ZMP
ENSDARG00000058556
Ensembl ID:
Human Orthologues:
MUC5AC, MUC6
Human Descriptions:
mucin 5AC, oligomeric mucus/gel-forming [Source:HGNC Symbol;Acc:7515]
mucin 6, oligomeric mucus/gel-forming [Source:HGNC Symbol;Acc:7517]
mucin 6, oligomeric mucus/gel-forming [Source:HGNC Symbol;Acc:7517]
Mouse Orthologues:
Muc5ac, Muc5b, Muc6
Mouse Descriptions:
mucin 5, subtype B, tracheobronchial Gene [Source:MGI Symbol;Acc:MGI:1921430]
mucin 5, subtypes A and C, tracheobronchial/gastric Gene [Source:MGI Symbol;Acc:MGI:104697]
mucin 6, gastric Gene [Source:MGI Symbol;Acc:MGI:2663233]
mucin 5, subtypes A and C, tracheobronchial/gastric Gene [Source:MGI Symbol;Acc:MGI:104697]
mucin 6, gastric Gene [Source:MGI Symbol;Acc:MGI:2663233]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa927 | Nonsense | Available for shipment | Available now |
sa38012 | Nonsense | Available for shipment | Available now |
sa24614 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa927
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 |
---|---|---|---|---|---|
ENSDART00000081428 | Nonsense | 231 | 1989 | 5 | 45 |
Genomic Location (Zv9):
Chromosome 25 (position 8624003)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 8338908 |
GRCz11 | 25 | 8415976 |
KASP Assay ID:
554-0832.1 (used for ordering genotyping assays)
KASP Sequence:
AATGTTACGGCAGCCATGACTGTCTGTGCAACACGCTAACAGAGATCTCA[C/T]GACAATGCACACATGCTGGAGGACAACCAGGAACATGGAGGACAGAACAG
Long Flanking Sequence:
AGTTTTCTAAGTACATTTTTGGGTACCTTTCAAGGCTTCCTAAATCCCTTTAATAAATTTGAAGCAATGGGTTTACTTACTTATTTAAGTACAGTCAACTAATTCAAAACAATGGCTTTATTCACTTATGTAAGTAAATTCGACTAAACTGTGATGTTTTACCAACTAAATCCTCAGGTCCAGCCACATGGAAGATCTCAACACCAACTGAATCCTGTGAAGACGTTATACTTCCACCCAAGGATCAGTGTGACCAGGTATTAGCCAAAATCGTGAGCATTTTAAAATGGAAATTTTGATGCTCGCAATTGAACGTTTGACCAATTTTCCATTTTTTTTTTCAGAACACAATGGTTTGCCAGCAGTACCTCAGCAGTCCAGGGTTTAGTGGCTGTTATGATGTGATGGACATGAAAATATTTGAAAAAGCCTGTGTGAGCGACATGTGCCAATGTTACGGCAGCCATGACTGTCTGTGCAACACGCTAACAGAGATCTCA[C/T]GACAATGCACACATGCTGGAGGACAACCAGGAACATGGAGGACAGAACAGCTCTGCCGTGAGTATCACTTCTAAAAAATAATGAAAAAGAAGGCATAAAATTTCATGTTTACATCGATTATAATCCTTACCCATTAAAACTATACTAGCATGACTTATTATCTGGTCATTTTAACACATTTAATACAAGACTAATTGTCTTATTTTGTGGAGCAGCAAAGATGTGTCCTATAAACCTGCAATACATGGAGTGTGGAGGTCCGTGTAAGAGCACTTGCTCTGATCCAACTGCACATCTAATGTGTAAAGATCACTGTGTGGATGGCTGCTTCTGCCCTGAAGGTAATTTTATGCAATATCAAGTGACTTTTTGTGCTTGTGAATAAAATATTATTAACTAAATTGCACCATCTGTTCTTTTTGTAAAGGGACCGTTGAAGACGACATTGGTCAGGGTGGTTGTGTTCCTGTAAACGAGTGTCCATGTGTGCATGATGGCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38012
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 |
---|---|---|---|---|---|
ENSDART00000081428 | Nonsense | 636 | 1989 | 14 | 45 |
Genomic Location (Zv9):
Chromosome 25 (position 8626427)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 8341332 |
GRCz11 | 25 | 8418400 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGCTGTGGCCTCACCTGCCGTTCTCTCAGTGGACAAGAAAACACCTGC[C/T]AAGGGTCCTTCACGCCTGTAGATGGCTGTGTTTGTTCTGAGGGAACCTAC
Long Flanking Sequence:
AAACTTGCTAAAGACTGGTGTTCCCGTCTGACTAACCAAAGTGGAGCCTTTTCTGCATGTCATTCAGAAATATGCCCAAAGATTTACTATGAAGTGAGTTCTTTTGTATATTTCCTTTTGAAATGAACTATATACAGTATTTATAGCAGACGCATTATCATTTTGTCACATCTGGGATTCATTGTCTGCAGAGGTGCGTCTATGACACCTGCAAGTGTGCAGATATCAGGAAGTGCATCTGTGCGGCTGTGTCCACTTATGCCCATGCTTGTGCTGCAAGAGGAATCATTCTCCAAGGCTGGATGGATTCAGACCCTTGTGGTATTATCTATATTATCTATTTGAATAACGTTCTGTTGATTTGGGGAAAAATAAACAATTCGTAATAAGTGTTCATTCTATGCATAGAATCTGAGTGTTCAGAGAACATGAAGCACTCCTACGGTATGACTGGCTGTGGCCTCACCTGCCGTTCTCTCAGTGGACAAGAAAACACCTGC[C/T]AAGGGTCCTTCACGCCTGTAGATGGCTGTGTTTGTTCTGAGGGAACCTACCTTAATGAAGAAGGCATCTGTGTGCCTGCTGACCAGTGTCCTTGTTACAGCGGTGACCAGGTCACAAAACCTTCGGAAGTATCCCACGTAGATGGTCTAACATGGTAAGTTCCTCAATTAACATCCAATGCATTGACGATAGTTTCCCAGAGATGGGTTGTGGCTGTAAGGGCATCCGCTGCGTAAAAAACTTGCTGGATAAGTTGGCGGTTCATTCCGCTGTGGCGACCCCGGATTAATAAAGGGACTAAGCTGACAAGAGAATGAATGAATGAATGCATTGACGATAGAATACCAATGCAACCATTAGTAACTCCTGATTTGCACAATTTTACAGCACCTGTAAACTTGGCAAACTGCACTGCTCCAATCCTGAAAGTAAGTTTCAACGTTTTTTATTCTGCAATTCCACCAGTCAAATTCCGACTTTAATCATCACTTGTGCAATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24614
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081428 | Essential Splice Site | 1879 | 1989 | 41 | 45 |
Genomic Location (Zv9):
Chromosome 25 (position 8649229)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 8364134 |
GRCz11 | 25 | 8441202 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAAGATCAAACCTAAATGCCCTGACTTTAATCCTGATGACTGTGAGGCT[G/T]TAAGTAGTGGTTGATAAGATATTACCATTAATCAAATTTCCACTTTGTTT
Long Flanking Sequence:
TTGCTCTGAGGTAATCATTTCAACTGATGTTAGTGATTAAAATACATTGGGAAAGATTTATATTCTGAATTCCAACAGTAATTTTTGAGTTCTGAAGCATACACATCATAAGCTCCTACATTCAATGTTTCCAAATGATTGAGTAAAATTTGATTGAATCTTTTTTGTGCTCCAAGGGCTTTGAGCTTGTGGAACAAGAAGGAGAGTGTTGTGGAACGTGCAAGCAGAAGTCCTGTATTTATACAGCGCCAGATAACACCACTCACACTCTTCAGGTACAAACCTTTCTTCATTTGTCTACGCATTTATTCAAACAAACCTTCTTTATTTGTTCTGCAGTACTTATTTCAGCCTATATCTCCCTTTAATTCTTTTAGCCTGGAGAGGTCAAAAGTCATCACAAATGTGAGACTCTTACCTGTCGTGAAATTGATGGTGTGTTTGTGACAGAGAAGATCAAACCTAAATGCCCTGACTTTAATCCTGATGACTGTGAGGCT[G/T]TAAGTAGTGGTTGATAAGATATTACCATTAATCAAATTTCCACTTTGTTTGCTGTTATATGTACTCTTCATGAATATGTATTAACTCAAGTTCTCAAAGAATATAGTCAAATTTCACTCAACCCAATTCTTAAGTAATCTTTATACAATTAAGTGAAGTTTATTTATAAACTAATTTCGAGAGGATCACGTTTGCTTGCAGCCGGTCCCGCATTATACAATTTCTGATTCGCCGATCAGACGATTCCTAAGCCACTATAAATACCCTAAGTTCCATATAATAGCCATATTCTAGGGATGTAACGGTATCAGAATTTCACGGTACGATAATACCTCGGTATGAATGGCACGGTACGGTATTTATTGAATAATTTACAGGAAAAAACAAAACTAATGAAAAGACTCGAAAAAAGTGCCAAAAGTGTTTATTTACCTTAGCACTGAACATATCAATGACATACAAATCAGCCATCTATCTGTAAGTTTCAAAACAGGAACTTC
Associated Phenotype:
Not determined