ZMP

serpinb1l2

Ensembl ID:

ENSDARG00000070396

ZFIN ID:

ZDB-GENE-041001-117

Description:

serpin peptidase inhibitor, clade B, member 1, like 2 [Source:RefSeq peptide;Acc:NP_001038636]

Human Orthologue:

SERPINB1

Human Description:

serpin peptidase inhibitor, clade B (ovalbumin), member 1 [Source:HGNC Symbol;Acc:3311]

Mouse Orthologues:

Serpinb1a, Serpinb1b, Serpinb1c

Mouse Descriptions:

serine (or cysteine) peptidase inhibitor, clade B, member 1a Gene [Source:MGI Symbol;Acc:MGI:1913472
serine (or cysteine) peptidase inhibitor, clade B, member 1b Gene [Source:MGI Symbol;Acc:MGI:2445361
serine (or cysteine) peptidase inhibitor, clade B, member 1c Gene [Source:MGI Symbol;Acc:MGI:2445363

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa16540	Splice Site, Nonsense	Available for shipment	Available now
sa43453	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa16540

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:

Splice Site, Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000077787	Splice Site, Nonsense	189	382	4	6

Genomic Location (Zv9):

Chromosome 20 (position 26948007)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	20	27019310
GRCz11	20	26918400

KASP Assay ID:

2261-4398.1 (used for ordering genotyping assays)

KASP Sequence:

TGCACACATTTKATRCACATGCGACTAAAGAAATGCCATTTAAAATAAAC[C/T]AGGTGTGACCCACANTTTTTTTTATTAGTGTGTTGAATTATTTWAWACTAT

Long Flanking Sequence:

TAATGCTCTCTCTCTCTCTCTCTGTGGTTTAAGTAGTCTTTATTTTGTCCGGCAGATGTATGTGGACTCCACTATGAAGCTTTATCACGCTGAACCTCAGACTGTGGACTTCATTAGAGCAGCAGATGACTCTCGCCAGTTCATTAACAAATGGGTGGAAAAGCAGACAGAGAGTGAGAAGATACAATTACACCTACGATAAAGTAAAATTATGTATGGTTCTTGGAAAAATCAGATTAAGCTTTATTGACACATGTGTGATAAAGGAATCATTTTAGTTTTCTCTTTATAACTTGTTAAAGAATGCTAAAAGGTCTAAAGTGTATAATTTAGTGGTGTTTTTGCTGTTTTTGTTTTTAGATCAAATTAAAGATCTTCTTCAGCCTGGTGTGGTAAATGAGATGACCAGACTACTTCTAGTTAATGCCATCTACTTCAAAGGGAACTGGATGCACACATTTGATGCACATGCGACTAAAGAAATGCCATTTAAAATAAAC[C/T]AGGTGTGACCCACATTTTTTTTATTAGTGTGTTGAATTATTTAAAACTATTTTTATTTTTAAACTTTATGCATTTCTTCACTTGTCTTCAATCAGAATGAGAGTCGGCCTGTGCAAATGATGGATCAGGTGGAAAATTTTCCCTACAGATGCATCCCAGAGTATAAACTGCAGGTGCTGGAGTTGCCATATACACAGCAGGAGCTCAGCATGTTGATCCTTCTTCCAGATGAAATCAAGTATGGATCTGATCCTCTTCTCAAGGTCAGCAAAGTGTTGTGAGCAGACAAAAGATGGATAGTTTTAATCCTGTGTGTGTTATTAACGTGTGTGTGCGTCTAACAGCTGGAGAGCGAGTTGAACCTCCAAAAGCTGCTTGACTGGACCAGTAGAGGCAAAATGGACACATGGAGAAAGATCATTGTCCGTCTGCCAAAGTTCAAGTTGGAGATTGAGAGCTGTCTATCAGAAACACTGGAAAAGATGGGCATGAGCTCTGTG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa43453

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
ENSDART00000077787	Nonsense	377	382	6	6

Genomic Location (Zv9):

Chromosome 20 (position 26948745)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	20	27020048
GRCz11	20	26919138

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TCATGTTCTTCATCAGACACAACCCCACTAACAGCATCCTTTTTCTGGGC[A/T]GATTCAGAGCCCCATCCTAGCTATGTAGTTCTTTTTCTTTGTTATATCAA

Long Flanking Sequence:

AGTATGGATCTGATCCTCTTCTCAAGGTCAGCAAAGTGTTGTGAGCAGACAAAAGATGGATAGTTTTAATCCTGTGTGTGTTATTAACGTGTGTGTGCGTCTAACAGCTGGAGAGCGAGTTGAACCTCCAAAAGCTGCTTGACTGGACCAGTAGAGGCAAAATGGACACATGGAGAAAGATCATTGTCCGTCTGCCAAAGTTCAAGTTGGAGATTGAGAGCTGTCTATCAGAAACACTGGAAAAGATGGGCATGAGCTCTGTGTTCCAGGAAACCAAGGCTGATCTGACAGGCATGAGCAGTAATGGTGGTCTCTTTCTTTCAGCAGTGATTCACAAGGCTTTTGTTGAGGTCAATGAGGAAGGAACTGAAGCAGCAGCAGCAACTGCATTGTTATTACCAATCAGTGCTTGTCAAGGTGCATTTCATGATTTCATAGCCGATCATCCCTTCATGTTCTTCATCAGACACAACCCCACTAACAGCATCCTTTTTCTGGGC[A/T]GATTCAGAGCCCCATCCTAGCTATGTAGTTCTTTTTCTTTGTTATATCAAAAGAAATATAATTCACATATTATTTAATAAGCTTTTCTCAATCTTAATCATGGAAAAATGCGTTGCATGTCTTCTGGTTTTACAAACTTACTATTTTAATGAGGTTATTTAGTTATGGGACATCTAAAATTACACCTTTATCTACACAAAGAGTCTTGAGAGTTTTATTTATCAGATGTCATTTCCAGCTCACAGTGTTAAAGTAATGCTAAATTCAGTGGCATGGAGATGGAGAAAGGTCAAGATGATTACAAGGGCCCGGAATAGTACTAAAAAGTAGTTTTATTTCCATTCTCAAAGATTGTAACCACATTTAACTTCTACCACATTTAAAATAAATATAAAATTGTAACATGTAAAATGTAAGCCACTCCTTTGCATAAAATAGAAAACACGTGCCACATTTTCAGATGTTTTAATTGATCTTATAAAATATGATACCTTAACCTA

Associated Phenotype:

Not determined