ZMP

treh

Ensembl ID:

ENSDARG00000077911

ZFIN ID:

ZDB-GENE-070912-84

Human Orthologue:

TREH

Human Description:

trehalase (brush-border membrane glycoprotein) [Source:HGNC Symbol;Acc:12266]

Mouse Orthologue:

Treh

Mouse Description:

trehalase (brush-border membrane glycoprotein) Gene [Source:MGI Symbol;Acc:MGI:1926230]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa23369	Essential Splice Site	Available for shipment	Available now
sa6532	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa23369

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
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Mutation:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000111309	Essential Splice Site	206	583	6	17

Genomic Location (Zv9):

Chromosome 18 (position 42261023)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	43866395
GRCz11	18	43859849

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTGAGACAGCCAGAGGAATGATTCTCAACTTTGTGTACTTGGTAGAAAGG[T/C]GCTTTCATTGTCTCCTATTTTAAAATGCTTGCAGACATAGAGAGCCCCAT

Long Flanking Sequence:

TGTCATCTATGTGATTTATGTGAAGATTGTCTCAAGAACACATTCGCACTTACCAATTTGTCCACAAGGTGGCAATTCTGAAATCGCCTGTTTAAAGAAGCACACTAATGTCTCAAGACATTTGATTTGCCAAAGATCTCAGATTAACTGCTTGAACAAGAAAAAGTGAAGACCTTTGTATAATGTTTATTGACAGGGTGGTTGTCACTTGGTACTGCAGAGATCATGGAAGTCAGTGGACTGAAAAGTGTGACAGCACCTTCACTCTGGTGCACATTGTACAAATAAACACTGTCATGGTGACTTAAAACAACAACAACACAGCAGCAGCCTGACAACTACTGTAACATCTTAATCCTGAGCTCTGTGCTTCAGTTAATTCCTCTTTTTCTTCTTCCTCTCTCAGGGACTCCTATTGGGTAATTAATGGTCTCCTTTTATCTGAGATGACTGAGACAGCCAGAGGAATGATTCTCAACTTTGTGTACTTGGTAGAAAGG[T/C]GCTTTCATTGTCTCCTATTTTAAAATGCTTGCAGACATAGAGAGCCCCATCATACACCCTGCGCAATAAGTGTATGGTGCTATTTGTTGCTTTTTTCAGACCAGTGCAACTGCAATATTCATGTTTTGCTCCACATGAATTAAATAGCACATTAATTTGTGCCAGTTTGTGGACTCATGGGTGTGCAGCTGGTGCTTTTTTCAGATTACTCATAACAATCCGCATTTGTAAAATGCTATTATAAATAGCAGTATCATTTATTATATGCATATTTATATTTGTTTTAATAAAAGCAAGTTTAGATTTGTCCACCTGTCGGGTTTTGGAGACATGCATGACCATATGGGGCACTACATGAGGACGTGTGTTTGGATATAACTCAGTTTTTTGAGCACACTTCATTATTATTGTTCATTTATTTATTTGCTCGAAATTAGAACTGAATGTAGAAATAGTTTTGAAACAAATCTTTGTGCTTAACAACCAAAAATAAATATTTA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa6532

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000111309	Nonsense	255	583	8	17

Genomic Location (Zv9):

Chromosome 18 (position 42259635)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	43865007
GRCz11	18	43858461

KASP Assay ID:

554-4898.1 (used for ordering genotyping assays)

KASP Sequence:

GCATGTGCTCGGTGGTTCAGGCAGGTTTTGCCAGCRCTGGAAAGAGAGTA[C/A]AGCTTTTGGATGCAGAATCGGTCGGTTGAYGTGRTGACGAGTGAACTGAC

Long Flanking Sequence:

AAGACTCTCCAGAAGAAAAAAAATATTGTAGGAAACACTGTGAAAAATGATTGCTCTGTAAAACATCATTTGTGACTTTAACTGTACAAAAGTTTCAAATATAATCCATTAAATAGCAAAAAAACAACTGAATGAAAATCACCTCACAATCATATTTTCATTTCCCAAAAGTCATTTTCTTGACAAATTATTGCATCAGTTTATGATATTAAATTCTTTATCATCATCATTATCTGTCCTCTCCGCCTCCATTCAGATATGGCATTGTCCCAAATGGTGGTCGTGTTTATTATGAGCGGCGCAGTCAGCCTCCATTTCTTCCTCTAATGGTGGAACGCTTCTACGAGGCCACCGGAGACAAAGACTTCCTCAGGTAACCTTTTCAGCTAAATTGGCCTCCTGCAGGTCTGTTGAATATTGAGTTGCTGCGCTGAATAACACCTCTGCTCTGCATGTGCTCGGTGGTTCAGGCAGGTTTTGCCAGCACTGGAAAGAGAGTA[C/A]AGCTTTTGGATGCAGAATCGGTCGGTTGATGTGATGACGAGTGAACTGACTCACATCCTGAATCGATATAATGTGCCGGTGGACCATCCCAGGTAAAAGCACTCGTTGACACTCAGTCACACTGAAAGAAAACATTAATAATGAGAAACTATTAATAGCATATTGAAATAATGTCAGTTTGTAACCTTGTAAATTAATCAATTGAGAAAATTAAGGCCCTTAAAATATATTAAAAAACCTTTTACATTTTATTCAAAAAGCTTGACTTCAAGTTCAAGAGCTTCAATTAACACTTTTGCCCAATTAATTTGACTTAATTTGACTACTTTATTATTATTATTATTATTTATTTTCGGCTTAGTTTCTTTATTAATCAGGGGTCGCCACAGCGGAATGAATCGGCAACTTATCCAGCATATGTTTTGCGCAGCGGATGCTCTTCCAGCTGCAACCCATCACTGGGAAACACGCATACACACTTATTCAAACGAACACTACGA

Associated Phenotype:

Not determined