MYADM (myeloid associated differentiation marker) - Rat Genome Database

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Gene: MYADM (myeloid associated differentiation marker) Homo sapiens
Analyze
Symbol: MYADM
Name: myeloid associated differentiation marker
RGD ID: 1353717
HGNC Page HGNC:7544
Description: Involved in several processes, including negative regulation of actin filament polymerization; negative regulation of heterotypic cell-cell adhesion; and positive regulation of substrate adhesion-dependent cell spreading. Located in several cellular components, including cortical actin cytoskeleton; membrane raft; and ruffle.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: myeloid upregulated protein; myeloid-associated differentiation marker; SB135
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Related Pseudogenes: MYADML  
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381953,865,628 - 53,876,435 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1953,864,763 - 53,878,125 (+)EnsemblGRCh38hg38GRCh38
GRCh371954,368,882 - 54,379,689 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361959,061,423 - 59,071,501 (+)NCBINCBI36Build 36hg18NCBI36
Build 341959,062,948 - 59,070,607NCBI
Celera1951,410,687 - 51,420,740 (+)NCBICelera
Cytogenetic Map19q13.42NCBI
HuRef1950,688,935 - 50,698,996 (+)NCBIHuRef
CHM1_11954,371,421 - 54,381,447 (+)NCBICHM1_1
T2T-CHM13v2.01956,945,407 - 56,956,143 (+)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
(-)-alpha-phellandrene  (EXP)
(-)-demecolcine  (EXP)
(1->4)-beta-D-glucan  (ISO)
1,2-dimethylhydrazine  (ISO)
1-naphthyl isothiocyanate  (ISO)
17beta-estradiol  (EXP)
2,3,7,8-tetrachlorodibenzodioxine  (EXP,ISO)
2,6-dinitrotoluene  (ISO)
2-hydroxypropanoic acid  (EXP)
2-methylcholine  (EXP)
3H-1,2-dithiole-3-thione  (ISO)
4,4'-diaminodiphenylmethane  (ISO)
4,4'-sulfonyldiphenol  (EXP,ISO)
5-methoxy-2-\{[(4-methoxy-3,5-dimethylpyridin-2-yl)methyl]sulfinyl\}-1H-benzimidazole  (ISO)
6-propyl-2-thiouracil  (ISO)
acetamide  (ISO)
aflatoxin B1  (EXP)
all-trans-retinoic acid  (EXP)
alpha-phellandrene  (EXP)
amiodarone  (ISO)
amitrole  (ISO)
amphetamine  (ISO)
atrazine  (ISO)
benzbromarone  (ISO)
benzo[a]pyrene  (EXP,ISO)
benzo[a]pyrene diol epoxide I  (EXP)
benzo[b]fluoranthene  (ISO)
bisphenol A  (EXP,ISO)
bisphenol AF  (EXP)
Bisphenol B  (EXP)
bisphenol F  (EXP,ISO)
cadmium atom  (EXP)
cadmium dichloride  (EXP,ISO)
cantharidin  (ISO)
carbamazepine  (EXP)
carbon nanotube  (ISO)
chlorpyrifos  (ISO)
chrysene  (ISO)
cisplatin  (EXP)
clofibrate  (ISO)
clozapine  (EXP)
cobalt dichloride  (EXP)
crocidolite asbestos  (EXP)
Cuprizon  (EXP)
cyclosporin A  (EXP)
cytarabine  (EXP)
Dibutyl phosphate  (EXP)
dibutyl phthalate  (ISO)
dicrotophos  (EXP)
dieldrin  (EXP)
flutamide  (ISO)
folic acid  (ISO)
furan  (ISO)
glafenine  (ISO)
haloperidol  (EXP)
hydrogen peroxide  (EXP)
inulin  (ISO)
isobutanol  (EXP)
ivermectin  (EXP)
L-ethionine  (ISO)
lead diacetate  (EXP)
lipopolysaccharide  (EXP)
menadione  (EXP)
N-nitrosodiethylamine  (ISO)
N-nitrosodimethylamine  (ISO)
nickel atom  (EXP)
nickel sulfate  (EXP)
omeprazole  (ISO)
oxaliplatin  (ISO)
paracetamol  (EXP,ISO)
perfluorohexanesulfonic acid  (ISO)
perfluorooctane-1-sulfonic acid  (ISO)
phenobarbital  (ISO)
pirinixic acid  (ISO)
progesterone  (EXP)
rac-lactic acid  (EXP)
rotenone  (ISO)
SB 431542  (EXP)
silicon dioxide  (EXP)
sodium arsenite  (EXP,ISO)
temozolomide  (EXP)
testosterone  (ISO)
tetrachloromethane  (ISO)
tetraphene  (ISO)
thioacetamide  (ISO)
thiram  (EXP)
topotecan  (ISO)
triphenyl phosphate  (EXP)
triptonide  (ISO)
urethane  (EXP)
valproic acid  (EXP)
vancomycin  (ISO)
vinclozolin  (ISO)

References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. Isolation of MYADM, a novel hematopoietic-associated marker gene expressed in multipotent progenitor cells and up-regulated during myeloid differentiation. Pettersson M, etal., J Leukoc Biol 2000 Mar;67(3):423-31.
3. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:12075932   PMID:12477932   PMID:12975309   PMID:14702039   PMID:15146197   PMID:15489334   PMID:15900300   PMID:16303743   PMID:16344560   PMID:17097684   PMID:19322201   PMID:21325632  
PMID:21516116   PMID:21873635   PMID:23264465   PMID:23376485   PMID:24623722   PMID:26186194   PMID:26496610   PMID:26760575   PMID:28443643   PMID:28514442   PMID:28784648   PMID:29117863  
PMID:29509190   PMID:31324722   PMID:31527615   PMID:31540324   PMID:31586073   PMID:32296183   PMID:32373233   PMID:32513696   PMID:32780723   PMID:32807901   PMID:33194618   PMID:33961781  
PMID:34862427   PMID:35013218   PMID:35156780   PMID:35676659   PMID:35696571   PMID:36215168   PMID:36244648   PMID:36526897   PMID:36724073   PMID:37002207   PMID:37132043   PMID:37616343  
PMID:38270169   PMID:38658526   PMID:38832511   PMID:39147351  


Genomics

Comparative Map Data
MYADM
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381953,865,628 - 53,876,435 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1953,864,763 - 53,878,125 (+)EnsemblGRCh38hg38GRCh38
GRCh371954,368,882 - 54,379,689 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361959,061,423 - 59,071,501 (+)NCBINCBI36Build 36hg18NCBI36
Build 341959,062,948 - 59,070,607NCBI
Celera1951,410,687 - 51,420,740 (+)NCBICelera
Cytogenetic Map19q13.42NCBI
HuRef1950,688,935 - 50,698,996 (+)NCBIHuRef
CHM1_11954,371,421 - 54,381,447 (+)NCBICHM1_1
T2T-CHM13v2.01956,945,407 - 56,956,143 (+)NCBIT2T-CHM13v2.0
Myadm
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm3973,337,563 - 3,347,871 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl73,337,605 - 3,348,958 (+)EnsemblGRCm39 Ensembl
GRCm3873,289,038 - 3,299,355 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl73,289,080 - 3,300,442 (+)EnsemblGRCm38mm10GRCm38
MGSCv3773,289,039 - 3,299,350 (+)NCBIGRCm37MGSCv37mm9NCBIm37
Celera73,239,892 - 3,250,194 (+)NCBICelera
Cytogenetic Map7A1NCBI
cM Map71.92NCBI
Myadm
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8174,779,616 - 74,796,752 (-)NCBIGRCr8
mRatBN7.2165,864,180 - 65,874,701 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl165,864,173 - 65,874,035 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx171,312,366 - 71,320,711 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0179,735,339 - 79,743,684 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0173,068,572 - 73,076,904 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0164,438,465 - 64,448,332 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl164,438,472 - 64,446,818 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0163,430,406 - 63,440,255 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4164,177,547 - 64,185,893 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1164,255,658 - 64,264,004 (-)NCBI
Celera163,588,895 - 63,597,242 (-)NCBICelera
Cytogenetic Map1q12NCBI
Myadm
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_004955604280,977 - 284,381 (-)EnsemblChiLan1.0
ChiLan1.0NW_004955604280,977 - 284,381 (-)NCBIChiLan1.0ChiLan1.0
MYADM
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v22059,878,608 - 59,888,754 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11961,800,611 - 61,810,691 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01950,807,615 - 50,817,196 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11959,656,521 - 59,666,643 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1959,663,790 - 59,664,758 (+)Ensemblpanpan1.1panPan2
MYADM
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11103,315,606 - 103,322,329 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1103,381,284 - 103,388,479 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01103,969,865 - 103,977,066 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1103,970,647 - 103,977,121 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11103,602,297 - 103,609,488 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01103,364,030 - 103,371,220 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01104,083,017 - 104,090,213 (-)NCBIUU_Cfam_GSD_1.0
Myadm
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_0244093492,854,208 - 2,858,812 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_00493699480,439 - 83,536 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_00493699478,989 - 83,536 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
MYADM
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl656,236,311 - 56,244,185 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1656,236,306 - 56,278,577 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2652,971,110 - 52,978,880 (+)NCBISscrofa10.2Sscrofa10.2susScr3
MYADM
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1646,559,943 - 46,568,057 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl646,566,968 - 46,567,936 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366607326,638,157 - 26,648,060 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Myadm
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046248322,568,128 - 2,573,544 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046248322,568,128 - 2,574,248 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in MYADM
21 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 19q13.33-13.43(chr19:50191219-58535818)x3 copy number gain See cases [RCV000050883] Chr19:50191219..58535818 [GRCh38]
Chr19:50694476..59047185 [GRCh37]
Chr19:55386288..63738997 [NCBI36]
Chr19:19q13.33-13.43
pathogenic
GRCh38/hg38 19q13.33-13.43(chr19:49907832-58557889)x3 copy number gain See cases [RCV000052925] Chr19:49907832..58557889 [GRCh38]
Chr19:50411089..59069256 [GRCh37]
Chr19:55102901..63761068 [NCBI36]
Chr19:19q13.33-13.43
pathogenic
GRCh38/hg38 19q13.41-13.43(chr19:51141518-58539965)x3 copy number gain See cases [RCV000052926] Chr19:51141518..58539965 [GRCh38]
Chr19:51644775..59051332 [GRCh37]
Chr19:56336587..63743144 [NCBI36]
Chr19:19q13.41-13.43
pathogenic
GRCh38/hg38 19q13.33-13.43(chr19:47908540-58539965)x3 copy number gain See cases [RCV000052914] Chr19:47908540..58539965 [GRCh38]
Chr19:48411797..59051332 [GRCh37]
Chr19:53103609..63743144 [NCBI36]
Chr19:19q13.33-13.43
pathogenic
GRCh38/hg38 19q13.33-13.43(chr19:47929575-58572206)x3 copy number gain See cases [RCV000052915] Chr19:47929575..58572206 [GRCh38]
Chr19:48432832..59083573 [GRCh37]
Chr19:53124644..63775385 [NCBI36]
Chr19:19q13.33-13.43
pathogenic
GRCh38/hg38 19q13.42(chr19:53553042-53899466)x3 copy number gain See cases [RCV000052593] Chr19:53553042..53899466 [GRCh38]
Chr19:54056296..54402720 [GRCh37]
Chr19:58748108..59094532 [NCBI36]
Chr19:19q13.42
uncertain significance
GRCh38/hg38 19q13.41-13.43(chr19:52612432-58581203)x3 copy number gain See cases [RCV000134174] Chr19:52612432..58581203 [GRCh38]
Chr19:53115685..59092570 [GRCh37]
Chr19:57807497..63784382 [NCBI36]
Chr19:19q13.41-13.43
pathogenic
GRCh38/hg38 19q13.41-13.43(chr19:52955056-58581203)x3 copy number gain See cases [RCV000134139] Chr19:52955056..58581203 [GRCh38]
Chr19:53458309..59092570 [GRCh37]
Chr19:58150121..63784382 [NCBI36]
Chr19:19q13.41-13.43
pathogenic
GRCh38/hg38 19q13.33-13.43(chr19:50152520-58581203)x3 copy number gain See cases [RCV000135843] Chr19:50152520..58581203 [GRCh38]
Chr19:50655777..59092570 [GRCh37]
Chr19:55347589..63784382 [NCBI36]
Chr19:19q13.33-13.43
pathogenic
GRCh38/hg38 19q13.41-13.43(chr19:52143873-58445521)x3 copy number gain See cases [RCV000142008] Chr19:52143873..58445521 [GRCh38]
Chr19:52647126..58956888 [GRCh37]
Chr19:57338938..63648700 [NCBI36]
Chr19:19q13.41-13.43
pathogenic
GRCh37/hg19 19q13.42(chr19:54280799-54486105)x3 copy number gain See cases [RCV000240206] Chr19:54280799..54486105 [GRCh37]
Chr19:19q13.42
uncertain significance
GRCh37/hg19 19q13.42(chr19:54082353-54486105)x3 copy number gain See cases [RCV000240228] Chr19:54082353..54486105 [GRCh37]
Chr19:19q13.42
uncertain significance
GRCh37/hg19 19q13.42(chr19:54280799-54635178)x1 copy number loss See cases [RCV000240343] Chr19:54280799..54635178 [GRCh37]
Chr19:19q13.42
pathogenic
GRCh37/hg19 19q13.33-13.43(chr19:50489390-59095359)x3 copy number gain See cases [RCV000445925] Chr19:50489390..59095359 [GRCh37]
Chr19:19q13.33-13.43
pathogenic
GRCh37/hg19 19q13.42-13.43(chr19:54344821-58956888)x3 copy number gain See cases [RCV000448186] Chr19:54344821..58956888 [GRCh37]
Chr19:19q13.42-13.43
pathogenic
NM_138373.5(MYADM):c.19C>T (p.Arg7Cys) single nucleotide variant not specified [RCV004304648] Chr19:53873548 [GRCh38]
Chr19:54376802 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_138373.5(MYADM):c.890C>T (p.Ala297Val) single nucleotide variant not specified [RCV004317359] Chr19:53874419 [GRCh38]
Chr19:54377673 [GRCh37]
Chr19:19q13.42
uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888) copy number gain See cases [RCV000512296] Chr19:260912..58956888 [GRCh37]
Chr19:19p13.3-q13.43
pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3 copy number gain See cases [RCV000511289] Chr19:260912..58956888 [GRCh37]
Chr19:19p13.3-q13.43
pathogenic|uncertain significance
NM_138373.5(MYADM):c.440C>T (p.Ala147Val) single nucleotide variant not specified [RCV004318088] Chr19:53873969 [GRCh38]
Chr19:54377223 [GRCh37]
Chr19:19q13.42
uncertain significance
GRCh37/hg19 19q13.42(chr19:54082504-54417191)x3 copy number gain not provided [RCV000684078] Chr19:54082504..54417191 [GRCh37]
Chr19:19q13.42
uncertain significance
GRCh37/hg19 19q13.42(chr19:53867570-55833460)x3 copy number gain not provided [RCV000684091] Chr19:53867570..55833460 [GRCh37]
Chr19:19q13.42
uncertain significance
GRCh37/hg19 19q13.42-13.43(chr19:54196216-58759679)x3 copy number gain not provided [RCV000684095] Chr19:54196216..58759679 [GRCh37]
Chr19:19q13.42-13.43
pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:68029-59110290)x3 copy number gain not provided [RCV000752439] Chr19:68029..59110290 [GRCh37]
Chr19:19p13.3-q13.43
pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:260912-59097160)x3 copy number gain not provided [RCV000752444] Chr19:260912..59097160 [GRCh37]
Chr19:19p13.3-q13.43
pathogenic
GRCh37/hg19 19q13.42(chr19:54314489-54373081)x3 copy number gain not provided [RCV000740243] Chr19:54314489..54373081 [GRCh37]
Chr19:19q13.42
benign
GRCh37/hg19 19q13.42(chr19:54346718-54379573)x3 copy number gain not provided [RCV000740244] Chr19:54346718..54379573 [GRCh37]
Chr19:19q13.42
benign
GRCh37/hg19 19q13.42(chr19:54357764-54373078)x1 copy number loss not provided [RCV000740247] Chr19:54357764..54373078 [GRCh37]
Chr19:19q13.42
benign
GRCh37/hg19 19q13.33-13.43(chr19:50740074-59097160)x3 copy number gain not provided [RCV000740208] Chr19:50740074..59097160 [GRCh37]
Chr19:19q13.33-13.43
pathogenic
NC_000019.10:g.53536530_53981185dup duplication Silver Russell Syndrome-related disorder [RCV000785667] Chr19:53536530..53981185 [GRCh38]
Chr19:54039784..54484439 [GRCh37]
Chr19:19q13.42
uncertain significance
GRCh37/hg19 19q13.32-13.42(chr19:47939842-54626871) copy number gain not provided [RCV001249294] Chr19:47939842..54626871 [GRCh37]
Chr19:19q13.32-13.42
not provided
NC_000019.10:g.(?_53873530)_(53893391_?)dup duplication not provided [RCV001032352] Chr19:54376784..54396645 [GRCh37]
Chr19:19q13.42
uncertain significance
GRCh37/hg19 19q13.42-13.43(chr19:54334195-56434037)x3 copy number gain not provided [RCV001259948] Chr19:54334195..56434037 [GRCh37]
Chr19:19q13.42-13.43
uncertain significance
GRCh37/hg19 19q13.33-13.43(chr19:48463931-57095254)x3 copy number gain not provided [RCV001259944] Chr19:48463931..57095254 [GRCh37]
Chr19:19q13.33-13.43
pathogenic
NC_000019.9:g.(?_54297303)_(54410149_?)dup duplication Familial cold autoinflammatory syndrome 2 [RCV001296829] Chr19:54297303..54410149 [GRCh37]
Chr19:19q13.42
uncertain significance
NC_000019.9:g.(?_54297303)_(55678016_?)dup duplication not provided [RCV001981426] Chr19:54297303..55678016 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_138373.5(MYADM):c.920A>C (p.Tyr307Ser) single nucleotide variant not specified [RCV004313023] Chr19:53874449 [GRCh38]
Chr19:54377703 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_138373.5(MYADM):c.642C>A (p.Phe214Leu) single nucleotide variant not specified [RCV004145381] Chr19:53874171 [GRCh38]
Chr19:54377425 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_138373.5(MYADM):c.718C>G (p.Leu240Val) single nucleotide variant not specified [RCV004097635] Chr19:53874247 [GRCh38]
Chr19:54377501 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_138373.5(MYADM):c.253G>A (p.Val85Met) single nucleotide variant not specified [RCV004169063] Chr19:53873782 [GRCh38]
Chr19:54377036 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_138373.5(MYADM):c.742G>A (p.Val248Ile) single nucleotide variant not specified [RCV004230062] Chr19:53874271 [GRCh38]
Chr19:54377525 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_138373.5(MYADM):c.394C>T (p.Arg132Cys) single nucleotide variant not specified [RCV004221825] Chr19:53873923 [GRCh38]
Chr19:54377177 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_138373.5(MYADM):c.118C>T (p.Arg40Cys) single nucleotide variant not specified [RCV004231374] Chr19:53873647 [GRCh38]
Chr19:54376901 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_138373.5(MYADM):c.295C>T (p.Arg99Cys) single nucleotide variant not specified [RCV004079942] Chr19:53873824 [GRCh38]
Chr19:54377078 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_138373.5(MYADM):c.583A>G (p.Asn195Asp) single nucleotide variant not specified [RCV004228581] Chr19:53874112 [GRCh38]
Chr19:54377366 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_138373.5(MYADM):c.553T>C (p.Cys185Arg) single nucleotide variant not specified [RCV004096187] Chr19:53874082 [GRCh38]
Chr19:54377336 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_138373.5(MYADM):c.798G>C (p.Lys266Asn) single nucleotide variant not specified [RCV004280948] Chr19:53874327 [GRCh38]
Chr19:54377581 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_138373.5(MYADM):c.782A>C (p.Tyr261Ser) single nucleotide variant not specified [RCV004275815] Chr19:53874311 [GRCh38]
Chr19:54377565 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_138373.5(MYADM):c.246C>G (p.Ile82Met) single nucleotide variant not specified [RCV004256469] Chr19:53873775 [GRCh38]
Chr19:54377029 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_138373.5(MYADM):c.409G>A (p.Ala137Thr) single nucleotide variant not specified [RCV004309195] Chr19:53873938 [GRCh38]
Chr19:54377192 [GRCh37]
Chr19:19q13.42
uncertain significance
GRCh37/hg19 19q13.33-13.43(chr19:49625130-57647352)x3 copy number gain not provided [RCV003485200] Chr19:49625130..57647352 [GRCh37]
Chr19:19q13.33-13.43
likely pathogenic
GRCh37/hg19 19q13.42(chr19:53963333-54421591)x3 copy number gain not provided [RCV003485201] Chr19:53963333..54421591 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_138373.5(MYADM):c.303C>G (p.Phe101Leu) single nucleotide variant not specified [RCV004443762] Chr19:53873832 [GRCh38]
Chr19:54377086 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_138373.5(MYADM):c.640T>C (p.Phe214Leu) single nucleotide variant not specified [RCV004443775] Chr19:53874169 [GRCh38]
Chr19:54377423 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_138373.5(MYADM):c.389A>G (p.His130Arg) single nucleotide variant not specified [RCV004443763] Chr19:53873918 [GRCh38]
Chr19:54377172 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_138373.5(MYADM):c.145G>A (p.Val49Met) single nucleotide variant not specified [RCV004826058] Chr19:53873674 [GRCh38]
Chr19:54376928 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_138373.5(MYADM):c.917C>T (p.Ala306Val) single nucleotide variant not specified [RCV004826061] Chr19:53874446 [GRCh38]
Chr19:54377700 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_138373.5(MYADM):c.341T>C (p.Leu114Pro) single nucleotide variant not specified [RCV004826062] Chr19:53873870 [GRCh38]
Chr19:54377124 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_138373.5(MYADM):c.916G>A (p.Ala306Thr) single nucleotide variant not specified [RCV004826057] Chr19:53874445 [GRCh38]
Chr19:54377699 [GRCh37]
Chr19:19q13.42
uncertain significance
NM_138373.5(MYADM):c.391G>A (p.Gly131Ser) single nucleotide variant not specified [RCV004826059] Chr19:53873920 [GRCh38]
Chr19:54377174 [GRCh37]
Chr19:19q13.42
uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:5107
Count of miRNA genes:936
Interacting mature miRNAs:1094
Transcripts:ENST00000336967, ENST00000391768, ENST00000391769, ENST00000391770, ENST00000391771, ENST00000414489, ENST00000421337, ENST00000439000, ENST00000448420
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.


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
1559110SCL22_HSerum cholesterol level QTL 22 (human)3.590.000241Lipid levelLDL cholesterol193190759457907594Human
597437384GWAS1533458_Hprostate cancer, disease progression measurement QTL GWAS1533458 (human)7e-08prostate cancer, disease progression measurementdisease progression measurement (CMO:0001110)195386921453869215Human
1331657COPD9_HChronic obstructive pulmonary disease QTL 9 (human)1.94Chronic airflow obstructionpost-bronchodilator FEV1193102176057021760Human

Markers in Region
ECD00756  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371954,372,171 - 54,373,062UniSTSGRCh37
Build 361959,063,983 - 59,064,874RGDNCBI36
Celera1951,413,247 - 51,414,138RGD
Cytogenetic Map19q13.42UniSTS
HuRef1950,691,495 - 50,692,386UniSTS
ECD02395  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371954,369,065 - 54,369,896UniSTSGRCh37
Build 361959,060,877 - 59,061,708RGDNCBI36
Celera1951,410,141 - 51,410,972RGD
Cytogenetic Map19q13.42UniSTS
HuRef1950,688,389 - 50,689,220UniSTS
ECD03413  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371954,370,249 - 54,371,045UniSTSGRCh37
Build 361959,062,061 - 59,062,857RGDNCBI36
Celera1951,411,325 - 51,412,121RGD
Cytogenetic Map19q13.42UniSTS
HuRef1950,689,573 - 50,690,369UniSTS
ECD11345  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371954,374,504 - 54,375,079UniSTSGRCh37
Build 361959,066,316 - 59,066,891RGDNCBI36
Celera1951,415,572 - 51,416,147RGD
Cytogenetic Map19q13.42UniSTS
HuRef1950,693,828 - 50,694,403UniSTS
ECD12650  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371954,377,270 - 54,377,808UniSTSGRCh37
Build 361959,069,082 - 59,069,620RGDNCBI36
Celera1951,418,338 - 51,418,876RGD
Cytogenetic Map19q13.42UniSTS
HuRef1950,696,594 - 50,697,132UniSTS
ECD12968  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371954,376,692 - 54,377,222UniSTSGRCh37
Build 361959,068,504 - 59,069,034RGDNCBI36
Celera1951,417,760 - 51,418,290RGD
Cytogenetic Map19q13.42UniSTS
HuRef1950,696,016 - 50,696,546UniSTS
ECD14772  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371954,371,578 - 54,372,064UniSTSGRCh37
Build 361959,063,390 - 59,063,876RGDNCBI36
Celera1951,412,654 - 51,413,140RGD
Cytogenetic Map19q13.42UniSTS
HuRef1950,690,902 - 50,691,388UniSTS
ECD17310  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371954,373,793 - 54,374,197UniSTSGRCh37
Build 361959,065,605 - 59,066,009RGDNCBI36
Celera1951,414,861 - 51,415,265RGD
Cytogenetic Map19q13.42UniSTS
HuRef1950,693,117 - 50,693,521UniSTS
ECD17827  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371954,379,121 - 54,379,504UniSTSGRCh37
Build 361959,070,933 - 59,071,316RGDNCBI36
Celera1951,420,174 - 51,420,557RGD
Cytogenetic Map19q13.42UniSTS
HuRef1950,698,430 - 50,698,813UniSTS
ECD21237  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371954,376,070 - 54,376,326UniSTSGRCh37
Build 361959,067,882 - 59,068,138RGDNCBI36
Celera1951,417,138 - 51,417,394RGD
Cytogenetic Map19q13.42UniSTS
HuRef1950,695,394 - 50,695,650UniSTS
ECD22699  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371954,371,152 - 54,371,363UniSTSGRCh37
Build 361959,062,964 - 59,063,175RGDNCBI36
Celera1951,412,228 - 51,412,439RGD
Cytogenetic Map19q13.42UniSTS
HuRef1950,690,476 - 50,690,687UniSTS
ECD23326  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371954,378,229 - 54,378,421UniSTSGRCh37
Build 361959,070,041 - 59,070,233RGDNCBI36
Celera1951,419,296 - 51,419,488RGD
Cytogenetic Map19q13.42UniSTS
HuRef1950,697,552 - 50,697,744UniSTS
ECD24142  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371954,378,613 - 54,378,771UniSTSGRCh37
Build 361959,070,425 - 59,070,583RGDNCBI36
Celera1951,419,666 - 51,419,824RGD
Cytogenetic Map19q13.42UniSTS
HuRef1950,697,922 - 50,698,080UniSTS
WI-17997  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371954,378,664 - 54,378,788UniSTSGRCh37
Build 361959,070,476 - 59,070,600RGDNCBI36
Celera1951,419,717 - 51,419,841RGD
Cytogenetic Map19q13.42UniSTS
HuRef1950,697,973 - 50,698,097UniSTS
GeneMap99-GB4 RH Map19280.16UniSTS
Whitehead-RH Map19357.9UniSTS
stSG605605  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371954,369,512 - 54,370,558UniSTSGRCh37
Build 361959,061,324 - 59,062,370RGDNCBI36
Celera1951,410,588 - 51,411,634RGD
HuRef1950,688,836 - 50,689,882UniSTS
stSG605606  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371954,370,632 - 54,371,733UniSTSGRCh37
Build 361959,062,444 - 59,063,545RGDNCBI36
Celera1951,411,708 - 51,412,809RGD
HuRef1950,689,956 - 50,691,057UniSTS
stSG605609  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371954,374,116 - 54,375,123UniSTSGRCh37
Build 361959,065,928 - 59,066,935RGDNCBI36
Celera1951,415,184 - 51,416,191RGD
HuRef1950,693,440 - 50,694,447UniSTS
stSG605610  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371954,375,105 - 54,376,168UniSTSGRCh37
Build 361959,066,917 - 59,067,980RGDNCBI36
Celera1951,416,173 - 51,417,236RGD
HuRef1950,694,429 - 50,695,492UniSTS
stSG605611  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371954,376,149 - 54,377,533UniSTSGRCh37
Build 361959,067,961 - 59,069,345RGDNCBI36
Celera1951,417,217 - 51,418,601RGD
HuRef1950,695,473 - 50,696,857UniSTS
stSG605612  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371954,377,514 - 54,378,552UniSTSGRCh37
GRCh37233,951,556 - 33,952,343UniSTSGRCh37
Build 361959,069,326 - 59,070,364RGDNCBI36
Celera233,790,266 - 33,791,053UniSTS
Celera1951,418,582 - 51,419,605RGD
Cytogenetic Map2p22.3UniSTS
Cytogenetic Map19q13.42UniSTS
HuRef233,685,509 - 33,686,302UniSTS
HuRef1950,696,838 - 50,697,861UniSTS
RH68540  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371954,379,438 - 54,379,619UniSTSGRCh37
Build 361959,071,250 - 59,071,431RGDNCBI36
Celera1951,420,491 - 51,420,670RGD
Cytogenetic Map19q13.42UniSTS
HuRef1950,698,747 - 50,698,926UniSTS
GeneMap99-GB4 RH Map19280.36UniSTS
NCBI RH Map19572.3UniSTS
RH48536  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371954,377,307 - 54,377,433UniSTSGRCh37
Build 361959,069,119 - 59,069,245RGDNCBI36
Celera1951,418,375 - 51,418,501RGD
Cytogenetic Map19q13.42UniSTS
HuRef1950,696,631 - 50,696,757UniSTS
GeneMap99-GB4 RH Map19303.47UniSTS
RH11539  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371954,379,384 - 54,379,504UniSTSGRCh37
Build 361959,071,196 - 59,071,316RGDNCBI36
Celera1951,420,437 - 51,420,557RGD
Cytogenetic Map19q13.42UniSTS
HuRef1950,698,693 - 50,698,813UniSTS
GeneMap99-GB4 RH Map19280.26UniSTS
A006V21  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371954,378,196 - 54,378,323UniSTSGRCh37
Build 361959,070,008 - 59,070,135RGDNCBI36
Celera1951,419,263 - 51,419,390RGD
Cytogenetic Map19q13.42UniSTS
HuRef1950,697,519 - 50,697,646UniSTS
GeneMap99-GB4 RH Map19280.26UniSTS


Expression

RNA-SEQ Expression

adipose tissue
alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
entire extraembryonic component
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
musculoskeletal system
nervous system
pharyngeal arch
renal system
reproductive system
respiratory system
sensory system
visual system
1204 2437 2788 2248 4972 1726 2341 6 624 1918 465 2268 7274 6442 52 3734 1 852 1744 1607 174 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001020818 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001020819 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001020820 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001020821 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001290188 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001290189 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001290190 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001290191 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001290192 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001290193 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001290194 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_138373 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC008440 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF087882 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI074232 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK027693 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK075276 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK093999 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK294400 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK316566 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL357205 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL524210 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AX775819 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY037147 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY358582 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC013995 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC095412 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BQ430033 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BQ716724 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX393859 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471135 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CN277531 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CN284532 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068259 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CQ783403 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CQ859714 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA027466 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA472260 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA677314 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA948116 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DB448983 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DC379591 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HY124929 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000336967   ⟹   ENSP00000337222
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1953,865,584 - 53,874,140 (+)Ensembl
Ensembl Acc Id: ENST00000391768   ⟹   ENSP00000375648
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1953,869,439 - 53,874,619 (+)Ensembl
Ensembl Acc Id: ENST00000391769   ⟹   ENSP00000375649
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1953,869,406 - 53,878,125 (+)Ensembl
Ensembl Acc Id: ENST00000391770   ⟹   ENSP00000375650
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1953,867,883 - 53,876,435 (+)Ensembl
Ensembl Acc Id: ENST00000391771   ⟹   ENSP00000375651
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1953,867,883 - 53,876,428 (+)Ensembl
Ensembl Acc Id: ENST00000414489   ⟹   ENSP00000404958
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1953,869,765 - 53,873,969 (+)Ensembl
Ensembl Acc Id: ENST00000421337   ⟹   ENSP00000398269
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1953,866,153 - 53,874,756 (+)Ensembl
Ensembl Acc Id: ENST00000422045
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1953,864,763 - 53,866,140 (+)Ensembl
Ensembl Acc Id: ENST00000439000   ⟹   ENSP00000416919
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1953,867,883 - 53,874,307 (+)Ensembl
Ensembl Acc Id: ENST00000448420   ⟹   ENSP00000399722
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1953,867,883 - 53,874,094 (+)Ensembl
Ensembl Acc Id: ENST00000651087   ⟹   ENSP00000498327
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1953,866,158 - 53,873,896 (+)Ensembl
RefSeq Acc Id: NM_001020818   ⟹   NP_001018654
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381953,869,391 - 53,876,435 (+)NCBI
GRCh371954,369,611 - 54,379,689 (+)RGD
Build 361959,064,593 - 59,071,501 (+)NCBI Archive
Celera1951,410,687 - 51,420,740 (+)RGD
HuRef1950,688,935 - 50,698,996 (+)ENTREZGENE
CHM1_11954,374,455 - 54,381,447 (+)NCBI
T2T-CHM13v2.01956,949,181 - 56,956,143 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001020819   ⟹   NP_001018655
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381953,867,883 - 53,876,435 (+)NCBI
GRCh371954,369,611 - 54,379,689 (+)RGD
Build 361959,062,949 - 59,071,501 (+)NCBI Archive
Celera1951,410,687 - 51,420,740 (+)RGD
HuRef1950,688,935 - 50,698,996 (+)ENTREZGENE
CHM1_11954,372,929 - 54,381,447 (+)NCBI
T2T-CHM13v2.01956,947,668 - 56,956,143 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001020820   ⟹   NP_001018656
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381953,866,371 - 53,876,435 (+)NCBI
GRCh371954,369,611 - 54,379,689 (+)RGD
Build 361959,061,423 - 59,071,501 (+)NCBI Archive
Celera1951,410,687 - 51,420,740 (+)RGD
HuRef1950,688,935 - 50,698,996 (+)ENTREZGENE
CHM1_11954,371,222 - 54,381,447 (+)NCBI
T2T-CHM13v2.01956,946,150 - 56,956,143 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001020821   ⟹   NP_001018657
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381953,869,391 - 53,876,435 (+)NCBI
GRCh371954,369,611 - 54,379,689 (+)RGD
Build 361959,064,472 - 59,071,501 (+)NCBI Archive
Celera1951,410,687 - 51,420,740 (+)RGD
HuRef1950,688,935 - 50,698,996 (+)ENTREZGENE
CHM1_11954,374,455 - 54,381,447 (+)NCBI
T2T-CHM13v2.01956,949,181 - 56,956,143 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001290188   ⟹   NP_001277117
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381953,866,371 - 53,876,435 (+)NCBI
CHM1_11954,371,222 - 54,381,447 (+)NCBI
T2T-CHM13v2.01956,946,150 - 56,956,143 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001290189   ⟹   NP_001277118
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381953,869,391 - 53,876,435 (+)NCBI
CHM1_11954,374,455 - 54,381,447 (+)NCBI
T2T-CHM13v2.01956,949,181 - 56,956,143 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001290190   ⟹   NP_001277119
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381953,868,545 - 53,876,435 (+)NCBI
CHM1_11954,373,609 - 54,381,447 (+)NCBI
T2T-CHM13v2.01956,948,330 - 56,956,143 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001290191   ⟹   NP_001277120
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381953,867,883 - 53,876,435 (+)NCBI
CHM1_11954,372,929 - 54,381,447 (+)NCBI
T2T-CHM13v2.01956,947,668 - 56,956,143 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001290192   ⟹   NP_001277121
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381953,867,883 - 53,876,435 (+)NCBI
CHM1_11954,372,929 - 54,381,447 (+)NCBI
T2T-CHM13v2.01956,947,668 - 56,956,143 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001290193   ⟹   NP_001277122
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381953,865,628 - 53,876,435 (+)NCBI
CHM1_11954,370,648 - 54,381,447 (+)NCBI
T2T-CHM13v2.01956,945,407 - 56,956,143 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001290194   ⟹   NP_001277123
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381953,867,883 - 53,876,435 (+)NCBI
CHM1_11954,372,929 - 54,381,447 (+)NCBI
T2T-CHM13v2.01956,947,668 - 56,956,143 (+)NCBI
Sequence:
RefSeq Acc Id: NM_138373   ⟹   NP_612382
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381953,867,883 - 53,876,435 (+)NCBI
GRCh371954,369,611 - 54,379,689 (+)RGD
Build 361959,062,949 - 59,071,501 (+)NCBI Archive
Celera1951,410,687 - 51,420,740 (+)RGD
HuRef1950,688,935 - 50,698,996 (+)ENTREZGENE
CHM1_11954,372,929 - 54,381,447 (+)NCBI
T2T-CHM13v2.01956,947,668 - 56,956,143 (+)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_001018654 (Get FASTA)   NCBI Sequence Viewer  
  NP_001018655 (Get FASTA)   NCBI Sequence Viewer  
  NP_001018656 (Get FASTA)   NCBI Sequence Viewer  
  NP_001018657 (Get FASTA)   NCBI Sequence Viewer  
  NP_001277117 (Get FASTA)   NCBI Sequence Viewer  
  NP_001277118 (Get FASTA)   NCBI Sequence Viewer  
  NP_001277119 (Get FASTA)   NCBI Sequence Viewer  
  NP_001277120 (Get FASTA)   NCBI Sequence Viewer  
  NP_001277121 (Get FASTA)   NCBI Sequence Viewer  
  NP_001277122 (Get FASTA)   NCBI Sequence Viewer  
  NP_001277123 (Get FASTA)   NCBI Sequence Viewer  
  NP_612382 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAH13995 (Get FASTA)   NCBI Sequence Viewer  
  AAH95412 (Get FASTA)   NCBI Sequence Viewer  
  AAK67628 (Get FASTA)   NCBI Sequence Viewer  
  AAP97182 (Get FASTA)   NCBI Sequence Viewer  
  AAQ88945 (Get FASTA)   NCBI Sequence Viewer  
  BAB55302 (Get FASTA)   NCBI Sequence Viewer  
  BAC04265 (Get FASTA)   NCBI Sequence Viewer  
  BAC11513 (Get FASTA)   NCBI Sequence Viewer  
  BAG38155 (Get FASTA)   NCBI Sequence Viewer  
  BAG57653 (Get FASTA)   NCBI Sequence Viewer  
  CAE11609 (Get FASTA)   NCBI Sequence Viewer  
  CAF86608 (Get FASTA)   NCBI Sequence Viewer  
  CAH25907 (Get FASTA)   NCBI Sequence Viewer  
  EAW72159 (Get FASTA)   NCBI Sequence Viewer  
  EAW72160 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000337222.4
  ENSP00000375648
  ENSP00000375648.2
  ENSP00000375649
  ENSP00000375649.2
  ENSP00000375650
  ENSP00000375650.4
  ENSP00000375651
  ENSP00000375651.1
  ENSP00000398269
  ENSP00000398269.2
  ENSP00000399722.1
  ENSP00000404958.1
  ENSP00000416919
  ENSP00000416919.1
  ENSP00000498327.1
GenBank Protein Q96S97 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_001018656   ⟸   NM_001020820
- UniProtKB: Q96SK9 (UniProtKB/Swiss-Prot),   Q96S97 (UniProtKB/Swiss-Prot),   Q96CS6 (UniProtKB/Swiss-Prot),   Q8N9R4 (UniProtKB/Swiss-Prot),   Q7Z507 (UniProtKB/Swiss-Prot),   Q542Z1 (UniProtKB/Swiss-Prot),   B2RE58 (UniProtKB/Swiss-Prot),   B4DG42 (UniProtKB/TrEMBL),   E9PBN6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_612382   ⟸   NM_138373
- UniProtKB: Q96SK9 (UniProtKB/Swiss-Prot),   Q96S97 (UniProtKB/Swiss-Prot),   Q96CS6 (UniProtKB/Swiss-Prot),   Q8N9R4 (UniProtKB/Swiss-Prot),   Q7Z507 (UniProtKB/Swiss-Prot),   Q542Z1 (UniProtKB/Swiss-Prot),   B2RE58 (UniProtKB/Swiss-Prot),   B4DG42 (UniProtKB/TrEMBL),   E9PBN6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001018655   ⟸   NM_001020819
- UniProtKB: Q96SK9 (UniProtKB/Swiss-Prot),   Q96S97 (UniProtKB/Swiss-Prot),   Q96CS6 (UniProtKB/Swiss-Prot),   Q8N9R4 (UniProtKB/Swiss-Prot),   Q7Z507 (UniProtKB/Swiss-Prot),   Q542Z1 (UniProtKB/Swiss-Prot),   B2RE58 (UniProtKB/Swiss-Prot),   B4DG42 (UniProtKB/TrEMBL),   E9PBN6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001018657   ⟸   NM_001020821
- UniProtKB: Q96SK9 (UniProtKB/Swiss-Prot),   Q96S97 (UniProtKB/Swiss-Prot),   Q96CS6 (UniProtKB/Swiss-Prot),   Q8N9R4 (UniProtKB/Swiss-Prot),   Q7Z507 (UniProtKB/Swiss-Prot),   Q542Z1 (UniProtKB/Swiss-Prot),   B2RE58 (UniProtKB/Swiss-Prot),   B4DG42 (UniProtKB/TrEMBL),   E9PBN6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001018654   ⟸   NM_001020818
- UniProtKB: Q96SK9 (UniProtKB/Swiss-Prot),   Q96S97 (UniProtKB/Swiss-Prot),   Q96CS6 (UniProtKB/Swiss-Prot),   Q8N9R4 (UniProtKB/Swiss-Prot),   Q7Z507 (UniProtKB/Swiss-Prot),   Q542Z1 (UniProtKB/Swiss-Prot),   B2RE58 (UniProtKB/Swiss-Prot),   B4DG42 (UniProtKB/TrEMBL),   E9PBN6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001277122   ⟸   NM_001290193
- UniProtKB: Q96SK9 (UniProtKB/Swiss-Prot),   Q96S97 (UniProtKB/Swiss-Prot),   Q96CS6 (UniProtKB/Swiss-Prot),   Q8N9R4 (UniProtKB/Swiss-Prot),   Q7Z507 (UniProtKB/Swiss-Prot),   Q542Z1 (UniProtKB/Swiss-Prot),   B2RE58 (UniProtKB/Swiss-Prot),   B4DG42 (UniProtKB/TrEMBL),   E9PBN6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001277117   ⟸   NM_001290188
- UniProtKB: Q96SK9 (UniProtKB/Swiss-Prot),   Q96S97 (UniProtKB/Swiss-Prot),   Q96CS6 (UniProtKB/Swiss-Prot),   Q8N9R4 (UniProtKB/Swiss-Prot),   Q7Z507 (UniProtKB/Swiss-Prot),   Q542Z1 (UniProtKB/Swiss-Prot),   B2RE58 (UniProtKB/Swiss-Prot),   B4DG42 (UniProtKB/TrEMBL),   E9PBN6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001277121   ⟸   NM_001290192
- UniProtKB: Q96SK9 (UniProtKB/Swiss-Prot),   Q96S97 (UniProtKB/Swiss-Prot),   Q96CS6 (UniProtKB/Swiss-Prot),   Q8N9R4 (UniProtKB/Swiss-Prot),   Q7Z507 (UniProtKB/Swiss-Prot),   Q542Z1 (UniProtKB/Swiss-Prot),   B2RE58 (UniProtKB/Swiss-Prot),   B4DG42 (UniProtKB/TrEMBL),   E9PBN6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001277120   ⟸   NM_001290191
- UniProtKB: Q96SK9 (UniProtKB/Swiss-Prot),   Q96S97 (UniProtKB/Swiss-Prot),   Q96CS6 (UniProtKB/Swiss-Prot),   Q8N9R4 (UniProtKB/Swiss-Prot),   Q7Z507 (UniProtKB/Swiss-Prot),   Q542Z1 (UniProtKB/Swiss-Prot),   B2RE58 (UniProtKB/Swiss-Prot),   B4DG42 (UniProtKB/TrEMBL),   E9PBN6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001277123   ⟸   NM_001290194
- UniProtKB: Q96SK9 (UniProtKB/Swiss-Prot),   Q96S97 (UniProtKB/Swiss-Prot),   Q96CS6 (UniProtKB/Swiss-Prot),   Q8N9R4 (UniProtKB/Swiss-Prot),   Q7Z507 (UniProtKB/Swiss-Prot),   Q542Z1 (UniProtKB/Swiss-Prot),   B2RE58 (UniProtKB/Swiss-Prot),   B4DG42 (UniProtKB/TrEMBL),   E9PBN6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001277119   ⟸   NM_001290190
- UniProtKB: Q96SK9 (UniProtKB/Swiss-Prot),   Q96S97 (UniProtKB/Swiss-Prot),   Q96CS6 (UniProtKB/Swiss-Prot),   Q8N9R4 (UniProtKB/Swiss-Prot),   Q7Z507 (UniProtKB/Swiss-Prot),   Q542Z1 (UniProtKB/Swiss-Prot),   B2RE58 (UniProtKB/Swiss-Prot),   B4DG42 (UniProtKB/TrEMBL),   E9PBN6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001277118   ⟸   NM_001290189
- UniProtKB: Q96SK9 (UniProtKB/Swiss-Prot),   Q96S97 (UniProtKB/Swiss-Prot),   Q96CS6 (UniProtKB/Swiss-Prot),   Q8N9R4 (UniProtKB/Swiss-Prot),   Q7Z507 (UniProtKB/Swiss-Prot),   Q542Z1 (UniProtKB/Swiss-Prot),   B2RE58 (UniProtKB/Swiss-Prot),   B4DG42 (UniProtKB/TrEMBL),   E9PBN6 (UniProtKB/TrEMBL)
- Sequence:
Ensembl Acc Id: ENSP00000416919   ⟸   ENST00000439000
Ensembl Acc Id: ENSP00000404958   ⟸   ENST00000414489
Ensembl Acc Id: ENSP00000337222   ⟸   ENST00000336967
Ensembl Acc Id: ENSP00000498327   ⟸   ENST00000651087
Ensembl Acc Id: ENSP00000375648   ⟸   ENST00000391768
Ensembl Acc Id: ENSP00000375649   ⟸   ENST00000391769
Ensembl Acc Id: ENSP00000375651   ⟸   ENST00000391771
Ensembl Acc Id: ENSP00000375650   ⟸   ENST00000391770
Ensembl Acc Id: ENSP00000399722   ⟸   ENST00000448420
Ensembl Acc Id: ENSP00000398269   ⟸   ENST00000421337
Protein Domains
MARVEL

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q96S97-F1-model_v2 AlphaFold Q96S97 1-322 view protein structure

Promoters
RGD ID:13205537
Promoter ID:EPDNEW_H26349
Type:initiation region
Name:MYADM_4
Description:myeloid associated differentiation marker
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H26350  EPDNEW_H26351  EPDNEW_H26352  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381953,865,628 - 53,865,688EPDNEW
RGD ID:13205539
Promoter ID:EPDNEW_H26350
Type:initiation region
Name:MYADM_3
Description:myeloid associated differentiation marker
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H26349  EPDNEW_H26351  EPDNEW_H26352  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381953,866,159 - 53,866,219EPDNEW
RGD ID:13205541
Promoter ID:EPDNEW_H26351
Type:initiation region
Name:MYADM_1
Description:myeloid associated differentiation marker
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H26349  EPDNEW_H26350  EPDNEW_H26352  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381953,867,883 - 53,867,943EPDNEW
RGD ID:13205543
Promoter ID:EPDNEW_H26352
Type:initiation region
Name:MYADM_2
Description:myeloid associated differentiation marker
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H26349  EPDNEW_H26350  EPDNEW_H26351  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381953,869,722 - 53,869,782EPDNEW
RGD ID:6795825
Promoter ID:HG_KWN:30886
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:HeLa_S3,   Lymphoblastoid
Transcripts:OTTHUMT00000134339
Position:
Human AssemblyChrPosition (strand)Source
Build 361959,061,131 - 59,061,631 (+)MPROMDB
RGD ID:6795826
Promoter ID:HG_KWN:30887
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   K562,   Lymphoblastoid,   NB4
Transcripts:NM_001020819,   OTTHUMT00000134336,   OTTHUMT00000134428
Position:
Human AssemblyChrPosition (strand)Source
Build 361959,062,574 - 59,063,074 (+)MPROMDB
RGD ID:6795843
Promoter ID:HG_KWN:30888
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   HeLa_S3,   K562,   Lymphoblastoid,   NB4
Transcripts:NM_001020821,   OTTHUMT00000134338,   OTTHUMT00000134347,   OTTHUMT00000318716
Position:
Human AssemblyChrPosition (strand)Source
Build 361959,063,081 - 59,064,747 (+)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:7544 AgrOrtholog
COSMIC MYADM COSMIC
Ensembl Genes ENSG00000179820 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000336967.8 UniProtKB/TrEMBL
  ENST00000391768 ENTREZGENE
  ENST00000391768.2 UniProtKB/Swiss-Prot
  ENST00000391769 ENTREZGENE
  ENST00000391769.3 UniProtKB/Swiss-Prot
  ENST00000391770 ENTREZGENE
  ENST00000391770.9 UniProtKB/Swiss-Prot
  ENST00000391771 ENTREZGENE
  ENST00000391771.1 UniProtKB/Swiss-Prot
  ENST00000414489.1 UniProtKB/TrEMBL
  ENST00000421337 ENTREZGENE
  ENST00000421337.6 UniProtKB/Swiss-Prot
  ENST00000439000 ENTREZGENE
  ENST00000439000.5 UniProtKB/TrEMBL
  ENST00000448420.5 UniProtKB/TrEMBL
  ENST00000651087.1 UniProtKB/TrEMBL
GTEx ENSG00000179820 GTEx
HGNC ID HGNC:7544 ENTREZGENE
Human Proteome Map MYADM Human Proteome Map
InterPro Marvel UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MYADM-like UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:91663 UniProtKB/Swiss-Prot
NCBI Gene MYADM ENTREZGENE
OMIM 609959 OMIM
PANTHER MYELOID-ASSOCIATED DIFFERENTIATION MARKER UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MYELOID-ASSOCIATED DIFFERENTIATION MARKER MYADM FAMILY MEMBER UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam MARVEL UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA31344 PharmGKB
PROSITE MARVEL UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A494C017_HUMAN UniProtKB/TrEMBL
  A0A499FIY8_HUMAN UniProtKB/TrEMBL
  B2RE58 ENTREZGENE
  B4DG42 ENTREZGENE, UniProtKB/TrEMBL
  C9JC07_HUMAN UniProtKB/TrEMBL
  C9JJV6_HUMAN UniProtKB/TrEMBL
  C9JZL8_HUMAN UniProtKB/TrEMBL
  E9PBN6 ENTREZGENE
  MYADM_HUMAN UniProtKB/Swiss-Prot
  Q542Z1 ENTREZGENE
  Q7Z507 ENTREZGENE
  Q8N9R4 ENTREZGENE
  Q96CS6 ENTREZGENE
  Q96S97 ENTREZGENE
  Q96SK9 ENTREZGENE
UniProt Secondary B2RE58 UniProtKB/Swiss-Prot
  E9PBN6 UniProtKB/TrEMBL
  Q542Z1 UniProtKB/Swiss-Prot
  Q7Z507 UniProtKB/Swiss-Prot
  Q8N9R4 UniProtKB/Swiss-Prot
  Q96CS6 UniProtKB/Swiss-Prot
  Q96SK9 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-06-28 MYADM  myeloid associated differentiation marker    myeloid-associated differentiation marker  Symbol and/or name change 5135510 APPROVED