ZMP
mycn
Ensembl ID:
ZFIN ID:
Description:
N-myc protein [Source:UniProtKB/Swiss-Prot;Acc:Q9PSJ0]
Human Orthologue:
MYCN
Human Description:
v-myc myelocytomatosis viral related oncogene, neuroblastoma derived (avian) [Source:HGNC Symbol;Acc
Mouse Orthologues:
Mycn, Mycs
Mouse Descriptions:
myc-like oncogene, s-myc protein Gene [Source:MGI Symbol;Acc:MGI:1332242]
v-myc myelocytomatosis viral related oncogene, neuroblastoma derived (avian) Gene [Source:MGI Symbol
v-myc myelocytomatosis viral related oncogene, neuroblastoma derived (avian) Gene [Source:MGI Symbol
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa1804 | Missense | F2 line generated | Not yet available |
sa13838 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa1804
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:
T > G
Consequence:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000024104 | Missense | 150 | 497 | 2 | 3 |
ENSDART00000112277 | Missense | 140 | 486 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 20 (position 33334433)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 33392673 |
GRCz11 | 20 | 33295552 |
KASP Assay ID:
554-1796.1 (used for ordering genotyping assays)
KASP Sequence:
TTTTACCGGGAGACGACATTTGGGGGGCGTCGGACGGGGACCTCTTTGGC[T/G]CCGTTTTGGATACTACGGACAATTCCATCATCATTCAGGACTGCATGTGG
Long Flanking Sequence:
TAAAAGTTTATCTTATCAAGTTAAAGAACAGTGTCACACTGTGAGACGGCAGGTAAAAAAAAAAAACAGTGAGAGTCATTAATAACAAAAGATGCTGTGCTTGCCTTTTTGCTGGAGGGAAGCTTTCATTTTGCAAGCTTATTCTAACACATCAGTTTGTGTCTTTCACAGGGAGAATGCCAGCTAAAACCATGAGCTCAGATCTGGAGTTTGACTCCTTGCAGCCGTGTTTCTACCCGGACGAGGATGACTTCTACTTCTGCAGACCAGACGCCGCACCGCCTGGTGAGGACATCTGGAAGAAATTCGAGCTGCTGCCCACTCCTCCTCTGTCCCCGAGCCGGGCAGCGCTTCCAGGGGACCCGGGGGAGCTGGGCGCGGTGGCTGGGGATTGCTCGCTGATGGGCTTTGGATTAACCGACCCGTTGGACTGGGCTTCCGAGCTTCTGCTTTTACCGGGAGACGACATTTGGGGGGCGTCGGACGGGGACCTCTTTGGC[T/G]CCGTTTTGGATACTACGGACAATTCCATCATCATTCAGGACTGCATGTGGAGCGGCTTCTCGGCGCGAGAGAAACTGGAGCGGGTTGTGAATGAGAAACTCGGCAAAGTCGTTCCTACTCCAACCTGTACTGAAGCCGGTAAAGACACGACAGTCAAAGCGCCCGAAGTGAGCCACTCTATACCGGAGTGTGTGGACCCTACCGTGGTTTTCCCTTATCCAGTCAACAAAAGAAACGGGAGCAGCAGCAGCCAAAGTGTGACACAACTGAGGAGCCAACAATTGCCTCAAGTCAGTGCAGGCGAGACTCCGAGCGACTCTGGTAAGAATCTCCTGACAATTAAAATCATTCACTAATGTCAACGCTTTTCTCATTCTGTATTTACAACTTGGTTTATAATAATCAAATAGATTTAATATCTTATCATAGTCCCTTGTTTTAATAGCCTGATGTTGATGATGATGCTAAACAGTTTGGCATTTTATAGTTTGGCCTAGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13838
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000024104 | Nonsense | 340 | 497 | 3 | 3 |
ENSDART00000112277 | Nonsense | 329 | 486 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 20 (position 33336811)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 33395051 |
GRCz11 | 20 | 33297930 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGCTCCGCAGGAACTCATTTTAAAGAGGACAGCAGCAGCCTCCATCCAC[C/T]AGCAGCAACATAACTACGCAGCCCCATCCCCTTACTYCGAACAGCAAGAC
Long Flanking Sequence:
GAAAGTCAGATCTGAGGTGGTCCGGTCTGGGGAGAATCCAGCTCCTCTGTGTTTGACAGAGCATGTTCAGATGATTGCACAGAGCAATTGTCTCATCTTCCCACACAAAGACATTAACTTAAGCACACACCCAAAAAAAAAAAAAAAAACACAGGCATGCTTCCGTTTGGCGTGCTTGTACATACCTGTGCATCTCAAATGGTGCAGTTGCACCACAAGCCTTCTAAACTAAATCTTCTTTTCTTCTTCTAGATGATGATGATGAGGATGACGAAGATGAGGATGATGAGGAAGAAGATGATGAAGAAGAGGAAGACGATGAAGAAGAGGAAGAGATTGATGTCGTAACGGTGGAGAAGAGGCGTTCCATCACCAGCAGGACAACCAGCACTGGACTGTCTGCTGTCTCCAACTCTCAGGCAGGAGGGCGACTGGGCTCAGGGGTGAGCAAAGCTCCGCAGGAACTCATTTTAAAGAGGACAGCAGCAGCCTCCATCCAC[C/T]AGCAGCAACATAACTACGCAGCCCCATCCCCTTACTCCGAACAGCAAGACGTTCCCAGCGCTCCTCCAAGCAAGAAACTCAGAATCGACAGCAGCACTATAACTCTACGCACTGGCAGGAACCAGAGCTCTTCTCCAAACTCCCCTACCAACAGCGTACCAAGTCAGCGCTTGAGGAAGAGCGACTCCAGCAGCCCCAGATGCTCCGACTCGGAGGACAGCGAACGCAGACGCAACCACAACATCTTGGAGCGCCAGCGGCGCAATGACCTGCGGTCTAGCTTCCTCACTCTGCGGGATCAGGTGCCTGAGCTCGCACACAACGACAAGGCAGCAAAGGTGGTCATCCTAAAGAAGGCCACTGATTACGTCAGCTCCCTGGAGGCTCAGGAGTTCCGACTCCAGCAGGAGAAAGACAGATTGCAAGCCAAACGACAACAGCTCCTCCGCAGACTTGAGCAGGCCAGGACTCGCTAACCCTTTACGCTCATTGGCTGAATG
Associated Phenotype:
Not determined