ZMP

senp5

Ensembl ID:

ENSDARG00000060646

ZFIN ID:

ZDB-GENE-050208-772

Description:

sentrin-specific protease 5 [Source:RefSeq peptide;Acc:NP_001073666]

Human Orthologue:

SENP5

Human Description:

SUMO1/sentrin specific peptidase 5 [Source:HGNC Symbol;Acc:28407]

Mouse Orthologue:

Senp5

Mouse Description:

SUMO/sentrin specific peptidase 5 Gene [Source:MGI Symbol;Acc:MGI:2443596]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa13930	Nonsense	Available for shipment	Available now
sa5974	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa13930

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
Order Allele From EZRC

Mutation:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000085701	Nonsense	55	487	1	10
ENSDART00000148051	None	None	229	None	8

Genomic Location (Zv9):

Chromosome 22 (position 41964126)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	38932119
GRCz11	22	38918864

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GGCCCAACGGAAAGCMCCACATGCCTGGACACGAGCAGGTTTCGAAGAAA[C/T]GAGGCCGCAAGAAGAAGGAGATGGTGAGCCAGGGAGAAGTGGCCGCGGAG

Long Flanking Sequence:

TTAATTTGCTGCAGGAGAAACTGCGTCAATCTTCATCTAATAAGTGACCTGCGCCTCAGGAGTCAGTCTCGATTACTTTTCGATGAATCCCCCAGCCCTGATGTGCAGCACGTTACGCTCTCTCGTTACGCTCCATGTCTTAAAGATTAATTATTAAATTATCCTAATTATTAAATAATCTAATTCTCTTTGTTTCTTTAACAGAGCTTTTAAACATCCCACTTACACGAATATATCCAATCTGCCAAGAATTCAAGCTCTGGATGTCGATGTTGGACTCTTTCTAAAGACACAAACAGCGGTGCGAGGACCCCGGGAGGAATGGGGTAGAGATTGCGATGAGGGTCCCGGCACCAAACAGCTCTGATCAGGCAGAATCGGGCTCAGGTAAGATGCCTGAGAATGGACGCTCAAGGAGGAAACGCGTGCCAAAGACGTGCGACTGCTGCGGGCCCAACGGAAAGCCCCACATGCCTGGACACGAGCAGGTTTCGAAGAAA[C/T]GAGGCCGCAAGAAGAAGGAGATGGTGAGCCAGGGAGAAGTGGCCGCGGAGGAGGAGGTGGTCTGGAGCACGTCCGGAGTCCTCACGCTGGAAGCCGACGCTGTGACTGCTGAGATGGAGGAGACGCCAGATGCCAGAGGAAAAGCAGACTTCATCCAGTCTGAGAGTGTGAGTGACAGCACTGTGATGGTGAACGGTTTGGAGAACAGCGCTCATGATAACTGTACTGATCCCGCCAAAGAGAACAGCCATCCAGTCCAGGCTGCTTCTGCTCTACTCAATGACCTAATGAAGAAACCCTCTGATTCTGCCTCGGTGGCTGCAGAGCCGGACGCTTCTCCTCATAGTAATGCGATGGAGACTGAACCGTCCAGCTTGTGTGTTCGTGTAGACAAGGCCTCCTGGGACCATCACTACTGCAAATCCAACCCTGCGGAGAACAGAAGCGACTCTGCAGAGGCGTCAGGACCACCGCCTGCTGAGTTTACAAGCGAGGGCATC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa5974

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 > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000085701	Essential Splice Site	398	487	6	10
ENSDART00000148051	Essential Splice Site	140	229	5	8

Genomic Location (Zv9):

Chromosome 22 (position 41971088)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	38939081
GRCz11	22	38925826

KASP Assay ID:

554-3733.1 (used for ordering genotyping assays)

KASP Sequence:

CATCAACTTCTACGACTCCCAGGGCATCCTGTTCAAGTTCGCTCTGGACG[T/C]GAGTGTTTTMTGAGCCGTGTGTTTGAGCWGAATCRCCACNNNNNNCTGAG

Long Flanking Sequence:

AAACTCATCTGACTGTGTTTTCTTTGCCCTTTTCTAGGTTCATTTCTTCAACAGTTTTTTTTACCGACAGTTCGTAGCAAAAGGCTATGAAGGAGTGAGGCGGTGGACCAAAAAGGTGAACGTCACGGCATGCAGAACTTCACTTCACTGTTATTGTTTGATTATTGCATGATGGAGGGCTCTATCATACACACGGTGCAATATAGCGCAGGATGTGCTGCTATTTTCAGACCAACACAACTCTAGTTTTCCACCACGCTGTGGACTCATGGGTGTTTCGATCTAGCAAAATAATCTTGTTTTTCAGTATTTAATAGTCCTTTCGCAAAGTGTCTTATTGGGTGTGTGTTGATGTGCTCAGGTTGATCTGTTTTCGAAGACACTGATTCTGATTCCTCTTCATCTGGAGATCCACTGGTCGCTCATCACTGTGGACGTTTCCAAGCAGAACATCAACTTCTACGACTCCCAGGGCATCCTGTTCAAGTTCGCTCTGGACG[T/C]GAGTGTTTTATGAGCCGTGTGTTTGAGCTGAATCGCCACACTGAGCTGAGCTGACGTGTGTCTCCTCTCCACAGAACGTCATGAAATACATCATGGAGGAAGCAAAAGAGAAGAAACAACCGCTCTTTCAGAAGGGCTGGAAGATGCTCATCAACAAGGTCTGGACAGGAAGCTTCCTAAAACAGTCAATTCAGTTCAGGTTTATTTGTGCTGCGCTTTTCACAATGATTACTGTTTTAAAGCAGCTTTACAAACTTTGCTCATTACATTACAGTGCAAATCAGAAAAGTTAAGGTAATTAGTTACTTGACTTTATTAGTTAGCTAGTAACTAAGAGCTTTTAACAGTTAAAGCTGTGATATACAGTGGGGAAAGTATTCAACATGTCACGTTCTTTACTTTAACTTTAGCTTGTAAAGGGGTCTGTTCCATAACCCAAGCTTAGAGAAAAAGCCAGGCTTATTTTGGTAAGTCAGGTTTATTAATGTCGGATTTTCATG

Associated Phenotype:

Not determined