ZMP

rheb

Ensembl ID:

ENSDARG00000039162

ZFIN ID:

ZDB-GENE-000510-1

Description:

ras homolog enriched in brain [Source:RefSeq peptide;Acc:NP_001070216]

Human Orthologue:

RHEBL1

Human Description:

Ras homolog enriched in brain like 1 [Source:HGNC Symbol;Acc:21166]

Mouse Orthologue:

Rhebl1

Mouse Description:

Ras homolog enriched in brain like 1 Gene [Source:MGI Symbol;Acc:MGI:1916409]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa13338	Splice Site, Nonsense	Available for shipment	Available now
sa20694	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa13338

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:

C > T

Consequence:

Splice Site, Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000057223	Splice Site, Nonsense	111	184	5	8

The following transcripts of ENSDARG00000039162 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 6 (position 23377048)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	6	19632494
GRCz11	6	21692716

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

AAGTTGTGCAGGTTCTTCACGAMAAGCTTCTTGATATGGTTGGAAAGATA[C/T]AGTAAGTRTGGGTTGAACATATGGTCAAAATTATTACATGGGGCAATAAA

Long Flanking Sequence:

CATTTGTAAGTTGCTTTGGATAAAAGCGTCTGCTAAATGACTAAATGTAAATGTAAATCTTCAACTACACACACATCAGGGCCATACCATTACATAAACTGTGTGGGGGTAAATCTGGACTAAACCAAAATTCACTGCTTTTACTACACTTCGTATGTTTTGCAGAGCTAAAAACAAGACGCTGTGGCTAGTGTGGCACAGATGCTAGAACCCGCCTTTATGGTTTATGCATGCGCGACATCGTAAATTGTATGGCAAGTGTAAACGCATGAATTGAATATGGGTCACAATGAAAACAAAGTGTAAACAGACAAGCTAACAAATCAGATATAGGCAACAAATCGTAATTGGGCATCAAGACCTGACAGTGTAAACGGAGCCTTAGATGCTGATATAATTTTAGAAGGCATTGTATTGTAAACATAATTTTTTTTTTGTCTTCCAGTTTTGAAGTTGTGCAGGTTCTTCACGACAAGCTTCTTGATATGGTTGGAAAGATA[C/T]AGTAAGTGTGGGTTGAACATATGGTCAAAATTATTACATGGGGCAATAAAACATGTAGTCATAAATATTGCATTTTTACCCAGGGTACCTACTGTTCTAGTTGGAAACAAAAAAGACCTTCACATGGAAAGGTAAGCATATACTACATGTTCACCTGTTGCATCTTGTAATCTTAACCTTATTAATTATGATTAGTTTGCACATGTTGTTTCATTTGCACATACAATTTTAACATTAGCTTTAAATCAGATTTTCTTGACAAAAGGTCACCAAAGGTGTGTGTTTTCTGTGGTAAATATGTTTGCGTGTTCAAAAATTGCACTAATATCTTTAATAACATGAATCTGATTTGACATCTAGAGTTAAATGATTCCAAAGTCCTATCAAGGCAAGTCTGTTCATATGACTTTAATATAGCTCCTTATTCAATGGGAAAATACAAAAAATCTCAACACTTAACAATGCTGAAATGATTGGTTTCAGTTAATAGAAATTACAAG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa20694

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 > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000057223	Essential Splice Site	154	184	None	8

The following transcripts of ENSDARG00000039162 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 6 (position 23377935)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	6	19633381
GRCz11	6	21693603

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGATTCCTGGGGTGCTGCTTTTATGGAGTCATCTGCGAAGGAAAATCAGG[T/C]ATAATAAACTTTTGTTTTTGGTAGCTTCAATTTATTTTTACAAAACGTGA

Long Flanking Sequence:

AGGCAAGTCTGTTCATATGACTTTAATATAGCTCCTTATTCAATGGGAAAATACAAAAAATCTCAACACTTAACAATGCTGAAATGATTGGTTTCAGTTAATAGAAATTACAAGAACTGGTATTGGCTGATTAAAATATGATATTTAACCCTTTGATGCACTACATGGGTGTAAAGTGACCAGCCTTAGTTAATTTTTTTCCTATATATATTTTATAGCTTGTGCATCAAAGGGTTAAAGGCCATTTAGGTAAAAGAGAAGAACAATTACTATTTTATTCATAAAACTAAATCCCTTTTGTGGTTTTAGAGCACTAAATCATCTAAATTCAAACTCTCGGGTTCACACACATTGAAGGGCAGCTGCTGTTTGGAAGGAAATGCTTTTTCACACTCATCTATGTTTTGTTTTTCATAGAGTGATTAAACCAGAAGAGGGAAAGAAGCTAGCTGATTCCTGGGGTGCTGCTTTTATGGAGTCATCTGCGAAGGAAAATCAGG[T/C]ATAATAAACTTTTGTTTTTGGTAGCTTCAATTTATTTTTACAAAACGTGATGCATTTCCACAATGTGTATTGTGTATTTTATAAGAAAAACATATACATTTTACAGACGGCTGTAGAGGTTTTCAAAAGGATTATTCTGGAAATGGAAAAAGTGGATGGAAACGCCCCATCAGAGGAGAAGAAGTGTGCTGTGATGTAAGGCATGCAGTGAACTCACATGCTGAAGATACAAACCACATCACCATGCCATTAATTATAACGGATCAGTTGAATAACAGGTCCTTACCTGATGAATAATGTCCAAATACAGTCAGATTTATAAATCAGTGCTCTTCAAAACCAATGTCTGCAAACCTATCAACAATCGTATTGGGAATATTAATGCTATTTGAGGCTAGAATTACTGAGGAATATTACTTTAAAAATCTCCCATCCCTTCTATCTTCAGCTTTACTACGCTGACTGACATTTAATTTTACAGGTATTAACCTGTCTACATA

Associated Phenotype:

Not determined