Incidental Mutation 'IGL01022:Slfn10-ps'
| ID |
53891 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Slfn10-ps
|
| Ensembl Gene |
ENSMUSG00000072621 |
| Gene Name |
schlafen 10, pseudogene |
| Synonyms |
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.073)
|
| Stock # |
IGL01022
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
11 |
| Chromosomal Location |
82919681-82926992 bp(-) (GRCm39) |
| Type of Mutation |
unclassified |
| DNA Base Change (assembly) |
C to T
at 82926353 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Gene Model |
predicted gene model for transcript(s):
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000100716
|
| SMART Domains |
Protein: ENSMUSP00000098282
Gene: ENSMUSG00000072621
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:AlbA_2
|
142 |
278 |
1.3e-13 |
PFAM |
|
Pfam:DUF2075
|
529 |
697 |
1.6e-7 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000152760
|
| SMART Domains |
Protein: ENSMUSP00000130353
Gene: ENSMUSG00000072621
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:AAA_4
|
142 |
280 |
1.8e-14 |
PFAM |
|
Pfam:DUF2075
|
529 |
693 |
1.8e-8 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000185158
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000215473
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 29 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adamts14 |
A |
G |
10: 61,038,721 (GRCm39) |
S927P |
probably benign |
Het |
| Arfgef1 |
G |
T |
1: 10,244,301 (GRCm39) |
F987L |
probably damaging |
Het |
| Asph |
A |
T |
4: 9,601,344 (GRCm39) |
N191K |
possibly damaging |
Het |
| Bmpr1b |
A |
T |
3: 141,577,099 (GRCm39) |
C71S |
probably damaging |
Het |
| Bod1l |
A |
T |
5: 41,951,652 (GRCm39) |
S2920T |
probably damaging |
Het |
| Camta2 |
G |
A |
11: 70,562,308 (GRCm39) |
R1030* |
probably null |
Het |
| Chd8 |
T |
C |
14: 52,474,450 (GRCm39) |
T194A |
probably benign |
Het |
| Col9a3 |
A |
T |
2: 180,258,227 (GRCm39) |
I549F |
probably damaging |
Het |
| Fstl4 |
A |
G |
11: 53,077,568 (GRCm39) |
N775S |
probably benign |
Het |
| Gm10800 |
T |
A |
2: 98,497,576 (GRCm39) |
|
probably benign |
Het |
| Gm5117 |
T |
A |
8: 32,228,515 (GRCm39) |
|
noncoding transcript |
Het |
| Hap1 |
A |
G |
11: 100,240,374 (GRCm39) |
L112P |
probably benign |
Het |
| Hcls1 |
C |
A |
16: 36,771,488 (GRCm39) |
|
probably benign |
Het |
| Kmt2c |
A |
G |
5: 25,507,699 (GRCm39) |
|
probably benign |
Het |
| Lct |
T |
A |
1: 128,228,596 (GRCm39) |
I966L |
probably benign |
Het |
| Myo1h |
A |
T |
5: 114,474,361 (GRCm39) |
I451F |
possibly damaging |
Het |
| Notch4 |
G |
A |
17: 34,784,671 (GRCm39) |
C128Y |
probably damaging |
Het |
| Oca2 |
T |
A |
7: 55,974,504 (GRCm39) |
N484K |
probably damaging |
Het |
| Or51f1e |
T |
G |
7: 102,747,077 (GRCm39) |
L43R |
probably damaging |
Het |
| Or7a42 |
A |
T |
10: 78,791,188 (GRCm39) |
I50F |
possibly damaging |
Het |
| Rprd2 |
T |
A |
3: 95,671,066 (GRCm39) |
R1362* |
probably null |
Het |
| Sema3a |
C |
T |
5: 13,523,433 (GRCm39) |
T134I |
probably damaging |
Het |
| Sfta2 |
C |
T |
17: 35,961,336 (GRCm39) |
T74I |
possibly damaging |
Het |
| Spag11a |
A |
T |
8: 19,208,005 (GRCm39) |
Q15H |
probably damaging |
Het |
| Tbc1d22a |
G |
A |
15: 86,185,756 (GRCm39) |
D282N |
probably damaging |
Het |
| Tmbim6 |
G |
A |
15: 99,300,003 (GRCm39) |
V40M |
possibly damaging |
Het |
| Tmem259 |
A |
G |
10: 79,819,808 (GRCm39) |
V22A |
probably damaging |
Het |
| Tnik |
T |
C |
3: 28,679,377 (GRCm39) |
|
probably null |
Het |
| Unc13c |
T |
C |
9: 73,424,610 (GRCm39) |
D2002G |
probably benign |
Het |
|
| Other mutations in Slfn10-ps |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00773:Slfn10-ps
|
APN |
11 |
82,926,355 (GRCm39) |
unclassified |
noncoding transcript |
|
|
IGL00826:Slfn10-ps
|
APN |
11 |
82,926,085 (GRCm39) |
unclassified |
noncoding transcript |
|
|
IGL01409:Slfn10-ps
|
APN |
11 |
82,926,322 (GRCm39) |
unclassified |
noncoding transcript |
|
|
IGL01664:Slfn10-ps
|
APN |
11 |
82,926,761 (GRCm39) |
unclassified |
noncoding transcript |
|
|
IGL01700:Slfn10-ps
|
APN |
11 |
82,919,938 (GRCm39) |
unclassified |
noncoding transcript |
|
|
IGL02093:Slfn10-ps
|
APN |
11 |
82,923,016 (GRCm39) |
unclassified |
noncoding transcript |
|
|
IGL02253:Slfn10-ps
|
APN |
11 |
82,919,890 (GRCm39) |
unclassified |
noncoding transcript |
|
|
IGL02364:Slfn10-ps
|
APN |
11 |
82,923,117 (GRCm39) |
unclassified |
noncoding transcript |
|
|
IGL02466:Slfn10-ps
|
APN |
11 |
82,921,090 (GRCm39) |
unclassified |
noncoding transcript |
|
|
IGL02636:Slfn10-ps
|
APN |
11 |
82,920,971 (GRCm39) |
unclassified |
noncoding transcript |
|
|
R0055:Slfn10-ps
|
UTSW |
11 |
82,921,126 (GRCm39) |
unclassified |
noncoding transcript |
|
|
R0055:Slfn10-ps
|
UTSW |
11 |
82,921,126 (GRCm39) |
unclassified |
noncoding transcript |
|
|
R0069:Slfn10-ps
|
UTSW |
11 |
82,926,368 (GRCm39) |
unclassified |
noncoding transcript |
|
|
R0069:Slfn10-ps
|
UTSW |
11 |
82,926,368 (GRCm39) |
unclassified |
noncoding transcript |
|
|
R0164:Slfn10-ps
|
UTSW |
11 |
82,926,128 (GRCm39) |
unclassified |
noncoding transcript |
|
|
R0362:Slfn10-ps
|
UTSW |
11 |
82,926,600 (GRCm39) |
unclassified |
noncoding transcript |
|
|
R0382:Slfn10-ps
|
UTSW |
11 |
82,920,360 (GRCm39) |
unclassified |
noncoding transcript |
|
|
R0597:Slfn10-ps
|
UTSW |
11 |
82,926,479 (GRCm39) |
unclassified |
noncoding transcript |
|
|
R0812:Slfn10-ps
|
UTSW |
11 |
82,926,388 (GRCm39) |
unclassified |
noncoding transcript |
|
|
R0904:Slfn10-ps
|
UTSW |
11 |
82,926,235 (GRCm39) |
unclassified |
noncoding transcript |
|
|
R1552:Slfn10-ps
|
UTSW |
11 |
82,920,676 (GRCm39) |
unclassified |
noncoding transcript |
|
|
R1703:Slfn10-ps
|
UTSW |
11 |
82,920,869 (GRCm39) |
unclassified |
noncoding transcript |
|
|
R2127:Slfn10-ps
|
UTSW |
11 |
82,921,168 (GRCm39) |
unclassified |
noncoding transcript |
|
|
R2151:Slfn10-ps
|
UTSW |
11 |
82,926,511 (GRCm39) |
unclassified |
noncoding transcript |
|
|
R2302:Slfn10-ps
|
UTSW |
11 |
82,919,756 (GRCm39) |
unclassified |
noncoding transcript |
|
|
R3114:Slfn10-ps
|
UTSW |
11 |
82,919,955 (GRCm39) |
unclassified |
noncoding transcript |
|
|
R4293:Slfn10-ps
|
UTSW |
11 |
82,926,260 (GRCm39) |
unclassified |
noncoding transcript |
|
|
R4929:Slfn10-ps
|
UTSW |
11 |
82,920,345 (GRCm39) |
unclassified |
noncoding transcript |
|
|
R4970:Slfn10-ps
|
UTSW |
11 |
82,921,207 (GRCm39) |
unclassified |
noncoding transcript |
|
|
R5083:Slfn10-ps
|
UTSW |
11 |
82,921,341 (GRCm39) |
unclassified |
noncoding transcript |
|
|
R5290:Slfn10-ps
|
UTSW |
11 |
82,919,851 (GRCm39) |
unclassified |
noncoding transcript |
|
|
R5306:Slfn10-ps
|
UTSW |
11 |
82,926,355 (GRCm39) |
unclassified |
noncoding transcript |
|
|
R5444:Slfn10-ps
|
UTSW |
11 |
82,926,113 (GRCm39) |
unclassified |
noncoding transcript |
|
|
| Posted On |
2013-06-28 |
Incidental Mutation