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Imported Disease Annotations - CTDObject Symbol | Species | Term | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | MYADM | Human | Experimental Liver Cirrhosis | | EXP | | 11554173 | CTD Direct Evidence: marker/mechanism | CTD | PMID:25380136 | |
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Imported Disease Annotations - CTDObject Symbol | Species | Term | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | MYADM | Human | Experimental Liver Cirrhosis | | EXP | | 11554173 | CTD Direct Evidence: marker/mechanism | CTD | PMID:25380136 | |
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# | 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 |
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 |
MYADM (Homo sapiens - human) |
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Myadm (Mus musculus - house mouse) |
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Myadm (Rattus norvegicus - Norway rat) |
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Myadm (Chinchilla lanigera - long-tailed chinchilla) |
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MYADM (Pan paniscus - bonobo/pygmy chimpanzee) |
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MYADM (Canis lupus familiaris - dog) |
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Myadm (Ictidomys tridecemlineatus - thirteen-lined ground squirrel) |
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MYADM (Sus scrofa - pig) |
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MYADM (Chlorocebus sabaeus - green monkey) |
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Myadm (Heterocephalus glaber - naked mole-rat) |
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Variants in MYADM
21 total 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 |
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. |
The following QTLs overlap with this region. | ![]() | Full Report | ![]() | CSV | ![]() | TAB | ![]() | Printer | ![]() | Gviewer |
ECD00756 |
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ECD02395 |
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ECD03413 |
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ECD11345 |
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ECD12650 |
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ECD12968 |
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ECD14772 |
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ECD17310 |
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ECD17827 |
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ECD21237 |
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ECD22699 |
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ECD23326 |
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ECD24142 |
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WI-17997 |
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stSG605605 |
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stSG605606 |
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stSG605609 |
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stSG605610 |
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stSG605611 |
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stSG605612 |
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RH68540 |
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RH48536 |
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RH11539 |
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A006V21 |
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adipose tissue
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alimentary part of gastrointestinal system
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appendage
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circulatory system
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ectoderm
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endocrine system
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endoderm
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entire extraembryonic component
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exocrine system
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hemolymphoid system
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hepatobiliary system
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integumental system
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mesenchyme
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mesoderm
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musculoskeletal system
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nervous system
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pharyngeal arch
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renal system
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reproductive system
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respiratory system
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sensory system
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visual system
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---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
1204 | 2437 | 2788 | 2248 | 4972 | 1726 | 2341 | 6 | 624 | 1918 | 465 | 2268 | 7274 | 6442 | 52 | 3734 | 1 | 852 | 1744 | 1607 | 174 | 1 |
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: |
|
Ensembl Acc Id: | ENST00000391768 ⟹ ENSP00000375648 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000391769 ⟹ ENSP00000375649 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000391770 ⟹ ENSP00000375650 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000391771 ⟹ ENSP00000375651 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000414489 ⟹ ENSP00000404958 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000421337 ⟹ ENSP00000398269 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000422045 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000439000 ⟹ ENSP00000416919 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000448420 ⟹ ENSP00000399722 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000651087 ⟹ ENSP00000498327 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | NM_001020818 ⟹ NP_001018654 | ||||||||||||||||||||||||||||||||
RefSeq Status: | VALIDATED | ||||||||||||||||||||||||||||||||
Type: | CODING | ||||||||||||||||||||||||||||||||
Position: |
|
||||||||||||||||||||||||||||||||
Sequence: |
RefSeq Acc Id: | NM_001020819 ⟹ NP_001018655 | ||||||||||||||||||||||||||||||||
RefSeq Status: | VALIDATED | ||||||||||||||||||||||||||||||||
Type: | CODING | ||||||||||||||||||||||||||||||||
Position: |
|
||||||||||||||||||||||||||||||||
Sequence: |
RefSeq Acc Id: | NM_001020820 ⟹ NP_001018656 | ||||||||||||||||||||||||||||||||
RefSeq Status: | VALIDATED | ||||||||||||||||||||||||||||||||
Type: | CODING | ||||||||||||||||||||||||||||||||
Position: |
|
||||||||||||||||||||||||||||||||
Sequence: |
RefSeq Acc Id: | NM_001020821 ⟹ NP_001018657 | ||||||||||||||||||||||||||||||||
RefSeq Status: | VALIDATED | ||||||||||||||||||||||||||||||||
Type: | CODING | ||||||||||||||||||||||||||||||||
Position: |
|
||||||||||||||||||||||||||||||||
Sequence: |
RefSeq Acc Id: | NM_001290188 ⟹ NP_001277117 | ||||||||||||||||
RefSeq Status: | VALIDATED | ||||||||||||||||
Type: | CODING | ||||||||||||||||
Position: |
|
||||||||||||||||
Sequence: |
RefSeq Acc Id: | NM_001290189 ⟹ NP_001277118 | ||||||||||||||||
RefSeq Status: | VALIDATED | ||||||||||||||||
Type: | CODING | ||||||||||||||||
Position: |
|
||||||||||||||||
Sequence: |
RefSeq Acc Id: | NM_001290190 ⟹ NP_001277119 | ||||||||||||||||
RefSeq Status: | VALIDATED | ||||||||||||||||
Type: | CODING | ||||||||||||||||
Position: |
|
||||||||||||||||
Sequence: |
RefSeq Acc Id: | NM_001290191 ⟹ NP_001277120 | ||||||||||||||||
RefSeq Status: | VALIDATED | ||||||||||||||||
Type: | CODING | ||||||||||||||||
Position: |
|
||||||||||||||||
Sequence: |
RefSeq Acc Id: | NM_001290192 ⟹ NP_001277121 | ||||||||||||||||
RefSeq Status: | VALIDATED | ||||||||||||||||
Type: | CODING | ||||||||||||||||
Position: |
|
||||||||||||||||
Sequence: |
RefSeq Acc Id: | NM_001290193 ⟹ NP_001277122 | ||||||||||||||||
RefSeq Status: | VALIDATED | ||||||||||||||||
Type: | CODING | ||||||||||||||||
Position: |
|
||||||||||||||||
Sequence: |
RefSeq Acc Id: | NM_001290194 ⟹ NP_001277123 | ||||||||||||||||
RefSeq Status: | VALIDATED | ||||||||||||||||
Type: | CODING | ||||||||||||||||
Position: |
|
||||||||||||||||
Sequence: |
RefSeq Acc Id: | NM_138373 ⟹ NP_612382 | ||||||||||||||||||||||||||||||||
RefSeq Status: | VALIDATED | ||||||||||||||||||||||||||||||||
Type: | CODING | ||||||||||||||||||||||||||||||||
Position: |
|
||||||||||||||||||||||||||||||||
Sequence: |
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 |
Name | Modeler | Protein Id | AA Range | Protein Structure |
AF-Q96S97-F1-model_v2 | AlphaFold | Q96S97 | 1-322 | view protein structure |
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: |
|
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: |
|
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: |
|
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: |
|
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: |
|
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: |
|
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: |
|
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 |
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 |