ZMP

si:ch211-288d18.1

Ensembl ID:

ENSDARG00000011088

ZFIN ID:

ZDB-GENE-060503-323

Description:

Novel protein similar to vertebrate USP6 N-terminal like (USP6NL) [Source:UniProtKB/TrEMBL;Acc:Q1LYR

Human Orthologues:

AC005702.1, AC053481.1, TBC1D26, TBC1D28, TBC1D3, TBC1D3B, TBC1D3C, TBC1D3F, TBC1D3G, TBC1D3H, USP6

Human Descriptions:

TBC1 domain family, member 26 [Source:HGNC Symbol;Acc:28745]
TBC1 domain family, member 28 [Source:HGNC Symbol;Acc:26858]
TBC1 domain family, member 3 [Source:HGNC Symbol;Acc:19031]
TBC1 domain family, member 3B [Source:HGNC Symbol;Acc:27011]
TBC1 domain family, member 3C [Source:HGNC Symbol;Acc:24889]
TBC1 domain family, member 3F [Source:HGNC Symbol;Acc:18257]
TBC1 domain family, member 3G [Source:HGNC Symbol;Acc:29860]
TBC1 domain family, member 3H [Source:HGNC Symbol;Acc:30708]
Uncharacterized protein [Source:UniProtKB/TrEMBL;Acc:A6NN51]
ubiquitin specific peptidase 6 (Tre-2 oncogene) [Source:HGNC Symbol;Acc:12629]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa34170	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa34170

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000098864	Nonsense	142	603	6	13
ENSDART00000145482	Nonsense	142	409	6	13

Genomic Location (Zv9):

Chromosome 7 (position 50487767)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	7	48758003
GRCz11	7	49030779

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATTTACAGAGAATGAAAGAGCAGGCTCAGCTTTACTCTCCAGAAATCAAG[C/T]AGATTGACCTCGATATCAACAGGACCTTTCGAAACCACATCATGTTTATG

Long Flanking Sequence:

TAACAAACCCTGTGCATCATGGAAACAAACACATACGACCCGTGCCATGCACGGACGCGGTCTCACCCATTTATTGTAACTCACAGCTTGGCAAGTCTGCCTTGCCTTCGGAAAGCACGTGCTCTCATGAGCGGATCTGTGCCATGTCACGGATTTTGATCTCGATTTTGATTTTGAAATTAGCTGACAAAAGTTCAAAATTATCCAGTTTTCTCCACAATTAAAGCTAACAGGTGCTAACGTTGTCTTAACTGATGCTCAACACACACAAATCTGTTCAAATCTCAGAAAATGTACTCCAGGGTGTCTCGAACATTTAAGTCAGAATTTGACAGGGGTATGAATACTTTTGGGCTTGACTGTATACCCATCTAACTTAAGAATTATAAACTTATGTTAGAAGTAAGATAACTTACAGTCAGCTTTATGATGAAGCCTTGTGTTTGTTTGATTTACAGAGAATGAAAGAGCAGGCTCAGCTTTACTCTCCAGAAATCAAG[C/T]AGATTGACCTCGATATCAACAGGACCTTTCGAAACCACATCATGTTTATGGATCGATTTGGTGTAAAGTAAGTAAAAGCATCTTCTTAAGCAAAGCTTGACTAATAAAATATTCTTCCCTCAGGCTTTCAGAGACATTAACTTACTCTGACTGACAAATAGCTCTTGAAGTTTCAGATAATGAGTAATGGCTTGTACTGTAAATATTTTATGTGAGTGCCTTAAAGTGATCCAAGATCCAAGCTTGATTTTGATTTTGCGTCTGTGCATATTTTCTTTTTCATTCAGTTGTCATGAACTAAACTGATGTTTGAAGGACTGATTTCAGAAGACCAAAATGGCACTCACAAAAAATTATGTGAAATGCTTTATTAACTTTACATTAACTTTACATTCCTGGTGGTGGCATGGAGAGACCCCCCTCATGATTGTGAAGCACTTTGGGTGTAGGCCATACAAAATAAACACGCTATATAAATAAACTTTACATTACATTACATT

Associated Phenotype:

Not determined