ZMP

ENSDARG00000087019

Ensembl ID:

ENSDARG00000087019

Human Orthologues:

CGN, CGNL1

Human Descriptions:

cingulin [Source:HGNC Symbol;Acc:17429]
cingulin-like 1 [Source:HGNC Symbol;Acc:25931]

Mouse Orthologues:

Cgn, Cgnl1

Mouse Descriptions:

cingulin Gene [Source:MGI Symbol;Acc:MGI:1927237]
cingulin-like 1 Gene [Source:MGI Symbol;Acc:MGI:1915428]

Alleles

There are 5 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa15716	Nonsense	Available for shipment	Available now
sa11668	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa15716

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:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000123347	Nonsense	293	507	6	14

Genomic Location (Zv9):

Chromosome 25 (position 29823931)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	25	28514025

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TRATAAAGTCCAGAARCTGGAGAAGCTGCTCTCAARGAAGGAAAAGGAAT[T/A]GATGGAAAAGTATGTACAKCTATCTATCTATCTAWCTATCTATCTATCTA

Long Flanking Sequence:

TATTGATCATCTGTGGAACCGTATTTAGCCACAATCTCAGGTAGTTTCAGATCAAGTTTAATTTTTAATTTTTAATATTTTGGAAGCCATTAGCCACTGACATCCAAAGTAGGAAAAATAAAACTGTCTTACAGCAAGAGGCTGATGTATATATGTGTGTGTTTATAAATTTATAATGCATTTAAAGGTGGTTCTTTCATAATGTCAGTTTGTAACAATGTAAGTACTGTTAATGCTCAAACTTTCTTCATAGGTGTCTTGTGAAGACCTGAATGGAGAGCTGGAGGAGGAGCTACTTAGGTTGAGAGACATGCTGAAGGTCAGAGATGCTGAGCTGCAGTCTGTTCTCAATCAGGTGAGGCCAGCAAACCTGACCTGAGATCTGTGAAATCCTGAAGAAGGACGGACATCAGATTTTTTCCCCCATGTTTTTCAGGAGTCACAACAGAGTAATAAAGTCCAGAAACTGGAGAAGCTGCTCTCAAAGAAGGAAAAGGAAT[T/A]GATGGAAAAGTATGTACATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTGTCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCATCACATTAGTATAGATGTAGAGGAAATGTTCTGTGAGATGTAAATTAGTGACACAGAGATAGGTCCAATTTAACAGACGTAACATCTGTTGCTGACACAAGGAAATGTGCTCCAGAAAAATTATTCTAAAATAGGGAACCTATTACAAGATATAAAATAAGTCTCTGATCTTGAGTGTGTATGTGAAGTTTCAGCTCAAAATATCCCACAAACAAATTGTTTTATATCTGTTTGAAACATCCCTTTTTAGGTTTTGATCCAAATTGTGCTTGTTATGGTGACTGTCACTTAAAAT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa11668

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
Order Allele From EZRC

Mutation:

C > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000123347	Nonsense	432	507	12	14

Genomic Location (Zv9):

Chromosome 25 (position 29839118)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	25	28529212
GRCz11	25	28972414

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TATGTGAAAYGTGTTCTATTCAGATCTTCAGTGTTCCCAAGAAGACCTTA[C/A]TTGGCTGATAATTTGGTCCAAAATGCTTCAGATATTAAGGTAAACAWGCA

Long Flanking Sequence:

ATATGTCCAGTACCTCGTTGAATGCCATGAAGGCAGAAGCCATGATTAAGGCAGTTCTGAAGACTAAAAGGGATCCAACCCAGTACTAATAAGGTGTACCTAATAATTTGGCCAGTGTGTATATATAAAAGTCAAACTCTTTGTTTCTAAATTGATATAATCGATATAAATCAAGATATTGTTTTTATTCAGGTAGTTTACATTTAACATTTTGTTTACTTTTTTTGTATTTTAGTTTAAGCTTTTGTTAATGATAATAACCTTCCTCCCAACTCTCCCTCAACGGATCAGTGAATGGTGTGAACCCTGGCTCAGGAAGAGGAGTGGGGGTGGGAATACTGGAATTTTCCCAATGTCATAATTCACATTTGGCATGTGGCGACGTTAAAACTGTCTTGGAAAAGAAGCTATGAATCAAATCTTATTGACATTTGACAGAAAACATATATGTATGTGAAACGTGTTCTATTCAGATCTTCAGTGTTCCCAAGAAGACCTTA[C/A]TTGGCTGATAATTTGGTCCAAAATGCTTCAGATATTAAGGTAAACAAGCACATTTTTCGTTTTTTAGGCCATAAATCGGGATGTCTTTTGATACGGAAATTAATAACAGCTGTGTGACACATTTAGAACTGGAATGCTGTTGACGTGAACCATCAGGGAAGAGAAACGCAGACACCGGAGCAAGATCCCCAACAGGGGGCAGCAAAACCATGTCCATCCCAGATCTCAGACGGAGGATCAGACAGGTCTGCAGGAGGGGTGGAGGATAAACAGCCAATCAGCGTCAAGCATTCCAGCAAGACTGCCCAGGTATGGTGAGAATCTGCGCTGCCGATCTTAGTTTGATAGCATTTTTGATTGGCTTATGGTGCTCTTCTAATTCAAGCTCAACTAAAAATTAATTGATTTTAATCTTTGAGTAAAGTTTAACAGAACAACTCACAAATCACATCATAGACTCTAATTATAGTGTCCTGATCTCACATTTTATGTTAATCAAA

Associated Phenotype:

Not determined