Wikidata:Database reports/Constraint violations/P1057

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Constraint violations report for chromosome (Discussion, uses, items, changes, related properties): chromosome on which an entity is localized
Data time stamp: (UTC) — Items processed: 634,876
The report is generated based on the settings on Property:P1057#P2302.
Updates overwrite this page. Some may already be fixed since the last update: check RecentChangesLinked.
When incremental dumps and the bot work as planned, items fixed before 07:00 UTC disappear in the next update. The report is not updated if only the item count changes.
The report can include false positives. There is no need to "fix" them.

"Value type chromosome (Q37748)" violations[edit]

Violations count: 365

Types statistics[edit]

Accepted Type Usage
Yes chromosome (Q37748) 634689
No cellular component (Q5058355) 315
No DNA (Q7430) 18
No natural number (Q21199) 2
No power of 1000 (Q41068772) 1
No automorphic number (Q2313686) 1
No stella octangula number (Q3879425) 1
No seventh power (Q37947505) 1
No sixth power (Q37947496) 1
No harshad number (Q375355) 1
No non-negative integer (Q28920052) 1
No pentagonal pyramidal number (Q2708903) 1
No nonagonal number (Q2702442) 1
No octagonal number (Q2634498) 1
No star number (Q2524197) 1
No triangular number (Q245102) 1
No unit (Q2198779) 1
No Fibonacci number (Q47577) 1
No square number (Q50705) 1
No heptagonal pyramidal number (Q606977) 1
No decagonal number (Q663029) 1
No pentagonal number (Q674928) 1
No multiplicative identity (Q68019776) 1
No coherent SI unit (Q69197847) 1
No fourth power (Q840676) 1
No eighth power (Q84752530) 1
No cube (Q861555) 1
No ninth power (Q91025251) 1
No centered heptagonal number (Q940343) 1
No heptagonal number (Q967999) 1
No tetrahedral number (Q975166) 1
No centered nonagonal number (Q1587799) 1
No fifth power (Q10549775) 1
No dodecagonal number (Q1081248) 1
No power of two (Q1136880) 1
No hexagonal number (Q1165838) 1
No repunit (Q1199125) 1
No {1} (Q125379148) 1
No odd number (Q13366129) 1
No icosahedral number (Q13823786) 1
No dodecahedral number (Q13825533) 1
No pentatope number (Q1403502) 1
No centered tetrahedral number (Q14390192) 1
No centered octahedral number (Q14390354) 1
No centered dodecahedral number (Q14390508) 1
No centered icosahedral number (Q14390666) 1
No Mersenne number (Q10338607) 1
No centered decagonal number (Q1587812) 1
No centered octagonal number (Q1589528) 1
No dimensionless unit (Q1618549) 1
No centered pentachoric number (Q16858648) 1
No power of 10 (Q184611) 1
No square triangular number (Q1885380) 1
No square pyramidal number (Q18949) 1
No centered triangular number (Q190890) 1
No centered pentagonal number (Q190891) 1
No centered cube number (Q190893) 1
No centered hexagonal number (Q190899) 1
No centered square number (Q190900) 1
No hexagonal pyramidal number (Q1990975) 1

"Type gene (Q7187), sequence variant (Q15304597), noncoding DNA (Q1458444), chromosome abnormality (Q744962)" violations[edit]

Violations count: 9011

Too many results. 4010 records skipped.

Types statistics[edit]

Accepted Type Usage
Yes gene (Q7187) 616433
Yes protein-coding gene (Q20747295) 484563
Yes pseudogene (Q277338) 37466
Yes coding region (Q3780824) 5921
No repetitive DNA (Q424473) 4288
No mature microRNA (Q23838648) 2588
No microRNA (Q310899) 1880
Yes missense mutation (Q2656896) 633
Yes sequence variant (Q15304597) 414
Yes transcript fusion (Q28419128) 129
Yes Frameshift Truncation (Q28371705) 66
No transfer RNA (Q201448) 66
Yes Loss Of Function Variant (Q27907094) 50
Yes Stop Gained (Q28371788) 46
No Transcript Amplification (Q27907091) 34
Yes Protein Altering Variant (Q27907087) 32
Yes Inframe Deletion (Q28371783) 24
Yes Frameshift Variant (Q28419131) 21
Yes Inframe Insertion (Q27908066) 20
Yes transcript variant (Q28371782) 19
Yes Gain Of Function Variant (Q28371786) 19
No non-coding RNA (Q427087) 17
No ribosomal RNA (Q215980) 16
No regulatory sequence (Q3238407) 15
Yes single-nucleotide polymorphism (Q501128) 14
Yes exon variant (Q27908063) 13
Yes gene variant (Q28381983) 12
No Synonymous Variant (Q28419125) 9
Yes Polymorphic Sequence Variant (Q28419136) 8
Yes Exon Loss Variant (Q28419122) 7
No Transcript Ablation (Q28381986) 7
No Splice Donor Variant (Q29937349) 7
No Stop Lost (Q28419141) 6
No splice acceptor variant (Q42866965) 6
No wild type (Q128723) 6
No 3 Prime UTR Variant (Q28419124) 4
Yes trisomy (Q844903) 4
No disruptive inframe deletion (Q42866969) 3
No Regulatory Region Variant (Q28381988) 3
No Plus 1 Frameshift Variant (Q28381736) 3
Yes Intron Variant (Q28419129) 3
No Frameshift Elongation (Q28381989) 3
Yes loss of heterozygosity (Q2617554) 3
No Start Lost (Q29938065) 3
Yes autosomal trisomy (Q55789081) 2
No Indel (Q32949508) 2
Yes total autosomal trisomy (Q55789082) 2
No microsatellite (Q265193) 2
Yes Coding Transcript Variant (Q29907183) 2
Yes noncoding DNA (Q1458444) 2
No protein (Q8054) 2
No Minus 1 Frameshift Variant (Q28419135) 2
No Coding Transcript Intron Variant (Q28419134) 2
Yes inframe variant (Q28419132) 2
Yes Coding Sequence Variant (Q28371787) 2
No Short Tandem Repeat Variation (Q28419126) 2
Yes unique-event polymorphism (Q4369985) 1
Yes ncRNA gene (Q1412309) 1
No DNA binding site (Q5205743) 1
No human (Q5) 1
Yes chromosome 10 anomaly (Q56742460) 1
No Insertion (Q32937968) 1
Yes deletion mutation (Q656732) 1
Yes deleterious mutation (Q120878399) 1
Yes chromosomal translocation (Q916504) 1
No inframe indel (Q42866966) 1
Yes frameshift mutation (Q1440688) 1
Yes insertion mutation (Q1650834) 1
No molecular chaperones (Q422496) 1
Yes tumor suppressor gene (Q422445) 1
Yes somatic mutation (Q2215243) 1
No variable number tandem repeat (Q2587423) 1
No Transfer-messenger RNA (Q285904) 1
No Nonsynonymous Variant (Q27905684) 1
No 3 Prime UTR Truncation (Q28419139) 1
No 5 Prime UTR Exon Variant (Q28419138) 1
No 5 Prime UTR Variant (Q27919343) 1
No Copy Number Change (Q28381984) 1
No Transcription Variant (Q28419121) 1
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