ZMP

sip1

Ensembl ID:

ENSDARG00000015638

ZFIN ID:

ZDB-GENE-030131-3756

Description:

survival of motor neuron protein-interacting protein 1 [Source:RefSeq peptide;Acc:NP_001017608]

Human Orthologue:

SIP1

Human Description:

survival of motor neuron protein interacting protein 1 [Source:HGNC Symbol;Acc:10884]

Mouse Orthologue:

Sip1

Mouse Description:

survival of motor neuron protein interacting protein 1 Gene [Source:MGI Symbol;Acc:MGI:1913853]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa13139	Essential Splice Site	Available for shipment	Available now
sa42885	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa42886	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa13139

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:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000013440	Essential Splice Site	185	253	7	10
ENSDART00000013440	Essential Splice Site	185	253	7	10

Genomic Location (Zv9):

Chromosome 17 (position 12957609)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	13083773
GRCz11	17	13094197

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TGAGTATTTRATTAATTGGTTTGAAGAGAGGGMCTTTGTTCCACAATTGG[T/C]AAGTGAAAAGTGTATTTCTGAGATGTATTTAATGATATGGKCACTCTAAA

Long Flanking Sequence:

GATCCCTAATCGTACCCTATAGCTAAACTCAATTACTACAATACTATTAATAAGCAGCTTATTAGTATTTTATTGTCTTAGTTAATCGTTTGCTAATAGCATTTATTAAAGATTCAAATAAAGTGTGAGCAGAAAAACTACATCTTCGATGACTTGAGTAAATTAACATCAAATTTTAATTTTGTGTGAACCGACCGGTTTAGTTGAATATATTTATTATCACATTATTTGAGCTATTTACAATTAATACATTTTTATGAATCCCTTTTATTAGACCGGTTTCCCACCTTTCCTGAGCATCGTCAGCAAACTAAGCCAGGTAACTTTCGATCGATAGCAGCTGTGGTTATTGTTCACATGTATCTGACATACATTCTGTTTAATATTCTGATAAATAATTAATTGTCATTTCATTACATTCTCTGTGCAGTCAACTGTGTCTGCTGTGCTTGAGTATTTGATTAATTGGTTTGAAGAGAGGGACTTTGTTCCACAATTGG[T/C]AAGTGAAAAGTGTATTTCTGAGATGTATTTAATGATATGGGCACTCTAAACGTTTGTGACAAATATATATGATAGTTTTGAAAGTTTCCCTGTTGTGTGTTTCCCCATATTACCTTACAAGTAGTTTATAAAGTACTGTAGCTGTTTGGGAATTTAAAAGGTCTGCAGTGTTTCAGAGATCTAAGAGGATAATAAATGGATGCTTTTTTCCCAAAAGAACACTCATTTATTTGACCATAGGTAATGCATGATGGCAGTCTTTGGTTGAAACAGCACAAAATGACTGTGTACACTCTTAAAACCCAACCATTGGGTTAAAAAGTGTAATTTAAGTGTAATTTAAATTCCATATTTGGCCCAATGTTGGGTTAAAACAACCCAGAATTATTTATAGTGTTTGGTTGTGGAAGCCACTGGAGATGGAGTTCACATGTCGTAATATTTATTGACATATATTTTATTTATTATTATATTTATTTTATTTTATTATAATTATTATA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa42885

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
ENSDART00000013440	Essential Splice Site	185	253	7	10
ENSDART00000013440	Essential Splice Site	185	253	7	10

Genomic Location (Zv9):

Chromosome 17 (position 12957609)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	13083773
GRCz11	17	13094197

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGAGTATTTGATTAATTGGTTTGAAGAGAGGGACTTTGTTCCACAATTGG[T/A]AAGTGAAAAGTGTATTTCTGAGATGTATTTAATGATATGGGCACTCTAAA

Long Flanking Sequence:

GATCCCTAATCGTACCCTATAGCTAAACTCAATTACTACAATACTATTAATAAGCAGCTTATTAGTATTTTATTGTCTTAGTTAATCGTTTGCTAATAGCATTTATTAAAGATTCAAATAAAGTGTGAGCAGAAAAACTACATCTTCGATGACTTGAGTAAATTAACATCAAATTTTAATTTTGTGTGAACCGACCGGTTTAGTTGAATATATTTATTATCACATTATTTGAGCTATTTACAATTAATACATTTTTATGAATCCCTTTTATTAGACCGGTTTCCCACCTTTCCTGAGCATCGTCAGCAAACTAAGCCAGGTAACTTTCGATCGATAGCAGCTGTGGTTATTGTTCACATGTATCTGACATACATTCTGTTTAATATTCTGATAAATAATTAATTGTCATTTCATTACATTCTCTGTGCAGTCAACTGTGTCTGCTGTGCTTGAGTATTTGATTAATTGGTTTGAAGAGAGGGACTTTGTTCCACAATTGG[T/A]AAGTGAAAAGTGTATTTCTGAGATGTATTTAATGATATGGGCACTCTAAACGTTTGTGACAAATATATATGATAGTTTTGAAAGTTTCCCTGTTGTGTGTTTCCCCATATTACCTTACAAGTAGTTTATAAAGTACTGTAGCTGTTTGGGAATTTAAAAGGTCTGCAGTGTTTCAGAGATCTAAGAGGATAATAAATGGATGCTTTTTTCCCAAAAGAACACTCATTTATTTGACCATAGGTAATGCATGATGGCAGTCTTTGGTTGAAACAGCACAAAATGACTGTGTACACTCTTAAAACCCAACCATTGGGTTAAAAAGTGTAATTTAAGTGTAATTTAAATTCCATATTTGGCCCAATGTTGGGTTAAAACAACCCAGAATTATTTATAGTGTTTGGTTGTGGAAGCCACTGGAGATGGAGTTCACATGTCGTAATATTTATTGACATATATTTTATTTATTATTATATTTATTTTATTTTATTATAATTATTATA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa42886

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:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000013440	Essential Splice Site	242	253	9	10

Genomic Location (Zv9):

Chromosome 17 (position 12960423)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	13086587
GRCz11	17	13097011

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GATGATGATCGTTTGTCAGCTCTTAACTTGATGATCTGTATTGTTGCCAG[G/A]TAACTGACACGGCGCTGTTTTGGCCAGATTTAGTGTTTCCTGAAATATGT

Long Flanking Sequence:

TTGTTTTCGATGGATTTAAAACTACTGTAGGAGGCCTCCAAAATATAATTGGACACATTTGAACTTTCAGCACTTCTAGATTGTTCAAGTACTATTATAACAACAATTTAAAGGTATTATTGAGCCATATTTTTCACTATGCATTGCTTAAACTTTAATCTTTATCTCCACAGGGCAGATGGTTATATGCATTACTAGCTTGCCTTGAGAAACCATTGCTTCCTGAAGCTCATTCCCTTATCAGGCAGTTGGCAAGACGGTGCTCAGCAGTCCGTGCCAATCTGGTAAACACTTATTTTACTCTGATCTGAATTAAAAGCTGAGGGTACCACTCAGATCGGGCCTCGCTTCGGCTGCAGCTTTAATACTGGAGCTTGTTTGCGAGAGCCTAAAATAGGTTGAATAGAACAGACAGAATATTTTATTTTCTTCCTCTTCTAGGAGAGCAAAGATGATGATCGTTTGTCAGCTCTTAACTTGATGATCTGTATTGTTGCCAG[G/A]TAACTGACACGGCGCTGTTTTGGCCAGATTTAGTGTTTCCTGAAATATGTGCAGATGGTTTTATGATGTATAATCACACGTCTCTCTGTTACAGGTATTTCGAGCAGAATGATTTGGCTGACAAAGAGTGAAGCAGGCCTTGGAAACAGATGGAAGAAAATTCGTAAGATTTTGTAAAATATAGATTATACAGTTACTTTGCCAATAGTTCAATGTAAAATAAAGTACGCCTGCCCTTTTGTAATGCAAATGATGTGTCATGTTAAACATTGGGATTGTCAAATAAAACTGGCTTCTTAGTATTGCACTGTCTTGTTTTTTGTGTGCTGTGAATGGCAATTAAACCGATTTATTAAAGGATTCACTAGAAATTTAATTTCTCTTTGCAAAGAAATGTCTATTGTTTTGTCCCTATTCGTTTGCTTATTAAAATAAAAGAAACACAATTTTCTCTTTAAAAAACAACAACTACGTGAGATGTTACTGTGTGGTTTTAATTA

Associated Phenotype:

Not determined