COL12A1 (collagen type XII alpha 1 chain)
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Gene
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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1303 |
Gene nameGene Name - the full gene name approved by the HGNC.
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Collagen type XII alpha 1 chain |
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
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COL12A1 |
SynonymsGene synonyms aliases
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BA209D8.1, BTHLM2, COL12A1L, DJ234P15.1, EDSMYP, UCMD2 |
ChromosomeChromosome number
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6 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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6q13-q14.1 |
SummarySummary of gene provided in NCBI Entrez Gene.
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This gene encodes the alpha chain of type XII collagen, a member of the FACIT (fibril-associated collagens with interrupted triple helices) collagen family. Type XII collagen is a homotrimer found in association with type I collagen, an association that i |
SNPsSNP information provided by dbSNP.
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SNP ID |
Visualize variation |
Clinical significance |
Consequence |
rs41266761 |
C>T |
Likely-benign, conflicting-interpretations-of-pathogenicity |
Coding sequence variant, missense variant |
rs151324784 |
C>T |
Conflicting-interpretations-of-pathogenicity |
Coding sequence variant, missense variant |
rs200201449 |
C>T |
Conflicting-interpretations-of-pathogenicity |
Coding sequence variant, missense variant |
rs200443479 |
G>A,T |
Conflicting-interpretations-of-pathogenicity |
Coding sequence variant, intron variant, missense variant |
rs200487396 |
G>A,T |
Uncertain-significance, pathogenic |
Coding sequence variant, missense variant |
rs201337277 |
G>A,T |
Uncertain-significance, likely-pathogenic |
Coding sequence variant, missense variant, synonymous variant |
rs371399251 |
G>A,T |
Pathogenic |
Synonymous variant, coding sequence variant, stop gained |
rs375760724 |
G>A |
Conflicting-interpretations-of-pathogenicity |
Synonymous variant, coding sequence variant |
rs755536829 |
T>C |
Uncertain-significance, likely-pathogenic |
Coding sequence variant, missense variant |
rs796052093 |
A>G |
Pathogenic, likely-pathogenic |
Missense variant, coding sequence variant |
rs796052094 |
C>T |
Pathogenic |
Missense variant, coding sequence variant |
rs875989819 |
C>T |
Pathogenic |
Splice donor variant |
rs984314526 |
G>A,C |
Pathogenic |
Stop gained, missense variant, coding sequence variant |
rs1064795770 |
A>G |
Likely-pathogenic |
Splice donor variant |
rs1064797326 |
C>T |
Likely-pathogenic |
Splice donor variant |
rs1131691587 |
G>A |
Likely-pathogenic |
Intron variant, coding sequence variant, missense variant |
rs1131691933 |
G>A |
Likely-pathogenic |
Stop gained, coding sequence variant |
rs1274606112 |
C>T |
Likely-pathogenic |
Splice donor variant |
rs1329022055 |
G>A |
Pathogenic |
Intron variant, stop gained, coding sequence variant |
rs1366112521 |
C>T |
Likely-pathogenic |
Splice donor variant |
rs1471550984 |
T>- |
Pathogenic |
Frameshift variant, coding sequence variant |
rs1554168326 |
C>T |
Likely-pathogenic |
Missense variant, coding sequence variant |
rs1554169319 |
C>T |
Likely-pathogenic |
Missense variant, coding sequence variant |
rs1554182935 |
C>- |
Pathogenic |
Coding sequence variant, frameshift variant |
rs1562223444 |
G>A |
Pathogenic |
Coding sequence variant, stop gained |
rs1562294703 |
G>A |
Likely-pathogenic |
Coding sequence variant, stop gained, intron variant |
rs1562310723 |
T>G |
Likely-pathogenic |
Splice acceptor variant, intron variant |
rs1582025807 |
->T |
Likely-pathogenic |
Coding sequence variant, frameshift variant |
rs1582068925 |
GT>- |
Pathogenic |
Coding sequence variant, frameshift variant |
rs1582133194 |
->A |
Pathogenic |
Coding sequence variant, frameshift variant |
rs1582139761 |
A>C |
Pathogenic |
Stop gained, coding sequence variant |
rs1582196903 |
->T |
Pathogenic |
Coding sequence variant, frameshift variant, intron variant |
rs1582208315 |
->T |
Likely-pathogenic |
Coding sequence variant, frameshift variant, intron variant |
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miRNAmiRNA information provided by mirtarbase database.
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Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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Protein
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UniProt ID |
Q99715 |
Protein name |
Collagen alpha-1(XII) chain |
Protein function |
Type XII collagen interacts with type I collagen-containing fibrils, the COL1 domain could be associated with the surface of the fibrils, and the COL2 and NC3 domains may be localized in the perifibrillar matrix. |
Family and domains |
Pfam
Accession |
ID |
Position in sequence |
Description |
Type |
PF00041 |
fn3 |
26 → 105 |
Fibronectin type III domain |
Domain |
PF00092 |
VWA |
140 → 311 |
von Willebrand factor type A domain |
Domain |
PF00041 |
fn3 |
335 → 416 |
Fibronectin type III domain |
Domain |
PF00092 |
VWA |
440 → 611 |
von Willebrand factor type A domain |
Domain |
PF00041 |
fn3 |
633 → 712 |
Fibronectin type III domain |
Domain |
PF00041 |
fn3 |
724 → 801 |
Fibronectin type III domain |
Domain |
PF00041 |
fn3 |
815 → 894 |
Fibronectin type III domain |
Domain |
PF00041 |
fn3 |
906 → 986 |
Fibronectin type III domain |
Domain |
PF00041 |
fn3 |
999 → 1077 |
Fibronectin type III domain |
Domain |
PF00041 |
fn3 |
1088 → 1168 |
Fibronectin type III domain |
Domain |
PF00092 |
VWA |
1199 → 1370 |
von Willebrand factor type A domain |
Domain |
PF00041 |
fn3 |
1386 → 1465 |
Fibronectin type III domain |
Domain |
PF00041 |
fn3 |
1475 → 1556 |
Fibronectin type III domain |
Domain |
PF00041 |
fn3 |
1567 → 1646 |
Fibronectin type III domain |
Domain |
PF00041 |
fn3 |
1656 → 1734 |
Fibronectin type III domain |
Domain |
PF00041 |
fn3 |
1754 → 1835 |
Fibronectin type III domain |
Domain |
PF00041 |
fn3 |
1845 → 1926 |
Fibronectin type III domain |
Domain |
PF00041 |
fn3 |
1937 → 2016 |
Fibronectin type III domain |
Domain |
PF00041 |
fn3 |
2026 → 2108 |
Fibronectin type III domain |
Domain |
PF00041 |
fn3 |
2117 → 2195 |
Fibronectin type III domain |
Domain |
PF00041 |
fn3 |
2205 → 2283 |
Fibronectin type III domain |
Domain |
PF00092 |
VWA |
2323 → 2495 |
von Willebrand factor type A domain |
Domain |
PF01391 |
Collagen |
2745 → 2802 |
Collagen triple helix repeat (20 copies) |
Repeat |
PF01391 |
Collagen |
2800 → 2853 |
Collagen triple helix repeat (20 copies) |
Repeat |
PF01391 |
Collagen |
2844 → 2902 |
Collagen triple helix repeat (20 copies) |
Repeat |
PF01391 |
Collagen |
2937 → 2994 |
Collagen triple helix repeat (20 copies) |
Repeat |
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Sequence |
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Sequence length |
3063 |
Interactions |
View interactions |
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
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Associated diseases
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Causal |
Disease name |
Disease term |
dbSNP ID |
References |
Alzheimer disease |
Alzheimer`s Disease |
rs63750215, rs28936379, rs63749851, rs63749884, rs28936380, rs63750048, rs63750579, rs63750264, rs63749964, rs63750671, rs281865161, rs63750066, rs63750399, rs63750734, rs63751039, rs63750973, rs63749810, rs63750643, rs193922916, rs63750306, rs63750590, rs63750526, rs63751235, rs661, rs63751037, rs63749885, rs63750231, rs63751229, rs63751272, rs63751223, rs63750391, rs63751163, rs281875357, rs63751141, rs63750082, rs121917807, rs63751399, rs63750265, rs63751144, rs63750886, rs63751068, rs121917808, rs63749891, rs63750083, rs63749824, rs63750577, rs267606983, rs63750218, rs63751287, rs63750900, rs145518263, rs63751475, rs63750450, rs63749805, rs63751278, rs63751106, rs63750004, rs63749806, rs63751024, rs63750248, rs63750779, rs63751139, rs63750219, rs63750298, rs63750687, rs63750851, rs1553268799, rs1561901881, rs1561905293, rs866101707, rs1566638673, rs63750009, rs1566656702, rs1566657804, rs1567885728, rs1568339995, rs1566630791, rs1555358260, rs63750964, rs1594998354, rs63751316 |
26830138 |
Bethlem myopathy |
BETHLEM MYOPATHY 2, BETHLEM MYOPATHY 1, Bethlem myopathy |
rs121434553, rs121434555, rs139260335, rs796052093, rs796052094, rs1768488927 |
24334769, 24334604, 27348394, 27159402, 24334604, 24334769 |
Congenital muscular dystrophy |
Congenital muscular dystrophy (disorder), Congenital muscular dystrophy, Ullrich type |
rs1565627745, rs774985604, rs1565629479, rs121913572, rs121913575, rs121913576, rs58932704, rs58912633, rs121912495, rs121912496, rs60458016, rs387906881, rs750764003, rs387907068, rs786205117, rs387907069, rs786205118, rs267607600, rs61672878, rs57629361, rs61444459, rs60872029, rs587780362, rs141554661, rs864309525, rs371751084, rs914395925, rs1060505038, rs766046008, rs1060505039, rs750781027, rs761612652, rs1060505040, rs749383757, rs776548207, rs1554269966, rs373091820, rs1553261891, rs1474512248, rs1333100080, rs1246940477, rs1554320168, rs372328960, rs1217190017, rs750756707, rs1555894289, rs1296761337, rs1562530132, rs1569054508, rs1565622052, rs1415944134, rs1565620275, rs752436924, rs1569054086, rs1583149141, rs17854600, rs757369551, rs755438542, rs1872274494, rs1874440714 |
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Microcephaly, epilepsy, and diabetes syndrome |
MICROCEPHALY, EPILEPSY, AND DIABETES SYNDROME |
rs387907012 |
27348394 |
Muscular dystrophy |
Muscular Dystrophy |
rs200198778, rs121908110, rs121908185, rs58932704, rs61672878, rs60458016, rs387906881, rs397509417, rs267607644, rs267607634, rs59332535, rs797045898, rs755660222, rs142908436, rs886039913, rs138945081, rs368970223, rs746855352, rs1553264624, rs1553265433, rs1553265436, rs1553265761, rs267607576, rs780302064, rs1557058294, rs1555352706, rs961440747, rs1185491348, rs1594796439, rs1603636710 |
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Myopathy |
Myopathy |
rs137854521, rs386834236, rs121908557, rs121909092, rs111033570, rs104894299, rs104894294, rs121909273, rs121909274, rs121909275, rs199474699, rs199476140, rs118192165, rs118192169, rs118192166, rs193922856, rs281865489, rs397514675, rs397514676, rs397514677, rs367543058, rs118192117, rs193922837, rs118192129, rs118192143, rs118192153, rs118192133, rs118192156, rs118192149, rs118192148, rs118192183, rs118192147, rs118192123, rs118192127, rs118192142, rs118192144, rs118192178, rs118192151, rs118192150, rs118192184, rs118192154, rs118192134, rs118192155, rs193922893, rs118192132, rs118192146, rs193922867, rs193922884, rs587777528, rs527236030, rs587777672, rs587777673, rs587777674, rs587777675, rs587783343, rs2754158, rs786204796, rs748277951, rs797046047, rs797046064, rs797046060, rs797045479, rs797045931, rs797045932, rs797045934, rs797045935, rs797045477, rs797045478, rs1057518851, rs1057518855, rs1057518773, rs1057518866, rs1555322610, rs1555806119, rs761483896, rs144071404, rs1198364572, rs1568614042, rs978984063, rs1568604308, rs1332371891, rs1601842249, rs777176261, rs1249621033, rs1278804520, rs1568613962, rs1568510406, rs1597512576, rs193922887, rs371455345, rs1603452200, rs1599634685, rs1575065895, rs1575201712, rs139715157, rs1974129338 |
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Hypotonia |
Neonatal Hypotonia |
rs141138948, rs397517172, rs869312824, rs1583169151 |
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Scoliosis |
Scoliosis, unspecified |
rs1057518828, rs147296805, rs758163506, rs1555613564, rs1596852902, rs1596853067, rs1596853085 |
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Ullrich congenital muscular dystrophy |
Ullrich congenital muscular dystrophy 1, ULLRICH CONGENITAL MUSCULAR DYSTROPHY 2 |
rs1601231322, rs748035948, rs1568931397, rs267606747, rs121912938, rs121912939, rs387906608, rs398122821, rs875989819, rs796052093, rs749974929, rs984314526, rs1582208315, rs1582196903 |
24334604, 24334769, 24334604, 27159402, 27348394 |
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Unknown |
Disease name |
Disease term |
dbSNP ID |
References |
Acquired kyphoscoliosis |
Acquired Kyphoscoliosis |
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Amyotrophy |
Generalized amyotrophy, Proximal amyotrophy |
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Congenital kyphoscoliosis |
Congenital kyphoscoliosis |
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Elbow flexion contracture |
Flexion contracture - elbow |
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Endometriosis |
Endometriosis |
rs1800629, rs1143634 |
28881265 |
Esotropia |
Esotropia |
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Facial paralysis |
Facial paralysis |
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High palate |
Byzanthine arch palate |
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Malignant mesothelioma |
Malignant mesothelioma |
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25756049 |
Micrognathism |
Micrognathism |
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Motor delay |
Clumsiness - motor delay |
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Myopathic ehlers-danlos syndrome |
Myopathic Ehlers-Danlos syndrome |
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Phrynoderma |
Phrynoderma |
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Respiratory failure |
Respiratory Failure |
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