ZMP

si:ch211-11m18.3

Ensembl ID:

ENSDARG00000007737

ZFIN ID:

ZDB-GENE-041014-17

Description:

Protein zyg-11 homolog [Source:UniProtKB/Swiss-Prot;Acc:Q5TYQ1]

Human Orthologues:

ZYG11A, ZYG11B

Human Descriptions:

zyg-11 homolog A (C. elegans) [Source:HGNC Symbol;Acc:32058]
zyg-11 homolog B (C. elegans) [Source:HGNC Symbol;Acc:25820]

Mouse Orthologues:

Zyg11a, Zyg11b

Mouse Descriptions:

zyg-11 homolog A (C. elegans) Gene [Source:MGI Symbol;Acc:MGI:2446208]
zyg-ll homolog B (C. elegans) Gene [Source:MGI Symbol;Acc:MGI:2685277]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa31042	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa43405	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa31042

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:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000104112	Essential Splice Site	445	746	None	16
ENSDART00000129633	None	446	445	7	7

Genomic Location (Zv9):

Chromosome 20 (position 16227463)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	20	16287416
GRCz11	20	16186999

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGCTCTCTCTGTGCAGTGATCGTATCTTGCAGGAGGTTCCCTTTAACAGG[T/C]GACACATTGCACATGATCTATAATTCATTGCACACACATAAACATGAGTT

Long Flanking Sequence:

TTTACTTAATTACTAGTTTAATAAATTAAGCAAATGATCATGAAAATCAGAAGTGATTATGAAATGAGAAGATCTTTTTGGAAACTTGGATGAGCTTATTAACAATTAAAATGCACATCAAAATCAACCTTGGTTTAGAATGTTGCTTATTATTATATTGCAAGTCATCGCATTACATAACATTTTGCTTATTTAATACATATTTTTTTCACCTAACTAGAGCAGTAGATGAAATGAATATGACTGAATTGTATAATGATGGTTTAATGCTGCCAGGTTGTGTACTCGGTTACAGGAAACATAACTGCACACAAAAGAGCATTTGTAACATAGTGTTCCCCATGTCATGGTGATGCAGAACTTCTTGTGGTGAATGAGGAAGAGAATTCTAGAGGGTTTCACAGGTGCTTTGATTTCCTCTATTTTTTTTTCAGCTTCAGAAGAACTGTCTGCTCTCTCTGTGCAGTGATCGTATCTTGCAGGAGGTTCCCTTTAACAGG[T/C]GACACATTGCACATGATCTATAATTCATTGCACACACATAAACATGAGTTTATTTATATAGCACATTTCACACACAATAGTAATTCAAAGTGCTTTACATGAACAAGAAGAAAAGTAATAATAAATACAAAAAGTTTGAGAATTAAAAATGGGTTCAAATTACATAGGATTGATTTATAAATATATGAAGAGTTCAGATGCAAAAGCTGCGAAACGCCACTTCTGTCAAAAATGAGCTAATGGCATTGAGCGAATGATTAAGGAACGTAGTACATGTTAAACCAATATTTTCACTTCAAAGCATCAGCGCTTTCAGAAATGACAGTTTGTTTGCAAAAGCCTCTGAACGGCACTTGCCTTTGACCCCAAAAGCCACTGTGTCCCGACGACCAATCAAAAGAGGTAGAATGTTTTCAATGTAGCAGTGTGCTGATGCGCCAGCTTTTATGAGGAGACTGTTTTATTCAGATTTATATTTTAAAAGACAGAGTTTGATGAAT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa43405

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:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000104112	Essential Splice Site	549	746	10	16
ENSDART00000129633	None	None	445	None	7

Genomic Location (Zv9):

Chromosome 20 (position 16234377)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	20	16294330
GRCz11	20	16193913

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ACACTTCATCGAGAACCAGGGGCTGGAGCTCTTCATCAAAGTGCTGGAGG[T/C]GAACATTGATTAAATGTGATTGTAATCTGATAAAGCTGTCCTGAACGAAG

Long Flanking Sequence:

TCCACATTAACATGCAGATTTTTTTTTTTTTAACAAAATACTGTGCAGAAATAGTAAAAAATGTCTGCAGATTCTGTCTGGCCCTACTGATATCACAACAACTATATTAATAACTATTAATAAGCAGGAGTTTATTAAGGCCAAACTTAATAACAGCGAGAATTGCATCCTAAAATAAAACATAATCCAATTTGTCTTTGACAGTTGTCCACTGAGCAAACCGCACAGTTGGGAGCCGAGCTTTTTATCGTCAAGGTATGTTTTTTGGAAGAGACTTTTTCTAATACCCTTGAATGGTAAAACTAGCAAACACTCACTCTCAAACTGTCTGCTTCAGCAACTCCTGCATATCGTGCGTCAGAAAACGTGTCAGTCGACGGTGGACGCCACGCTGAAGTTTACCCTCAGTGCCCTGTGGAACCTCACAGACGAGTCTCCGACCACATGCAGACACTTCATCGAGAACCAGGGGCTGGAGCTCTTCATCAAAGTGCTGGAGG[T/C]GAACATTGATTAAATGTGATTGTAATCTGATAAAGCTGTCCTGAACGAAGCCCTCATTCCTGAATCTCTCTGTTTTTTATAGTCTTTTCCATCAGAGTCATCCATTCAGCAGAAGGTGCTGGGGTTACTGGTAAGAAATGTATCTTGTGTAGTTGTGTCTAGCATAAAAATACATCAAAATAGCCTAAAGTGACCTTAAATAAAAGATTACTTTATTAACTTTCACGAACTAATCATAAAAAAAATGTATTATGGATTCATGTTTACCTTTTTATTTAAAATCAAATCATCATGTTTAAATGATTTCCAGAGGTTTGTGTAACCCTAAAGTTTGCTGTAATGTGCTAAAAAATCTACTTTGCTTCACACAAATAAACATTTAAAATGTATTAAGATAGGCAGCAAACTGGCTCAGTGGTTAACACTGTCGCCTCCCAGCAAGAAGTTCGATGGTTTAAGTCCTGGCTAGGTCAGTTGGCATTTCTTTGTGGAGTTTGCAT

Associated Phenotype:

Not determined