ZMP

cadm2a

Ensembl ID:

ENSDARG00000009930

ZFIN ID:

ZDB-GENE-040426-1614

Description:

cell adhesion molecule 2a [Source:RefSeq peptide;Acc:NP_956958]

Human Orthologue:

CADM2

Human Description:

cell adhesion molecule 2 [Source:HGNC Symbol;Acc:29849]

Mouse Orthologue:

Cadm2

Mouse Description:

cell adhesion molecule 2 Gene [Source:MGI Symbol;Acc:MGI:2442722]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa21731	Essential Splice Site	Available for shipment	Available now
sa34900	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa4371	Essential Splice Site	F2 line generated	Not yet available

Mutation Details

Allele Name:

sa21731

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 > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000056369	Essential Splice Site	56	324	2	8
ENSDART00000135475	Essential Splice Site	102	332	2	7

Genomic Location (Zv9):

Chromosome 10 (position 23543677)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	10	23314970
GRCz11	10	23284422

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTCTTCACCATGCCTGTCAAAACAGCCAAGGCTTTCCTCACCGTCCTGGG[T/C]AAGACATCATTTCATTTACATCCTAATTCAACCAGCTGGAGCGATGAGGT

Long Flanking Sequence:

GAATCTTATGAGCTCAGGGATTCTCTCCCAGGACAGCATGCCAAACAAGCTTCATTATCAATCATCAACTAAGTGTGAACTCTTGAAACCAGCATGTGCACTGGGGGGAAAAGTTATATAGCTCAGTACCTTTGTGGATACGTCATAATGAACTAGGAATTGCAGAAGTGTCAAAGTCACACATTTCCAATAATCCAGAGTGGGTCTTGTCTGTTAAGCCAGTGTTCATGCATTAAAACTTTGGGTTGTTTGGGAAAAGCGGGAATATTACCTTGAACCATTATGGTACATGCTTATTAAGGTGTCATAATTAATATCAGTGTGTGAATTGTTTGTTTTCCGGCAGCTCTGAGAGATAACCGGATTGAACTGGTCAGAGCCACGTCGCAGGAGTTGACGATCAGCATCAGCGAGGTCTCGCTGTCAGACGAGGGGCTCTACACCTGCTCCCTCTTCACCATGCCTGTCAAAACAGCCAAGGCTTTCCTCACCGTCCTGGG[T/C]AAGACATCATTTCATTTACATCCTAATTCAACCAGCTGGAGCGATGAGGTAGTTAGTTAGCCTTGACTTGTCACATCACTAAACTGGAAATAGACAGTTTGGTTCATGTTAATCCTAAGTTTGGCGGAGTCTACATCAGGGTTCCTGTAAAATTTATGGAATTTTTAGAATATAATAGAATATTAGAAGGTCTATTCCAAACATTGAAAGTCGTGGAATTGTATCCAAGTCATGGAATATCAGGGATTTTTTGGTTGTTGTTTGTTTGTAAAAATAATAATAATTCTAATAAAGTCTATAATAAATTAATAAAGTCTATTGTTATGGTCAGATTATTTTTCAGCTTTATTTTATTTCTTTCAAACTTATCAGCTGGCAATTTACATACTTTGTTTTTTTTTAGGATTTTCAAATAGTACAAACAACAAAGACAATCAGACAACAGACAAACAAACCAAACCCAAGCACTGCAAATCAAATAAACATTTACAAATGTACGT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa34900

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:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000056369	Essential Splice Site	102	324	3	8
ENSDART00000135475	Essential Splice Site	148	332	3	7

Genomic Location (Zv9):

Chromosome 10 (position 23534454)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	10	23305747
GRCz11	10	23275199

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AAACCTGCGGCTGACGTCCGATGGTTCAAAAATGAGATGGAGGTCAAAGG[T/C]GAGGAAAGCTGGTAAAATATGCGATCATTGAAAGTAAACTTTTAAAAGCT

Long Flanking Sequence:

AATTTATTTTAATTTGTTAATTAGTCAGCATATGTAATTCATTCGATTTGAAATCTTAGATTGATTGACGTTCCAAATTAGAAGCTAAATTTAATCGTAAATACCCTGCTGCTTTTAAAAACTCTGCAATAATAGGATCAAATAACCACTAAATGAAAGAGTCTAAATTTAAATTAACCCCAGTGAACGACAAAAAGCCTCAGGCAAAACAAAAGGTGGTTCACAGAAGATATAAATAAAATCTCTAATCGTTCTCTATTAACGTTACATTCACCTACTGTTTATATTTAGAGCTGCCATAAAGAATTGAGTTCCACCTCTCTACCTTTCTCTCTAAATCACATGTCTGCTTCTTTTTCAGGGGTGCCTAAGAAACCAGAGATCAATGGACTCACCAAGCCGGTCCTGGAGGGAGATCACATCACTCTGACCTGCGTGACCTCTGGCAGCAAACCTGCGGCTGACGTCCGATGGTTCAAAAATGAGATGGAGGTCAAAGG[T/C]GAGGAAAGCTGGTAAAATATGCGATCATTGAAAGTAAACTTTTAAAAGCTGTTTGGACAGAAATCTATGTAGGTAAAGTGTGCCCATGGTCATATTGGAGTGATATAAACACAACACATCCCTTTTTTACATTAAAATATGATTCAAATCCCAGTGATTTTTGGGCCCACCACAAAACATAGAAGTGCAGTTTTCCCTGCCTGCCAATATTGATTGACAGTCACATTTTACCATGTCTTAGGATTTATTTGTATTGTCATGTATACAATACAGGATTTGCAAAGAAACTGGGATTAAAAGATCTGTTCCAACTCTCTTTGATCCAACTGCACTTCAAGAAGCAGTAATTGGTACACTTAGTATTTTTATAGCATTTTAAACTATACTTTTGAGCTATGTATTTCATCATTGCTGGACCAACTGCACAGTGTACACAATCATAAACGAGGATTCTTCGTTAAATCAGGTTTATTTTGTACACTAACTTAGCTGTACTGGAT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa4371

Status:

F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

T > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000056369	Essential Splice Site	246	324	6	8
ENSDART00000135475	Essential Splice Site	292	332	6	7

Genomic Location (Zv9):

Chromosome 10 (position 23505199)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	10	23276492
GRCz11	10	23245944

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

ACCAATCACCTCGGCACCAGTCATGCTGAATTCAAACTGGTTATTTATGG[T/G]GAGTGACAGATGGATTACATTAACATGTCTGTTAAGCAAACACAGCCCTT

Long Flanking Sequence:

ATTGTAGTATGGAAACTTTCAGAAGTCAAAACCTTCAGAACTTTTCTCTGTCAAAAAGAAAGTTTGTTTTAACTTACGCTGCAAAAGCTTACTATGGATTTCTAGAATAATTTCTGCAAACATATGATAAACCTGTTTCTCATATTAATGAAAAAAAGGGTTAGATGTTAGCATCTATGGCTCTGGAGACCCCTAAACAATAGAATAAAACTAATAAAAAAAAAGATATGATATGAAAAATTTATGTGAGTGCTTCATTAAGCATCATGGAAAAGAAGCTGAATTATGCTGTTAGAAGCTAAAAATGAGTGTTTCCCCAGGCCAGACCCTGTGCTGTGGACTAAAGATGGAGGAGAGCTGCCAGACATGGACAGGATGATTGTTGATGGAAGAGATCTCACATTCACGTCACTGAACAAAACAGACAACGGCACCTACCGCTGTGAAGCCACCAATCACCTCGGCACCAGTCATGCTGAATTCAAACTGGTTATTTATGG[T/G]GAGTGACAGATGGATTACATTAACATGTCTGTTAAGCAAACACAGCCCTTGCTGCTGTCTTGGAAAGCATCTGCATCGCTAATCAAACCTACGTTTCCTCCCTGCTAATAACTGTCATTTTATTTTCAAGCCACTGAAAGCTGCAGTGCCTTAAATGATTGCTGATTTGAAAGATCAAAGGGATAAATCAAACATTTTTTTATGGCATTTGTTTCTAAATTCATGTTTTGAATGTTATTTGGGGCTTAATATGGAAGTCAGTGGGACCCAAAACTGTTACATTTGTGTTGTCATATTTTATTTAGTCTTTATATATTACTTACTCACAGGGCCATTTTTATATTGAAGTTGATATTTAACCGCACGATGTTGGTGTTTCATAACATAACATTTTTACGAGGTGAGTCATTAGCCCCTTTCACACATACAGACCTTTCCGGAAAATTGCCGGCAATTTTCCGGAAAGGGTGTATGTGTGAACAGGTCCTTTTTGAAAATAC

Associated Phenotype:

Not determined