ZMP

grn2

Ensembl ID:

ENSDARG00000088641

ZFIN ID:

ZDB-GENE-050522-264

Description:

granulin 2 [Source:RefSeq peptide;Acc:NP_997921]

Human Orthologue:

GRN

Human Description:

granulin [Source:HGNC Symbol;Acc:4601]

Mouse Orthologue:

Grn

Mouse Description:

granulin Gene [Source:MGI Symbol;Acc:MGI:95832]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa13899	Essential Splice Site	Available for shipment	Available now
sa43332	Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa13899

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 > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000051970	Essential Splice Site	None	147	1	5

Genomic Location (Zv9):

Chromosome 19 (position 41159381)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	40611919
GRCz11	19	40199039

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

ACAGACAGCAGCAGAAGCATCCCRAACAGAAGGAAAMCCAGCCAGAAAGG[T/G]AAATATTRCTATCACTCTCAGCAAATTTGCTTTGGGAAARGTAAACTATR

Long Flanking Sequence:

AACATTATTGACTTCTGTGGAAATGGTCATCTGATTTATGTACAATGCAGTTTGTACAGAATTATTTTTTGTCTTTTACTAGATATATAATATGACAAACTTGCTCTTTTTACCAAATAAAGTGAATCTAATTGGATTTGCATTTTAAACATTAAATAAAAGTTAAAAAGAAATTATTTTTCATTTCATATATTAAGGTTTTAATTATAATACTCCCAAAACAATTCCGCAGAAATCCGCAGACTATTACCAAAATTCTCAGCAGAAATAGCAAAAAACGTCCGCAGATTCCGTCTGGCCCTAGGCATGGGTCACAATTTGACTGAAGAGATTTCCTGTTTTTACAGTTGGTATAAATCCCAACAACAAATCTGATGAAGTTTCCAGTAATTACACTGGGAGGAGTCTGTCTACAAATATAAGAGGTATAGAATCACCGGACAGAATGACACAGACAGCAGCAGAAGCATCCCGAACAGAAGGAAAACCAGCCAGAAAGG[T/G]AAATATTACTATCACTCTCAGCAAATTTGCTTTGGGAAAAGTAAACTATGTCTAATATCTAATTCTAATAGGTAGTCTTATATACTTAGTTACCTTAAAAAAATAATAAATAATAAATAAAAAAAAAAATAATAATAAATAAATAAATAAATAAATAATGGTAAAATTAACATTAATAATAATAATAATAATAATAATAAGTAGAAGAAGAAGAAGTAGAAGAAGAAGAAGCAAAAAATAAAACAAAATTTAAAAGTTCTAAAATAAAATAAAAAAATAAAATAAAATAAAATAAAAGGATCGCCTCAAAGCAAGAAGGTTGCTGGTTCGAGCCCCAGCTGGGTCAGTTGGCATTTCTGTGTGGAGTTTACATGTTCTCCCCATGTTCGCGTGGGTTTCCCCAGATTAATAAGGGGACTAAGCCGAAAAGAAAATGAAGAAATGATAAAAAAATAAAAAAACCTGATATTACAAATGAGAGATCTGTACTTATTTATGAT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa43332

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:

A > T

Consequence:

Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000051970	Splice Site	None	147	None	5

Genomic Location (Zv9):

Chromosome 19 (position 41157096)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	40609634
GRCz11	19	40196754

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGAAGTTTTGCTGCAAGACTGGAACTGGCCAGTGGGGCTGCTGCAGCGGT[A/T]AAACAGACTTCATATCACTGTATTAATAAGCATGGCTAATCAAGAAGCAT

Long Flanking Sequence:

AAAAAATATAATTATAAAGATTTAGTCAAATGCACACTTCAGTGTATAAAAAACCAAACTGAACAATTAGCTCTTAATGTATTTGAGAAGTCACTGTCGGTAATAACAAACAACAATTTTTTTTACATAATTTTTATAAAATAAAGCCATCAAGTAAAGCTTAACTCACACACTTTTTCTTGAAAATAAATCAAAAACCAAAATATTACATTTTGCACCTGCTGCTTGCCTGATTATATTCATAAACTTGACTGCTTAAGGTTAAGATGATTACTAATCTTAAAAATAAGTTGACTTTGCAGCAAGTCAACACCACATTCTGTCTGTGTTAGTTTGAATTATGTGAGCTGCAATCATTTAAATTAGTCAGACTAATGTAATTCTTGTGAATGTAAATTTAGACCCAGGCTGAGACTGTCCAATGTGAAGGAAATTTCTACTGCCCGGCTGAGAAGTTTTGCTGCAAGACTGGAACTGGCCAGTGGGGCTGCTGCAGCGGT[A/T]AAACAGACTTCATATCACTGTATTAATAAGCATGGCTAATCAAGAAGCATAATATAATACAATTCACTTACAACCTGTATTTCTGTTGTTTATAGAGTTGGAGTTGTAAGCAAACAACCACTGTTACACTGGTTCACCTCTTACTGAAGACTGTCAAAATGCAAGAGGCTCCAAACTTCATTCATGTTTCAGGCTATAGTTTACTCTTACTGAATTAGTGTGAAATAAAAACTAAAAGAATTACTGTCAAAATGCACCGTCATTTAATAAATCTTTGTGATTAGTGGGAAAAGAGATTGTTTTTATTCATTTGTTTGTGGTATTTTTATGAAGTAATCTATGGTTATGAATAGTTCCTTTACTTGTCTCAACCATATACTGCACAACAGTTTTGGGATGACTGACGATATGATGACGGACAAATGTAATGTTGCGTTTCTGATTTAAATGAGAACGACTAACAAAACAATCACAACTGCTGCAGTCACATTTTGTAGTAT

Associated Phenotype:

Not determined