ZMP
LOC100147849
Ensembl ID:
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]
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 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15145 | Nonsense | Available for shipment | Available now |
sa34253 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa41088 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa34252 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa34251 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa34250 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa41087 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa15145
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000127798 | Nonsense | 276 | 4915 | 7 | 55 |
Genomic Location (Zv9):
Chromosome 7 (position 74897803)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 72080165 |
GRCz11 | 7 | 72329456 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTCATCCTTGCCCAGAAACYATGGTGTACAGCCAGTGTGGAAATCCCTG[C/A]ACAGACACCTGTACCARCTCTGAAAGAGGACAAGTGTGTGCGCAGCACTG
Long Flanking Sequence:
GAATGGAGAACTGAGTATTTCTGCCGTGAGTTGCCTCATCTTTGTAGTCCTGCATTCATGTTGGTTTAATATTAAATTTTAGCTGTCAGAGCCGGGTAGTAGTGGATTTTACACTGCAAAAATCAAGTTTTTGACTTGTTTCAAGCCCGAATATCTAAAAATTCTTAAATCAAGAATAGTGTTCTAGACATCAGAAAAGCATGGTCTCGTTTTCAGAAATAATATGTCAAAATGTATTTTTTGCCCTTAAAACAAGCTAAATAATCTGCCAGAGGGGTAAGAAAAAACTAAAATCGTATATAAAACCGAAAACAAGATTACTTTGCTCACCCCATTGGCAGATTATTTCTAGAGCAGAGGTTTCTAAAATAATAACAATAATAATAATCTGAAGTTTAAGCACAAAACTGCACTGCAACTGACTTTTATTTGTTTGTTTTGTATATCACAGCTCATCCTTGCCCAGAAACCATGGTGTACAGCCAGTGTGGAAATCCCTG[C/A]ACAGACACCTGTACCAACTCTGAAAGAGGACAAGTGTGTGCGCAGCACTGCATTGATGGATGCTTCTGCCCTCCTGGTACAGTTTTTTTTAACCATGGCTTTCTTTACGGACACTTTATTCAAAAACATGTTGATTTACATTTTTACCTTCCTAATCAAAAGTCTTTAGTCAGATTCTGATGCTAAACCACAAATTCCCATTTAAACACAATATACTTAGTGAAGTTTACTTATAGACTAATTTCGAGAGGATCATATGCTTATGCTGCCGGTCCTGCATTATTCCATTTATAATTGACCAATCAGACGATTCCCAAGCACTATAAACACCCTAAGCTTCATATAACAGCTATCTTCATTTTGAAGAATCCCCCCTTCCACCCCTACACCTCCTCTTTTCCTAGATGGGGACACGGTGGTGCAGTGGTTATCGCTGTTGCCTCACAGCAAGAAAGTCACTGGTTCTAGTCCTTACCAAGCCAGCCAAGTTTCTGTGCCGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34253
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000127798 | Essential Splice Site | 496 | 4915 | 12 | 55 |
Genomic Location (Zv9):
Chromosome 7 (position 74894041)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 72076403 |
GRCz11 | 7 | 72325694 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGCAGCTTTACATCACAGCCAATTCAGTGTATCAAGGAGAAACATGTGG[T/A]ATTTATCTCTATTCTTTCTTTATTTATTACATGTTTGTTATATTTAACCC
Long Flanking Sequence:
ATAACAGCTTTACAACCCCTTTATAAACCTTTTATGCACACAGGTTATTAATGTGGACTCCAGCGGAAACGTTGAGGTCAACAGAATAGTTGCTCAACTTCCACTTTTTACATGTAAGTCTATGGCAAAGCAACAAAATCAAAGCATCAGTTTCTGCTACAATAATGCAGTTACTTTTGTCCCCCCTACGTTAACACAATACAGCACAATGTGAATAAATAGAATGAAATACATTGATAACAAAGATAAGATGTATATTATCTATGCAAATGATGCAACTATGCAAAATTAACTATTACAAAAAATCAAATCTTCCCTCATGTATTAATAATGTTGCATGCTGTTATCTGATTTCCAGCTTCAGTGAGTGTTTTCAAGCCCTCCTCATTCTACATCATCATTGAAGCTCCGCTGATTGGGCTTCGTCTGGAGATCCAGCTGGTGCCAATAATGCAGCTTTACATCACAGCCAATTCAGTGTATCAAGGAGAAACATGTGG[T/A]ATTTATCTCTATTCTTTCTTTATTTATTACATGTTTGTTATATTTAACCCTTTCATGCACTATCAACTAGCAGAATCAACTATAGTTATAAAAACATCCATCTGGAAATTTCAAACAGGATTTTTAATGTTTTGTACGTATAGATTTGATCAAGTGGTATTTGCCTACATACAAGTCTGAATATTTTCTGGCTTAAAAGTGAAGAAACAACTCTGTCCTAATTTGAACTCTTTTATGAAGTAAACCACCCGATTCAAATGTTATCATTTGATTGAATGGGTGTTATTAGTGGTTATAAGCTGATATATATGGGCCAGTAGGGGCCTTCTGCGCCTACTAGTAGGCTCAGAAGGCTGTAATCATCCATCCACATGGTTAATCAGCTATACTAATAGAGAAGACTCCAGATCCAGATCTGTTTTTACATTACTGTGACGGTTGGGTTTTGGTTTGGCGTAGTAAAATACAATTAATGGGAAATTTAATAAATAATATAAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41088
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 |
---|---|---|---|---|---|
ENSDART00000127798 | Nonsense | 668 | 4915 | 16 | 55 |
Genomic Location (Zv9):
Chromosome 7 (position 74890117)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 72072479 |
GRCz11 | 7 | 72321770 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCCAGGCTGACGGTTCCTGCACCCATGATCATGTGCTGGTGGACGGCTG[C/A]GGCTGTGCTGAAGGAAAGTACATGAATGAGAACGGAGACTGTGTTGAAGC
Long Flanking Sequence:
TATTAAGCTTAAAGTGACATTTAAAAAACTTCACTATTAAGGTTAATTAGGCAAGTTAGGGAAGGCAAGTCATTGTAAGTGGTTTGTTTTGTAGACAATTAAAAGAAAAGCTTAAGGCGGCTAATAATATTGACCTTAAAATAGTTTTAAATTGAAAAAACAAAACAAAAATTATTCTAGCCAAAATAAAGCAAATAATAATTTCTTAAAATTATTATAAAAAATATCAGAAATACTGTAAAAATTTCCTTGCACTTGAGAAATATTTAAAAAGGAACAAATATTTCAGAGGAGGGTGAATAATTTCGCCCTTAACTGTATTTTTGCGTATGCTCATCAGGTTGATGAATCTTCCTATTTTTCCCCTCAGTGAAATACACAGAAACCTGCGCCGCCACCACAGTTTACTCATATCAGATGACGAGCTGCGGGCGCACATGCAGGTCTCTCAGCCAGGCTGACGGTTCCTGCACCCATGATCATGTGCTGGTGGACGGCTG[C/A]GGCTGTGCTGAAGGAAAGTACATGAATGAGAACGGAGACTGTGTTGAAGCTGCCGCCTGCTCCTGTTACGATTCAGGCAAAGTCGTTGCTTTAGGAGAGACCATCTCCAAAGACGGAGGATCATGGTATGCACATTTCTGCTAAATTCAATATTTGTGGGGTCACACTTCAGAATATTGGACAACTGTTTAATCAATGTATTTTAATCGCATGTATGTTTAAATTTCAGTATTTGCCAGCAAGGGAAACTGAGCTGCTCTGGTGTATCAAATGGAGAAGGTATGTATGTGAATCAGGGTCGCTCCAGCCAATTGCATAACAGCTACTACTGGGGAGGCAGGACTAAAGATAGCACAGCCCAATCTGATTGGACGAATTTAGATAACTAATGCATAAAGTAAAAGGATGGGTCAGCAGTGTAATTAAGGATGCTATAACATGCAGTTATCCAATCAATCTAAAGTACAATGTAAAAAACTATTTACACATTCAGTACAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34252
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000127798 | Nonsense | 908 | 4915 | 22 | 55 |
Genomic Location (Zv9):
Chromosome 7 (position 74885223)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 72067585 |
GRCz11 | 7 | 72316876 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCAGAGCAATGAGCTGAGACTGACTGATGGATCCTTCCAAGTTGTTCGC[A/T]GAGACGCGGGAGAGGAGATTCCCTACCAGATGCGAACCATGGGGCTTTAC
Long Flanking Sequence:
TTTGATGACAAAAGATACGTCTTTAGTGGAAACTGCGAATACAGCCTCGTTCAGGTATTCACTCTGCACTTAAAATAATTGTAAAATTTCCAAAAGCCTCCAGATAATTCTAGAGTCCTTTGCTAGAGATCTTTCGGTTTGTTTTGGTGGGTTTTTGCATGCGTATTTGGTTGTTTTTGTTCTGTTTTCTGTTACTTTCAATAAAAATGAAATAAAATACAACAAATAATTAACAAAAATCTAACCTTTACACCCTGTGCAGGACTTCTGCAACAGCACCTCCGGCACTTTCAGAGTCATCACTGAAAACATTCCCTGCGGATCCACCGGCACCACTTGCTCCAAGGCGATCAAGCTTTTCCTTGGAGTGGGTTAACTCTTGACATTCACTAAAGCCATCATAGCAAACATTAAAATACTACAGATTAAACATCGACATGTCTTTTATATTTCAGAGCAATGAGCTGAGACTGACTGATGGATCCTTCCAAGTTGTTCGC[A/T]GAGACGCGGGAGAGGAGATTCCCTACCAGATGCGAACCATGGGGCTTTACTTGGTGATCGAGACCAAAAATGGCCTGATGCTCATATGGGACAGAAAAACAACTATACACATCAAACTGGGACCAGAGTATAATGTGAGTAAGATAAAAGGTCTATTATCATTCATGTCAGTCCTCAGGATTTTGGATTTGAGTCAGAAGAGATCCATAAAAATCAATCAATGATCAAATCTTTACTTTAGGACATCCAAAACATACAATGCATTTTGTTAAGTGTTTGTTTACAATTGTTTTTATTTAATATTATCTCTGGATTTTAGCATATTACCATTCTTAAAACATGTTTCTTTTCTAGTTCAGTTTAGAGTTTAAACATATATGGACTCGAGTCTTTTTGTAAATATATAGATTCATTTTATACTTTTATATTTTTTTGTGCCTAAAAAACAACAACAACTTTTCCCCAAATCTCACACATTTTTGTGACTTAATGTTGTTGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34251
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000127798 | Nonsense | 2299 | 4915 | 34 | 55 |
Genomic Location (Zv9):
Chromosome 7 (position 74876455)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 72058817 |
GRCz11 | 7 | 72308108 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCACTACACTTGTGTCCACAACAGTAACTGTTGAATCGTCCACTGAATTT[G/T]AGGTCAGCACCCAGAGTCCATCTTCAACAACAAAACCAATCAAAGCTGAA
Long Flanking Sequence:
CCCAGGGTCCATCTTCAACAACAAAACCAATCAAAGCTGAAACAACACTTTCAACCACCACAGCAGAGACTCCATCCACCACTGTCCTTGTAGAGGGAAGCAGTACTGTCCAACAACCCACAGAAACATCAGCTCCAAGCATTTTGTCAACAACATCCAAATCATCTACAGTAACTGAAACAACTGGAGTAGTAACATCAACTGAGACAGTTACTGAGAACGAACTGAGCACTTCTGAGACAACATTGTCCACCACCAGGCCACCGAAGGTGGTAACAACTGGCCAAACAATCGAGCCGACAACTACAGCCACAACAACCGTGGAGGAGCTTACGCCAACTTCACCTGAATCTTCAACACCATCAAGCACATTGGTTCCTGTGAGACAAACCTCACCAGCCATAACATCCACTCAACCAACAACACTAACAAAGACAACTGCTGTACCAGTCACTACACTTGTGTCCACAACAGTAACTGTTGAATCGTCCACTGAATTT[G/T]AGGTCAGCACCCAGAGTCCATCTTCAACAACAAAACCAATCAAAGCTGAAACAACACTTTCAACCACCACCGCAGAGACCCCATCCACCACTGTCCTTGTAGAGGGAAGCAGTACTGTCCAACAACCCACAGAAACATCAGCTCCAAGCATTTTGTCAACAACATCCAAATCATCTACAGTAACTGAAACAACTGGAGTAGTAACAACAACTGAGACAGTTACTGAGAACGAACTGAGCACTTCTGAGACAACGTTGTCCACCACCAGGCCACCGAAGGTGGTAACAACTGGGCAGACAATCCAGCCGACAACTACTGCCACAACAACCGTGGAGGAGCTTACGGCAACATCACCTGAATCTTCAACACCATCAAGCACATCTGTCCCTCTGAGACAAACCTCACCAGCCATAACATCCACTCAACCAACAACACTAACAAAGACGACTGCTGTACCAGTCACTACACTTGTGTCCACAACAGTGAGTGTTGAATCATCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34250
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000127798 | Essential Splice Site | 4501 | 4915 | 45 | 55 |
Genomic Location (Zv9):
Chromosome 7 (position 74868375)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 72050737 |
GRCz11 | 7 | 72300028 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATTGCCCCCATTACAAAAACACTACCATTTTTCACTCTCACCATTCCAG[T/C]GACTACAGACTCCTCTCTTTTCTCAACTACCTCAGAGTTTTGTTGCTTTG
Long Flanking Sequence:
CACAACAGTGAGTGTTGAATCATCCACTGAATTTGAGGTCAGTACCCAGGGTCCATCTTCAACAACAAAACCAATCAAAGCTGAAACAACACTTTCAACCACCACAGCAGCCATCCCATCCACGACTTTTAGTGTTGTGGAGGGAAGTACCACTGTGCAGCCATCAGCTCCAAGCATTTTGTCCACAACATCCAAATCATCTACAGTAACTGAAACAACTGGAGTAGTAACAACAACTGAGACAGTTACTGAGAACGAACTGAGCACTTCTGAGACAACGTTGTCCACCACCAGGCCACCGAAGGTGGTAACAACTGGCCAAACAATCCAGCCGACAACTACAGCCACAACTACTTCAGAAGAAGGAACAACATTAGAAACAACCAAATCTACAATTTCACCAGTTGTTACTACAAATGTTTTCTACTTTTCTACATCCATGGAGACCTCAATTGCCCCCATTACAAAAACACTACCATTTTTCACTCTCACCATTCCAG[T/C]GACTACAGACTCCTCTCTTTTCTCAACTACCTCAGAGTTTTGTTGCTTTGTGAATGAGACAAATTTCCATTCAGGTATCAACACATTATTTGCTCCTGTTTTTCTTTTGAGTATTTGATAACTTGAAACTGAAAATGTCTGAATTTTATTCTCAGGTGATATCATTTATAATGTTACCGATGGCTTTGGTTGGTGCTTCACTGCATACTGTGATGAAAGTTGTAATATCGTGAAGATTTCAACATCTTGTGTAACCAGTCCTTCACCATCTATTCCTCCCGAAACAACCACGTATTCTAGTTCATCAACAGCAGGCACAAATGAGCCAGAGACAATAATCTCGACAACTAATACAATCACTGAAGAAACTACACCCTCTCTGCCTAGGTGTGACGCCATTGATCCACCTAGACAGGTACATTTTTAAATAATCTGTTTTTTTTATATGTGAAATGTCAATGGGAAAACAAAATCTAAATGCATTGTACCTATAGCCTGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41087
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000127798 | Nonsense | 4673 | 4915 | 48 | 55 |
Genomic Location (Zv9):
Chromosome 7 (position 74867292)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 72049654 |
GRCz11 | 7 | 72298945 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGATTCACACTTACCCCAGTCATAACTGCAGATGCCTGCTGTCCAGAGTA[T/A]ACTTGCTGTGAGTATATGATCCACTTATTCTCAGTAAACACTGCAGTTCT
Long Flanking Sequence:
TTCTTGCCATTTGTTATTTGGTCAAATTATGATTATTTTTAAATAACCTGACAAGATTTATTGGTTTTGCAGCCCAATGAGGCTTGGTGGAGTGAATGTCAAAAGTGTGAGTGTGACAGCCAAACACTGACGGTCATTTGCCGGCCTGTAAACTGTCCTGTTTCACCACCTATTACCTGCGATAAACCTGGACAAATGCTTATCACAGTAGCAACAGTCGACTGCTGTGAGATCCAAGATTGCAGTAAGTTTTAGAACAGATCATACCACATAACATGTTAAGTAATATTAATTTAATAAATTTCATAAGCAGTATTTCTCCACTATTAAGCTAGAACCAAAAAAGAAGTCTAAAGAAATAATGTGGAATTACTTAACAATAATGTTAACTATCTGTCTCCAGCTTGCAATTCGAGTCTGTGTCCTACTCCACCACAGCAATGCCAACCGGGATTCACACTTACCCCAGTCATAACTGCAGATGCCTGCTGTCCAGAGTA[T/A]ACTTGCTGTGAGTATATGATCCACTTATTCTCAGTAAACACTGCAGTTCTTCGATGTTGTACGTTGCATTCATTCATTTGTTATTGTCTACAGCACCCATGGAAGTCTGTGTCCAAAATAACACAGTATATCAGGTACAACAAGTTAGGATTGGTTCATAATAGAAATATGTTTCTTAGAAAATATCTAAAACACCTTTATCCCCTTTATTTAGCCCGGCTCGAACATACCAAGTGATGATCCCTGTACGCAGTGTCTGTGCGGACAGGACACTGATCCTGAAACAAATCTTCTTGCTCCAGAGTGTCATTCATTGGCCTGCATGATGTACTGTCCTGAGGAGGTATGGGATATTTAGATATGAATGAAAGACTAGTTCTGTTGGTTTATAAATGCTGCTGTTTAAAAATAATCAAACCTGTTTGAACCAAGGTGTCCTTTAGGTCAAATATTGATTCGCTGACTGTTCTCACTGAATAAAAAGCTGAACTTTCATGACC
Associated Phenotype:
Not determined