ZMP
LOC100330214
Ensembl ID:
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17280 | Nonsense | Available for shipment | Available now |
sa7270 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa17280
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 |
---|---|---|---|---|---|
ENSDART00000144513 | Nonsense | 229 | 407 | 5 | 9 |
Genomic Location (Zv9):
Chromosome 4 (position 34191310)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 39986610 |
GRCz11 | 4 | 40528473 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTTCTCAAGCCTTCCTCCTCCACCATCTTTCCCAAACCTTTCTCCWCCA[C/T]AAACTTCCTCCAGCTTTTCTCCTTCATCTGCTGYTCTTCTACCATYTTTC
Long Flanking Sequence:
TCTTTTACTTTGATAATGCAGATTTGCTACAAATGTATCTGGGATGTTTGTGCTAATATTATGATTATATTGCATTTTTCTATACTGTTTTTATGTATTTATTTTTCAGGTTAAGAAATTGGAAATGCTGGGCTACAAGCCATTGTTGTTTATTTCAAAAGAAAAGAAAAAAGGATTCAACGCAGAGCTTATAACAACAATGGGTCCATTTGGAGAGGGACCACAGCAAAAAATTATAGATAAAATGACCAGCCTGTACGAAGTTTTTATTAAAAGTAAGAGTTGTGGTCATTTGATTACAAAATTCACAAAATTTCAAAGAAATCTCTAACTTTATTTTAAAATTGTTTATAGATTTCCAGAGGTTTCAGAATTTGGCTGCAACAGACCCTGATGTCTGCCAAAACCTACCATCATCCGTTTCTCCTCCAGCTTCTATTCCTCCATCATCTTTCTCAAGCCTTCCTCCTCCACCATCTTTCCCAAACCTTTCTCCTCCA[C/T]AAACTTCCTCCAGCTTTTCTCCTTCATCTGCTGTTCTTCTACCATCTTTCCCAAATCTTCCTCCTCCACAATCTTCATCCAGCTTTCCTCCTTCATCTGCTCCTCCATCTTTATCTTCCAACCTTATTCCTCCAACTAATTCCTCAAGCTTCAGTCCTCCTACCTCCTCTTACATTACCCCTCTTCCACCTGCCTCTTCATACAAAACACTTCTTGCTCCACCGCCTACTTCCCTCACTACTACACCTACTTCCTCTCTATCAAGTCCTGCAGTCCAGTGCATGACTACAGATTCCGGTGATTCAGGTGACTTTATTTTGAACTTTTACACAGCATTTTTCCCATTTTAGTTGGGACAAACAATTTATATAGAAATTTAAAATTAAAACATTAGTTGTGTAAATACAGTTGAATTCTGAATTATTTGCCCCCTTTAAATTTTTTTCTTTTTAAAGTATTTTTAACATCTTTAAATGATGTTTAAAAGAGCAAGGACATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7270
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000144513 | Nonsense | 296 | 407 | 5 | 9 |
Genomic Location (Zv9):
Chromosome 4 (position 34191107)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 39986407 |
GRCz11 | 4 | 40528270 |
KASP Assay ID:
554-4936.1 (used for ordering genotyping assays)
KASP Sequence:
AGTCCTCCTACCTCCTCTTACATYACCCCTCTTCCACCTGCCTCTTCATA[C/A]AAAACACTTCYTGCTCCACCGCCTACTTCCCTCACTACTACACCTACTTC
Long Flanking Sequence:
GTCCATTTGGAGAGGGACCACAGCAAAAAATTATAGATAAAATGACCAGCCTGTACGAAGTTTTTATTAAAAGTAAGAGTTGTGGTCATTTGATTACAAAATTCACAAAATTTCAAAGAAATCTCTAACTTTATTTTAAAATTGTTTATAGATTTCCAGAGGTTTCAGAATTTGGCTGCAACAGACCCTGATGTCTGCCAAAACCTACCATCATCCGTTTCTCCTCCAGCTTCTATTCCTCCATCATCTTTCTCAAGCCTTCCTCCTCCACCATCTTTCCCAAACCTTTCTCCTCCACAAACTTCCTCCAGCTTTTCTCCTTCATCTGCTGTTCTTCTACCATCTTTCCCAAATCTTCCTCCTCCACAATCTTCATCCAGCTTTCCTCCTTCATCTGCTCCTCCATCTTTATCTTCCAACCTTATTCCTCCAACTAATTCCTCAAGCTTCAGTCCTCCTACCTCCTCTTACATTACCCCTCTTCCACCTGCCTCTTCATA[C/A]AAAACACTTCTTGCTCCACCGCCTACTTCCCTCACTACTACACCTACTTCCTCTCTATCAAGTCCTGCAGTCCAGTGCATGACTACAGATTCCGGTGATTCAGGTGACTTTATTTTGAACTTTTACACAGCATTTTTCCCATTTTAGTTGGGACAAACAATTTATATAGAAATTTAAAATTAAAACATTAGTTGTGTAAATACAGTTGAATTCTGAATTATTTGCCCCCTTTAAATTTTTTTCTTTTTAAAGTATTTTTAACATCTTTAAATGATGTTTAAAAGAGCAAGGACATTTTGTTTTTTACAGTGTAAAGAGTAAGTGTTTTTTTTTTTTATCTGGAAAAAGTCTTATTTGTTTAATTTAGGCTAGAATAAAAGCAGTTTTTAATTTTTTAAAACCATTTTAGGGACAAAATTATTAGCCCCTTTAAGCTATATATTTTTTTCAACAGAACAAACCATCGTTAAAAATAACTTGCCTAATTATCCTAACCTGCC
Associated Phenotype:
Not determined