Incidental Mutation 'IGL01485:Ttc21b'
| ID |
88735 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Ttc21b
|
| Ensembl Gene |
ENSMUSG00000034848 |
| Gene Name |
tetratricopeptide repeat domain 21B |
| Synonyms |
Thm1, line 158, aln, 2410066K11Rik |
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
IGL01485
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
2 |
| Chromosomal Location |
66014671-66086961 bp(-) (GRCm39) |
| Type of Mutation |
splice site |
| DNA Base Change (assembly) |
G to A
at 66082234 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000131758
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000102718]
[ENSMUST00000125446]
|
| AlphaFold |
Q0HA38 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000102718
|
| SMART Domains |
Protein: ENSMUSP00000099779
Gene: ENSMUSG00000034848
| Domain | Start | End | E-Value | Type |
|---|
|
Blast:TPR
|
109 |
141 |
5e-12 |
BLAST |
|
Blast:TPR
|
178 |
211 |
3e-12 |
BLAST |
|
TPR
|
324 |
357 |
4.21e1 |
SMART |
|
low complexity region
|
379 |
390 |
N/A |
INTRINSIC |
|
TPR
|
492 |
525 |
8.51e0 |
SMART |
|
TPR
|
526 |
559 |
5.92e1 |
SMART |
|
TPR
|
563 |
596 |
7.69e1 |
SMART |
|
TPR
|
721 |
754 |
3.07e-5 |
SMART |
|
TPR
|
755 |
788 |
9.45e0 |
SMART |
|
TPR
|
790 |
821 |
9.24e1 |
SMART |
|
TPR
|
830 |
863 |
3.05e0 |
SMART |
|
TPR
|
883 |
916 |
1.55e-1 |
SMART |
|
TPR
|
917 |
950 |
8.74e0 |
SMART |
|
TPR
|
951 |
984 |
6.75e1 |
SMART |
|
Blast:TPR
|
1023 |
1054 |
5e-13 |
BLAST |
|
Blast:TPR
|
1156 |
1189 |
1e-12 |
BLAST |
|
TPR
|
1196 |
1229 |
9.7e0 |
SMART |
|
TPR
|
1265 |
1298 |
1.02e1 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000125446
|
| SMART Domains |
Protein: ENSMUSP00000131758
Gene: ENSMUSG00000034848
| Domain | Start | End | E-Value | Type |
|---|
|
Blast:TPR
|
108 |
141 |
3e-12 |
BLAST |
|
Blast:TPR
|
178 |
211 |
3e-12 |
BLAST |
|
TPR
|
324 |
357 |
4.21e1 |
SMART |
|
low complexity region
|
379 |
390 |
N/A |
INTRINSIC |
|
TPR
|
492 |
525 |
8.51e0 |
SMART |
|
TPR
|
526 |
559 |
5.92e1 |
SMART |
|
TPR
|
563 |
596 |
7.69e1 |
SMART |
|
TPR
|
721 |
754 |
3.07e-5 |
SMART |
|
TPR
|
755 |
788 |
9.45e0 |
SMART |
|
TPR
|
790 |
821 |
9.24e1 |
SMART |
|
TPR
|
830 |
863 |
3.05e0 |
SMART |
|
TPR
|
883 |
916 |
1.55e-1 |
SMART |
|
TPR
|
917 |
950 |
8.74e0 |
SMART |
|
TPR
|
951 |
984 |
6.75e1 |
SMART |
|
Blast:TPR
|
1023 |
1054 |
4e-13 |
BLAST |
|
Blast:TPR
|
1156 |
1189 |
9e-13 |
BLAST |
|
TPR
|
1196 |
1229 |
9.7e0 |
SMART |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000131503
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of TTC21 family, containing several tetratricopeptide repeat (TPR) domains. This protein is localized to the cilium axoneme, and may play a role in retrograde intraflagellar transport in cilia. Mutations in this gene are associated with various ciliopathies, nephronophthisis 12, and asphyxiating thoracic dystrophy 4. [provided by RefSeq, Oct 2011]
PHENOTYPE: Homozygous mutation of this gene is embryonic lethal. Mutant embryos exhibit several deformities including polydactyly, microphthalmia, irregular shape of the long bones, rib fusion and truncation, neural tube defects, and abnormal brain structure. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 34 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4930590J08Rik |
C |
T |
6: 91,927,003 (GRCm39) |
L888F |
probably damaging |
Het |
| Aftph |
G |
T |
11: 20,642,507 (GRCm39) |
A842E |
probably damaging |
Het |
| Ankrd13d |
A |
T |
19: 4,323,592 (GRCm39) |
M257K |
probably benign |
Het |
| Anks1 |
T |
C |
17: 28,270,558 (GRCm39) |
F786L |
probably damaging |
Het |
| Cd2ap |
A |
T |
17: 43,163,365 (GRCm39) |
I20N |
probably damaging |
Het |
| Cdh20 |
C |
T |
1: 104,861,832 (GRCm39) |
T4M |
probably benign |
Het |
| Dnah5 |
C |
T |
15: 28,331,872 (GRCm39) |
R2153C |
probably damaging |
Het |
| Fap |
G |
A |
2: 62,374,655 (GRCm39) |
P248L |
possibly damaging |
Het |
| Hps4 |
T |
A |
5: 112,512,377 (GRCm39) |
|
probably benign |
Het |
| Igdcc4 |
C |
A |
9: 65,029,889 (GRCm39) |
T313K |
probably benign |
Het |
| Klhl30 |
G |
A |
1: 91,281,761 (GRCm39) |
V121I |
probably damaging |
Het |
| Ldb3 |
C |
A |
14: 34,264,519 (GRCm39) |
E526D |
probably damaging |
Het |
| Ldc1 |
T |
A |
4: 130,109,218 (GRCm39) |
Y274F |
probably benign |
Het |
| Lhfpl4 |
T |
A |
6: 113,171,082 (GRCm39) |
I35F |
probably benign |
Het |
| Lpin1 |
A |
G |
12: 16,612,358 (GRCm39) |
|
probably benign |
Het |
| Nek1 |
T |
A |
8: 61,502,860 (GRCm39) |
C436S |
probably benign |
Het |
| Nek5 |
C |
A |
8: 22,573,385 (GRCm39) |
A524S |
probably benign |
Het |
| Nkx2-3 |
C |
T |
19: 43,601,094 (GRCm39) |
T52M |
possibly damaging |
Het |
| Or1e33 |
A |
G |
11: 73,738,036 (GRCm39) |
I305T |
probably benign |
Het |
| Or2w2 |
A |
T |
13: 21,758,627 (GRCm39) |
|
probably null |
Het |
| Or8b56 |
G |
A |
9: 38,739,895 (GRCm39) |
V303I |
possibly damaging |
Het |
| Pappa |
T |
C |
4: 65,107,536 (GRCm39) |
V649A |
probably damaging |
Het |
| Parp4 |
T |
A |
14: 56,859,661 (GRCm39) |
Y920N |
possibly damaging |
Het |
| Pdgfra |
G |
A |
5: 75,324,313 (GRCm39) |
S56N |
probably benign |
Het |
| Pigg |
T |
C |
5: 108,484,067 (GRCm39) |
V438A |
possibly damaging |
Het |
| Ptn |
A |
T |
6: 36,720,298 (GRCm39) |
C85S |
probably damaging |
Het |
| Sh3rf1 |
A |
C |
8: 61,782,365 (GRCm39) |
E169A |
possibly damaging |
Het |
| Slc30a10 |
T |
A |
1: 185,187,616 (GRCm39) |
V119E |
probably damaging |
Het |
| Speg |
A |
G |
1: 75,364,471 (GRCm39) |
E178G |
probably damaging |
Het |
| Sspo |
A |
G |
6: 48,455,665 (GRCm39) |
Y3105C |
probably damaging |
Het |
| Supt3 |
A |
G |
17: 45,430,045 (GRCm39) |
E366G |
possibly damaging |
Het |
| Top2a |
A |
T |
11: 98,901,856 (GRCm39) |
L458Q |
probably damaging |
Het |
| Usp24 |
T |
C |
4: 106,219,429 (GRCm39) |
F542L |
probably benign |
Het |
| Vmn1r234 |
T |
A |
17: 21,449,171 (GRCm39) |
D28E |
possibly damaging |
Het |
|
| Other mutations in Ttc21b |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00465:Ttc21b
|
APN |
2 |
66,073,119 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL00467:Ttc21b
|
APN |
2 |
66,018,708 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL00721:Ttc21b
|
APN |
2 |
66,057,122 (GRCm39) |
missense |
probably benign |
0.06 |
|
IGL00837:Ttc21b
|
APN |
2 |
66,065,915 (GRCm39) |
critical splice donor site |
probably null |
|
|
IGL01317:Ttc21b
|
APN |
2 |
66,018,700 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL01739:Ttc21b
|
APN |
2 |
66,068,200 (GRCm39) |
missense |
probably benign |
|
|
IGL02282:Ttc21b
|
APN |
2 |
66,022,081 (GRCm39) |
missense |
probably damaging |
0.96 |
|
IGL02431:Ttc21b
|
APN |
2 |
66,082,229 (GRCm39) |
splice site |
probably benign |
|
|
IGL02478:Ttc21b
|
APN |
2 |
66,018,624 (GRCm39) |
missense |
probably benign |
0.05 |
|
IGL02487:Ttc21b
|
APN |
2 |
66,065,500 (GRCm39) |
missense |
probably benign |
0.02 |
|
IGL03327:Ttc21b
|
APN |
2 |
66,068,192 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
IGL03346:Ttc21b
|
APN |
2 |
66,068,192 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
plus-sized
|
UTSW |
2 |
66,073,023 (GRCm39) |
missense |
probably damaging |
1.00 |
|
puffer
|
UTSW |
2 |
66,057,244 (GRCm39) |
missense |
probably benign |
0.12 |
|
PIT4696001:Ttc21b
|
UTSW |
2 |
66,061,563 (GRCm39) |
splice site |
probably null |
|
|
R0049:Ttc21b
|
UTSW |
2 |
66,053,908 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0049:Ttc21b
|
UTSW |
2 |
66,053,908 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0373:Ttc21b
|
UTSW |
2 |
66,018,670 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0440:Ttc21b
|
UTSW |
2 |
66,066,726 (GRCm39) |
missense |
probably benign |
0.03 |
|
R0504:Ttc21b
|
UTSW |
2 |
66,053,142 (GRCm39) |
splice site |
probably benign |
|
|
R0600:Ttc21b
|
UTSW |
2 |
66,069,914 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0621:Ttc21b
|
UTSW |
2 |
66,056,355 (GRCm39) |
missense |
probably benign |
0.07 |
|
R0633:Ttc21b
|
UTSW |
2 |
66,066,577 (GRCm39) |
missense |
probably benign |
|
|
R0863:Ttc21b
|
UTSW |
2 |
66,073,117 (GRCm39) |
missense |
probably benign |
|
|
R1617:Ttc21b
|
UTSW |
2 |
66,056,379 (GRCm39) |
missense |
probably benign |
0.22 |
|
R1837:Ttc21b
|
UTSW |
2 |
66,028,106 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1844:Ttc21b
|
UTSW |
2 |
66,053,921 (GRCm39) |
nonsense |
probably null |
|
|
R2120:Ttc21b
|
UTSW |
2 |
66,057,098 (GRCm39) |
missense |
probably benign |
0.12 |
|
R2205:Ttc21b
|
UTSW |
2 |
66,065,467 (GRCm39) |
missense |
possibly damaging |
0.51 |
|
R2392:Ttc21b
|
UTSW |
2 |
66,037,794 (GRCm39) |
critical splice donor site |
probably null |
|
|
R3689:Ttc21b
|
UTSW |
2 |
66,054,488 (GRCm39) |
missense |
probably benign |
0.22 |
|
R3810:Ttc21b
|
UTSW |
2 |
66,082,577 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
R3847:Ttc21b
|
UTSW |
2 |
66,073,023 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3897:Ttc21b
|
UTSW |
2 |
66,065,413 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4561:Ttc21b
|
UTSW |
2 |
66,016,562 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4671:Ttc21b
|
UTSW |
2 |
66,057,257 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R5161:Ttc21b
|
UTSW |
2 |
66,059,367 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5274:Ttc21b
|
UTSW |
2 |
66,066,627 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R5594:Ttc21b
|
UTSW |
2 |
66,066,579 (GRCm39) |
missense |
probably benign |
0.39 |
|
R6210:Ttc21b
|
UTSW |
2 |
66,066,698 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6305:Ttc21b
|
UTSW |
2 |
66,018,614 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6456:Ttc21b
|
UTSW |
2 |
66,018,675 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R6482:Ttc21b
|
UTSW |
2 |
66,057,244 (GRCm39) |
missense |
probably benign |
0.12 |
|
R6645:Ttc21b
|
UTSW |
2 |
66,066,721 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6800:Ttc21b
|
UTSW |
2 |
66,038,994 (GRCm39) |
splice site |
probably null |
|
|
R6815:Ttc21b
|
UTSW |
2 |
66,057,134 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6959:Ttc21b
|
UTSW |
2 |
66,061,656 (GRCm39) |
missense |
probably benign |
0.05 |
|
R7125:Ttc21b
|
UTSW |
2 |
66,066,670 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7265:Ttc21b
|
UTSW |
2 |
66,040,517 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R7283:Ttc21b
|
UTSW |
2 |
66,039,062 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R7560:Ttc21b
|
UTSW |
2 |
66,047,548 (GRCm39) |
missense |
possibly damaging |
0.69 |
|
R7561:Ttc21b
|
UTSW |
2 |
66,047,548 (GRCm39) |
missense |
possibly damaging |
0.69 |
|
R7816:Ttc21b
|
UTSW |
2 |
66,077,705 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
R8172:Ttc21b
|
UTSW |
2 |
66,082,500 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8179:Ttc21b
|
UTSW |
2 |
66,031,824 (GRCm39) |
missense |
probably benign |
|
|
R9047:Ttc21b
|
UTSW |
2 |
66,031,596 (GRCm39) |
missense |
|
|
|
R9282:Ttc21b
|
UTSW |
2 |
66,056,349 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
R9336:Ttc21b
|
UTSW |
2 |
66,057,287 (GRCm39) |
missense |
probably benign |
|
|
R9464:Ttc21b
|
UTSW |
2 |
66,053,866 (GRCm39) |
missense |
probably damaging |
1.00 |
|
X0013:Ttc21b
|
UTSW |
2 |
66,056,294 (GRCm39) |
nonsense |
probably null |
|
|
| Posted On |
2013-11-18 |
Incidental Mutation