Incidental Mutation 'R8074:Idua'
| ID |
620405 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Idua
|
| Ensembl Gene |
ENSMUSG00000033540 |
| Gene Name |
iduronidase, alpha-L |
| Synonyms |
|
| MMRRC Submission |
067508-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.147)
|
| Stock # |
R8074 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
5 |
| Chromosomal Location |
108808197-108832423 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to A
at 108828441 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Alanine to Glutamic Acid
at position 265
(A265E)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000071577
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000071650]
[ENSMUST00000112563]
[ENSMUST00000119212]
[ENSMUST00000139734]
[ENSMUST00000140620]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000071650
AA Change: A265E
PolyPhen 2
Score 0.650 (Sensitivity: 0.87; Specificity: 0.91)
|
| SMART Domains |
Protein: ENSMUSP00000071577
Gene: ENSMUSG00000033540
AA Change: A265E
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Glyco_hydro_39
|
22 |
542 |
1.4e-223 |
PFAM |
|
SCOP:d1bpv__
|
546 |
643 |
3e-8 |
SMART |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000112563
AA Change: A265E
PolyPhen 2
Score 0.650 (Sensitivity: 0.87; Specificity: 0.91)
|
| SMART Domains |
Protein: ENSMUSP00000108182
Gene: ENSMUSG00000033540
AA Change: A265E
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Glyco_hydro_39
|
22 |
542 |
2.1e-224 |
PFAM |
|
SCOP:d1bpv__
|
546 |
643 |
3e-8 |
SMART |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000119212
AA Change: A218E
PolyPhen 2
Score 0.807 (Sensitivity: 0.84; Specificity: 0.93)
|
| SMART Domains |
Protein: ENSMUSP00000113190
Gene: ENSMUSG00000033540
AA Change: A218E
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
25 |
N/A |
INTRINSIC |
|
Pfam:Glyco_hydro_39
|
48 |
495 |
2.4e-193 |
PFAM |
|
SCOP:d1bpv__
|
499 |
596 |
3e-8 |
SMART |
|
| Predicted Effect |
unknown
Transcript: ENSMUST00000139734
AA Change: Q232K
|
| SMART Domains |
Protein: ENSMUSP00000117694
Gene: ENSMUSG00000033540
AA Change: Q232K
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Glyco_hydro_39
|
22 |
199 |
6.8e-80 |
PFAM |
|
low complexity region
|
235 |
260 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000140620
|
| SMART Domains |
Protein: ENSMUSP00000119624
Gene: ENSMUSG00000033540
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Glyco_hydro_39
|
22 |
150 |
3.4e-52 |
PFAM |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 99.2%
|
| Validation Efficiency |
98% (62/63) |
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes an enzyme that hydrolyzes the terminal alpha-L-iduronic acid residues of two glycosaminoglycans, dermatan sulfate and heparan sulfate. This hydrolysis is required for the lysosomal degradation of these glycosaminoglycans. Mutations in this gene that result in enzymatic deficiency lead to the autosomal recessive disease mucopolysaccharidosis type I (MPS I). [provided by RefSeq, Jul 2008]
PHENOTYPE: Targeted mutants show lysosomal storage in multiple tissues, increased urinary GAG, craniofacial and skeletal defects, increased body weight, impaired habituation and long-term memory for aversive training, reduced ventricular function with valve insufficiency, and progressive hearing loss. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 62 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abca8b |
T |
A |
11: 109,829,320 (GRCm39) |
I1380L |
probably benign |
Het |
| Adcy3 |
T |
C |
12: 4,184,420 (GRCm39) |
V32A |
probably benign |
Het |
| Ano3 |
T |
A |
2: 110,780,577 (GRCm39) |
|
probably benign |
Het |
| Arhgef12 |
G |
A |
9: 42,882,399 (GRCm39) |
R1482* |
probably null |
Het |
| Cd300lg |
T |
G |
11: 101,932,427 (GRCm39) |
L4R |
probably damaging |
Het |
| Cfap57 |
T |
A |
4: 118,426,822 (GRCm39) |
K1072M |
possibly damaging |
Het |
| Clasp1 |
G |
T |
1: 118,390,213 (GRCm39) |
M132I |
probably benign |
Het |
| Clec18a |
T |
G |
8: 111,798,230 (GRCm39) |
D489A |
probably damaging |
Het |
| Cngb1 |
A |
G |
8: 95,978,801 (GRCm39) |
S551P |
|
Het |
| Efna4 |
G |
A |
3: 89,242,633 (GRCm39) |
T87M |
probably benign |
Het |
| Fam229b |
T |
C |
10: 38,996,255 (GRCm39) |
R42G |
probably null |
Het |
| Gm17175 |
C |
T |
14: 51,809,080 (GRCm39) |
M95I |
probably damaging |
Het |
| Grk4 |
A |
G |
5: 34,833,482 (GRCm39) |
E96G |
probably benign |
Het |
| Helb |
A |
C |
10: 119,925,321 (GRCm39) |
F1019V |
probably benign |
Het |
| Hsd17b2 |
T |
C |
8: 118,485,440 (GRCm39) |
V301A |
possibly damaging |
Het |
| Htr1b |
A |
G |
9: 81,513,582 (GRCm39) |
F342L |
probably benign |
Het |
| Jup |
T |
G |
11: 100,277,113 (GRCm39) |
T32P |
probably damaging |
Het |
| Kidins220 |
A |
G |
12: 25,107,715 (GRCm39) |
K1632E |
probably benign |
Het |
| Lef1 |
G |
A |
3: 130,997,954 (GRCm39) |
|
probably null |
Het |
| Lypla2 |
A |
G |
4: 135,697,112 (GRCm39) |
|
probably null |
Het |
| Mall |
A |
G |
2: 127,571,785 (GRCm39) |
M1T |
probably null |
Het |
| Mettl25 |
G |
T |
10: 105,661,941 (GRCm39) |
A343E |
probably benign |
Het |
| Mpdz |
T |
C |
4: 81,267,324 (GRCm39) |
N940S |
probably benign |
Het |
| Nsun4 |
A |
T |
4: 115,908,631 (GRCm39) |
V643D |
possibly damaging |
Het |
| Nupr1 |
A |
T |
7: 126,224,109 (GRCm39) |
F70Y |
possibly damaging |
Het |
| Or1e17 |
T |
A |
11: 73,831,213 (GRCm39) |
V47D |
possibly damaging |
Het |
| Or52b4i |
A |
G |
7: 102,191,830 (GRCm39) |
H229R |
probably benign |
Het |
| Or52e8 |
A |
T |
7: 104,624,934 (GRCm39) |
I90N |
probably damaging |
Het |
| Or5ac20 |
A |
G |
16: 59,104,549 (GRCm39) |
F104L |
probably benign |
Het |
| Or8g32 |
A |
T |
9: 39,305,242 (GRCm39) |
I49F |
probably damaging |
Het |
| Or8k3 |
C |
G |
2: 86,058,473 (GRCm39) |
V281L |
possibly damaging |
Het |
| Pabpc4 |
A |
T |
4: 123,180,508 (GRCm39) |
M77L |
probably benign |
Het |
| Phactr3 |
A |
G |
2: 177,944,589 (GRCm39) |
E429G |
probably damaging |
Het |
| Polr3b |
A |
G |
10: 84,549,523 (GRCm39) |
D915G |
probably damaging |
Het |
| Pramel14 |
A |
T |
4: 143,718,424 (GRCm39) |
F340I |
probably benign |
Het |
| Prkcg |
T |
A |
7: 3,372,037 (GRCm39) |
M501K |
probably damaging |
Het |
| Prkch |
G |
A |
12: 73,747,041 (GRCm39) |
A307T |
possibly damaging |
Het |
| Ptprt |
A |
G |
2: 161,769,581 (GRCm39) |
V428A |
possibly damaging |
Het |
| Rnf145 |
C |
A |
11: 44,448,263 (GRCm39) |
D373E |
probably damaging |
Het |
| Scfd2 |
G |
T |
5: 74,680,257 (GRCm39) |
Q299K |
probably benign |
Het |
| Septin2 |
A |
G |
1: 93,433,283 (GRCm39) |
D315G |
probably benign |
Het |
| Sf3a1 |
T |
A |
11: 4,125,435 (GRCm39) |
Y408* |
probably null |
Het |
| Siglecf |
A |
T |
7: 43,001,214 (GRCm39) |
N61Y |
possibly damaging |
Het |
| Sis |
A |
T |
3: 72,824,531 (GRCm39) |
I1334K |
probably damaging |
Het |
| Slc38a6 |
A |
T |
12: 73,391,658 (GRCm39) |
T307S |
possibly damaging |
Het |
| Spag9 |
T |
A |
11: 94,002,877 (GRCm39) |
F1129Y |
probably damaging |
Het |
| Sra1 |
G |
A |
18: 36,808,064 (GRCm39) |
A388V |
possibly damaging |
Het |
| Srpk1 |
T |
G |
17: 28,840,990 (GRCm39) |
K12T |
probably damaging |
Het |
| Stam2 |
A |
T |
2: 52,596,438 (GRCm39) |
I333K |
probably damaging |
Het |
| Tle1 |
GAA |
GA |
4: 72,057,216 (GRCm39) |
|
probably null |
Het |
| Tmem121b |
T |
C |
6: 120,469,869 (GRCm39) |
K283E |
possibly damaging |
Het |
| Tmem200a |
T |
C |
10: 25,868,850 (GRCm39) |
E473G |
probably damaging |
Het |
| Tnxb |
T |
A |
17: 34,922,955 (GRCm39) |
S2513T |
probably benign |
Het |
| Ttc16 |
A |
T |
2: 32,664,135 (GRCm39) |
|
probably benign |
Het |
| Ttll8 |
C |
T |
15: 88,799,578 (GRCm39) |
C621Y |
probably damaging |
Het |
| Ubn2 |
T |
A |
6: 38,417,475 (GRCm39) |
M171K |
probably benign |
Het |
| Vmn2r19 |
T |
A |
6: 123,312,904 (GRCm39) |
V658D |
probably damaging |
Het |
| Vmn2r6 |
A |
T |
3: 64,455,064 (GRCm39) |
|
probably benign |
Het |
| Vwa3a |
A |
T |
7: 120,398,321 (GRCm39) |
I941L |
probably benign |
Het |
| Zbtb24 |
A |
G |
10: 41,327,228 (GRCm39) |
D38G |
probably damaging |
Het |
| Zfp628 |
T |
C |
7: 4,923,205 (GRCm39) |
C476R |
probably damaging |
Het |
| Zfp831 |
A |
C |
2: 174,486,528 (GRCm39) |
N401T |
possibly damaging |
Het |
|
| Other mutations in Idua |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01335:Idua
|
APN |
5 |
108,828,737 (GRCm39) |
missense |
probably benign |
0.34 |
|
IGL01575:Idua
|
APN |
5 |
108,829,973 (GRCm39) |
missense |
possibly damaging |
0.71 |
|
IGL02402:Idua
|
APN |
5 |
108,827,657 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03145:Idua
|
APN |
5 |
108,829,362 (GRCm39) |
missense |
probably benign |
|
|
Cooper
|
UTSW |
5 |
108,828,180 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0208:Idua
|
UTSW |
5 |
108,829,618 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1572:Idua
|
UTSW |
5 |
108,828,455 (GRCm39) |
missense |
probably benign |
|
|
R1731:Idua
|
UTSW |
5 |
108,829,538 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2024:Idua
|
UTSW |
5 |
108,828,600 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2126:Idua
|
UTSW |
5 |
108,829,304 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R3760:Idua
|
UTSW |
5 |
108,817,978 (GRCm39) |
unclassified |
probably benign |
|
|
R4747:Idua
|
UTSW |
5 |
108,828,902 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R4832:Idua
|
UTSW |
5 |
108,817,247 (GRCm39) |
missense |
probably benign |
|
|
R5140:Idua
|
UTSW |
5 |
108,828,180 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5543:Idua
|
UTSW |
5 |
108,818,095 (GRCm39) |
missense |
probably benign |
0.22 |
|
R5643:Idua
|
UTSW |
5 |
108,828,090 (GRCm39) |
utr 3 prime |
probably benign |
|
|
R5821:Idua
|
UTSW |
5 |
108,827,600 (GRCm39) |
missense |
probably benign |
0.29 |
|
R6004:Idua
|
UTSW |
5 |
108,828,510 (GRCm39) |
missense |
probably benign |
|
|
R6330:Idua
|
UTSW |
5 |
108,829,574 (GRCm39) |
missense |
probably benign |
0.21 |
|
R6963:Idua
|
UTSW |
5 |
108,827,641 (GRCm39) |
missense |
possibly damaging |
0.84 |
|
R7180:Idua
|
UTSW |
5 |
108,828,761 (GRCm39) |
missense |
probably benign |
0.43 |
|
R7453:Idua
|
UTSW |
5 |
108,829,362 (GRCm39) |
missense |
probably benign |
|
|
R7575:Idua
|
UTSW |
5 |
108,829,565 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7712:Idua
|
UTSW |
5 |
108,829,388 (GRCm39) |
missense |
probably benign |
0.10 |
|
R7923:Idua
|
UTSW |
5 |
108,828,449 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7980:Idua
|
UTSW |
5 |
108,828,486 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8026:Idua
|
UTSW |
5 |
108,818,115 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8029:Idua
|
UTSW |
5 |
108,817,278 (GRCm39) |
missense |
probably benign |
0.23 |
|
R8089:Idua
|
UTSW |
5 |
108,829,646 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8384:Idua
|
UTSW |
5 |
108,829,305 (GRCm39) |
missense |
possibly damaging |
0.70 |
|
R9040:Idua
|
UTSW |
5 |
108,828,929 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9717:Idua
|
UTSW |
5 |
108,818,037 (GRCm39) |
nonsense |
probably null |
|
|
Z1177:Idua
|
UTSW |
5 |
108,828,489 (GRCm39) |
frame shift |
probably null |
|
|
Z1177:Idua
|
UTSW |
5 |
108,827,450 (GRCm39) |
missense |
probably null |
0.80 |
|
| Predicted Primers |
PCR Primer
(F):5'- AGGTCACCAATGTGCTGGAG -3'
(R):5'- TATCACTGGCCACTGGTACTG -3'
Sequencing Primer
(F):5'- AATGTGCTGGAGCCTCCTG -3'
(R):5'- GCATGATGGCAAGGACCCAC -3'
|
| Posted On |
2020-01-23 |
Incidental Mutation