Incidental Mutation 'R7589:Ttc8'
| ID |
587315 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Ttc8
|
| Ensembl Gene |
ENSMUSG00000021013 |
| Gene Name |
tetratricopeptide repeat domain 8 |
| Synonyms |
BBS8, 0610012F22Rik |
| MMRRC Submission |
045637-MU
|
| Accession Numbers |
|
| Essential gene? |
Possibly non essential
(E-score: 0.393)
|
| Stock # |
R7589 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
12 |
| Chromosomal Location |
98886833-98949497 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 98942696 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Aspartic acid to Valine
at position 412
(D412V)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000078148
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000079146]
[ENSMUST00000085109]
|
| AlphaFold |
Q8VD72 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000079146
AA Change: D412V
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000078148
Gene: ENSMUSG00000021013
AA Change: D412V
| Domain | Start | End | E-Value | Type |
|---|
|
Blast:TPR
|
4 |
37 |
5e-12 |
BLAST |
|
TPR
|
225 |
258 |
2.35e-1 |
SMART |
|
TPR
|
292 |
325 |
9.68e-3 |
SMART |
|
Blast:TPR
|
326 |
359 |
3e-14 |
BLAST |
|
TPR
|
360 |
393 |
2.26e-3 |
SMART |
|
TPR
|
397 |
430 |
1.91e-1 |
SMART |
|
TPR
|
431 |
464 |
1.81e-2 |
SMART |
|
Blast:TPR
|
465 |
498 |
7e-14 |
BLAST |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000085109
AA Change: D402V
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000082190
Gene: ENSMUSG00000021013
AA Change: D402V
| Domain | Start | End | E-Value | Type |
|---|
|
Blast:TPR
|
4 |
37 |
4e-12 |
BLAST |
|
TPR
|
215 |
248 |
2.35e-1 |
SMART |
|
TPR
|
282 |
315 |
9.68e-3 |
SMART |
|
Blast:TPR
|
316 |
349 |
3e-14 |
BLAST |
|
TPR
|
350 |
383 |
2.26e-3 |
SMART |
|
TPR
|
387 |
420 |
1.91e-1 |
SMART |
|
TPR
|
421 |
454 |
1.81e-2 |
SMART |
|
Blast:TPR
|
455 |
488 |
7e-14 |
BLAST |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.7%
- 20x: 99.0%
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein that has been directly linked to Bardet-Biedl syndrome. The primary features of this syndrome include retinal dystrophy, obesity, polydactyly, renal abnormalities and learning disabilities. Experimentation in non-human eukaryotes suggests that this gene is expressed in ciliated cells and that it is involved in the formation of cilia. A mutation in this gene has also been implicated in nonsyndromic retinitis pigmentosa. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]
PHENOTYPE: Mice homozygous for a null mutation display partial postnatal lethality with slow postnatal weight gain, age related obesity, impaired olfation, loss of cilia from the olfactory epithelium, impaired targeting of olfactory sensory neuron axons, retinal degeneration, and mild renal tubule dilation. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 44 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 2610021A01Rik |
T |
G |
7: 41,276,396 (GRCm39) |
C700G |
probably damaging |
Het |
| 4930486L24Rik |
T |
C |
13: 60,990,747 (GRCm39) |
K316E |
probably damaging |
Het |
| Akap6 |
A |
T |
12: 53,188,846 (GRCm39) |
K2087* |
probably null |
Het |
| Alpk2 |
A |
T |
18: 65,433,144 (GRCm39) |
H1320Q |
probably damaging |
Het |
| Aox1 |
A |
T |
1: 58,080,643 (GRCm39) |
R31W |
probably damaging |
Het |
| Asnsd1 |
G |
T |
1: 53,387,126 (GRCm39) |
A167E |
probably benign |
Het |
| Atg14 |
T |
C |
14: 47,780,547 (GRCm39) |
D409G |
probably benign |
Het |
| Atp13a3 |
T |
A |
16: 30,163,433 (GRCm39) |
E574D |
probably benign |
Het |
| Bicd1 |
A |
T |
6: 149,415,165 (GRCm39) |
Y626F |
possibly damaging |
Het |
| Cdc5l |
C |
T |
17: 45,721,707 (GRCm39) |
R521Q |
probably benign |
Het |
| Dglucy |
T |
C |
12: 100,807,660 (GRCm39) |
F160L |
probably damaging |
Het |
| Enpp5 |
G |
A |
17: 44,396,155 (GRCm39) |
G356S |
probably damaging |
Het |
| Fmo9 |
T |
A |
1: 166,501,997 (GRCm39) |
K209N |
possibly damaging |
Het |
| Gsdmc2 |
C |
A |
15: 63,696,892 (GRCm39) |
L426F |
probably damaging |
Het |
| Hip1 |
T |
C |
5: 135,443,165 (GRCm39) |
D956G |
probably benign |
Het |
| Kif28 |
C |
T |
1: 179,558,965 (GRCm39) |
V248I |
probably benign |
Het |
| Klk10 |
T |
C |
7: 43,433,051 (GRCm39) |
V149A |
probably benign |
Het |
| Krt40 |
G |
T |
11: 99,430,983 (GRCm39) |
N255K |
probably damaging |
Het |
| Map4k4 |
T |
A |
1: 40,060,251 (GRCm39) |
Y1013* |
probably null |
Het |
| Mcur1 |
T |
C |
13: 43,705,101 (GRCm39) |
Y185C |
probably damaging |
Het |
| Mzt1 |
T |
C |
14: 99,273,948 (GRCm39) |
|
probably null |
Het |
| Naip5 |
G |
T |
13: 100,356,205 (GRCm39) |
Q1137K |
not run |
Het |
| Naip5 |
T |
C |
13: 100,356,204 (GRCm39) |
Q1137R |
probably benign |
Het |
| Nkx1-2 |
T |
C |
7: 132,201,204 (GRCm39) |
I18V |
probably damaging |
Het |
| Ofcc1 |
T |
A |
13: 40,408,960 (GRCm39) |
Q155L |
probably benign |
Het |
| Or1ad1 |
A |
T |
11: 50,875,857 (GRCm39) |
M110L |
probably damaging |
Het |
| Or4a2 |
A |
G |
2: 89,248,724 (GRCm39) |
V11A |
possibly damaging |
Het |
| Or4k38 |
T |
C |
2: 111,165,719 (GRCm39) |
K235E |
probably damaging |
Het |
| Or51q1 |
T |
C |
7: 103,628,998 (GRCm39) |
Y200H |
probably damaging |
Het |
| Or9s15 |
G |
A |
1: 92,524,781 (GRCm39) |
R180H |
probably benign |
Het |
| Prnp |
A |
G |
2: 131,778,786 (GRCm39) |
D146G |
probably benign |
Het |
| Rhbdf1 |
C |
T |
11: 32,162,903 (GRCm39) |
V455I |
probably benign |
Het |
| Rnf6 |
G |
A |
5: 146,148,239 (GRCm39) |
R260W |
possibly damaging |
Het |
| Rtl1 |
T |
C |
12: 109,560,279 (GRCm39) |
N520S |
possibly damaging |
Het |
| Setbp1 |
A |
T |
18: 78,899,707 (GRCm39) |
M1320K |
probably benign |
Het |
| Slc39a8 |
A |
G |
3: 135,590,123 (GRCm39) |
T338A |
probably damaging |
Het |
| Tcf4 |
A |
G |
18: 69,815,890 (GRCm39) |
*693W |
probably null |
Het |
| Ush2a |
G |
T |
1: 188,275,046 (GRCm39) |
A1840S |
probably benign |
Het |
| Vmn1r60 |
A |
T |
7: 5,547,688 (GRCm39) |
S137R |
|
Het |
| Vmn1r91 |
T |
A |
7: 19,835,802 (GRCm39) |
H240Q |
probably benign |
Het |
| Vmn2r107 |
A |
T |
17: 20,595,634 (GRCm39) |
H729L |
probably benign |
Het |
| Yme1l1 |
C |
T |
2: 23,050,274 (GRCm39) |
T35I |
probably benign |
Het |
| Zfp292 |
A |
G |
4: 34,806,777 (GRCm39) |
V2094A |
probably damaging |
Het |
| Zfp934 |
A |
T |
13: 62,666,130 (GRCm39) |
N202K |
|
Het |
|
| Other mutations in Ttc8 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00925:Ttc8
|
APN |
12 |
98,942,277 (GRCm39) |
missense |
probably damaging |
0.96 |
|
IGL01139:Ttc8
|
APN |
12 |
98,930,804 (GRCm39) |
nonsense |
probably null |
|
|
IGL02179:Ttc8
|
APN |
12 |
98,930,796 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
IGL02715:Ttc8
|
APN |
12 |
98,910,179 (GRCm39) |
splice site |
probably benign |
|
|
IGL02958:Ttc8
|
APN |
12 |
98,930,803 (GRCm39) |
missense |
probably benign |
0.03 |
|
IGL03249:Ttc8
|
APN |
12 |
98,910,080 (GRCm39) |
splice site |
probably benign |
|
|
P0035:Ttc8
|
UTSW |
12 |
98,942,675 (GRCm39) |
splice site |
probably benign |
|
|
R0606:Ttc8
|
UTSW |
12 |
98,909,718 (GRCm39) |
splice site |
probably benign |
|
|
R1005:Ttc8
|
UTSW |
12 |
98,903,403 (GRCm39) |
missense |
probably benign |
0.11 |
|
R1584:Ttc8
|
UTSW |
12 |
98,887,023 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1628:Ttc8
|
UTSW |
12 |
98,948,780 (GRCm39) |
missense |
probably benign |
0.07 |
|
R1706:Ttc8
|
UTSW |
12 |
98,910,142 (GRCm39) |
missense |
probably benign |
0.02 |
|
R4585:Ttc8
|
UTSW |
12 |
98,948,789 (GRCm39) |
missense |
probably benign |
|
|
R4720:Ttc8
|
UTSW |
12 |
98,946,068 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R4879:Ttc8
|
UTSW |
12 |
98,908,562 (GRCm39) |
missense |
possibly damaging |
0.55 |
|
R5110:Ttc8
|
UTSW |
12 |
98,908,562 (GRCm39) |
missense |
probably benign |
0.25 |
|
R6272:Ttc8
|
UTSW |
12 |
98,948,753 (GRCm39) |
missense |
possibly damaging |
0.63 |
|
R6465:Ttc8
|
UTSW |
12 |
98,930,829 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6620:Ttc8
|
UTSW |
12 |
98,923,579 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R6708:Ttc8
|
UTSW |
12 |
98,909,791 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6772:Ttc8
|
UTSW |
12 |
98,909,848 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6901:Ttc8
|
UTSW |
12 |
98,927,735 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7060:Ttc8
|
UTSW |
12 |
98,909,726 (GRCm39) |
missense |
probably benign |
|
|
R7117:Ttc8
|
UTSW |
12 |
98,942,761 (GRCm39) |
missense |
possibly damaging |
0.63 |
|
R7174:Ttc8
|
UTSW |
12 |
98,940,960 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R7385:Ttc8
|
UTSW |
12 |
98,908,547 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
R7447:Ttc8
|
UTSW |
12 |
98,910,131 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R8517:Ttc8
|
UTSW |
12 |
98,909,594 (GRCm39) |
missense |
probably benign |
|
|
R9397:Ttc8
|
UTSW |
12 |
98,942,692 (GRCm39) |
nonsense |
probably null |
|
|
R9629:Ttc8
|
UTSW |
12 |
98,886,965 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
| Predicted Primers |
PCR Primer
(F):5'- TATATCCTCAAGTCAAATCCATGCC -3'
(R):5'- AAGTCCAATGTCCAATTCTGGC -3'
Sequencing Primer
(F):5'- GTCAAATCCATGCCCGGAC -3'
(R):5'- GGCCTGTAAGACTCTAGAGCTAC -3'
|
| Posted On |
2019-10-24 |
Incidental Mutation