ZMP

si:dkey-197c15.6

Ensembl ID:

ENSDARG00000079401

ZFIN ID:

ZDB-GENE-060810-147

Human Orthologue:

HARBI1

Human Description:

harbinger transposase derived 1 [Source:HGNC Symbol;Acc:26522]

Mouse Orthologue:

Harbi1

Mouse Description:

harbinger transposase derived 1 Gene [Source:MGI Symbol;Acc:MGI:2443194]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa24444	Nonsense	Available for shipment	Available now
sa30044	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa24444

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Order Allele From ZIRC

Mutation:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000112777	Nonsense	71	395	1	2

Genomic Location (Zv9):

Chromosome 24 (position 7939569)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	24	7796861
GRCz11	24	7826180

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GGACTGGACGATCACTTCCTTTCACGCTGGTTACATCTCAACCGACAGTG[T/A]CTGCGGTTCATCATCGATTTCATCCAGGCCCGTTTTAAAAAAGACATATT

Long Flanking Sequence:

TGCCTCTCATTCATTTCGTGTTTTTTCGTTTGTTTTGAAGGTAAAGTGTTGGCTTTTCTTTCCAAATTACGTAAACCAAACGCAGATGAGATGTTTTAAGTACTACCCGGTCGTCATTCCATTCAGTTAATACTTTATTTTCATGGACTAATCTGATGTTTGAAGATACTGACGCTTTATGGTCCAGTTCACGCGAAGTTTTCTTGTAGACAGTAATCGAGATAACGTTAGTCAACTGAAACACAACCCAGAGGAGGACTTCAACAGTTTCCCCCCCTGCTGCTCATAATGTCTTTAGCTGGTGCGCTGTGGTTTGCAGTTCAGGATGATTTATTAACAAATGGTGTATGTAACAACACAACATCATCCAACATCAGCAACAAAAAACCAGACAAACAGCCCAGCACCAGCGAGCCCATCTCTGCTCCCGAGATCCACTCTGTGCTGGGCGGACTGGACGATCACTTCCTTTCACGCTGGTTACATCTCAACCGACAGTG[T/A]CTGCGGTTCATCATCGATTTCATCCAGGCCCGTTTTAAAAAAGACATATTTGCGTCCAGCCACAAGCCGAACTTGTCCGAGGCCAACATTCTGGCCGCACTTGCCTACTACGCACAGGGGTCTCTGCCAAATAAAGTCACAGACCGTCTGAGAATCGATCAGAAAACAGCATGCGAGGCGGTGAAGGCCACCACCAAACTCTTATCAGACTTAACCCCCGAATTCATCACATTCCCGAACAGTTATAACGACCGCATGGGTGCCGCACAAGCCTTCAAGAACCTGAGCGGCATCCCGCATGTGGTGGGAGTGTTGGGGTATTTGCACATAAGGGTGAGACCTCCCGTCTTGGAGGAACGCATGTATGTGAATACTCTGGGTTATCATTCAATCATGGTGCAGGTCATATTCGACGCGGACGGGAATCTCTTTAGTGTGGAGCAGTGCTGTCCTGGGGGAACTCCTGAACACTCTGTTTGGGAAAACTCGGACATTGGCAG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa30044

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 > G

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000112777	Nonsense	142	395	1	2

Genomic Location (Zv9):

Chromosome 24 (position 7939357)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	24	7796649
GRCz11	24	7825968

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GAAAACAGCATGCGAGGCGGTGAAGGCCACCACCAAACTCTTATCAGACT[T/G]AACCCCCGAATTCATCACATTCCCGAACAGTTATAACGACCGCATGGGTG

Long Flanking Sequence:

GTAATCGAGATAACGTTAGTCAACTGAAACACAACCCAGAGGAGGACTTCAACAGTTTCCCCCCCTGCTGCTCATAATGTCTTTAGCTGGTGCGCTGTGGTTTGCAGTTCAGGATGATTTATTAACAAATGGTGTATGTAACAACACAACATCATCCAACATCAGCAACAAAAAACCAGACAAACAGCCCAGCACCAGCGAGCCCATCTCTGCTCCCGAGATCCACTCTGTGCTGGGCGGACTGGACGATCACTTCCTTTCACGCTGGTTACATCTCAACCGACAGTGTCTGCGGTTCATCATCGATTTCATCCAGGCCCGTTTTAAAAAAGACATATTTGCGTCCAGCCACAAGCCGAACTTGTCCGAGGCCAACATTCTGGCCGCACTTGCCTACTACGCACAGGGGTCTCTGCCAAATAAAGTCACAGACCGTCTGAGAATCGATCAGAAAACAGCATGCGAGGCGGTGAAGGCCACCACCAAACTCTTATCAGACT[T/G]AACCCCCGAATTCATCACATTCCCGAACAGTTATAACGACCGCATGGGTGCCGCACAAGCCTTCAAGAACCTGAGCGGCATCCCGCATGTGGTGGGAGTGTTGGGGTATTTGCACATAAGGGTGAGACCTCCCGTCTTGGAGGAACGCATGTATGTGAATACTCTGGGTTATCATTCAATCATGGTGCAGGTCATATTCGACGCGGACGGGAATCTCTTTAGTGTGGAGCAGTGCTGTCCTGGGGGAACTCCTGAACACTCTGTTTGGGAAAACTCGGACATTGGCAGACAGTTCAGCATATTTCAACACGGGCACACGTGGATCATTGGTAAGAACCATTGGGAACAACTAATAAACCTTTAGTTTTCTTATTTTACCTTAAATCCTATAGGTCAGGGGTTCCCAAAGTTTTCAGCCCACGACCCCCAAAATAACAACGTCAGTGACTCACGACCCCCACTAATTTCAAAGGTGGTTGTAAACACAAATGTTCAATGCA

Associated Phenotype:

Not determined