ZMP

sb:cb54

Ensembl ID:

ENSDARG00000016945

ZFIN ID:

ZDB-GENE-030131-9886

Description:

Sb:cb54 protein [Source:UniProtKB/TrEMBL;Acc:A4IG06]

Human Orthologues:

SIPA1, SIPA1L1, SIPA1L2, SIPA1L3

Human Descriptions:

signal-induced proliferation-associated 1 [Source:HGNC Symbol;Acc:10885]
signal-induced proliferation-associated 1 like 1 [Source:HGNC Symbol;Acc:20284]
signal-induced proliferation-associated 1 like 2 [Source:HGNC Symbol;Acc:23800]
signal-induced proliferation-associated 1 like 3 [Source:HGNC Symbol;Acc:23801]

Mouse Orthologues:

Sipa1, Sipa1l1, Sipa1l2, Sipa1l3

Mouse Descriptions:

signal-induced proliferation associated gene 1 Gene [Source:MGI Symbol;Acc:MGI:107576]
signal-induced proliferation-associated 1 like 1 Gene [Source:MGI Symbol;Acc:MGI:2443679]
signal-induced proliferation-associated 1 like 2 Gene [Source:MGI Symbol;Acc:MGI:2676970]
signal-induced proliferation-associated 1 like 3 Gene [Source:MGI Symbol;Acc:MGI:1921456]

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa42303	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa42303

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
ENSDART00000003390	Essential Splice Site	123	281	3	6

Genomic Location (Zv9):

Chromosome 13 (position 49855474)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	48627711
GRCz11	13	48987800

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGTGATGTGTGCAGCCGCTCATCCTTCTGTCTCTCTCTCTCTGTCTCTTC[A/T]GATGAGTTCTGGTTCTCTGACGGCTCTCTCGCCGACCGGGCCAAGTTCAG

Long Flanking Sequence:

TATTTTCAGTAAATATAAAACATCAAATACATTTATTAAACAATGTTTTTAAAAAGGTTTCTTTTATTGTAAATGCACCTTTTCCATTCACAATAAAGAATAAAAAATACTTCAACATAAATGAAAAGATCTATGTTTTTGCTAAACATTTTACAACACTTTCCACAGAAACGCATTCTCCCATCTACAATATAAAACTTTGTTTTGCCAATTTTCACATAAAACCTTTGTAATCATGTAAAAGTTAATTTAATTTACTTAATTTCAAAATAGCAATAGAATTATGCAAAAGTATTGTAATGAAGTAGGGCCACTGGTTATGTGTGGGATGTTTTCTGATCTTGTGTTTGAAAAAGCACTAGCTGTTTATTCCTCGTGCTGTTTCTCTTCAGGGTGGTCATTATCGTGACCTTTTGGCCTCCTGGAAGCGTCTTTCCTCAGAGTGCTCACAGTGATGTGTGCAGCCGCTCATCCTTCTGTCTCTCTCTCTCTGTCTCTTC[A/T]GATGAGTTCTGGTTCTCTGACGGCTCTCTCGCCGACCGGGCCAAGTTCAGTGACCCGGGCCTCATGCCTCTGCCAGACACGGCCAGCGGACTCGACTGGTCACACCTCGTGGATGCAGCCAGAGCCTTCGAAGGTACAGCAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATATGTCAGAGATGATTCACAATGCTTTTTGAGCCACAAAATACACTCTTCTTCTATACTGACTACTCAGTTTATGTTTTCTGTATTTGAAGTGCACTATAGGGCAGCACTTCGAACAGAGTAGTCCTGGCCCACAAGGGGGCCTCAGCGAGCTCTGTGGGGGGTTGCATCATATTTTAAAACATTTTTAGCAGTGGACAATTAGGAGAACAATCATCTTGCCTGAGTTTTTCCCCTGGCCTCCACATAAAAGACAGAGAGCTCTATTTTGACAATCTAGGCGCAAAGTCTAAAGCG

Associated Phenotype:

Not determined