System Message

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Gene Symbol:
MCL1
Entrez Gene ID
4170
Gene Name:
BCL2 family apoptosis regulator
Gene Aliases
BCL2L3, EAT, MCL1-ES, MCL1L, MCL1S, Mcl-1, TM, bcl2-L-3, mcl1/EAT
Gene Chromosome Location
Chr.1: on Build GRCh38
UniGene
Hs.632486
Species:
Human
Primer Chromosome Location
Chr.1: 150579005-150579250 on Build GRCh38
Amplicon Length
246
Primer Sequences
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Ampliseq ID's
Primer ID Hs00592031_CE
Primer 5'-tail Option
Purification
Primer Pair /FWD/REV
Synthesis Scale 25 nmol
Availability Made To Order
Catalog #'s A15629,A15630
Price (USD) USD 16.46,USD 16.46

Genomic Map

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Assay Details

Gene Information


MCL1
Accession Protein COSMIC ID Mutation AA
RefSeq NM_001197320.1 NP_001184249.1 - - -
NM_021960.4 NP_068779.1 675537 c.367G>A p.E123K
6946930 c.305C>T p.T102I
895585 c.520T>C p.L174L
2182389 c.402C>G p.L134L
6945793 c.308G>T p.R103L
6709742 c.420C>A p.V140V
5609333 c.297C>T p.F99F
5651527 c.372G>A p.E124E
895586 c.441C>T p.V147V
3473463 c.461C>T p.T154I
6987358 c.451_452GG>CA p.G151H
6940011 c.433G>C p.E145Q
6254901 c.526C>A p.R176R
4990451 c.365C>T p.P122L
5014148 c.482C>A p.P161H
6243190 c.321G>T p.P107P
2182388 c.430C>T p.L144L
1724575 c.513_515delGGA p.E171delE
6347292 c.516C>A p.D172E
1726576 c.465T>G p.S155R
7241732 c.355A>G p.I119V
1160858 c.481C>T p.P161S
6976746 c.302C>T p.P101L
6120938 c.315G>T p.A105A
6923155 c.416C>T p.A139V
6978710 c.328_330delGAG p.E110delE
6919929 c.297C>A p.F99L
6212585 c.285G>C p.R95S
6928871 c.526C>T p.R176W
4990450 c.522G>T p.L174F
6983753 c.307C>T p.R103C
1294995 c.282G>C p.A94A
4847432 c.485C>G p.S162W
1214709 c.442G>A p.G148R
6925508 c.505G>A p.E169K
6208338 c.375G>C p.E125D
6981286 c.330G>C p.E110D
3984197 c.390G>A p.E130E
6912244 c.325G>A p.E109K
6909708 c.376C>A p.L126M
3774406 c.522G>A p.L174L
6918187 c.516C>G p.D172E
4629737 c.329A>G p.E110G
6917657 c.472G>C p.G158R
NM_182763.2 NP_877495.1 - - -
GenBank AF118124.1 AAD13299.1 - - -
AF203373.1 AAG00904.1 - - -
AK294462.1 - - -
AK297217.1 - - -
AK300499.1 - - -
AK304775.1 - - -
AK312508.1 - - -
AK316267.1 - - -
BC017197.2 AAH17197.1 - - -
BC071897.1 AAH71897.1 - - -
BC107735.1 AAI07736.1 - - -
BT006640.1 AAP35286.1 - - -
ENST00000369026.0 - - -
FJ917536.1 - - -
L08246.1 - - -


Phenotype

MIM: 159552

Literature Links:

MCL1 PubMed Links

SNP ID

rs751936394 rs751523069 rs758318152 rs748263149 rs746792176 rs773866164 rs749913949 rs770123858 rs769996178 rs751406920 rs778171830 rs1802504 rs587719450 rs753534510 rs147383002 rs754863720 rs587652007 rs147150688 rs755770114 rs587684336 rs758375227 rs764786930 rs369059511 rs771094920 rs377087381 rs138713477 rs932315539 rs752513670 rs767724723 rs778329513 rs199711529 rs776618436 rs756444423 rs772557216 rs973804470 rs778045091 rs945056615 rs779873561 rs959415730 rs771542364 rs1055106408 rs768299859 rs149932083 rs757424648 rs752950171 rs754817818 rs587756150 rs372948653 rs151065075 rs768904402 rs900035249 rs775612047 rs756812136 rs773052989 rs587760643 rs774942478 rs145728752 rs748466480 rs771817704 rs148702277 rs750040895 rs749347699 rs763609710 rs780780459 rs778855545

Submission count

1

Allele Nomenclature



Chromosome Location

Chr.1: 150579064-150579064 on Build GRCh38

Allele Frequency



1000Genome Applied Biosystems® HapMap
Global - Not Available Caucasian - Not Available CEPH (CEU) - Not Available
EAS - Not Available African American - Not Available YRI (Yoruba) - Not Available
SAS - Not Available Chinese - Not Available CHB (Han Chinese) - Not Available
AFR - Not Available Japanese - Not Available JPT (Japanese) - Not Available
EUR - Not Available
AMR - Not Available


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