Busch Lab

ZMP

LOC569425

Ensembl ID:
ENSDARG00000086283
Human Orthologue:
CNST
Human Description:
consortin, connexin sorting protein [Source:HGNC Symbol;Acc:26486]
Mouse Orthologue:
Cnst
Mouse Description:
consortin, connexin sorting protein Gene [Source:MGI Symbol;Acc:MGI:2445141]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa39150 Nonsense Mutation detected in F1 DNA Not yet available
sa7431 Missense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa39150
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000126501 Nonsense 478 575 9 10
Genomic Location (Zv9):
Chromosome 17 (position 11996876)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 11979398
GRCz11 17 12133464
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCCAGCTGCTGGTCTCGTGTCCATTTTGAAGAGGAGAGTCTCTCTGGAG[G/T]GAGAAAACAGCTCAGCTCCTGCTGCTCCCAAACCTGTGTCCAAAAGAAAG
Long Flanking Sequence:
TCGGCAGATATAGAGAGCACAGATACGTGGTAAGTGTTCACAAGACACTTCCCTCTTAACATAGATGTTTATATCTATATATAGCATACTATTAGAGCATACTGCTTTTGACCTACAGTAACCCTCCAAAACAGCTAATCAGAGGTCAGCATACACTGAAAATACACTGACAACTTATGTGTGTTTTATTAATAAATTACCTGCAATTTAGATAAATTCATAAATTTGATTCACTGAAGCATTCATTACACAAACTCCCATTGCAAAACGGTTTTTATATCTAAACCACAGAACAAAACAGTTCTTTGCAAAACAGTGTATTTTACATCACCTGCCCACGCAGCTTATAGTGACCTCTAGTGGGTAAAGTCTGTCAGCGCACATCTTTTCTGGAGATTTGTAAATGACTGAAGAGCGTGTGGTCTGTCTGTGTTTGTGTCCGTCAGATCACTCCAGCTGCTGGTCTCGTGTCCATTTTGAAGAGGAGAGTCTCTCTGGAG[G/T]GAGAAAACAGCTCAGCTCCTGCTGCTCCCAAACCTGTGTCCAAAAGAAAGGTCCGTTTCCGAGAGCCTGACGAGGGATTGGACCACGGTAAGAGCTAGTTTTCTAAAAGTCTCGAAGGAAGAGTTCACGCAAAAATGAAAATTTCTTTTTGAAAAAAAATTTTTTTTAGCTAAATTAGCTTGTCGAATTGTCATTATAACCAAAAATATTTAGAAAAAAGAAATATAGCAAATATTTATTTTTAAACACAATTGTTTTACATTATAAATTATTAGAAAAAAATGTTTTAAATTAAAAACTAAAACCTATTGTAATTTATTGAGCAAATAACAAACGTTAAACACATTCACACTTTTTTCAGTCAGAATTTGTCCATTTAAATAATATATACATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATGTATATATATATATATATATATATATATATATATATATATATTTGTGTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa7431
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 > G
Consequence:
Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000126501 Missense 513 575 10 10
Genomic Location (Zv9):
Chromosome 17 (position 11998020)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 11980542
GRCz11 17 12134608
KASP Assay ID:
554-4376.1 (used for ordering genotyping assays)
KASP Sequence:
CAATATTATTGTTGCTNCTNCNTTAATATGCAGATGAKGTGGCCGGTGAC[T/G]CGTGGCTGCTYCTCCTCCTGCTGTGTTTGGCTACAGTGGTRATCAGTGTG
Long Flanking Sequence:
GGGGGGGGGAAACGGAGCTGTCAAGCCGGACACTTCGGGGCTCAAAGTTGTTGCAGTCATCATGACCGATCACAAGGCATCATCATCATTTTTTTATTTATAATACCGAAAGATTTACAGTAAATAAAACAGAAAAACAGAATACAGTCTCTACAAACTAGTTCATTTTTAAACAAAAGGGGAATTATAAATTAAATTTATAGCAAACGCATGAGAAAAATAAGAAGAAACAAGAGGGAAATACAAACAAAAATGAAAAGGCCTATTAAATACAAAGCAATACGCACAAATTCTAGGAGTTTAAACATCCATAAAAACATCTATATAAAGAAACCAATCAATCGATTGAGTGTGACTAAGTAGTGAGTAATAGTTCATTTTAAGGTGAGCTATACCTTTAAATTACAGCTTATATTTTTTTGCAGCATTCACATCATCTGTGTTCTCATCCAATATTATTGTTGCTCCTCCTTTAATATGCAGATGAGGTGGCCGGTGAC[T/G]CGTGGCTGCTCCTCCTCCTGCTGTGTTTGGCTACAGTGGTGATCAGTGTGGGCGGGACCGCGCTTTACTGCTCATTCGGAGACACTCAGTCCAGCGTTTGCACAGACTTCTCTCACAACATGGACTTCTATGTGGGACGAGTGCAGCGTGGCATGGATGAACTCAAACACTGGCTGTCCCCGAGCTCATAGCAGGACAACAGAGAATATAAAATATACAGGCCTTTGCTGGAAGAAGCCCGAAGGATCCCTGTCTGTGTGGGGACGTCCGGTTTGTGGTAAACACAGGAAAAACCACTTTGGCCAGTTTTTTTGACTCGAGTAGCCCACTGTTTACTGCCATCAACTGAACCTCATTTGAAGAGACTTCATTTTTAAAGTCTTAAAGCTCAGATCTTAATACGGATTATGGTCTTATATTTGTTTAAATTACGGTACTGAAGGTATATTAATAATAATAATAATGGACATAGTCATCTGTAGCCTGGACGTAGCATTTTT
Associated Phenotype:
Not determined