ZMP

NP_001038711.1

Ensembl ID:

ENSDARG00000057013

Description:

cell adhesion molecule 3 [Source:RefSeq peptide;Acc:NP_001038711]

Human Orthologue:

CADM3

Human Description:

cell adhesion molecule 3 [Source:HGNC Symbol;Acc:17601]

Mouse Orthologue:

Cadm3

Mouse Description:

cell adhesion molecule 3 Gene [Source:MGI Symbol;Acc:MGI:2137858]

Alleles

There are 4 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa38354	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa44546	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa33009	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa38354

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
ENSDART00000079596	None	None	373	None	8
ENSDART00000111246	Essential Splice Site	None	393	None	11
ENSDART00000124222	None	None	413	None	9

The following genes are also affected by this mutation:

ENSDARG00000094421

Genomic Location (Zv9):

Chromosome 2 (position 44244756)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	44330257
GRCz11	2	44183255

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ACTCCTGAACCGACGGAGCCATCGGGCATCACGAGGAGCGCTTATATCGG[T/C]GAGTATCGTAATCTGCCCTCCTTTTGAGCTCACAGACACGCAGGGGCATT

Long Flanking Sequence:

TAGAACGAAGTTTCATGGGATTAGCCTACTGTAAAAACCGATTGTCCACTAACTTCATGCAGGATATTGTTATAAACAAAACAACAACAACAACAACAACAACAATTTATAACAACAACAACAACAACATAATAACAATAATAATAACAAAACTCTCTCAGTCAGTATGGTCTGGTCCTGTTATTCAAATGGTATGGCCAAATCGTATTAAAATCCCCACCCCTCCCCCTCCGCCCCGCGCGCCTGCCCCTTCCCTCCCTCCCTTCCTCACTTCCTCTCCCTCCCTTTCTCCGTGCTTTCAGACAGACTGTTTTGCTGCAGTGAACGGTAGCCGTGGAGAGAGGAAAAGGCAAGAAAAACAAGAAGACAGCGGAGGGCGGAACGAGAACCAAGACAGACAGATCCATTGGGACCTTAGCGTGAGCGCCAGCAGGCACAGACGCTTCCAACACTCCTGAACCGACGGAGCCATCGGGCATCACGAGGAGCGCTTATATCGG[T/C]GAGTATCGTAATCTGCCCTCCTTTTGAGCTCACAGACACGCAGGGGCATTATTGTCGTTGGCGTCCCGGCGCTTATACGGAATGGGTGGGGGGGTGGGGGGGGACACCTGTCAGGTTTGTAAATAGGGACACGCTCGTGCTCTGGAATGCGCCTGCATCCGCGCGCGCGCCAGGCGCACCGGGAACAAATCCGCGAGCTCGGAGGTGTAAAACTATGAGCGCTGATGGTAAAGTGTGCTTAGGCTACTGTTAATGCGCTGGTGCTCGCTTTGCCCCTCGCGTTTCCCCTCCCCTCCTTCCACTAGCATCCCTGCCGCTCCTTCTGCATTCAGCGCGCTCGGACTGTGTGCACCTGCTACTGTTTTCCGTGGTTCGGTGGGGCGTCCCGGTTGGGACTGGTACTCATAGGGAGTGAGGGATGGAAATAAAGAGAAGTGCAAGAGAAGAGCCGATGATGAGTGAGGGATGCTGCTGGCTCCGTCTCAGGTTGCGTGTTATTG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa44546

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:

A > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000079596	Essential Splice Site	51	373	2	8
ENSDART00000111246	Essential Splice Site	64	393	4	11
ENSDART00000124222	Essential Splice Site	91	413	3	9

Genomic Location (Zv9):

Chromosome 2 (position 44155380)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	44240881
GRCz11	2	44093879

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TACGGCACCTATGTAGTGTATGTGTTCCTCTTATCGGTTCTGTCTTTTTC[A/T]GCACTGAGAGATAACCGTATCCAGTTGGTAAAGTCCACGGCCACGGAGCT

Long Flanking Sequence:

CGTTACGCTGTTCACTACATGGTGAACATCACATGGCTCGCTAGATGCAAGCAAAAAGGAAAGTATTTGGATCAGACAATATTGCGCACTCTGCATGATGTTGTAAACGTCACATTGCTGAATAATAAATGAAAAAAAAGAGCTTTGAAATCTGATCTGACCTTTCAAACTAAGGGGTGTACTTAAAAAAAACCCACACTTTAATTGGATCTCAGAGGCATTGGAACATTGTGTGCATGGGGTTTGTACAGATAAGACTGCTTATGTTCTGTTTTGTTGTTGCTGTCGTCGTTTTGCTTGTGATACAGCAAGGAAATGTAAATGTTACAGAGAGAGATGGTGGAAAGCAATCACATAAATCTAAATCACAATGGTTTTGCTGCCAGATATTTTGACTTGTGTTATCAGCCGACTTCAGGGGAGGGAAATAAAATGCTAAAACTTGTAATGTACGGCACCTATGTAGTGTATGTGTTCCTCTTATCGGTTCTGTCTTTTTC[A/T]GCACTGAGAGATAACCGTATCCAGTTGGTAAAGTCCACGGCCACGGAGCTGATAATCACCATCGGGGATGTTCAGCTGTCAGATGATGGAGAATATACCTGTTCCATTTTTACCATGCCTGTACGGACCGCACGAGCCACAGTTACTGTACTCGGTAAGTGTGTATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCCTTTTCTCTCAGAGTGGGAGCTGTCAGTAGAAATTGCTATTGCTACAGTACATCAAGCCTGTAAGTAGTGATGTGCTCATTCCGATTGCCGATTTGTTTATAAGCAACAGGCCAATTCCAATATCTATTTGTGGTTATTTATTTATTTATTTTTACTTTACATAAATCGTAAAATTGATTCATCCAGTACTTTAAGATAAAAACAACAAAATTTGGCCAAAATGCCAATTCAGTGGACATTATTTGTGTAATTATGAGAGCATGTACACAGAGACAAGGTTCTCTATCTATCTATCTATCTATC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa33009

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
ENSDART00000079596	Essential Splice Site	335	373	7	8
ENSDART00000111246	Essential Splice Site	355	393	10	11
ENSDART00000124222	Essential Splice Site	375	413	8	9

Genomic Location (Zv9):

Chromosome 2 (position 44117885)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	44203386
GRCz11	2	44056384

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATGCTCTGTCTCCTCCTTGTCCTCGGCAGATACCTCATCAGACACAAAGG[T/C]AACACACACACACACATACAAGGCAAATCAGACAAAGAAATCTCTTACTC

Long Flanking Sequence:

CAGTCATTTAAGTCATTTTGTAGCATTCAACCTGAAGTATTCTGAGAAACACACACATTTCCATCCGCTGCACAGCATCCATATATAAAGGACAAAAGCAAATCAAAATACATTCAGCTTCACGCCATCGCATTGTGACTCTCTGAATCAAACACAGATTGGATTCCCGAAGTTACTGTACATGCGGCACCTTTGTAAAAAAAAAAAAAAAGTGAGGTGGAGATGAATAAGAATTGTACAGTTTGTCAGTTTCAGCTGAAGTTTCTCTCAGAGTCTTCTCTGATTTTGCCTGGTGTGTATTGTTGAAGTGATTCTGATTGTGCGTGGTCGTGACTGTCTACAGCAGCTGTCTGTCTGTCTGTCCCGTCTGCAGACCCTACAGCGATGTCCACTGGTTCGGGAGTCGACCATGCTGTGATTGGTGGAGTGGTCGCTGTCATTGTCTTCATCATGCTCTGTCTCCTCCTTGTCCTCGGCAGATACCTCATCAGACACAAAGG[T/C]AACACACACACACACATACAAGGCAAATCAGACAAAGAAATCTCTTACTCACACACATACACACACAGAGACCTAATCAGACACAAAGAGACTGCACACACACACACACACTTTATAACCTTTTGGGACTGTCTTCAAATTCCTGAAAGAGGGTCTGGCAGCAATCGCCCCATCAGCAGCTTTTTTTAAATGATTTTTTCACGGATTTTGTCTTTCAATTTAAGCATCAACAAACATTGTGGACGCTTGACTCAAGATCTCATTGTTGACTGGGATATTTTACTTGTAAATGAGTCACGTGTCTCGCTGCAGTGGTGCACCTAAAACGCAGGAGGAAAAAGGGTTGGGGGAAAATATGAAAAAGAGAAATATGAATAAACAGCTGCTGAGTCTGTCAACTTATAAGACAATGAAGTACACACACTCACACACACTTTATGACCTTGCTGTTTAGAAATGTATATTCATTGGTCAATATGAATGTATATCCAATATCTTGC

Associated Phenotype:

Not determined