Incidental Mutation 'S24628:Tnc'
ID |
385650 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Tnc
|
Ensembl Gene |
ENSMUSG00000028364 |
Gene Name |
tenascin C |
Synonyms |
TN, TN-C, hexabrachion, tenascin-C, C130033P17Rik, cytotactin, Hxb |
Accession Numbers |
|
Is this an essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
S24628 ()
of strain
waterfowl
|
Quality Score |
222 |
Status
|
Not validated
|
Chromosome |
4 |
Chromosomal Location |
63959785-64047015 bp(-) (GRCm38) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
C to T
at 64018012 bp (GRCm38)
|
Zygosity |
Homozygous |
Amino Acid Change |
Glycine to Aspartic acid
at position 229
(G229D)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000103000
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000030056]
[ENSMUST00000107371]
[ENSMUST00000107372]
[ENSMUST00000107377]
|
AlphaFold |
Q80YX1 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000030056
AA Change: G229D
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000030056 Gene: ENSMUSG00000028364 AA Change: G229D
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
22 |
N/A |
INTRINSIC |
low complexity region
|
121 |
138 |
N/A |
INTRINSIC |
EGF
|
189 |
217 |
1.87e1 |
SMART |
EGF_like
|
220 |
248 |
3.5e1 |
SMART |
EGF
|
251 |
280 |
4.89e0 |
SMART |
EGF
|
283 |
311 |
3.23e0 |
SMART |
EGF_like
|
314 |
342 |
2.98e1 |
SMART |
EGF
|
345 |
373 |
1.87e1 |
SMART |
EGF
|
376 |
404 |
3.97e0 |
SMART |
EGF
|
407 |
435 |
8.52e0 |
SMART |
EGF
|
438 |
466 |
3.01e0 |
SMART |
EGF
|
469 |
497 |
3.46e0 |
SMART |
EGF
|
500 |
528 |
3.71e0 |
SMART |
EGF
|
531 |
559 |
4.32e-1 |
SMART |
EGF
|
562 |
590 |
1.84e1 |
SMART |
EGF
|
593 |
621 |
3.82e-2 |
SMART |
FN3
|
623 |
701 |
8.9e-8 |
SMART |
FN3
|
712 |
794 |
1.53e-6 |
SMART |
FN3
|
803 |
884 |
7.23e-8 |
SMART |
FN3
|
893 |
974 |
1.71e-9 |
SMART |
FN3
|
985 |
1062 |
2.56e-8 |
SMART |
FN3
|
1074 |
1152 |
8.58e-1 |
SMART |
FN3
|
1165 |
1245 |
2.72e-3 |
SMART |
FN3
|
1256 |
1334 |
5.36e-2 |
SMART |
FN3
|
1347 |
1427 |
4.93e0 |
SMART |
FN3
|
1438 |
1517 |
3.4e-4 |
SMART |
FN3
|
1528 |
1606 |
1.55e-7 |
SMART |
FN3
|
1617 |
1694 |
1.53e-6 |
SMART |
FN3
|
1705 |
1782 |
7.75e-8 |
SMART |
FBG
|
1797 |
2007 |
4.08e-124 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000107371
AA Change: G229D
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000102994 Gene: ENSMUSG00000028364 AA Change: G229D
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
22 |
N/A |
INTRINSIC |
low complexity region
|
121 |
138 |
N/A |
INTRINSIC |
Pfam:hEGF
|
173 |
185 |
4e-4 |
PFAM |
EGF
|
189 |
217 |
1.87e1 |
SMART |
EGF_like
|
220 |
248 |
3.5e1 |
SMART |
EGF
|
251 |
280 |
4.89e0 |
SMART |
EGF
|
283 |
311 |
3.23e0 |
SMART |
EGF_like
|
314 |
342 |
2.98e1 |
SMART |
EGF
|
345 |
373 |
1.87e1 |
SMART |
EGF
|
376 |
404 |
3.97e0 |
SMART |
EGF
|
407 |
435 |
8.52e0 |
SMART |
EGF
|
438 |
466 |
3.01e0 |
SMART |
EGF
|
469 |
497 |
3.46e0 |
SMART |
EGF
|
500 |
528 |
3.71e0 |
SMART |
EGF
|
531 |
559 |
4.32e-1 |
SMART |
EGF
|
562 |
590 |
1.84e1 |
SMART |
EGF
|
593 |
621 |
3.82e-2 |
SMART |
FN3
|
623 |
701 |
8.9e-8 |
SMART |
FN3
|
712 |
794 |
1.53e-6 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000107372
AA Change: G229D
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000102995 Gene: ENSMUSG00000028364 AA Change: G229D
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
22 |
N/A |
INTRINSIC |
low complexity region
|
121 |
138 |
N/A |
INTRINSIC |
EGF
|
189 |
217 |
1.87e1 |
SMART |
EGF_like
|
220 |
248 |
3.5e1 |
SMART |
EGF
|
251 |
280 |
4.89e0 |
SMART |
EGF
|
283 |
311 |
3.23e0 |
SMART |
EGF_like
|
314 |
342 |
2.98e1 |
SMART |
EGF
|
345 |
373 |
1.87e1 |
SMART |
EGF
|
376 |
404 |
3.97e0 |
SMART |
EGF
|
407 |
435 |
8.52e0 |
SMART |
EGF
|
438 |
466 |
3.01e0 |
SMART |
EGF
|
469 |
497 |
3.46e0 |
SMART |
EGF
|
500 |
528 |
3.71e0 |
SMART |
EGF
|
531 |
559 |
4.32e-1 |
SMART |
EGF
|
562 |
590 |
1.84e1 |
SMART |
EGF
|
593 |
621 |
3.82e-2 |
SMART |
FN3
|
623 |
701 |
8.9e-8 |
SMART |
FN3
|
712 |
794 |
1.53e-6 |
SMART |
FN3
|
803 |
884 |
7.23e-8 |
SMART |
FN3
|
893 |
974 |
1.71e-9 |
SMART |
FN3
|
985 |
1062 |
2.56e-8 |
SMART |
FN3
|
1074 |
1152 |
8.58e-1 |
SMART |
FN3
|
1165 |
1245 |
2.72e-3 |
SMART |
FN3
|
1256 |
1334 |
5.36e-2 |
SMART |
FN3
|
1347 |
1427 |
4.93e0 |
SMART |
FN3
|
1438 |
1517 |
2.75e0 |
SMART |
FN3
|
1529 |
1608 |
3.4e-4 |
SMART |
FN3
|
1619 |
1697 |
1.55e-7 |
SMART |
FN3
|
1708 |
1785 |
1.53e-6 |
SMART |
FN3
|
1796 |
1873 |
7.75e-8 |
SMART |
FBG
|
1888 |
2098 |
4.08e-124 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000107377
AA Change: G229D
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000103000 Gene: ENSMUSG00000028364 AA Change: G229D
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
22 |
N/A |
INTRINSIC |
low complexity region
|
121 |
138 |
N/A |
INTRINSIC |
EGF
|
189 |
217 |
1.87e1 |
SMART |
EGF_like
|
220 |
248 |
3.5e1 |
SMART |
EGF
|
251 |
280 |
4.89e0 |
SMART |
EGF
|
283 |
311 |
3.23e0 |
SMART |
EGF_like
|
314 |
342 |
2.98e1 |
SMART |
EGF
|
345 |
373 |
1.87e1 |
SMART |
EGF
|
376 |
404 |
3.97e0 |
SMART |
EGF
|
407 |
435 |
8.52e0 |
SMART |
EGF
|
438 |
466 |
3.01e0 |
SMART |
EGF
|
469 |
497 |
3.46e0 |
SMART |
EGF
|
500 |
528 |
3.71e0 |
SMART |
EGF
|
531 |
559 |
4.32e-1 |
SMART |
EGF
|
562 |
590 |
1.84e1 |
SMART |
EGF
|
593 |
621 |
3.82e-2 |
SMART |
FN3
|
623 |
701 |
8.9e-8 |
SMART |
FN3
|
712 |
794 |
1.53e-6 |
SMART |
FN3
|
803 |
884 |
7.23e-8 |
SMART |
FN3
|
893 |
974 |
1.71e-9 |
SMART |
FN3
|
985 |
1062 |
2.56e-8 |
SMART |
FN3
|
1074 |
1152 |
8.58e-1 |
SMART |
FN3
|
1165 |
1245 |
2.72e-3 |
SMART |
FN3
|
1256 |
1334 |
5.36e-2 |
SMART |
FN3
|
1347 |
1427 |
4.93e0 |
SMART |
FN3
|
1438 |
1517 |
3.4e-4 |
SMART |
FN3
|
1528 |
1606 |
1.55e-7 |
SMART |
FN3
|
1617 |
1694 |
1.53e-6 |
SMART |
FN3
|
1705 |
1782 |
7.75e-8 |
SMART |
FBG
|
1797 |
2007 |
4.08e-124 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000135042
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000141428
|
Coding Region Coverage |
- 1x: 98.1%
- 3x: 97.0%
- 10x: 94.3%
- 20x: 88.0%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes an extracellular matrix protein with a spatially and temporally restricted tissue distribution. This protein is homohexameric with disulfide-linked subunits, and contains multiple EGF-like and fibronectin type-III domains. It is implicated in guidance of migrating neurons as well as axons during development, synaptic plasticity, and neuronal regeneration. [provided by RefSeq, Jul 2011] PHENOTYPE: Mice homozygous for several different targeted mutations show variable behavioral and nervous system phenotypes such as abnormal circadian rhythm, anxiety behavior, novelty-induced activity, swimming, impaired synaptic plasticity, long term potentiation and serotonin and dopamine neurotransmission. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 30 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgre4 |
G |
A |
17: 55,852,288 |
V658I |
probably benign |
Het |
Ccdc40 |
T |
C |
11: 119,232,118 |
Y249H |
possibly damaging |
Het |
D6Ertd527e |
C |
G |
6: 87,111,524 |
T223S |
unknown |
Homo |
Gbp4 |
G |
A |
5: 105,121,106 |
R394C |
possibly damaging |
Het |
Gpr183 |
C |
A |
14: 121,954,476 |
C211F |
probably damaging |
Homo |
Lcp1 |
A |
T |
14: 75,227,006 |
I556F |
possibly damaging |
Het |
Letm1 |
G |
A |
5: 33,747,444 |
P513S |
probably benign |
Het |
Letm1 |
G |
A |
5: 33,747,446 |
P512L |
probably benign |
Het |
Msh3 |
A |
G |
13: 92,346,786 |
V283A |
possibly damaging |
Het |
Nfkb2 |
G |
T |
19: 46,307,567 |
E170D |
probably benign |
Het |
Npr3 |
C |
A |
15: 11,848,563 |
M439I |
probably benign |
Het |
Olfr1023 |
A |
T |
2: 85,887,438 |
I213F |
possibly damaging |
Het |
Olfr1034 |
A |
T |
2: 86,047,055 |
H191L |
probably benign |
Het |
Pax5 |
G |
A |
4: 44,691,886 |
A120V |
probably damaging |
Het |
Plcb1 |
A |
G |
2: 135,337,499 |
Y609C |
probably damaging |
Het |
Plxna1 |
G |
A |
6: 89,357,336 |
H104Y |
probably benign |
Homo |
Rnf213 |
A |
T |
11: 119,414,469 |
I509F |
probably damaging |
Het |
Ryr2 |
T |
C |
13: 11,869,156 |
S213G |
probably damaging |
Homo |
Spint1 |
A |
G |
2: 119,245,615 |
T231A |
probably damaging |
Het |
Tbcel |
C |
A |
9: 42,444,500 |
C139F |
probably benign |
Het |
Thbs2 |
A |
C |
17: 14,679,973 |
S573A |
probably benign |
Het |
Tmem43 |
C |
A |
6: 91,482,318 |
P257Q |
probably benign |
Homo |
Tmprss13 |
A |
G |
9: 45,337,132 |
|
probably null |
Het |
Ugt1a10 |
TTCATCA |
TTCA |
1: 88,216,158 |
|
probably benign |
Het |
Vmn1r196 |
T |
A |
13: 22,293,836 |
V215D |
probably damaging |
Homo |
Vmn1r22 |
G |
T |
6: 57,900,332 |
T220K |
probably benign |
Homo |
Vmn2r116 |
G |
A |
17: 23,387,279 |
M388I |
possibly damaging |
Het |
Zap70 |
A |
G |
1: 36,770,811 |
M1V |
probably null |
Homo |
Zfp282 |
A |
G |
6: 47,897,881 |
D340G |
probably damaging |
Homo |
Zfp282 |
T |
A |
6: 47,905,053 |
I558N |
possibly damaging |
Homo |
|
Other mutations in Tnc |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00229:Tnc
|
APN |
4 |
64016824 |
splice site |
probably benign |
|
IGL00531:Tnc
|
APN |
4 |
63971153 |
splice site |
probably benign |
|
IGL00674:Tnc
|
APN |
4 |
63965607 |
missense |
probably damaging |
1.00 |
IGL01015:Tnc
|
APN |
4 |
64017334 |
missense |
probably benign |
0.19 |
IGL01090:Tnc
|
APN |
4 |
64000080 |
missense |
probably damaging |
1.00 |
IGL01310:Tnc
|
APN |
4 |
64013077 |
missense |
probably benign |
0.03 |
IGL01331:Tnc
|
APN |
4 |
63982875 |
missense |
probably damaging |
0.99 |
IGL01393:Tnc
|
APN |
4 |
64014054 |
splice site |
probably benign |
|
IGL01411:Tnc
|
APN |
4 |
64000722 |
missense |
probably damaging |
0.96 |
IGL01472:Tnc
|
APN |
4 |
64006419 |
missense |
probably benign |
0.00 |
IGL01552:Tnc
|
APN |
4 |
63970408 |
missense |
probably damaging |
1.00 |
IGL01661:Tnc
|
APN |
4 |
63970307 |
splice site |
probably benign |
|
IGL01669:Tnc
|
APN |
4 |
64000701 |
missense |
probably damaging |
1.00 |
IGL01912:Tnc
|
APN |
4 |
64008740 |
missense |
probably damaging |
1.00 |
IGL02028:Tnc
|
APN |
4 |
63966672 |
splice site |
probably benign |
|
IGL02100:Tnc
|
APN |
4 |
64000161 |
missense |
possibly damaging |
0.84 |
IGL02549:Tnc
|
APN |
4 |
64015072 |
missense |
probably damaging |
1.00 |
IGL02642:Tnc
|
APN |
4 |
63965579 |
splice site |
probably benign |
|
IGL02712:Tnc
|
APN |
4 |
63975256 |
missense |
probably damaging |
1.00 |
IGL02876:Tnc
|
APN |
4 |
64015101 |
missense |
possibly damaging |
0.56 |
IGL02886:Tnc
|
APN |
4 |
64000107 |
missense |
probably damaging |
0.96 |
IGL02972:Tnc
|
APN |
4 |
63976478 |
missense |
probably benign |
0.11 |
IGL03073:Tnc
|
APN |
4 |
63971224 |
missense |
possibly damaging |
0.58 |
IGL03116:Tnc
|
APN |
4 |
64014033 |
missense |
probably damaging |
1.00 |
IGL03181:Tnc
|
APN |
4 |
63967306 |
missense |
possibly damaging |
0.95 |
IGL03358:Tnc
|
APN |
4 |
64017615 |
nonsense |
probably null |
|
tancredo
|
UTSW |
4 |
63993297 |
nonsense |
probably null |
|
BB009:Tnc
|
UTSW |
4 |
64008620 |
missense |
probably benign |
|
BB019:Tnc
|
UTSW |
4 |
64008620 |
missense |
probably benign |
|
P0020:Tnc
|
UTSW |
4 |
64008857 |
missense |
possibly damaging |
0.63 |
PIT4377001:Tnc
|
UTSW |
4 |
64017736 |
missense |
probably damaging |
1.00 |
PIT4403001:Tnc
|
UTSW |
4 |
63964667 |
missense |
probably damaging |
1.00 |
PIT4468001:Tnc
|
UTSW |
4 |
63964667 |
missense |
probably damaging |
1.00 |
R0243:Tnc
|
UTSW |
4 |
63970420 |
missense |
probably damaging |
0.98 |
R0362:Tnc
|
UTSW |
4 |
64017442 |
missense |
probably damaging |
1.00 |
R0410:Tnc
|
UTSW |
4 |
64007694 |
missense |
probably benign |
0.00 |
R0420:Tnc
|
UTSW |
4 |
64000159 |
missense |
probably benign |
0.00 |
R0540:Tnc
|
UTSW |
4 |
64020455 |
missense |
probably damaging |
1.00 |
R0650:Tnc
|
UTSW |
4 |
64008734 |
missense |
probably benign |
0.00 |
R1019:Tnc
|
UTSW |
4 |
63962082 |
missense |
probably damaging |
1.00 |
R1102:Tnc
|
UTSW |
4 |
64020468 |
missense |
probably benign |
0.05 |
R1126:Tnc
|
UTSW |
4 |
64018120 |
missense |
probably damaging |
0.99 |
R1141:Tnc
|
UTSW |
4 |
64013994 |
missense |
probably damaging |
1.00 |
R1142:Tnc
|
UTSW |
4 |
64013994 |
missense |
probably damaging |
1.00 |
R1307:Tnc
|
UTSW |
4 |
64008859 |
missense |
probably damaging |
0.98 |
R1322:Tnc
|
UTSW |
4 |
64013994 |
missense |
probably damaging |
1.00 |
R1414:Tnc
|
UTSW |
4 |
63965695 |
splice site |
probably benign |
|
R1470:Tnc
|
UTSW |
4 |
63966574 |
missense |
probably damaging |
1.00 |
R1470:Tnc
|
UTSW |
4 |
63966574 |
missense |
probably damaging |
1.00 |
R1499:Tnc
|
UTSW |
4 |
63964754 |
missense |
probably benign |
0.15 |
R1506:Tnc
|
UTSW |
4 |
64007684 |
missense |
possibly damaging |
0.90 |
R1597:Tnc
|
UTSW |
4 |
64006384 |
missense |
probably benign |
|
R1750:Tnc
|
UTSW |
4 |
63972735 |
missense |
probably damaging |
1.00 |
R1765:Tnc
|
UTSW |
4 |
64013994 |
missense |
probably damaging |
1.00 |
R1783:Tnc
|
UTSW |
4 |
64018096 |
missense |
probably damaging |
0.98 |
R1808:Tnc
|
UTSW |
4 |
63999931 |
missense |
probably damaging |
1.00 |
R1903:Tnc
|
UTSW |
4 |
64000062 |
missense |
probably benign |
0.00 |
R1932:Tnc
|
UTSW |
4 |
63993025 |
critical splice donor site |
probably null |
|
R1941:Tnc
|
UTSW |
4 |
64014964 |
missense |
probably damaging |
1.00 |
R1983:Tnc
|
UTSW |
4 |
63984630 |
missense |
possibly damaging |
0.95 |
R2024:Tnc
|
UTSW |
4 |
63964621 |
missense |
probably damaging |
1.00 |
R2075:Tnc
|
UTSW |
4 |
63995666 |
missense |
possibly damaging |
0.94 |
R2327:Tnc
|
UTSW |
4 |
63975238 |
missense |
possibly damaging |
0.78 |
R2444:Tnc
|
UTSW |
4 |
64014963 |
missense |
probably damaging |
1.00 |
R2982:Tnc
|
UTSW |
4 |
64020519 |
missense |
possibly damaging |
0.81 |
R3874:Tnc
|
UTSW |
4 |
64008710 |
missense |
probably damaging |
1.00 |
R4110:Tnc
|
UTSW |
4 |
64014951 |
missense |
probably damaging |
1.00 |
R4360:Tnc
|
UTSW |
4 |
64016924 |
missense |
probably benign |
0.35 |
R4371:Tnc
|
UTSW |
4 |
63970351 |
missense |
probably damaging |
1.00 |
R4434:Tnc
|
UTSW |
4 |
64007829 |
missense |
possibly damaging |
0.91 |
R4438:Tnc
|
UTSW |
4 |
64007829 |
missense |
possibly damaging |
0.91 |
R4570:Tnc
|
UTSW |
4 |
63995672 |
missense |
probably damaging |
0.99 |
R4595:Tnc
|
UTSW |
4 |
63995745 |
missense |
probably damaging |
1.00 |
R4749:Tnc
|
UTSW |
4 |
63995639 |
missense |
possibly damaging |
0.56 |
R4756:Tnc
|
UTSW |
4 |
63967343 |
missense |
probably damaging |
0.99 |
R4824:Tnc
|
UTSW |
4 |
64017620 |
nonsense |
probably null |
|
R4957:Tnc
|
UTSW |
4 |
63976556 |
missense |
probably damaging |
1.00 |
R4977:Tnc
|
UTSW |
4 |
64006248 |
missense |
possibly damaging |
0.82 |
R5001:Tnc
|
UTSW |
4 |
63984489 |
missense |
probably damaging |
1.00 |
R5001:Tnc
|
UTSW |
4 |
64000062 |
missense |
probably benign |
0.16 |
R5015:Tnc
|
UTSW |
4 |
64006502 |
missense |
probably damaging |
1.00 |
R5049:Tnc
|
UTSW |
4 |
64017986 |
missense |
probably damaging |
1.00 |
R5066:Tnc
|
UTSW |
4 |
63975229 |
missense |
probably damaging |
0.96 |
R5073:Tnc
|
UTSW |
4 |
64020411 |
missense |
probably damaging |
1.00 |
R5116:Tnc
|
UTSW |
4 |
63967215 |
critical splice donor site |
probably null |
|
R5195:Tnc
|
UTSW |
4 |
63967252 |
missense |
probably damaging |
1.00 |
R5200:Tnc
|
UTSW |
4 |
63971278 |
missense |
probably damaging |
1.00 |
R5221:Tnc
|
UTSW |
4 |
63993297 |
nonsense |
probably null |
|
R5237:Tnc
|
UTSW |
4 |
63962096 |
missense |
probably damaging |
1.00 |
R5265:Tnc
|
UTSW |
4 |
63993206 |
missense |
probably benign |
0.00 |
R5275:Tnc
|
UTSW |
4 |
63964730 |
nonsense |
probably null |
|
R5346:Tnc
|
UTSW |
4 |
64008655 |
missense |
probably benign |
|
R5409:Tnc
|
UTSW |
4 |
63966536 |
missense |
probably damaging |
1.00 |
R5409:Tnc
|
UTSW |
4 |
64007417 |
missense |
probably damaging |
1.00 |
R5469:Tnc
|
UTSW |
4 |
64013925 |
splice site |
probably null |
|
R5518:Tnc
|
UTSW |
4 |
64017679 |
missense |
probably damaging |
1.00 |
R5560:Tnc
|
UTSW |
4 |
64008709 |
missense |
probably damaging |
1.00 |
R5588:Tnc
|
UTSW |
4 |
64006422 |
missense |
possibly damaging |
0.57 |
R5686:Tnc
|
UTSW |
4 |
64007730 |
splice site |
probably null |
|
R5686:Tnc
|
UTSW |
4 |
64008795 |
missense |
possibly damaging |
0.78 |
R5837:Tnc
|
UTSW |
4 |
64013214 |
missense |
probably damaging |
1.00 |
R5976:Tnc
|
UTSW |
4 |
64018166 |
missense |
probably benign |
0.17 |
R6156:Tnc
|
UTSW |
4 |
63970352 |
missense |
probably damaging |
1.00 |
R6182:Tnc
|
UTSW |
4 |
64008796 |
missense |
probably damaging |
0.99 |
R6360:Tnc
|
UTSW |
4 |
64000733 |
missense |
probably damaging |
1.00 |
R6416:Tnc
|
UTSW |
4 |
64007816 |
missense |
probably benign |
0.05 |
R6778:Tnc
|
UTSW |
4 |
63995598 |
missense |
probably benign |
0.12 |
R6798:Tnc
|
UTSW |
4 |
63965604 |
missense |
probably benign |
0.02 |
R6799:Tnc
|
UTSW |
4 |
63965604 |
missense |
probably benign |
0.02 |
R6943:Tnc
|
UTSW |
4 |
63982745 |
missense |
probably damaging |
0.97 |
R7027:Tnc
|
UTSW |
4 |
63984589 |
missense |
probably benign |
0.02 |
R7183:Tnc
|
UTSW |
4 |
64013128 |
missense |
probably damaging |
1.00 |
R7204:Tnc
|
UTSW |
4 |
63971155 |
splice site |
probably null |
|
R7317:Tnc
|
UTSW |
4 |
63972722 |
missense |
probably damaging |
0.99 |
R7323:Tnc
|
UTSW |
4 |
63971232 |
missense |
probably damaging |
0.96 |
R7327:Tnc
|
UTSW |
4 |
63964762 |
splice site |
probably null |
|
R7382:Tnc
|
UTSW |
4 |
64014043 |
nonsense |
probably null |
|
R7399:Tnc
|
UTSW |
4 |
64020657 |
start gained |
probably benign |
|
R7479:Tnc
|
UTSW |
4 |
64017628 |
missense |
possibly damaging |
0.95 |
R7585:Tnc
|
UTSW |
4 |
64020411 |
missense |
probably damaging |
1.00 |
R7932:Tnc
|
UTSW |
4 |
64008620 |
missense |
probably benign |
|
R7947:Tnc
|
UTSW |
4 |
64017343 |
missense |
probably damaging |
1.00 |
R7974:Tnc
|
UTSW |
4 |
64000724 |
missense |
possibly damaging |
0.84 |
R7991:Tnc
|
UTSW |
4 |
64008746 |
missense |
probably benign |
0.42 |
R8004:Tnc
|
UTSW |
4 |
63984657 |
missense |
probably benign |
0.04 |
R8080:Tnc
|
UTSW |
4 |
63976469 |
missense |
possibly damaging |
0.52 |
R8109:Tnc
|
UTSW |
4 |
64008763 |
missense |
probably benign |
0.11 |
R8145:Tnc
|
UTSW |
4 |
64017479 |
missense |
probably benign |
|
R8340:Tnc
|
UTSW |
4 |
64007799 |
missense |
probably damaging |
1.00 |
R8360:Tnc
|
UTSW |
4 |
63967274 |
missense |
probably benign |
0.00 |
R8671:Tnc
|
UTSW |
4 |
64017446 |
missense |
probably damaging |
1.00 |
R8691:Tnc
|
UTSW |
4 |
63962076 |
missense |
probably damaging |
1.00 |
R8759:Tnc
|
UTSW |
4 |
64006264 |
missense |
possibly damaging |
0.86 |
R8864:Tnc
|
UTSW |
4 |
63993059 |
missense |
probably damaging |
0.98 |
R8927:Tnc
|
UTSW |
4 |
64007358 |
missense |
probably damaging |
1.00 |
R8928:Tnc
|
UTSW |
4 |
64007358 |
missense |
probably damaging |
1.00 |
R8949:Tnc
|
UTSW |
4 |
64008850 |
missense |
probably damaging |
1.00 |
R8956:Tnc
|
UTSW |
4 |
64000733 |
missense |
probably damaging |
1.00 |
R9016:Tnc
|
UTSW |
4 |
64017094 |
missense |
probably benign |
0.23 |
R9049:Tnc
|
UTSW |
4 |
64000010 |
missense |
possibly damaging |
0.83 |
R9097:Tnc
|
UTSW |
4 |
63970385 |
missense |
possibly damaging |
0.62 |
R9114:Tnc
|
UTSW |
4 |
63972736 |
missense |
probably benign |
0.03 |
R9151:Tnc
|
UTSW |
4 |
64020449 |
missense |
possibly damaging |
0.46 |
R9488:Tnc
|
UTSW |
4 |
63995705 |
missense |
probably damaging |
0.99 |
R9537:Tnc
|
UTSW |
4 |
63966584 |
missense |
probably damaging |
0.99 |
R9666:Tnc
|
UTSW |
4 |
64007808 |
missense |
probably damaging |
1.00 |
R9700:Tnc
|
UTSW |
4 |
64014949 |
missense |
probably damaging |
0.99 |
R9703:Tnc
|
UTSW |
4 |
63971175 |
missense |
probably benign |
0.00 |
R9771:Tnc
|
UTSW |
4 |
64007363 |
missense |
probably damaging |
1.00 |
Z1177:Tnc
|
UTSW |
4 |
63960544 |
critical splice acceptor site |
probably null |
|
Z1177:Tnc
|
UTSW |
4 |
64007426 |
nonsense |
probably null |
|
|
Predicted Primers |
PCR Primer
(F):5'- ATTGTAGCAGTTGTTGAGGCAAAG -3'
(R):5'- TCAATGCAGGTCGTCTGGAC -3'
Sequencing Primer
(F):5'- AAAGGGGCTCGTTGCAGTC -3'
(R):5'- ACGGGGCAACTTCAGTG -3'
|
Posted On |
2016-05-10 |