ZMP
ENSDARG00000091834
Ensembl ID:
Human Orthologues:
MUC12, MUC16, MUC17, MUC20, MUC4, MUC5B
Human Descriptions:
mucin 12, cell surface associated [Source:HGNC Symbol;Acc:7510]
mucin 16, cell surface associated [Source:HGNC Symbol;Acc:15582]
mucin 17, cell surface associated [Source:HGNC Symbol;Acc:16800]
mucin 20, cell surface associated [Source:HGNC Symbol;Acc:23282]
mucin 4, cell surface associated [Source:HGNC Symbol;Acc:7514]
mucin 5B, oligomeric mucus/gel-forming [Source:HGNC Symbol;Acc:7516]
mucin 16, cell surface associated [Source:HGNC Symbol;Acc:15582]
mucin 17, cell surface associated [Source:HGNC Symbol;Acc:16800]
mucin 20, cell surface associated [Source:HGNC Symbol;Acc:23282]
mucin 4, cell surface associated [Source:HGNC Symbol;Acc:7514]
mucin 5B, oligomeric mucus/gel-forming [Source:HGNC Symbol;Acc:7516]
Mouse Orthologues:
Muc20, Muc4
Mouse Descriptions:
mucin 20 Gene [Source:MGI Symbol;Acc:MGI:2385039]
mucin 4 Gene [Source:MGI Symbol;Acc:MGI:2153525]
mucin 4 Gene [Source:MGI Symbol;Acc:MGI:2153525]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa33255 | Nonsense | Available for shipment | Available now |
| sa6908 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa33254 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa33255
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 |
|---|---|---|---|---|---|
| ENSDART00000127483 | Nonsense | 775 | 1105 | 4 | 13 |
Genomic Location (Zv9):
Chromosome 3 (position 38717280)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 38580640 |
| GRCz11 | 3 | 38722498 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCCTTTTAGGTACTTGTCCTACAGTGCCCTGCCCATCACTCAGTGTCTG[T/A]GTGAACTCCGTCTGCCAGTGCTTGGCAGGAACTGTTCTTTTAAATAATGT
Long Flanking Sequence:
TACTACACCAGGGAGCAACACAACAGTAAATGCTACAACACCACCCATTACTACACCAGGGAGCAACACAACAGTAAATGCTACAACACCAGCCATTACTACACCAGGGAGCAACACAACAGTAAATGCTACTACACCAGCCATTACTACACCAGGGAGCAATACCACAGTAAATGCTACAACAACACCCATTACTACACCAGGGAGCAATACAACAGTAAATGCTACCACACCACCACAATCTACTCCAGGAAATACTACTCTACCACCTATAACCAACTCAACAACTGGACCCATCGTATCTACTACTAACCCAACTAACACCACCACACCAGGTGTGTTTGAATGAATGTGATTGTGTACTTCTCAAATATAATGTGCATGCAGTGTTGTACATAAATGTCTTTAATATGTCCCACATTCATAAACACTAAGTTCCATTCCTTTTCCCCCCTTTTAGGTACTTGTCCTACAGTGCCCTGCCCATCACTCAGTGTCTG[T/A]GTGAACTCCGTCTGCCAGTGCTTGGCAGGAACTGTTCTTTTAAATAATGTTTGTGTGGAAAGTAAGTACCTGTTGTCAAGCCTCTTTCATTCACTTGCCCTATTTGTCCTCACATGGGGCCATCATACTGAATCACTCTTATTTTAAGTTGCATTTCACCAGCATAAACCATGCCACACTTTGAGCTAGACTTTATTGTAGGGATGAAGGGGATGTTAAGAGAACAGTGGAATGAACGGGAGGGGAAATAAGAGGATAAACATTGAACAGGTAGGTAGGTTGATCGGACATCCTACGATGATGCCCAGAGACTCAGAGTCAGGGTACCGTCTCTGTAATATTTTGGTAGACTGATTGAACCCCCGATTCAACCTAGGAGTGAAGAGAGGGTTGTGAATGGGAAGCAAGGAAACAGAGGAGGGGAGGGTGGGTTCTAAAGAATGAGACGAACAACGCTAGAGGGCTGGTCTGCCTTAAATACATTTTACGAAGTAGGTGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6908
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 |
|---|---|---|---|---|---|
| ENSDART00000127483 | Nonsense | 933 | 1105 | 8 | 13 |
Genomic Location (Zv9):
Chromosome 3 (position 38710971)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 38574331 |
| GRCz11 | 3 | 38716189 |
KASP Assay ID:
554-5451.1 (used for ordering genotyping assays)
KASP Sequence:
GTGTGTAATACTAAAGATGGGTCTGCCATCTGTACCTGTGTAACTGGTTA[C/A]ATCCSCAGTCCTTACCAGATCAAAAGCTGCAGTGGTGAGTTTTTATTACT
Long Flanking Sequence:
AGCACCTGGAGGAAACCCATGCAAAGGCAGGGAGAACATGCAAACTCCTCACTGAAACGCTAACTGAGCCGAGGCTCGAACCAGCGACCCAGCAACCTTCTTGCTGTGAGGCGACAGCACTACCTACTGCGCCACTGCTTCGCCTTTAAGTAGTTGTATCTCGGCCAAATTTTCTCCTAACAAATCATACATCAACTTTCAGATACATACATCTCAGTTTTCGAGGAATTACACCAATGGCTTCTTTTGTTGTCCATTTACAGTAGCTTTTTAGGACATAAATCTATTACTTTACATTACAAGTCCTTTAGTTGCATGGTAGGCAGAGAAAGCATTCTTATGATGAAATATCTAATATATGTATACTGGGCTCTGTTTCTTTATGATTGTCTATTTCTAGAAACTAGTCTGTGTGCTCAAAATCCTCCTCCTTGTGATACCGAAACTACAGTGTGTAATACTAAAGATGGGTCTGCCATCTGTACCTGTGTAACTGGTTA[C/A]ATCCCCAGTCCTTACCAGATCAAAAGCTGCAGTGGTGAGTTTTTATTACTGCATAAAAAAAATCACATGAGCTACCATGTATGTTTATGTTTGCATATAATATTCATTGCTGACCTTTGAGTTTGACGTGGTTTCTGCCATGGCAACAGACATATTAATCCTGATCTGGGGACATCAGTGTTTATAATGTACTCTACTCTCTTCACCAATTGATTCGGTTTATTTTCTGTCTTTTTTTTTTCACAGCTTGCCCAAGTGGCTCCAAAGCATATGAAAATAAATGTGTGCCGTGAGTAGAATTTCATTCTTTTTTTAATACACACCAGTGTCAAGTTTGTTTCTGTCTAGACGAGTTGAAGTTAAAGTCATGATGTCAATATATAGGGCAACCTATAAGACATTAGTATAGCAGTTTTTGTTTAGGTATAGTCAACATTTAAAGTGGATTTTTCATCAAAGTTGGACTAAAACTATTGAACATCAATCACTTTAGTCTTTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33254
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:
T > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000127483 | Essential Splice Site | 945 | 1105 | 8 | 13 |
Genomic Location (Zv9):
Chromosome 3 (position 38710935)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 38574295 |
| GRCz11 | 3 | 38716153 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGTAACTGGTTACATCCCCAGTCCTTACCAGATCAAAAGCTGCAGTGG[T/G]GAGTTTTTATTACTGCATAAAAAAAATCACATGAGCTACCATGTATGTTT
Long Flanking Sequence:
CATGCAAACTCCTCACTGAAACGCTAACTGAGCCGAGGCTCGAACCAGCGACCCAGCAACCTTCTTGCTGTGAGGCGACAGCACTACCTACTGCGCCACTGCTTCGCCTTTAAGTAGTTGTATCTCGGCCAAATTTTCTCCTAACAAATCATACATCAACTTTCAGATACATACATCTCAGTTTTCGAGGAATTACACCAATGGCTTCTTTTGTTGTCCATTTACAGTAGCTTTTTAGGACATAAATCTATTACTTTACATTACAAGTCCTTTAGTTGCATGGTAGGCAGAGAAAGCATTCTTATGATGAAATATCTAATATATGTATACTGGGCTCTGTTTCTTTATGATTGTCTATTTCTAGAAACTAGTCTGTGTGCTCAAAATCCTCCTCCTTGTGATACCGAAACTACAGTGTGTAATACTAAAGATGGGTCTGCCATCTGTACCTGTGTAACTGGTTACATCCCCAGTCCTTACCAGATCAAAAGCTGCAGTGG[T/G]GAGTTTTTATTACTGCATAAAAAAAATCACATGAGCTACCATGTATGTTTATGTTTGCATATAATATTCATTGCTGACCTTTGAGTTTGACGTGGTTTCTGCCATGGCAACAGACATATTAATCCTGATCTGGGGACATCAGTGTTTATAATGTACTCTACTCTCTTCACCAATTGATTCGGTTTATTTTCTGTCTTTTTTTTTTCACAGCTTGCCCAAGTGGCTCCAAAGCATATGAAAATAAATGTGTGCCGTGAGTAGAATTTCATTCTTTTTTTAATACACACCAGTGTCAAGTTTGTTTCTGTCTAGACGAGTTGAAGTTAAAGTCATGATGTCAATATATAGGGCAACCTATAAGACATTAGTATAGCAGTTTTTGTTTAGGTATAGTCAACATTTAAAGTGGATTTTTCATCAAAGTTGGACTAAAACTATTGAACATCAATCACTTTAGTCTTTGGGCGATATTGAAAAACTGTTTTGATCCACTTTGTGAT
Associated Phenotype:
Not determined