ZMP

tmprss13a

Ensembl ID:

ENSDARG00000057040

ZFIN ID:

ZDB-GENE-090309-3

Description:

transmembrane protease, serine 13a [Source:RefSeq peptide;Acc:NP_001152984]

Human Orthologue:

TMPRSS13

Human Description:

transmembrane protease, serine 13 [Source:HGNC Symbol;Acc:29808]

Mouse Orthologue:

Tmprss13

Mouse Description:

transmembrane protease, serine 13 Gene [Source:MGI Symbol;Acc:MGI:2682935]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa18225	Nonsense	Available for shipment	Available now
sa42499	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa18225

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
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Mutation:

C > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000101332	Nonsense	257	506	7	13
ENSDART00000128387	Nonsense	257	506	7	13

Genomic Location (Zv9):

Chromosome 15 (position 13118136)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	15	12412681
GRCz11	15	12344098

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

YATTTGTTCAGCTCGGGTTGTTTGGAYGAYAAAKCGGTCTCACTTCAGTG[C/A]TCCGGTRAGAATTAAACTTCAYTCACTWAYTACTGTGAYGCATTGTTGAA

Long Flanking Sequence:

GTACTACGGTAATTAACCTAATTAAGCCTTAAAAATAGACTTTAAGCTGAATACTGGTGTCTTAAAAAAAGCAAATAGTAAAATATTATTTACTGCCATCATTCAAATATAAAACTAATCAGTAATTAGAAATTAGTTTTTAAAACAAATATGTTTTGAAATGAGGTGAAAAAAATATATTTCCATTACACAGGAATAGGGGGAAAAATAAACAGGGGGCTAATAATTCAATTGGGCTAATAATTCTGACTTCAACTGTAACTTGATTTTTTTCCTCAGGTCTTATGAATCAAGTGCACTGAATAGCAAGAGCTCCGAAGCCCTTATTTTAGAACCAACATCAGGCTTACTTATACAGGGACTGGCCAATGTCAGGTAAGAGAAGATTGTAGAAAGAGTGTTAAATATTTTGCTTTGTCTGTGGCTTCATCAACCGTACATAATATCTTTCATTTGTTCAGCTCGGGTTGTTTGGACGACAAATCGGTCTCACTTCAGTG[C/A]TCCGGTAAGAATTAAACTTCACTCACTAATTACTGTGATGCATTGTTGAATGAGGCATCACAGTAAACATGCCATTCTTATTTCCTCCATTTGTAAGTTAGTGAGGGACATATTGTGTGGATAAGTGAAATAATGACCTGTTTTTTTTTTTCTTTTCTTTGTTTACTCTTCCAGCTTTATTTAGTGCATAACGTAGTTATTGTTAGAATATATGGTTCAAATACTGTAACTGTAGTCTTGAGTTTTCTCCCAGGAATGTGCACATCAAATATATTTCATTCAAAAAATTACTTCTTTGTTTTGTCATAGTTTCACGTCCCACTTTATATAGTTACCTCAATTACATTGTACTTACATTTAAGTTAATCATTTGGTACGAGGCACTTATTATGTATATGCATCCCAGCAAACATTTATGTGTTTAAAAGACATCTAATAGACATCAAACATAGACAGCTCGGGTAAAACAAAGCTAAACTTGGGCTGGTAATGAAAATTTA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa42499

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000101332	Nonsense	446	506	11	13
ENSDART00000128387	Nonsense	446	506	11	13

Genomic Location (Zv9):

Chromosome 15 (position 13130981)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	15	12399836
GRCz11	15	12331253

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTGGCCTCATCACCAATAATATGATCTGTGCTGGAGATCTGAAGGGAGGA[C/T]GAGACTCCTGTCAGGTGGGTTTATTCAGCCAGACACTGTCCCAATAATAC

Long Flanking Sequence:

TTTATTTATGTATTTATGTATTTATTTATTTATATTAGCAGTCTATATTCGGGACAAAAATCAGTCTAGACCAGGGGTACTCAATCCTGTTCCTAGAGATCTACCTTCCTGCAGATTTCAGTTGCTACCCATATCAAACACACCTGAACCAATTAATTAGGACCTGAACACCACTTGATAATTACAGGCAGGTGTGTTTGATATGAGTAGCAACTGAAATCTGCAGCAAGGTAGATCTCCAGGAACAGGATTGAGCACCCCTGGTCTAGACACATTGAAATCTAATGATTTGAGCTTAGAAGTCTGTCCAAATCACAATATTCAATTAATATAATATTGTTCTAAATTCTGCTTTTTTTCCTTGTCTGGTAGATCGTGCCTCGAGCAGCCTCATGAGTGTGAGTGTGAACATCATAGACTCCAGTGTGTGCAACAGCTGTCAGATTTATTGTGGCCTCATCACCAATAATATGATCTGTGCTGGAGATCTGAAGGGAGGA[C/T]GAGACTCCTGTCAGGTGGGTTTATTCAGCCAGACACTGTCCCAATAATACTAGACCTGATGTAAATACATTATTTACTGGCTAAAACTGGTCCAGTGTATCTCTGTATTATGTCACTGATTTATTCGAGTGTTTGGTTCAAGCTGATGCAACTATGTTTTGTTCAACCAAGTATCTACATCCATTATAACCTTTGCATTAAGAAGAACTTTTGAAAGTATGGGTAAATCAGAATTTTTTTACATGTTCCAATTTAGTGACCACACTGTGTAAAATTGGTGTAAAAAGTACTAAATAAATAATTGAAGTAAAAAAATTATGTCTCAAAACAGTATTAATTAAACAGCATTAATCTTCCTAGAAACTTTATTTTATTAGAACAATTATACAATGTTATCATAAAAAGTCATGAAGATTTATTGTTCTAGTAAAAAAAAAAGATGATTGGCATCATAATTTACTACTTTTCATTGTATTTATTAATAAATTGTGTTATTTAGA

Associated Phenotype:

Not determined