Busch Lab

ZMP

LOC100333859

Ensembl ID:
ENSDARG00000088432
Human Orthologues:
MUC16, MUC20
Human Descriptions:
mucin 16, cell surface associated [Source:HGNC Symbol;Acc:15582]
mucin 20, cell surface associated [Source:HGNC Symbol;Acc:23282]
Mouse Orthologue:
Muc20
Mouse Description:
mucin 20 Gene [Source:MGI Symbol;Acc:MGI:2385039]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa20842 Nonsense Available for shipment Available now
sa33992 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa38588 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa20842
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000126123 Nonsense 1915 3161 7 17
Genomic Location (Zv9):
Chromosome 7 (position 953145)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 835744
GRCz11 7 990622
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACCCAGTCAACAATGACCACATCACAACTTCCAACAGAAACAACCCAGT[C/A]AACAATCTCAACAAGTGCCCAGCCTACAAATACACCCCAGTCTGTAACTA
Long Flanking Sequence:
TTAAAGAAACTTTCTATTTAAATGATTTAGACTAAATTAACATCTATTTTTTTTTTATCAACAATAATTCAAAAATCTACAAAACACCCAACCATTCAATCTATGATAAAAAACAACAGTCAGGCCAGATGAAAATGCTACTACAAGTGAAACCCAGTCAACGATGACCACATCACAACTTCCAACAGATACAACACAGTCAACATTCTCAACAAGTGCTCAGTCTACAAATACACCTCAGTCTGTAACTACTTCACAACCAATACAAACCGAAACCCAAAGTACAAGTGAAACCCAAACTACAACGGAAGGCCAGTCAACATCGACCACATCACAACTTCCAACAGGTACAACCCAGTCAACCTTCTCATCAAGTGCTCAGTCTACAAATACACCCCAGTCATCAACTACTTTACAACCCATACAAACTGAAATCCAAAGTACAAGTGAAACCCAGTCAACAATGACCACATCACAACTTCCAACAGAAACAACCCAGT[C/A]AACAATCTCAACAAGTGCCCAGCCTACAAATACACCCCAGTCTGTAACTACTTCACCAACCACACAAACTGAAACCCAAACTACAACGGAAGGTCAGTCAACATCAACCACATCACAACTTCCAACAGAAGCAACCCAGTCAACCTTCTCAACAAGTGCCCAGCCTACAAATACACCCCAGTCATTAACTACTTCACCAACCATACAAACTGAAATCCAAACTACAACGGAAGGCCAGTCAACAATGACCACATCACAACTTCCAACAGATACAACCCAGTCAACAATGACCACATCACAAATTCCAACAGAAACAACCCAGTCAGCAATCTCAACAAGTGCCCAGCCTACAAATACACCCCAGTCTGTAACTACTTCACAACCCATACAAACTGAAATCCAAAGTACAAGTGAAACCCAGTCAACAATGACCACATCACAACTTCCAACAGATACAACCCAGTCCACATTCTCAACAAGTGCCCAGCCAACAACTACAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33992
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000126123 Essential Splice Site 2951 3161 13 17
Genomic Location (Zv9):
Chromosome 7 (position 958781)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 841380
GRCz11 7 996258
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCACCACTTCCACATGCGCAGACTTTAACACAAACTTTGTGTTTTCTTTC[A/T]GAGCTGTGAACAAAATAAGGGCAGTAGAACAAAATGTACTGGTGGACCTA
Long Flanking Sequence:
CATCCGCTGTGTAAACCATCTGTATATAAGTTGGCAGTTGATTCTGCTATGGTGTATCCTGATTAATAAAGGGACTGAGCCAAAAAGAAAATCTCTAAAATCTCAAAAAGAATTCTCTAAATCTGCGTCTCAATTCGAGACTGCTACAGCCCTCCAGAGGTCACATTTACATGGTTACAATAAAATACACTGTTTTTCACCAACGCAACCCAAAGTGCTTAAATATAATTGGTTAAATTGGCAGTGGGCGGAGTTACAGAGACCAAAACAAAACAGACATGTCGAAACGCACATTTTTAAAGCAGAATATCTGACTTTAGCATTGTTTCACAGATAAACAAGAATGTTCACTCAACATGTTTCTTAAATTTTTGCAAACATATCATGGTATTTTTATGATTCAGGACAGTCACAAACTTACATATAGCACCTTAAAAAAAGACAAAATCTTCACCACTTCCACATGCGCAGACTTTAACACAAACTTTGTGTTTTCTTTC[A/T]GAGCTGTGAACAAAATAAGGGCAGTAGAACAAAATGTACTGGTGGACCTAGAAATAGTGTTTAACCAGAACTCCACTGAACAGATTCCCGACAACAATGACATTGTGCAGACTCTAAAAGATGCAGCGGTAAATCCGACCTCAGGGTTCAACCTCAGCGTGGATGTCGGCACTATTATGGTTATCAGTAAGTTTGCAGGAATCGGTCTTCTGATATATTCAATGTCCACATCTATTGAAGACTGCAACCGATGAACTGTTTTATCTGTACAGAATCGCTGCAGATCATTCCAGTGATAATCCTGACCAATGGAACCTTTACGGCTGCACTTTCAAATAAGACTAAGACCGATTTTCAGACCAGGGCAATGATGATAAAAACTGGGGTATGTGTGAAGAATTCATTAAGGAATTTGGTGTATCATCTTCCAAAACAGAAAACCAATTTTGCTTAACTGCTCTTGTTTTACAGCTTGAGCCCTTTTTCTTCTACGACTACCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38588
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000126123 Essential Splice Site 3072 3161 16 17
Genomic Location (Zv9):
Chromosome 7 (position 959610)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 842209
GRCz11 7 997087
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTTAACAGTCTGTTTTTATGACTAAATCTGGATTAAACACACTCTCTCT[A/C]GTGATGCCGGTGTGAAATCAAAGATTGTGCCGTCGATCAGGAACAGCATG
Long Flanking Sequence:
CTTTCAAATAAGACTAAGACCGATTTTCAGACCAGGGCAATGATGATAAAAACTGGGGTATGTGTGAAGAATTCATTAAGGAATTTGGTGTATCATCTTCCAAAACAGAAAACCAATTTTGCTTAACTGCTCTTGTTTTACAGCTTGAGCCCTTTTTCTTCTACGACTACCCAGTGTCATTCAGCACCATATCTTTAACAAACTTCAGGTAGGCATATGTATGCTTGTGTGTTCTAATCCCTCCTGTTGTCTAACGATAAACACTATTCGGACTGTAGGTCAAGATGGCCCTCCTTGACTAAACCAATTTAATTTCAAGCCTCAAATCTATTTTAATAAATCTTGTGAATGTCCAGGTTTTCCCTTATTAGCGTTTTATCAATGGACAACATTCGTTTCTGACTGCAGTAGTGTTTACATCCAACAGGAGGGTTAAACCCAGCTTTGACTATTTAACAGTCTGTTTTTATGACTAAATCTGGATTAAACACACTCTCTCT[A/C]GTGATGCCGGTGTGAAATCAAAGATTGTGCCGTCGATCAGGAACAGCATGGATTTAGCATTCTCAGCCGGCACAATTCTGCCCAATGACACCCAGATAGTGAACACTATAGTCCGAGCAGCCAGAAACAACACGCTACCCTTCGAGATCTACACTTATTCAATAATAGTAAATAACACAGGTAAGTGGGGTCAAATAATCTTGTACTACAGCCAAACATTAATTACATTGACACTGTATTAAGTGAAGGATAATGTACATCCAGCTGGTGGTTGTTGTAGGATAAAGTACACCAGATTTATCAGCAGCTGTAGTGAAGGCTGGAGGGTTTATTTTACAATTACCACCGGCTGGATGTACATTATCCTGATTATTACATGGCTACTGGACACAGAACTAAACCATTAGACACAAGACCATGATCTGAGCTGTAATAATCTACTAGCTCTTTAATTAAATGTGCAAGCTTGCAGAAAGAAAAACTGAATGTAGAACAACCTA
Associated Phenotype:
Not determined