ZMP

si:ch211-80h18.1

Ensembl ID:

ENSDARG00000078522

ZFIN ID:

ZDB-GENE-070705-257

Description:

hypothetical protein LOC555593 [Source:RefSeq peptide;Acc:NP_001121804]

Alleles

There are 5 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa29129	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa36757	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa36756	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa29129

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 > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000108914	None	None	359	None	24
ENSDART00000122816	Essential Splice Site	148	638	10	41

The following transcripts of ENSDARG00000078522 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 19 (position 3673359)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	3169932
GRCz11	19	3110830

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CGCAAGTTACGATGGACAAGATGGGTCCAAATCTGAGATAGCCCCTCCAG[G/A]TACATGATGAATGAGTGAATGAATCAATGAACAAATGAATGAATGAATAA

Long Flanking Sequence:

TATTTGAAACCAGGATCTAGTTCTGCAACATTTTCCCTTAACAATAGTTTTCAAAATGAAATATGCTACACAAATGTGTAAATATTACAATAAATCTGGGCCTATTTCTAATATTGGCAATGCACAATAAATAAAAGCTAGTATTTAATTCAGAACATACTTATAATGTGGGCAGCGAATAAGGTTTTGTTGTGTAATTAAGCCGTGGTTGTGATATTGGATTACTGTTAGTGTTGAGACAGGTGTCTGGGTTTTATTACTGTAGAAAGAAAGGGCCCTCAGTAGTGCTCAAGTGTTTTTGTTTTTTACAGGAGGTAACGGTAGAGACGGGTATTCACATTCATCTGGCTCAAGTTCTCAAGGTACTGAATTCACCTGTGAAAAACAGGACTTTCTTTTTCTCTCTAACACATTTTCGTGCCTAATGGCTGTATTTATTTCACTTACAGACGCAAGTTACGATGGACAAGATGGGTCCAAATCTGAGATAGCCCCTCCAG[G/A]TACATGATGAATGAGTGAATGAATCAATGAACAAATGAATGAATGAATAAGTGAGTAAAGTAACAAGTGAGTGAGAGAGTGAATGAATGAATCAATCAATGAACTAATAAATGAATGAATGAGTGAGTGAATGAACAAACCAATGAGTAAGTGAATGAATCAATCAATAAATTAATAAACAAATGAATGAATGAGTGAGTGAATTAATTAATAATAATCAATCAATAAATGAATAAACAAATGTGTATATGAATGAATGAACTAACAAATGAATGATGGAGTGAGTGAATGAATGAATCAGTCAATCAATGAACGAATTAATGAAGAAATGAACAAATGTATTAATGAGTCAAACAAACAAATGAATGAACTAACAAATGAATGAATGAGTGAGTAAGTTAATGAATGAATCAATTAATGAACGAATGCATAAAGAAATAAACAAATGTATTAATGAGTCAAACAAACAAATGAATGAATGAGTGAGTAAGGTAATGAAC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa36757

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 > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000108914	None	None	359	None	24
ENSDART00000122816	Essential Splice Site	237	638	14	41

The following transcripts of ENSDARG00000078522 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 19 (position 3669573)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	3166146
GRCz11	19	3107044

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGCATGTATTTGTTCAGGGTCGGATGGATTCTCTCCACAATATGAAAATG[G/A]TATGTGAATAACAGGGTTAGTTCTTACTTTAAATGCTGTATGAAATATTA

Long Flanking Sequence:

AAAATAGTAAACGTTTAGTATCATTTACCATCAGACATTTTTGTTTTTAAATAGTTATGTTCCTTTTTTTAGAGTGTATGGAAACTTCTGGTTTCAACTGTGTATTACTGGATAAAATTAGGATGAAATGCATTATTTACGTTAAGAAGGATTATGATTGATATTGTAATTAGTGTGTTTTGCGTAAGCTAAAGGCTGAATGTTGGTGGCGGTTTGTCTTTTATGGACTTCATAATGTCAATCTGTCAGTGTCATCAGGTCAAGGGTCATCAGGCCACATATCAGCAGGTCATGGGTCAGTGATGTCATCAAGCCAGTCGTCTGGCAGGCCTTCAGCAGGACAGACATCAGACGCTGCAGGTGTCGTTTCATCCGAGGTCCAGCCTACAGGTGCTTCAGGTGCTTCACAACGACATGAGTATTTCAGTGTAAAAGGTATAATAATATCCATGCATGTATTTGTTCAGGGTCGGATGGATTCTCTCCACAATATGAAAATG[G/A]TATGTGAATAACAGGGTTAGTTCTTACTTTAAATGCTGTATGAAATATTAAAACAGATCTTGTGTTCGTCCATCAGGAGAAACATCTCAAGATGGATCTCAGATCGAGCCTCCAGGTGATGATACACATCATTTATGGAAATGTGTTCAGTTAAAAACAAGAATTGATTTCACCACTGTGTTATTTGTGTCTTGTGAATTCAGAAATCCCTGAGACAGAATCTAACGGTGAGTATTATGCTGTTTTAATGCACACACACACACACACACTGTCATTCTACAGTATGCAGAATGAGAGATTACGTTTGCATGGACACCAATTCTCTGATTTTAATACGATTAACACAATACTCTGATCAAAAATCGAATGTGTTATCAGAGATTTTTGACTACCTTCATCCCACTAAAAGTCATAATAGCACAAATCGAGTTAAGACGTATTCATATTTTATATTTATATTTTAGGTAATGGACATAAACAGCTACTGAATGGAGGGGAAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa36756

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000108914	Nonsense	95	359	7	24
ENSDART00000122816	Nonsense	374	638	24	41

The following transcripts of ENSDARG00000078522 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 19 (position 3663920)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	3160493
GRCz11	19	3101391

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTTGATAAGCGTCTCTTGTTCTGTCCTCTAGACTCTGCAGGACCGGATTA[T/A]CTCTCTGTTGACAATGGGAACGGTGATTATAGCCACTCAGTCAGTAAGTC

Long Flanking Sequence:

TAGATAGATAGATAGATAGATAGATAGACAGACAGATAAACAGATGGACAGACAGACAAAGAGATAGATAGATAGACAGACAGACAGATAAACAGATTAACAAAGACAGATATTTAGACAGACATATGGTCAGACAGACAGATGCATAGATTGACAGACAGACCAATAGACTGACAGACGGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGGGTGTGGGTGTATGGATGGATGGATGATGGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATCTGTCTTGATAAGCGTCTCTTGTTCTGTCCTCTAGACTCTGCAGGACCGGATTA[T/A]CTCTCTGTTGACAATGGGAACGGTGATTATAGCCACTCAGTCAGTAAGTCAAGCACATCTGTTGACTAGCAGTAGATTAATAGTGTGCTGATATCTGGTTGAATAATTGCTTATGTCCTCAGGCACGTCTGATAATGGAGCACCATCAAAATTACCGGCCGATACAACAGGTAAACTGACTAAAGTACTTACTTTGAACTACTTACCAAAGTTCTTCATGCTCTGTCAGAGAGCATAAAGTTGAAACAGAAACTGAAATCTCAGACTGGTGATGTTTGCAGATTCATCAGTAGTGTTGGACACAGCGTCACATCCGGCTCATTCCTTCATAGACTATTCAGGTAAGACACCTGGCTTAGTAACACTTAATCATTTTCTATAATAATTGTTATTAAGGGTGTCATGGTGGCGCAGTGGGTAGCACATTCACCTCACAGCAAAAAGGTTGCTGGTTTGAGCCTCAACTAAGCCAGTTGGCATTTCTGTGTGGAGTTTGCATG

Associated Phenotype:

Not determined