ZMP
ENSDARG00000075951
Ensembl ID:
Human Orthologues:
MUC17, MUC5B
Human Descriptions:
mucin 17, cell surface associated [Source:HGNC Symbol;Acc:16800]
mucin 5B, oligomeric mucus/gel-forming [Source:HGNC Symbol;Acc:7516]
mucin 5B, oligomeric mucus/gel-forming [Source:HGNC Symbol;Acc:7516]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa6599 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa39654 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa32725 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa6599
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 |
---|---|---|---|---|---|
ENSDART00000114414 | Nonsense | 3172 | 4056 | 34 | 35 |
Genomic Location (Zv9):
Chromosome 1 (position 41083064)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 39969843 |
GRCz11 | 1 | 40687916 |
KASP Assay ID:
554-4964.1 (used for ordering genotyping assays)
KASP Sequence:
AGAAACATCAACAACTGTAGATGTGAACCTCACAACCACTCTTATACCMT[C/A]AGAAACTACAACAACAACACTATCTTCAACATCTGAAACTGCAGAAACCA
Long Flanking Sequence:
AAATGCAAATAAAAAGAAGAGTCTAAATGACATTTTAGGAGGTTAAACGAAAATTATGAAATATGTTTGTTATTTCTTGACAGTATATGTATGGTGTACCCTATGTGGAGCTTCATCTTTAACTACTGATGCACCAACCACACAGATTTTACAAACAGCCAATGATGTTTGTACAATAAAAACTAAAGGATCTATTGGCACACCTATGACCACTAAACAAAATCCCAAATGTACAGCTGTGACTTTCACACCTACACTTCCTACAACAGGTCCAAATTCAATGTCTACAATGTTACCTTTGATTACAACAGAATCTGTAATTATAACAACAACAGATATGATTCCCACGTCTATACTCGGATCCTTATCAGCTACAACGGCACCTCCAACAGCGACAGATGCTGCTTCAACAACAAATCTTACTTCAACATTAACAGAATCTTTGACAACAGAAACATCAACAACTGTAGATGTGAACCTCACAACCACTCTTATACCAT[C/A]AGAAACTACAACAACAACACTATCTTCAACATCTGAAACTGCAGAAACCACAACTGTGACTCCCACAATCATTCTTATATCATCAGAAGCTACAACAGTCAGTGCTACTTCTACAACAACAACACCATCTTTACCAACTGAAACTTTAACAGACACAGTTGGATCTTCCACAAACGCTCCTATATCCTCAGAAGCTGCAACAACAGTTAGTGCTACTACAACAACAGCATCTTCAGCAACTGAAGCTTTCACAACATCATATGCGGAGCCTAATACAACACCTAAATTCCCAGAATCCACAACTGCACCTCAAGCCACAGAGAGTACTAGTGCCACAATCCCACCTTCAACAACTGAAACTTTAACACCTACAGCTGTATCTTCCACAGTCACTTTTATAACCACAGAAACTACATTAACAGATGCTACTTCAGCAACTACACTATCTTCCACATCTGAAACTGCAGAAACCACATTTGTGACTCCCACAACCACTCTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39654
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 |
---|---|---|---|---|---|
ENSDART00000114414 | Nonsense | 3712 | 4056 | 34 | 35 |
Genomic Location (Zv9):
Chromosome 1 (position 41081444)
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCCACAGAAAGTGCTGGTGCCACAATCCCATCTTCAACAACTGAAACTT[C/A]AACATCTACAGTTGTATCTTCCCACAGTCACTTTTATACCCACAGAAACT
Long Flanking Sequence:
TACATTCCCAGAATCCACAACTGCACCTCAAGTCACAGAAAGTGCTGGTGCCACAGTCCCATCTTCAACAACTGAAGCATCAACATCTACAGTTGTATCTTCCACAGTCACTTTTATACCCACAGAAACTACATCAACAGATGCTACTCCAGCAACAGCACTGTCTTCAACATCTGAAACTTCAGAAACCACATTTGTAACATCCACAACCACTCTCATATCCTCAGAAGCTTCAACAGTCAGTGCTACTTCTACAACAACACCATCTTCAACAACTGAAACTTCAACAGACACAGTTGTATCTTCCACAACCGCTCCTATATCCTCAGAAGCCACAACAACAGTTAGTGCTACTACAACAACAGCATCTTCAGCAACTGAAGCTTTCACAACATCATATGTGGAGCCTAATACCACAGCTTTATTCTCAGGATCCACAACTGCAACTCAAGCCACAGAAAGTGCTGGTGCCACAATCCCATCTTCAACAACTGAAACTT[C/A]AACATCTACAGTTGTATCTTCCCACAGTCACTTTTATACCCACAGAAACTACATCAACAGATGCTACTCCAGCAACAGCACTGTCTTCAACATCTGAAACTGCAGAAACCACATTTGTGACACCCACAACCACTCTCATATCCTCTGAAGCTACAACAGTCAGTGCTACTTCTACAACAACACCATCTTCAACAACTGAAACTTCAACAGAAGCAGTTGTATCTTCCACAACCGCTCCTATATCCTCAGAAGCTACAACAACAGTTAGTGCTACTACAACAACAGAATCTTCAGCAACTGAAGCTTTCACAACATCATATGTGGAGCCTAATACCACACCTTTATTCTCAGGATCCACAACTGCACCTCAAGCCACAGAAAGTGCTGGTGCCACAATACTACCTTCAACAACTGAAACTTCAGTGGCCGCTGTTGTGACTCCTGTAACCACTCATATATCCTCAGAAACTACAACAATAAATGTTACTCCAACAACAGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32725
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 |
---|---|---|---|---|---|
ENSDART00000114414 | Nonsense | 4043 | 4056 | 35 | 35 |
Genomic Location (Zv9):
Chromosome 1 (position 41080436)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 39973097 |
GRCz11 | 1 | 40691170 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGCAGCCACATCTTTGCAAAATGAAACTACAAATGCAGTGACTTCAATT[C/T]AAATTACAGACACTCAAAAGCCAACAATGTCAATAACAAGCCCTGAACCG
Long Flanking Sequence:
CTACTGTGCCTTTCGAAACCACAGATGTAAACCCCAATACAATTCCTGCATCATTTACAGCTGCACCTCCAGCAACAGAAAATCCTGATAAAACAACTCCATTATCAACAACAAATGAGGTTTCAGTAACAACAGATGTAACTCCTACTTCCAAGTCTTCATCCTCAGAACCTGCACCTTCAACCTCCTCAAATGCTGCTCCTACTGCATCTTCCACCAGTGAAGGTTATAGCACAACATCTGTGACCTCCATCCCTACTCTAATACCATCTGAGATTACAGCAACAAATGAAGCTTCAATATATTCAACTTCACTAGTATCCTTAAACACAACAAATATGTATCCCACCAATACACCAGTTTACAAGACAACAACTAAAACTGGCACAGCAACAACATTTGTCACTCCTACAACTATGCCAATGTTCTCAGAAATTACGACATCCTTTCTAGCAGCCACATCTTTGCAAAATGAAACTACAAATGCAGTGACTTCAATT[C/T]AAATTACAGACACTCAAAAGCCAACAATGTCAATAACAAGCCCTGAACCGACGGTCATAATTGTTACACAAGAGACCACTATATCATTGCCAGTGTCAACAACTGATTCTACCCAAAGAACAAACCAAACAACAGCTGTGGTCACAAGCAGACTGTTATTCAACTCTTCATCTCCAGTCCCCAGTGAAGCTCAGGTCCTGAATGCTGTCAACGCTCTTCTCACATCCAGACAGTTGTGGCTTGATAAATCAGTGGAAATTGTCAATGTCACCTTCGAGGGTAAGTTTTATTAGCTTAATTACACATACTGTACATTAGAAAATGGTTAAGCTGAAATAATTGGATGTTTCTTTGCCAACAGAACTCTCAGACACCTCATATGCCATCATCTTTATATTTGATCTGACAAATATCAGCATTCCTGAAGACCCTGTACTCAAAAACAAGAGCTACAATCAAGTGGAAAGTAATGTCAATAATGCAGTAAGTAATTTATATTA
Associated Phenotype:
Not determined