AMMECR1
type: Thing
description: protein-coding gene in the species Homo sapiens
additional property: PropertyValue
  property ID: P31
  value: gene
additional property: PropertyValue
  property ID: P279
  value: protein-coding gene
additional property: PropertyValue
  property ID: P351
  value: 9949
additional property: PropertyValue
  property ID: P353
  value: AMMECR1
additional property: PropertyValue
  property ID: P354
  value: 467
additional property: PropertyValue
  property ID: P492
  value: 300195
additional property: PropertyValue
  property ID: P593
  value: 68944
additional property: PropertyValue
  property ID: P594
  value: ENSG00000101935
additional property: PropertyValue
  property ID: P639
  value: NM_015365
additional property: PropertyValue
  property ID: P639
  value: NM_001025580
additional property: PropertyValue
  property ID: P639
  value: NM_001171689
additional property: PropertyValue
  property ID: P644
  value: 110194186
additional property: PropertyValue
  property ID: P644
  value: 109437414
additional property: PropertyValue
  property ID: P645
  value: 109683461
additional property: PropertyValue
  property ID: P645
  value: 110440318
additional property: PropertyValue
  property ID: P684
  value: Ammecr1
additional property: PropertyValue
  property ID: P684
  value: Ammecr1
additional property: PropertyValue
  property ID: P684
  value: ammecr1
additional property: PropertyValue
  property ID: P688
  value: AMMECR nuclear protein 1
additional property: PropertyValue
  property ID: P703
  value: Homo sapiens
additional property: PropertyValue
  property ID: P704
  value: ENST00000262844
additional property: PropertyValue
  property ID: P704
  value: ENST00000372057
additional property: PropertyValue
  property ID: P704
  value: ENST00000372059
additional property: PropertyValue
  property ID: P1057
  value: human X chromosome
additional property: PropertyValue
  property ID: P2293
  value: midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis
additional property: PropertyValue
  property ID: P2293
  value: Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome
additional property: PropertyValue
  property ID: P2548
  value: reverse strand
additional property: PropertyValue
  property ID: P2671
  value: /g/11gbldq5kc
additional property: PropertyValue
  property ID: P2888
  value: http://identifiers.org/ncbigene/9949
additional property: PropertyValue
  property ID: P2892
  value: C1412386
confidence:
  popularity graph score:
    score: 0.001
    score pct: 0
    tier: established
    components:
      sitelinks: 0
      sitelinks norm: 0.0
      unique citations: 10
      unique citations norm: 0.004
      monthly pageviews: 0
      monthly pageviews norm: 0.0
  sitelinks: 0
  unique citations: 10
  monthly pageviews: 0
  yearly pageviews: 0
  tier: established
claims:
  P31:
    value: Q7187
    source count: 1
    confidence: 0.2
    value label: gene
  P279:
    value: Q20747295
    source count: 1
    confidence: 0.2
    value label: protein-coding gene
  P351:
    value: 9949
    source count: 1
    confidence: 0.2
  P353:
    value: AMMECR1
    source count: 1
    confidence: 0.2
  P354:
    value: 467
    source count: 1
    confidence: 0.2
  P492:
    value: 300195
    source count: 1
    confidence: 0.2
  P593:
    value: 68944
    source count: 1
    confidence: 0.2
  P594:
    value: ENSG00000101935
    source count: 1
    confidence: 0.2
  P639:
    value: NM_015365
    source count: 1
    confidence: 0.2
  P639:
    value: NM_001025580
    source count: 1
    confidence: 0.2
  P639:
    value: NM_001171689
    source count: 1
    confidence: 0.2
  P644:
    value: 110194186
    source count: 1
    confidence: 0.2
  P644:
    value: 109437414
    source count: 1
    confidence: 0.2
  P645:
    value: 109683461
    source count: 1
    confidence: 0.2
  P645:
    value: 110440318
    source count: 1
    confidence: 0.2
  P684:
    value: Q18258276
    source count: 2
    confidence: 0.4
    value label: Ammecr1
  P684:
    value: Q24408967
    source count: 2
    confidence: 0.4
    value label: Ammecr1
  P684:
    value: Q29743331
    source count: 2
    confidence: 0.4
    value label: ammecr1
  P684:
    value: Q29723019
    source count: 1
    confidence: 0.2
    value label: CG5902
  P684:
    value: Q29672307
    source count: 1
    confidence: 0.2
    value label: R166.3
  P688:
    value: Q21112662
    source count: 1
    confidence: 0.2
    value label: AMMECR nuclear protein 1

value: Q15978631
source count: 1
confidence: 0.2
value label: Homo sapiens

value: ENST00000262844
source count: 1
confidence: 0.2

value: ENST00000372057
source count: 1
confidence: 0.2

value: ENST00000372059
source count: 1
confidence: 0.2

value: ENST00000473662
source count: 1
confidence: 0.2

value: ENST00000496695
source count: 1
confidence: 0.2

value: Q29867336
source count: 1
confidence: 0.2
value label: human X chromosome

value: Q55782525
source count: 1
confidence: 0.2
value label: midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis

value: Q55782425
source count: 1
confidence: 0.2
value label: Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome

value: Q22809711
source count: 1
confidence: 0.2
value label: reverse strand

value: /g/11gbldq5kc
source count: 0
confidence: 0.0

value: http://identifiers.org/ncbigene/9949
source count: 1
confidence: 0.2

value: C1412386
source count: 1
confidence: 0.2

value: Xq23
source count: 1
confidence: 0.2

value: Q116529247
source count: 1
confidence: 0.2
value label: buccal mucosa cell

value: Q1759640
source count: 1
confidence: 0.2
value label: trabecular bone

value: Q66558726
source count: 1
confidence: 0.2
value label: gingival epithelium

value: Q8124
source count: 1
confidence: 0.2
value label: human penis

value: Q1635319
source count: 1
confidence: 0.2
value label: germinal epithelium

source: Bgee
stated in qid: Q54985720
retrieved: 2024-06-07

source: Orthologous MAtrix
stated in qid: Q7104801

source: Identifiers.org
stated in qid: Q16335166

source: Q20641742
stated in qid: Q20641742
retrieved: 2022-05-15

source: Online Mendelian Inheritance in Man
stated in qid: Q241953
retrieved: 2019-08-19

source: UniProt
stated in qid: Q905695
retrieved: 2017-07-06

source: UMLS 2023
stated in qid: Q118645236
retrieved: 2023-06-15

source: ensembl Release 106
stated in qid: Q111699881

source: Ensembl Release 87
stated in qid: Q27975061

source: HomoloGene build68
stated in qid: Q20976936

wikidata id: Q18034906
domain: gene
level: standard
html url: https://4ort.xyz/entity/ammecr1-q18034906
markdown url: https://4ort.xyz/entity/ammecr1-q18034906.md
facts url summary: https://4ort.xyz/entity/ammecr1-q18034906/facts.json
facts url standard: https://4ort.xyz/entity/ammecr1-q18034906/facts.json
facts url full: https://4ort.xyz/entity/ammecr1-q18034906/facts.json
data source: Wikidata (CC0 / public domain)
license: https://creativecommons.org/publicdomain/zero/1.0/
api version: v1
served at: 2026-08-13T12:08:25.167010Z
entity updated at: 2026-05-03T18:28:36.114423+00:00Z
entity created at: 2026-05-03T15:11:31.713622+00:00Z