ZMP

CDH19

Ensembl ID:

ENSDARG00000074991

Description:

cadherin 19, type 2 [Source:HGNC Symbol;Acc:1758]

Human Orthologue:

CDH19

Human Description:

cadherin 19, type 2 [Source:HGNC Symbol;Acc:1758]

Mouse Orthologue:

Cdh19

Mouse Description:

cadherin 19, type 2 Gene [Source:MGI Symbol;Acc:MGI:3588198]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa16067	Essential Splice Site	Available for shipment	Available now
sa37802	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa16067

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:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000114853	Essential Splice Site	69	693	1	11

Genomic Location (Zv9):

Chromosome 24 (position 12604)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	24	15810
GRCz11	24	15810

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CCAGATATTTGTTGAAGAGGAAGATTCAACCCCGARGAACATTGGTCAGG[T/C]ATTCATTCACAAGCAGCTCTTACACATACACATGCATACAGGTGCTGGTC

Long Flanking Sequence:

CGTTGTAGTGGTTTAATATATTAAACACCTCGTCTGAACATTTCAGTATGTTTGAATGCAGTCATTTATTTAAGCCTGAGTTGTGTTTTCTGTGGAATTGCTCAGACCTGTAAATCATTCAGACAATCTCTCTCTCTCTCTACTTTGCTTTCCCATAACAGAAGATCTATCATTTCCTTCTCATTGCATTCTTCTTTATGTACTGTCTGAGTCCATCTCCTCCTTTGGCATCTTCAACATGACATCAAGTCCTAGTGTTCACTGAAGGCCCTACTGAAGGATCTCCTCCACAATGGTCCACTGCTGTGTTCTTCGTGTGCTTCTCATGCTTTCCTGCACTCCTGCATGGCCCGCGGCCGTGTTCATCATCTCAGAACAGCAGCAGGAGAAGCTTTTCAGACCAGAGTCTCGTGGGTCCCATCTCAGAGTCAGACGAGGCTGGATCTGGAGCCAGATATTTGTTGAAGAGGAAGATTCAACCCCGAGGAACATTGGTCAGG[T/C]ATTCATTCACAAGCAGCTCTTACACATACACATGCATACAGGTGCTGGTCAAACATATCCATTCAAGAACTAAAGCTGGTGCTGTGTGTACATTTATTCCACACAGACTGATATATTTCAAGTGTTTATTTCTTTTTATTTTTATTGTTTTAATGTCAAACTTCAAATTCACTATCTCAGAAAATTAGATTATTGTGAAAAGGTTGACACTCTTATAGTGACTCTCCACGCTGCATTGCTGCAGTAATACAGGCAGAGGGAGCTCACGCTGGGTATTGAGTGCTGTGCATGCTCAGACTGTCCGTCTTCACACTTCAGTTGGACGAGATTTTTAAAAATCCTGTCTTGAATTGGTCAGAAGTAATCTTGTAATTTTCTGAGATACTGAATTTGGCGTTTTCATTAGTAGTCTACTCATCGATCATCAAAATTAAAAGAAATAAACACTTGAAATATATCAGTGTGTGTGGATTGAGCACGTTAGGCAAGTTTCACTTAAG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa37802

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:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000114853	Nonsense	517	693	9	11

Genomic Location (Zv9):

Chromosome 24 (position 4898)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	24	23516
GRCz11	24	23516

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTGATCAGCGCCACTGATGCAGATGATCCTGTGGATGGACAACATTTCTA[T/A]TTCTCCATGATCCCAGACAAGCACATCAACCCCAACTTCACAATCAGAGA

Long Flanking Sequence:

CTTTCCCTAATAATTATCTGTGTTATGAAAGACGCAGACTAGCGCACTTCACCATCCTCCTCACAGTGTTCCTGACCCATCCTGATCTCCACACTGTCATCTGTTATAATCCACGTGACAATAAGCCGCTCTGGTTTTAGTTGAAGCGTCTTTCTTCCATCAACAGTGTGAAAATGATCTGTGCTGTTTTATACCTTGCTGTACTTCAGTGTCATGTGAACCCCTNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNCATGGGAATCTGGATTTGGGGCACACACAAGATCTGATCCAGAACAGCAAAGCAAAGCATTTCCAGATCTGGCTCTTGTTTAAACACTCACATGTTCTGTGTGTTTCTGACTTCAGCTTATTGAGCTGATCAGCGCCACTGATGCAGATGATCCTGTGGATGGACAACATTTCTA[T/A]TTCTCCATGATCCCAGACAAGCACATCAACCCCAACTTCACAATCAGAGACAACCAAGGTATGTCACAATGTGAGCTTTATAAATGCAGAATATGCAATTTCACTAACACTGAGTCGGGTCCACATTGGTGTTATTTACAAGTCTTTTACAGGTGTAGCTATTCAGACGCAGTGAACTAGAGCAGGGATGCCCAGTGCTGTTCCTGGAGATCTACCTTCCTGTTCCTGAGTCCTGAGATCAGCTCCATTGCTGCTCAAACACACCTAACCCAAGAGCGCTCCTCGGTTCTTATTTGTGCATCCGCATTTCCTCTCCTCATGTCTCAGCTCCACTCTTCAGGATTTGAGGGAAAAACACAAGAACAAAAAGATGCGAAGACGGAGGAGTTAAATCAAGTGAAACACATCGTCTGCTCCTTTCACTTCAAGGCAATCAATTCATCAACACTGTCCATCACTGATGGTGCTTACATTTCTGCATTCTTGAAGAATATAGATGC

Associated Phenotype:

Not determined