AMHR2 (NM_001164690) Human 3' UTR Clone

Specifications

Product Data
Product Name	AMHR2 (NM_001164690) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	AMHR; MISR2; MISRII; MRII
ACCN	NM_001164690
Insert Size	510 bp
Sequence Data	Insert Sequence (showhide) >SC204563 3’UTR clone of NM_001164690 The sequence shown below is from the reference sequence of NM_001164690. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GCTGCTTTGCCACAGACCCTGATGGGCTGAGGGAGCTCCTAGAAGACTGTTGGGATGCAGACCCAGAAG CACGGCTGACAGCTGAGTGTGTACAGCAGCGCCTGGCTGCCTTGGCCCATCCTCAAGAGAGCCACCCCT TTCCAGAGAGCTGTCCACGTGGCTGCCCACCTCTCTGCCCAGAAGACTGTACTTCAATTCCTGCCCCTA CCATCCTCCCCTGTAGGCCTCAGCGGAGTGCCTGCCACTTCAGCGTTCAGCAAGGCCCTTGTTCCAGGA ATCCTCAGCCTGCCTGTACCCTTTCTCCTGTGTAAATATGCAGTTTATGTGTCATCAATGTACATGCCA ACATAAATATGGCGATTGTATAGCTGTCTTGTCTGCCTCATCACTGCATTTCCCACCTGCCGAATCCTT GGATTCTTCTGCGGGCATCCAGTCCACATCAGTTCTGACCAGTGACTTGGGGTAGGTGTGCACAGGAAA GAGAATAAAGTCAGCTTTCCTGATGCA ACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCGACCAAGCGACGCCCAACCTGCCATCA CGAGATTTCGATTCCACCGCCGCCTTCTATGAAAGG
Restriction Sites	SgfI-MluI
OTI Disclaimer	Our molecular clone sequence data has been matched to the sequence identifier above as a point of reference. Note that the complete sequence of this clone is largely the same as the reference sequence but may contain minor differences , e.g., single nucleotide polymorphisms (SNPs).
Reference Data
RefSeq	NM_001164690.2
Synonyms	AMHR; MISR2; MISRII; MRII
Summary	This gene encodes the receptor for the anti-Mullerian hormone (AMH) which, in addition to testosterone, results in male sex differentiation. AMH and testosterone are produced in the testes by different cells and have different effects. Testosterone promotes the development of male genitalia while the binding of AMH to the encoded receptor prevents the development of the mullerian ducts into uterus and Fallopian tubes. Mutations in this gene are associated with persistent Mullerian duct syndrome type II. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Sep 2009]
Locus ID	269
MW	18.4

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