Incidental Mutation 'IGL02831:Acrbp'
| ID |
361453 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Acrbp
|
| Ensembl Gene |
ENSMUSG00000072770 |
| Gene Name |
proacrosin binding protein |
| Synonyms |
OY-TES-1, sp32 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.085)
|
| Stock # |
IGL02831
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
6 |
| Chromosomal Location |
125026890-125040228 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to A
at 125038212 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Threonine to Asparagine
at position 471
(T471N)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000085632
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000088294]
|
| AlphaFold |
Q3V140 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000088294
AA Change: T471N
PolyPhen 2
Score 0.891 (Sensitivity: 0.82; Specificity: 0.94)
|
| SMART Domains |
Protein: ENSMUSP00000085632
Gene: ENSMUSG00000072770
AA Change: T471N
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:PBP_sp32
|
1 |
239 |
1.6e-139 |
PFAM |
|
KAZAL
|
466 |
506 |
1.42e0 |
SMART |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000136100
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is similar to proacrosin binding protein sp32 precursor found in mouse, guinea pig, and pig. This protein is located in the sperm acrosome and is thought to function as a binding protein to proacrosin for packaging and condensation of the acrosin zymogen in the acrosomal matrix. This protein is a member of the cancer/testis family of antigens and it is found to be immunogenic. In normal tissues, this mRNA is expressed only in testis, whereas it is detected in a range of different tumor types such as bladder, breast, lung, liver, and colon. [provided by RefSeq, Jul 2008]
PHENOTYPE: Homozygous mutation of this gene results in delayed fertilization due to a delay in sperm penetration of the zona pellucida. Homozygous sperm also show reduced fertilization rates of oocytes with a thick or hardened zona pellucida. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 43 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abca8a |
C |
T |
11: 109,943,907 (GRCm39) |
V1121M |
probably damaging |
Het |
| Blnk |
C |
T |
19: 40,950,873 (GRCm39) |
D93N |
probably damaging |
Het |
| Casp7 |
A |
G |
19: 56,392,855 (GRCm39) |
D3G |
probably benign |
Het |
| Coro1c |
A |
T |
5: 113,982,469 (GRCm39) |
C456S |
probably benign |
Het |
| Dlec1 |
T |
G |
9: 118,972,983 (GRCm39) |
L1499R |
probably damaging |
Het |
| Dnah8 |
T |
C |
17: 30,931,250 (GRCm39) |
S1422P |
probably benign |
Het |
| Exd1 |
T |
C |
2: 119,359,235 (GRCm39) |
D216G |
probably damaging |
Het |
| Fhit |
T |
C |
14: 9,870,080 (GRCm38) |
T130A |
probably benign |
Het |
| Frem1 |
A |
T |
4: 82,874,395 (GRCm39) |
M1409K |
probably benign |
Het |
| Fut2 |
C |
T |
7: 45,300,193 (GRCm39) |
G193E |
possibly damaging |
Het |
| Glb1l2 |
A |
G |
9: 26,678,746 (GRCm39) |
V465A |
probably benign |
Het |
| Ints8 |
T |
C |
4: 11,245,896 (GRCm39) |
Q194R |
possibly damaging |
Het |
| Ip6k2 |
C |
T |
9: 108,681,733 (GRCm39) |
|
probably benign |
Het |
| Kctd2 |
T |
A |
11: 115,321,166 (GRCm39) |
*264K |
probably null |
Het |
| Krt34 |
C |
A |
11: 99,930,973 (GRCm39) |
|
probably benign |
Het |
| Lamc1 |
A |
G |
1: 153,122,801 (GRCm39) |
S760P |
probably benign |
Het |
| Lrp1b |
T |
C |
2: 41,083,603 (GRCm39) |
N1702S |
probably damaging |
Het |
| Lrrc8e |
T |
A |
8: 4,285,429 (GRCm39) |
S551R |
probably damaging |
Het |
| Map3k20 |
T |
C |
2: 72,202,071 (GRCm39) |
V139A |
probably damaging |
Het |
| Mrtfa |
A |
G |
15: 80,988,994 (GRCm39) |
L9P |
probably benign |
Het |
| Napsa |
A |
G |
7: 44,236,184 (GRCm39) |
T408A |
probably benign |
Het |
| Or2h15 |
T |
C |
17: 38,441,403 (GRCm39) |
K227E |
probably benign |
Het |
| Or2w6 |
T |
C |
13: 21,843,074 (GRCm39) |
I140V |
probably benign |
Het |
| Or5l13 |
T |
C |
2: 87,780,020 (GRCm39) |
|
probably null |
Het |
| Panx1 |
A |
G |
9: 14,918,944 (GRCm39) |
L305P |
probably damaging |
Het |
| Pkhd1l1 |
A |
G |
15: 44,364,889 (GRCm39) |
H676R |
probably benign |
Het |
| Pld1 |
T |
A |
3: 28,130,574 (GRCm39) |
V458E |
probably damaging |
Het |
| Ppp5c |
A |
G |
7: 16,742,570 (GRCm39) |
L256P |
probably damaging |
Het |
| Pyroxd2 |
G |
T |
19: 42,724,342 (GRCm39) |
T307K |
probably damaging |
Het |
| Scart1 |
G |
T |
7: 139,808,434 (GRCm39) |
V782L |
probably benign |
Het |
| Sin3b |
A |
G |
8: 73,471,190 (GRCm39) |
E379G |
probably damaging |
Het |
| Slc22a23 |
T |
C |
13: 34,483,052 (GRCm39) |
T276A |
possibly damaging |
Het |
| Slc26a3 |
T |
C |
12: 31,502,628 (GRCm39) |
I283T |
probably damaging |
Het |
| Sltm |
A |
G |
9: 70,492,147 (GRCm39) |
D712G |
probably damaging |
Het |
| Slu7 |
C |
T |
11: 43,333,480 (GRCm39) |
Q367* |
probably null |
Het |
| Srbd1 |
T |
C |
17: 86,311,299 (GRCm39) |
N706S |
probably damaging |
Het |
| Supt16 |
A |
T |
14: 52,408,335 (GRCm39) |
M870K |
possibly damaging |
Het |
| Tnxb |
T |
C |
17: 34,922,545 (GRCm39) |
Y2453H |
possibly damaging |
Het |
| Tomm40 |
A |
G |
7: 19,437,014 (GRCm39) |
Y274H |
probably damaging |
Het |
| Utp20 |
A |
T |
10: 88,651,770 (GRCm39) |
D404E |
probably benign |
Het |
| Vmn2r23 |
T |
A |
6: 123,681,344 (GRCm39) |
M84K |
probably benign |
Het |
| Wdr70 |
A |
G |
15: 7,913,787 (GRCm39) |
Y621H |
possibly damaging |
Het |
| Wfdc8 |
C |
T |
2: 164,447,685 (GRCm39) |
|
probably null |
Het |
|
| Other mutations in Acrbp |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00096:Acrbp
|
APN |
6 |
125,027,477 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01656:Acrbp
|
APN |
6 |
125,030,675 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
IGL02095:Acrbp
|
APN |
6 |
125,030,919 (GRCm39) |
nonsense |
probably null |
|
|
IGL02186:Acrbp
|
APN |
6 |
125,031,773 (GRCm39) |
splice site |
probably null |
|
|
IGL02473:Acrbp
|
APN |
6 |
125,031,661 (GRCm39) |
missense |
probably benign |
|
|
IGL03110:Acrbp
|
APN |
6 |
125,039,436 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0071:Acrbp
|
UTSW |
6 |
125,027,915 (GRCm39) |
unclassified |
probably benign |
|
|
R0071:Acrbp
|
UTSW |
6 |
125,027,915 (GRCm39) |
unclassified |
probably benign |
|
|
R0279:Acrbp
|
UTSW |
6 |
125,030,917 (GRCm39) |
critical splice donor site |
probably null |
|
|
R0483:Acrbp
|
UTSW |
6 |
125,031,759 (GRCm39) |
missense |
possibly damaging |
0.61 |
|
R1017:Acrbp
|
UTSW |
6 |
125,038,223 (GRCm39) |
splice site |
probably benign |
|
|
R1486:Acrbp
|
UTSW |
6 |
125,027,585 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4679:Acrbp
|
UTSW |
6 |
125,037,881 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R4898:Acrbp
|
UTSW |
6 |
125,027,501 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R4987:Acrbp
|
UTSW |
6 |
125,030,725 (GRCm39) |
missense |
probably benign |
0.23 |
|
R5249:Acrbp
|
UTSW |
6 |
125,037,885 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5458:Acrbp
|
UTSW |
6 |
125,027,013 (GRCm39) |
unclassified |
probably benign |
|
|
R5579:Acrbp
|
UTSW |
6 |
125,038,062 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6491:Acrbp
|
UTSW |
6 |
125,028,442 (GRCm39) |
unclassified |
probably benign |
|
|
R7643:Acrbp
|
UTSW |
6 |
125,030,795 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R8217:Acrbp
|
UTSW |
6 |
125,037,921 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9167:Acrbp
|
UTSW |
6 |
125,039,942 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9280:Acrbp
|
UTSW |
6 |
125,039,938 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R9492:Acrbp
|
UTSW |
6 |
125,038,062 (GRCm39) |
missense |
probably benign |
0.00 |
|
| Posted On |
2015-12-18 |
Incidental Mutation