ZMP

zgc:91835

Ensembl ID:

ENSDARG00000008170

ZFIN ID:

ZDB-GENE-040704-42

Description:

drebrin-like [Source:RefSeq peptide;Acc:NP_001002201]

Human Orthologue:

DBNL

Human Description:

drebrin-like [Source:HGNC Symbol;Acc:2696]

Mouse Orthologue:

Dbnl

Mouse Description:

drebrin-like Gene [Source:MGI Symbol;Acc:MGI:700006]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa41734	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa44732	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa41734

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:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000025691	Essential Splice Site	311	496	10	15

The following transcripts of ENSDARG00000008170 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 10 (position 43731611)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	10	42538106
GRCz11	10	42366486

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GAGAAGCTTGGTCAATGATGCAACATCTTCTCCATCAAGCAGCCGACAGG[G/T]TACAACTAAAACTTCTCCAGCATTTCATAACCCAGAACCTCATTTTTAAA

Long Flanking Sequence:

GAGTTTTTTTAGTAAAATATTACTAAAAATACTGCCTGCCTTAAAGGGATAGTTCACGTCACAATTCATTCACCCTTTAGCTCTTTCAACCCTGTTTGAGTTTCTTTCTTCTGTTGATCGCAAAAGAAGACATTTTGAAAAATATTGGAAACCGGTAACCATCGACATCCATTGTATTTGTTTTTTGCTACTACGGAAGTCAATGGTTACCGGTTTTCAACTTACTCCAAAATATTTTATTTTGCATTTAACAGAAGAAACTCATAAAGGTTTGGCACCACTTGAGGAAGAACAAATAGTGGGTAAATTTAGATGTTTGGGTGAACTACCCCTTTAAATTAAAGTGTTATCATTATTCCTTACATATTCTACCTTTTCTGTCCCCCAGGAGGCGGCATCGATTATCTCCCAGCGATCCACCAATCCCAGAGAGCTGTTTATGAAGAAAGAGAGAAGCTTGGTCAATGATGCAACATCTTCTCCATCAAGCAGCCGACAGG[G/T]TACAACTAAAACTTCTCCAGCATTTCATAACCCAGAACCTCATTTTTAAAACATGTGCACAATCCTTTCATCCCGGAGTTCAGATGACTCTCATCTTTTCCCCTTAGGTCAGCTAAGAAGCCCATTTTTATCCCAGCAAGCAGTAAGCACTCCCAGTGAGAGCAGATCTCAGCCTTTATCTCCTCTTCAGCCTGTGGCTTCAGTTTCACATGTTCCAGCTAAAGTCTCTCCTGTGCGCGAAACTCAGACTTTCCCAGTTAAAACCGCAGGTGAGGATGAGATTGCAGGCACATTTCAGAGATTGCCTGTTCATTGTTCTTAAAGGGGACCTATAATGCTGAAATAATTTTTATAAGGGGGTTAAACACAGTTGTGTGGCAGCAGTGTGTGAATATAAGCAGCTTCTAATAGTAAAATGTATTCATTTTATGTTTTATAATCAGACTGGATAGAAACAGTCTGCAGAAACACTTTGATTGACATTCTCCCTTTGTAGGTGT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa44732

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:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000025691	Essential Splice Site	451	496	14	15

The following transcripts of ENSDARG00000008170 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 10 (position 43735522)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	10	42542017
GRCz11	10	42370397

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGGCGACAACCAGAACATCTGCGCAAGAGCACTATATGACTATCAGGCTT[G/T]TGAGTGCCTTTTACTGCATCATATAAAGTCATTAATTTCCCTTCGGCTTA

Long Flanking Sequence:

ATATAGAAATCTGATACATGCTAATATATGCAAATCACATATTTAACATACCAGATATTGTTTTTATTTGACAGGCATACAGTCAACATATATTTCAAAATATTGCAAAAATGTTGTTTATATATTCATTTTCAATCATTAGAATTACAAACATGCACAAATGAGTTTAAATACAGTATATGAACTATCCTTTTTATAGGCAGTATATGTTCATATTTAGCCACATACAGTGTTAGAATTTTATATAGGCCATAAAACACACAATTAATTGCTTAATTTTTAGACAATTAATACAGTTTTATAATCAGCCCTACTTGCTTGACATGGTAGCCATTATTTGTTGTAATCTTTCAACTGCATGTCAAATATTGTGCACCGAAAAGATTCTTGTCATGTAAGTGTCATTGTATATTTGAAGGATTTCCAATCTCCGGCGGATGAAGAGGAGAATGGCGACAACCAGAACATCTGCGCAAGAGCACTATATGACTATCAGGCTT[G/T]TGAGTGCCTTTTACTGCATCATATAAAGTCATTAATTTCCCTTCGGCTTAGTCTGTTTTTCAGTGGTCACCACAGCAGAATGAACCGCCAACTAATCCGGCATATGTTTTACGCTTAAGATGGTGCTAAGTGTCAGTGGCGCCTGCAGCTGTACGCACTGTGCGTAGCTATCATGAGAGGGCTGGAATTAATGCCGGTTTTTTATTTATTTATTTGTGACATCATTTAAATTGATGATTAAACAGTATACACTACAGCTGCCTGCTTTCCCTCTATTGTGCCAAATCGCTGCAGCACTGCATTTGGTAGCACAAAAACTCGTTTTTGAGAACTTGATCAACAGCTACATGCGCTGCTGAAAGACTTTTTTTCTGCTGCGCATCGAATAAAGACACACTTAACATCATCGATGTCCACAATACATCCTATATCCATGAATCAGGAACATGCAGACTCTGAACAACGAGCAAATAACTGCACTTCAGTCAAGCCAGATGGCT

Associated Phenotype:

Not determined