ZMP
ENSDARG00000090335
Ensembl ID:
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa41074 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa15587 | Nonsense | Available for shipment | Available now |
sa17505 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa41074
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000122698 | Essential Splice Site | 52 | 584 | 1 | 10 |
Genomic Location (Zv9):
Chromosome 7 (position 69942044)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 67664713 |
GRCz11 | 7 | 67888065 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCTCAAGACGACACAACTCCAGCGAGACACAGACTGTCTTCACAAACAG[G/A]TAAACACACACACACTCACACACACACAAAAACACAGAGAGACAGAGCAA
Long Flanking Sequence:
TAGTTAAGGCCACTTAATATAAAGTAAGACCTAAAAAGTCTTACAACACACTGTAAGCGTCTAGGGCAAGGGTGGCCAACCCTGTTCCTGAAGAGCCACCTTCCTGCAGATTTCAGTTGTAACCCATATCAAACACACCTGGCTGTAATTATCACGTGGTGTTCAGGTCCTAATTAATTGGTTCAGGTGTGTTTGGTATGGGTAGCAACTGAAATCTGCAGGAAGGTGGCTCTCCAGGAACAGGGTTGGCCACCCCTGGTCTAGGGCCACATATATTGGTACTGGCTGTCAGATAGTAGTTGAGCAATATTTTCTGTCTGTGTTGTGTTTAGATAGCAGGGCAGATGCAGGAGGTCTGGTCCAGCAGAGAGAAGGCTGCGGCCCTGCAGAAAGAGTTGAGCAGACTTCAGGTGATCCTGAAACACAGAGAAGAGCTGATAGAAGAAAACAACCTCAAGACGACACAACTCCAGCGAGACACAGACTGTCTTCACAAACAG[G/A]TAAACACACACACACTCACACACACACAAAAACACAGAGAGACAGAGCAAACATACTAAAAATCACAAATTGGCCAGTCTGGGTATTGAGAGCTGAAAAATGTATGACGTAAGCATGAGTTTGGCGATGTTGTTGTGTGTGTGTTTTTGCTGAAGGGTGTTTGTGAGATCTCTCGTGTGTAATATTTCCTGTCTGCAGCATCCACAGACCTCACATAGGCATGGAATTCCAATTAACTCCTTTAATTAGGCCCTCCCTTGCTCATGGCAGCGTTCCTTCATTTATTTTAATCTTGTTTATTCACCTTGATTGTTTCGCCATATAGATTTTTTTTAATTAGGTTAGATTGATTAAATTGCATTGATTCTCTGTCCTTATTAAAATGAAACAGACCCCCCCCCCCAATCTACTCTCTCCAGACCACTGTTATTTTTCATAATTAGTGACTGTGCCTACAGCGTGACTTTAAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15587
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 |
---|---|---|---|---|---|
ENSDART00000122698 | Nonsense | 396 | 584 | 7 | 10 |
Genomic Location (Zv9):
Chromosome 7 (position 69915832)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 67638501 |
GRCz11 | 7 | 67861853 |
KASP Assay ID:
2259-9785.1 (used for ordering genotyping assays)
KASP Sequence:
AGAAAAGGCAGAAGGAGAAAGAGTGCGCCTCSCTCMAAACACAACTGCTT[C/T]AGYTCAGAGAACAACTGAAAGAGGCCAACACCACCTGCAGAGACACYGGT
Long Flanking Sequence:
TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTAGAAGAGATGCAGCGACTGCAGGAGCAGCTGAGGAAGCTCCAGGCAGACGCAGCAGATGAAGTCCACAGACAAGCACAAGTTGATTCTCTGGAGCAGAAGGTTGCCAATCTGGAAGGAGAACTGCAGGCTGCTCAAAGGCAGTGCGACCAGGTAAACAAGTACACACACACATAAACAGACACAGCGCAGATCAAAAAGGCTTTGCCTGTGGCTGACTCTTATAGACATTCTCTCTCAGGCTATCCAAAAGAGAGACGCCCTACTGAGACAGTCCGAGGCTGATCTTCTGCAGGCTCGGGACAAGATCCGAGGCAGGGCGGCGGAGGCTGAGAGGCAGGCGGCGGCTGCTCGAGGGCTGGAAGCTGATCTGCAGAGAGCCAAGAAAGAGAAAAGGCAGAAGGAGAAAGAGTGCGCCTCCCTCAAAACACAACTGCTT[C/T]AGCTCAGAGAACAACTGAAAGAGGCCAACACCACCTGCAGAGACACCGGTAACACACACTGGCAAACAAATGCTGGCTTCCACACAATCGATTTGTATACTGGCACAACATGAAGGAATTAGGTTGACTTAGTAGTTTTTACTAATTTAAGTTGATTGATTATAACACTATATAACCCCAAATACAGTTTTTCTCAGTCGCTTTGGTGCTTTTCTCACAACACTAGTGCATTTCTCAAAACAATTAGTGCATTTCTCAAAACAATTAGTACAAATTGCAAAACCTAGCTGATAACCTGCAAAAGTGCATCACATGCTTAAAATGAATAGTTCATTCCTTACAAGCAAGTATTCATGTCAATCAAAGTGTCAGTATTATCAAAATGAAAAGTCCTGACACCATTTTTTATGAACAAGATAGTCAAATGGCTTTGTCATGTTTTCATTATGACAGTTTACTCTGGACATTATTTCAATGCAAAAAAGTCAGATATTGGTGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17505
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 |
---|---|---|---|---|---|
ENSDART00000122698 | Nonsense | 458 | 584 | 8 | 10 |
Genomic Location (Zv9):
Chromosome 7 (position 69912522)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 67635191 |
GRCz11 | 7 | 67858543 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGAGCTGCTGGAGGCTGAAAAAGCCCACAGAAAACTCCAGGCTGAGCTC[A/T]AGAGAACCACAGACRGTCTGGAAAACACCCAGCTGGAGCTGCAGGACTCA
Long Flanking Sequence:
GCGTGCACCTGTTTGTGTTCTCCTGCAGTCTGAGTGTCCCGTCTGAAATGAAACAGCCCATCAATTCAGAGCCTCAAGCCATCAGATACACACTCTACTGTGGGAATGATGCTCATTAAAAACTACATCCTCATCCCAGATGAACAGGGGCAGATGTAGCCATAGTAAACCATGCAATGGGATTAGTGTGTTTTTTTAATATAGGCTTTATCATCAATAACAAAAAAAGAAAAACATGAAATTCTAAATGTTGCCGTCAATTTTATTTCTTTTATATTCAGCAAAAAAAAACTAAAATGCATGAGTTTTCCCATTCAGAACTTTCTGGAAGTGTATTGTTCAGGGATGGTCTGTGTGTTTCAGGCCAGGAGCTGATGCGGCAGCAGGAGAAGCTGCAGCTATTGGAGGGAGGTCAGCGTCTGACTCAGGATCAGCTCTCAGAGCGGGTGGCAGAGCTGCTGGAGGCTGAAAAAGCCCACAGAAAACTCCAGGCTGAGCTC[A/T]AGAGAACCACAGACAGTCTGGAAAACACCCAGCTGGAGCTGCAGGACTCACGGTAAACTCACAACCAGGAGGCAAGCTGCCCAGCTACCAAAATATTCTTACAACATTTCATAACGTTTTATAAATGTTTGCGTATAACATTACTGAAATAATATTATGGGAACATTCTCGTAAAGTTGATAGGACGTTTTTTTAGATGTTAGTATGAATATGTTAGTCTTAAGGATATCTTTAAGCGCCAAAACATGGACAGGGTAACAGGGACGATGAGATATAAACATCCAAAGCTTGCAGTTTTCCACTTTTGCCTAAATTAATCAAATTTATTTTCACGTGGGGCGTCACGGTGGCGCTGTGAGTTGCTCAATCACCTCACAGCAAGAAGTTTGCTAGTTCGAGCTTCAGCTGGGTCAGTTGGCATTTCTGTGTGGAGTTTGCATGTTCTCCCCATGTTGGTGTGGGTTTCCTCCGGGTGCTCCGGTTTCCCCCACAAGGCCAAA
Associated Phenotype:
Not determined