early conceptus |
embryo ectoderm |
embryo endoderm |
embryo mesoderm |
embryo mesenchyme |
extraembryonic component |
alimentary system |
auditory system |
branchial arches |
cardiovascular system |
connective tissue |
endocrine system |
exocrine system |
hemolymphoid system |
integumental system |
limbs |
liver and biliary system |
musculoskeletal system |
nervous system |
olfactory system |
reproductive system |
respiratory system |
urinary system |
visual system |
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Transcription Start Site | Location | Distance from Gene 5'-end |
Tssr10084 | Chr1:171594463-171594481 (+) | -228 bp |
Tssr10085 | Chr1:171594493-171594509 (+) | -199 bp |
Tssr10086 | Chr1:171594691-171594706 (+) | -1 bp |
Tssr10087 | Chr1:171594712-171594738 (+) | 25 bp |
Tssr10088 | Chr1:171602727-171602730 (+) | 8,029 bp |
Tssr10089 | Chr1:171602932-171602940 (+) | 8,236 bp |
Tssr10090 | Chr1:171604744-171604755 (+) | 10,050 bp |
Tssr10091 | Chr1:171606166-171606207 (+) | 11,487 bp |
Tssr10092 | Chr1:171615547-171615553 (+) | 20,850 bp |
Tssr10093 | Chr1:171627183-171627195 (+) | 32,489 bp |
Tssr10094 | Chr1:171628024-171628035 (+) | 33,330 bp |
QTL | Genetic Location* | Genome Location (GRCm39) | Reference | QTL Note |
Nktcn1 | Chr1, 76.25 cM | Chr1:168186243-171632257 | J:137521 | Microarray analysis was performed on thymus RNA from 4 week old NOD.Nkrp1.Nkt1 congenic animals and NOD.Nkrp1 congenic animals to screen candidate genes for Nktcn1. The NOD.Nkrp1 congenic carries C57BL/6J-derived DNA from D6Mit105 (45.5 cM) toD6Mit135 (62.3 cM) on a NOD genetic background. The NOD.Nkrp.Nkt1 congenic carries C57BL/6J-derived DNA from D1Mit369 (73 cM) to D1Mit155 (telomere) on a NOD genetic background in addition to the NOD-derived chromosome 6 interval. The formal QTL designation for Nkt1 is Nktcn1. Nkrp1 is synonymous with Klrb1c. Previously identified lupus susceptibility locus Sle1b (89.5 cM) maps near Nktcn1. Twenty-one genes displaying expression differences between NOD and C57BL/6J mapped to the Nktcn1 region, 15of which are located in the 95% confidence interval. The most promising candidate genes for controlling NKT cell number are Slamf1 (93.3 cM) and Slamf6 (89.5 cM). Gene expression of Slamf1 and Slamf6 was examined in thymic and splenic lymphocytes from congenic animals. It was observed that NOD.Nkrp.Nkt1 animals expressed significantly higher amounts of SLAM proteins on cell sufaces compared to NOD.Nkt1 parentals. Authors hypothesize control of NKT cell numbers may be mediated by differentialexpression of Slamf1 with additionial influence by Slamf6. |
Sle1b | Chr1, 75.10 cM | J:94686 | Congenic and physical mapping was used to show that Sle1b mapped within an interval containing SLAM family members ordered as Cd244 - Ly9 - Slamf7 - Cd48 - Slamf1 - Cd84 - Slamf6. Haplotype analysis of the aformentioned region were suggestive that the markers contained within the region as contributing to the Sle1b phenotype. The strongest contribution may come from Slamf6. |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 12/10/2024 MGI 6.24 |
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