Busch Lab

ZMP

ENSDARG00000087843

Ensembl ID:
ENSDARG00000087843
Human Orthologues:
CNTN1, CNTN2
Human Descriptions:
contactin 1 [Source:HGNC Symbol;Acc:2171]
contactin 2 (axonal) [Source:HGNC Symbol;Acc:2172]
Mouse Orthologues:
Cntn1, Cntn2
Mouse Descriptions:
contactin 1 Gene [Source:MGI Symbol;Acc:MGI:105980]
contactin 2 Gene [Source:MGI Symbol;Acc:MGI:104518]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa6784 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa6784
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000128281 Essential Splice Site 105 491 7 17
Genomic Location (Zv9):
Chromosome 25 (position 167990)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 146990
GRCz11 25 10822
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGGTATGCKCTGTGTAAAACATATGCTGGAATAGYTGTTGGTTCATTCC[A/G]CTGTGRCRACCCCTGATRAATAAAGRGAYTMAGCTGGAGGASAGTGAGTG
Long Flanking Sequence:
TCTCCTCGCTGCACAGAGCTGGTGTGGAGGGTGAAGTGAAGGTCAACACTGCTGTAAACCTGCGCTCGTGCTGGATGATGAGGGTCTGATGTGTTTATTCACCTTCAGCACAAACACCTCAGCCAGCATCTCACACTGCCACAGCCTGACATGACATGAGCTATTATTCTGAATATTAGAAATGGAAGGGGTGACACGGTGGCTCAGTGGTGTCGCTCTGTGGCCTCACAGCACTCAGGTCTCTGGTTTGAGTCTCGGCTGGGTCAGTTGGTGTTTCTGTGTGGAGTTTGCATGTTCTCCCCGTGTTGGTGTGGGTTTCCTCCGGGTGCTCCGGTTTCCCCCACAGTCCAAACACATGCGCTATAGGGGAACTGATCAACTACACTGACACTAGTGTGTGTGTGAGAATGAGTGTGTATGGGTGTTTCCCAGTACTGGGTTGCAGCTGAAAGGGTATGCGCTGTGTAAAACATATGCTGGAATAGTTGTTGGTTCATTCC[A/G]CTGTGGCGACCCCTGATAAATAAAGGGACTCAGCTGGAGGAGAGTGAGTGAGTGAGTGTTTGTTTCTTCTGGGGAAATGTTATTTATTTAAGATTCTCTGGATTAAATGGAGTTTATGCAACACTCAGGTCAGGGTTATGATGTGTTCTACAGCTGTGTTGACTACAGGAATTCTGACTTCAGCTGTTTGAACATCCGTCTGTAAACAAGACTCAGATCATCTGAATAATGTCTGTCAGCTGTGTAGATCAGATTATCATCCTAAACATGTGTGTGTGTGTGTGTGTTGGTGAACAGTAACTGGTGTGTGTGTGTGTGTGTGTTAATAAGATCAGATCATGATAAACCCCGCGCAGCGCTGCTCTGATGAAACCCCTGATGATGAATTATTCATGTCTGATCAGAAGACTCATTTACAGTCAGACTGACTCAATCTGCTGGACGGAGACACACACACACACACACACACACACACATGCACACACACACACACACACACA
Associated Phenotype:
Not determined