ZMP

ranbp10

Ensembl ID:

ENSDARG00000062138

ZFIN ID:

ZDB-GENE-070705-86

Description:

Ran-binding protein 10 [Source:UniProtKB/Swiss-Prot;Acc:Q1LUS8]

Human Orthologue:

RANBP10

Human Description:

RAN binding protein 10 [Source:HGNC Symbol;Acc:29285]

Mouse Orthologue:

Ranbp10

Mouse Description:

RAN binding protein 10 Gene [Source:MGI Symbol;Acc:MGI:1921584]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa23301	Essential Splice Site	Available for shipment	Available now
sa39200	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa23301

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:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000089507	Essential Splice Site	524	604	12	14
ENSDART00000146261	Essential Splice Site	529	609	12	15

Genomic Location (Zv9):

Chromosome 18 (position 21788645)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	22018868
GRCz11	18	22007934

KASP Assay ID:

2261-2195.1 (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGCTCTGCCGCCAGTATGGCAAGAATGCCACTCACAAGAAGATGCTGCAG[G/A]TAGGAGGAATAGAAGGGGAAAAGGAGGATAAGCTTGAGAAAGAGATGAAT

Long Flanking Sequence:

TCACTCATAATACAGAGACATCTAGTAAAGGAGACAGGGCTGCAGACATTCACCTTTCTGATTGGGACCTTTTCCTCAATATTAAGTGCATAATTTGCAGTCTTGCATTCTTTTCTTGTAAGTTCAGACTTCAGAAGTGACAGAGTGTGTGTATGGTCACGTGATGTGTGTTTTCAGCTGTGTAGTGTGCACTGAGAACTTTTCAAAAATGCTAGGTGAAACAACAGTGTGGTTAAGGATCATTTTCATTCTAAAATGCCATTTTAAATCTAAAACAGATTAGTGTAAACGGGGCCTTATTATTGTAAACTTGCCTGTTTTTGAGGTGTGATTGTGCCATCTCTGCTCCTCTAGATGACACCTGCAGCTCCAGACAGCTGTGTGGAGGAAACCAGGCGGCCACGGAGAGAATGATCCAGTTCGGCAGAGAGCTTCAGACCCTCAGCGAACAGCTCTGCCGCCAGTATGGCAAGAATGCCACTCACAAGAAGATGCTGCAG[G/A]TAGGAGGAATAGAAGGGGAAAAGGAGGATAAGCTTGAGAAAGAGATGAATAGCTGGAGGCTTGAAATGATGACAGGGCTTGACACAGACGTTTTTGCCTGTGGTGTACATTCGAAGACTTTAAATGTTAAAATCTCTATGTTGTATCTGTCATTTTCTTGTAAAAAATAGCATTTTTCTTAGCCCCTTATGTTTATATTCAGTTTTTTTTATGTTAAAAGCAATAAAAAATAACCGATTCTTTGCCATAAATGTGAAATTACTAAATTAAGACAAGAGAACAAATTCATGGCATTTAGAGTTTTTTGCATCTGAACATTTGTTTCTAATTTGAAAGATTTAGAAGCTTTGGTATATCTCAAGTCCAGGCTTGGAACAAGTGTAGTATGAGTAAGGCCTTGATTACACCAAACACAATCTCTGCGATAAGAAGTGCCTTTTTAAAATGGTTTTCTAATGGCAATGGGTGTTTTCAGCGTTGTTTATGCACCCTGCGCACCT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa39200

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 > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000089507	Essential Splice Site	562	604	13	14
ENSDART00000146261	Essential Splice Site	567	609	13	15

Genomic Location (Zv9):

Chromosome 18 (position 21790589)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	22020812
GRCz11	18	22009878

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CCCATGCAAAGAGAGGCGATCTGCTCTGCTCTCAACAGTGCTATTCTGGG[T/A]AAGAAATAAGCTCTGTGAACATGATCGCTTTAATAGGCTTCACAATTTAA

Long Flanking Sequence:

GCACGTTACAAAACCACAAATTTTAGTGTGTGTTTTATGTGTGATTTTAACATGCAGTTAAACCTTTAATGCATTTCTATTTCTATAAGGCACAGTTTTGGCACCCAAGTACGTTAAATTCTTTGCACAGATCTATTTCTAGTCACAAATGAACTCATTTAGTTGTGTTATGCTGATATTGTGCAATTAAGTTTGATTGTCGTATTTTATATTAAATATCAGTAAAATGGTCTTTTGTTTTGAGACTTGTAAACTAATCTGTTCAGCTTCTCAGCCTCATGTTTGATGCAAATACACACTCAAAGTGCAAATACTGAGTAGCCCAGTTGGTAGCAGCACTCTTGCATCTTTTGTACCCACTTGCCATTATCTATGTTTGTGTTTTAGGATGCATTCAGTCTGCTGGCATATTCAGACCCCTGGAACTGCCCCGTGGGCCAGCAGTTGGACCCCATGCAAAGAGAGGCGATCTGCTCTGCTCTCAACAGTGCTATTCTGGG[T/A]AAGAAATAAGCTCTGTGAACATGATCGCTTTAATAGGCTTCACAATTTAAATGTGGCTGCAGATAAATGAGCCTGTAAGGGCCTGGTAATGTGGCCACAGGTTGTTACGGTCATTCATACATATTTAATAGTTGTAATGAATTCATATGTGTGATGTGTTCCCTCATTCAGAGTCTCAGAATCTGCCTAAACAGCCGCCTCTTATGCTGGCTCTGGGTCAGGCCACTGAGTGCGTGCAGCTGATGGCCAGGGTTCGCTCTGGGTCTTGCTCCTTCGCCAGAGTCGACAACTTTTTGCACTAGCACCAGTACAGGTGAGAACACTAGAGGTGATTAGAGAAATGAATTCTATTGTTGTTATTTTCAATATTATCATTACTTGGCTGCAGTTAGTATTCTGTTTTAATCCAATTCATACTATTTGTATTATGATATAATATAAAAAACATTATGAAAGAAAATACATCATCAAAAGTGTTTTATAAAATATTATTATATTAT

Associated Phenotype:

Not determined