ZMP
wu:fb77e12
Ensembl ID:
ZFIN IDs:
Human Orthologue:
NCKAP5L
Human Description:
NCK-associated protein 5-like [Source:HGNC Symbol;Acc:29321]
Mouse Orthologue:
Nckap5l
Mouse Description:
NCK-associated protein 5-like Gene [Source:MGI Symbol;Acc:MGI:3609653]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa31089 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa43983 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa24336 | Nonsense | Available for shipment | Available now |
sa30740 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa31089
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109062 | Essential Splice Site | 25 | 1275 | 2 | 15 |
ENSDART00000110841 | Essential Splice Site | 11 | 1234 | 2 | 19 |
ENSDART00000134978 | Essential Splice Site | 41 | 1480 | 3 | 12 |
Genomic Location (Zv9):
Chromosome 23 (position 24939095)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 24725215 |
GRCz11 | 23 | 24651756 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTTACTTTTCTTCCTTGACTTGCTGTTTAAACTGGACTATTTTTGTAT[A/C]GGCAGAGAACTCTGCCCTTTCATTAGCAAACGAGAGTCAGAGAGAAGCAT
Long Flanking Sequence:
CAAGTTTTGTTATAGTCTCCCAATAGTTGGTTATATACATTATGTAGTAACTTGCTGTTTCAGGCTGTTTAAACACAAGGATCAGTGTTTTATGAGTTTTCACATTTGACTTATAGTTTTCTCTTTATGTTGGGACAGAATCATCTGTATTGAAGACAAGAACATTTGCCACTAATAATCAAAATAGTTTTATTTATAATATTTACCGCACTTTCCTTTCAGTATGGGGTGGGGGAACTATAAAAGAATGCCACACTAAAAATTCTAATCTCTTTGTTCTTGTTAGGTTGAGACAATGTCGGAAGAGGCTCAAAATAGAGTAGATGAGGACTTTGAGTCTGAGGAGGGTGATTTGGAGTCCTATCTAGAGGAAGAGAGTAGCAGTGAGCTTCTGGAGCGAGTGAGAGAACTTCAAGTAAGTGCCATATACTTTCACCAAGAATGCAGTTTTGTTTACTTTTCTTCCTTGACTTGCTGTTTAAACTGGACTATTTTTGTAT[A/C]GGCAGAGAACTCTGCCCTTTCATTAGCAAACGAGAGTCAGAGAGAAGCATATGAACGATGCTTGGATGAGGTGAGTTGAATGTTGTTCCTTACCAATCTATGCATTTGACTTTTTTAGATATCGGATCGTTTTTCCTAATGCAGACAGTCAATTAGTCAGATAAATAAATAAAATATCCCTGAAAGTACACAATGTTAACATCATGTCTTTGATGTAGGTGGCCAACCATGTTGTCCAGGCTTTACTCAATCAAAAGGTACAAAAATTGTGTTTTTTCTTCAGCAACATGTTTGTAAGGTTTATTTAAACGGCAAAGATAAAAGGTTCTTTTTTATTTAATATGTTTATTAATTTATTATTATTTGTTATAAATAATCGATAATGATGATTTTTTTTTAAATTTGTGGTTGTATATTTTATAACTGCCATGCATATTTTAGCCATATGTTTTTCAGATGATTTATTTAATATTATGAATTATTCTTTTAGGATCTCAGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43983
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109062 | Essential Splice Site | 61 | 1275 | 4 | 15 |
ENSDART00000110841 | Essential Splice Site | 47 | 1234 | 4 | 19 |
ENSDART00000134978 | Essential Splice Site | 77 | 1480 | 5 | 12 |
Genomic Location (Zv9):
Chromosome 23 (position 24939584)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 24725704 |
GRCz11 | 23 | 24652245 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGCCATATGTTTTTCAGATGATTTATTTAATATTATGAATTATTCTTTT[A/G]GGATCTCAGAGAGGAATGCATCAAACTGAAAATGCGTGTTTTTGATTTGG
Long Flanking Sequence:
TATTTTTGTATAGGCAGAGAACTCTGCCCTTTCATTAGCAAACGAGAGTCAGAGAGAAGCATATGAACGATGCTTGGATGAGGTGAGTTGAATGTTGTTCCTTACCAATCTATGCATTTGACTTTTTTAGATATCGGATCGTTTTTCCTAATGCAGACAGTCAATTAGTCAGATAAATAAATAAAATATCCCTGAAAGTACACAATGTTAACATCATGTCTTTGATGTAGGTGGCCAACCATGTTGTCCAGGCTTTACTCAATCAAAAGGTACAAAAATTGTGTTTTTTCTTCAGCAACATGTTTGTAAGGTTTATTTAAACGGCAAAGATAAAAGGTTCTTTTTTATTTAATATGTTTATTAATTTATTATTATTTGTTATAAATAATCGATAATGATGATTTTTTTTTAAATTTGTGGTTGTATATTTTATAACTGCCATGCATATTTTAGCCATATGTTTTTCAGATGATTTATTTAATATTATGAATTATTCTTTT[A/G]GGATCTCAGAGAGGAATGCATCAAACTGAAAATGCGTGTTTTTGATTTGGAGAGGCAGAACAGAACACTGTGTGAGCTTCTGCAGGAGAAACTGCACAGTCAGTCTTGTGTACATCAGCAGGTAAATGATTAAAACTTGCAATGGAAAATGCACAGTGCATGCCTTCTAAGTTGATGTTTTTCACAAAACATTCTTCAAACTCCACTGGGATGACCTATTAGGTTTGTTTGCAAATTGGAGAAAATGGCTCAATTAACGTCTTCCTGTTTAATTTCCCTGTGCTCCTCAGGCAGCATTTTTTTTCCCTGTAATTACAAGAAATTTGTTTGTAAATGGGCAAATACCCTTGTTTTACATGCATTCCTGTGATACCCTTGTTGTGCATGAATACTTGGGATGTTCTGCATAATCCAATAATTGATTCATATAATAAGAAGCTTAAGGCTTACCTGATGTTTCTTATCAAAGCAGCCAGGACCCTGTCTGGAGCACATTGGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24336
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109062 | Nonsense | 226 | 1275 | 6 | 15 |
ENSDART00000110841 | None | None | 1234 | None | 19 |
ENSDART00000134978 | Nonsense | 236 | 1480 | 7 | 12 |
Genomic Location (Zv9):
Chromosome 23 (position 24940493)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 24726613 |
GRCz11 | 23 | 24653154 |
KASP Assay ID:
2261-7770.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACAATACATCCAGGTGCAATGCACCCAAAGCACATTGTTCCCATTCCTG[T/A]CCAGATGTTTGCACACATCAGCATTTGAATGGAGGAGAGCACAGCAATGT
Long Flanking Sequence:
AATCCAATAATTGATTCATATAATAAGAAGCTTAAGGCTTACCTGATGTTTCTTATCAAAGCAGCCAGGACCCTGTCTGGAGCACATTGGTGAGCTACAGCAGAGTGAATCTACCAAACTGATTGAGGCTCAAAGGAATGCACAGGCCAAGGTAGGAGCCATACACAAAATCTTTGTTGAATCAATCTGAGATGACAAATTCCTTATTCTTAGGATTTGTTTTCACAGGGTAACAGCGAATGTGCACAAAATTCCGTACCCGAGACTCAAGGCTCGTCCACATCCATGGAGGCCATGTCCCCATTCTTGAAGAAGAAAGCACACATTTTGGAGGTTCTCCGCAAACTTGAAGAAACAGATCCACTTCGGTACCATCGTTCCTCTGGCATTCCCTCCATCTGTGACTACAGTCAGGCTCTTGCCTCTAAGGAGGCTGTATTAGCCTGCAGAGACAATACATCCAGGTGCAATGCACCCAAAGCACATTGTTCCCATTCCTG[T/A]CCAGATGTTTGCACACATCAGCATTTGAATGGAGGAGAGCACAGCAATGTAAAGTGTGGTAGTTGTAGCACATGTTTGATGCTGTCCAATAAAGATTCCGTCAGCTTAGCCAAGAGTAGCCACAACTGTTGCACTTCAACCCCCATTACCATTGATAACCTCAATTTGGCTCGGCCCGATTTCCAAGAGAATGTGGAAATGCAGAGCCTTGTGAAACCTGCCACAGGTACAAGTGAACTGTTTGTAAACAGGACTTCTGGAGATATGTCGATTCTTTCAGCAGAGCAAGGTCTTATACCGTCAGTTGATCCTCACTCATTAGAAGCCCCTGAATCATACTCAAGATTGACTATTTCAGAAAGAGATCAGCCAAGGGGAGTCTCTGACCATGTGTTGGTAGATACAAGAGAAAAGAATAGGTTGTCTGATCTTCTCCTTGAGTGTCAATCCAACAGGTCAAGCAGCAGCACCTGTAATGAGACTATTTGTGACGATGGCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30740
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109062 | Nonsense | 1032 | 1275 | 10 | 15 |
ENSDART00000110841 | Nonsense | 982 | 1234 | 13 | 19 |
ENSDART00000134978 | Nonsense | 1215 | 1480 | 8 | 12 |
Genomic Location (Zv9):
Chromosome 23 (position 24943872)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 24729992 |
GRCz11 | 23 | 24656533 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATCCAGACCTGTTTTTAGTCACCAGAGTGCTGCCATTGCTAGTCAGACA[C/T]GAAGCAGTGATGACATGGAAAAGGTAAGTTCAATTCTTTATTGTAGTACG
Long Flanking Sequence:
CTTTTTTATTTTTTTTGCATTAGTCAGAAAAGCAACCCACAAATTAAAGGCCAAATTAGTTCATTCATAGTTGTAGTTCAGGTTTGTAAGTGATGAAAGGTATTTGAAATAACTTCTGAGTGAGTAAGGTGAGAAAATATGCTTCGAGACATAATTTGTATATGATTTGTAAGTCATCTGTTTGAGTTACTGGGAATTTGCGTCATTGTAAAGGCTGGGCTTTTTGGATTGGCTTAATAAATTTAAATGCATGAATTTGATTACAACCAAAATGTAAAATTTACTTTTATTTAAAAGTTTCTTTTTAAATTTTTTAATTTTTTTTTTTTTTACCAAACAACAACTAAGGGTGTATTGACATTCATTTTTTTTTTACTTTTTCCACAAGGGTTGATGGGAAGGATACTAGTGGCATCAGTATGGCACATAGACGTCTCTCATTTGACTGTAAATCCAGACCTGTTTTTAGTCACCAGAGTGCTGCCATTGCTAGTCAGACA[C/T]GAAGCAGTGATGACATGGAAAAGGTAAGTTCAATTCTTTATTGTAGTACGTGTTGTTTTTGCACTTGGCAATACTTTTAATGTTACCTCGGCTATTTTTTTCACAGGTCTCTGCATTACTAAGTAAAGACGTCACGTCGGACGACAACCTGGCTGAGACAATTCATCATGAACACTTTGCAGGTCAGGCACTAGTACAATGCATGACATCATGGCTTTCAGTGTTCCCAGAGGCAGGAATTTTGACCGATTAGCATGTAGCAGCAAAAACGGGTTTTAACCTGTCATTGATGATGAGTAATCTAGGTGCGTCTGAATTTTCTCTGGCTTCCATATGCAAGTAATCCGGTAACATCTGTGTAGCACACATTTTATTGCTTATATACTTAGAGTGTGATGGTTTGTTACCTGGTTACATTGCCTTATAAATAAACATTTTTAATACATTTTTAGTTATATATTTTATATATAAATGCAGTTATATAATAATCAGAGGTGGAA
Associated Phenotype:
Not determined