ZMP
MUC17
Ensembl ID:
Description:
mucin 17, cell surface associated [Source:HGNC Symbol;Acc:16800]
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 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa38871 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa15291 | Nonsense | Available for shipment | Available now |
sa6232 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa41955 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa38871
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 |
---|---|---|---|---|---|
ENSDART00000110641 | Nonsense | 212 | 2043 | 3 | 7 |
Genomic Location (Zv9):
Chromosome 12 (position 6027932)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 4795106 |
GRCz11 | 12 | 4830063 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAAAGAATCAAGGCCCCTCAATGCTGTTAAGGATCTATTTCAAAGGCTG[C/A]TATGCTCAAAACTGGGTAAGACATTCTCCTTGCAATAGCAATTTAAATTA
Long Flanking Sequence:
ATTTCGCTTTTTAAATGCCTGAATTCAGTCCACAGTAATTGGCTGTTCAAATGATGCTGCAGATGTAATAATGCTGAAGATTCAGCTTTAAATCAAAAGAACGAGGTACCATTTGAAATACTTTAATAAAACAATCATATTAAGAAAACTTAACGTTAGCACACTATTTTGACCATTGTGTAAAGTCATATTTAAAACAAATAAGCAACTAAAAGTGATATAATTGGTCTGATTACCTGCAGATCAAACTCCCTGCTTGGGTCAACATAGATGGCATTTGTCATTTTAAGTCTTTCCTCAACAACTTGAAAATAAAGATTGCATATCAGTGTTTATTGTTTGAATCAGTGGTGTTTACAAGTAAACATGAATTTCTCTGAATTGCTTCACATGCTTATTGCAGATTCAGAACAGAATGCTTCACCCTCCCAAAAGCAGTGTCGGTGCATCAAAAAGAATCAAGGCCCCTCAATGCTGTTAAGGATCTATTTCAAAGGCTG[C/A]TATGCTCAAAACTGGGTAAGACATTCTCCTTGCAATAGCAATTTAAATTATGTATTTTTTAAAGATTTATGTACAAAATTGTATTTTTACTCAATTTGGTGAACCATTTTTTAATAAATAGTTTGTGTATTGTCAGGCTTGCCAGGTTTTTGCCAAAGCAACAAAAACATATCCCAATGACTAATCAAATCTAGCTCAATAATACCAAAACTTGATTAAAAACATTTACACCAACCTATTTATTATACACCATTTCATGTTTAAAAAAATAATGGTTTATTTGTTCATTTTCAATGTTTTGTTTTTGTCATAAGGAATCTTGATACTCATGTGATGTCGAGTTGAAATATAGTGGATGTGAGAAAAAACAGAAAACTCTGGCAGAAGTAAACCCCAAACTTATGAAATGAAATAATTTTAATTTAAACATCACGTCCCTTAAGTTGTAAATTGTCTGACTTAAAATATAGGTAATTTATACAAATATATTTTAAAATATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15291
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110641 | Nonsense | 358 | 2043 | 6 | 7 |
Genomic Location (Zv9):
Chromosome 12 (position 6030420)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 4792618 |
GRCz11 | 12 | 4827575 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTCAAAAAGGGCAGTAGAAAACGAAGACAAGATGYATTTGATTTTGAYT[G/A]GGAGTTTGATTCAGTTCCGACGGATTCCTTTATACCGAAGATTGCAAAAT
Long Flanking Sequence:
GGGTGAGTATTTGTCATTGGTGGATTACACTATTATTTTCGTGACTGCAGCAATTTAAAAGTTTGTCGGATTCAATGTTTTTTAAAAATTGTCCATGACTTTGTAATTTGCATAAAAATAATGAAAACAAAGATGTGAACTGGTACCTTAAACATTTAAGCCTCTTAAATATGTAAAAGAAGCTTTGTCAATCTCTGTTCTAAAGATGTTTCCAGGCAATTCCCTCATCTAATCATGTGGAAACATCACAATGCTGTGATTGTCAAAGTTAAACGCTCTGAGATTAAGGTATAACCCTTTCACAGTTTTTTTTCTTTGCTTTTTCAAAGGTATTGATTTTTAAAAAAGTTTTATTACTTTTTGAAAGGGTGATGTTCTTCGGCTGAGTTATCTTGATTTGACTGGAAAATCACAGATGATCAGAGTGTCCTGTGTTCACCACATGATCCCTTTCAAAAAGGGCAGTAGAAAACGAAGACAAGATGTATTTGATTTTGATT[G/A]GGAGTTTGATTCAGTTCCGACGGATTCCTTTATACCGAAGATTGCAAAATTCACTGTCCCCTTACAGATCATCCAACCTGGGATTTCTTCTTCTTCTTCAGAGTCTAAATCTCCTAGTGCTGTCACTACTGAATTACTTGACTTTCCTCCTGATACAGTAGAAACTGATTATCTAGATTTTGATTATTTCGATTTGAGGAAAGACCATGTCAACCCCTCATTTTTTTTTGAGCCAGCTGAGCAAAATCTTGGTACGTCTCTGACAGAAAAAACACAAGCAAAAACAGACATATCATCAAGCACACCTGTGGATCCAGACCCCACTACAGGCACCATTTCCATTAGGCCAACCACTGTATCTCTTGATACAACCCATAAGACAAAAAACAGTAATAAATCTTGTGATGTTAATGCCATTGTAGGTTCTGAGACTGATTCTCTACTTTGGGAATTTGAAGACATACCCACTGCTCAATATGAGGCGTTTGAAGTAGCTCCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6232
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110641 | Nonsense | 415 | 2043 | 6 | 7 |
Genomic Location (Zv9):
Chromosome 12 (position 6030592)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 4792446 |
GRCz11 | 12 | 4827403 |
KASP Assay ID:
554-4690.1 (used for ordering genotyping assays)
KASP Sequence:
GTCACTACTGAATTACTTGACTTTCCTCCTGATACAGTAGAAACTGATTA[T/G]CTAGATTTTGATTATTTCGATTTGAGGAAAGACCATGTCAACCCCTCATT
Long Flanking Sequence:
GTAAAAGAAGCTTTGTCAATCTCTGTTCTAAAGATGTTTCCAGGCAATTCCCTCATCTAATCATGTGGAAACATCACAATGCTGTGATTGTCAAAGTTAAACGCTCTGAGATTAAGGTATAACCCTTTCACAGTTTTTTTTCTTTGCTTTTTCAAAGGTATTGATTTTTAAAAAAGTTTTATTACTTTTTGAAAGGGTGATGTTCTTCGGCTGAGTTATCTTGATTTGACTGGAAAATCACAGATGATCAGAGTGTCCTGTGTTCACCACATGATCCCTTTCAAAAAGGGCAGTAGAAAACGAAGACAAGATGTATTTGATTTTGATTGGGAGTTTGATTCAGTTCCGACGGATTCCTTTATACCGAAGATTGCAAAATTCACTGTCCCCTTACAGATCATCCAACCTGGGATTTCTTCTTCTTCTTCAGAGTCTAAATCTCCTAGTGCTGTCACTACTGAATTACTTGACTTTCCTCCTGATACAGTAGAAACTGATTA[T/G]CTAGATTTTGATTATTTCGATTTGAGGAAAGACCATGTCAACCCCTCATTTTTTTTTGAGCCAGCTGAGCAAAATCTTGGTACGTCTCTGACAGAAAAAACACAAGCAAAAACAGACATATCATCAAGCACACCTGTGGATCCAGACCCCACTACAGGCACCATTTCCATTAGGCCAACCACTGTATCTCTTGATACAACCCATAAGACAAAAAACAGTAATAAATCTTGTGATGTTAATGCCATTGTAGGTTCTGAGACTGATTCTCTACTTTGGGAATTTGAAGACATACCCACTGCTCAATATGAGGCGTTTGAAGTAGCTCCAAAAACCACCCCGAAGTCACCTCAATTATCAAGCATGCCTGCATACATAGACCCTACTATGAGTACAAGCTCTATTTCCTTCAAGCCATCTGATTTAACTCTTGGTGTAACCCAGAAAGCTGAAGAATCAAGTGCTGCTACAAAGCCAGGCAGAATCACCAAAATTGCAACTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41955
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110641 | Nonsense | 627 | 2043 | 6 | 7 |
Genomic Location (Zv9):
Chromosome 12 (position 6031228)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 4791810 |
GRCz11 | 12 | 4826767 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCCCTTCAAGTCCAGACTATACTATACAAACAAACACTGTTACCTTCTG[G/A]CCCCCCGATGTACTTGGTACCACCAAAACATCAAGTGATGTTGCAAAACC
Long Flanking Sequence:
GTGGATCCAGACCCCACTACAGGCACCATTTCCATTAGGCCAACCACTGTATCTCTTGATACAACCCATAAGACAAAAAACAGTAATAAATCTTGTGATGTTAATGCCATTGTAGGTTCTGAGACTGATTCTCTACTTTGGGAATTTGAAGACATACCCACTGCTCAATATGAGGCGTTTGAAGTAGCTCCAAAAACCACCCCGAAGTCACCTCAATTATCAAGCATGCCTGCATACATAGACCCTACTATGAGTACAAGCTCTATTTCCTTCAAGCCATCTGATTTAACTCTTGGTGTAACCCAGAAAGCTGAAGAATCAAGTGCTGCTACAAAGCCAGGCAGAATCACCAAAATTGCAACTTCTGCTGTTGATGCCGATGTCGAGTTAGATTTTGGTTTTTGGGATTTGGATGTCATACCCACTGTTCCATTTGAGGAATTTTCAAGCACCCCTTCAAGTCCAGACTATACTATACAAACAAACACTGTTACCTTCTG[G/A]CCCCCCGATGTACTTGGTACCACCAAAACATCAAGTGATGTTGCAAAACCAAGCACTGAAACTGCAACTGCTACTACTAATGTGCAGTCTGAGACAGATTATGGTCTTTGGGGCTTTAGTGTTATTCCAACTGTTACAACTGCTACTACACTGGAATCCACTTTGGGAGAAACTACAATGCTAGGTAGCAGTTTGCTTGAAACAACTACCCCAGCCACTATTTATGAAGAAACAAATACCCTGGAACCCATTTTGGCAGAAGCTACTATGCTGGGCTGGTTTGAAATTACTACCCCAGCCACTCCTTCTGCTGACACTGTACTAGACACTAGCACCACATCTGACAAAACTACTACTACTTTAAAAGAATATACTATGATGGAAACTGCTACCACTTCAGGAGAAATCACTATCATGGATACAACTCTGACAAAAATAGCTACCCCAAGCCTCACATCTGCAATAAGTTTTCCAGTCACCGCTTCTATAGGGACTACTGC
Associated Phenotype:
Not determined