(Q5145896)

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_14330&ncbiId=1305

http://www.genome.gov/gwastudies/index.cfm?gene=COL13A1

Parkinson disease loci in the mid-western Amish

Phenocarta

genome-wide association study

25 May 2020

fatty liver disease

determination method

TAS

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_9452&ncbiId=1305

http://www.genome.gov/gwastudies/index.cfm?gene=COL13A1

Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease

Phenocarta

congenital myasthenic syndrome 19

25 May 2020

1 reference

13 August 2019

congenital myasthenic syndrome

1 reference

Open Targets Platform

24 August 2023

https://platform.opentargets.org/evidence/ENSG00000197467/Orphanet_590

based on heuristic

inferred from an Open Targets association score over 0.7

chromosome

human chromosome 10

genomic assembly

1 reference

1 reference

71561644

1 reference

69801880

1 reference

69964275

1 reference

71724031

1 reference

10q22.1

1 reference

15 May 2022

22421

1 reference

15 May 2022

PBB GE COL13A1 211809 x at fs.png
732 × 530; 12 KB

0 references

PBB GE COL13A1 208535 x at fs.png
732 × 530; 12 KB

0 references

PBB GE COL13A1 211343 s at fs.png
732 × 530; 11 KB

0 references

1 reference

22421

1 reference

22421

1 reference

22421

cerebellar hemisphere

1

1 reference

28 April 2022

periodontal fiber

2

1 reference

28 April 2022

tibia

3

1 reference

28 April 2022

corpus epididymis

4

1 reference

28 April 2022

ascending aorta

5

1 reference

28 April 2022

cerebellar vermis

6

1 reference

28 April 2022

popliteal artery

7

1 reference

28 April 2022

lower lobe of lung

8

1 reference

28 April 2022

stromal cell of endometrium

9

1 reference

28 April 2022

spongy bone

10

1 reference

28 April 2022

http://identifiers.org/ncbigene/1305

exact match

1 reference

Identifiers.org

http://www.ebi.ac.uk/miriam/main/collections/MIR:00000069

Identifiers

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

15 May 2022

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15 May 2022

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15 May 2022

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15 May 2022

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15 May 2022

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15 May 2022

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15 May 2022

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15 May 2022

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15 May 2022

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15 May 2022

1 reference

15 May 2022

1 reference

15 May 2022

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15 May 2022

1 reference

15 May 2022

1 reference

15 May 2022

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15 May 2022

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

15 May 2022

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15 May 2022

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15 May 2022

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15 May 2022

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15 May 2022

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15 May 2022

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15 May 2022

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

10 April 2022

1 reference

10 April 2022

1 reference

10 April 2022

1 reference

10 April 2022

1 reference

10 April 2022

1 reference

10 April 2022

1 reference

10 April 2022

1 reference

10 April 2022

1 reference

10 April 2022

1 reference

10 April 2022

1 reference

10 April 2022

1 reference

10 April 2022

1 reference

10 April 2022

1 reference

10 April 2022

1 reference

10 April 2022

1 reference

10 April 2022

1 reference

10 April 2022

1 reference

10 April 2022

1 reference

10 April 2022

1 reference

15 May 2022

1 reference

1 reference

Ensembl transcript ID

1 reference

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1 reference

1 reference

1 reference

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

Online Mendelian Inheritance in Man

19 August 2019

1 reference

inferred by common HGNC mappings on source and on Wikidata

UMLS 2023