Incidental Mutation 'IGL02066:Gba2'
| ID |
185666 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Gba2
|
| Ensembl Gene |
ENSMUSG00000028467 |
| Gene Name |
glucosidase beta 2 |
| Synonyms |
bile acid |
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
IGL02066
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
4 |
| Chromosomal Location |
43566928-43578873 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to A
at 43570175 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Threonine to Isoleucine
at position 373
(T373I)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000030189
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000030189]
[ENSMUST00000102944]
[ENSMUST00000130443]
[ENSMUST00000132631]
[ENSMUST00000167751]
|
| AlphaFold |
Q69ZF3 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000030189
AA Change: T373I
PolyPhen 2
Score 0.184 (Sensitivity: 0.92; Specificity: 0.87)
|
| SMART Domains |
Protein: ENSMUSP00000030189
Gene: ENSMUSG00000028467
AA Change: T373I
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:GBA2_N
|
142 |
446 |
9.4e-106 |
PFAM |
|
Pfam:DUF608
|
512 |
879 |
1.3e-153 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000102944
|
| SMART Domains |
Protein: ENSMUSP00000100008
Gene: ENSMUSG00000028466
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
54 |
83 |
N/A |
INTRINSIC |
|
low complexity region
|
132 |
147 |
N/A |
INTRINSIC |
|
BRLZ
|
158 |
222 |
2.03e-15 |
SMART |
|
low complexity region
|
240 |
253 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000126277
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000128403
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000130443
|
| SMART Domains |
Protein: ENSMUSP00000119589
Gene: ENSMUSG00000028467
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:GBA2_N
|
142 |
180 |
5.6e-13 |
PFAM |
|
Pfam:GBA2_N
|
178 |
227 |
1.5e-13 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000132631
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000138623
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000152251
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000139606
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000144968
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000159923
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000148426
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000167751
|
| SMART Domains |
Protein: ENSMUSP00000129401
Gene: ENSMUSG00000028466
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
54 |
83 |
N/A |
INTRINSIC |
|
low complexity region
|
156 |
171 |
N/A |
INTRINSIC |
|
BRLZ
|
182 |
246 |
2.03e-15 |
SMART |
|
low complexity region
|
264 |
277 |
N/A |
INTRINSIC |
|
| 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 microsomal beta-glucosidase that catalyzes the hydrolysis of bile acid 3-O-glucosides as endogenous compounds. Studies to determine subcellular localization of this protein in the liver indicated that the enzyme was mainly enriched in the microsomal fraction where it appeared to be confined to the endoplasmic reticulum. This putative transmembrane protein is thought to play a role in carbohydrate transport and metabolism. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit accumulation of glucosylceramides in multiple tissues, and show impaired male fertility associated with globozoospermia, oligozoospermia, reduced sperm motility, and male germ cell apoptosis. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 59 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| A2m |
T |
A |
6: 121,626,854 (GRCm39) |
C569S |
probably damaging |
Het |
| Adck5 |
T |
C |
15: 76,479,406 (GRCm39) |
V487A |
probably damaging |
Het |
| Agfg1 |
A |
G |
1: 82,871,279 (GRCm39) |
T483A |
probably damaging |
Het |
| Akr1c12 |
T |
C |
13: 4,326,236 (GRCm39) |
T82A |
probably damaging |
Het |
| Ano2 |
T |
A |
6: 125,667,702 (GRCm39) |
L6Q |
probably benign |
Het |
| Anp32a |
G |
A |
9: 62,284,615 (GRCm39) |
|
probably benign |
Het |
| Bltp2 |
G |
A |
11: 78,164,058 (GRCm39) |
R1133H |
probably damaging |
Het |
| Cep250 |
C |
A |
2: 155,818,441 (GRCm39) |
A871D |
probably damaging |
Het |
| Chl1 |
T |
C |
6: 103,675,185 (GRCm39) |
V624A |
probably benign |
Het |
| Clasp1 |
G |
A |
1: 118,492,990 (GRCm39) |
|
probably null |
Het |
| Clca3a2 |
T |
G |
3: 144,519,216 (GRCm39) |
D320A |
probably benign |
Het |
| Cnot9 |
A |
G |
1: 74,566,212 (GRCm39) |
Q201R |
possibly damaging |
Het |
| Cox4i2 |
C |
T |
2: 152,602,602 (GRCm39) |
R99C |
probably damaging |
Het |
| Csmd1 |
A |
T |
8: 15,976,594 (GRCm39) |
F2875I |
probably damaging |
Het |
| Dpagt1 |
A |
G |
9: 44,243,203 (GRCm39) |
Y246C |
probably damaging |
Het |
| Dsc1 |
A |
G |
18: 20,241,860 (GRCm39) |
|
probably benign |
Het |
| Eef1d |
G |
A |
15: 75,768,704 (GRCm39) |
T464I |
probably benign |
Het |
| Efna2 |
C |
T |
10: 80,024,500 (GRCm39) |
|
probably benign |
Het |
| Entrep3 |
C |
T |
3: 89,095,903 (GRCm39) |
R545* |
probably null |
Het |
| Etaa1 |
C |
A |
11: 17,896,687 (GRCm39) |
V477L |
probably benign |
Het |
| Fam83d |
C |
T |
2: 158,627,793 (GRCm39) |
T494M |
probably benign |
Het |
| Fbxo24 |
C |
T |
5: 137,611,132 (GRCm39) |
V553M |
probably damaging |
Het |
| Gal3st2 |
A |
G |
1: 93,801,379 (GRCm39) |
T12A |
probably damaging |
Het |
| Kitl |
T |
A |
10: 99,912,744 (GRCm39) |
C154S |
probably damaging |
Het |
| Lrp1b |
A |
T |
2: 41,001,091 (GRCm39) |
C2044* |
probably null |
Het |
| Lrp6 |
G |
T |
6: 134,427,900 (GRCm39) |
S1564* |
probably null |
Het |
| Manea |
A |
T |
4: 26,340,965 (GRCm39) |
|
probably benign |
Het |
| Myt1 |
T |
C |
2: 181,438,982 (GRCm39) |
L168P |
probably damaging |
Het |
| Notch1 |
T |
C |
2: 26,350,408 (GRCm39) |
E2244G |
possibly damaging |
Het |
| Nsd3 |
T |
G |
8: 26,203,515 (GRCm39) |
V1343G |
probably damaging |
Het |
| Nup155 |
T |
C |
15: 8,187,250 (GRCm39) |
|
probably benign |
Het |
| Obox6 |
T |
C |
7: 15,568,628 (GRCm39) |
I83V |
probably benign |
Het |
| Or12k5 |
A |
T |
2: 36,895,321 (GRCm39) |
F102I |
probably damaging |
Het |
| Or13a24 |
A |
T |
7: 140,154,413 (GRCm39) |
T116S |
possibly damaging |
Het |
| Pdgfra |
T |
C |
5: 75,331,241 (GRCm39) |
V282A |
possibly damaging |
Het |
| Pkd1l2 |
A |
G |
8: 117,736,303 (GRCm39) |
|
probably benign |
Het |
| Pmfbp1 |
A |
T |
8: 110,268,365 (GRCm39) |
I971F |
possibly damaging |
Het |
| Ppp6c |
T |
C |
2: 39,089,683 (GRCm39) |
T199A |
probably benign |
Het |
| Ptpra |
A |
G |
2: 30,333,308 (GRCm39) |
T3A |
possibly damaging |
Het |
| Rb1 |
A |
T |
14: 73,435,974 (GRCm39) |
M897K |
probably benign |
Het |
| Rptn |
A |
C |
3: 93,304,436 (GRCm39) |
S590R |
probably benign |
Het |
| Rreb1 |
A |
G |
13: 38,115,482 (GRCm39) |
D947G |
probably benign |
Het |
| Samd9l |
T |
C |
6: 3,376,575 (GRCm39) |
T229A |
probably damaging |
Het |
| Slc5a9 |
A |
T |
4: 111,744,719 (GRCm39) |
M423K |
probably damaging |
Het |
| Slc6a12 |
T |
A |
6: 121,329,015 (GRCm39) |
I111N |
probably damaging |
Het |
| Slc6a15 |
T |
A |
10: 103,252,519 (GRCm39) |
L561I |
probably damaging |
Het |
| Spag5 |
A |
G |
11: 78,195,358 (GRCm39) |
N222D |
probably benign |
Het |
| Spp2 |
G |
A |
1: 88,344,965 (GRCm39) |
M54I |
probably benign |
Het |
| Sptbn4 |
T |
C |
7: 27,063,940 (GRCm39) |
E847G |
possibly damaging |
Het |
| Timd2 |
T |
A |
11: 46,569,050 (GRCm39) |
N203Y |
probably damaging |
Het |
| Togaram1 |
G |
T |
12: 65,030,195 (GRCm39) |
D1000Y |
probably damaging |
Het |
| Usp47 |
C |
T |
7: 111,663,604 (GRCm39) |
R258C |
probably damaging |
Het |
| Uts2r |
A |
C |
11: 121,051,523 (GRCm39) |
D129A |
probably damaging |
Het |
| Vmn2r102 |
G |
A |
17: 19,914,191 (GRCm39) |
M585I |
probably benign |
Het |
| Vmn2r77 |
A |
T |
7: 86,452,836 (GRCm39) |
R518* |
probably null |
Het |
| Wdfy4 |
C |
T |
14: 32,871,523 (GRCm39) |
R296K |
probably benign |
Het |
| Xirp2 |
A |
T |
2: 67,356,415 (GRCm39) |
K3725N |
probably benign |
Het |
| Xntrpc |
T |
C |
7: 101,727,036 (GRCm39) |
S142P |
probably benign |
Het |
| Zfat |
T |
C |
15: 68,052,678 (GRCm39) |
H372R |
probably damaging |
Het |
|
| Other mutations in Gba2 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00501:Gba2
|
APN |
4 |
43,568,477 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01577:Gba2
|
APN |
4 |
43,573,753 (GRCm39) |
nonsense |
probably null |
|
|
IGL02126:Gba2
|
APN |
4 |
43,567,918 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
IGL02243:Gba2
|
APN |
4 |
43,568,719 (GRCm39) |
missense |
probably benign |
0.13 |
|
IGL02474:Gba2
|
APN |
4 |
43,568,538 (GRCm39) |
missense |
possibly damaging |
0.69 |
|
IGL02567:Gba2
|
APN |
4 |
43,567,281 (GRCm39) |
missense |
probably benign |
|
|
IGL02628:Gba2
|
APN |
4 |
43,568,919 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL02706:Gba2
|
APN |
4 |
43,567,257 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL02795:Gba2
|
APN |
4 |
43,578,331 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0389:Gba2
|
UTSW |
4 |
43,570,832 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0555:Gba2
|
UTSW |
4 |
43,569,927 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0650:Gba2
|
UTSW |
4 |
43,570,424 (GRCm39) |
splice site |
probably null |
|
|
R1603:Gba2
|
UTSW |
4 |
43,567,823 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1628:Gba2
|
UTSW |
4 |
43,570,118 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1664:Gba2
|
UTSW |
4 |
43,578,080 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1686:Gba2
|
UTSW |
4 |
43,573,869 (GRCm39) |
splice site |
probably benign |
|
|
R1730:Gba2
|
UTSW |
4 |
43,578,242 (GRCm39) |
missense |
probably benign |
0.01 |
|
R2036:Gba2
|
UTSW |
4 |
43,568,118 (GRCm39) |
unclassified |
probably benign |
|
|
R2061:Gba2
|
UTSW |
4 |
43,574,029 (GRCm39) |
nonsense |
probably null |
|
|
R2259:Gba2
|
UTSW |
4 |
43,570,107 (GRCm39) |
missense |
probably benign |
|
|
R2847:Gba2
|
UTSW |
4 |
43,568,000 (GRCm39) |
splice site |
probably null |
|
|
R3026:Gba2
|
UTSW |
4 |
43,578,308 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R3617:Gba2
|
UTSW |
4 |
43,573,803 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4225:Gba2
|
UTSW |
4 |
43,569,464 (GRCm39) |
unclassified |
probably benign |
|
|
R4346:Gba2
|
UTSW |
4 |
43,571,337 (GRCm39) |
missense |
probably benign |
0.04 |
|
R4601:Gba2
|
UTSW |
4 |
43,573,810 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4611:Gba2
|
UTSW |
4 |
43,568,092 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4664:Gba2
|
UTSW |
4 |
43,568,619 (GRCm39) |
unclassified |
probably benign |
|
|
R4784:Gba2
|
UTSW |
4 |
43,568,315 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4785:Gba2
|
UTSW |
4 |
43,568,315 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5079:Gba2
|
UTSW |
4 |
43,568,640 (GRCm39) |
unclassified |
probably benign |
|
|
R5327:Gba2
|
UTSW |
4 |
43,574,063 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5746:Gba2
|
UTSW |
4 |
43,568,465 (GRCm39) |
splice site |
probably null |
|
|
R6052:Gba2
|
UTSW |
4 |
43,568,330 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6485:Gba2
|
UTSW |
4 |
43,574,118 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7073:Gba2
|
UTSW |
4 |
43,573,753 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7112:Gba2
|
UTSW |
4 |
43,568,453 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7472:Gba2
|
UTSW |
4 |
43,568,967 (GRCm39) |
missense |
probably benign |
0.44 |
|
R8220:Gba2
|
UTSW |
4 |
43,568,510 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8315:Gba2
|
UTSW |
4 |
43,569,937 (GRCm39) |
frame shift |
probably null |
|
|
R8476:Gba2
|
UTSW |
4 |
43,569,944 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8477:Gba2
|
UTSW |
4 |
43,569,944 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8794:Gba2
|
UTSW |
4 |
43,568,077 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R9087:Gba2
|
UTSW |
4 |
43,568,304 (GRCm39) |
missense |
probably benign |
0.09 |
|
R9193:Gba2
|
UTSW |
4 |
43,578,112 (GRCm39) |
missense |
probably benign |
0.26 |
|
R9753:Gba2
|
UTSW |
4 |
43,568,716 (GRCm39) |
missense |
probably damaging |
1.00 |
|
RF007:Gba2
|
UTSW |
4 |
43,569,894 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Posted On |
2014-05-07 |
Incidental Mutation