EntrezGene: 9949: Difference between revisions

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{{GenePage
{{GenePage
|ensembl=Ensembl:ENSG00000101935
|gencode_transcripts=ENST00000262844.9 ENST00000372059.6 ENST00000372057.1 ENST00000473662.1 ENST00000496695.1
|gene_id=9949
|gene_id=9949
|gene_name=Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1
|gene_name=Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1
Line 6: Line 8:
|gene_type=protein-coding
|gene_type=protein-coding
|hgnc_mgi_id=HGNC:467
|hgnc_mgi_id=HGNC:467
|hprd=HPRD:02182
|imgt_gene-db=
|mim=MIM:300195
|mirbase=
|old_gene_ids=23656 286505
|old_gene_ids=23656 286505
|other_mrnas=BC065214 BC051895 AK055321 BC037983 BC024762 BC060813 AK023637 BX648797 AK001703 AK091430 AJ007014 AK314596 HQ448514 KU178496 KU178497 CU687440
|refSeq_transcripts=NM_015365 NM_001171689 NM_001025580
|species=human
|species=human
|ucsc_genes=uc004eoo.4 uc004eop.4 uc004eoq.4 uc065arq.1 uc065art.1
|vega=Vega:OTTHUMG00000022197
}}
}}

Latest revision as of 08:16, 14 June 2018



Related TSS IDs


rfhg_238367.1
rfhg_238368.1
rfhg_238369.1
rfhg_238378.1
rfhg_238379.1
rfhg_238380.1


Basic information


GeneID:9949
Species:human
Gene name:Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1
Gene symbol:AMMECR1
Gene synonyms:AMMERC1
Gene type:protein-coding
Old GeneIDs:23656 286505


Links to external databases


HGNC/MGI_ID:HGNC:467
Ensembl:Ensembl:ENSG00000101935
Vega:Vega:OTTHUMG00000022197
HPRD:HPRD:02182
miRBase:
IMGT/GENE-DB:
MIM:MIM:300195


Transcripts


Gencode transcripts:ENST00000262844.9
ENST00000372059.6
ENST00000372057.1
ENST00000473662.1
ENST00000496695.1
RefSeq transcripts:NM_015365
NM_001171689
NM_001025580
UCSC genes:uc004eoo.4
uc004eop.4
uc004eoq.4
uc065arq.1
uc065art.1
Other_mRNAs:BC065214
BC051895
AK055321
BC037983
BC024762
BC060813
AK023637
BX648797
AK001703
AK091430
AJ007014
AK314596
HQ448514
KU178496
KU178497
CU687440