ZMP

CDH22

Ensembl ID:

ENSDARG00000075268

Description:

cadherin 22, type 2 [Source:HGNC Symbol;Acc:13251]

Human Orthologue:

CDH22

Human Description:

cadherin 22, type 2 [Source:HGNC Symbol;Acc:13251]

Mouse Orthologue:

Cdh22

Mouse Description:

cadherin 22 Gene [Source:MGI Symbol;Acc:MGI:1341843]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa20832	Nonsense	Available for shipment	Available now
sa18858	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa20832

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:

G > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000110855	Nonsense	314	519	5	8

Genomic Location (Zv9):

Chromosome 6 (position 56731739)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	6	56784891
GRCz11	6	56781932

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGGGTGAGAATACGGATATGAGTTACCTGATCAAAGACGAGGAGGGAGGA[G/T]AGCTGTTCAGAGTGTCCACTGATGGAGACACACAGGAGGCCGTCATCGCC

Long Flanking Sequence:

CTGCCTAGTTAACCTAATTACCCTAGCCTTTAAGCCTTTAAATGTCACTTTAGGCTGTATAGAAGTGTCTTGAAAAATATCTAGTCTAATATTATTTACTGTCATCATGGCAAAAATAAAATAAATCAGGAATTAGAGGTGAGAAATTAAAACTATTATATTTAGAAATGTGCTGAAATAACTTCCCTACATTAAACAGAAATTGGAGGAAAAAATAAACAGGGGGCGCATAATTCTGACTTCATGTATGTATTATACAAACATAACACAGATTGCTATATTCCCCAGGGCTAATATGCATATATTCTCAGGCCAGCGTGTGAACATGAATGGAGCTGATCTGAAAGTATCATCTTCTCTTTTCTGTCACAGAGATGTATCAGTTTTCGGTCTCGGAGGGCGCCGCCGTCGGGACAGCGATCGGTCGGGTGATCGCGACAGATGCAGACATGGGTGAGAATACGGATATGAGTTACCTGATCAAAGACGAGGAGGGAGGA[G/T]AGCTGTTCAGAGTGTCCACTGATGGAGACACACAGGAGGCCGTCATCGCCATCAGAAAGGTACAGGAGACCTTCAGACCTGTCGTTTTACACTCTGAAGGTCATGCGCTTGTTTATAGCATTAAGTACTGATCAAAAAGCACCAGAACTGATTACCAAACTAAAATATGTAAACACTTTAGCTGTAAAAATGCGTAAAAAGCACATTAAAATATATTTTTTTATAATCCTAAAACATGTTTACAAATTATTTTATTATGCATTCATTTGTTCGTTCAGTTTGTTTGTTTATCATTCATTTATTTATTCATTCATTCATTCATTCATTCATTCATTCTTTATTTATTTATTCATTTATTCTTTCATTCATTTATTTATTTATTTAGTAAGTTATAGTTTATTTAATTATTTTTATTTACTTATTTAATTATTTTTTGTCTATATATATTTTTTATTTGTCTATATATATATTTTTTTGTATTAAATATTTGTTTATTTATC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa18858

Status:

Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000110855	Essential Splice Site	419	519	6	8

Genomic Location (Zv9):

Chromosome 6 (position 56729490)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	6	56782642
GRCz11	6	56779683

KASP Assay ID:

2259-8250.1 (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTGGGAATCGTGACAGCCAGAGATCCAGATATGGACAACGTCCCCATCAG[G/A]TGTGGTTTAATACAGTTCAAGTTTATTTGTATAGACACACACTTGAAACA

Long Flanking Sequence:

TGTCTGACAAGTTATGTTATGCTTGCTTGATATGAATCAGTCAAGATTTCACACATGAAGCACTAGCTGGAGATGGACATTTGTACAGCAATACAAGCATTTTACTGTATTTTCATTAACTAACGTTAACAGATACTGTAATAAATGTAATGTTCATTGTTTGTTCAAGTTTGTAAATGCATTAATAAACAATAACTAATACAAGCTTTTTGTAAAGTTTTACTGATGTCCTTTTCTCTTCAGCCTCTAGACTTTGAGCACAAGCGCACACATAATGTGGTGGTGGAGGCTGTAAACAAGCACGTGGACCCTCGTTTTGTTGATCTGGGGTCTTTCCGGGACCAGACCATCGTGAGAGTCAGTGTTTCTGATGTGGACGAGCCGCCGATCTTCATGCCACCCGCTGGAACCATCATGGAGGTTCAGGAGGATGCTCGGCTAGGAGCGCTGGTGGGAATCGTGACAGCCAGAGATCCAGATATGGACAACGTCCCCATCAG[G/A]TGTGGTTTAATACAGTTCAAGTTTATTTGTATAGACACACACTTGAAACACACTTTACGTAATGTATATCAGATTTGCAAAAATGTCGACAGCGGCCTCTAGTGGATTTTACATCTGAAATGGGCAACAAAACATGCCCAGGGTCATGGGGGCCACTTGGGGGTGAACGTTAGGATGATTACAAGGCCTCATGCAGTTCATCAACCCCAAAACCCACAACACCTCCACCCAACAACTCCACCCACCCCCTCTTCACTTTCATTTGGGACACATTGACACCCCCCCCCCACCACTACCTTTTTGCTACTAAACCCCAGCTCTTTACTTTCGTCCGTGACATAAACATCACGACCTAAATCTAACCCTAATATCATCGTCTTATGACGTTGTGTGCCCGCTGGGCAATAACTACATGCACTACAGAATGTTACGTTTACACACATCCACAAACTACATGTAAATGCATCAGCTTTTACAGCGTAATACTCACTACTATTTTA

Associated Phenotype:

Not determined