ZMP

zgc:113263

Ensembl ID:

ENSDARG00000045842

ZFIN ID:

ZDB-GENE-050306-34

Description:

hypothetical protein LOC503753 [Source:RefSeq peptide;Acc:NP_001013349]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa6046	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa30606	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa6046

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
ENSDART00000067371	None	None	430	None	8
ENSDART00000123375	Essential Splice Site	937	1111	16	20

Genomic Location (Zv9):

Chromosome 4 (position 5232176)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	4	5350357
GRCz11	4	5358927

KASP Assay ID:

554-3883.1 (used for ordering genotyping assays)

KASP Sequence:

CAGTGCCACTCGCGTATCAAAAGACTCAAGTCCCAGTTCTACTACGATGG[G/A]TGAGCGAGATGTGACTAGTATTGTRTAMTCTAATTGCATGCATATACAAT

Long Flanking Sequence:

ATTTTGGTCTGTCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATTTACCATGCCATTCTTTTATCTACCCATCCATTCAGCTTTTCTGTCCTTTTTGATTTCATCCATCCATCCATCCATCCTCCTATAAACAGGCTTTATTTCAATGTATTTCAATAGATGTCCAATGTGATGTATTGCTTTGATGTTTGTTTCTTCCCTAACCCAAAACTCGTCAACCTTTTAGATTACCAGCCGACTGCCATGGTAGCCGTTTCTGAATCGGGCAGGAAAATGACCTGGTCAGACCAGGAGACGCTTGCCCTGCTGGAGATCTGGGGTGATGACCGTGTGCAGCACAGCCTGATGTCCTGCCCTAAAAACAGGCACATCTACAGATATATTTCTAAGAGAATGATTGCATTGGGCTTCAACAGAACGGGCGTGCAGTGCCACTCGCGTATCAAAAGACTCAAGTCCCAGTTCTACTACGATGG[G/A]TGAGCGAGATGTGACTAGTATTGTGTACTCTAATTGCATGCATATACAATATGTTGTCTAGTATGAAACTGATATTATATATAATGTATTCATGTGTTTTTCAGCAGGGAGGAGTGTAAATTTTATGATCAACTGGAAAAGATTCTTTTAAAGGACAGAACGTCTGAGGACAAGGAGATGAGTGAGCTGGAGTCCATAACTGATTCGGATTCAGGTATCTGTCTGTAAAACTGGCCACACTCATTTTTTTATTTTACTTTTAAGATCCAATAGAGAAATATAGAATTTGTCTACTCTACATTAATCTGGAGACCTTTGAAAATGTCATTTATTTTCTGATGATGCATTTACTAGTAATAGCAGCTTTCGAAGCATTGCTTCTTGAAGCTTTGGTTCCTTTACCAATCATTTGTTTCGAATCAGTGGTTCAGAGTATGCATTAAATTGACAAAGTCTCATCATTCCAATTGTTAGATTTTGCTGTATTTGGCTTAACTGTT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa30606

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
ENSDART00000067371	None	None	430	None	8
ENSDART00000123375	Essential Splice Site	974	1111	18	20

Genomic Location (Zv9):

Chromosome 4 (position 5234142)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	4	5352323
GRCz11	4	5360893

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GCTTACATTTCCCATCTCATTTACTCTTTTGAAATGTATTTGCATTTTCA[G/A]ACTCCCTCGCTCTCTCCAAACCTCTCACCACGGACGGGCCGAAGCTGGCG

Long Flanking Sequence:

TCTTTCACAGTAAACTGGGCTTTGTTACATTAAAACAGTTTCAAAGCATTTAGCAGATTCGGTAGTTCTCCACTAGAGGGTGATCAGTGTAATAATAATATCGTAAAATCTACATTAATACATTTCACTGGATTTACTGGATCTCGGATCAGTTTTATGGGGTTGTAGTAGGGCTGCACGTTGTTGGAAAAATCGGACATTGTAATATTTAGTTTTTGTGTGATAAATATCGTGATATACGGTATATACAATTTCACCAGATGACTTGAAAACTGCTATCTGGAAGGACTGCCTGCCTTTATCAGTGTCACACTATTTTCATTTCATTTTTCTGACAGCCTAGAGAACACTAGTTTTGACTGGAATGGTGTCCCTAGCATATGGTGTTTAAATGCCTTGAAACAGTGAATCATTTTGCAAAGCAATTGGTTTGTTTTGAAGCTTTAGAAAGCTTACATTTCCCATCTCATTTACTCTTTTGAAATGTATTTGCATTTTCA[G/A]ACTCCCTCGCTCTCTCCAAACCTCTCACCACGGACGGGCCGAAGCTGGCGTGGGGTGACAGCGAGACACACACTCTAATATCCATTTGGGGCAGCGATGGCATCCAGGAGAGGCTGAAAGGCTGCGTCAAACGTAAACCAGTTTTCCAGCAGATCGCGTTGATTATGGCTGAGAAAGGCTACAGCAGGACTGATGAACAGTGTCGCTCCAGGATCAAAAGACTGAAGGCCAGTTACCGCCAGCACCTTGACAATTACAGGTAAGCACAGTACATCACTGATGATAAAAGTGGAATATTTAAATGTTTAAAACTGTGAATGAATTGTAATTTTTGCTGTCCTCATCCCATAGGAATGAAGGAGAGCAGGTTGAGTGGAAGTTCTACAAACAGCTTAATAAAATATTTCAGAAATACCCTCTAGATGATACCGAAACTACAGTGCAGGAGACAAAGGCAGTTTGGAGGAAAAACCCAAGCAGGTCTGCAAAAGCACACAGCT

Associated Phenotype:

Not determined