FAM186A (family with sequence similarity 186 member A) - Rat Genome Database

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Gene: FAM186A (family with sequence similarity 186 member A) Homo sapiens
Analyze
Symbol: FAM186A
Name: family with sequence similarity 186 member A
RGD ID: 2301117
HGNC Page HGNC:26980
Description: ASSOCIATED WITH genetic disease; INTERACTS WITH aflatoxin B1; antirheumatic drug; aristolochic acid A
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: family with sequence similarity 186, member A
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381250,327,309 - 50,396,609 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1250,326,230 - 50,396,622 (-)EnsemblGRCh38hg38GRCh38
GRCh371250,721,092 - 50,790,392 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361249,007,362 - 49,076,672 (-)NCBINCBI36Build 36hg18NCBI36
Celera1249,516,875 - 49,586,366 (-)NCBICelera
Cytogenetic Map12q13.12NCBI
HuRef1247,754,259 - 47,823,307 (-)NCBIHuRef
CHM1_11250,687,064 - 50,756,579 (-)NCBICHM1_1
T2T-CHM13v2.01250,290,439 - 50,359,662 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

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

References - curated
# Reference Title Reference Citation
1. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
2. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:11329013   PMID:12477932   PMID:16541075   PMID:28065597   PMID:31586073   PMID:36243803  


Genomics

Comparative Map Data
FAM186A
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381250,327,309 - 50,396,609 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1250,326,230 - 50,396,622 (-)EnsemblGRCh38hg38GRCh38
GRCh371250,721,092 - 50,790,392 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361249,007,362 - 49,076,672 (-)NCBINCBI36Build 36hg18NCBI36
Celera1249,516,875 - 49,586,366 (-)NCBICelera
Cytogenetic Map12q13.12NCBI
HuRef1247,754,259 - 47,823,307 (-)NCBIHuRef
CHM1_11250,687,064 - 50,756,579 (-)NCBICHM1_1
T2T-CHM13v2.01250,290,439 - 50,359,662 (-)NCBIT2T-CHM13v2.0
Fam186a
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391599,816,226 - 99,864,974 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1599,816,229 - 99,864,942 (-)EnsemblGRCm39 Ensembl
GRCm381599,918,345 - 99,967,093 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1599,918,348 - 99,967,061 (-)EnsemblGRCm38mm10GRCm38
MGSCv371599,748,779 - 99,764,144 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361599,746,382 - 99,761,747 (-)NCBIMGSCv36mm8
MGSCv3615100,846,382 - 100,861,852 (-)NCBIMGSCv36mm8
Celera15102,072,903 - 102,088,234 (-)NCBICelera
Cytogenetic Map15F1NCBI
cM Map1556.13NCBI
Fam186a
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr87132,922,410 - 132,981,466 (-)NCBIGRCr8
mRatBN7.27131,043,586 - 131,102,312 (-)NCBImRatBN7.2mRatBN7.2
Rnor_6.07141,592,629 - 141,627,652 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
RGSC_v3.47138,670,220 - 138,718,690 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
Celera7127,553,869 - 127,581,135 (-)NCBICelera
Cytogenetic Map7q36NCBI
Fam186a
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0NW_004955547870,511 - 930,908 (-)NCBIChiLan1.0ChiLan1.0
FAM186A
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21043,790,150 - 43,862,696 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11243,786,922 - 43,859,456 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01238,359,142 - 38,429,634 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11239,258,123 - 39,326,876 (+)NCBIpanpan1.1PanPan1.1panPan2
FAM186A
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1274,326,268 - 4,421,267 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl274,390,459 - 4,421,586 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha2741,836,726 - 41,929,426 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0274,377,343 - 4,470,157 (+)NCBIROS_Cfam_1.0
UMICH_Zoey_3.1274,340,792 - 4,434,758 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0274,330,454 - 4,423,432 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.02742,231,195 - 42,324,097 (-)NCBIUU_Cfam_GSD_1.0
Fam186a
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440494565,143,019 - 65,202,906 (+)NCBIHiC_Itri_2
SpeTri2.0NW_0049365127,961,924 - 8,021,682 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
FAM186A
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl516,233,993 - 16,279,903 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1516,233,752 - 16,280,685 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2516,886,467 - 16,920,132 (+)NCBISscrofa10.2Sscrofa10.2susScr3
FAM186A
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11146,553,669 - 46,612,478 (-)NCBIChlSab1.1ChlSab1.1chlSab2
Vero_WHO_p1.0NW_023666037199,489,755 - 199,563,131 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Fam186a
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_0046248161,954,349 - 2,021,566 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in FAM186A
123 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_001145475.1(FAM186A):c.6696+678A>G single nucleotide variant Lung cancer [RCV000111100] Chr12:50333233 [GRCh38]
Chr12:50727016 [GRCh37]
Chr12:12q13.12		 uncertain significance
GRCh38/hg38 12p13.33-q24.33(chr12:121271-133196807)x3 copy number gain See cases [RCV000139555] Chr12:121271..133196807 [GRCh38]
Chr12:282465..133773393 [GRCh37]
Chr12:100698..132283466 [NCBI36]
Chr12:12p13.33-q24.33		 pathogenic
GRCh38/hg38 12q13.12-13.13(chr12:50122359-53248460)x1 copy number loss See cases [RCV000142033] Chr12:50122359..53248460 [GRCh38]
Chr12:50516142..53642244 [GRCh37]
Chr12:48802409..51928511 [NCBI36]
Chr12:12q13.12-13.13		 pathogenic
GRCh37/hg19 12p13.33-q24.33(chr12:1-133851895)x3 copy number gain See cases [RCV000258805] Chr12:1..133851895 [GRCh37]
Chr12:12p13.33-q24.33		 pathogenic|likely pathogenic
GRCh37/hg19 12p13.33-q24.33(chr12:173787-133777902)x3 copy number gain See cases [RCV000510482] Chr12:173787..133777902 [GRCh37]
Chr12:12p13.33-q24.33		 pathogenic
GRCh37/hg19 12p13.33-q24.33(chr12:173787-133777902) copy number gain See cases [RCV000511643] Chr12:173787..133777902 [GRCh37]
Chr12:12p13.33-q24.33		 pathogenic
NC_000012.11:g.26370251_54361538inv inversion not specified [RCV000714265] Chr12:26370251..54361538 [GRCh37]
Chr12:12p12.1-q13.13		 uncertain significance
NM_001145475.3(FAM186A):c.1699G>T (p.Val567Leu) single nucleotide variant Inborn genetic diseases [RCV003281096] Chr12:50355133 [GRCh38]
Chr12:50748916 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.6263C>T (p.Pro2088Leu) single nucleotide variant Inborn genetic diseases [RCV003295571] Chr12:50350569 [GRCh38]
Chr12:50744352 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.6149T>C (p.Leu2050Pro) single nucleotide variant Inborn genetic diseases [RCV003240398] Chr12:50350683 [GRCh38]
Chr12:50744466 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.3065G>C (p.Arg1022Pro) single nucleotide variant Inborn genetic diseases [RCV003285482] Chr12:50353767 [GRCh38]
Chr12:50747550 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.2726A>T (p.Gln909Leu) single nucleotide variant Inborn genetic diseases [RCV003252661] Chr12:50354106 [GRCh38]
Chr12:50747889 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.1610G>A (p.Ser537Asn) single nucleotide variant Inborn genetic diseases [RCV003254650] Chr12:50355222 [GRCh38]
Chr12:50749005 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.1654C>T (p.Arg552Cys) single nucleotide variant Inborn genetic diseases [RCV003254780] Chr12:50355178 [GRCh38]
Chr12:50748961 [GRCh37]
Chr12:12q13.12		 uncertain significance
GRCh37/hg19 12p13.33-q24.33(chr12:621220-133779118)x3 copy number gain not provided [RCV000750253] Chr12:621220..133779118 [GRCh37]
Chr12:12p13.33-q24.33		 pathogenic
GRCh37/hg19 12p13.33-q24.33(chr12:191619-133777645)x3 copy number gain not provided [RCV000750246] Chr12:191619..133777645 [GRCh37]
Chr12:12p13.33-q24.33		 pathogenic
NM_001145475.3(FAM186A):c.414T>C (p.Asn138=) single nucleotide variant not provided [RCV000959267] Chr12:50360925 [GRCh38]
Chr12:50754708 [GRCh37]
Chr12:12q13.12		 benign
NM_001145475.3(FAM186A):c.849C>A (p.Asn283Lys) single nucleotide variant Inborn genetic diseases [RCV003240974] Chr12:50355983 [GRCh38]
Chr12:50749766 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.6579G>A (p.Met2193Ile) single nucleotide variant not provided [RCV001639240] Chr12:50334028 [GRCh38]
Chr12:50727811 [GRCh37]
Chr12:12q13.12		 benign
NM_001145475.3(FAM186A):c.2724G>T (p.Lys908Asn) single nucleotide variant Inborn genetic diseases [RCV003252660] Chr12:50354108 [GRCh38]
Chr12:50747891 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.559A>C (p.Lys187Gln) single nucleotide variant not provided [RCV001695063] Chr12:50360780 [GRCh38]
Chr12:50754563 [GRCh37]
Chr12:12q13.12		 benign
NM_001145475.3(FAM186A):c.3253A>G (p.Ile1085Val) single nucleotide variant Inborn genetic diseases [RCV003196975] Chr12:50353579 [GRCh38]
Chr12:50747362 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.1626G>A (p.Met542Ile) single nucleotide variant Inborn genetic diseases [RCV003276903] Chr12:50355206 [GRCh38]
Chr12:50748989 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.3754G>A (p.Gly1252Arg) single nucleotide variant Inborn genetic diseases [RCV003256924] Chr12:50353078 [GRCh38]
Chr12:50746861 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.4109C>A (p.Ala1370Asp) single nucleotide variant Inborn genetic diseases [RCV003286178] Chr12:50352723 [GRCh38]
Chr12:50746506 [GRCh37]
Chr12:12q13.12		 uncertain significance
GRCh37/hg19 12q13.12(chr12:50690609-50743492)x1 copy number loss not provided [RCV002474866] Chr12:50690609..50743492 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.140T>C (p.Val47Ala) single nucleotide variant Inborn genetic diseases [RCV002901780] Chr12:50396345 [GRCh38]
Chr12:50790128 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.5441C>T (p.Pro1814Leu) single nucleotide variant Inborn genetic diseases [RCV002774065] Chr12:50351391 [GRCh38]
Chr12:50745174 [GRCh37]
Chr12:12q13.12		 likely benign
NM_001145475.3(FAM186A):c.101G>A (p.Ser34Asn) single nucleotide variant Inborn genetic diseases [RCV002776711] Chr12:50396384 [GRCh38]
Chr12:50790167 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.5879C>G (p.Ser1960Cys) single nucleotide variant Inborn genetic diseases [RCV002858815] Chr12:50350953 [GRCh38]
Chr12:50744736 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.4255T>G (p.Leu1419Val) single nucleotide variant Inborn genetic diseases [RCV002683153] Chr12:50352577 [GRCh38]
Chr12:50746360 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.5503G>C (p.Gly1835Arg) single nucleotide variant Inborn genetic diseases [RCV002794501] Chr12:50351329 [GRCh38]
Chr12:50745112 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.5039C>T (p.Ala1680Val) single nucleotide variant Inborn genetic diseases [RCV002883976] Chr12:50351793 [GRCh38]
Chr12:50745576 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.1670A>T (p.Asp557Val) single nucleotide variant Inborn genetic diseases [RCV002793350] Chr12:50355162 [GRCh38]
Chr12:50748945 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.647G>A (p.Arg216His) single nucleotide variant Inborn genetic diseases [RCV002684501] Chr12:50356185 [GRCh38]
Chr12:50749968 [GRCh37]
Chr12:12q13.12		 likely benign
NM_001145475.3(FAM186A):c.5912C>T (p.Pro1971Leu) single nucleotide variant Inborn genetic diseases [RCV002684877] Chr12:50350920 [GRCh38]
Chr12:50744703 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.4936G>A (p.Ala1646Thr) single nucleotide variant Inborn genetic diseases [RCV002993094] Chr12:50351896 [GRCh38]
Chr12:50745679 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.768T>G (p.Asn256Lys) single nucleotide variant Inborn genetic diseases [RCV002682044] Chr12:50356064 [GRCh38]
Chr12:50749847 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.4238C>T (p.Pro1413Leu) single nucleotide variant Inborn genetic diseases [RCV002818607] Chr12:50352594 [GRCh38]
Chr12:50746377 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.6309G>T (p.Lys2103Asn) single nucleotide variant Inborn genetic diseases [RCV002837027] Chr12:50350523 [GRCh38]
Chr12:50744306 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.4090A>G (p.Thr1364Ala) single nucleotide variant Inborn genetic diseases [RCV002849314] Chr12:50352742 [GRCh38]
Chr12:50746525 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.3272A>T (p.Gln1091Leu) single nucleotide variant Inborn genetic diseases [RCV002911281] Chr12:50353560 [GRCh38]
Chr12:50747343 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.4102G>T (p.Ala1368Ser) single nucleotide variant Inborn genetic diseases [RCV002782982] Chr12:50352730 [GRCh38]
Chr12:50746513 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.6827C>T (p.Ser2276Phe) single nucleotide variant Inborn genetic diseases [RCV002844931] Chr12:50331691 [GRCh38]
Chr12:50725474 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.5386C>T (p.Arg1796Cys) single nucleotide variant Inborn genetic diseases [RCV002758680] Chr12:50351446 [GRCh38]
Chr12:50745229 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.1302C>A (p.Ser434Arg) single nucleotide variant Inborn genetic diseases [RCV002924504] Chr12:50355530 [GRCh38]
Chr12:50749313 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.5569T>G (p.Ser1857Ala) single nucleotide variant Inborn genetic diseases [RCV002662278] Chr12:50351263 [GRCh38]
Chr12:50745046 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.3995C>T (p.Ala1332Val) single nucleotide variant Inborn genetic diseases [RCV002691804] Chr12:50352837 [GRCh38]
Chr12:50746620 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.4895C>T (p.Ala1632Val) single nucleotide variant Inborn genetic diseases [RCV002693044] Chr12:50351937 [GRCh38]
Chr12:50745720 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.3224T>C (p.Leu1075Pro) single nucleotide variant Inborn genetic diseases [RCV002799988] Chr12:50353608 [GRCh38]
Chr12:50747391 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.2704G>A (p.Glu902Lys) single nucleotide variant Inborn genetic diseases [RCV002886833] Chr12:50354128 [GRCh38]
Chr12:50747911 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.2054A>T (p.Asp685Val) single nucleotide variant Inborn genetic diseases [RCV002822264] Chr12:50354778 [GRCh38]
Chr12:50748561 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.4751C>T (p.Ala1584Val) single nucleotide variant Inborn genetic diseases [RCV002955548] Chr12:50352081 [GRCh38]
Chr12:50745864 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.650C>T (p.Ala217Val) single nucleotide variant Inborn genetic diseases [RCV002713535] Chr12:50356182 [GRCh38]
Chr12:50749965 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.4253A>T (p.Glu1418Val) single nucleotide variant Inborn genetic diseases [RCV002931630] Chr12:50352579 [GRCh38]
Chr12:50746362 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.542C>T (p.Thr181Ile) single nucleotide variant Inborn genetic diseases [RCV002767929] Chr12:50360797 [GRCh38]
Chr12:50754580 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.3734C>T (p.Pro1245Leu) single nucleotide variant Inborn genetic diseases [RCV002665450] Chr12:50353098 [GRCh38]
Chr12:50746881 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.3964G>A (p.Ala1322Thr) single nucleotide variant Inborn genetic diseases [RCV002697089] Chr12:50352868 [GRCh38]
Chr12:50746651 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.3599C>A (p.Ala1200Asp) single nucleotide variant Inborn genetic diseases [RCV002789923] Chr12:50353233 [GRCh38]
Chr12:50747016 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.4109C>T (p.Ala1370Val) single nucleotide variant Inborn genetic diseases [RCV002701851] Chr12:50352723 [GRCh38]
Chr12:50746506 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.3985C>A (p.Pro1329Thr) single nucleotide variant Inborn genetic diseases [RCV002708943] Chr12:50352847 [GRCh38]
Chr12:50746630 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.488C>T (p.Pro163Leu) single nucleotide variant Inborn genetic diseases [RCV002892975] Chr12:50360851 [GRCh38]
Chr12:50754634 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.6779T>C (p.Phe2260Ser) single nucleotide variant Inborn genetic diseases [RCV002827845] Chr12:50331739 [GRCh38]
Chr12:50725522 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.6601G>A (p.Gly2201Arg) single nucleotide variant Inborn genetic diseases [RCV002981925] Chr12:50334006 [GRCh38]
Chr12:50727789 [GRCh37]
Chr12:12q13.12		 likely benign
NM_001145475.3(FAM186A):c.2252A>T (p.Lys751Ile) single nucleotide variant Inborn genetic diseases [RCV002698318] Chr12:50354580 [GRCh38]
Chr12:50748363 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.934G>A (p.Glu312Lys) single nucleotide variant Inborn genetic diseases [RCV002699163] Chr12:50355898 [GRCh38]
Chr12:50749681 [GRCh37]
Chr12:12q13.12		 likely benign
NM_001145475.3(FAM186A):c.3715T>A (p.Leu1239Met) single nucleotide variant Inborn genetic diseases [RCV002712521] Chr12:50353117 [GRCh38]
Chr12:50746900 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.6148C>G (p.Leu2050Val) single nucleotide variant Inborn genetic diseases [RCV002641008] Chr12:50350684 [GRCh38]
Chr12:50744467 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.6206G>A (p.Arg2069Gln) single nucleotide variant Inborn genetic diseases [RCV002668519] Chr12:50350626 [GRCh38]
Chr12:50744409 [GRCh37]
Chr12:12q13.12		 likely benign
NM_001145475.3(FAM186A):c.247C>T (p.Arg83Cys) single nucleotide variant Inborn genetic diseases [RCV002714355] Chr12:50363310 [GRCh38]
Chr12:50757093 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.4335G>C (p.Met1445Ile) single nucleotide variant Inborn genetic diseases [RCV002988163] Chr12:50352497 [GRCh38]
Chr12:50746280 [GRCh37]
Chr12:12q13.12		 likely benign
NM_001145475.3(FAM186A):c.4822G>A (p.Ala1608Thr) single nucleotide variant Inborn genetic diseases [RCV002988211] Chr12:50352010 [GRCh38]
Chr12:50745793 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.5221G>A (p.Ala1741Thr) single nucleotide variant Inborn genetic diseases [RCV002669147] Chr12:50351611 [GRCh38]
Chr12:50745394 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.3715T>G (p.Leu1239Val) single nucleotide variant Inborn genetic diseases [RCV002748180] Chr12:50353117 [GRCh38]
Chr12:50746900 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.6363G>C (p.Gln2121His) single nucleotide variant Inborn genetic diseases [RCV002672385] Chr12:50350469 [GRCh38]
Chr12:50744252 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.5473C>T (p.Leu1825Phe) single nucleotide variant Inborn genetic diseases [RCV002961384] Chr12:50351359 [GRCh38]
Chr12:50745142 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.5387G>C (p.Arg1796Pro) single nucleotide variant Inborn genetic diseases [RCV002648970] Chr12:50351445 [GRCh38]
Chr12:50745228 [GRCh37]
Chr12:12q13.12		 likely benign
NM_001145475.3(FAM186A):c.5935G>A (p.Ala1979Thr) single nucleotide variant Inborn genetic diseases [RCV002898200] Chr12:50350897 [GRCh38]
Chr12:50744680 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.1967T>C (p.Val656Ala) single nucleotide variant Inborn genetic diseases [RCV002920326] Chr12:50354865 [GRCh38]
Chr12:50748648 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.1340A>G (p.Tyr447Cys) single nucleotide variant Inborn genetic diseases [RCV002941506] Chr12:50355492 [GRCh38]
Chr12:50749275 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.2863C>T (p.His955Tyr) single nucleotide variant Inborn genetic diseases [RCV002831745] Chr12:50353969 [GRCh38]
Chr12:50747752 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.1681A>G (p.Thr561Ala) single nucleotide variant Inborn genetic diseases [RCV002940171] Chr12:50355151 [GRCh38]
Chr12:50748934 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.3661C>T (p.Pro1221Ser) single nucleotide variant Inborn genetic diseases [RCV002939374] Chr12:50353171 [GRCh38]
Chr12:50746954 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.6127C>A (p.Pro2043Thr) single nucleotide variant Inborn genetic diseases [RCV002677649] Chr12:50350705 [GRCh38]
Chr12:50744488 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.3613G>T (p.Val1205Phe) single nucleotide variant Inborn genetic diseases [RCV002680091] Chr12:50353219 [GRCh38]
Chr12:50747002 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.539G>A (p.Ser180Asn) single nucleotide variant Inborn genetic diseases [RCV002722492] Chr12:50360800 [GRCh38]
Chr12:50754583 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.4823C>T (p.Ala1608Val) single nucleotide variant Inborn genetic diseases [RCV002723304] Chr12:50352009 [GRCh38]
Chr12:50745792 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.4835G>C (p.Gly1612Ala) single nucleotide variant Inborn genetic diseases [RCV003202391] Chr12:50351997 [GRCh38]
Chr12:50745780 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.5293G>C (p.Val1765Leu) single nucleotide variant Inborn genetic diseases [RCV003179839] Chr12:50351539 [GRCh38]
Chr12:50745322 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.2548T>A (p.Leu850Met) single nucleotide variant Inborn genetic diseases [RCV003179838] Chr12:50354284 [GRCh38]
Chr12:50748067 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.161T>C (p.Ile54Thr) single nucleotide variant Inborn genetic diseases [RCV003191787] Chr12:50396324 [GRCh38]
Chr12:50790107 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.1862A>T (p.Glu621Val) single nucleotide variant Inborn genetic diseases [RCV003220834] Chr12:50354970 [GRCh38]
Chr12:50748753 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.5737T>C (p.Trp1913Arg) single nucleotide variant Inborn genetic diseases [RCV003214468] Chr12:50351095 [GRCh38]
Chr12:50744878 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.3295C>T (p.Leu1099Phe) single nucleotide variant Inborn genetic diseases [RCV003198174] Chr12:50353537 [GRCh38]
Chr12:50747320 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.6862C>A (p.Gln2288Lys) single nucleotide variant Inborn genetic diseases [RCV003194145] Chr12:50330745 [GRCh38]
Chr12:50724528 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.5755G>A (p.Ala1919Thr) single nucleotide variant Inborn genetic diseases [RCV003338250] Chr12:50351077 [GRCh38]
Chr12:50744860 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.1353G>C (p.Glu451Asp) single nucleotide variant Inborn genetic diseases [RCV003339957] Chr12:50355479 [GRCh38]
Chr12:50749262 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.5992G>A (p.Glu1998Lys) single nucleotide variant Inborn genetic diseases [RCV003359329] Chr12:50350840 [GRCh38]
Chr12:50744623 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.5486G>A (p.Arg1829Gln) single nucleotide variant Inborn genetic diseases [RCV003376307] Chr12:50351346 [GRCh38]
Chr12:50745129 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.5425A>G (p.Thr1809Ala) single nucleotide variant Inborn genetic diseases [RCV003383322] Chr12:50351407 [GRCh38]
Chr12:50745190 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.6280C>A (p.Pro2094Thr) single nucleotide variant Inborn genetic diseases [RCV003354551] Chr12:50350552 [GRCh38]
Chr12:50744335 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.3461C>T (p.Ala1154Val) single nucleotide variant Inborn genetic diseases [RCV003372008] Chr12:50353371 [GRCh38]
Chr12:50747154 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.6379G>A (p.Gly2127Arg) single nucleotide variant Inborn genetic diseases [RCV003348195] Chr12:50350453 [GRCh38]
Chr12:50744236 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.6980T>G (p.Leu2327Arg) single nucleotide variant Inborn genetic diseases [RCV003369413] Chr12:50330627 [GRCh38]
Chr12:50724410 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.2026A>T (p.Ile676Leu) single nucleotide variant Inborn genetic diseases [RCV003348349] Chr12:50354806 [GRCh38]
Chr12:50748589 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.1336T>G (p.Phe446Val) single nucleotide variant Inborn genetic diseases [RCV003367174] Chr12:50355496 [GRCh38]
Chr12:50749279 [GRCh37]
Chr12:12q13.12		 likely benign
NM_001145475.3(FAM186A):c.88C>G (p.Gln30Glu) single nucleotide variant Inborn genetic diseases [RCV003374044] Chr12:50396397 [GRCh38]
Chr12:50790180 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.6490A>T (p.Ile2164Phe) single nucleotide variant Inborn genetic diseases [RCV003385645] Chr12:50350342 [GRCh38]
Chr12:50744125 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.4800G>T (p.Gly1600=) single nucleotide variant not provided [RCV003456811] Chr12:50352032 [GRCh38]
Chr12:50745815 [GRCh37]
Chr12:12q13.12		 likely benign
NM_001145475.3(FAM186A):c.2168A>G (p.Gln723Arg) single nucleotide variant Inborn genetic diseases [RCV003385717] Chr12:50354664 [GRCh38]
Chr12:50748447 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001145475.3(FAM186A):c.1973A>G (p.Glu658Gly) single nucleotide variant Inborn genetic diseases [RCV003375795] Chr12:50354859 [GRCh38]
Chr12:50748642 [GRCh37]
Chr12:12q13.12		 likely benign
NM_001145475.3(FAM186A):c.4449C>G (p.Leu1483=) single nucleotide variant not provided [RCV003390237] Chr12:50352383 [GRCh38]
Chr12:50746166 [GRCh37]
Chr12:12q13.12		 likely benign
NM_001145475.3(FAM186A):c.3621C>A (p.Leu1207=) single nucleotide variant not provided [RCV003390238] Chr12:50353211 [GRCh38]
Chr12:50746994 [GRCh37]
Chr12:12q13.12		 likely benign
NM_001145475.3(FAM186A):c.*8A>G single nucleotide variant not provided [RCV003391808] Chr12:50327375 [GRCh38]
Chr12:50721158 [GRCh37]
Chr12:12q13.12		 likely benign
NM_001145475.3(FAM186A):c.4860C>G (p.Ala1620=) single nucleotide variant not provided [RCV003456810] Chr12:50351972 [GRCh38]
Chr12:50745755 [GRCh37]
Chr12:12q13.12		 likely benign
NM_001145475.3(FAM186A):c.4680T>G (p.Ala1560=) single nucleotide variant not provided [RCV003391811] Chr12:50352152 [GRCh38]
Chr12:50745935 [GRCh37]
Chr12:12q13.12		 likely benign
NM_001145475.3(FAM186A):c.4362G>A (p.Glu1454=) single nucleotide variant not provided [RCV003391812] Chr12:50352470 [GRCh38]
Chr12:50746253 [GRCh37]
Chr12:12q13.12		 likely benign
NM_001145475.3(FAM186A):c.4290T>C (p.Ala1430=) single nucleotide variant not provided [RCV003391813] Chr12:50352542 [GRCh38]
Chr12:50746325 [GRCh37]
Chr12:12q13.12		 likely benign
NM_001145475.3(FAM186A):c.4284A>C (p.Ala1428=) single nucleotide variant not provided [RCV003391814] Chr12:50352548 [GRCh38]
Chr12:50746331 [GRCh37]
Chr12:12q13.12		 likely benign
NM_001145475.3(FAM186A):c.3636T>C (p.Ala1212=) single nucleotide variant not provided [RCV003391815] Chr12:50353196 [GRCh38]
Chr12:50746979 [GRCh37]
Chr12:12q13.12		 likely benign
NM_001145475.3(FAM186A):c.4500C>G (p.Ala1500=) single nucleotide variant not provided [RCV003390236] Chr12:50352332 [GRCh38]
Chr12:50746115 [GRCh37]
Chr12:12q13.12		 likely benign
NM_001145475.3(FAM186A):c.4723C>T (p.Leu1575=) single nucleotide variant not provided [RCV003456812] Chr12:50352109 [GRCh38]
Chr12:50745892 [GRCh37]
Chr12:12q13.12		 likely benign
NM_001145475.3(FAM186A):c.4728G>T (p.Gly1576=) single nucleotide variant not provided [RCV003391809] Chr12:50352104 [GRCh38]
Chr12:50745887 [GRCh37]
Chr12:12q13.12		 likely benign
NM_001145475.3(FAM186A):c.4687T>C (p.Leu1563=) single nucleotide variant not provided [RCV003391810] Chr12:50352145 [GRCh38]
Chr12:50745928 [GRCh37]
Chr12:12q13.12		 likely benign
NM_001145475.3(FAM186A):c.3276C>T (p.Ala1092=) single nucleotide variant not provided [RCV003391816] Chr12:50353556 [GRCh38]
Chr12:50747339 [GRCh37]
Chr12:12q13.12		 likely benign
NM_001145475.3(FAM186A):c.4788G>T (p.Ala1596=) single nucleotide variant not provided [RCV003390234] Chr12:50352044 [GRCh38]
Chr12:50745827 [GRCh37]
Chr12:12q13.12		 likely benign
NM_001145475.3(FAM186A):c.4543T>C (p.Leu1515=) single nucleotide variant not provided [RCV003390235] Chr12:50352289 [GRCh38]
Chr12:50746072 [GRCh37]
Chr12:12q13.12		 likely benign
NM_001145475.3(FAM186A):c.4872G>T (p.Gly1624=) single nucleotide variant not provided [RCV003886289] Chr12:50351960 [GRCh38]
Chr12:50745743 [GRCh37]
Chr12:12q13.12		 likely benign
NM_001145475.3(FAM186A):c.4866T>C (p.Ala1622=) single nucleotide variant not provided [RCV003885683] Chr12:50351966 [GRCh38]
Chr12:50745749 [GRCh37]
Chr12:12q13.12		 likely benign
NM_001145475.3(FAM186A):c.148A>G (p.Ile50Val) single nucleotide variant Inborn genetic diseases [RCV003343317] Chr12:50396337 [GRCh38]
Chr12:50790120 [GRCh37]
Chr12:12q13.12		 likely benign
NM_001145475.3(FAM186A):c.6397C>T (p.His2133Tyr) single nucleotide variant Inborn genetic diseases [RCV003342461] Chr12:50350435 [GRCh38]
Chr12:50744218 [GRCh37]
Chr12:12q13.12		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1010
Count of miRNA genes:468
Interacting mature miRNAs:506
Transcripts:ENST00000327337, ENST00000539751, ENST00000543096, ENST00000543111
Prediction methods:Miranda, Rnahybrid, Targetscan
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
D8S2279  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q22.12UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map15q22.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map17q24.2UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map15q13.2UniSTS
Cytogenetic Map12q24.1UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map3p24.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map5q14UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map7q21.11UniSTS
Cytogenetic Map9q34.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map6p21.1-p12UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map7p21.3UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map1q12UniSTS
Cytogenetic Map8p23UniSTS
Cytogenetic Map11q13.2-q13.3UniSTS
Cytogenetic Map13q14.1-q14.3UniSTS
Cytogenetic Map3q22-q24UniSTS
Cytogenetic Map3q13.1-q13.2UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map17p13.1-p12UniSTS
Cytogenetic Map18q21.33UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map17p12-p11.2UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map2q32UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map2q33UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map14q31-q32UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map1q23.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map4q32.2UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map5q14.2UniSTS
Cytogenetic Map4q32.1UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map19q13.11UniSTS
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Cytogenetic Map17q11.1UniSTS
Cytogenetic Map15q25.1UniSTS
Cytogenetic Map13q12.3UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map12q12-q13UniSTS
Cytogenetic Map12q14UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map2q32-q34UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic Map2p15-p13UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic Map19q13.33-q13.41UniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map6q23-q24UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map2p13UniSTS
Cytogenetic Map13q11-q12UniSTS
Cytogenetic Map6p12.3-p11.2UniSTS
Cytogenetic Map6q16.1-q16.3UniSTS
Cytogenetic Map22q11UniSTS
Cytogenetic Map7q31.2UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map3q25.2UniSTS
Cytogenetic Map3p21.1-p14.3UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map3q23-q24UniSTS
Cytogenetic Map3q12UniSTS
Cytogenetic Map7q11.1UniSTS
Cytogenetic Map3q22.3UniSTS
Cytogenetic Map7q21.3UniSTS
Cytogenetic Map4q31.1UniSTS
Cytogenetic Map22q12-q13UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map18q21.3UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map11q21UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map4q28-q32UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map8p11UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map1q24.3UniSTS
Cytogenetic Map9q33.1UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map2p16.2UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map1p36.2UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map13q22.1UniSTS
Cytogenetic Map2q12.2UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map4q21UniSTS
Cytogenetic Map13q12.2UniSTS
Cytogenetic Map9q31-q33UniSTS
Cytogenetic Map6p24.1UniSTS
Cytogenetic Map1q23UniSTS
Cytogenetic Map11q12-q13UniSTS
Cytogenetic Map11q13.3UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map11q12.1UniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map8p21UniSTS
Cytogenetic Map19q13.1-q13.2UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map7q36.2UniSTS
Cytogenetic Map4q32.3UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map10q26.1UniSTS
Cytogenetic Map9q32-q33.3UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map5q31-q34UniSTS
Cytogenetic Map9q33-q34UniSTS
Cytogenetic Map5q11.2-q13.2UniSTS
Cytogenetic Map13q32UniSTS
Cytogenetic Map9q22.32UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map5q22UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic MapXq13.3UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map3p26.3UniSTS
Cytogenetic Map2q11.1UniSTS
Cytogenetic Map21q11.2UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map12q24.23UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map2q31.1-q31.2UniSTS
Cytogenetic MapXp22.31UniSTS
Cytogenetic MapXp21.3UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map4q28.2UniSTS
Cytogenetic Map3p14.2UniSTS
Cytogenetic Map3q24UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map20q13.2UniSTS
Cytogenetic Map14q11.2-q12UniSTS
Cytogenetic Map3p24UniSTS
Cytogenetic Map12q23.3UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map11q14.3UniSTS
Cytogenetic Map10q25.2UniSTS
Cytogenetic Map3q25.1UniSTS
Cytogenetic Map8q13UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map3p22.3UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map8q23.3UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic Map11cen-q12UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map12q21UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map7q22-q31UniSTS
Cytogenetic Map11q22UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map1p35-p34UniSTS
Cytogenetic Map4p13-p12UniSTS
Cytogenetic Map10q21-q22UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map7p13-p11.1UniSTS
Cytogenetic Map9q31-q34UniSTS
Cytogenetic Map7q21.1-q22UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map3q13.13-q13.2UniSTS
Cytogenetic MapXp22.13UniSTS
Cytogenetic Map13q12.12UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map1pUniSTS
Cytogenetic Map16pUniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map2qUniSTS
Cytogenetic Map5q13.1UniSTS
Cytogenetic Map11p14.1UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map2p22UniSTS
Cytogenetic Map5q14.3UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map5q23.2UniSTS
Cytogenetic Map2p24.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map9p21.1UniSTS
Cytogenetic Map9q34.2-q34.3UniSTS


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
High
Medium 317
Low 7 8 199 5 40 5 25 11 388 40 141 13 1 23
Below cutoff 2325 2721 1420 531 1463 369 4037 2104 3251 312 900 1446 168 1196 2687

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000327337   ⟹   ENSP00000329995
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1250,327,309 - 50,396,609 (-)Ensembl
RefSeq Acc Id: ENST00000539751   ⟹   ENSP00000437706
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1250,327,309 - 50,334,103 (-)Ensembl
RefSeq Acc Id: ENST00000543096   ⟹   ENSP00000443703
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1250,326,230 - 50,350,885 (-)Ensembl
RefSeq Acc Id: ENST00000543111   ⟹   ENSP00000441337
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1250,326,230 - 50,396,622 (-)Ensembl
RefSeq Acc Id: NM_001145475   ⟹   NP_001138947
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381250,327,309 - 50,396,609 (-)NCBI
GRCh371250,721,095 - 50,790,405 (-)RGD
Celera1249,516,875 - 49,586,366 (-)RGD
HuRef1247,754,259 - 47,823,307 (-)RGD
CHM1_11250,687,064 - 50,756,579 (-)NCBI
T2T-CHM13v2.01250,290,439 - 50,359,662 (-)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_001138947 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein A6NE01 (Get FASTA)   NCBI Sequence Viewer  
  AAI40704 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000329995
  ENSP00000329995.5
  ENSP00000437706.1
  ENSP00000441337.1
  ENSP00000443703.1
Reference Protein Sequences
RefSeq Acc Id: NP_001138947   ⟸   NM_001145475
- UniProtKB: A6NE01 (UniProtKB/Swiss-Prot),   F5GYN0 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000441337   ⟸   ENST00000543111
RefSeq Acc Id: ENSP00000443703   ⟸   ENST00000543096
RefSeq Acc Id: ENSP00000329995   ⟸   ENST00000327337
RefSeq Acc Id: ENSP00000437706   ⟸   ENST00000539751
Protein Domains
FAM186A/B C-terminal   FAM186A/B N-terminal

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-A6NE01-F1-model_v2 AlphaFold A6NE01 1-2351 view protein structure


Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:26980 AgrOrtholog
COSMIC FAM186A COSMIC
Ensembl Genes ENSG00000185958 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000327337 ENTREZGENE
  ENST00000327337.6 UniProtKB/Swiss-Prot
  ENST00000539751.1 UniProtKB/TrEMBL
  ENST00000543096.5 UniProtKB/TrEMBL
  ENST00000543111.5 UniProtKB/TrEMBL
GTEx ENSG00000185958 GTEx
HGNC ID HGNC:26980 ENTREZGENE
Human Proteome Map FAM186A Human Proteome Map
InterPro FAM186A_B_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  FAM186A_B_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  FAM186A_PQQAQ UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:121006 UniProtKB/Swiss-Prot
NCBI Gene 121006 ENTREZGENE
PANTHER GLUTENIN, HIGH MOLECULAR WEIGHT SUBUNIT PW212-RELATED PROTEIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR33590:SF2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam FAM186A-B_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  FAM186A-B_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  FAM186A_PQQAQ UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA164719869 PharmGKB
UniProt A6NE01 ENTREZGENE
  B9EIJ5_HUMAN UniProtKB/TrEMBL
  F186A_HUMAN UniProtKB/Swiss-Prot
  F5GYN0 ENTREZGENE, UniProtKB/TrEMBL
  F5H8C1_HUMAN UniProtKB/TrEMBL
  H0YFA1_HUMAN UniProtKB/TrEMBL


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2015-11-24 FAM186A  family with sequence similarity 186 member A    family with sequence similarity 186, member A  Symbol and/or name change 5135510 APPROVED