Incidental Mutation 'IGL00815:Adal'
ID |
8565 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Adal
|
Ensembl Gene |
ENSMUSG00000027259 |
Gene Name |
adenosine deaminase-like |
Synonyms |
4930578F03Rik |
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
IGL00815
|
Quality Score |
|
Status
|
|
Chromosome |
2 |
Chromosomal Location |
120970909-120987161 bp(+) (GRCm39) |
Type of Mutation |
splice site |
DNA Base Change (assembly) |
A to G
at 120981699 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000113052
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000028702]
[ENSMUST00000066155]
[ENSMUST00000110662]
[ENSMUST00000110665]
[ENSMUST00000119031]
|
AlphaFold |
Q80SY6 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000028702
|
SMART Domains |
Protein: ENSMUSP00000028702 Gene: ENSMUSG00000027259
Domain | Start | End | E-Value | Type |
Pfam:A_deaminase
|
1 |
276 |
1.8e-37 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000066155
|
SMART Domains |
Protein: ENSMUSP00000067133 Gene: ENSMUSG00000027259
Domain | Start | End | E-Value | Type |
Pfam:A_deaminase
|
16 |
343 |
1.6e-36 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000110662
|
SMART Domains |
Protein: ENSMUSP00000106290 Gene: ENSMUSG00000027259
Domain | Start | End | E-Value | Type |
Pfam:A_deaminase
|
2 |
200 |
1.1e-28 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000110665
|
SMART Domains |
Protein: ENSMUSP00000106293 Gene: ENSMUSG00000027259
Domain | Start | End | E-Value | Type |
Pfam:A_deaminase
|
2 |
236 |
4.3e-24 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000119031
|
SMART Domains |
Protein: ENSMUSP00000113052 Gene: ENSMUSG00000027259
Domain | Start | End | E-Value | Type |
Pfam:A_deaminase
|
16 |
343 |
3e-44 |
PFAM |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000147271
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000152164
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000156132
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 33 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Arhgap20 |
A |
G |
9: 51,760,713 (GRCm39) |
N819D |
probably benign |
Het |
Cenpe |
A |
G |
3: 134,965,112 (GRCm39) |
I2061V |
probably benign |
Het |
Chrna4 |
T |
C |
2: 180,671,184 (GRCm39) |
I191V |
probably benign |
Het |
Crim1 |
A |
G |
17: 78,677,520 (GRCm39) |
E907G |
probably damaging |
Het |
Cyp2d9 |
T |
A |
15: 82,340,576 (GRCm39) |
D175E |
possibly damaging |
Het |
Eml4 |
A |
G |
17: 83,758,219 (GRCm39) |
|
probably benign |
Het |
Faim |
G |
A |
9: 98,874,218 (GRCm39) |
G15R |
probably damaging |
Het |
Fam3c |
A |
T |
6: 22,318,947 (GRCm39) |
D151E |
probably damaging |
Het |
Far1 |
G |
A |
7: 113,139,896 (GRCm39) |
V115I |
probably benign |
Het |
Gfap |
T |
C |
11: 102,779,516 (GRCm39) |
D427G |
possibly damaging |
Het |
Hdac5 |
A |
G |
11: 102,088,168 (GRCm39) |
F934S |
probably damaging |
Het |
Hyou1 |
A |
G |
9: 44,296,443 (GRCm39) |
E456G |
probably benign |
Het |
Kl |
G |
A |
5: 150,904,315 (GRCm39) |
E356K |
possibly damaging |
Het |
Morc1 |
T |
C |
16: 48,281,055 (GRCm39) |
I198T |
possibly damaging |
Het |
Mroh9 |
C |
T |
1: 162,866,700 (GRCm39) |
V679M |
probably damaging |
Het |
Pigr |
T |
A |
1: 130,762,167 (GRCm39) |
M1K |
probably null |
Het |
Pkn3 |
C |
A |
2: 29,971,212 (GRCm39) |
P260T |
possibly damaging |
Het |
Pld5 |
T |
G |
1: 175,967,585 (GRCm39) |
D28A |
probably damaging |
Het |
Plekhg2 |
G |
A |
7: 28,060,294 (GRCm39) |
Q1012* |
probably null |
Het |
Ppp1ca |
A |
G |
19: 4,243,143 (GRCm39) |
I104V |
probably benign |
Het |
Rad21l |
A |
G |
2: 151,509,909 (GRCm39) |
V64A |
probably damaging |
Het |
Rbm20 |
A |
G |
19: 53,803,948 (GRCm39) |
D427G |
probably damaging |
Het |
Rev3l |
A |
G |
10: 39,735,149 (GRCm39) |
I2792V |
possibly damaging |
Het |
Sec23a |
C |
T |
12: 59,039,068 (GRCm39) |
C248Y |
possibly damaging |
Het |
Sf3b1 |
A |
T |
1: 55,036,090 (GRCm39) |
|
probably benign |
Het |
Slc30a1 |
A |
G |
1: 191,641,191 (GRCm39) |
N279S |
probably damaging |
Het |
Slit2 |
G |
A |
5: 48,146,493 (GRCm39) |
E95K |
possibly damaging |
Het |
Spic |
T |
C |
10: 88,511,729 (GRCm39) |
N176D |
probably damaging |
Het |
Tlk2 |
C |
T |
11: 105,137,621 (GRCm39) |
Q184* |
probably null |
Het |
Tpm4 |
T |
C |
8: 72,897,347 (GRCm39) |
I107T |
probably benign |
Het |
Ttll11 |
A |
T |
2: 35,792,732 (GRCm39) |
C186* |
probably null |
Het |
Txlnb |
A |
T |
10: 17,718,711 (GRCm39) |
H514L |
probably damaging |
Het |
Zfpm2 |
T |
A |
15: 40,962,887 (GRCm39) |
M183K |
probably benign |
Het |
|
Other mutations in Adal |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01917:Adal
|
APN |
2 |
120,973,035 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02487:Adal
|
APN |
2 |
120,985,877 (GRCm39) |
missense |
probably benign |
0.12 |
R0004:Adal
|
UTSW |
2 |
120,982,966 (GRCm39) |
missense |
probably damaging |
1.00 |
R0234:Adal
|
UTSW |
2 |
120,978,798 (GRCm39) |
missense |
probably benign |
0.01 |
R0234:Adal
|
UTSW |
2 |
120,978,798 (GRCm39) |
missense |
probably benign |
0.01 |
R1376:Adal
|
UTSW |
2 |
120,983,011 (GRCm39) |
missense |
probably damaging |
1.00 |
R1376:Adal
|
UTSW |
2 |
120,983,011 (GRCm39) |
missense |
probably damaging |
1.00 |
R4989:Adal
|
UTSW |
2 |
120,986,030 (GRCm39) |
utr 3 prime |
probably benign |
|
R6532:Adal
|
UTSW |
2 |
120,976,604 (GRCm39) |
splice site |
probably null |
|
R6606:Adal
|
UTSW |
2 |
120,980,769 (GRCm39) |
missense |
probably damaging |
1.00 |
R6750:Adal
|
UTSW |
2 |
120,973,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R6819:Adal
|
UTSW |
2 |
120,978,794 (GRCm39) |
missense |
probably damaging |
0.99 |
R7035:Adal
|
UTSW |
2 |
120,985,942 (GRCm39) |
missense |
probably benign |
0.00 |
R8210:Adal
|
UTSW |
2 |
120,985,236 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9373:Adal
|
UTSW |
2 |
120,980,703 (GRCm39) |
missense |
probably benign |
0.21 |
R9446:Adal
|
UTSW |
2 |
120,976,530 (GRCm39) |
missense |
probably null |
0.99 |
|
Posted On |
2012-12-06 |