ZMP

scin

Ensembl ID:

ENSDARG00000010728

ZFIN ID:

ZDB-GENE-060503-6

Description:

adseverin [Source:RefSeq peptide;Acc:NP_001038583]

Human Orthologue:

SCIN

Human Description:

scinderin [Source:HGNC Symbol;Acc:21695]

Mouse Orthologue:

Scin

Mouse Description:

scinderin Gene [Source:MGI Symbol;Acc:MGI:1306794]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa36864	Nonsense	Mutation detected in F1 DNA	Not yet available
sa39252	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa36864

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:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000046609	Nonsense	579	733	12	16

Genomic Location (Zv9):

Chromosome 19 (position 32594621)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	31761910
GRCz11	19	31349223

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTGAAGAAGAGGAAAAAGCTGCAAAGTACATGAGCGAGAAGCTGAACTGC[A/T]AAACCAAAATGGTTGTTGAAGGAAAGGAGCCAGGTAAAGCTAATATGGAT

Long Flanking Sequence:

GAACCTGGGAACCATTACAAGGATTAGTGAGGTGAGTCCTGGTTTGCACATGGAGACAACGCTGTTCTAGCACAATGTCCAAGACAAATGAGTTTGGTCATCAGAAAATGATAGATGGAGATAAATCAAATGTTCAAGTTAACCTGATCTTGCAAAATGGTGAAAGATGGTTAATTCACTAGACTGCAATGTGGTGGTAACCTGATAAATTTCTAGGTCATCTGTTTAGCACAGGAAGATTGTCTAGGCCAAGATGGTGGAGATTTGCCTGATTCTCCAAATCAGTGTTGACCATTTGTGGTTGGAGTGGCCTATTTTGATGTATCCTCTGAGTGTGTTGGTTTGTGGTCTAACAGGTGGATGCTAAAGCATCAAGTTTGAACAGCAATGATGTCTATCTGCTGAAGTTACCTCAGGGAGATGGGTACATTTGGAAGGGAAAGGGGGCCAGTGAAGAAGAGGAAAAAGCTGCAAAGTACATGAGCGAGAAGCTGAACTGC[A/T]AAACCAAAATGGTTGTTGAAGGAAAGGAGCCAGGTAAAGCTAATATGGATTCAATGACATACTTTTGACTAGGGCTTTATTATACAAGGAACATTTGTGATGTACAATATTGATGTTAAGTATTGCAGATGTTTTGATACTTCAACTTTGTCGCCTTCTCCTTTCACTTTCAGGACCGGTCTATCCAATAGCATAATAGCACTTAATGATAGTAAGACCCAATCTGATTGGTAGAATTTGGATAAACAATACACAAATGCTTGGCACATAAAATATTTTTAAATTTGATCACATCTTTGAGACCTGGACATTGAATGTACTGTAATCACAATAACATATTGTGATTACAGTGCATATAAACACAAAAACATTATTTATTGTCCAACTTTACTTTTAACTAAGATCATTAGACTTAAACACACTAATTCCTCATTTCCCCTTTAAAAGATGTCTTTTGGATGGCTCTGGGTGGAAAGACAGAGTATCAGACGTCTGGCTTG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa39252

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:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000046609	Essential Splice Site	677	733	None	16

Genomic Location (Zv9):

Chromosome 19 (position 32593247)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	31760536
GRCz11	19	31347849

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TAACTAATAAATATGATCATTTAACTTTCTGAATATTGTTGTACTTTTGC[A/T]GCAAAGATCTACATTGAGACAGACCCATCAGGACGGGACAAGGGGACTCC

Long Flanking Sequence:

TGGAGCCAATGCTGACCATGTATAACAGAACCTGTCTGTGCTTAATGATCAGATATAAACGGTCAAACTGAACTACTGATTGAAAACTGACTTTTACAACTATAGATCGAAGAAGTACCTGGTGAGTTTAACCAAGATGATCTGGCTGAAGATGATGTCATGCTGCTGGATGTCTGGGATTCGGTTAGACGCTTATCTCTCTTTATGACTTCCTCATGGATTATGTTTAAGATTCAAAGGTATCTCCTGCCTTGGGTGTAGCCATGATGACTCTTGATTTCCCTCTCAGGTTTTTGTGTGGATTGGGAAGGATGCCAATGAGGTGGAGAGGACTGAGTCTGTGAAATCCGGTGAGAAGCCTCAGGCACACATTCATTTGAGTCAAATTAAAGGGATAAACATGAAATTTAAAATACAAAAATCAACATTTTCAATATGTCGTCTTTTTGCTAACTAATAAATATGATCATTTAACTTTCTGAATATTGTTGTACTTTTGC[A/T]GCAAAGATCTACATTGAGACAGACCCATCAGGACGGGACAAGGGGACTCCTTTGGTTGTGGTAAAGCAGGGACATGAGCCCCCCACCTTCACCGGCTGGTTCCTGGCATGGGACGCCTCTCGATGGGACGGTGACCTCATGGCAAGAGCACTGAATTCCCTCTCTGTAGTTTAATGAAAGACTCAGTTCTGAACTCAATGGACTTCACTGGAAATATAAAACAGATGTTTGTTTATGGAGGCATGAAGAGTGAACTATATTAAAATATTCTATGAAAATCTTTTTAAAAATACTCCTCCACCCATCCTAAATACTCCAATTCACTTTTGATCATAAAGTTGTGCACATCATTTAGAAGGGTTCGCCCAGTTTTATTTCTTCTCTGAATTTCTGTAAGCATGATTTGAAAATTTATTATTAAAGAATCAATACACTTTTGAAAATGATTTTGTCTTTGTTAATGCAGCACACCAGAGCCCCCTAGAGACACAAGATACATT

Associated Phenotype:

Not determined