Incidental Mutation 'IGL02012:Tuft1'
| ID |
183407 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Tuft1
|
| Ensembl Gene |
ENSMUSG00000005968 |
| Gene Name |
tuftelin 1 |
| Synonyms |
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
IGL02012
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
3 |
| Chromosomal Location |
94520064-94566179 bp(-) (GRCm39) |
| Type of Mutation |
unclassified |
| DNA Base Change (assembly) |
A to G
at 94529462 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000143473
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000006123]
[ENSMUST00000196655]
[ENSMUST00000196733]
[ENSMUST00000200407]
|
| AlphaFold |
O08970 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000006123
|
| SMART Domains |
Protein: ENSMUSP00000006123
Gene: ENSMUSG00000005968
| Domain | Start | End | E-Value | Type |
|---|
|
coiled coil region
|
88 |
125 |
N/A |
INTRINSIC |
|
coiled coil region
|
164 |
347 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000196655
|
| SMART Domains |
Protein: ENSMUSP00000142537
Gene: ENSMUSG00000005968
| Domain | Start | End | E-Value | Type |
|---|
|
coiled coil region
|
109 |
292 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000196733
|
| SMART Domains |
Protein: ENSMUSP00000143278
Gene: ENSMUSG00000005968
| Domain | Start | End | E-Value | Type |
|---|
|
coiled coil region
|
63 |
100 |
N/A |
INTRINSIC |
|
coiled coil region
|
139 |
322 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000200407
|
| SMART Domains |
Protein: ENSMUSP00000143473
Gene: ENSMUSG00000005968
| Domain | Start | End | E-Value | Type |
|---|
|
coiled coil region
|
29 |
66 |
N/A |
INTRINSIC |
|
coiled coil region
|
105 |
174 |
N/A |
INTRINSIC |
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: Tuftelin is an acidic protein that is thought to play a role in dental enamel mineralization and is implicated in caries susceptibility. It is also thought to be involved with adaptation to hypoxia, mesenchymal stem cell function, and neurotrophin nerve growth factor mediated neuronal differentiation. [provided by RefSeq, Aug 2014]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 29 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| A2m |
A |
G |
6: 121,651,820 (GRCm39) |
N1296S |
probably damaging |
Het |
| Adprh |
A |
T |
16: 38,266,214 (GRCm39) |
D309E |
possibly damaging |
Het |
| Armc1 |
A |
T |
3: 19,211,701 (GRCm39) |
C40S |
possibly damaging |
Het |
| Cops8 |
T |
C |
1: 90,539,956 (GRCm39) |
V204A |
probably damaging |
Het |
| Cstdc5 |
T |
G |
16: 36,187,802 (GRCm39) |
D21A |
possibly damaging |
Het |
| Dchs1 |
T |
G |
7: 105,413,504 (GRCm39) |
T1104P |
probably damaging |
Het |
| Ddi2 |
A |
T |
4: 141,435,529 (GRCm39) |
|
probably null |
Het |
| Ehbp1 |
G |
A |
11: 22,051,218 (GRCm39) |
P420S |
probably damaging |
Het |
| Eif1ad |
T |
G |
19: 5,418,687 (GRCm39) |
V80G |
probably damaging |
Het |
| Fat1 |
T |
C |
8: 45,480,577 (GRCm39) |
Y3004H |
possibly damaging |
Het |
| Fbxo11 |
C |
T |
17: 88,320,079 (GRCm39) |
R211Q |
probably benign |
Het |
| Foxf2 |
A |
G |
13: 31,810,499 (GRCm39) |
N146S |
probably damaging |
Het |
| Fsd2 |
A |
T |
7: 81,199,662 (GRCm39) |
N334K |
probably benign |
Het |
| Gm45234 |
C |
A |
6: 124,723,011 (GRCm39) |
|
probably benign |
Het |
| Itpr3 |
T |
A |
17: 27,323,069 (GRCm39) |
F1157I |
probably benign |
Het |
| Jph1 |
C |
A |
1: 17,167,638 (GRCm39) |
W64L |
probably benign |
Het |
| Lmo7 |
T |
C |
14: 102,126,152 (GRCm39) |
|
probably benign |
Het |
| Man2a1 |
T |
C |
17: 64,973,894 (GRCm39) |
I390T |
probably damaging |
Het |
| Marveld3 |
C |
T |
8: 110,674,764 (GRCm39) |
V351M |
probably damaging |
Het |
| Minar1 |
T |
C |
9: 89,483,491 (GRCm39) |
I635M |
probably benign |
Het |
| Mycn |
A |
G |
12: 12,987,104 (GRCm39) |
L431P |
probably damaging |
Het |
| Naip5 |
T |
C |
13: 100,359,847 (GRCm39) |
N463S |
probably benign |
Het |
| Npnt |
A |
G |
3: 132,614,158 (GRCm39) |
C182R |
probably damaging |
Het |
| Obscn |
A |
G |
11: 58,967,333 (GRCm39) |
V3068A |
probably benign |
Het |
| Pggt1b |
A |
T |
18: 46,396,022 (GRCm39) |
S88T |
probably benign |
Het |
| Prx |
A |
G |
7: 27,217,326 (GRCm39) |
E748G |
probably damaging |
Het |
| Scrn3 |
T |
C |
2: 73,148,773 (GRCm39) |
|
probably null |
Het |
| Trmt10b |
G |
A |
4: 45,315,045 (GRCm39) |
R292H |
probably benign |
Het |
| Wfdc8 |
T |
C |
2: 164,445,070 (GRCm39) |
|
probably benign |
Het |
|
| Other mutations in Tuft1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00655:Tuft1
|
APN |
3 |
94,530,091 (GRCm39) |
missense |
possibly damaging |
0.96 |
|
IGL00816:Tuft1
|
APN |
3 |
94,523,138 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL01339:Tuft1
|
APN |
3 |
94,535,594 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL01364:Tuft1
|
APN |
3 |
94,542,810 (GRCm39) |
splice site |
probably benign |
|
|
IGL02332:Tuft1
|
APN |
3 |
94,523,075 (GRCm39) |
critical splice donor site |
probably null |
|
|
IGL02400:Tuft1
|
APN |
3 |
94,542,809 (GRCm39) |
splice site |
probably benign |
|
|
IGL03155:Tuft1
|
APN |
3 |
94,541,821 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
R4246:Tuft1
|
UTSW |
3 |
94,522,108 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4911:Tuft1
|
UTSW |
3 |
94,542,750 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R5261:Tuft1
|
UTSW |
3 |
94,546,712 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R6622:Tuft1
|
UTSW |
3 |
94,542,726 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6639:Tuft1
|
UTSW |
3 |
94,539,930 (GRCm39) |
missense |
probably benign |
|
|
R6790:Tuft1
|
UTSW |
3 |
94,535,537 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R6986:Tuft1
|
UTSW |
3 |
94,521,461 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7944:Tuft1
|
UTSW |
3 |
94,539,909 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8008:Tuft1
|
UTSW |
3 |
94,521,440 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8200:Tuft1
|
UTSW |
3 |
94,523,977 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8546:Tuft1
|
UTSW |
3 |
94,529,420 (GRCm39) |
missense |
probably benign |
0.08 |
|
R9232:Tuft1
|
UTSW |
3 |
94,529,445 (GRCm39) |
missense |
probably benign |
0.06 |
|
X0022:Tuft1
|
UTSW |
3 |
94,542,735 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Posted On |
2014-05-07 |
Incidental Mutation