ZMP
si:ch73-150k18.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to contactin associated protein-like 5 (CNTNAP5) [Source:UniProtKB/TrEMBL;Acc:
Human Orthologue:
CNTNAP5
Human Description:
contactin associated protein-like 5 [Source:HGNC Symbol;Acc:18748]
Mouse Orthologues:
Cntnap5a, Cntnap5b, Cntnap5c
Mouse Descriptions:
contactin associated protein-like 5A Gene [Source:MGI Symbol;Acc:MGI:3643623]
contactin associated protein-like 5B Gene [Source:MGI Symbol;Acc:MGI:3664583]
contactin associated protein-like 5C Gene [Source:MGI Symbol;Acc:MGI:3646013]
contactin associated protein-like 5B Gene [Source:MGI Symbol;Acc:MGI:3664583]
contactin associated protein-like 5C Gene [Source:MGI Symbol;Acc:MGI:3646013]
Alleles
There are 10 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32391 | Nonsense | Available for shipment | Available now |
sa24108 | Nonsense | Available for shipment | Available now |
sa12112 | Essential Splice Site | Available for shipment | Available now |
sa24107 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa32391
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110136 | Nonsense | 291 | 1306 | 6 | 24 |
ENSDART00000134035 | None | None | 158 | None | 3 |
Genomic Location (Zv9):
Chromosome 22 (position 13670421)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 13501639 |
GRCz11 | 22 | 13526416 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTCCGTCCTGATTGAGCGATTTAACAAACAGATCAACTTCACTGTGGAC[A/T]GACTGACCAAACACGTCAGGACGGGTGGACTGGACGATTCTCTGGAGGTC
Long Flanking Sequence:
GCCCTTTGGTAAGTAAGTGGATGGTGATGGAGTGAGTGAATGGATGAGTGAAGGTAGAGTGTGAAGAAGTGAGTAAGCATATGTATATATTATTAGATTAGAAATAGGTAAGTGATTAAATAAGCATACAAATGGGTACTTGGATTGGGTACTTGTTTTATAAATAGATTTACTAAGGTAATGGATGAATGAATGAGGGGATAATTGTGTGAGGATTTTAAAGTAATATATTACTGGCCAAAACATAAACACTGACCAATTCAAAATATGAACACGCAGACGAACAGGAACTGCAGTAAAGCTGTTCTAAGAGGAATTCTGGTGATGGAAATGCTCAAACTGAATTCTTTTCTCTGATTGTGTTTTTGTCTGAAGACGATGCTAAGACGCACCCAAGCAGCGGCCATGTGTCAGTGTTTTTGGGTGGTCTTCTGGATGACCAGCACTGGCACTCCGTCCTGATTGAGCGATTTAACAAACAGATCAACTTCACTGTGGAC[A/T]GACTGACCAAACACGTCAGGACGGGTGGACTGGACGATTCTCTGGAGGTCGATTATGAGGTGAGAATGTTCTTAATTACTTGTCTTGTTCTAGTTTGTTTGGTTTGCATATGAAATTGTGTTCTTTTGTTTTTTATTATTGAGTTTTATTAAGGACATTTAAAATGAATGTTTTTAGAAGATAATTATGTCTTTTAAATATAAAATATGACTAAAACTTGTGATGGATTAAAGATTTTTTTTTCGGCCAGTGAAATGCTACACTTAGTTTATAATAAATTGTGCATATTTTATTAATATTTACTTGAAACAAAGCCTTGGTAAATAGTTTAATCATTTACAACTTTTCAATAGAAAAATGTAATTACATTTTTATTCACTTTGCAAACTCTTTTGTTTGTTTGCTTGTTTGCAATAATGGAAATAAATGTTAGTGTTTTTTAACAGTTTTTTGTATATATAGATTTTTCATTTTATTTGATTGATTGATTGATTGATCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24108
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110136 | Nonsense | 349 | 1306 | 7 | 24 |
ENSDART00000134035 | None | None | 158 | None | 3 |
Genomic Location (Zv9):
Chromosome 22 (position 13668503)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 13499721 |
GRCz11 | 22 | 13524498 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTGCATGGAGAACCTCTACTACAACGGCGTCAACATCATCGACCTGGCC[A/T]AACGCCGCAAACCACAGATCTACAGTGTGGTGAGGATGTTCATCTCGTAC
Long Flanking Sequence:
TTTTATTTGTCTATACCTCTACCTAAATCCAACCCTCACAAAAAATATGCTATATTGACGCGAATATCTTCAGCTGTATCCCATCTAGACTTCACCCACTTCTCTAGCATGGTGAAGTCTAGATGAATTATTATTATTATTTTTTTTGTGACACTGTACAATAATAATAGTTGTGGTAATACTGTGAATTGTGACCTAAACTAAAACCCTAATAATTTGTCCACCTGCTAACATGTTGGTTTAAAGATTGGCAGCATGTTGACCACAATCAAGTGCATTGATTGGTTAAGAGTGCTTCAAGCACCAAATCCCTCAACTAATAATTGACCCCAGTCCATGTTGTAAAACCTCTCCAATGCTGTTGTTTGTCCATTCATTTCACAAAGCTCAGCTTCGGCGGCATCCCTCTTCCTGGAAAACCAGGCACGTTCCTGCGCAAAAACTTCCATGGCTGCATGGAGAACCTCTACTACAACGGCGTCAACATCATCGACCTGGCC[A/T]AACGCCGCAAACCACAGATCTACAGTGTGGTGAGGATGTTCATCTCGTACATTTATTATTGATAATCTCACACATTTGTTATTGTTGTTATGATCGGATATTTGAAAATAAGAAAAATGACCACAGGATTTGATGAATGAGCGGTCCTATCCTATCCTATTTATAATAAATGCTTCTTGACCCCAGTGTTTAGTGATTTTTTTTATTTCTGTGGAGAGATGCCAAAACGTTCTGCTGCACAGTTTGTGGATTATGATGAATTTTTGCAGTTGGGAGTGCAAACCGTGTTTATAAGGAGATTGATTTCTATTTTCGTTCTCATTAGTTTTTACCTGCATTTTTAACTCTGGCGTGGTTCTCTGTGGAACCGGGCAGCGAAATAGAGCCATTTCGAAGGGTTTTTTGAGCCGTCGCCAGTATACTAAGACAACACGAGGGAGCTTTTTAAGGGAATGAATTGTGGTTTTGTCCACATTATTCCCACGGCGCTGAGAGCGGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12112
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:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110136 | Essential Splice Site | 588 | 1306 | 11 | 24 |
ENSDART00000134035 | None | None | 158 | None | 3 |
Genomic Location (Zv9):
Chromosome 22 (position 13638207)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 13472676 |
GRCz11 | 22 | 13497453 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCTGCGACTGCTCGGGAACAGGATACACYGGAGCCACCTGTCATAACTG[T/G]GAGTTGGCATGTAACCCATACAAAARAAACAACAATAACAAKATACTGTT
Long Flanking Sequence:
GTCCACCAGTTGTATTTGCGAATATGGCGCATCATAACAGAGCCACCAAGAATGAGTTTGTTTCTTGGCTTCAGATTTAACTTCATCACAATCACAATCTTTCATCGCTTGTCCGCCGTCCTCATCCTTGAGTGCGCGTTCAGTCTGTCGCAAAATTGATTCATCCTTCGCGAGCTTTCAGCCCCTGCCATCTATTTCCTAATAGTCACTTGCGGTTATTGATTGATCGCCACGTCCTTAAATCCCTCCGAGCACAAAATGCATTACCGTTCGGTATTGTGCCGTATGTCGCAGTGTGTCGTTTGTGTGATTTGTGTAATTCGATAATGTATTCTCCCACCCGCTGTAAGTACCGTGAAAGTTTAATCAGAAGTCTTTTTTTTTTCCTGCAGATGTCTTCCTAACTACTGCGAGCATGATGGAGTGTGCTCTCAATCCTGGAGCACGTTTTTCTGCGACTGCTCGGGAACAGGATACACCGGAGCCACCTGTCATAACTG[T/G]GAGTTGGCATGTAACCCATACAAAAAAAACAACAATAACAATATACTGTTCACTTTTTTATCTAATTTTGTAGCTGTAGTTGTTGAGAAAATAACTAAAAGGTATCTTTTGAAATCTCTAAAGTTTTATTTATTTTCAAAACTTTTGTTTGTCTGGTTTTGAGATTTTTTTAGGTATATTTAAATGTAAATATTTAATTGTGTATTTATTTATTTGCTTTTTGTCTAAAATCTCTTTCATCATGTAGTTTGGTATTAATGAGTAAATGTCATGTTTATTAATTTATTTAACTAACTTTTGTTGTTTTATGAAACTATATATTTTTTCTAATTTATTTATTTATTTATTTATTTACTTATTTATTTACTTATTTATTTGTTTAACTTTCATGATTTGGATTGATGATGAGCCACCTACATAACTGTAAGTTGGCAAATAACATACAAAAATCAACAATATCGTTCAACTGTTTGCTTCGTTTTGTTGTTGTTGTTGAGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24107
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 |
---|---|---|---|---|---|
ENSDART00000110136 | Essential Splice Site | 1000 | 1306 | 19 | 24 |
ENSDART00000134035 | None | None | 158 | None | 3 |
Genomic Location (Zv9):
Chromosome 22 (position 13612367)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 13447884 |
GRCz11 | 22 | 13472661 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTGCCCACGAGCGTTTGTGACAATGCTTTTTGTGTTTTTCTTCCTTTGC[A/T]GAGGTTTCCGTGTCATTTGAAAGCGGGTCCTCGGTGACCTACACCTTCCA
Long Flanking Sequence:
GCAGTTCTGGATACGACTTGCGTCAATGACCATGAACCGCGGTTGTTTGGATGAATTTCGCTCAAAGGGCTGCAACCTGAGCGGTCCCAGCAGAGCATCCCTGCCCATCACATTCAATGCTAAACCTCTCGCCTGTCAATACAGCCTTTATCACATTTGATCCTGCGATACGCCAGACAGCCGAGCCATTCAGCACTCCGTGAATGAGGCTTTGCGTTTTCTTTATTGGACTCCAGAGGGATGGTGTTTCCATCCTGATAATATTATGAGTAAATGAACACCATGAGATGCCCCAGGGGTCGGTTTCAGTCCAAGCATAATTTTGCATTCATTTAAAGTTTAAATGATTCATTTCCTCCGCATTTGTCCACTCAGCAGCGTGTCCTTGGTGTTCGACAGCGCATTAATATGCTGATATGGAAACAAAAACAGCAAAATCGCTGTCTAGGATCTGCCCACGAGCGTTTGTGACAATGCTTTTTGTGTTTTTCTTCCTTTGC[A/T]GAGGTTTCCGTGTCATTTGAAAGCGGGTCCTCGGTGACCTACACCTTCCAGGAGCCGTTTTCTGTGATGCGCAACCACAGCCGTCAGTCCTCCGCGATCTTCGCCCAAAGCAGCAATTCACGGGAGAGCATCGCTTTCAGTTTCCTCACAACTCAGACGCCTGCCATGCTTCTGACCGTCAACACCTATCATCAGCAGTACATGGCCATTATTCTGGCTCACAATGGTATTTATAGTTTATATTGATTTTGATGGGCTCAAGTCGTTGTTTTTTCATCCCTTTAAATGAAATGAATGCAATATTATTTGACTTTTTCAAAACAAAATGGTATTTCTCCATCCATTTTTAGTGTAACAAGCGTATTGCTTCAAGTTAACAAATATTGTGCTGCATAGTTTATTGTAATATACTTTTTGAATCCTAACATTGTTTGTTCTACAGCCTTAATTATTTGTTTATATATATATATATATATATATATATATATATATATATATAT
Associated Phenotype:
Not determined