Incidental Mutation 'IGL03115:Asah1'
| ID |
419382 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Asah1
|
| Ensembl Gene |
ENSMUSG00000031591 |
| Gene Name |
N-acylsphingosine amidohydrolase 1 |
| Synonyms |
2310081N20Rik, acid ceramidase |
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
IGL03115
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
8 |
| Chromosomal Location |
41793234-41827810 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 41813336 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Tryptophan to Arginine
at position 26
(W26R)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000034000
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000034000]
[ENSMUST00000110417]
[ENSMUST00000143057]
|
| AlphaFold |
Q9WV54 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000034000
AA Change: W26R
PolyPhen 2
Score 0.938 (Sensitivity: 0.80; Specificity: 0.94)
|
| SMART Domains |
Protein: ENSMUSP00000034000
Gene: ENSMUSG00000031591
AA Change: W26R
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
20 |
N/A |
INTRINSIC |
|
Pfam:NAAA-beta
|
44 |
138 |
4.2e-35 |
PFAM |
|
Pfam:CBAH
|
142 |
389 |
1e-58 |
PFAM |
|
| Predicted Effect |
unknown
Transcript: ENSMUST00000110417
AA Change: V27E
|
| SMART Domains |
Protein: ENSMUSP00000106047
Gene: ENSMUSG00000031591
AA Change: V27E
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:NAAA-beta
|
24 |
118 |
8.8e-39 |
PFAM |
|
Pfam:CBAH
|
122 |
216 |
7.9e-24 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000143057
|
| SMART Domains |
Protein: ENSMUSP00000117362
Gene: ENSMUSG00000031591
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
26 |
N/A |
INTRINSIC |
|
Pfam:NAAA-beta
|
68 |
120 |
6.4e-18 |
PFAM |
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: This gene encodes acid ceramidase, an enzyme that plays a central role in ceramide metabolism. The encoded protein undergoes proteolytic processing to generate a heterodimeric enzyme comprised of alpha and beta subunits that catalyzes the hydrolysis of sphingolipid ceramide into sphingosine and free fatty acid. The homozygous disruption of this gene leads to embryonic lethality in mice whereas the heterozygous animals exhibit a progressive lipid storage disease phenotype. [provided by RefSeq, Oct 2015]
PHENOTYPE: Nullizygous mutation of this gene causes embryonic lethality. Homozygotes for the P361R mutation die prematurely with growth defects, low acid ceramidase activity, high ceramide levels, histiocyte infiltrates into various organs, Farber bodies, short femur growth plates and altered ovary morphology. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 51 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adamdec1 |
T |
A |
14: 68,808,802 (GRCm39) |
H302L |
probably damaging |
Het |
| Adamts12 |
T |
A |
15: 11,263,422 (GRCm39) |
C595S |
probably damaging |
Het |
| Arid2 |
G |
A |
15: 96,268,154 (GRCm39) |
V756I |
probably damaging |
Het |
| Brinp1 |
C |
T |
4: 68,822,973 (GRCm39) |
|
probably null |
Het |
| Cers2 |
A |
G |
3: 95,228,663 (GRCm39) |
D162G |
probably damaging |
Het |
| Clasp1 |
G |
T |
1: 118,429,053 (GRCm39) |
E106* |
probably null |
Het |
| Col12a1 |
T |
C |
9: 79,588,719 (GRCm39) |
E1132G |
probably damaging |
Het |
| Dhdds |
G |
T |
4: 133,710,182 (GRCm39) |
H196N |
probably benign |
Het |
| Eps8 |
T |
C |
6: 137,504,379 (GRCm39) |
D118G |
probably damaging |
Het |
| Fmo9 |
A |
G |
1: 166,505,220 (GRCm39) |
S7P |
probably damaging |
Het |
| Gamt |
A |
G |
10: 80,094,272 (GRCm39) |
L197P |
probably damaging |
Het |
| Grb7 |
A |
G |
11: 98,341,945 (GRCm39) |
I82V |
probably damaging |
Het |
| Hectd2 |
T |
C |
19: 36,577,121 (GRCm39) |
|
probably null |
Het |
| Ilk |
T |
C |
7: 105,389,542 (GRCm39) |
V83A |
probably damaging |
Het |
| Kif21a |
T |
A |
15: 90,869,598 (GRCm39) |
I418F |
probably damaging |
Het |
| Kndc1 |
A |
G |
7: 139,501,425 (GRCm39) |
I905V |
probably benign |
Het |
| Lyl1 |
C |
T |
8: 85,429,300 (GRCm39) |
P3L |
possibly damaging |
Het |
| Morc3 |
T |
C |
16: 93,667,971 (GRCm39) |
I710T |
probably damaging |
Het |
| Nefm |
T |
C |
14: 68,357,728 (GRCm39) |
|
probably benign |
Het |
| Or10d5 |
T |
C |
9: 39,862,040 (GRCm39) |
E9G |
probably damaging |
Het |
| Or2f2 |
A |
G |
6: 42,767,599 (GRCm39) |
T209A |
probably benign |
Het |
| Or8g23 |
C |
A |
9: 38,971,259 (GRCm39) |
R234S |
probably damaging |
Het |
| Pard6g |
T |
G |
18: 80,123,068 (GRCm39) |
L34W |
probably damaging |
Het |
| Patj |
C |
T |
4: 98,332,040 (GRCm39) |
S562L |
probably damaging |
Het |
| Pcsk4 |
A |
G |
10: 80,164,883 (GRCm39) |
I61T |
probably damaging |
Het |
| Pcsk7 |
T |
A |
9: 45,825,670 (GRCm39) |
H300Q |
probably damaging |
Het |
| Pip5kl1 |
A |
G |
2: 32,470,033 (GRCm39) |
D288G |
probably damaging |
Het |
| Plxnb2 |
T |
A |
15: 89,046,641 (GRCm39) |
|
probably benign |
Het |
| Poldip2 |
T |
C |
11: 78,411,970 (GRCm39) |
|
probably benign |
Het |
| Ralgapa2 |
T |
C |
2: 146,266,734 (GRCm39) |
Y614C |
probably damaging |
Het |
| Rarres1 |
C |
A |
3: 67,403,145 (GRCm39) |
|
probably null |
Het |
| Samd3 |
C |
T |
10: 26,147,606 (GRCm39) |
T427M |
probably damaging |
Het |
| Skap1 |
A |
G |
11: 96,593,446 (GRCm39) |
I98V |
probably benign |
Het |
| Skint11 |
T |
C |
4: 114,101,820 (GRCm39) |
S87P |
probably damaging |
Het |
| Slc22a22 |
T |
G |
15: 57,126,670 (GRCm39) |
E133A |
probably damaging |
Het |
| Slc23a2 |
T |
C |
2: 131,933,185 (GRCm39) |
Y91C |
probably damaging |
Het |
| Slc6a20b |
T |
A |
9: 123,426,403 (GRCm39) |
E494V |
possibly damaging |
Het |
| Slco1a4 |
A |
T |
6: 141,765,329 (GRCm39) |
D304E |
probably benign |
Het |
| Slco1a4 |
A |
C |
6: 141,763,585 (GRCm39) |
M377R |
probably damaging |
Het |
| Srpk2 |
T |
C |
5: 23,729,616 (GRCm39) |
|
probably null |
Het |
| Supt3 |
T |
G |
17: 45,352,114 (GRCm39) |
C271W |
probably damaging |
Het |
| Taar7d |
C |
A |
10: 23,903,539 (GRCm39) |
F140L |
probably benign |
Het |
| Tmbim7 |
T |
C |
5: 3,729,158 (GRCm39) |
*225Q |
probably null |
Het |
| Tpst1 |
T |
C |
5: 130,130,752 (GRCm39) |
I74T |
probably damaging |
Het |
| Utp3 |
T |
C |
5: 88,703,179 (GRCm39) |
V236A |
possibly damaging |
Het |
| Vmn2r55 |
A |
T |
7: 12,404,558 (GRCm39) |
F282I |
probably damaging |
Het |
| Vwa5b1 |
A |
T |
4: 138,327,460 (GRCm39) |
I372N |
possibly damaging |
Het |
| Wtip |
C |
T |
7: 33,824,958 (GRCm39) |
A209T |
probably damaging |
Het |
| Zbbx |
T |
C |
3: 74,985,867 (GRCm39) |
D395G |
probably benign |
Het |
| Zfp273 |
A |
T |
13: 67,973,769 (GRCm39) |
H299L |
probably damaging |
Het |
| Zfp459 |
G |
A |
13: 67,556,796 (GRCm39) |
R96* |
probably null |
Het |
|
| Other mutations in Asah1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01824:Asah1
|
APN |
8 |
41,802,580 (GRCm39) |
unclassified |
probably benign |
|
|
IGL02512:Asah1
|
APN |
8 |
41,813,344 (GRCm39) |
intron |
probably benign |
|
|
IGL02523:Asah1
|
APN |
8 |
41,804,984 (GRCm39) |
missense |
probably benign |
|
|
IGL03357:Asah1
|
APN |
8 |
41,799,233 (GRCm39) |
splice site |
probably benign |
|
|
PIT4366001:Asah1
|
UTSW |
8 |
41,796,783 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R0593:Asah1
|
UTSW |
8 |
41,802,619 (GRCm39) |
missense |
probably benign |
0.02 |
|
R1451:Asah1
|
UTSW |
8 |
41,807,049 (GRCm39) |
critical splice donor site |
probably null |
|
|
R1977:Asah1
|
UTSW |
8 |
41,796,554 (GRCm39) |
critical splice donor site |
probably null |
|
|
R2200:Asah1
|
UTSW |
8 |
41,796,765 (GRCm39) |
critical splice donor site |
probably null |
|
|
R3429:Asah1
|
UTSW |
8 |
41,804,925 (GRCm39) |
unclassified |
probably benign |
|
|
R4002:Asah1
|
UTSW |
8 |
41,801,176 (GRCm39) |
splice site |
probably benign |
|
|
R4078:Asah1
|
UTSW |
8 |
41,807,119 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4470:Asah1
|
UTSW |
8 |
41,796,761 (GRCm39) |
splice site |
probably null |
|
|
R4471:Asah1
|
UTSW |
8 |
41,796,761 (GRCm39) |
splice site |
probably null |
|
|
R4968:Asah1
|
UTSW |
8 |
41,807,067 (GRCm39) |
missense |
|
|
|
R4970:Asah1
|
UTSW |
8 |
41,813,314 (GRCm39) |
nonsense |
probably null |
|
|
R5643:Asah1
|
UTSW |
8 |
41,813,332 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R5644:Asah1
|
UTSW |
8 |
41,813,332 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R6128:Asah1
|
UTSW |
8 |
41,807,092 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6419:Asah1
|
UTSW |
8 |
41,796,803 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7059:Asah1
|
UTSW |
8 |
41,800,106 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R7442:Asah1
|
UTSW |
8 |
41,796,602 (GRCm39) |
missense |
possibly damaging |
0.60 |
|
R7587:Asah1
|
UTSW |
8 |
41,827,578 (GRCm39) |
missense |
probably benign |
0.43 |
|
R7663:Asah1
|
UTSW |
8 |
41,794,664 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R7980:Asah1
|
UTSW |
8 |
41,807,067 (GRCm39) |
missense |
|
|
|
R8122:Asah1
|
UTSW |
8 |
41,796,767 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8275:Asah1
|
UTSW |
8 |
41,801,159 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8700:Asah1
|
UTSW |
8 |
41,813,312 (GRCm39) |
missense |
probably benign |
0.03 |
|
R8752:Asah1
|
UTSW |
8 |
41,813,314 (GRCm39) |
missense |
possibly damaging |
0.47 |
|
R8960:Asah1
|
UTSW |
8 |
41,800,061 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9131:Asah1
|
UTSW |
8 |
41,807,049 (GRCm39) |
critical splice donor site |
probably null |
|
|
R9539:Asah1
|
UTSW |
8 |
41,827,584 (GRCm39) |
missense |
probably benign |
0.00 |
|
| Posted On |
2016-08-02 |
Incidental Mutation