL01760:Odf2
|
APN |
2 |
29,804,472 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02487:Odf2
|
APN |
2 |
29,810,851 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL03057:Odf2
|
APN |
2 |
29,813,657 (GRCm39) |
intron |
probably benign |
|
IGL03064:Odf2
|
APN |
2 |
29,791,091 (GRCm39) |
missense |
probably benign |
0.28 |
3-1:Odf2
|
UTSW |
2 |
29,794,087 (GRCm39) |
nonsense |
probably null |
|
IGL02837:Odf2
|
UTSW |
2 |
29,816,725 (GRCm39) |
missense |
probably damaging |
0.99 |
R4025:Odf2
|
UTSW |
2 |
29,816,827 (GRCm39) |
missense |
probably damaging |
1.00 |
R4227:Odf2
|
UTSW |
2 |
29,791,296 (GRCm39) |
intron |
probably benign |
|
R4357:Odf2
|
UTSW |
2 |
29,782,256 (GRCm39) |
missense |
probably benign |
0.00 |
R4417:Odf2
|
UTSW |
2 |
29,805,333 (GRCm39) |
splice site |
probably benign |
|
R4512:Odf2
|
UTSW |
2 |
29,816,109 (GRCm39) |
splice site |
probably null |
|
R4705:Odf2
|
UTSW |
2 |
29,794,046 (GRCm39) |
missense |
probably damaging |
1.00 |
R4815:Odf2
|
UTSW |
2 |
29,792,252 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5325:Odf2
|
UTSW |
2 |
29,802,583 (GRCm39) |
missense |
probably benign |
0.19 |
R5614:Odf2
|
UTSW |
2 |
29,810,879 (GRCm39) |
missense |
probably damaging |
0.99 |
R6998:Odf2
|
UTSW |
2 |
29,802,629 (GRCm39) |
missense |
probably benign |
0.43 |
R7740:Odf2
|
UTSW |
2 |
29,820,636 (GRCm39) |
missense |
probably damaging |
1.00 |
R7963:Odf2
|
UTSW |
2 |
29,816,112 (GRCm39) |
missense |
probably benign |
0.44 |
R8548:Odf2
|
UTSW |
2 |
29,783,526 (GRCm39) |
critical splice donor site |
probably null |
|
R9096:Odf2
|
UTSW |
2 |
29,783,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R9157:Odf2
|
UTSW |
2 |
29,816,815 (GRCm39) |
missense |
probably benign |
0.05 |
R9313:Odf2
|
UTSW |
2 |
29,816,815 (GRCm39) |
missense |
probably benign |
0.05 |
R9383:Odf2
|
UTSW |
2 |
29,791,249 (GRCm39) |
missense |
probably damaging |
1.00 |
R9658:Odf2
|
UTSW |
2 |
29,779,813 (GRCm39) |
missense |
probably benign |
0.01 |
R9722:Odf2
|
UTSW |
2 |
29,813,594 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
Posted On |
2016-08-02 |