ZMP

ENSDARG00000089358

Ensembl ID:

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]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa25674	Nonsense	Mutation detected in F1 DNA	Not yet available
sa25675	Nonsense	Mutation detected in F1 DNA	Not yet available
sa19600	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa25674

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:

G > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000128834	Nonsense	509	5002	4	16

Genomic Location (Zv9):

Chromosome 1 (position 52843507)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	1	51714366
GRCz11	1	52343378

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CAGGAGAAACATCTGCCAAAACGACAGAGCTCTTAACAACAACTCCTACT[G/T]AAATATCAACCACTGCTATCGAAGAAACATCTACTGCAACATCAGAGCCC

Long Flanking Sequence:

CCACTACAGCAGCAGTAATATCTGCCACAACAGCAGAGCCCTCAACAACAATTCATACTGAAACATCTACCACTGCTGCAGAAGAAACATCTACAACAACATCAGAGCCCCCCACAACGACAACTGAACCATCCACCACAACAACAGAAGCCTCCAAAACAACACCTGAACAATCCACCACTACAGCAGGAGAAACATCTGCCACAACAACAACTGAACCATCCACTGCAACAGAAGAACTCTCCACAATAGCAGCTGAACCATCCACCAACACGGTAGAATTAACATCTACTACAACAACTCGTACTGAAACCTCCACCATCGCAATAGAAGAAACATCTACTACAACATCACAGCCCCTCACAACAACTGAACCATCAACCACTACAACAGAGGCCTCCACAACAACAGAGACTTCCACAACAACACCTGAACCATCCACCACTACAGCAGGAGAAACATCTGCCAAAACGACAGAGCTCTTAACAACAACTCCTACT[G/T]AAATATCAACCACTGCTATCGAAGAAACATCTACTGCAACATCAGAGCCCCCCACAACAACAACTGAACCATCCACCACAACAACTGAACTCTCCACAACAACAGCTGAACCATCCACCAGTGCGGTAGAATTAACATCTACTACAACAACTTCTACTGAACCATCCACCACAACAGAAGCCTCCACAACAACTGAACCATCCACCACAACAACAGAAGCCTCCACAACAACACCTGAACAATCGACCACTACGGCAGGAGAAACATCTGCCACAACAACAGAGCCCTCAACAACAATTTATACTGAAACATCTACCACTGCTGCAGAAGAAACATCTACTGCAACATCAGAGCCCCCCACAACAACAACTGAACCATCCACTGCAACAACAGAACTCTCCACAACAACAGCTGAACAATCCACCAGTGCGGTAGAATTAACATCTACTACAACAACTCCTACTAAAACATCTACCACAGCTGCAGAAGAAACATCTACT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa25675

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:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000128834	Nonsense	1743	5002	10	16

Genomic Location (Zv9):

Chromosome 1 (position 52851642)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	1	51722501
GRCz11	1	52351513

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CCACAACAACTCTTGCTGAAGAATCCACCAGTACGGCAGTAGTAACATCT[A/T]AAATAACAACATCAACTACAACAACAGAGCCTTCGACAACCACTCCTGCC

Long Flanking Sequence:

CTACAACAACAGCATTTACAACTACAACAGAGCCATCCACAACAATTCCCGTGGAAACATCCACAACTGCTGCAGAAGTAACATCTACTACAACAGAGCCAACATCAACTTTTGCTGAAGCATCCACCAGTACTGCAGTAGTAACATCTGCAACAACTACAACAGAGCCCACCACAACAACTTCTGGAACATCCACCACTGTTGCAGCAATAACATCTACCACGACAACAGAGCCATCAACAACAACAGCTGAAACATCTACCACTGCTGTAGAAGTAACATCTACTACAACAACAGAGCCCTCCACAACAACTCTTGCTGAAACATCCACCAGTAATGCACCAGTAACATCTACAACAACCGCATTTACAACTACAACAGAGCCATCCANNCACATTACTATGGAAACATCCACAACTGCTGCAGAAGTAACATCTACTACAACAGAGCCCACAACAACTCTTGCTGAAGAATCCACCAGTACGGCAGTAGTAACATCT[A/T]AAATAACAACATCAACTACAACAACAGAGCCTTCGACAACCACTCCTGCCAAAACATCCACCACTGCTACAGAAGTAACATCTACTACAACAACAGAGCCCTACACAACAACTCCTCCAGAGACATCCACTAGTACTGTAGCAATAACATCCTCAACGAAAACAGAGCCAGCAACAACAACAACAACAGCTGAAACATCCACCACTGCTGCAGAAGAAACATCTACAACAACCGAGCCCTCCACAACAACTCTTAAAGAATCATCCACCACGACAACAGAGCCCTCCACAACAACTATTGAAGAAACATCCTTGATAACTGCAGAAAAAACATCTACTACAACAACAGAGCCCTCAACCACTACAGCAGAAATAATATCTACCACATCAGAGCGCTTAACAACTCTTTATGAAACATCCACAAGTAATGCAGCAGAAACATCTACAACAAGTACAACAGAGCCCTCCACAACTCTTGCTGAAACATCCGCCACTACTGCA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa19600

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:

G > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000128834	Nonsense	3633	5002	16	16

Genomic Location (Zv9):

Chromosome 1 (position 52862583)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	1	51733442
GRCz11	1	52368446

KASP Assay ID:

2259-1151.1 (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AAGCAGAAACATCTACTATAAATACAGAGCCCTCCACAACAACTCCTGCT[G/T]AAACATCTTCCACTGCTGCAGAAGAAACATCTACTACAACAGAGGCCTCC

Long Flanking Sequence:

TACCTTTTTGTTTAAGTCATCTTAAATTAAAAAAAAGTTTAACAAATATATATTTTCCATTAGAAATATCATCGATTACTGAACCAACAACGGAATACTCAACACCCACAACAACATCTGCTCAAACATTCACCCCTACTGCAGCAGAAACATCTACAACAACAGAGTCCTCCACAGCAGAGGCCTCCACAACAACTCCTGTGGAAACGTCTACTACTACCATAGCAGTAACATCTACTACAGCAACAGAAGCTTCCACAGCTCCGGCTGAAACACCAGTGACCTCCACAACAACTGGTGATGAAACGTCCACAACTACCAGTGGAGTGAAATCTTCTACGACAACAGAGTATTTAACAACAACTGTGGAAACATTCACCACTATAACAGATATTCTATCTACCACAACAGAGCCCTTAACAACTCTTAATGAAGCATCTACCACCACTGAAGCAGAAACATCTACTATAAATACAGAGCCCTCCACAACAACTCCTGCT[G/T]AAACATCTTCCACTGCTGCAGAAGAAACATCTACTACAACAGAGGCCTCCACAACTCTTGAAGAAACATCGACCACCACTGAAGCAGTAACATCAACCACAACAACAGAGGCCCCCACAACAACTTTTGCTGAAACATCTACCACTGCTGCAGAAGAAACATCTACTACAACAACAGAGGCCTCTACAACAACTTTTGCTGAAACATCTACAACTGCTGTAGAAGAAACATCTACCACAACAACAGAGGCCTCCACAACTCTAGAAGAAACATCCACCACCACTGAAGCAGTAACATCAACCACAACAACAGAGGCATCCACAACAACTTCTGCTGAAACATCTACAACTGCTGCAGAAGAAACATCTACCACAACAACAGTGGCCTCCACAACTCTTGAGGAAACATCCACCACTACTGAAGCAGTATTATCAACCACAACAACAGAGCCCTCCACAACAACTTCTGCTAAAACATCTACCACTGCTGAAGAAACGTCT

Associated Phenotype:

Not determined