FAHD2CP (fumarylacetoacetate hydrolase domain containing 2C, pseudogene) - Rat Genome Database

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Gene: FAHD2CP (fumarylacetoacetate hydrolase domain containing 2C, pseudogene) Homo sapiens
Analyze
Symbol: FAHD2CP
Name: fumarylacetoacetate hydrolase domain containing 2C, pseudogene
RGD ID: 6766683
HGNC Page HGNC:44135
Description: INTERACTS WITH acrylamide; benzo[a]pyrene; fipronil
Type: pseudo (Ensembl: transcribed_unprocessed_pseudogene)
RefSeq Status: VALIDATED
Related Functional Gene: FAHD2A  
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38296,010,551 - 96,023,136 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl296,013,730 - 96,021,608 (+)EnsemblGRCh38hg38GRCh38
GRCh37296,676,299 - 96,688,884 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36296,040,026 - 96,052,611 (+)NCBINCBI36Build 36hg18NCBI36
Celera291,117,235 - 91,129,823 (+)NCBICelera
Cytogenetic Map2q11.2NCBI
HuRef290,644,074 - 90,656,675 (+)NCBIHuRef
CHM1_1296,680,695 - 96,693,255 (+)NCBICHM1_1
T2T-CHM13v2.0296,308,064 - 96,320,649 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
References

References - curated
# Reference Title Reference Citation
1. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:15146197   PMID:16341674  


Genomics

Variants

.
Variants in FAHD2CP
7 total Variants
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1347
Count of miRNA genes:709
Interacting mature miRNAs:836
Transcripts:ENST00000427863, ENST00000443258, ENST00000467292, ENST00000483000, ENST00000535464, ENST00000607780
Prediction methods:Miranda, Rnahybrid
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.

Markers in Region
RH26381  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37297,747,791 - 97,747,974UniSTSGRCh37
GRCh37296,688,933 - 96,689,116UniSTSGRCh37
Build 36296,052,660 - 96,052,843RGDNCBI36
Celera291,129,872 - 91,130,055RGD
Celera292,189,945 - 92,190,128UniSTS
Cytogenetic Map2q11.1UniSTS
Cytogenetic Map2q11.2UniSTS
HuRef291,707,446 - 91,707,629UniSTS
HuRef290,656,724 - 90,656,907UniSTS
D2S1603E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37296,078,476 - 96,078,744UniSTSGRCh37
GRCh37296,687,177 - 96,687,447UniSTSGRCh37
Build 36295,442,203 - 95,442,471RGDNCBI36
Celera291,128,118 - 91,128,385UniSTS
Celera290,431,597 - 90,431,865RGD
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map2q11.1UniSTS
HuRef291,709,112 - 91,709,377UniSTS
HuRef290,105,418 - 90,105,686UniSTS
HuRef290,654,970 - 90,655,237UniSTS
D2S1692E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37296,679,231 - 96,679,517UniSTSGRCh37
GRCh37296,071,062 - 96,071,349UniSTSGRCh37
Build 36295,434,789 - 95,435,076RGDNCBI36
Celera290,424,183 - 90,424,470RGD
Celera291,120,167 - 91,120,453UniSTS
Cytogenetic Map2q11.1UniSTS
Cytogenetic Map2q11.2UniSTS
HuRef290,647,006 - 90,647,292UniSTS
HuRef290,098,019 - 90,098,306UniSTS
D2S2136  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37297,747,780 - 97,747,959UniSTSGRCh37
GRCh37296,688,948 - 96,689,127UniSTSGRCh37
Build 36296,052,675 - 96,052,854RGDNCBI36
Celera291,129,887 - 91,130,066RGD
Celera292,189,934 - 92,190,113UniSTS
Cytogenetic Map2q11.1UniSTS
Cytogenetic Map2q11.2UniSTS
HuRef291,707,435 - 91,707,614UniSTS
HuRef290,656,739 - 90,656,918UniSTS
SHGC-105076  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37297,747,664 - 97,747,868UniSTSGRCh37
GRCh37296,689,039 - 96,689,261UniSTSGRCh37
Build 36296,052,766 - 96,052,988RGDNCBI36
Celera292,189,818 - 92,190,022UniSTS
Celera291,129,978 - 91,130,200RGD
Cytogenetic Map2q11.1UniSTS
Cytogenetic Map2q11.2UniSTS
HuRef290,656,830 - 90,657,052UniSTS
HuRef291,707,319 - 91,707,523UniSTS
TNG Radiation Hybrid Map257614.0UniSTS
SGC35015  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37296,687,429 - 96,687,578UniSTSGRCh37
GRCh37296,078,726 - 96,078,875UniSTSGRCh37
Build 36295,442,453 - 95,442,602RGDNCBI36
Celera291,128,368 - 91,128,517UniSTS
Celera290,431,847 - 90,431,996RGD
Cytogenetic Map2q11.1UniSTS
Cytogenetic Map2q11.2UniSTS
HuRef290,105,668 - 90,105,817UniSTS
HuRef290,655,220 - 90,655,369UniSTS
Whitehead-RH Map2489.7UniSTS
RH35908  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37296,687,320 - 96,687,496UniSTSGRCh37
GRCh37296,078,617 - 96,078,793UniSTSGRCh37
Build 36295,442,344 - 95,442,520RGDNCBI36
Celera291,128,261 - 91,128,435UniSTS
Celera290,431,738 - 90,431,914RGD
Cytogenetic Map2q11.1UniSTS
Cytogenetic Map2q11.2UniSTS
HuRef290,105,559 - 90,105,735UniSTS
HuRef290,655,113 - 90,655,287UniSTS
GeneMap99-GB4 RH Map2338.13UniSTS
RH79204  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37297,747,934 - 97,748,064UniSTSGRCh37
GRCh37296,688,843 - 96,688,973UniSTSGRCh37
Build 36296,052,570 - 96,052,700RGDNCBI36
Celera291,129,782 - 91,129,912RGD
Celera292,190,088 - 92,190,218UniSTS
Cytogenetic Map2q11.1UniSTS
Cytogenetic Map2q11.2UniSTS
HuRef291,707,589 - 91,707,719UniSTS
HuRef290,656,634 - 90,656,764UniSTS


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system adipose tissue appendage entire extraembryonic component
High
Medium 126 56 48 18 45 18 591 113 1913 17 564 32 1 1 514
Low 2302 2570 1630 578 1543 420 3759 2070 1792 398 877 1560 169 1203 2273 1
Below cutoff 4 357 42 24 358 24 5 10 2 2 3 14 1 2

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000427863
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,013,730 - 96,021,608 (+)Ensembl
RefSeq Acc Id: ENST00000443258
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,593 - 96,023,385 (+)Ensembl
RefSeq Acc Id: ENST00000467292
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,526 - 96,023,398 (+)Ensembl
RefSeq Acc Id: ENST00000483000
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,551 - 96,023,385 (+)Ensembl
RefSeq Acc Id: ENST00000607780
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,557 - 96,021,834 (+)Ensembl
RefSeq Acc Id: ENST00000684860
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,564 - 96,023,382 (+)Ensembl
RefSeq Acc Id: ENST00000684890
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,593 - 96,023,385 (+)Ensembl
RefSeq Acc Id: ENST00000685061
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,564 - 96,023,382 (+)Ensembl
RefSeq Acc Id: ENST00000685203
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,593 - 96,023,385 (+)Ensembl
RefSeq Acc Id: ENST00000685309
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,571 - 96,023,385 (+)Ensembl
RefSeq Acc Id: ENST00000685321
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,564 - 96,023,385 (+)Ensembl
RefSeq Acc Id: ENST00000685451
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,554 - 96,023,385 (+)Ensembl
RefSeq Acc Id: ENST00000685578
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,552 - 96,023,385 (+)Ensembl
RefSeq Acc Id: ENST00000685821
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,613 - 96,023,382 (+)Ensembl
RefSeq Acc Id: ENST00000685912
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,564 - 96,023,385 (+)Ensembl
RefSeq Acc Id: ENST00000686031
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,554 - 96,021,834 (+)Ensembl
RefSeq Acc Id: ENST00000686146
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,564 - 96,023,385 (+)Ensembl
RefSeq Acc Id: ENST00000686333
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,596 - 96,023,376 (+)Ensembl
RefSeq Acc Id: ENST00000686450
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,564 - 96,023,385 (+)Ensembl
RefSeq Acc Id: ENST00000686549
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,563 - 96,023,386 (+)Ensembl
RefSeq Acc Id: ENST00000686616
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,571 - 96,023,385 (+)Ensembl
RefSeq Acc Id: ENST00000686623
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,548 - 96,023,385 (+)Ensembl
RefSeq Acc Id: ENST00000686703
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,602 - 96,023,382 (+)Ensembl
RefSeq Acc Id: ENST00000686766
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,563 - 96,021,834 (+)Ensembl
RefSeq Acc Id: ENST00000687200
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,530 - 96,023,386 (+)Ensembl
RefSeq Acc Id: ENST00000687277
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,535 - 96,023,385 (+)Ensembl
RefSeq Acc Id: ENST00000687350
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,532 - 96,021,834 (+)Ensembl
RefSeq Acc Id: ENST00000687421
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,554 - 96,023,385 (+)Ensembl
RefSeq Acc Id: ENST00000687514
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,564 - 96,023,382 (+)Ensembl
RefSeq Acc Id: ENST00000687567
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,553 - 96,023,385 (+)Ensembl
RefSeq Acc Id: ENST00000687767
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,564 - 96,023,382 (+)Ensembl
RefSeq Acc Id: ENST00000687808
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,564 - 96,023,382 (+)Ensembl
RefSeq Acc Id: ENST00000688019
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,554 - 96,023,385 (+)Ensembl
RefSeq Acc Id: ENST00000688439
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,545 - 96,023,385 (+)Ensembl
RefSeq Acc Id: ENST00000688767
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,563 - 96,021,834 (+)Ensembl
RefSeq Acc Id: ENST00000688890
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,545 - 96,023,385 (+)Ensembl
RefSeq Acc Id: ENST00000689054
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,551 - 96,023,385 (+)Ensembl
RefSeq Acc Id: ENST00000689101
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,545 - 96,021,834 (+)Ensembl
RefSeq Acc Id: ENST00000689299
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,543 - 96,023,385 (+)Ensembl
RefSeq Acc Id: ENST00000689315
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,545 - 96,023,386 (+)Ensembl
RefSeq Acc Id: ENST00000689487
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,551 - 96,023,385 (+)Ensembl
RefSeq Acc Id: ENST00000689599
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,551 - 96,023,385 (+)Ensembl
RefSeq Acc Id: ENST00000690132
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,564 - 96,023,385 (+)Ensembl
RefSeq Acc Id: ENST00000690226
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,593 - 96,023,382 (+)Ensembl
RefSeq Acc Id: ENST00000690506
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,545 - 96,023,385 (+)Ensembl
RefSeq Acc Id: ENST00000690531
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,532 - 96,023,385 (+)Ensembl
RefSeq Acc Id: ENST00000690546
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,564 - 96,023,385 (+)Ensembl
RefSeq Acc Id: ENST00000690894
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,563 - 96,023,385 (+)Ensembl
RefSeq Acc Id: ENST00000690986
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,613 - 96,023,381 (+)Ensembl
RefSeq Acc Id: ENST00000691037
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,532 - 96,023,385 (+)Ensembl
RefSeq Acc Id: ENST00000691311
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,564 - 96,023,385 (+)Ensembl
RefSeq Acc Id: ENST00000691480
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,564 - 96,023,385 (+)Ensembl
RefSeq Acc Id: ENST00000691683
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,564 - 96,023,385 (+)Ensembl
RefSeq Acc Id: ENST00000691870
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,545 - 96,023,385 (+)Ensembl
RefSeq Acc Id: ENST00000692100
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,548 - 96,021,834 (+)Ensembl
RefSeq Acc Id: ENST00000692114
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,593 - 96,023,385 (+)Ensembl
RefSeq Acc Id: ENST00000692128
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,564 - 96,023,382 (+)Ensembl
RefSeq Acc Id: ENST00000692153
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,564 - 96,023,382 (+)Ensembl
RefSeq Acc Id: ENST00000692284
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,596 - 96,023,380 (+)Ensembl
RefSeq Acc Id: ENST00000692364
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,564 - 96,023,382 (+)Ensembl
RefSeq Acc Id: ENST00000692639
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,574 - 96,023,385 (+)Ensembl
RefSeq Acc Id: ENST00000692942
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,532 - 96,023,385 (+)Ensembl
RefSeq Acc Id: ENST00000692960
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,545 - 96,023,385 (+)Ensembl
RefSeq Acc Id: ENST00000693304
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,558 - 96,023,385 (+)Ensembl
RefSeq Acc Id: ENST00000693333
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,596 - 96,023,385 (+)Ensembl
RefSeq Acc Id: ENST00000693624
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,564 - 96,021,834 (+)Ensembl
RefSeq Acc Id: ENST00000700796
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,529 - 96,023,382 (+)Ensembl
RefSeq Acc Id: ENST00000700806
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,574 - 96,021,831 (+)Ensembl
RefSeq Acc Id: ENST00000701113
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,551 - 96,023,380 (+)Ensembl
RefSeq Acc Id: ENST00000701149
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,548 - 96,023,381 (+)Ensembl
RefSeq Acc Id: ENST00000701505
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,554 - 96,023,380 (+)Ensembl
RefSeq Acc Id: ENST00000701589
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,564 - 96,023,382 (+)Ensembl
RefSeq Acc Id: ENST00000701677
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,596 - 96,023,385 (+)Ensembl
RefSeq Acc Id: ENST00000701738
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,564 - 96,023,382 (+)Ensembl
RefSeq Acc Id: ENST00000701869
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,611 - 96,021,834 (+)Ensembl
RefSeq Acc Id: ENST00000701887
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,593 - 96,023,385 (+)Ensembl
RefSeq Acc Id: ENST00000702185
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,602 - 96,023,380 (+)Ensembl
RefSeq Acc Id: ENST00000702348
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,611 - 96,023,380 (+)Ensembl
RefSeq Acc Id: ENST00000702452
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,564 - 96,021,831 (+)Ensembl
RefSeq Acc Id: ENST00000702710
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,574 - 96,023,380 (+)Ensembl
RefSeq Acc Id: ENST00000702739
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,596 - 96,023,382 (+)Ensembl
RefSeq Acc Id: ENST00000702789
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,613 - 96,023,385 (+)Ensembl
RefSeq Acc Id: ENST00000702836
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,596 - 96,023,382 (+)Ensembl
RefSeq Acc Id: ENST00000702843
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,596 - 96,023,382 (+)Ensembl
RefSeq Acc Id: ENST00000702875
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl296,010,564 - 96,023,385 (+)Ensembl
RefSeq Acc Id: NR_003698
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38296,010,551 - 96,023,136 (+)NCBI
GRCh37296,676,299 - 96,688,884 (+)NCBI
HuRef290,644,074 - 90,656,675 (+)NCBI
CHM1_1296,680,695 - 96,693,255 (+)NCBI
T2T-CHM13v2.0296,308,064 - 96,320,649 (-)NCBI
Sequence:
Protein Sequences
GenBank Protein AAH15216 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences


Additional Information

Database Acc Id Source(s)
COSMIC FAHD2CP COSMIC
Ensembl Genes ENSG00000231584 Ensembl
GTEx ENSG00000231584 GTEx
HGNC ID HGNC:44135 ENTREZGENE
Human Proteome Map FAHD2CP Human Proteome Map
NCBI Gene FAHD2CP ENTREZGENE