ZMP
ENSDARG00000053454
Ensembl ID:
Human Orthologues:
CNTN1, CNTN2, CNTN5
Human Descriptions:
contactin 1 [Source:HGNC Symbol;Acc:2171]
contactin 2 (axonal) [Source:HGNC Symbol;Acc:2172]
contactin 5 [Source:HGNC Symbol;Acc:2175]
contactin 2 (axonal) [Source:HGNC Symbol;Acc:2172]
contactin 5 [Source:HGNC Symbol;Acc:2175]
Mouse Orthologues:
Cntn1, Cntn2, Cntn5
Mouse Descriptions:
contactin 1 Gene [Source:MGI Symbol;Acc:MGI:105980]
contactin 2 Gene [Source:MGI Symbol;Acc:MGI:104518]
contactin 5 Gene [Source:MGI Symbol;Acc:MGI:3042287]
contactin 2 Gene [Source:MGI Symbol;Acc:MGI:104518]
contactin 5 Gene [Source:MGI Symbol;Acc:MGI:3042287]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa26814 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9424 | Essential Splice Site | Available for shipment | Available now |
sa2281 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa26814
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000055035 | Nonsense | 247 | 1029 | 6 | 22 |
Genomic Location (Zv9):
Chromosome 6 (position 44586098)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 44654669 |
GRCz11 | 6 | 44651188 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTACGAGCCTAAAATAGAGCTTCATTTCCCCGACACCATTCCAGCTGCT[A/T]AAGGATCCGCGCTGAAGCTCGAATGCTTCGCCTTGGGAAAGTAAGTCCGC
Long Flanking Sequence:
TGAAGTTACATATGCAAAACATATTGTTTTTACTCATCTACAGTCATTACATTTACACCAGATCTCACAGATGTTTTAAAGTTAGTCTCACAAGTCATTAAATCATCCAACATTTTTCTTGAGATCTTCATTCATAAATGTTAGATGCACATTTATGCCCTATAGGAACCCTAACCTGCACTCTTGACAATGCCTCCAAGAAAGCTGCATTACTATTTGAGAAGGATCCTGATTTTACTATGTGTGTTCCATAAATCTTTAATAACATGTCTGCGTATTTTTGGCACTGTCTTCTCAGCTCTCCTTCTCATTGACAGGTCTTTGTGTTTTGCCATTTGTTGTTGTTTTGCTTGTATTTCTGGAGTACAAAGCTTGTATGTCGTAAATCATGAATGACAAAGCCGTATGCATCTGTGGTGTATTGTCTGCCCGTGGCAGGAGCGATGGGAGAGTACGAGCCTAAAATAGAGCTTCATTTCCCCGACACCATTCCAGCTGCT[A/T]AAGGATCCGCGCTGAAGCTCGAATGCTTCGCCTTGGGAAAGTAAGTCCGCTGTTTGTGCACCTGCGTCTGTCTGCGTCCTCCCGCAAACTGTTGCCTGAGTTCACACCCTCTCTTAGCGCCATTTATTTTTATCCCATCATATGAAATACACCCAATTTGTGATCAGCACTTCAAGTTCATTCTTAATGCGATTTGCAGACTGTCACGGAAGCTTTTTACAGAGGCCTTTTCAGTAAAATGGCCTGCTTTGCAGAGAGCAATGACCCGTAAGATTTACTCCTTAAATAGTGAGGAAATAGAGCTCCATGCTTCTTTTCAAAGGAAGAGCAGAAGTGCTGTCGTTTTAGAGAGGGGGTAATGCTGGTTTTTTTACAAAAAGCGGGAGATGATAGCTTTTCACACTATACAGGGAGTGTGTCACCCCAGATTCAAACGTGAATCAGATCCTTTTACACTCAGATTTCTTAATGGGGTTCAGCTTTAAAGAAACAAGAGAGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9424
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000055035 | Essential Splice Site | 260 | 1029 | 7 | 22 |
Genomic Location (Zv9):
Chromosome 6 (position 44583409)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 44651980 |
GRCz11 | 6 | 44648499 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAAAAAGTTTGACATYGATAACTAATTGTGGCCTTGTTCTGYTTAAAAC[A/T]GTCCAGTTCCTAGGATCAGCTGGAGAAGAACCAGTGACGTTTCMTTCCCA
Long Flanking Sequence:
TTAACTACTAACTACTTGCTTATTAGCAGAAAACTATTATAATATTGGCTTTTTATTATTATATTTGTTGCAAAAAAAAATCTAACATTATTAAAAACATCAGTAAAAAATTAGACATCAAAGGTATGTCTGATAATGTAATTGATTGAATGGAAAAAGAAGACTGTGTAGCTGTAGAACATTGTCTATGCAATGCCAAGGTCTTTGATTTTGTCCCTATGCATCAGTGATTAAATACCTTGAAAGCTTTGAATAATACTGTCTGCTAAATGCAAAAAAAAAAGTAAGTGCTACATCTTCACATATTAAAATGCAAAGCTTGGATGAAATGTACATCTCTTTGAATATAAGTCCTAAGGATGAGAAAAAGTAAATCCTACAGTAGTTATGCCAAGGTCATGGATTTGACTCCATGTAATAAACGCACTAATTAAAAAGTATATGGACTTAAGAAAAAGTTTGACATCGATAACTAATTGTGGCCTTGTTCTGTTTAAAAC[A/T]GTCCAGTTCCTAGGATCAGCTGGAGAAGAACCAGTGACGTTTCATTCCCAAATAAAGTCAAACTAAAGAATTCCAATGCAATTCTGGAAATTCCCAGTTTTCAACAAGAGGACACAGGAACGTATGAGTGCATTGCTGAAAACAGTCGTGGAAAAAATGCTGCAAGAGGTCGGGTGTCTTTCCATGGTGAGTTATTCTTGATTTTTTTTAGGTGTTTTTTAATTTAACAATTCTTTTTGCAATCTTTTAATCTTTATTAAAACAAATATCTTATACATTTATGATTCACAAACACCTTTATCAGGATGTCATTGCTGGTATGTGTGTACTGCATACAGTATGTATGTATTTCTTCTGCCTCTAGAGGTCTTTTATTGGTATAAATAGATATTTTTGACAGTTCATACTGTTGTTTTACAGATTGATGTTACCATATGGCTCTTGTACAGCATTGAAACCACAGTGATAAATCATTATATAGAACTATTGGTTATTTTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2281
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000055035 | Nonsense | 865 | 1029 | 19 | 22 |
Genomic Location (Zv9):
Chromosome 6 (position 44532199)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 44600770 |
GRCz11 | 6 | 44597659 |
KASP Assay ID:
554-2436.1 (used for ordering genotyping assays)
KASP Sequence:
GATGACACCAAGCCGGATACAGTGGGTAAAGTTCGAATCACTGGAAACTA[C/A]ACAGCAGTGAATGTCAGCGGCCTGCAGGGGAACACTCAATATTACCTRGC
Long Flanking Sequence:
AAAATAAAAAGAAAATAAAAAAATGAAAGGGGGCCTAATAATTCTGGCTTTTATTTATATTACTGTATATTTGGCAGATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTATTGTTTGTTTATTTATTTATTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTATTTATTTTAGCATTAGCTTTGTGGATTTGACTAAACATTGTAAACCCAATTAACATTCATTTAGTTCAAAAACATGCCAAAAACCTATTTGTGTAGTAGCACATCTTTTGACAAAAATTAGCATATTTAGGGTCACAGCGGGTTACAGGAGTGTGTAATTGTTCTGGCACAAGAGCTGTTTACATCTAAATCATAGTCAAGGATATATAAAATGCCCTTGTTGTGTGTCCTGGTGAACAGGTGGTGTACTGGGAAGATGACACCAAGCCGGATACAGTGGGTAAAGTTCGAATCACTGGAAACTA[C/A]ACAGCAGTGAATGTCAGCGGCCTGCAGGGGAACACTCAATATTACCTAGCGGTGTGCGCCTTCAATACAGCAGGAACCGGCCCACAGTCTGCACCGGTCAACATTACCACTAAGAAACCACGTAAGTAAGCCCTTGTCTAAGAAAACCCCATTTTTTGTGCAATCTTTTAAAGACAAACCAAATCAACTCAATTATAACTTGACTCAAAAGTATGACTTACTAACTTGTTATTATGAGTAAGTCAAAGTTATATTGTGTTTCCTGAAACAGTGCATGCAAAATGATTTGATTAAATATTATATGATTATTTTGATGCAGGTTTAGCTCTTAGCTCTTATTGCCTTCCATTTTGATAAAAACTCAAGAAGGGTTTGTAAAACCATGTTTAAAACGCTTCCGACCATAAAAATATTTGTAAATTAACAGGTTACATATTTCATGGTTTACAGGGGTTTTTATGTTTATTTACATTTGTTTATTGTATTATGGGATGTTGATC
Associated Phenotype:
Not determined