ZMP

sc:d812

Ensembl ID:

ENSDARG00000017217

ZFIN ID:

ZDB-GENE-080303-21

Description:

cDNA, clone cssl:d0812 [Source:UniProtKB/TrEMBL;Acc:A4JYF4]

Human Orthologues:

C1orf204, IGSF11

Human Descriptions:

chromosome 1 open reading frame 204 [Source:HGNC Symbol;Acc:27647]
immunoglobulin superfamily, member 11 [Source:HGNC Symbol;Acc:16669]

Mouse Orthologue:

Igsf11

Mouse Description:

immunoglobulin superfamily, member 11 Gene [Source:MGI Symbol;Acc:MGI:2388477]

Alleles

There are 4 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa1863	Essential Splice Site	F2 line generated	Not yet available
sa42630	Nonsense	Mutation detected in F1 DNA	Not yet available
sa19127	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa1863

Status:

F2 line generated
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
ENSDART00000099202	Essential Splice Site	21	442	2	7

Genomic Location (Zv9):

Chromosome 15 (position 45907556)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	15	46329579
GRCz11	15	46564096

KASP Assay ID:

554-1854.1 (used for ordering genotyping assays)

KASP Sequence:

TTTTTCCATGCATTTATTTGACTATGTGWATATGTGTGTGTTTTCTCTGC[A/T]GTGTGTGTGTATGCGCTAGAAGTGACGGTCAGTCAGAGCAGTGTCCAGGT

Long Flanking Sequence:

TCTAGCCAAAATAAAACAAATAAGACCTTCTCCAGACGAAAAAATTTTATCAGACATACTGTGAACATTTCTTTGCTCTGTTAAACATTATTTTGGAAATATTTAAAGAAGAAAAAAAAATCAAAAGGGGGCGAATAATTCTGACTTCAACTGTATATATATATATATATATATATATATATATATATACAGTTGAAGTCAGAATTATTAGCCCCTTTTGATTTTTTTTCTTTAAAAAATACATATATATATATATATATATATATATTTTTTTTTTTTAAATGCTGAAAATTTGGACAAAACATGTGAAATCTCTCCACAAAATCACTCCATTTAATTACAAAAATCTGATTTTTTTTTCCCCAGAAATCCTGTAGGGACTGATATTGCATTGAATATGCTAAATGCAATTGTGTGTGTATTCTAGCCTGTTGCCATTGTGTGGACTGTTTTTTCCATGCATTTATTTGACTATGTGTATATGTGTGTGTTTTCTCTGC[A/T]GTGTGTGTGTATGCGCTAGAAGTGACGGTCAGTCAGAGCAGTGTCCAGGTGGCCAGAGGTCAGGCGGCCGTCTTGCCCTGTACTTTCAGCACCAGCGCCGCTCTCAATAATCTCTACATCATATGGATGGTCACACCGCTAGCCAACGCCAACCAGCCGGAGCAGGTGAGAAAACACAGCACCACACACACACTGACAGTGTATAAAACACACTCTTCATTGCCCTCACTGTAACGTCTGACTCTGCTCAGAATAAAGTCTCATCACTGAACAGAAATAATGTCCAGTCTAGAATATAAAGTCCTGCTGCAGTGGAGACAGAATGAATATTGTGTCTGACTCCATCATGAGCTTGGAGGACTGCATCCATACATCTCTGACATGACTCAAATCACTGATTAATAAAGTCATCTGGAATGAAGAAGAAAGCGTTCAGCAGGATCCCAGAGTTCATCAAGACTCTTTGTGTTCATCTTCAACACCTCCTCCATCTTACCCCA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa42630

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:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000099202	Nonsense	24	442	2	7

Genomic Location (Zv9):

Chromosome 15 (position 45907568)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	15	46329591
GRCz11	15	46564108

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTTATTTGACTATGTGTATATGTGTGTGTTTTCTCTGCAGTGTGTGTGTA[T/A]GCGCTAGAAGTGACGGTCAGTCAGAGCAGTGTCCAGGTGGCCAGAGGTCA

Long Flanking Sequence:

AAAACAAATAAGACCTTCTCCAGACGAAAAAATTTTATCAGACATACTGTGAACATTTCTTTGCTCTGTTAAACATTATTTTGGAAATATTTAAAGAAGAAAAAAAAATCAAAAGGGGGCGAATAATTCTGACTTCAACTGTATATATATATATATATATATATATATATATATATACAGTTGAAGTCAGAATTATTAGCCCCTTTTGATTTTTTTTCTTTAAAAAATACATATATATATATATATATATATATATTTTTTTTTTTTAAATGCTGAAAATTTGGACAAAACATGTGAAATCTCTCCACAAAATCACTCCATTTAATTACAAAAATCTGATTTTTTTTTCCCCAGAAATCCTGTAGGGACTGATATTGCATTGAATATGCTAAATGCAATTGTGTGTGTATTCTAGCCTGTTGCCATTGTGTGGACTGTTTTTTCCATGCATTTATTTGACTATGTGTATATGTGTGTGTTTTCTCTGCAGTGTGTGTGTA[T/A]GCGCTAGAAGTGACGGTCAGTCAGAGCAGTGTCCAGGTGGCCAGAGGTCAGGCGGCCGTCTTGCCCTGTACTTTCAGCACCAGCGCCGCTCTCAATAATCTCTACATCATATGGATGGTCACACCGCTAGCCAACGCCAACCAGCCGGAGCAGGTGAGAAAACACAGCACCACACACACACTGACAGTGTATAAAACACACTCTTCATTGCCCTCACTGTAACGTCTGACTCTGCTCAGAATAAAGTCTCATCACTGAACAGAAATAATGTCCAGTCTAGAATATAAAGTCCTGCTGCAGTGGAGACAGAATGAATATTGTGTCTGACTCCATCATGAGCTTGGAGGACTGCATCCATACATCTCTGACATGACTCAAATCACTGATTAATAAAGTCATCTGGAATGAAGAAGAAAGCGTTCAGCAGGATCCCAGAGTTCATCAAGACTCTTTGTGTTCATCTTCAACACCTCCTCCATCTTACCCCAGACACACTCAAT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa19127

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 > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000099202	Essential Splice Site	76	442	3	7

Genomic Location (Zv9):

Chromosome 15 (position 45926875)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	15	46348808
GRCz11	15	46583025

KASP Assay ID:

2260-9038.1 (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTC[A/G]GGTGATCATCTACCAGAGTGGTCAGGTATTCAGTTTAGCCAATCACATGA

Long Flanking Sequence:

TAATGTGGCAGATCACAGGGGGTTTTAGTGAGGATCAAAGTGCTGTAAAATGCTTTATTCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGCGCTGGACATGCTAACACTCACAGCAGAATGTGCTGCATATTTAAACTCTTCAATAATTGATCATTTCAGGCACATTTACACCTTTCAGCTAAACACTCCAAACCTCTGCGTCTGACCGCTCTGACCGTCACTGAGGTGATCTAGAGCTCCACAGGGCCAGATGTCGAAAGTTTTGCTGTTTTTGTCTCTCTCTCTCTATGTGTGTGTGTGTGTTTAGTTTTGAGCTAATTAGATATCTCTGAAATGCCTAATGTCTGTTTGTTGTTGTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTC[A/G]GGTGATCATCTACCAGAGTGGTCAGGTATTCAGTTTAGCCAATCACATGAATGGGCGTGTGGGTTTCGTGTCCACCATGCCCAGCACAAGTGCCTCCATCTTCATCAATAACACTCAGCTGTCGGACACCGGGACGTACCAGTGCCTGGTCAACAACCTGCCGGACCGCGGAGGACGCAATATAGGAGTGATCGGCCTGACGGTGCTCGGTGAGTGACTTCACTCTGCTCTATGACTGCTCCATGTGCTGTATCTGCTTCAGACAGTGCCTGTTATTTGGGACGAAACACAGTAAACACTTGCACAATATGTTTGCTCGTACAGTACTGTGCTGCAAAAGTTTAGGCCAGCATTGAATCTGCTGTTTTACTGTTGGTATAATGGATATTAGTGGCCCTTTACCACAAAACCACTCATAAGTCTACAATTTATTTGTCTTTTTAAAATTTTTTATTAAGATTTCAGGGTGAATACACTCTAATTTAATGATCTAGGCGCAA

Associated Phenotype:

Not determined