ZMP

cnnm2a

Ensembl ID:

ENSDARG00000061195

ZFIN ID:

ZDB-GENE-050208-36

Description:

cyclin M2a [Source:RefSeq peptide;Acc:NP_001138257]

Human Orthologue:

CNNM2

Human Description:

cyclin M2 [Source:HGNC Symbol;Acc:103]

Mouse Orthologue:

Cnnm2

Mouse Description:

cyclin M2 Gene [Source:MGI Symbol;Acc:MGI:2151054]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa14149	Nonsense	Available for shipment	Available now
sa22317	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa14149

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Order Allele From ZIRC
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Mutation:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000087001	Nonsense	672	811	6	8

Genomic Location (Zv9):

Chromosome 13 (position 28859743)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	28505691
GRCz11	13	28636141

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TCTCTCTCTTTTTTCCGTCCTCTTGCTSTCCAGTTCCTCTCTCCTTGTCT[C/T]GAACCTTCGTGGTCAGCAGGGCAGAATCACTGGCAGRATCTCCAGGTATG

Long Flanking Sequence:

TTCTGATGTTTGGTCTGAGCTGTCCTGCAATGGTTACCAGTTGTAGTCTTACGCAAGAAATAGCATATGTTCTTGTGGTATTTCTTTGTGGAGCAGACAGAGTTGTGTCTGATAATTTCTATTATTAAAGTCACTCACTTCTGTTGCTGATCCATTGTGCAATGTGAGCACAGCAGCAACTGAATGCTACCAATGATAGTCATGCAGTGTGAAAACGACTGTAGTCCCACAACTCGTGCATCATGCCGTCAGTGTGAACTCATCATAAGTCTTTCTACCTAATTGTGCAGGACACTCTTTGCTCTCAGATTTCTTATTGGATTTTTTTAAGCATGCATTCTTCTGACTCCTCTACCGCTAATCAATCACATTATGCTAATGATTGCTGTTTTGTCTCCTGGAGGAATTCTGCTTAAATTGTATTTTCCTCGCCATGATTTCCTTTTGTCTTCTCTCTCTTTTTTCCGTCCTCTTGCTCTCCAGTTCCTCTCTCCTTGTCT[C/T]GAACCTTCGTGGTCAGCAGGGCAGAATCACTGGCAGGATCTCCAGGTATGATAATGGTTTCTTCACCCATCACTTCTTCCTCTGAACGCCTGATGGTTTGAGAATCAAACAATTTGATGAATACTTTTTAACAGTTTTGCAGAGAAAGGCTTGATAATAAAAATGGGAGCTGAAAAAGAAAATGACAGATAAAAACAACATTTTCAATATATTCAAGGTTCAGAATAGTGCTAAAATGCACCTACACCTACAGTGACATTTAGTGGCTCTTCATTCCAGTCAGTTGAGAGGTGCCATGAAGTAGTTGTGTTTTTGTTGGCTTGTGTTTTCATCAAATTCAACAAATTTCACCTCTGTAAAGTTAGTTTTAGGTTGAAATATATGCTTTACATCCACATCGCTGTACATCCACAGTGCAAAATGCTCGCTCTTAGCTTTTCCAAATGTGTCTATTTATATTATAAACAGTACACAATTACTGTAGGATTAAACAAAAACCC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa22317

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Order Allele From ZIRC

Mutation:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000087001	Nonsense	751	811	8	8

Genomic Location (Zv9):

Chromosome 13 (position 28866377)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	28512325
GRCz11	13	28642775

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CCAAAACGGCTGATTGATTCTAAATCTCCATTTTTCAGGTGACCCGCCAG[C/T]AATACCAGAATGCCCTGATGGCATCTCGCATGGACAAAACACCTCAATCC

Long Flanking Sequence:

AAAATCTTTATAAATGTTATCAGTATATATTTTTAGCATTGTAGTTGTCCCTGCTTGAAGGGGTCTGAAATGTCACGTTTTTATTTATTTTTTTACATTTTGTATACAAAGCCAGGGTTATCTAGGATTTTTAATTTCGGTCCAGATAGTACTTTTATTATTTTTTAGTGCAGATCATTTAAACATTTTGCAGTATAAATGAGCAGAAATACTTAAAGAAACACTCATACTCATGACTCATAAATCATTGAATCGGATTAAAACATTAGCATCTTGCTCAAAAATTTCAAAAAAAGTTTTGGTCAGTTTGCTATTTCAAGCCTGACTCTTCTGTTGGTCATAGTACCCAGTGTAGAGTCAAGCTTTAAGTGAGAAAATTATCAAAGCTCCACTTTCCAAAAAAGTGTTTAAAGCAAGAAGAAAGTTAACCTTTTAAAAGCACTAAAATGTCCAAAACGGCTGATTGATTCTAAATCTCCATTTTTCAGGTGACCCGCCAG[C/T]AATACCAGAATGCCCTGATGGCATCTCGCATGGACAAAACACCTCAATCCACAGACAGTGAGTTCACCAAGATCGAACTGACCTTCACCGAGCACCAGGACGGACCATTGGAAGAATCGGCCACACTTTTGACCACCAACTCACACAAACCCAACCACACTGCCCACAACGACGGGGTAGTTTAAGCACCCTCTGCGAAAGAGAGAGAGAGATGCCTCTTTCCACAGAGTGAGTGAGAGGCACTGGGCAGCTTCATACGAGTCCTCTCATCACGCTCCAATTCAAAGGGGAACGTACAGCGTGAAGGGCCACACATCCCACAATGCATGCACTAATGACCTTAACACCTTTTGTAGGCAGCGGATCAGTCAGGGACCACCAAATCATTCTCGCTCACTCGATCGAGGAAGGACACACTTGAAATACACACTACGAAGGAGCAAGGAGACGACCCACGCCACACCTTGAGCAGACACGACCATAACAGAAGGACAAAGAAA

Associated Phenotype:

Not determined