Incidental Mutation 'IGL00427:Rec8'
| ID |
4186 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Rec8
|
| Ensembl Gene |
ENSMUSG00000002324 |
| Gene Name |
REC8 meiotic recombination protein |
| Synonyms |
Rec8L1, mrec |
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
IGL00427
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
14 |
| Chromosomal Location |
55855494-55862852 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 55856108 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Threonine to Serine
at position 17
(T17S)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000002395
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000002395]
|
| AlphaFold |
Q8C5S7 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000002395
AA Change: T17S
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000002395
Gene: ENSMUSG00000002324
AA Change: T17S
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Rad21_Rec8_N
|
1 |
117 |
2.2e-26 |
PFAM |
|
low complexity region
|
235 |
249 |
N/A |
INTRINSIC |
|
low complexity region
|
329 |
347 |
N/A |
INTRINSIC |
|
coiled coil region
|
423 |
458 |
N/A |
INTRINSIC |
|
low complexity region
|
497 |
521 |
N/A |
INTRINSIC |
|
Pfam:Rad21_Rec8
|
536 |
590 |
9.2e-23 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000140335
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000141425
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000227922
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the kleisin family of SMC (structural maintenance of chromosome) protein partners. The protein localizes to the axial elements of chromosomes during meiosis in both oocytes and spermatocytes. In the mouse, the homologous protein is a key component of the meiotic cohesion complex, which regulates sister chromatid cohesion and recombination between homologous chromosomes. Multiple alternatively spliced variants, encoding the same protein, have been found for this gene. [provided by RefSeq, Jul 2008]
PHENOTYPE: Homozygous null mice are infertile and exhibit small ovaries and testes. Females show absence of ovarian follicles and abnormal meiosis, while males exhibit abnormal chromosome pairing during meiosis, abnormal synaptonemal complex formation, and arrest of male meiosis. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 42 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adcy3 |
A |
G |
12: 4,244,357 (GRCm39) |
D289G |
probably damaging |
Het |
| Adnp |
C |
T |
2: 168,024,482 (GRCm39) |
D938N |
probably benign |
Het |
| Arpin |
T |
A |
7: 79,577,423 (GRCm39) |
N208I |
probably benign |
Het |
| Cby3 |
A |
G |
11: 50,248,638 (GRCm39) |
|
probably benign |
Het |
| Cmklr2 |
A |
T |
1: 63,222,497 (GRCm39) |
I246N |
probably damaging |
Het |
| Cnih4 |
T |
A |
1: 180,981,312 (GRCm39) |
S28T |
probably damaging |
Het |
| D130052B06Rik |
G |
T |
11: 33,573,558 (GRCm39) |
V97L |
possibly damaging |
Het |
| Dchs1 |
T |
C |
7: 105,407,631 (GRCm39) |
E2067G |
probably damaging |
Het |
| Dennd6a |
C |
T |
14: 26,329,768 (GRCm39) |
T113I |
probably damaging |
Het |
| Dock4 |
T |
A |
12: 40,882,305 (GRCm39) |
F1590L |
possibly damaging |
Het |
| Dop1a |
G |
T |
9: 86,403,553 (GRCm39) |
Q1582H |
probably benign |
Het |
| Dop1a |
A |
T |
9: 86,403,552 (GRCm39) |
Q1582L |
probably damaging |
Het |
| Dop1a |
C |
A |
9: 86,403,551 (GRCm39) |
Q1582K |
possibly damaging |
Het |
| Ebna1bp2 |
A |
T |
4: 118,483,018 (GRCm39) |
K291M |
probably damaging |
Het |
| Evpl |
G |
T |
11: 116,125,331 (GRCm39) |
Q73K |
probably benign |
Het |
| Fam131b |
G |
T |
6: 42,295,895 (GRCm39) |
T139K |
probably damaging |
Het |
| Golga3 |
A |
G |
5: 110,368,753 (GRCm39) |
T1358A |
probably damaging |
Het |
| Hgf |
G |
A |
5: 16,783,484 (GRCm39) |
D265N |
probably benign |
Het |
| Homer1 |
A |
G |
13: 93,538,622 (GRCm39) |
N333S |
probably benign |
Het |
| Igkv17-134 |
A |
T |
6: 67,697,968 (GRCm39) |
|
probably benign |
Het |
| Il16 |
T |
C |
7: 83,301,666 (GRCm39) |
D152G |
probably benign |
Het |
| Ireb2 |
T |
C |
9: 54,806,766 (GRCm39) |
|
probably benign |
Het |
| Itgb2 |
C |
T |
10: 77,393,790 (GRCm39) |
T410I |
probably benign |
Het |
| Kctd14 |
C |
A |
7: 97,106,919 (GRCm39) |
A111E |
possibly damaging |
Het |
| Lmod3 |
A |
C |
6: 97,229,258 (GRCm39) |
V92G |
probably damaging |
Het |
| Lmtk2 |
A |
G |
5: 144,070,973 (GRCm39) |
D83G |
probably damaging |
Het |
| Myh1 |
A |
G |
11: 67,111,691 (GRCm39) |
E1682G |
probably damaging |
Het |
| Myo9a |
T |
A |
9: 59,750,342 (GRCm39) |
|
probably benign |
Het |
| Nlrc4 |
T |
C |
17: 74,754,087 (GRCm39) |
N99D |
probably benign |
Het |
| P2rx3 |
A |
G |
2: 84,865,616 (GRCm39) |
Y10H |
probably damaging |
Het |
| Pcsk7 |
C |
A |
9: 45,838,958 (GRCm39) |
D623E |
probably benign |
Het |
| Plxna1 |
A |
G |
6: 89,297,980 (GRCm39) |
I1766T |
probably damaging |
Het |
| Ptk7 |
T |
C |
17: 46,885,353 (GRCm39) |
Y691C |
probably damaging |
Het |
| Rtraf-ps |
A |
C |
3: 88,484,230 (GRCm39) |
|
probably benign |
Het |
| Ryr1 |
T |
C |
7: 28,804,162 (GRCm39) |
|
probably benign |
Het |
| Scg3 |
T |
G |
9: 75,570,519 (GRCm39) |
K345T |
probably damaging |
Het |
| Serpina3b |
A |
T |
12: 104,099,200 (GRCm39) |
K238N |
probably benign |
Het |
| Slc38a9 |
T |
A |
13: 112,838,152 (GRCm39) |
S306T |
probably damaging |
Het |
| Txndc16 |
A |
G |
14: 45,382,547 (GRCm39) |
|
probably benign |
Het |
| Vmn1r238 |
T |
A |
18: 3,123,243 (GRCm39) |
Y57F |
probably benign |
Het |
| Vmn2r104 |
A |
T |
17: 20,258,501 (GRCm39) |
S548T |
probably damaging |
Het |
| Xrcc1 |
T |
A |
7: 24,247,309 (GRCm39) |
|
probably null |
Het |
|
| Other mutations in Rec8 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00233:Rec8
|
APN |
14 |
55,860,972 (GRCm39) |
nonsense |
probably null |
|
|
IGL02116:Rec8
|
APN |
14 |
55,862,336 (GRCm39) |
splice site |
probably null |
|
|
R1349:Rec8
|
UTSW |
14 |
55,856,431 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1372:Rec8
|
UTSW |
14 |
55,856,431 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1564:Rec8
|
UTSW |
14 |
55,859,732 (GRCm39) |
splice site |
probably null |
|
|
R1667:Rec8
|
UTSW |
14 |
55,856,253 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1970:Rec8
|
UTSW |
14 |
55,861,599 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3157:Rec8
|
UTSW |
14 |
55,862,763 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R3625:Rec8
|
UTSW |
14 |
55,859,954 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R3919:Rec8
|
UTSW |
14 |
55,858,716 (GRCm39) |
missense |
probably benign |
0.02 |
|
R4280:Rec8
|
UTSW |
14 |
55,856,091 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4282:Rec8
|
UTSW |
14 |
55,856,091 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4283:Rec8
|
UTSW |
14 |
55,856,091 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4622:Rec8
|
UTSW |
14 |
55,862,215 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4894:Rec8
|
UTSW |
14 |
55,862,787 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5488:Rec8
|
UTSW |
14 |
55,860,283 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5489:Rec8
|
UTSW |
14 |
55,860,283 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6113:Rec8
|
UTSW |
14 |
55,859,935 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6264:Rec8
|
UTSW |
14 |
55,856,636 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6439:Rec8
|
UTSW |
14 |
55,856,076 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R7952:Rec8
|
UTSW |
14 |
55,862,760 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
Z1088:Rec8
|
UTSW |
14 |
55,862,604 (GRCm39) |
missense |
probably damaging |
0.96 |
|
| Posted On |
2012-04-20 |
Incidental Mutation