ZMP
si:ch211-169k21.2
Ensembl ID:
ZFIN IDs:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:A2CEB9]
Human Orthologue:
NAV2
Human Description:
neuron navigator 2 [Source:HGNC Symbol;Acc:15997]
Mouse Orthologue:
Nav2
Mouse Description:
neuron navigator 2 Gene [Source:MGI Symbol;Acc:MGI:2183691]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa14333 | Nonsense | Available for shipment | Available now |
| sa14752 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa14333
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 |
|---|---|---|---|---|---|
| ENSDART00000073629 | Nonsense | 759 | 1110 | 8 | 12 |
| ENSDART00000131502 | None | None | 174 | None | 3 |
| ENSDART00000143666 | None | None | 518 | None | 6 |
The following transcripts of ENSDARG00000001879 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 25 (position 14809091)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 14452014 |
| GRCz11 | 25 | 14548414 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTGTCGATGAWGGATACCTTCCCCCAAGTGCTCGGACGACACTTCAGTA[T/A]CGGAGTTTACCAAGACCTAGCCGAACCRGTGCCACTCGCTGTTCAAATCG
Long Flanking Sequence:
AGTAGATTCCTGAGGCATAACAGGCAAAAGATCTCTATCTGCTCACACACAGAACTATAACACCTACATTATCTTGAGCTGTGTGCTCAGATAAGGCTTATTTTCAGACGAGTCTTGACACGGACCATGCATTTGTATTCAAAACCATCAAAATCATTCTGCTTGACAGTTCATGTCCTTTATCATCCCACAGGTAAGACAGATGACGCCAAGGTATCAGAAAAAGGACGCTCTAACAGCACCCACTCCATAACTGTAGACGACAGCAAGAAACCTCCTCTCAATTCCACCGCACGCACACCAACCAGCACTTTTGGCTTCAAGAAAGCCCCGGGAACAATGGCGACAATTACCGCGAGTGGTGCTGTGGTAACTAGTGGCTCCGCTACTGTGGGAAAGATACCTAAATCTGTCGGCTTCTCTGGGAGTCGAATTGGTTGTCGGCAGACAGCTGTCGATGATGGATACCTTCCCCCAAGTGCTCGGACGACACTTCAGTA[T/A]CGGAGTTTACCAAGACCTAGCCGAACCAGTGCCACTCGCTGTTCAAATCGCCCCAACATCTCAAACTTTGATTCAAATTTTTGTAACAAAAGCACTGCCACACTTCCCAACCCTAAGAGTCGCAACTTAGTCAAGTCCCCTGTGGGAGCTACTAACCAGACAGACCGGGAAAAGGGGATCTTTTCGGATGTGGATAACCAGGTACTTAAGACTAGTCAGTCGGGGATGCAAACTGGAAGGCAAACAGGAGGAAAGTATCCAGAAATGTCTTCACCAACTTTTCGTAGGTAAGTTGAAATATTCGCACAGCAGTTCTTGACTTTGTGAGTGAAAAAGCATAAGTTGTCATGTCTGTGTAAACACATGAAAATGAGTCTTTACAAACAATGGTCATGCACAGTACATGTTTGGGGTGGTGTAGGTTAAGCGCAATTGCAAACAAACACACAGCAATGGCGGAGTATATGGTGGTGTTACTGCTGTTACTCAAGTGTTTGCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14752
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:
G > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000073629 | Nonsense | 963 | 1110 | 9 | 12 |
| ENSDART00000131502 | None | None | 174 | None | 3 |
| ENSDART00000143666 | None | None | 518 | None | 6 |
The following transcripts of ENSDARG00000001879 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 25 (position 14803969)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 14446892 |
| GRCz11 | 25 | 14543292 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAAGCTCCAACCACACCAATAGTGACTCCATAGATGTTTGCTTGGGAAAA[G/T]AAGATTTRTGTCTTAATCGTGTCAACAGTGCCCGAACCGGCCTCTCAGAC
Long Flanking Sequence:
CAGGTCTGTGTCAGCAACAAACCAAGAGAAATCTTCTTCAACAGTTTCTTGAGTCAATAATAAAATGTGTTCATAACAATCATTTGTTTGCAGTTCCGTCATTGCAACCTGTAATATTACCACAGTCTGGTTTTCAATCTGTCTCATTGTTAAATCTCTCTACACACTTTGCATCCAGACTCTTTGGTGGTAAATCATGCAACAAGCAAGTGCCGGTCACCACCATGGAGAACATGAAGAACTCCACAGTCATCTCCAATCCCCATGCCACATCCACCCAACAGAATGGATCACTGGACTCAAAATCTGTCGCCAGCGGTCCAGATTATGGCGAAAATCTAACGGTGCCCTCTGGAGGTCATGGAGAACAGACCCTTTCCTCTGTAATCTCCAGTCCAGGATCAGCTTTCTCTCCTTGGGGAGGCAAGGCTGGATTGGATTTCCCTTCTCAAAGCTCCAACCACACCAATAGTGACTCCATAGATGTTTGCTTGGGAAAA[G/T]AAGATTTATGTCTTAATCGTGTCAACAGTGCCCGAACCGGCCTCTCAGACAGGTGAGATACTGGTTGTTTGTTTTAACTCAGCTGTTTATGACTTGTAAGTAGGGTTTACATCTGTACTCATGATCTGTCTTCCTCTCCTGTTACGCCTCTTTAATCATTTCTTTATCTCCTCTCCTTTCTTCTGTCTCTTTTTATCTGCTTCTTTTTTGTTTTGTCTGCCCTGTGCCCTCTTCTAGCCCTCACTCCTCTCCCTCTGCTAGCCCTAAATTTACCCACAACACTCTGCCGCGGAAGCAGGACAGGTAAAGCTATATTTGTGGTCAAATGATCAGTTGTGCTTTGTGAGTTTGTCTTGCACGTGTTCAACTGTGATCAGGGTTGCCAGTTGGAACCGATTTACAAAAGAATTTAAAAATTAGGAAATCTCTGTGTGGTTTATATATTTGGCTTGATTTCATTGTGTCCTACATGTTGCAGATGTTGTGTGAGCATTGATTTA
Associated Phenotype:
Not determined