ZMP

ssrp1b

Ensembl ID:

ENSDARG00000016994

ZFIN ID:

ZDB-GENE-041008-209

Description:

Structure specific recognition protein 1b [Source:UniProtKB/TrEMBL;Acc:B8A5B7]

Human Orthologue:

SSRP1

Human Description:

structure specific recognition protein 1 [Source:HGNC Symbol;Acc:11327]

Mouse Orthologue:

Ssrp1

Mouse Description:

structure specific recognition protein 1 Gene [Source:MGI Symbol;Acc:MGI:107912]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa14765	Nonsense	Available for shipment	Available now
sa39668	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa14765

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000003895	Nonsense	93	531	4	14
ENSDART00000100268	Nonsense	93	543	4	16
ENSDART00000131296	Nonsense	93	681	4	17
ENSDART00000142187	Nonsense	93	533	4	15

Genomic Location (Zv9):

Chromosome 1 (position 45167385)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	1	44010604
GRCz11	1	44711907

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CTTTTTGCGCAGGACCTTGAGAAGATCTCAGAATACTTCAAAGACAACTA[C/A]AAAGTGGAGCTRACAGAGAAAGACATGTGTGTTAAGGGCTGGAATTGGGG

Long Flanking Sequence:

AGCTTTTAAACGTCACAGGTCCATTCTGTCTACTCTGACATGAGTGACACTTTGGAGTTCAATGAAATTTATCAGGAGGTCAAGGGCTCATGGGTGAGTTAAAAAAGGTTTTGTTCTCTAACTTGAGGTGTTTTTCTATCAAACTCTCAATAAAGTTGACCGACTGTCTTTTCTTGTAGAATGACGGCCGCCTGCGCTTCAGTAAGCAGACAGTGGTGTATAAAAACAGTAAGACCGGGAAGGTGGACACTATTCCGGTCCCTGAACTCACTCAGGCCCAGTGGAGGAGAGTCTGTCTGGGTCACGGCATCAAACTATGGACCAGCACTGGCCACATCTACAAATATGATGGCTTTAAAGACGCAGTGAGTCTGAGATGCAAATTACAGATCAATTGATCACTCAGTTTGATCCGCTGTTTCATTCCAGGTCTTAAATTTTCATCCGTTTCTTTTTGCGCAGGACCTTGAGAAGATCTCAGAATACTTCAAAGACAACTA[C/A]AAAGTGGAGCTAACAGAGAAAGACATGTGTGTTAAGGGCTGGAATTGGGGCACTGCTAAATTTAATGGTCAGTGCATTCCTGTTGCAACGCTTTTTGTCTGAGATATTCAGTTAAAGTCAGAATTATTAGCCATTCTGAATTATTAGCCCCCCTGTTTATTTTTTCCCCCAATTTCTGTTTAACAGAGAGATTTTCTCAACACATTTCTAAACATAATAGTTTTAATAACTCATTTCTAATAACTGATTTATTTTATCTTTACCATGATGCCAGTAAATAATATTTAACTAGATATTTGTAAGACACTTCTATACAGCTTAAAGTGACATTTAAAGGCTTAACTAGGTCAATTAGGTTAACTAGGCAGGTTAGGGTAATTAGGCAAGTTATTGTATAGTGATGGTTTGTTCTGTAGACCATCGGACACAAATAGCTTAAAGGGGCTAATAACTTTGTCTTTGAAGTGTTTTTAAAAAATGTAAAACTGCTTTTCTTCTAG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa39668

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
ENSDART00000003895	Essential Splice Site	409	531	10	14
ENSDART00000100268	Essential Splice Site	409	543	10	16
ENSDART00000131296	Essential Splice Site	409	681	10	17
ENSDART00000142187	Essential Splice Site	409	533	10	15

Genomic Location (Zv9):

Chromosome 1 (position 45179571)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	1	44022790
GRCz11	1	44724093

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGATCGAGACCAAGCAAGGCAATCAGTACACCTTCAGCAGCATCGAGAGG[T/C]ACCCAGAACCCCCGATGATACTCTTGTCTGGCTGTCGGGAACATCACTTT

Long Flanking Sequence:

CAACAGGAAGATCACAGTGCCTGGAAATTTCCAAGGGTAAAACGCATATTTACACTGTAGAAAACGATACAGTAAAACACTGAAAACACTCAATGACATTTGCATTCAACACTGACATATATATACATACATATATATATATATATATATATATATATATATATATATATATATATATATATATAGTGTTTGCATTCATACTGAACAATTACTTGATAATGTGGTAATTTATTGTAATAAAAGTGTCTAATTTCCTGTCTCTCTCTGTTCTCTGTAGTCACTCAGGAGCTCAGTGTATAACCTGCTCCTATAAGGCCAGTTCAGGGCTGCTGTATCCCCTGGAAAGAGGTTTCATCTACGTGCACAAGCCCCCAGTGCACCTGCGTTTTGAGGAGATCGCCTGTGTGAACTTCGCCCGCGGGACCACCACGACCCGCTCCTTCGATTTCGAGATCGAGACCAAGCAAGGCAATCAGTACACCTTCAGCAGCATCGAGAGG[T/C]ACCCAGAACCCCCGATGATACTCTTGTCTGGCTGTCGGGAACATCACTTTGAAGGGAACTAGATCACAGCAGTAATGAAAAGAGCATTGTTCATACCCTTTTCCAGGCACTTCCAGCTATTATGTCATTGAGCACTTAACCCCCATCTGCCATTGAAAATCAATGCCTGCTCTTTGTGGTCATTCTCTCTGTTTTTGTCTTAACACTGGTGTAAAAGAGCCCCTCTCTTTTAGTGACCTGACCCCCATCTGCACGTTGAGGGGGCAAAAACTAAGCTGCTTTATGGACATTATTGTATTTTCTGTTGGGTGCACATTATGACTGAATCAATACAGCAAGGCATCAGTTAATCACATCACACTAATGTGCCAGAAACAATGTGTCCGGAAAACTTTTAAGGGACCGTTCACACAGAAGACGTTTTTTATATTCCAGTGTGCAACTTTTCCATTGTCTTTCTATGTAATATGTGCTTGATGTGTACATAGACTTTAAGACGC

Associated Phenotype:

Not determined