Gene: FAM95C (family with sequence similarity 95 member C) Homo sapiens
Analyze
Symbol:
FAM95C (Ensembl: ANKRD18A)
Name:
family with sequence similarity 95 member C (Ensembl:ankyrin repeat domain 18A)
RGD ID:
7242150
HGNC Page
HGNC:45272
Description:
INTERACTS WITH aristolochic acid A; lipopolysaccharide; propofol
Type:
ncrna (Ensembl: protein-coding)
RefSeq Status:
VALIDATED
RGD Orthologs
Alliance Orthologs
More Info
more info ...
More Info
Allele / Splice:
See ClinVar data
Latest Assembly:
GRCh38 - Human Genome Assembly GRCh38
Position:
Human Assembly Chr Position (strand) Source Genome Browsers JBrowse NCBI UCSC Ensembl GRCh38 9 38,540,567 - 38,545,372 (-) NCBI GRCh38 GRCh38 hg38 GRCh38 GRCh38.p14 Ensembl 9 38,540,567 - 38,620,596 (-) Ensembl GRCh38 hg38 GRCh38 GRCh37 9 38,540,564 - 38,545,369 (-) NCBI GRCh37 GRCh37 hg19 GRCh37 Cytogenetic Map 9 p13.1 NCBI HuRef 9 38,492,875 - 38,497,680 (-) NCBI HuRef CHM1_1 9 38,542,343 - 38,547,148 (-) NCBI CHM1_1 T2T-CHM13v2.0 9 38,564,763 - 38,569,568 (-) NCBI T2T-CHM13v2.0
JBrowse:
View Region in Genome Browser (JBrowse)
Model
References
Additional References at PubMed
Genomics
Comparative Map Data
FAM95C Human Assembly Chr Position (strand) Source Genome Browsers JBrowse NCBI UCSC Ensembl GRCh38 9 38,540,567 - 38,545,372 (-) NCBI GRCh38 GRCh38 hg38 GRCh38 GRCh38.p14 Ensembl 9 38,540,567 - 38,620,596 (-) Ensembl GRCh38 hg38 GRCh38 GRCh37 9 38,540,564 - 38,545,369 (-) NCBI GRCh37 GRCh37 hg19 GRCh37 Cytogenetic Map 9 p13.1 NCBI HuRef 9 38,492,875 - 38,497,680 (-) NCBI HuRef CHM1_1 9 38,542,343 - 38,547,148 (-) NCBI CHM1_1 T2T-CHM13v2.0 9 38,564,763 - 38,569,568 (-) NCBI T2T-CHM13v2.0
Gm57858 Mouse Assembly Chr Position (strand) Source Genome Browsers JBrowse NCBI UCSC Ensembl GRCm39 3 36,061,396 - 36,107,676 (-) NCBI GRCm39 GRCm39 mm39 GRCm39 Ensembl 3 36,061,393 - 36,107,696 (-) Ensembl GRCm39 Ensembl GRCm38 3 36,007,247 - 36,053,547 (-) NCBI GRCm38 GRCm38 mm10 GRCm38 GRCm38.p6 Ensembl 3 36,007,244 - 36,053,547 (-) Ensembl GRCm38 mm10 GRCm38 MGSCv37 3 35,906,169 - 35,952,469 (-) NCBI GRCm37 MGSCv37 mm9 NCBIm37 MGSCv36 3 36,198,796 - 36,245,096 (-) NCBI MGSCv36 mm8 Celera 3 35,889,674 - 35,936,124 (-) NCBI Celera Cytogenetic Map 3 B NCBI cM Map 3 17.41 NCBI
4921524L21Rikl2 Rat Assembly Chr Position (strand) Source Genome Browsers JBrowse NCBI UCSC Ensembl GRCr8 17 59,376,110 - 59,416,150 (-) NCBI GRCr8 mRatBN7.2 17 54,681,040 - 54,721,106 (-) NCBI mRatBN7.2 mRatBN7.2 mRatBN7.2 Ensembl 17 54,681,044 - 54,720,740 (-) Ensembl mRatBN7.2 Ensembl Rnor_6.0 17 57,507,650 - 57,526,428 (-) NCBI Rnor6.0 Rnor_6.0 rn6 Rnor6.0 Rnor_6.0 Ensembl 17 57,507,659 - 57,526,461 (-) Ensembl Rnor6.0 rn6 Rnor6.0 Cytogenetic Map 17 q12.1 NCBI
Markers in Region
RH12064
Human Assembly Chr Position (strand) Source JBrowse GRCh37 9 38,540,653 - 38,540,811 UniSTS GRCh37 Build 36 9 38,530,653 - 38,530,811 RGD NCBI36 Celera 9 38,473,595 - 38,473,753 RGD Cytogenetic Map 9 p13.1 UniSTS HuRef 9 38,492,964 - 38,493,122 UniSTS GeneMap99-GB4 RH Map 9 148.92 UniSTS NCBI RH Map 9 549.6 UniSTS
Expression
RNA-SEQ Expression
Click on a value in the shaded box below the category label to view a detailed expression data table for that system.
alimentary part of gastrointestinal system
1
18
31
15
18
15
214
15
264
232
31
16
30
3
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Sequence
Ensembl Acc Id:
ENST00000625242
Type:
CODING
Position:
Human Assembly Chr Position (strand) Source GRCh38.p14 Ensembl 9 38,540,569 - 38,545,372 (-) Ensembl
Ensembl Acc Id:
ENST00000636756
Type:
CODING
Position:
Human Assembly Chr Position (strand) Source GRCh38.p14 Ensembl 9 38,543,253 - 38,577,156 (-) Ensembl
Ensembl Acc Id:
ENST00000637288 ⟹ ENSP00000489798
Type:
CODING
Position:
Human Assembly Chr Position (strand) Source GRCh38.p14 Ensembl 9 38,540,683 - 38,577,203 (-) Ensembl
Ensembl Acc Id:
ENST00000637322 ⟹ ENSP00000489764
Type:
CODING
Position:
Human Assembly Chr Position (strand) Source GRCh38.p14 Ensembl 9 38,540,569 - 38,571,152 (-) Ensembl
Ensembl Acc Id:
ENST00000637556 ⟹ ENSP00000490788
Type:
CODING
Position:
Human Assembly Chr Position (strand) Source GRCh38.p14 Ensembl 9 38,540,569 - 38,577,207 (-) Ensembl
RefSeq Acc Id:
NR_047651
RefSeq Status:
VALIDATED
Type:
NON-CODING
Position:
Human Assembly Chr Position (strand) Source GRCh38 9 38,540,567 - 38,545,372 (-) NCBI GRCh37 9 38,540,564 - 38,545,369 (-) NCBI HuRef 9 38,492,875 - 38,497,680 (-) NCBI CHM1_1 9 38,542,343 - 38,547,148 (-) NCBI T2T-CHM13v2.0 9 38,564,763 - 38,569,568 (-) NCBI
Sequence:
TGCTGGGAGGTCAGACCCTGTGAGGGCTGTGGGGGCATCAGGCGCAGTGGGCTCCAGGGAGCCT
hide sequence
Additional Information
Nomenclature History
Date
Current Symbol
Current Name
Previous Symbol
Previous Name
Description
Reference
Status
2015-11-24
FAM95C
family with sequence similarity 95 member C
family with sequence similarity 95, member C
Symbol and/or name change
5135510 APPROVED
