Global Variome shared LOVD
LINC00242 (long intergenic non-protein coding RNA 242)
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Phenotypes for disease #02997 (CLN7 (lipofuscinosis, ceroid, neuronal, type 7 (CLN7)), OMIM:610951)
Legend
Please note that a short description of a certain column can be displayed when you move your mouse cursor over the column's header and hold it still. Below, a more detailed description is shown per column.
Phenotype details
: additional information on the phenotype of the individual, preferably use HPO terms only (http://www.human-phenotype-ontology.org/)
Diagnosis/Initial
: initial diagnosis, before molecular testing
Diagnosis/Definite
: phenotype individual after molecular testing (OMIM abbreviation)
Inheritance
: Indicates the inheritance of the phenotype in the family; unknown, familial (autosomal/X-linked, dominant/ recessive), paternal (Y-linked), maternal (mitochondrial), isolated (sporadic) or complex
All options:
Unknown
Familial
Familial, autosomal dominant
Familial, autosomal recessive
Familial, X-linked
Familial, X-linked dominant
Familial, X-linked dominant, male sparing
Familial, X-linked recessive
Paternal, Y-linked
Maternal, mitochondrial
Isolated (sporadic)
Di-genic
Complex
- = Not applicable
Age/Examination
: age at which the individual was examined.
35y = 35 years
04y08m = 4 years and 8 months
00y00m01d12h = 1 day and 12 hours
18y? = around 18 years
30y-40y = between 30 and 40 years
>54y = older than 54
? = unknown
Age/Diagnosis
: age diagnosis was confirmed
35y = 35 years
04y08m = 4 years and 8 months
00y00m01d12h = 1 day and 12 hours
18y? = around 18 years
30y-40y = between 30 and 40 years
>54y = older than 54
? = unknown
Age/Onset
: Age first symptoms disease appeared in individual:
35y = 35 years
04y08m = 4 years and 8 months
00y00m01d12h = 1 day and 12 hours
18y? = around 18 years
30y-40y = between 30 and 40 years
>54y = older than 54
? = unknown
Phenotype/Onset
: individual's phenotype at Age/Onset described using HPO
Protein
: result from protein staining
How to query this table
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Column type
Example
Matches
Text
Arg
all entries containing 'Arg'
space
Text
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|
Text
Arg|Ser
all entries containing 'Arg' or 'Ser'
!
Text
!fs
all entries not containing 'fs'
^
Text
^p.(Arg
all entries beginning with 'p.(Arg'
$
Text
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all entries ending with 'Ser)'
=""
Text
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all entries with this field empty
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Text
="p.0"
all entries exactly matching 'p.0'
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Text
!=""
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!=""
Text
!="p.0"
all entries not exactly matching 'p.0?'
combination
Text
*|Ter !fs
all entries containing '*' or 'Ter' but not containing 'fs'
Date
2020
all entries matching the year 2020
|
Date
2020-03|2020-04
all entries matching March or April, 2020
!
Date
!2020-03
all entries not matching March, 2020
<
Date
<2020
all entries before the year 2020
<=
Date
<=2020-06
all entries in or before June, 2020
>
Date
>2020-06
all entries after June, 2020
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Date
>=2020-06-15
all entries on or after June 15th, 2020
combination
Date
2019|2020 <2020-03
all entries in 2019 or 2020, and before March, 2020
Numeric
23
all entries exactly matching 23
|
Numeric
23|24
all entries exactly matching 23 or 24
!
Numeric
!23
all entries not exactly matching 23
<
Numeric
<23
all entries lower than 23
<=
Numeric
<=23
all entries lower than, or equal to, 23
>
Numeric
>23
all entries higher than 23
>=
Numeric
>=23
all entries higher than, or equal to, 23
combination
Numeric
>=20 <30 !23
all entries with values from 20 to 29, but not equal to 23
Some more advanced examples:
Example
Matches
Asian
all entries containing 'Asian', 'asian', including 'Caucasian', 'caucasian', etc.
Asian !Caucasian
all entries containing 'Asian' but not containing 'Caucasian'
Asian|African !Caucasian
all entries containing 'Asian' or 'African', but not containing 'Caucasian'
"South Asian"
all entries containing 'South Asian', but not containing 'South East Asian'
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81 entries on 1 page. Showing entries 1 - 81.
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How to query
Phenotype ID
Phenotype details
Diagnosis/Initial
Diagnosis/Definite
Inheritance
Age/Examination
Age/Diagnosis
Age/Onset
Phenotype/Onset
Protein
Owner
Individual ID
0000060506
Ceroid lipofuscinosis, neuronal, 7 (OMIM:610951)
-
-
Familial, autosomal recessive
-
-
-
-
-
Daniel Trujillano
00080937
0000060625
Ceroid lipofuscinosis, neuronal, 7 (OMIM:610951)
-
-
Familial, autosomal recessive
-
-
-
-
-
Daniel Trujillano
00081056
0000172891
Fingerprint/Curvilinear/Granular Osmiophilic Deposits
-
-
-
-
-
5y
late infantile
-
Sara Mole
00229684
0000172893
Fingerprint
-
-
-
-
-
-
late infantile
-
Sara Mole
00229686
0000172894
Fingerprint/Curvilinear
-
-
-
-
-
2y6m
late infantile
-
Sara Mole
00229687
0000172895
Fingerprint/Curvilinear
-
-
-
-
-
5y6m
late infantile
-
Sara Mole
00229688
0000172896
-
-
-
-
-
-
3y
late infantile
-
Sara Mole
00229689
0000172897
-
-
-
-
-
-
-
late infantile
-
Sara Mole
00229690
0000172898
Fingerprint/Curvilinear
-
-
-
-
-
3y
late infantile
-
Sara Mole
00229691
0000172899
-
-
-
-
-
-
-
late infantile
-
Sara Mole
00229692
0000172900
-
-
-
-
-
-
?
late infantile
-
Sara Mole
00229693
0000172902
no visual failure reported
-
-
-
-
-
5y
late infantile
-
Sara Mole
00229695
0000172903
no visual failure reported
-
-
-
-
-
5y
late infantile
-
Sara Mole
00229696
0000172904
no visual failure reported
-
-
-
-
-
5y
late infantile
-
Sara Mole
00229697
0000172905
Fingerprint/Curvilinear/Granular Osmiophilic Deposits
-
-
-
-
-
2y9m
late infantile
-
Sara Mole
00229698
0000172906
n.a.
-
-
-
-
-
-
late infantile
-
Sara Mole
00229699
0000172907
-
-
-
-
-
-
11y
juvenile
-
Sara Mole
00229700
0000172909
Fingerprint
-
-
-
-
-
-
late infantile
-
Sara Mole
00229702
0000172910
-
-
-
-
-
-
3y
late infantile
-
Sara Mole
00229703
0000172911
-
-
-
-
-
-
4y
late infantile
-
Sara Mole
00229704
0000172912
Fingerprint/Curvilinear
-
-
-
-
-
4y
late infantile
-
Sara Mole
00229705
0000172913
Fingerprint
-
-
-
-
-
3y
late infantile
-
Sara Mole
00229706
0000172914
-
-
-
-
-
-
-
late infantile
-
Sara Mole
00229707
0000172915
-
-
-
-
-
-
5y
late infantile
-
Sara Mole
00229708
0000172916
Fingerprint
-
-
-
-
-
3y
late infantile
-
Sara Mole
00229709
0000172917
-
-
-
-
-
-
2y6m
late infantile
-
Sara Mole
00229710
0000172918
Fingerprint/Curvilinear/Rectilinear
-
-
-
-
-
3y6m
late infantile
-
Sara Mole
00229711
0000172919
-
-
-
-
-
-
-
late infantile
-
Sara Mole
00229712
0000172920
-
-
-
-
-
-
-
late infantile
-
Sara Mole
00229713
0000172921
-
-
-
-
-
-
3y
late infantile
-
Sara Mole
00229714
0000172922
-
-
-
-
-
-
-
late infantile
-
Sara Mole
00229715
0000172923
-
-
-
-
-
-
-
late infantile
-
Sara Mole
00229716
0000172924
-
-
-
-
-
-
-
late infantile
-
Sara Mole
00229717
0000172925
-
-
-
-
-
-
-
late infantile
-
Sara Mole
00229718
0000172926
-
-
-
-
-
-
-
late infantile
-
Sara Mole
00229719
0000172927
-
-
-
-
-
-
5y
late infantile
-
Sara Mole
00229720
0000172928
Fingerprint/Curvilinear
-
-
-
-
-
2y
late infantile
-
Sara Mole
00229721
0000172929
Fingerprint/Curvilinear
-
-
-
-
-
6y
late infantile
-
Sara Mole
00229722
0000172930
-
-
-
-
-
-
3y6m
late infantile
-
Sara Mole
00229723
0000172931
-
-
-
-
-
-
4y
late infantile
-
Sara Mole
00229724
0000172932
Fingerprint/Curvilinear/Rectilinear
-
-
-
-
-
4y
late infantile
-
Sara Mole
00229725
0000172933
Fingerprint/Curvilinear/Rectilinear
-
-
-
-
-
2y6m
late infantile
-
Sara Mole
00229726
0000172934
Fingerprint/Curvilinear/Rectilinear
-
-
-
-
-
3y6m
late infantile
-
Sara Mole
00229727
0000172935
Fingerprint/Curvilinear/Rectilinear
-
-
-
-
-
2y6m
late infantile
-
Sara Mole
00229728
0000172936
Fingerprint/Curvilinear/Rectilinear
-
-
-
-
-
4y
late infantile
-
Sara Mole
00229729
0000172937
Fingerprint/Curvilinear/Rectilinear
-
-
-
-
-
4y
late infantile
-
Sara Mole
00229730
0000172938
Fingerprint/Curvilinear/Rectilinear
-
-
-
-
-
2y
late infantile
-
Sara Mole
00229731
0000172939
Fingerprint/Curvilinear/Rectilinear
-
-
-
-
-
5y
late infantile
-
Sara Mole
00229732
0000172940
Fingerprint/Curvilinear/Rectilinear
-
-
-
-
-
4y
late infantile
-
Sara Mole
00229733
0000172941
Fingerprint/Curvilinear/Rectilinear
-
-
-
-
-
4y6m
late infantile
-
Sara Mole
00229734
0000172942
Fingerprint/Curvilinear/Rectilinear
-
-
-
-
-
1y6m
late infantile
-
Sara Mole
00229735
0000172943
Fingerprint/Curvilinear/Rectilinear
-
-
-
-
-
2y
late infantile
-
Sara Mole
00229736
0000172944
Fingerprint/Curvilinear/Rectilinear
-
-
-
-
-
2y
late infantile
-
Sara Mole
00229737
0000172945
Fingerprint/Curvilinear/Rectilinear
-
-
-
-
-
2y
late infantile
-
Sara Mole
00229738
0000172946
-
-
-
-
-
-
3y
late infantile
-
Sara Mole
00229739
0000172947
Fingerprint/Curvilinear/Rectilinear
-
-
-
-
-
4y
late infantile
-
Sara Mole
00229740
0000172948
Fingerprint/Granular Osmiophilic Deposits
-
-
-
-
-
2y
late infantile
-
Sara Mole
00229741
0000172949
-
-
-
-
-
-
-
late infantile
-
Sara Mole
00229742
0000172950
-
-
-
-
-
-
-
late infantile
-
Sara Mole
00229743
0000172951
-
-
-
-
-
-
4y
late infantile
-
Sara Mole
00229744
0000172952
-
-
-
-
-
-
3y
late infantile
-
Sara Mole
00229745
0000172953
Fingerprint
-
-
-
-
-
6y
late infantile
-
Sara Mole
00229746
0000172954
-
-
-
-
-
-
-
late infantile
-
Sara Mole
00229747
0000172955
?
-
-
-
-
-
?
late infantile
-
Sara Mole
00229748
0000172957
No vacuoles
-
-
-
-
-
3y6m
late infantile
-
Sara Mole
00229750
0000172958
Fingerprint/Curvilinear
-
-
-
-
-
2y
late infantile
-
Sara Mole
00229751
0000172959
No inclusions
-
-
-
-
-
6y
late infantile
-
Sara Mole
00229752
0000172960
No inclusions
-
-
-
-
-
7y
late infantile
-
Sara Mole
00229753
0000172961
No inclusions
-
-
-
-
-
7y
late infantile
-
Sara Mole
00229754
0000172963
Fingerprint
-
-
-
-
-
5y
late infantile
-
Sara Mole
00229756
0000172964
Fingerprint/Curvilinear
-
-
-
-
-
4y6m
late infantile
-
Sara Mole
00229757
0000172965
Fingerprint/Curvilinear/Rectilinear
-
-
-
-
-
4y6m
late infantile
-
Sara Mole
00229758
0000172968
Fingerprint
-
-
-
-
-
-
late infantile
-
Sara Mole
00229761
0000233303
Hearing impairment, Optic atrophy, Dementia, Intellectual disability, Failure to thrive, Abnormal facial shape, Developmental regression, Scoliosis, Multiple joint contractures, Respiratory failure, Myoclonic spasms, Gastrostomy tube feeding in infancy, Brain atrophy, Neurodevelopmental delay, Abnormality of movement
-
-
Familial, autosomal recessive
-
18y05m
?
-
-
Corina-Marcela Rus
00307878
0000233304
Hypertelorism, Delayed speech and language development, Global developmental delay, Cerebellar atrophy, Cerebral atrophy, Unsteady gait, Abnormality of the cerebral white matter, Lower limb muscle weakness, Abnormal thalamic MRI signal intensity
-
-
Familial, autosomal recessive
-
04y08m
03y06m
-
-
Corina-Marcela Rus
00307879
0000233305
Seizures, Motor delay, Developmental regression, Abnormality of the cerebral white matter
-
-
Familial, autosomal recessive
-
01y02m
?
-
-
Corina-Marcela Rus
00307880
0000344148
HP:0003678 (present);HP:0000572 (present);HP:0002180 (present);HP:0002353 (present);HP:0002373 (present);HP:0000708 (present);HP:0000752 (present);HP:0001249 (present);HP:0030891 (present);HP:0007207 (present);HP:0011147 (present);HP:0001336 (present) (present);HP:0011813 (present);HP:0002059 (present)
-
-
Familial, autosomal recessive
-
05y
03y
HP:0002373;HP:0000708;HP:0001249;HP:0002359
-
Favio Pesaola
00455537
0000344149
HP:0000750 (present);HP:0001272 (present);HP:0030891 (present);HP:0002353 (present);HP:0002312 (present);HP:0006887 (present)
-
-
Familial, autosomal recessive
-
06y
04y
HP:0000750;HP:0002361
-
Favio Pesaola
00455615
0000344150
HP:0003678 (present);HP:0000572 (present);HP:0002180 (present);HP:0002353 (present);HP:0002373 (present);HP:0000708 (present);HP:0000752 (present);HP:0001249 (present);HP:0030891 (present);HP:0007207 (present);HP:0011147 (present);HP:0001336 (present) (present);HP:0011813 (present);HP:0002059 (present)
-
-
Familial, autosomal recessive
-
04y
03y
HP:0000750;HP:0001249;HP:0000708
-
Favio Pesaola
00455616
0000344152
HP:0030891 (present);HP:0001272 (present);HP:0002353 (present);HP:0008035 (present);HP:0000543 (present);HP:0007965 (present);HP:0002123 (present);HP:0007270 (present);HP:0001336 (present);HP:0001347 (present)
-
-
Familial, autosomal recessive
-
04y
03y
HP:0001288
-
Favio Pesaola
00455618
0000344153
HP:0000750 (present);HP:0001272 (present);HP:0030891 (present);HP:0002353 (present);HP:0002312 (present);HP:0006887 (present);HP:0001251 (present)
-
-
Familial, autosomal recessive
-
16y
08y
HP:0010818
-
Favio Pesaola
00455619
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