ZMP
LOC100148804
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 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24613 | Nonsense | Available for shipment | Available now |
sa15547 | Essential Splice Site | Available for shipment | Available now |
sa32517 | Nonsense | Available for shipment | Available now |
sa44236 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa8866 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa24613
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000073410 | Nonsense | 284 | 2870 | 8 | 47 |
Genomic Location (Zv9):
Chromosome 25 (position 8572249)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 8287154 |
GRCz11 | 25 | 8364222 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATGTGATGGACATGAGAATATTTCAGAAAGCCTGTGTGAGCGACCTGTG[T/A]CAATGTTATGGCAACCATGACTGTCTGTGCAACACACTAACAGAGATCTC
Long Flanking Sequence:
CAGAAACTGGGGAAAAAAATAAATAAGGGTGCTAATAATTCTGGGGGGGCTAATAATTCTGACTTCAACTGTATATATACTTGCATTTTCTATTATTTCTGTTTTACAAATAAAGTCTAGACCAACTAGACAACTAACTGGATATAACTCAAGAAATAACTCATAATAAAACAGCACAAGTCAACAAAAACAAACCACATCAGTTACGTCAACAACATGTCTTGCGCCTCTTGACACACTAAAAATCTAAATGCAGGTTTTTGCATTCGAATGTGTTTTCTTTTTTTTTTTTTTCAAATTAATTCTTCTAGGACCCTTCAAACTGTTAAACCTCACTGATTGAAGCATTGGTGGTGTTGAGACAGTCAGTCCTATAATAATCTATTTTGTTTCAACTAGGCAAGCTTTTGCGAGGAGTACCTCATCAGTCCAGGGTTTAGTGGCTGTTATGATGTGATGGACATGAGAATATTTCAGAAAGCCTGTGTGAGCGACCTGTG[T/A]CAATGTTATGGCAACCATGACTGTCTGTGCAACACACTAACAGAGATCTCACGACAATGCACACATGCTGGAGGACAACCAGGAACATGGAGAACAGAACAGCTCTGTCGTGAGTATCTTTTCTGGAAGATGACATTCATCAGAAGCCATTCAAATGATGTGCAATGTATTTATTGATTTCAGTGTACAAAGCCTAAATGAACAATAAAAAAACATTCATTATCTACCAATAATGATGCAGAGAAAAATAAATCTTAAGGGATATAATTTTACTATGCTGTTTTTTTTTTTTTTTTTCCCAGGAAACAATTTTAATAACAATTACATTAACAATTACTATTCCAGAAATTAATACTATGAATAAACAAAAATAAATAAAGCTTTTAAAGTAGACACAAAATATATGTTAGTTTTTAAAGGGATAGTGTAATTTACTGAAATTTTACTTACCCTCAAGTGGTTCCACAACATTTTTTGTTCAAGATATTTTAAAGAATGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15547
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000073410 | Essential Splice Site | 553 | 2870 | 14 | 47 |
Genomic Location (Zv9):
Chromosome 25 (position 8575405)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 8290310 |
GRCz11 | 25 | 8367378 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGCAGTTGTACATTGTAGCCAGCACTGAAGAGAAAGGAAAAATGACTGG[T/C]GAGWYTATAAAAGYCTTTGGGAAATGTGTATAGTTTTCTGAAAATGCATA
Long Flanking Sequence:
TGCCGTTGTGGGAAATCTGGCAAAGTGTGAAGCATCCCGAACAGACACCTGCTTACACTCAGTTACCCTTGTCATCTCTGGGACCACTGTAAGCGCTGGGTTTAATTAGTTATGCATAATTCTTGCTAATAACAATACTGACTACCACTAATTATTAAAATAATCGTATTAATAATATATTTTTGCTGATGTTTTACTTGTTAAACAGATTAGTTTTTCCTCCAGTGGAGATGTGACATTAAATAACATCAATTCAAAAGAGCTTCCTTTCAGCATTGGTGGGTCAAAAATAAAGGATTGTTTTTATAATTTTACAAAAGAAATGACATCAGAAATAAATATATAAATAAAATTATTATACCAGGTCCTGTGAGTATCTTCCAGCCCTCTTCATCCTTCATTATTGTTGATTTGACGAGCGTTCGTCTGGAGATTCAGCTGGCTCCAGTCATGCAGTTGTACATTGTAGCCAGCACTGAAGAGAAAGGAAAAATGACTGG[T/C]GAGTTTATAAAAGCCTTTGGGAAATGTGTATAGTTTTCTGAAAATGCATATAAACATTTTTAAAATAGTCAAAGAGCAGAAATAATCTAGTAAACTTTTAACCTTCCTTGTTTTAGGTCTTTGTGGGAACTATAATGATGTCCAAACAGATGATTTTAAAACTGAATCAGGCATTATCGAGGGCACCCCAACATCCTTTGTCAACTTTTGGAAACAAAACTGTCCAGATCTTGAAATCACATTTGACAACCCATGCAGCTTGAACATGGACACAGGTGCTTATTCCATTTCCGCTCAGAACATTCATATTGCACTTGATCATTCTTCCCGGGATTGATCCTGTTTCTTTGTTTTTTTGCCTCATAGAGAAACTTGCCAAAGACTGGTGCTCCCGCCTTACAAATCCAAATGGCACCTTTTCCGAGTGTCACTCAGAAATATGTCCTGAGATGTACTACCAAGTAAGTCATCCTGCAGAAATGTTTAGTTTCCTTTTAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32517
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000073410 | Nonsense | 601 | 2870 | 15 | 47 |
Genomic Location (Zv9):
Chromosome 25 (position 8575666)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 8290571 |
GRCz11 | 25 | 8367639 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAACAAAACTGTCCAGATCTTGAAATCACATTTGACAACCCATGCAGCT[T/A]GAACATGGACACAGGTGCTTATTCCATTTCCGCTCAGAACATTCATATTG
Long Flanking Sequence:
GCTTCCTTTCAGCATTGGTGGGTCAAAAATAAAGGATTGTTTTTATAATTTTACAAAAGAAATGACATCAGAAATAAATATATAAATAAAATTATTATACCAGGTCCTGTGAGTATCTTCCAGCCCTCTTCATCCTTCATTATTGTTGATTTGACGAGCGTTCGTCTGGAGATTCAGCTGGCTCCAGTCATGCAGTTGTACATTGTAGCCAGCACTGAAGAGAAAGGAAAAATGACTGGTGAGTTTATAAAAGCCTTTGGGAAATGTGTATAGTTTTCTGAAAATGCATATAAACATTTTTAAAATAGTCAAAGAGCAGAAATAATCTAGTAAACTTTTAACCTTCCTTGTTTTAGGTCTTTGTGGGAACTATAATGATGTCCAAACAGATGATTTTAAAACTGAATCAGGCATTATCGAGGGCACCCCAACATCCTTTGTCAACTTTTGGAAACAAAACTGTCCAGATCTTGAAATCACATTTGACAACCCATGCAGCT[T/A]GAACATGGACACAGGTGCTTATTCCATTTCCGCTCAGAACATTCATATTGCACTTGATCATTCTTCCCGGGATTGATCCTGTTTCTTTGTTTTTTTGCCTCATAGAGAAACTTGCCAAAGACTGGTGCTCCCGCCTTACAAATCCAAATGGCACCTTTTCCGAGTGTCACTCAGAAATATGTCCTGAGATGTACTACCAAGTAAGTCATCCTGCAGAAATGTTTAGTTTCCTTTTAAATTTACTTTGCGGTTGTGTTCACTGGCCACCATAAAATCAAATAATAATAGAAAATTGTCCTAGAAAAAGTATAAATTTTTTTTTCGTTAATGTGCCCTTCCTAATCTTCAATCAAAACAAATTCTCCTCCTTTTCATGCAACATCGTCTCTTTCTCTGATGATTTGTTTTTAAGTGAAGTTTGTTTATAAACTCATTTTGAGAGGATCACATGCTTATGATTGATCACAGCTGGTCCTGCATTACCCAATTTATTATTCACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44236
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 |
---|---|---|---|---|---|
ENSDART00000073410 | Nonsense | 1801 | 2870 | 29 | 47 |
Genomic Location (Zv9):
Chromosome 25 (position 8591578)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 8306483 |
GRCz11 | 25 | 8383551 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACAACTGCATCCACTACTTCACCAACTACTGAAACATCAACGCCTACTT[C/A]AACAGAGACACCATCCACAATCACATCCACTATTACACCAACTACTGGAA
Long Flanking Sequence:
CACTATTACACCAACTACTGGAACTTCAACACCAACTTCTACAGAAACACCAATCACAACAACATCCATTACTTCACCAACGACTGAAACATCGACACCAACTTCTACAGAAACACCATCCACAACAGCATCCACTACTTCACCAACTACTGAAACAGCAACGCCTACTTCAACAGAGACACCATCCACAATCACATCTACTGTTACACCTACTACTGGAACACTGACACCAACTTCTACAGAAACACCATCCACAACTGCATCCACTACTTCACCTACTACTGAAACATTAACCCCTACTTCAACAGAAACACCATCCACAATCACATCAACTGTTACACCAACTACTGGAACGTCGACACCAACTTCTACAGAAACACCAATCACAACAACATCCATTACTTCACCAACTACTGAAACATCGACACCAACTTCTACAGAAACACCATCCACAACTGCATCCACTACTTCACCAACTACTGAAACATCAACGCCTACTT[C/A]AACAGAGACACCATCCACAATCACATCCACTATTACACCAACTACTGGAACTTCAACACCAACTTCTACAGAAACACCATCCACAACTGCATCCACTACTTCACCAACGACTGAAACATCGACACCTACATCAACAGAAACACCATCCACAACAGCATCCACTACTTCACCAACGACTGAAATATCGACACCTACATCAACAGAAACACCATCCCTAGGCACATCCACTGTTACACCAACTACTGGAACTTCGGCACCAACTTCTACAGAAACACCATCCACAACAACATCCATTACTTCACCAACGACTGAAACATCAACACCAACTTCTACAGAAACACCATCCACAATCACATCCACTGTTACACCAACTACTGAAACATCAACACCTACTTCAACAGAAACTACATCTACAACAATTCCAGTAACAACTATACCAACAGAAACTCCATCTACAGTTGTTACAGTAACAACTTTATCAACAGAAACCCCATCTACAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8866
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 |
---|---|---|---|---|---|
ENSDART00000073410 | Nonsense | 2302 | 2870 | 33 | 47 |
Genomic Location (Zv9):
Chromosome 25 (position 8595045)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 8309950 |
GRCz11 | 25 | 8387018 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCNNGTTTCCCACAGGTYTATGTTAATGATGAWTTGAAACAACTAACTTA[C/A]GTCAATAACAACTTCTTCATCACCACCTCTGGCATTGGAGTCATTTTGAA
Long Flanking Sequence:
TTATAACAATGGCTGCTGCTCTAGATATGAATGCGAATGTGAGTTTAAACCATGCTTATTTACATTAAATTTATCTTTAATACTTATGAGTAAATGTTAAATAACATGCCCTGTTCCTTGGTTTGAAAGGTAAATGCAGTGGTTGGGGTGACCCACATTACCAAATGTTTGATGGAACATACTATGACTTCCAAGGAAATTGCACTTACGTCTTGTTCAAAGAAATCGTCCCAAGATATAACATCAGTGCCTATGTTAAAAACTACTTATGTGATCTTCAAAATAATCTTGCCTGCCCAGAGTATGTGATTGTGAACTACAAATCATATAGCATTAAGCTGACAAGCAACACCAAAGAGATTGAGGTAAGTCTGCAAAACATTCCTAAAAACATTTTACGTCCCATAATGACAAAATGACAGTGCACTAGAGCATCGTTTTGAAAAGACCCCGTGTTTCCCACAGGTCTATGTTAATGATGATTTGAAACAACTAACTTA[C/A]GTCAATAACAACTTCTTCATCACCACCTCTGGCATTGGAGTCATTTTGAACATCACTGAAATCAATGTCGAGATTACTGTGAATCATCAAGGCTTTGTGATCAATCTCCCATTCTCCTACTTCAGTGGTAATACAGAGGGGCAGTGTGGTGAGTACAGATCCGAGATCATTTCTATGAGATGTGCATTAAGCAAAATGAAGTTTCACAAACTAGTTTCGAGAGAAGCAAGTGATATAATTGAGTTGAGCTGTTCTTTCATCTGTAATCATTAGTAAGCCAATCCGATCATTCCAAACTCACTATAAATAGCCTGACTAGCATTACTCCCTTCGTTTTTTTAAGAATCCACCCCATTTCCTCCCTTACCAGGATGAGCTCTTGAGAACTACCTGATCTCAGACCCCCTTACCTGCTAATTGACCAGGCGGGAGCCCTGGGCTCAATTATCTCTGAGCTCAGGGTTCTCTCCCGGGACAGCATGCCAAACCTGTTATTAATA
Associated Phenotype:
Not determined